GENR
{
RETE|ID 1 FBgn0025724	CLA 1 Gene	NAM 1 &bgr;'-coatomer protein	GSYM 1 &bgr;'Cop	DT 1 25 Dec 04	RESZ 3956	PDOM 2 INTERPRO:IPR001680 == WD-40 repeat	PTD 1	DBA 15	FNC 7 ER to Golgi transport	CEL 1 COPI vesicle coat	CLOC 1 34B9	ALESR 1	REF 8	
GSYM|&bgr;'Cop
PTD
DT|25 Dec 04
ID|FBgn0025724
UAB|Duplication: Dp(2;2)GYL (inferred from cytology)
SYN|CG6699
|CG6699
|beta'-COP
|d&bgr;'COP
|beta'Cop
NAM|&bgr;'-coatomer protein
CLOC|34B9
|Limits computationally determined from genome sequence between @P{lacW}l(2)k00302<up>k00302</up>@ and @P{PZ}kuz<up>03782</up>@&@P{lacW}kuz<up>k14817</up>@
CYC|Experimentally determined: 34B5--9
FNC|ER to Golgi transport ; GO:0006888
|Golgi vesicle budding ; GO:0048194
|cell surface receptor linked signal transduction ; GO:0007166
|endocytosis ; GO:0006897
|exocytosis ; GO:0006887
|intracellular protein transport ; GO:0006886
|retrograde transport, Golgi to ER ; GO:0006890
CEL|COPI vesicle coat ; GO:0030126
PDOM|IPR001680 == WD-40 repeat
|IPR006692 == Coatomer WD associated region
ENZ|protein transporter activity ; GO:0008565
|protein transporter activity ; GO:0008565 | inferred from electronic annotation
DBA|NA:AA264134
|BDGP:LD07733
|NA:AE003639
|PA:AAF53294
|NA:AI293311
|BDGP-DGC:GH16479
|NA:AJ006523
|PA:CAA07084
|NA:AJ006524
|PA:CAA07085
|NA:AW940627
|BDGP-DGC:GH16479
|NA:AY119527
|PA:AAM50181
|BDGP-DGC:GH16479
PAC|UniProt_Swiss_Prot:O62621
ASQ|FBan0006699
REF
{
REFM|FBrf0126702
|Zheng
|1999.11
|9
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|FBrf0106031
|Merdes
|1998.12.20
|9
REFM|FBrf0131779
|Swiss-Prot Project Members
|2000.10.1
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0126671
|Guan
|1999.11
|9
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
}

REFDSR
{
RDID|FBrf0106031
|Merdes
|1998.12.20
CLOC|34B5--9 (determined by in situ hybridization)
}

REFDSR
{
RDID|FBrf0118011
|Merdes
|1998.6.2
FNC|ER to Golgi transport ; GO:0006888 | non-traceable author statement
|Golgi vesicle budding ; GO:0048194 | non-traceable author statement
|retrograde transport, Golgi to ER ; GO:0006890 | non-traceable author statement
CEL|COPI vesicle coat ; GO:0030126 | non-traceable author statement
SYN|beta'-COP
}

REFDSR
{
RDID|FBrf0118012
|Merdes
|1998.6.2
FNC|retrograde transport, Golgi to ER ; GO:0006890 | non-traceable author statement
CEL|COPI vesicle coat ; GO:0030126 | non-traceable author statement
GPD|coatomer, &bgr;'-subunit
SYN|beta'-COP
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: GH16479 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0126671
|Guan
|1999.11
AM|Source for identity of: &bgr;'Cop CG6699
}

REFDSR
{
RDID|FBrf0131779
|Swiss-Prot Project Members
|2000.10.1
FNC|retrograde transport, Golgi to ER ; GO:0006890 | non-traceable author statement
CEL|COPI vesicle coat ; GO:0030126 | non-traceable author statement
}

REFDSR
{
RDID|FBrf0146969
|Dunne et al.
|2002
MD|Identified with: LD07733
SYN|CG6699
|d&bgr;'COP
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
FNC|cell surface receptor linked signal transduction ; GO:0007166 | inferred from electronic annotation
|endocytosis ; GO:0006897 | inferred from electronic annotation
|exocytosis ; GO:0006887 | inferred from electronic annotation
|intracellular protein transport ; GO:0006886 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
SYN|beta'Cop
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|protein transporter activity ; GO:0008565 | inferred from electronic annotation
FNC|intracellular protein transport ; GO:0006886 | inferred from electronic annotation
}

ALESR
{
ASYM|&bgr;'Cop<up>+</up>
ID|FBal0093738
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070058	CLA 1 foreign safe element	GSYM 1 &lgr;\attP	DT 1 25 Dec 04	RESZ 1004	FSQ 1 <I>Bacteriophage lambda</I> attP', recombination target site'.	ALESR 2	REF 1	
GSYM|&lgr;\attP
DT|25 Dec 04
ID|FBgn0070058
CLA|foreign_safe_element
FSQ|species == Bacteriophage lambda; sequence == attP', recombination target site'.
OTH|The &lgr; recombination proteins mediate site-specific and
|directional recombination between recombination sites;
|@Ecol\attB@ x @&lgr;\attP@ <=> @Ecol\attL@ and @Ecol\attR@.
REF
{
REFM|FBrf0179058
|Murphy
|2003-
|9
}

ALESR
{
ASYM|&lgr;\attP<up>1</up>
SYN|attP1
ID|FBal0157551
REF|FBrf0179058
REFDSR
{
RDID|FBrf0179058
|Murphy
|2003-
OTH|@Ecol\attR<up>1</up>@ will recombine with @Ecol\attL<up>1</up>@ to produce @Ecol\attB<up>1</up>@
|and @&lgr;\attP<up>1</up>@.
SYN|attP1
}

}

ALESR
{
ASYM|&lgr;\attP<up>2</up>
SYN|attP2
ID|FBal0157550
REF|FBrf0179058
REFDSR
{
RDID|FBrf0179058
|Murphy
|2003-
OTH|@Ecol\attR<up>2</up>@ will recombine with @Ecol\attL<up>2</up>@ to produce @Ecol\attB<up>2</up>@
|and @&lgr;\attP<up>2</up>@.
SYN|attP2
}

}

}
# EOR
GENR
{
RETE|ID 1 FBgn0043467	CLA 1 Gene	GSYM 1 064Ya	DT 1 25 Dec 04	RESZ 1217	FNC 1 behavioral response to ethanol	CEL 1 cellular_component unknown	CLOC 1 XLt--XRt	ALESR 2	REF 2	
GSYM|064Ya
DT|25 Dec 04
ID|FBgn0043467
FNC|behavioral response to ethanol ; GO:0048149
CEL|cellular_component unknown ; GO:0008372
CLOC|XLt--XRt
ENZ|molecular_function unknown ; GO:0005554
|molecular_function unknown ; GO:0005554 | no biological data available
REF
{
REFM|FBrf0159398
|FlyBase Curators
|2002-
|9
REFM|FBrf0131396
|Scholz et al.
|2000
|-1
}

REFDSR
{
RDID|FBrf0131396
|Scholz et al.
|2000
CLOC|XLt--XRt
FNC|behavioral response to ethanol ; GO:0048149 | inferred from mutant phenotype
SYN|unnamed
}

REFDSR
{
RDID|FBrf0159398
|FlyBase Curators
|2002-
ENZ|molecular_function unknown ; GO:0005554 | no biological data available
CEL|cellular_component unknown ; GO:0008372 | no biological data available
}

ALESR
{
ASYM|064Ya<up>064Ya</up>
SYN|064Y
ID|FBal0119724
PHC|chemical sensitive
PHI|Mutants exhibit a reduced tolerance to ethanol.
REF|FBrf0131396
REFDSR
{
RDID|FBrf0131396
|Scholz et al.
|2000
TRN|FBti0016904 == P{GAL4}064Ya<up>064Ya</up>
MU|P-element activity
PHC|chemical sensitive
PHI|Mutants exhibit a reduced tolerance to ethanol.
SYN|064Y
}

}

ALESR
{
ASYM|064Ya<up>+</up>
ID|FBal0120253
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0010347	CLA 1 Gene	GSYM 1 1.28	DT 1 25 Dec 04	RESZ 5347	PDOM 1 INTERPRO:IPR000194 == H+-transporting two-sector ATPase, alpha/beta subunit, central	PTD 1	DBA 4	FNC 2 ATP synthesis coupled proton transport	CEL 1 proton-transporting two-sector ATPase complex	CLOC 1 42B3	ALESR 3	REF 14	
GSYM|1.28
PTD
DT|25 Dec 04
ID|FBgn0010347
UAB|Deficiency: Df(2R)cn88b (inferred from cytology)
|Duplication: Dp(2;Y)cn<up>+</up> (inferred from cytology)
SYN|CG9397
|CG9397
|CG9397
|deformed
CLOC|42B3
|Limits computationally determined from genome sequence between @P{lacW}l(2)k09848<up>k09848</up>@&@P{EP}EP407@ and @P{lacW}geminin<up>k14019</up>@&@P{PZ}Adf1<up>01349</up>@
CYC|Experimentally determined: 42B
FNC|ATP synthesis coupled proton transport ; GO:0015986
|specification of segmental identity, maxillary segment ; GO:0007382
CEL|proton-transporting two-sector ATPase complex ; GO:0016469
PDOM|IPR000194 == H+-transporting two-sector ATPase, alpha/beta subunit, central
ENZ|ATP binding ; GO:0005524
|ATP binding ; GO:0005524 | inferred from electronic annotation
|hydrogen-transporting ATP synthase activity, rotational mechanism ; GO:0046933
|hydrogen-transporting ATPase activity, rotational mechanism ; GO:0046961
|hydrogen-transporting ATP synthase activity, rotational mechanism ; GO:0046933 | inferred from electronic annotation
|hydrogen-transporting ATPase activity, rotational mechanism ; GO:0046961 | inferred from electronic annotation
DBA|NA:AE003789
|PA:AAF57355
|NA:L07262
|PA:AAA03084
PAC|UniProt_TrEMBL:Q24300
|UniProt_TrEMBL:Q9V9D6
WTI|Dfd
ASQ|FBan0009397
REF
{
REFM|FBrf0079168
|Pederson and Mahaffey
|1995
|1
REFM|FBrf0076134
|Mohler et al.
|1995
|0
REFM|FBrf0068222
|Mahaffey et al.
|1994
|1
REFM|FBrf0092336
|LaFollette et al.
|1997
|1
REFM|FBrf0075267
|Mahaffey
|1993
|9
REFM|FBrf0064596
|Mahaffey et al.
|1993
|0
REFM|FBrf0132330
|Mahaffey et al.
|2001
|0
REFM|FBrf0068424
|Botas
|1993
|2
REFM|FBrf0130258
|Pederson et al.
|2000
|0
REFM|FBrf0090735
|Pederson et al.
|1996
|0
REFM|FBrf0078949
|Mahato and Mahaffey
|1995
|1
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0085725
|Pederson et al.
|1996
|1
}

REFDSR
{
RDID|FBrf0064596
|Mahaffey et al.
|1993
CLOC|42B (determined by in situ hybridization)
FNC|specification of segmental identity, maxillary segment ; GO:0007382 | inferred from expression pattern
|specification of segmental identity, maxillary segment ; GO:0007382 | inferred from genetic interaction with FLYBASE:Dfd; FB:FBgn0000439
WT|Identified in an enhancer trap screen for target genes of homeoproteins.
|The 1.28 gene is a target gene that is activated by @Dfd@. @Dfd@ is required
|to activate 1.28 in the maxillary segment, but ectopic expression of
|@Dfd@ is incapable of activating @1.28@ elsewhere.
WTI|Dfd
}

REFDSR
{
RDID|FBrf0079168
|Pederson and Mahaffey
|1995
WT|The @1.28@ gene is directly activated by @Dfd@ in the maxillary segment
|but not in the mandibular segment. Four @Dfd@-product binding sites
|have been identified within a 664bp fragment of the @1.28@ regulatory
|region, in addition to a @Dfd@ epidermal autoactivation element (DEAE).
WTI|Dfd
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
}

REFDSR
{
RDID|FBrf0117645
|Mahaffey
|1992
CLOC|42B
SYN|deformed
}

REFDSR
{
RDID|FBrf0136026
|Dobie and Karpen
|2001.4.18
AM|"1.28" may correspond to "Scim21".
|Sequence analysis off ends of @P{SUPor-P}@ in Scim insertion mutant
|places "Scim21" near/in "1.28".
SYN|CG9397
}

REFDSR
{
RDID|FBrf0137489
|Mount
|2001.8.14
SYN|CG9397
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|ATP binding ; GO:0005524 | inferred from electronic annotation
|hydrogen-transporting ATP synthase activity, rotational mechanism ; GO:0046933 | inferred from electronic annotation
|hydrogen-transporting ATPase activity, rotational mechanism ; GO:0046961 | inferred from electronic annotation
FNC|ATP synthesis coupled proton transport ; GO:0015986 | inferred from electronic annotation
CEL|proton-transporting two-sector ATPase complex ; GO:0016469 | inferred from electronic annotation
}

ALESR
{
ASYM|1.28<up>P</up>
ID|FBal0121022
REF|FBrf0130258
REFDSR
{
RDID|FBrf0130258
|Pederson et al.
|2000
MD|@P{lacW}@ insertion into the @Deaf1@ binding region of the @1.28@ regulatory
|sequences.
TRN|FBti0003587 == P{lacW}1.28<up>P</up>
MU|P-element activity
}

}

ALESR
{
ASYM|1.28<up>rv13</up>
SYN|line 13
ID|FBal0121021
REF|FBrf0130258
REFDSR
{
RDID|FBrf0130258
|Pederson et al.
|2000
MD|Mobilization of the @P{lacW}@ element, resulting in a deletion of approximately
|1kb upstream of the original @P{lacW}@ element insertion site.
PRG|1.28<up>P</up>
MU|&Dgr;2-3
SYN|line 13
}

}

ALESR
{
ASYM|1.28<up>+</up>
ID|FBal0066314
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0026615	CLA 1 Gene	GSYM 1 10-4	DT 1 25 Dec 04	RESZ 1135	ALESR 1	REF 1	
GSYM|10-4
DT|25 Dec 04
ID|FBgn0026615
MD|In dividing precursor cells of the developing nervous system the
|correct asymmetric apical localization of @10-4@ mRNA  depends on
|@insc@.  @10-4@ protein localization to the apical cytoplasm occurs
|when @insc@ protein disappears, in anaphase.  In telophase @10-4@
|protein forms a tight apical crescent.
REF
{
REFM|FBrf0106275
|Bulgheresi and Knoblich
|1999
|1
}

REFDSR
{
RDID|FBrf0106275
|Bulgheresi and Knoblich
|1999
MD|In dividing precursor cells of the developing nervous system the
|correct asymmetric apical localization of @10-4@ mRNA  depends on
|@insc@.  @10-4@ protein localization to the apical cytoplasm occurs
|when @insc@ protein disappears, in anaphase.  In telophase @10-4@
|protein forms a tight apical crescent.
OTH|Identification: Defined in a yeast two hybrid assay for genes whose
|products interact with the 364 amino acid domain of @insc@ that
|are required and sufficient for all the known @insc@ functions.
}

ALESR
{
ASYM|10-4<up>+</up>
ID|FBal0096586
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067637	CLA 1 Gene	GSYM 1 106y	DT 1 25 Dec 04	RESZ 2191	ALESR 2	REF 1	
GSYM|106y
DT|25 Dec 04
ID|FBgn0067637
REF
{
REFM|FBrf0141372
|Ejima et al.
|2001
|0
}

ALESR
{
ASYM|106y<up>106y</up>
SYN|106y
ID|FBal0151008
PHC|viable
|fertile
|courtship defective | female
PHI|@106y<up>106y</up>@ virgin females show elevated ovulation; 27% of the virgin
|females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @106y<up>106y</up>@ virgin females are mated
|to wild-type males is lower than that seen when wild-type virgin females
|are mated to wild-type males, but is higher than that seen when wild-type
|mated females are mated to wild-type males. @106y<up>106y</up>@ mutant virgin
|females show ovipositor extrusion towards courting wild-type males
|(this extrusion behavior is normally observed in mated wild-type females
|but not in virgin wild-type females).
REF|FBrf0141372
REFDSR
{
RDID|FBrf0141372
|Ejima et al.
|2001
TRN|FBti0037977 == P{GawB}106y<up>106y</up>
MU|P-element activity
PHC|viable
|fertile
|courtship defective | female
PHI|@106y<up>106y</up>@ virgin females show elevated ovulation; 27% of the virgin
|females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @106y<up>106y</up>@ virgin females are mated
|to wild-type males is lower than that seen when wild-type virgin females
|are mated to wild-type males, but is higher than that seen when wild-type
|mated females are mated to wild-type males. @106y<up>106y</up>@ mutant virgin
|females show ovipositor extrusion towards courting wild-type males
|(this extrusion behavior is normally observed in mated wild-type females
|but not in virgin wild-type females).
SYN|106y
}

}

ALESR
{
ASYM|106y<up>+</up>
ID|FBal0151314
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0011557	CLA 1 Gene	GSYM 1 107.1	DT 1 25 Dec 04	RESZ 1143	ALESR 1	REF 3	
GSYM|107.1
DT|25 Dec 04
ID|FBgn0011557
WTI|tub
REF
{
REFM|FBrf0068202
|West and Anderson
|1994
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0079611
|West and Anderson
|1995
|1
}

REFDSR
{
RDID|FBrf0068202
|West and Anderson
|1994
WTI|tub
PHP|@107.1@ behaves as a dominant gain of function enhancer of all alleles
|of @tub@, @107.1@ regulates @tub@ at post-transcriptional level. @107.1@
|acts in trans to disrupt accumulation of maternal @tub@ transcript.
|Females homozygous for @107.1@ lack maternal @tub@ transcript and
|yield completely dorsalized embryos.
}

REFDSR
{
RDID|FBrf0079611
|West and Anderson
|1995
PHP|@107.1@ may define a regulator of @tub@ transcript levels, the recessive
|maternal effect dorsalizing mutation exhibits loss of @tub@ message
|that can be completely rescued with excess @tub@.
}

ALESR
{
ASYM|107.1<up>+</up>
ID|FBal0066315
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070057	CLA 1 Gene	GSYM 1 11	DT 1 25 Dec 04	RESZ 300	ALESR 1	
GSYM|11
DT|25 Dec 04
ID|FBgn0070057
SYN|#1
REFDSR
{
RDID|FBrf0173481
|Pistillo et al.
|2004
OTH|Identification: In a screen for mutations affecting R7/R8 photoreceptor subtype specification.
SYN|#1
}

ALESR
{
ASYM|11<up>+</up>
ID|FBal0158438
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0010339	CLA 1 Gene	NAM 1 upstream of RpIII128	GSYM 1 128up	DT 1 25 Dec 04	RESZ 4734	PDOM 5 INTERPRO:IPR002917 == GTP-binding protein, HSR1-related	PTD 1	DBA 10	CLOC 1 48D8	ALESR 1	REF 13	
GSYM|128up
PTD
MMP
DT|25 Dec 04
ID|FBgn0010339
UAB|Duplication: Dp(2;2)Y3b (inferred from cytology)
SYN|CG8340
|CG8340
|GTP-bp
|X71866
ID2|FBgn0010196
NAM|upstream of RpIII128
GLOC|2-
CLOC|48D8
|Limits computationally determined from genome sequence between @P{lacW}l(2)k06612<up>k06612</up>@ and @P{lacW}jeb<up>k05644</up>@
CYC|Experimentally determined: 48E
PDOM|IPR002917 == GTP-binding protein, HSR1-related
|IPR004095 == TGS
|IPR005225 == Small GTP-binding protein domain
|IPR006073 == GTP1/OBG
|IPR006074 == GTP1/OBG domain
MD|Identified with: SD05004 (BDGP-DGC)
ENZ|GTP binding ; GO:0005525
|GTP binding ; GO:0005525 | inferred from direct assay
|GTP binding ; GO:0005525 | non-traceable author statement
|hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides ; GO:0016818 ; EC:3.6.1.- | inferred from electronic annotation
|hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides ; GO:0016818 ; EC:3.6.1.-
|GTP binding ; GO:0005525 | inferred from sequence similarity with UniProt:P43690
DBA|NA:AE003823
|PA:AAF58591
|NA:AI533247
|BDGP-DGC:SD05004
|NA:AX093898
|NA:AY069810
|PA:AAL39955
|BDGP-DGC:SD05004
|NA:X71866
|PA:CAA50701
PAC|PIR:S33467
|PIR:S42582
|UniProt_Swiss_Prot:P32234
|UniProt_TrEMBL:Q9V648
ASQ|FBan0008340
REF
{
REFM|FBrf0067209
|Sommer et al.
|1994
|0
REFM|FBrf0126686
|Milshina
|1999.11
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|-1505380982
|0
|Patent: WO 0118547-A 15-MAR-2001;
REFM|FBrf0058389
|Sommer et al.
|1993
|1
REFM|FBrf0147137
|Brody et al.
|2002
|0
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0146674
|Roth and Foulger
|2002.4.24
|9
REFM|FBrf0155515
|Ptak and Petrov
|2002
|0
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0156694
|Swiss-Prot Project Members
|1993.10.1
|9
REFM|FBrf0090923
|Seifarth
|1991
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0058389
|Sommer et al.
|1993
WT|@RpIII128@ gene is flanked by an upstream transcription unit, @128up@.
|@128up@ is transcribed in the same direction as @RpIII128@ and they
|are separated by a short intergenic region. Bacterially expressed
|@128up@, in fusion with maltose binding protein (MBP), specifically
|binds GTP.
}

REFDSR
{
RDID|995280021
|Davies
|2001.3.30
OTH|Area matching Drosophila GTP-binding protein, Acc. No. X71866.
}

REFDSR
{
RDID|FBrf0067209
|Sommer et al.
|1994
ENZ|GTP binding ; GO:0005525 | inferred from direct assay
WT|Bacterially expressed @128up@ is capable of binding GTP and the protein
|is primarily located in the perinuclear region.
GPD|GTP binding protein
}

REFDSR
{
RDID|FBrf0090923
|Seifarth
|1991
CLOC|48E (determined by in situ hybridization)
}

REFDSR
{
RDID|FBrf0102347
|Kliman and Eyre-Walker
|1998
OTH|In a sample of 79 genes with multiple introns, 33 showed significant
|heterogeneity in G+C content among introns of the same gene and significant
|positive correspondence between the intron and the third codon position
|G+C content within genes. These results are consistent with selection
|adding against preferred codons at the start of genes.
SYN|GTP-bp
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ENZ|GTP binding ; GO:0005525 | inferred from sequence similarity with UniProt:P43690
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: SD05004 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0146674
|Roth and Foulger
|2002.4.24
ENZ|hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides ; GO:0016818 ; EC:3.6.1.- | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0147137
|Brody et al.
|2002
SYN|CG8340
}

REFDSR
{
RDID|FBrf0155515
|Ptak and Petrov
|2002
SYN|X71866
}

REFDSR
{
RDID|FBrf0156694
|Swiss-Prot Project Members
|1993.10.1
ENZ|GTP binding ; GO:0005525 | non-traceable author statement
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

ALESR
{
ASYM|128up<up>+</up>
ID|FBal0066316
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0005673	CLA 1 transposable element	NAM 1 1360 element	GSYM 1 1360	DT 1 25 Dec 04	RESZ 8855	DBA 19	WT 5 In situ hybridization to polytene chromosomes shows variable	REF 48	
GSYM|1360
MMP
DT|25 Dec 04
ID|FBgn0005673
CLA|transposable_element
SYN|hoppel
|hopel
|Hoppel
|hoppel-like
|Dr. D
|protop
|protop_b
|Hoppel-like
|DmHoppel
|ProtoP
|ProtoP_B
|1360/Hoppel
|Dm1360
|EG:23E12.4
|anon-CH(3)336
|CR31276
|CR31011
|CR31553
ID2|FBgn0004180
|FBgn0013399
|FBgn0051011
|FBgn0051276
|FBgn0051553
NAM|1360 element
TE|element type: IR
|terminal repeat length in bp: 37
|total length in bp: 1176
|target site duplication length in bp: 6
|number of copies in genome: >25
WT|In situ hybridization to polytene chromosomes shows variable,
|strain-specific location in the euchromatic parts of the arms and heavy
|labeling of the 12E region of the X chromosome, chromosome bases
|(20A--20F, 40A--40F, 41A--41F, 80A--80C and 81F), the chromocenter and
|chromosome 4.
DBA|NA:AF533772
|NA:AF540061
|NA:AJ000473
|NA:AJ441085
|NA:AL031884
|NA:AY138841
|NA:L36596
|NA:M55078
|NA:U66884
|NA:X59157
|NA:X78388
|NA:Z11734
|NA:Z11735
|NA:Z31905
|dbSTS:4444
|NA:Z32073
|dbSTS:4624
|NA:Z32074
|dbSTS:4625
ASQ|FBan0031276
REF
{
REFM|FBrf0111489
|Spradling et al.
|1999
|0
REFM|FBrf0134799
|van Steensel et al.
|2001
|9
REFM|FBrf0155828
|Kaminker et al.
|2002
|0
REFM|FBrf0053529
|Leibovich et al.
|1991
|0
REFM|FBrf0053528
|Leibovich
|1991
|0
REFM|FBrf0159203
|Reiss et al.
|2003
|0
REFM|FBrf0155823
|Celniker et al.
|2002
|0
REFM|FBrf0162162
|Lerat et al.
|2003
|0
REFM|FBrf0105803
|Cryderman et al.
|1998
|0
REFM|FBrf0155500
|Maggert and Golic
|2002
|0
REFM|FBrf0144916
|Rizzon et al.
|2002
|0
REFM|FBrf0071734
|EDGP Project Members
|1994-
|9
REFM|FBrf0046087
|Kholodilov et al.
|1987
|0
REFM|FBrf0105798
|Coelho et al.
|1998
|0
REFM|FBrf0149015
|Yan et al.
|2002
|0
REFM|FBrf0106872
|Locke et al.
|1999
|9
REFM|FBrf0137315
|Galindo et al.
|2001
|0
REFM|FBrf0106421
|Dimitri et al.
|1999
|1
REFM|FBrf0080514
|Zhang and Spradling
|1995
|0
REFM|FBrf0080225
|Madueno et al.
|1995
|0
REFM|FBrf0135796
|Pardue and Debaryshe
|2000
|2
REFM|FBrf0149106
|Bartolome et al.
|2002
|0
REFM|FBrf0125039
|Bejarano and Gonzalez
|1999
|0
REFM|FBrf0135794
|Wallrath
|2000
|2
REFM|FBrf0167608
|Greil et al.
|2003
|0
REFM|FBrf0135792
|Gvozdev et al.
|2000
|2
REFM|FBrf0162058
|Aravin et al.
|2003
|0
REFM|FBrf0101830
|Locke et al.
|1998
|1
REFM|FBrf0083001
|Almeida Coelho and Sunkel
|1995
|1
REFM|FBrf0057400
|Balakireva et al.
|1992
|0
REFM|FBrf0174713
|Myster et al.
|2004
|0
REFM|FBrf0126011
|Aravin et al.
|2000
|1
REFM|FBrf0137496
|Misra
|2001.8.16
|9
REFM|FBrf0151627
|Ashburner
|2002.8.15
|9
REFM|FBrf0135823
|Benos et al.
|2001
|0
REFM|FBrf0047691
|Kholodilov et al.
|1988
|0
REFM|FBrf0117093
|Kurenova
|1994.5.6
|9
REFM|FBrf0112417
|Ahmed
|1996.8.14
|9
REFM|FBrf0121135
|Sunkel
|1997.7.15
|9
REFM|FBrf0109548
|Cryderman et al.
|1999
|0
REFM|FBrf0101859
|Wallrath et al.
|1998
|1
REFM|FBrf0100583
|Kalmykova et al.
|1998
|0
REFM|FBrf0151719
|Tulin et al.
|2002
|0
REFM|FBrf0117473
|Livak
|1992.2.24
|9
REFM|FBrf0117472
|Livak
|1992.2.24
|9
REFM|FBrf0158965
|Tritto et al.
|2003
|0
REFM|FBrf0137199
|Aravin et al.
|2001
|0
REFM|FBrf0099762
|Deak et al.
|1997
|0
}

REFDSR
{
RDID|FBrf0047691
|Kholodilov et al.
|1988
WT|In situ hybridization to polytene chromosomes shows variable,
|strain-specific location in the euchromatic parts of the arms and heavy
|labeling of the 12E region of the X chromosome, chromosome bases
|(20A--20F, 40A--40F, 41A--41F, 80A--80C and 81F), the chromocenter and
|chromosome 4.
}

REFDSR
{
RDID|FBrf0052018
|Kurenova et al.
|1990
PHP|A @1360@ element has been cloned and sequenced. It is flanked by short
|inverted repeats. The @1360@ element is present in approximately 10-30
|euchromatic sites and also in numerous heterochromatic sites (in the
|chromocenter, pericentric heterochromatin, the fourth chromosome and
|at the telomeres) in the D.melanogaster genome. At least 6 variant
|@1360@ elements differing in the length of the central region have
|been detected. The @1360@ element has ARS activity, similar to the
|@P-element@.
SYN|hoppel
}

REFDSR
{
RDID|FBrf0053528
|Leibovich
|1991
SYN|hopel
}

REFDSR
{
RDID|FBrf0053529
|Leibovich et al.
|1991
SYN|hopel
}

REFDSR
{
RDID|FBrf0080514
|Zhang and Spradling
|1995
}

REFDSR
{
RDID|FBrf0083001
|Almeida Coelho and Sunkel
|1995
SYN|Hoppel
}

REFDSR
{
RDID|FBrf0099762
|Deak et al.
|1997
SYN|hoppel
}

REFDSR
{
RDID|FBrf0101830
|Locke et al.
|1998
SYN|Hoppel
}

REFDSR
{
RDID|FBrf0101859
|Wallrath et al.
|1998
SYN|hoppel
}

REFDSR
{
RDID|FBrf0105803
|Cryderman et al.
|1998
SYN|hoppel
}

REFDSR
{
RDID|FBrf0106421
|Dimitri et al.
|1999
SYN|hoppel
}

REFDSR
{
RDID|FBrf0106872
|Locke et al.
|1999
SYN|Hoppel
}

REFDSR
{
RDID|FBrf0109548
|Cryderman et al.
|1999
SYN|hoppel
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
SYN|hoppel
}

REFDSR
{
RDID|FBrf0112417
|Ahmed
|1996.8.14
SYN|unnamed
}

REFDSR
{
RDID|FBrf0117093
|Kurenova
|1994.5.6
SYN|hoppel
}

REFDSR
{
RDID|FBrf0117472
|Livak
|1992.2.24
SYN|unnamed
}

REFDSR
{
RDID|FBrf0117473
|Livak
|1992.2.24
SYN|unnamed
}

REFDSR
{
RDID|FBrf0121135
|Sunkel
|1997.7.15
SYN|hoppel-like
}

REFDSR
{
RDID|FBrf0123109
|Locke et al.
|1999
TE|The "Dr. D" repetitive sequence (described in FBrf0048918) contains
|sequences of both @INE-1@ and @1360@ transposable elements.
SYN|hoppel
}

REFDSR
{
RDID|FBrf0125039
|Bejarano and Gonzalez
|1999
SYN|hoppel
}

REFDSR
{
RDID|FBrf0126011
|Aravin et al.
|2000
SYN|hoppel
}

REFDSR
{
RDID|FBrf0128554
|Locke et al.
|2000
SYN|Dr. D
|Hoppel
}

REFDSR
{
RDID|FBrf0134799
|van Steensel et al.
|2001
SYN|hoppel
}

REFDSR
{
RDID|FBrf0135792
|Gvozdev et al.
|2000
SYN|hoppel
}

REFDSR
{
RDID|FBrf0135794
|Wallrath
|2000
SYN|hoppel
}

REFDSR
{
RDID|FBrf0135796
|Pardue and Debaryshe
|2000
SYN|Hoppel
}

REFDSR
{
RDID|FBrf0137199
|Aravin et al.
|2001
SYN|hoppel
}

REFDSR
{
RDID|FBrf0144916
|Rizzon et al.
|2002
SYN|Hoppel
}

REFDSR
{
RDID|FBrf0151607
|Kapitonov and Jurka
|1997-
SYN|protop
|protop_b
}

REFDSR
{
RDID|FBrf0151719
|Tulin et al.
|2002
SYN|hoppel
}

REFDSR
{
RDID|FBrf0155500
|Maggert and Golic
|2002
SYN|hoppel
}

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
TE|element type: IR
|total length in bp: 1177
|number of copies in genome: 105 in euchromatin of Release 3 genome annotation, of which 10 are full length.
}

REFDSR
{
RDID|FBrf0158933
|Marsano et al.
|2003
SYN|Hoppel-like
|DmHoppel
}

REFDSR
{
RDID|FBrf0158965
|Tritto et al.
|2003
SYN|Hoppel
}

REFDSR
{
RDID|FBrf0160656
|Kapitonov and Jurka
|2003
TE|total length in bp: 4480
|number of copies in genome: 17
SYN|ProtoP
|ProtoP_B
}

REFDSR
{
RDID|FBrf0162058
|Aravin et al.
|2003
}

REFDSR
{
RDID|FBrf0162162
|Lerat et al.
|2003
SYN|hoppel
}

REFDSR
{
RDID|FBrf0167608
|Greil et al.
|2003
}

REFDSR
{
RDID|FBrf0174713
|Myster et al.
|2004
SYN|1360/Hoppel
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0066320	CLA 1 transposable element gene	GSYM 1 1360\T	DT 1 25 Dec 04	RESZ 290	DBA 2	ALESR 1	REF 1	
GSYM|1360\T
DT|25 Dec 04
ID|FBgn0066320
CLA|transposable_element_gene
DBA|NA:AF533772
|PA:AAN39288
PAC|UniProt_TrEMBL:Q86BW1
REF
{
REFM|FBrf0159203
|Reiss et al.
|2003
|0
}

ALESR
{
ASYM|1360\T<up>+</up>
ID|FBal0146588
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0020238	CLA 1 Gene	GSYM 1 14-3-3&egr;	DT 1 25 Dec 04	RESZ 35909	PDOM 1 INTERPRO:IPR000308 == 14-3-3 protein	PTD 1	DBA 11	FNC 10 DNA damage checkpoint	CEL 4 chromosome	WT 2 @14-3-3&egr;@ is required to time mitosis in undisturbed post-blastoderm	CLOC 1 90F10	ALESR 12	SK 6	REF 46	
GSYM|14-3-3&egr;
PTD
ARGS
DT|25 Dec 04
ID|FBgn0020238
UAB|Deficiency: Df(3R)P14
|Duplication: Dp(3;3)C123.3 (inferred from cytology)
SYN|CG31196
|SR3-9
|14-3-3
|d14-3-3&egr;
|14-3-3epsilon
|14-3-3e
|CT24092
|EK3-5
|D14-3-3&egr;
|14-3-3-e
|D14-3-3e
|par-5
|Par-5
|Su(Raf)3B
|l(3)j2B10
|Suppressor of Ras85D 3-9
ID2|FBgn0011329
|FBgn0016739
|FBgn0016743
|FBgn0051196
|FBgn0064146
CLOC|90F10
|Limits computationally determined from genome sequence between @P{EP}cpo<up>EP3679</up>@ and @P{EP}Dlc90F<up>EP3634</up>@
CYC|Experimentally determined: 90E--F, 90F6--7
FNC|DNA damage checkpoint ; GO:0000077
|Ras protein signal transduction ; GO:0007265
|imaginal disc development ; GO:0007444
|maintenance of oocyte identity (sensu Insecta) ; GO:0016350
|mitotic checkpoint ; GO:0007093
|nonassociative learning ; GO:0046958
|oocyte microtubule cytoskeleton polarization (sensu Insecta) ; GO:0048129
|regulation of mitosis ; GO:0007088
|response to external stimulus ; GO:0009605
|response to radiation ; GO:0009314
CEL|chromosome ; GO:0005694
|cytoplasm ; GO:0005737
|nucleus ; GO:0005634
|ring canal (sensu Insecta) ; GO:0045172
PDOM|IPR000308 == 14-3-3 protein
GLC|Maps 0.4 +/- 0.2 cM from a P{w<up>+</up>} insertion into 90E.
WT|@14-3-3&egr;@ is required to time mitosis in undisturbed post-blastoderm
|cell cycles and to delay mitosis following irradiation in embryos.
ENZ|transcription regulator activity ; GO:0030528 | inferred from electronic annotation
|transcription regulator activity ; GO:0030528
|diacylglycerol-activated phospholipid-dependent protein kinase C inhibitor activity ; GO:0004863
|diacylglycerol-activated phospholipid-dependent protein kinase C inhibitor activity ; GO:0004863 | non-traceable author statement
|protein domain specific binding ; GO:0019904
|protein domain specific binding ; GO:0019904 | inferred from electronic annotation
DBA|NA:AE003721
|PA:AAF55519
|PA:AAN13764
|PA:AAN13765
|PA:AAN13766
|NA:AQ026302
|BDGP:l(3)j2B10
|NA:U84897
|PA:AAC47519
|NA:U84898
|PA:AAC47520
PAC|UniProt_Swiss_Prot:P92177
|UniProt_TrEMBL:Q8IN86
ASQ|FBan0031196
REV|FBrf0158832
|FBrf0111327
|FBrf0127283
REF
{
REFM|FBrf0111489
|Spradling et al.
|1999
|-1
REFM|FBrf0179731
|Bilder
|2004
|2
REFM|FBrf0151902
|Benton et al.
|2002
|0
REFM|FBrf0091142
|Perrimon et al.
|1996
|0
REFM|FBrf0158832
|Ahringer
|2003
|2
REFM|FBrf0173208
|Benton and St. Johnston
|2003
|0
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0111327
|Baek and Lee
|1999
|2
REFM|FBrf0131405
|Therrien et al.
|2000
|-1
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|FBrf0179660
|Jaramillo et al.
|2004
|1
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0126669
|Gong
|1999.11
|9
REFM|FBrf0126349
|Su
|2000
|1
REFM|FBrf0104946
|FlyBase
|1996-
|9
REFM|FBrf0127357
|Teeter et al.
|2000
|0
REFM|FBrf0104620
|Rommel and Hafen
|1998
|2
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
|9
REFM|FBrf0133450
|Acevedo and Skoulakis
|2001
|1
REFM|FBrf0083714
|Meister and Braun
|1995.10
|9
REFM|FBrf0145821
|Acevedo and Skoulakis
|2002
|1
REFM|FBrf0173511
|Skoulakis et al.
|2004
|1
REFM|FBrf0139721
|Su et al.
|2001
|0
REFM|FBrf0151887
|Rebay
|2002
|2
REFM|FBrf0159706
|Hacker et al.
|2003
|0
REFM|FBrf0127283
|Raabe
|2000
|2
REFM|FBrf0113722
|Chang
|1997.1.11
|9
REFM|FBrf0108153
|Chen and Chien
|1999
|0
REFM|FBrf0102393
|Rubin et al.
|1997
|2
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
REFM|FBrf0126651
|Ashburner
|1999.11
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0126680
|Lei
|1999.11
|9
REFM|FBrf0127025
|Brodsky et al.
|2000
|0
REFM|FBrf0149093
|Johannes and Preiss
|2002
|0
REFM|FBrf0173982
|Wang and Cooley
|2004
|1
REFM|FBrf0124174
|Swiss-Prot Project Members
|1998.2.1
|9
REFM|FBrf0159690
|Chen et al.
|2003
|0
REFM|FBrf0087493
|Karim et al.
|1996
|-1
REFM|FBrf0133630
|Purdy et al.
|2001
|1
REFM|FBrf0129944
|Li et al.
|2000
|0
REFM|FBrf0086382
|Dickson et al.
|1996
|0
REFM|FBrf0167337
|de Morais Guedes et al.
|2003
|0
REFM|FBrf0130073
|Sekelsky et al.
|2000
|0
REFM|FBrf0158996
|Li and Li
|2003
|0
REFM|FBrf0093395
|Chang and Rubin
|1997
|0
}

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
CLOC|90F6--7
LOI|14-3-3&egr;<up>j2B10</up>
BMD|Df(3R)P14
}

REFDSR
{
RDID|FBrf0086382
|Dickson et al.
|1996
GLC|Maps 0.4 +/- 0.2 cM from a P{w<up>+</up>} insertion into 90E.
WTI|phl (data from @14-3-3&egr;<up>18A2</up>@)
PHP|Identified in a genetic screen for modifiers of the @phl::tor<up>12D.sev</up>@
|rough eye mutant phenotype.
}

REFDSR
{
RDID|FBrf0087493
|Karim et al.
|1996
GLOC|3-
CLOC|90E--F
CYC|On basis of meiotic mapping (details unspecified).
WTI|Dsor1 (data from @14-3-3&egr;<up>S-1259</up>@, @14-3-3&egr;<up>S-696</up>@)
|Ras85D (data from @14-3-3&egr;<up>S-1259</up>@, @14-3-3&egr;<up>S-696</up>@)
|aop (data from @14-3-3&egr;<up>S-1259</up>@, @14-3-3&egr;<up>S-696</up>@)
|phl (data from @14-3-3&egr;<up>S-1259</up>@, @14-3-3&egr;<up>S-696</up>@)
PHP|Identified on the basis of genetic interaction with @Ras85D<up>V12.sev</up>@.
SYN|SR3-9: Suppressor of Ras85D 3-9
}

REFDSR
{
RDID|FBrf0091142
|Perrimon et al.
|1996
CLOC|90F6--7 (determined by in situ hybridization)
PHP|The autosomal "FLP-DFS" technique (using the @P{ovoD1-18}@ @P{FRT(w<up>hs</up>)}@
|@P{hsFLP}@ chromosomes) has been used to identify the specific maternal
|effect phenotype for the zygotic lethal mutation. @14-3-3&egr;@ gene
|expression during oogenesis is not critical to embryonic development,
|but the gene function may be essential for fertilization and/or completion
|of meiosis.
}

REFDSR
{
RDID|FBrf0093395
|Chang and Rubin
|1997
GLOC|3-62.0
WTI|14-3-3&zgr; (data from @14-3-3&egr;<up>j2B10</up>@)
|Ras85D (data from @14-3-3&egr;<up>S-1259</up>@, @14-3-3&egr;<up>S-696</up>@, @14-3-3&egr;<up>j2B10</up>@)
|phl (data from @14-3-3&egr;<up>18A2</up>@, @14-3-3&egr;<up>S-1259</up>@, @14-3-3&egr;<up>S-696</up>@, @14-3-3&egr;<up>j2B10</up>@)
PHP|@14-3-3&egr;@ has been cloned and characterized. Genetic studies suggest
|that @14-3-3&egr;@ functions in multiple receptor tyrosine kinase pathways,
|acting downstream or parallel to @phl@, but upstream of @aop@ and @phyl@,
|two nuclear factors involved in @Ras85D@ signaling.
}

REFDSR
{
RDID|FBrf0104620
|Rommel and Hafen
|1998
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0108031
|Tien et al.
|1999
BMD|Df(3R)P14
SYN|d14-3-3&egr;
}

REFDSR
{
RDID|FBrf0108153
|Chen and Chien
|1999
SYN|d14-3-3&egr;
}

REFDSR
{
RDID|FBrf0111327
|Baek and Lee
|1999
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
CLOC|90F6--7 (determined by in situ hybridization)
LOI|14-3-3&egr;<up>j2B10</up>
BMD|Df(3R)P14
SYN|14-3-3epsilon
}

REFDSR
{
RDID|FBrf0113721
|Chang
|1997.1.10
ENZ|diacylglycerol-activated phospholipid-dependent protein kinase C inhibitor activity ; GO:0004863 | non-traceable author statement
CLOC|90F6--7
FNC|Ras protein signal transduction ; GO:0007265 | non-traceable author statement
GPD|14-3-3-protein
SYN|14-3-3e
}

REFDSR
{
RDID|FBrf0113722
|Chang
|1997.1.11
SYN|14-3-3e
}

REFDSR
{
RDID|FBrf0124174
|Swiss-Prot Project Members
|1998.2.1
FNC|Ras protein signal transduction ; GO:0007265 | non-traceable author statement
}

REFDSR
{
RDID|FBrf0126669
|Gong
|1999.11
AM|Source for identity of: 14-3-3&egr; CG8045
}

REFDSR
{
RDID|FBrf0126913
|Bayraktaroglu
|2000.4.13
SYN|CT24092
}

REFDSR
{
RDID|FBrf0127025
|Brodsky et al.
|2000
FNC|DNA damage checkpoint ; GO:0000077 | inferred from mutant phenotype
}

REFDSR
{
RDID|FBrf0127283
|Raabe
|2000
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0129944
|Li et al.
|2000
WTI|phl (data from @14-3-3&egr;<up>&Dgr;24</up>@)
}

REFDSR
{
RDID|FBrf0130073
|Sekelsky et al.
|2000
FNC|DNA damage checkpoint ; GO:0000077 | traceable author statement
}

REFDSR
{
RDID|FBrf0131405
|Therrien et al.
|2000
WTI|ksr
|Ras85D (data from @14-3-3&egr;<up>unspecified</up>@)
|phl (data from @14-3-3&egr;<up>unspecified</up>@)
SYN|EK3-5
}

REFDSR
{
RDID|FBrf0133450
|Acevedo and Skoulakis
|2001
SYN|D14-3-3&egr;
}

REFDSR
{
RDID|FBrf0134532
|Walworth
|2000
FNC|imaginal disc development ; GO:0007444 | traceable author statement
|mitotic checkpoint ; GO:0007093 | traceable author statement
|response to radiation ; GO:0009314 | traceable author statement
SYN|14-3-3e
}

REFDSR
{
RDID|FBrf0139721
|Su et al.
|2001
FNC|DNA damage checkpoint ; GO:0000077 | inferred from mutant phenotype
|regulation of mitosis ; GO:0007088 | inferred from mutant phenotype
CEL|chromosome ; GO:0005694 | inferred from direct assay
|cytoplasm ; GO:0005737 | inferred from direct assay
|nucleus ; GO:0005634 | inferred from direct assay
WT|@14-3-3&egr;@ is required to time mitosis in undisturbed post-blastoderm
|cell cycles and to delay mitosis following irradiation in embryos.
}

REFDSR
{
RDID|FBrf0145821
|Acevedo and Skoulakis
|2002
SYN|D14-3-3&egr;
}

REFDSR
{
RDID|FBrf0145847
|Skoulakis and Acevedo
|2002
FNC|response to external stimulus ; GO:0009605 | inferred from mutant phenotype
SYN|D14-3-3&egr;
}

REFDSR
{
RDID|FBrf0149093
|Johannes and Preiss
|2002
SYN|14-3-3-e
}

REFDSR
{
RDID|FBrf0151887
|Rebay
|2002
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0151902
|Benton et al.
|2002
FNC|maintenance of oocyte identity (sensu Insecta) ; GO:0016350 | inferred from mutant phenotype
|oocyte microtubule cytoskeleton polarization (sensu Insecta) ; GO:0048129 | inferred from mutant phenotype
CEL|ring canal (sensu Insecta) ; GO:0045172 | inferred from direct assay
BMD|Df(3R)P14
WTI|14-3-3&zgr; (data from @14-3-3&egr;<up>S-1259</up>@, @14-3-3&egr;<up>j2B10</up>@)
|par-1 (data from @14-3-3&egr;<up>j2B10</up>@)
}

REFDSR
{
RDID|FBrf0154848
FNC|nonassociative learning ; GO:0046958 | non-traceable author statement
SYN|D14-3-3e
}

REFDSR
{
RDID|FBrf0155512
|Pellettieri and Seydoux
|2002
SYN|par-5
}

REFDSR
{
RDID|FBrf0158996
|Li and Li
|2003
WTI|tor (data from @14-3-3&egr;<up>&Dgr;24</up>@)
}

REFDSR
{
RDID|FBrf0159706
|Hacker et al.
|2003
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
ENZ|transcription regulator activity ; GO:0030528 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
SYN|14-3-3epsilon
}

REFDSR
{
RDID|FBrf0167337
|de Morais Guedes et al.
|2003
}

REFDSR
{
RDID|FBrf0173208
|Benton and St. Johnston
|2003
WTI|14-3-3&zgr; (data from @14-3-3&egr;<up>j2B10</up>@)
}

REFDSR
{
RDID|FBrf0173511
|Skoulakis et al.
|2004
SYN|D14-3-3&egr;
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|protein domain specific binding ; GO:0019904 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0179050
|Macara
|2004
SYN|14-3-3
|Par-5
}

REFDSR
{
RDID|FBrf0179255
|Huynh and St. Johnston
|2004
SYN|par-5
|14-3-3
}

REFDSR
{
RDID|FBrf0179660
|Jaramillo et al.
|2004
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0179731
|Bilder
|2004
SYN|14-3-3
}

ALESR
{
ASYM|14-3-3&egr;<up>&Dgr;24</up>
ID|FBal0122336
REF|FBrf0158996
|FBrf0129944
REFDSR
{
RDID|FBrf0129944
|Li et al.
|2000
GIC2|lethal with @phl<up>Su2</up>@
}

REFDSR
{
RDID|FBrf0158996
|Li and Li
|2003
GIA|suppressor | maternal effect of embryonic/first instar larval cuticle | maternal effect phenotype of @tor<up>12D</up>@
}

}

ALESR
{
ASYM|14-3-3&egr;<up>18A2</up>
SYN|14-3-3&egr;<up>Y214F</up>
|18A2
ID|FBal0049166
REF|FBrf0093395
|FBrf0086382
REFDSR
{
RDID|FBrf0086382
|Dickson et al.
|1996
MU|ethyl methanesulfonate
GIC|suppressor | dominant of visible phenotype of @phl::tor<up>12D.sev</up>@
GIA|suppressor | dominant of eye phenotype of @phl::tor<up>12D.sev</up>@
|suppressor | dominant of photoreceptor cell R7 phenotype of @phl::tor<up>12D.sev</up>@
GIC2|lethal | dominant with @phl<up>12</up>@
GII|Dominantly suppresses the rough eye phenotype of
|@phl::tor<up>12D.sev</up>@. Synthetic lethal in combination with @phl<up>12</up>@.
PHC|viable
|female fertile
ALC|antimorph
PHI|Homozygous viable with no obvious defects in eye development.
}

REFDSR
{
RDID|FBrf0093395
|Chang and Rubin
|1997
MD|Amino acid replacement: Y214F.
MU|ethyl methanesulfonate
GIC2|lethal | dominant with @phl<up>12</up>@
PHC|viable
|fertile
PHI|Homozygotes have no detectable phenotype in a wild-type background.
SYN|14-3-3&egr;<up>Y214F</up>
|18A2
}

}

ALESR
{
ASYM|14-3-3&egr;<up>EP3423</up>
ID|FBal0157549
REF|FBrf0104946
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
TRN|FBti0011566 == P{EP}14-3-3&egr;<up>EP3423</up>
MU|P-element activity
}

SK|FBst0102382
|P{EP}14-3-3epsilon[EP3423]
|FBst0017126
|w[1118]; P{w[+mC]=EP}14-3-3epsilon[EP3423]
}

ALESR
{
ASYM|14-3-3&egr;<up>EP3578</up>
ID|FBal0157548
REF|FBrf0104946
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
TRN|FBti0011678 == P{EP}14-3-3&egr;<up>EP3578</up>
MU|P-element activity
}

SK|FBst0103552
|P{EP}14-3-3epsilon[EP3578]
|FBst0017142
|w[1118]; P{w[+mC]=EP}14-3-3epsilon[EP3578]/TM6B, Tb[1]
}

ALESR
{
ASYM|14-3-3&egr;<up>ex4</up>
ID|FBal0148514
ALC|loss of function
REF|FBrf0159690
REFDSR
{
RDID|FBrf0159690
|Chen et al.
|2003
MD|Imprecise mobilization of the @P{lacW}14-3-3&egr;<up>j2B10</up>@ element has
|created this allele.
PRG|14-3-3&egr;<up>j2B10</up>
MU|P-element activity
ALC|loss of function
}

}

ALESR
{
ASYM|14-3-3&egr;<up>j2B10</up>
SYN|l(3)j2B10
|l(3)2B10
|14-3-3&egr;<up>j2b10</up>
|14-3-3-e<up>j2B10</up>
ID|FBal0010913
TRN|FBti0004920 == P{lacW}14-3-3&egr;<up>j2B10</up>
|BDGP:l(3)j2B10
MU|P-element activity
REF|FBrf0067338
|FBrf0173208
|FBrf0151902
|FBrf0127025
|FBrf0093395
|FBrf0108153
|FBrf0159690
|FBrf0149093
|FBrf0083714
|FBrf0091142
|FBrf0111489
|FBrf0139721
REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
OTH|Complements: @repo<up>03702</up>@.
|Complements: @l(3)05822<up>05822</up>@.
|Complements: @Trap80<up>s2956</up>@.
TRN|FBti0004920 == P{lacW}14-3-3&egr;<up>j2B10</up>
|BDGP:l(3)j2B10
}

REFDSR
{
RDID|FBrf0091142
|Perrimon et al.
|1996
PHC|lethal | larval | recessive
|lethal | embryonic | maternal effect
PHM|cuticle | embryonic | maternal effect
PHI|Germline clones produce normal eggs with no cuticle development.
}

REFDSR
{
RDID|FBrf0093395
|Chang and Rubin
|1997
AFC|14-3-3&egr;<up>S-696</up>
MD|Insertion of a @P{lacW}@ element within the first intron.
OTH|The rough eye and missing photoreceptor cell phenotype of @14-3-3&egr;<up>S-696</up>@/@14-3-3&egr;<up>j2B10</up>@
|flies is reverted by mobilization of the @P-element@ in @14-3-3&egr;<up>j2B10</up>@.
|The recessive lethality of the @14-3-3&egr;<up>j2B10</up>@ chromosome is not
|associated with the @P-element@ insertion.
TRN|FBti0004920 == P{lacW}14-3-3&egr;<up>j2B10</up>
|BDGP:l(3)j2B10
MU|P-element activity
GIC|suppressor | recessive of visible phenotype of @Ras85D<up>V12.sev</up>@
GIC2|lethal | recessive with @14-3-3&zgr;<up>P2355</up>@/+
|visible | recessive with @14-3-3&zgr;<up>X1</up>@/+
|visible | recessive with @14-3-3&zgr;<up>2.3</up>@/+
|lethal | dominant with @phl<up>12</up>@
GIA|suppressor | recessive of eye phenotype of @Ras85D<up>V12.sev</up>@
|suppressor | recessive of ommatidium phenotype of @Ras85D<up>V12.sev</up>@
GIA2|ommatidium with @14-3-3&zgr;<up>X1</up>@/+
|ommatidium with @14-3-3&zgr;<up>2.3</up>@/+
|posterior crossvein with @14-3-3&zgr;<up>2.3</up>@
|eye with @14-3-3&zgr;<up>2.3</up>@
|photoreceptor cell with @14-3-3&zgr;<up>2.3</up>@
|posterior crossvein with @14-3-3&zgr;<up>X1</up>@
|eye with @14-3-3&zgr;<up>X1</up>@
|photoreceptor cell with @14-3-3&zgr;<up>X1</up>@
GII|Homozygotes but not heterozygotes suppress the @Ras85D<up>V12.sev</up>@
|rough eye phenotype.
|@14-3-3&zgr;<up>X1</up>@/+ @14-3-3&egr;<up>j2B10</up>@/@14-3-3&egr;<up>j2B10</up>@ or
|@14-3-3&zgr;<up>2.3</up>@/+ @14-3-3&egr;<up>j2B10</up>@/@14-3-3&egr;<up>j2B10</up>@ flies
|have slightly roughened eyes, a low penetrance of missing
|photoreceptors and a gap in the posterior crossvein of the wings in
|more than 50% of cases.
PHC|viable
|sterile | recessive
|(with 14-3-3&egr;<up>S-696</up>) visible
PHM|(with 14-3-3&egr;<up>S-696</up>) eye
|(with 14-3-3&egr;<up>S-696</up>) photoreceptor cell
|(with 14-3-3&egr;<up>S-696</up>) ommatidium
ALC|loss of function
PHI|Homozygotes have normal eyes but are sterile.
|@14-3-3&egr;<up>S-696</up>@/@14-3-3&egr;<up>j2B10</up>@ flies have rough eyes and
|a low penetrance of missing photoreceptors in the ommatidia.
SYN|l(3)j2B10
}

REFDSR
{
RDID|FBrf0108153
|Chen and Chien
|1999
GIA2|(with Df(3R)P14) photoreceptor cell R8 with @Egfr<up>E1</up>@
GII|R8 photoreceptor cells fail to form in @Egfr<up>E1</up>@/+ ; @14-3-3&egr;<up>j2B10</up>@/@Df(3R)P14@
|eye discs.
SYN|l(3)2B10
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
TRN|FBti0004920 == P{lacW}14-3-3&egr;<up>j2B10</up>
|BDGP:l(3)j2B10
PHC|lethal | recessive
SYN|l(3)j2B10
}

REFDSR
{
RDID|FBrf0127025
|Brodsky et al.
|2000
PHI|In the absence of irradiation, @14-3-3&egr;<up>j2B10</up>@ animals have a
|normal external appearance, normal imaginal disc morphology and normal
|numbers of mitotic cells in the discs. After irradiation, the number
|of mitotic cells in @14-3-3&egr;<up>j2B10</up>@ discs is greater than the
|number found in irradiated wild-type discs.
SYN|14-3-3&egr;<up>j2b10</up>
}

REFDSR
{
RDID|FBrf0139721
|Su et al.
|2001
TRN|FBti0004920 == P{lacW}14-3-3&egr;<up>j2B10</up>
|BDGP:l(3)j2B10
PHC|mitotic | recessive
PHM|embryonic cycle 14
PHI|Embryos derived from a cross of @14-3-3&egr;<up>j2B10</up>@/@Df(3R)Cha7@ females
|to @14-3-3&egr;<up>j2B10</up>@/@Df(3R)Cha7@ males progress through the first
|13 mitotic cycles and cellularize without obvious defects. Cells enter
|mitosis 14 prematurely compared to wild type so that the division pattern
|of mutant embryos in gastrulation is more advanced than in wild-type
|embryos of similar gastrulation but is similar to wild-type embryos
|of more advanced gastrulation. The entire schedule of mitosis is advanced
|without disrupting the relative order of mitosis in different positions
|within the embryo. The rate of germ-band elongation is indistinguishable
|from wild type. Mutant embryos do not show a delay of entry into mitosis
|14 after irradiation, in contrast to wild-type embryos.
SYN|l(3)j2B10
}

REFDSR
{
RDID|FBrf0149093
|Johannes and Preiss
|2002
SYN|14-3-3-e<up>j2B10</up>
}

REFDSR
{
RDID|FBrf0151902
|Benton et al.
|2002
GIA2|nurse cell | ectopic | germ-line clone, enhanceable by @14-3-3&zgr;<up>P1188</up>@
|oocyte, enhanceable by @par-1<up>W3</up>@/+
|oocyte | germ-line clone with @14-3-3&zgr;<up>P1188</up>@
GIA|enhancer of oocyte phenotype of @par-1<up>W3</up>@
GIA2|oocyte | germ-line clone, enhanceable by @14-3-3&zgr;<up>P1188</up>@
GII|The penetrance of the oocyte to nurse cell transformation phenotype
|seen in @14-3-3&egr;<up>j2B10</up>@ germ-line clones (80% n=106) is dominantly
|enhanced to 100% by @14-3-3&zgr;<up>P1188</up>@.
|In @14-3-3&egr;<up>j2B10</up>@ mutant egg chambers that develop an oocyte,
|the penetrance of oocyte polarization defects in oocytes at stage 10
|is dominantly enhanced by @par-1<up>W3</up>@.
|Many @14-3-3&zgr;<up>P1188</up>@ germ-line clones in @14-3-3&egr;<up>j2B10</up>@/+
|females have defects in oocyte specification and polarization.
PHC|viable
|female sterile | recessive
|(with Df(3R)P14) viable
|(with Df(3R)P14) female sterile
PHM|oocyte
|nurse cell | ectopic
|(with Df(3R)P14) oocyte
|(with Df(3R)P14) nurse cell | ectopic
|oocyte | germ-line clone
|nurse cell | ectopic | germ-line clone
|microtubule organizing center
|oocyte
|oocyte
|centrosome
|microtubule
|oocyte
ALC|loss of function
PHI|In @14-3-3&egr;<up>j2B10</up>@ homozygotes or @14-3-3&egr;<up>j2B10</up>@/@Df(3R)P14@
|females most egg chambers lack a differentiated oocyte: both of the
|nurse cells with four ring canals develop as nurse cells. The same
|phenotype is caused by @14-3-3&egr;<up>j2B10</up>@ germ-line clones, but not
|@14-3-3&egr;<up>j2B10</up>@ somatic clones in the ovarian follicle cells.
|The microtubule organizing center which is visible in the posterior
|of the prospective oocyte as early as stage 2 in wild-type, is absent
|from @14-3-3&egr;<up>j2B10</up>@ mutants at this stage. The centrosomes do
|not undergo the anterior-to-posterior movement and eventually diffuse
|away as this cell exits meiosis and adopts a nurse cell fate. In @14-3-3&egr;<up>j2B10</up>@
|mutant egg chambers where oocyte specification does occur, marker analysis
|at stage 10 shows a partially penetrant oocyte polarization phenotype,
|although migration of the oocyte nucleus occurs normally. These oocytes
|also show defects in microtubule organization.
}

REFDSR
{
RDID|FBrf0159690
|Chen et al.
|2003
TRN|FBti0004920 == P{lacW}14-3-3&egr;<up>j2B10</up>
|BDGP:l(3)j2B10
}

REFDSR
{
RDID|FBrf0173208
|Benton and St. Johnston
|2003
GIA2|follicle cell with @14-3-3&zgr;<up>P1188</up>@/@14-3-3&zgr;<up>P1375</up>@
GII|Follicular epithelium morphogenesis is normal in @14-3-3&zgr;<up>P1188</up>@/@14-3-3&zgr;<up>P1375</up>@
|; @14-3-3&egr;<up>j2B10</up>@/+ egg chambers up to stage 4, but the follicle
|cells subsequently lose their regular cuboidal shape.
}

SK|FBst0012142
|y[1] w[*]; P{w[+mC]=lacW}14-3-3epsilon[j2B10]/TM3, Sb[1]
}

ALESR
{
ASYM|14-3-3&egr;<up>PL00784</up>
SYN|l(3)PL00784
ID|FBal0148516
PHC|lethal | embryonic | maternal effect | germ-line clone
PHM|embryo | maternal effect | germ-line clone
PHI|@14-3-3&egr;<up>PL00784</up>@ germ-line clones produce embryos that die before
|they produce a larval cuticle and appear as 'empty eggs'.
REF|FBrf0159706
REFDSR
{
RDID|FBrf0159706
|Hacker et al.
|2003
MD|The @PBac{GAL4D,EYFP}@ insertion is in the first
|intron of @14-3-3&egr;@.
TRN|FBti0038117 == PBac{GAL4D,EYFP}14-3-3&egr;<up>PL00784</up>
MU|piggyBac transposase
PHC|lethal | embryonic | maternal effect | germ-line clone
PHM|embryo | maternal effect | germ-line clone
PHI|@14-3-3&egr;<up>PL00784</up>@ germ-line clones produce embryos that die before
|they produce a larval cuticle and appear as 'empty eggs'.
SYN|l(3)PL00784
}

}

ALESR
{
ASYM|14-3-3&egr;<up>S-696</up>
SYN|14-3-3&egr;<up>E183K</up>
|SR3-9<up>696</up>
ID|FBal0048994
REF|FBrf0151902
|FBrf0093395
|FBrf0087493
|FBrf0131405
REFDSR
{
RDID|FBrf0087493
|Karim et al.
|1996
MU|ethyl methanesulfonate
GIC|suppressor of visible phenotype of @Ras85D<up>V12.sev</up>@
|suppressor of @phl::tor<up>13D.hs.sev</up>@
|suppressor of @Ras85D::Src64B<up>V12.&Dgr;CAAX.sev</up>@
|enhancer of @Ras85D<up>N17.sev</up>@
|enhancer of lethal phenotype of @phl<up>12</up>@
|enhancer of visible phenotype of @phl<up>12</up>@
|enhancer of visible phenotype of @Dsor1<up>XS520</up>@
|enhancer of visible phenotype of @aop<up>S2382</up>@
GIA|suppressor of eye phenotype of @Ras85D<up>V12.sev</up>@
|enhancer of eye phenotype of @phl<up>12</up>@
|enhancer of eye phenotype of @Dsor1<up>XS520</up>@
|enhancer of eye phenotype of @aop<up>S2382</up>@
GII|Suppresses the rough eye phenotype of @Ras85D<up>V12.sev</up>@.
PHC|viable | poor
PHI|Homozygotes are subviable.
}

REFDSR
{
RDID|FBrf0093395
|Chang and Rubin
|1997
AFC|14-3-3&egr;<up>j2B10</up>
MD|Amino acid replacement: E183K.
MU|ethyl methanesulfonate
GIC|suppressor | dominant of @Ras85D<up>V12.sev</up>@
GIC2|lethal | dominant with @phl<up>12</up>@
GIC|suppressor | dominant of @phl::tor<up>13D.hs.sev</up>@
GII|@14-3-3&egr;<up>S-696</up>@ does not show any dominant interaction with @aop<up>yan-1</up>@
|or @phyl<up>hs.sev</up>@.
PHC|lethal | recessive | partially
|(with 14-3-3&egr;<up>j2B10</up>) visible
PHM|(with Df(3R)P14) ommatidium
|(with 14-3-3&egr;<up>j2B10</up>) eye
|(with 14-3-3&egr;<up>j2B10</up>) photoreceptor cell
|(with 14-3-3&egr;<up>j2B10</up>) ommatidium
|ommatidium
|photoreceptor cell
|posterior crossvein
PHI|62.5% of ommatidia are normal in homozygous escapers, with the remaining
|ommatidia lacking some photoreceptor cells, and 69.1% of ommatidia
|are normal in @14-3-3&egr;<up>S-696</up>@/@Df(3R)P14@ flies. Homozygous escapers
|often have gaps in the posterior crossveins of the wings.
|@14-3-3&egr;<up>S-696</up>@/@14-3-3&egr;<up>j2B10</up>@ flies have rough eyes and
|a low penetrance of missing photoreceptors in the ommatidia.
SYN|14-3-3&egr;<up>E183K</up>
|SR3-9<up>696</up>
}

REFDSR
{
RDID|FBrf0151902
|Benton et al.
|2002
PHM|oocyte
ALC|antimorph
PHI|@14-3-3&egr;<up>S-696</up>@ mutant females have oocyte determintaion and polarity
|defects with a much higher penetrance than @14-3-3&egr;<up>j2B10</up>@, suggesting
|that this allele is antimorphic (dominant negative).
SYN|14-3-3&egr;<up>E183K</up>
}

SK|FBst0006565
|14-3-3epsilon[S-696]/TM3, P{ry[+t7.2]=sevRas1.V12}FK2, Sb[1]
}

ALESR
{
ASYM|14-3-3&egr;<up>S-1259</up>
SYN|14-3-3&egr;<up>F199Y</up>
|SR3-9<up>1259</up>
ID|FBal0048993
REF|FBrf0151902
|FBrf0093395
|FBrf0087493
REFDSR
{
RDID|FBrf0087493
|Karim et al.
|1996
MU|ethyl methanesulfonate
GIC|suppressor of visible phenotype of @Ras85D<up>V12.sev</up>@
|suppressor of @phl::tor<up>13D.hs.sev</up>@
|suppressor of @Ras85D::Src64B<up>V12.&Dgr;CAAX.sev</up>@
|enhancer of lethal phenotype of @phl<up>12</up>@
|enhancer of visible phenotype of @phl<up>12</up>@
|enhancer of @Ras85D<up>N17.sev</up>@
|enhancer of visible phenotype of @Dsor1<up>XS520</up>@
|enhancer of visible phenotype of @aop<up>S2382</up>@
|suppressor | dominant of @Ras85D<up>V12.sev</up>@
GIA|suppressor of eye phenotype of @Ras85D<up>V12.sev</up>@
|enhancer of eye phenotype of @phl<up>12</up>@
|enhancer of eye phenotype of @Dsor1<up>XS520</up>@
|enhancer of eye phenotype of @aop<up>S2382</up>@
GII|Suppresses the rough eye phenotype of @Ras85D<up>V12.sev</up>@.
PHC|viable | poor
PHI|Homozygotes are subviable.
}

REFDSR
{
RDID|FBrf0093395
|Chang and Rubin
|1997
MD|Amino acid replacement: F199Y.
MU|ethyl methanesulfonate
GIC|suppressor | dominant of @Ras85D<up>V12.sev</up>@
GIC2|lethal | dominant with @phl<up>12</up>@
PHC|viable
|fertile
PHI|Homozygotes have no detectable phenotype in a wild-type background.
SYN|14-3-3&egr;<up>F199Y</up>
|SR3-9<up>1259</up>
}

REFDSR
{
RDID|FBrf0151902
|Benton et al.
|2002
GIA2|oocyte | germ-line clone with @14-3-3&zgr;<up>P1188</up>@
GII|Many @14-3-3&zgr;<up>P1188</up>@ germ-line clones in @14-3-3&egr;<up>S-1259</up>@/+
|females have defects in oocyte specification.
SYN|14-3-3&egr;<up>F199Y</up>
}

}

ALESR
{
ASYM|14-3-3&egr;<up>Scer\UAS.cCa</up>
ID|FBal0148515
PHI|When @14-3-3&egr;<up>Scer\UAS.cCa</up>@ is driven by @Scer\GAL4<up>GMR.PF</up>@ no
|deleterious effects are seen.
REF|FBrf0159690
REFDSR
{
RDID|FBrf0159690
|Chen et al.
|2003
NAM|Saccharomyces cerevisiae UAS construct a of Chen
MD|@Scer\UAS@ sequences drive expression of @14-3-3&egr;@.
CNS|FBtp0017453 == P{UAS-14-3-3&egr;.C}
GIC2|lethal with @Hsap\ATX1<up>82Q.Scer\UAS</up>@
|lethal with @Hsap\ATX1<up>82Q.Scer\UAS</up>@, @Scer\GAL4<up>GMR.PF</up>@
|lethal with @Hsap\ATX1<up>82Q.Scer\UAS</up>@
|lethal with @Hsap\ATX1<up>82Q.Scer\UAS</up>@, @Scer\GAL4<up>GMR.PF</up>@
GIA|enhancer of eye phenotype of @Hsap\ATX1<up>82Q.Scer\UAS</up>@, @Scer\GAL4<up>GMR.PF</up>@
|enhancer of retina phenotype of @Hsap\ATX1<up>82Q.Scer\UAS</up>@, @Scer\GAL4<up>GMR.PF</up>@
|enhancer of rhabdomere phenotype of @Hsap\ATX1<up>82Q.Scer\UAS</up>@, @Scer\GAL4<up>GMR.PF</up>@
GII|The addition of @14-3-3&egr;<up>Scer\UAS.cCa</up>@ enhances the eye phenotypes
|seen in @Hsap\ATX1<up>82Q.Scer\UAS</up>@, @Scer\GAL4<up>GMR.PF</up>@ animals alone.
|They have profoundly disordered ommatidia, a thin and disorganized
|retina layer, and grossly abnormal rhabdomeres.
PHI|When @14-3-3&egr;<up>Scer\UAS.cCa</up>@ is driven by @Scer\GAL4<up>GMR.PF</up>@ no
|deleterious effects are seen.
}

}

ALESR
{
ASYM|14-3-3&egr;<up>unspecified</up>
ID|FBal0121020
PHC|lethal | recessive
REF|FBrf0131405
REFDSR
{
RDID|FBrf0131405
|Therrien et al.
|2000
GIA|enhancer | dominant of eye phenotype of @ksr::tor<up>&Dgr;Nksr.hs.sev</up>@
|suppressor | dominant of eye phenotype of @Ras85D<up>V12.sev</up>@
GIC|enhancer | dominant of lethal phenotype of @phl<up>12</up>@
|enhancer | dominant of visible phenotype of @ksr::tor<up>&Dgr;Nksr.hs.sev</up>@
|suppressor | dominant of visible phenotype of @Ras85D<up>V12.sev</up>@
PHC|lethal | recessive
}

}

ALESR
{
ASYM|14-3-3&egr;<up>+</up>
ID|FBal0079281
CLA|wild-type generic
REF|FBrf0105495
}

SK|FBst0006565
|14-3-3epsilon[S-696]/TM3, P{ry[+t7.2]=sevRas1.V12}FK2, Sb[1]
|FBst0102382
|P{EP}14-3-3epsilon[EP3423]
|FBst0103552
|P{EP}14-3-3epsilon[EP3578]
|FBst0017126
|w[1118]; P{w[+mC]=EP}14-3-3epsilon[EP3423]
|FBst0017142
|w[1118]; P{w[+mC]=EP}14-3-3epsilon[EP3578]/TM6B, Tb[1]
|FBst0012142
|y[1] w[*]; P{w[+mC]=lacW}14-3-3epsilon[j2B10]/TM3, Sb[1]
SKC|6
}
# EOR
GENR
{
RETE|ID 1 FBgn0004907	CLA 1 Gene	GSYM 1 14-3-3&zgr;	DT 1 25 Dec 04	RESZ 68867	PDOM 1 INTERPRO:IPR000308 == 14-3-3 protein	PTD 1	DBA 42	FNC 11 Ras protein signal transduction	CEL 2 nucleus	CLOC 1 46E6--8	ALESR 31	SK 2	REF 82	
GSYM|14-3-3&zgr;
PTD
ARGS
DT|25 Dec 04
ID|FBgn0004907
UAB|Deficiency: Df(2R)stan1 (inferred from cytology)
|Duplication: Dp(2;2)Y3b (inferred from cytology)
SYN|CG17870
|CG17870
|549
|2G1
|5.11
|leonardo
|leo: leonardo
|D14-3-3&zgr;
|K
|14-3-3
|14-3-3zeta
|Leonardo-13-3-3
|Complementation group K
|leonardo 14-3-3
|4-3-3 zeta
|par-5
|Par-5
|l(2)46CFe
|l(2)46Ee
|D14-3-3: D14 3 3 protein
|l(2)07103
|BEST:GH05075
|leo
|D14 3 3 protein
ID2|FBgn0010635
|FBgn0019723
|FBgn0023038
|FBgn0046306
|FBgn0064146
CLOC|46E6--8
|Limits computationally determined from genome sequence between @P{lacW}Adam<up>k13906</up>@/@P{EP}Pka-R2<up>EP2162</up>@ and @P{PZ}14-3-3&zgr;<up>07103</up>@
CYC|Experimentally determined: 46C8--F6, 46E, 46E--F, 46E4--8
FNC|Ras protein signal transduction ; GO:0007265
|cell proliferation ; GO:0008283
|chromosome segregation ; GO:0007059
|learning and/or memory ; GO:0007611
|maintenance of oocyte identity (sensu Insecta) ; GO:0016350
|mitotic cell cycle, embryonic ; GO:0045448
|olfactory learning ; GO:0008355
|oocyte microtubule cytoskeleton polarization (sensu Insecta) ; GO:0048129
|photoreceptor differentiation (sensu Endopterygota) ; GO:0007467
|regulation of cell cycle ; GO:0000074
|tryptophan hydroxylase activation ; GO:0006588
CEL|nucleus ; GO:0005634
|ring canal (sensu Insecta) ; GO:0045172
PDOM|IPR000308 == 14-3-3 protein
ENZ|protein kinase C inhibitor activity ; GO:0008426 | non-traceable author statement
|transcription regulator activity ; GO:0030528 | inferred from electronic annotation
|transcription regulator activity ; GO:0030528
|protein binding ; GO:0005515
|protein binding ; GO:0005515 | inferred from physical interaction with FLYBASE:Slob; FB:FBgn0024290
|diacylglycerol-activated phospholipid-dependent protein kinase C inhibitor activity ; GO:0004863
|protein kinase C inhibitor activity ; GO:0008426
|tryptophan hydroxylase activator activity ; GO:0016483
|diacylglycerol-activated phospholipid-dependent protein kinase C inhibitor activity ; GO:0004863 | inferred from sequence similarity with UniProt:P35215
|tryptophan hydroxylase activator activity ; GO:0016483 | inferred from sequence similarity with UniProt:P35215
|protein domain specific binding ; GO:0019904
|protein domain specific binding ; GO:0019904 | inferred from electronic annotation
DBA|NA:AA538817
|BDGP-DGC:LD18434
|NA:AC005469
|BDGP:DS05181
|NA:AC005974
|BDGP:DS05181
|NA:AE003831
|PA:AAM71060
|PA:AAM71061
|PA:AAF58843
|PA:AAM71062
|PA:AAF58842
|PA:AAS64884
|PA:AAM71063
|PA:AAM71064
|NA:AI064611
|BDGP:GH05075.3prime
|NA:AQ025662
|BDGP:l(2)07103
|NA:AW942482
|BDGP-DGC:LD18434
|NA:AY095521
|PA:AAM12253
|BDGP-DGC:LD18434
|NA:BH840513
|BDGP:KG02642
|NA:BI564632
|BDGP-DGC:RH61958
|NA:BI629143
|BDGP-DGC:RH57960
|NA:BT001855
|PA:AAN71617
|BDGP-DGC:RH61958
|NA:CC060506
|NA:CL632153
|NA:M77518
|PA:AAA28324
|NA:Y12573
|PA:CAA73153
|PA:CAA73152
|NA:Z32177
|dbSTS:4728
PAC|PIR:JC1122
|UniProt_Swiss_Prot:P29310
|UniProt_TrEMBL:Q8IGB9
|UniProt_TrEMBL:Q8MKV5
|UniProt_TrEMBL:Q8SWR6
ASQ|FBan0017870
REV|FBrf0158832
|FBrf0137068
|FBrf0127283
REF
{
REFM|FBrf0093395
|Chang and Rubin
|1997
|-1
REFM|FBrf0159690
|Chen et al.
|2003
|0
REFM|FBrf0173208
|Benton and St. Johnston
|2003
|-1
REFM|FBrf0102616
|Connolly and Tully
|1998
|2
REFM|FBrf0101184
|Hermon et al.
|1998
|1
REFM|FBrf0084992
|Edwards and Wasserman
|1996
|1
REFM|FBrf0178762
|Rana
|2004.7.8
|9
REFM|FBrf0102121
|Broadie
|1998
|2
REFM|FBrf0101416
|Amanai et al.
|1998
|1
REFM|FBrf0056086
|Swanson and Ganguly
|1992
|0
REFM|FBrf0057515
|Ganguly et al.
|1992
|0
REFM|FBrf0179660
|Jaramillo et al.
|2004
|1
REFM|FBrf0173651
|Grammenoudi et al.
|2004
|1
REFM|FBrf0126651
|Ashburner
|1999.11
|9
REFM|FBrf0151902
|Benton et al.
|2002
|-1
REFM|FBrf0145821
|Acevedo and Skoulakis
|2002
|1
REFM|FBrf0099136
|Broadie et al.
|1997
|1
REFM|FBrf0133630
|Purdy et al.
|2001
|1
REFM|FBrf0145131
|Goldstein et al.
|2001
|-1
REFM|FBrf0096484
|Tully et al.
|1996
|2
REFM|FBrf0134535
|Zars
|2000
|2
REFM|FBrf0147137
|Brody et al.
|2002
|0
REFM|FBrf0099525
|Skoulakis et al.
|1997
|1
REFM|FBrf0090801
|Skoulakis and Davis
|1996
|0
REFM|FBrf0129944
|Li et al.
|2000
|0
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
REFM|FBrf0058506
|McConnell and Hodges
|1993
|9
REFM|FBrf0159674
|Whitfield et al.
|2002
|9
REFM|FBrf0108310
|Zhou et al.
|1999
|0
REFM|FBrf0139731
|Philip et al.
|2001
|-1
REFM|FBrf0159020
|Zhou et al.
|2003
|0
REFM|FBrf0055263
|Swanson and Ganguly
|1992
|1
REFM|FBrf0178744
|Goldstein
|2004.3.15
|9
REFM|FBrf0083714
|Meister and Braun
|1995.10
|9
REFM|FBrf0137492
|Oliver
|2001.8.16
|9
REFM|FBrf0100355
|Grotewiel et al.
|1998
|0
REFM|FBrf0141665
|Sokolowski
|2001
|2
REFM|FBrf0139721
|Su et al.
|2001
|0
REFM|FBrf0104946
|FlyBase
|1996-
|9
REFM|FBrf0093851
|Mlodzik
|1997.5.10
|9
REFM|FBrf0110590
|Prokop
|1999
|2
REFM|FBrf0092060
|Amanai et al.
|1997
|1
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
REFM|FBrf0123915
|Swiss-Prot Project Members
|1992.12.1
|9
REFM|FBrf0089671
|Han et al.
|1996
|0
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
|9
REFM|FBrf0098203
|Broadie et al.
|1997
|-1
REFM|FBrf0130073
|Sekelsky et al.
|2000
|0
REFM|FBrf0132177
|Gene Disruption Project members
|2001-
|9
REFM|FBrf0099365
|Li et al.
|1997
|-1
REFM|FBrf0126031
|Johnson Hamlet and Perkins
|2000
|1
REFM|FBrf0101895
|Dubnau and Tully
|1998
|2
REFM|FBrf0099854
|Belvin and Yin
|1997
|2
REFM|FBrf0151992
|Jauch et al.
|2002
|0
REFM|FBrf0107641
|Casci et al.
|1999
|0
REFM|FBrf0085952
|Skoulakis and Davis
|1996
|1
REFM|FBrf0111489
|Spradling et al.
|1999
|-1
REFM|FBrf0085951
|Skoulakis and Davis
|1996
|1
REFM|FBrf0093549
|Kockel et al.
|1997
|-1
REFM|FBrf0079774
|Skoulakis
|1995
|9
REFM|FBrf0111327
|Baek and Lee
|1999
|2
REFM|FBrf0167437
|Brembs
|2003
|2
REFM|FBrf0084657
|Amanai and Shearn
|1996
|1
REFM|FBrf0079419
|Skoulakis and Davis
|1995
|1
REFM|FBrf0127283
|Raabe
|2000
|2
REFM|FBrf0076706
|Currie and Sullivan
|1994
|0
REFM|FBrf0092345
|Li et al.
|1997
|1
REFM|FBrf0099843
|Isaksson et al.
|1997
|0
REFM|FBrf0158996
|Li and Li
|2003
|-1
REFM|FBrf0107534
|Zhang et al.
|1999
|-1
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0158832
|Ahringer
|2003
|2
REFM|FBrf0103626
|Amanai et al.
|1998
|1
REFM|FBrf0133552
|Skoulakis and Philip
|2001
|1
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0174700
|Janody et al.
|2004
|0
REFM|FBrf0098932
|Anonymous
|1997
|2
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0104620
|Rommel and Hafen
|1998
|2
REFM|FBrf0137068
|Davis
|2001
|2
REFM|FBrf0095439
|Kockel et al.
|1997
|0
}

REFDSR
{
RDID|FBrf0037868
|Levy et al.
|1982
CLOC|46E (determined by in situ hybridization)
PHP|Identified as a cDNA clone that is expressed at a low frequency in
|the body but abundantly in the head of the adult.
SYN|549
}

REFDSR
{
RDID|FBrf0037869
|Levy and Manning
|1982
PHP|Developmental expression pattern of the cDNA clone is examined.
SYN|549
}

REFDSR
{
RDID|FBrf0050680
|Palazzolo et al.
|1989
PHP|Identified as a cDNA clone that is expressed exclusively or predominantly
|in the adult visual system.
SYN|unnamed
}

REFDSR
{
RDID|FBrf0052826
|Hyde et al.
|1990
CLOC|46E (determined by in situ hybridization)
PHP|Identified as a cDNA clone that is expressed exclusively or predominantly
|in the adult visual system.
SYN|2G1
|549
}

REFDSR
{
RDID|FBrf0056086
|Swanson and Ganguly
|1992
CLOC|46E (determined by in situ hybridization)
PHP|D14-3-3 has been characterized: gene expression is developmentally
|regulated and predominantly expressed in the neural tissues of the
|fly.
}

REFDSR
{
RDID|FBrf0057515
|Ganguly et al.
|1992
SYN|549
}

REFDSR
{
RDID|FBrf0058506
|McConnell and Hodges
|1993
PHP|The alternate 5' end of @Egfr@ reported by Schejter et al. (Cell 46:
|1091--1101) is a cloning artefact and is actually from D14-3-3 of Swanson
|and Ganguly (Gene 113: 183--190).
}

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
CLOC|46E4--8
LOI|14-3-3&zgr;<up>07103</up>
MD|Identified with: D1325
BMD|Df(2R)X1
BMDD|Df(2R)12
BMDD|Df(2R)X3
}

REFDSR
{
RDID|FBrf0076706
|Currie and Sullivan
|1994
SYN|5.11
}

REFDSR
{
RDID|FBrf0079774
|Skoulakis
|1995
CLOC|46E--F (determined by in situ hybridization)
}

REFDSR
{
RDID|FBrf0085951
|Skoulakis and Davis
|1996
SYN|leonardo
}

REFDSR
{
RDID|FBrf0085952
|Skoulakis and Davis
|1996
SYN|leonardo
}

REFDSR
{
RDID|FBrf0089671
|Han et al.
|1996
SYN|unnamed
}

REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
CLOC|46E (determined by in situ hybridization)
LOI|14-3-3&zgr;<up>P1.3H</up>
|14-3-3&zgr;<up>P1188</up>
|14-3-3&zgr;<up>P1375</up>
PHP|@14-3-3&zgr;@ has a biological role in mushroom body-mediated learning and
|memory processes.
}

REFDSR
{
RDID|FBrf0092060
|Amanai et al.
|1997
SYN|leo
}

REFDSR
{
RDID|FBrf0092792
|Goldstein et al.
|1993
CLOC|46C8--F6
CYC|Complementation data from unspecified deficiency chromosomes.
OTH|Complementation group identified in an EMS and DEB screen to isolate
|deficiencies that uncover @Jra@.
SYN|unnamed
}

REFDSR
{
RDID|FBrf0093395
|Chang and Rubin
|1997
WTI|14-3-3&egr; (data from @14-3-3&zgr;<up>2.3</up>@, @14-3-3&zgr;<up>P2355</up>@, @14-3-3&zgr;<up>X1</up>@)
SYN|leo
}

REFDSR
{
RDID|FBrf0093549
|Kockel et al.
|1997
PHP|Genetic studies indicate that @14-3-3&zgr;@ acts downstream of @Ras85D@
|and upstream of @phl@ in the developing eye disc.
SYN|D14-3-3&zgr;
}

REFDSR
{
RDID|FBrf0095439
|Kockel et al.
|1997
BMD|Df(2R)E73
}

REFDSR
{
RDID|FBrf0098203
|Broadie et al.
|1997
WT|@14-3-3&zgr;@ may function in the activity-dependent regulation of synaptic
|vesicle dynamics to control the pool of releaseable transmitter vesicles
|at presynaptic fusion sites.
OTH|@14-3-3&zgr;@ is strongly and specifically expressed in the presynaptic
|boutons of the neuro muscular junction.
PHP|In mutants the basic processes of synaptogenesis and excitation-secretion
|coupling are not perturbed, but properties of synaptic modulation such
|as transmission augmentation, high frequency transmission fidelity
|and post-tetanic potentiation (PTP) are strongly impaired.
SYN|leo
}

REFDSR
{
RDID|FBrf0098753
|Carney et al.
|1997
BMD|Df(2R)X1
BMDD|Df(2R)12
BMDD|Df(2R)X3
SYN|K: Complementation group K
|K
}

REFDSR
{
RDID|FBrf0099136
|Broadie et al.
|1997
SYN|leonardo
}

REFDSR
{
RDID|FBrf0099365
|Li et al.
|1997
WTI|faf
|tor (data from @14-3-3&zgr;<up>hs.PL</up>@)
SYN|leo
}

REFDSR
{
RDID|FBrf0099525
|Skoulakis et al.
|1997
SYN|leo
}

REFDSR
{
RDID|FBrf0099843
|Isaksson et al.
|1997
WTI|faf (data from @14-3-3&zgr;<up>E16</up>@)
}

REFDSR
{
RDID|FBrf0101184
|Hermon et al.
|1998
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0101416
|Amanai et al.
|1998
SYN|leo
}

REFDSR
{
RDID|FBrf0101626
|Skoulakis
|1998
SYN|14-3-3
|leonardo
}

REFDSR
{
RDID|FBrf0102121
|Broadie
|1998
SYN|leo
}

REFDSR
{
RDID|FBrf0102616
|Connolly and Tully
|1998
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0104620
|Rommel and Hafen
|1998
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ENZ|diacylglycerol-activated phospholipid-dependent protein kinase C inhibitor activity ; GO:0004863 | inferred from sequence similarity with UniProt:P35215
|tryptophan hydroxylase activator activity ; GO:0016483 | inferred from sequence similarity with UniProt:P35215
FNC|Ras protein signal transduction ; GO:0007265 | inferred from sequence similarity with SGD_LOCUS:BMH2; SGD:S0002506
|tryptophan hydroxylase activation ; GO:0006588 | inferred from sequence similarity with UniProt:P35215
MD|Maps to clone: DS05181
GPD|14-3-3-protein
}

REFDSR
{
RDID|FBrf0107534
|Zhang et al.
|1999
WTI|Src42A (data from @14-3-3&zgr;<up>07103</up>@)
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0107641
|Casci et al.
|1999
SYN|leo
}

REFDSR
{
RDID|FBrf0108310
|Zhou et al.
|1999
ENZ|protein binding ; GO:0005515 | inferred from physical interaction with FLYBASE:Slob; FB:FBgn0024290
MD|@14-3-3&zgr;@ can interact with and modulate @slo@ via @Slob@. The
|binding between @14-3-3&zgr;@ and @Slob@ is regulated by calcium/calmodulin-dependent
|kinase II phosphorylation.
}

REFDSR
{
RDID|FBrf0110590
|Prokop
|1999
SYN|leo
}

REFDSR
{
RDID|FBrf0111327
|Baek and Lee
|1999
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
CLOC|46E4--8 (determined by in situ hybridization)
LOI|14-3-3&zgr;<up>07103</up>
BMD|Df(2R)X1
BMDD|Df(2R)12
BMDD|Df(2R)X3
SYN|14-3-3zeta
}

REFDSR
{
RDID|FBrf0123915
|Swiss-Prot Project Members
|1992.12.1
FNC|Ras protein signal transduction ; GO:0007265 | non-traceable author statement
|cell proliferation ; GO:0008283 | non-traceable author statement
|photoreceptor differentiation (sensu Endopterygota) ; GO:0007467 | non-traceable author statement
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: LD18434 (BDGP-DGC)
|Identified with: RH61958 (BDGP-DGC)
|Identified with: RH57960 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0125895
|Tallman et al.
|2000
MD|Gene order: Overall orientation not stated: Pfk? 14-3-3&zgr;?
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0126031
|Johnson Hamlet and Perkins
|2000
SYN|leonardo
}

REFDSR
{
RDID|FBrf0127283
|Raabe
|2000
SYN|14-3-3
}

REFDSR
{
RDID|FBrf0129944
|Li et al.
|2000
SYN|leo
}

REFDSR
{
RDID|FBrf0133450
|Acevedo and Skoulakis
|2001
SYN|D14-3-3&zgr;
|leo
}

REFDSR
{
RDID|FBrf0133552
|Skoulakis and Philip
|2001
SYN|leo
}

REFDSR
{
RDID|FBrf0134535
|Zars
|2000
SYN|Leonardo-13-3-3
}

REFDSR
{
RDID|FBrf0137068
|Davis
|2001
SYN|leo
}

REFDSR
{
RDID|FBrf0137171
|Roman and Davis
|2001
FNC|olfactory learning ; GO:0008355 | non-traceable author statement
SYN|leo
}

REFDSR
{
RDID|FBrf0137492
|Oliver
|2001.8.16
MD|Identified with: GH05075.3prime
}

REFDSR
{
RDID|FBrf0139721
|Su et al.
|2001
FNC|chromosome segregation ; GO:0007059 | inferred from mutant phenotype
|mitotic cell cycle, embryonic ; GO:0045448 | inferred from mutant phenotype
CEL|nucleus ; GO:0005634 | non-traceable author statement
WT|@14-3-3&zgr;@ is required for normal chromosome separation during syncytial
|mitoses in the embryo.
}

REFDSR
{
RDID|FBrf0139731
|Philip et al.
|2001
FNC|learning and/or memory ; GO:0007611 | inferred from mutant phenotype
WT|Both isoforms of the @14-3-3&zgr;@ gene are required acutely (as opposed
|to developmentally) for normal learning and memory.
SYN|leo
}

REFDSR
{
RDID|FBrf0141665
|Sokolowski
|2001
ENZ|protein kinase C inhibitor activity ; GO:0008426 | non-traceable author statement
FNC|learning and/or memory ; GO:0007611 | non-traceable author statement
}

REFDSR
{
RDID|FBrf0141765
|Waddell and Quinn
|2001
SYN|leo: leonardo
}

REFDSR
{
RDID|FBrf0144737
|Morley and Montgomery
|2001
SYN|leonardo
|14-3-3
}

REFDSR
{
RDID|FBrf0145131
|Goldstein et al.
|2001
AM|Source for merge of: 14-3-3&zgr; l(2)46Ee
BMD|Df(2R)X1
BMDD|Ab(2R)55-20
BMDD|Ab(2R)89-22
BMDD|Df(2R)520
BMDD|Df(2R)61-25
BMDD|Df(2R)64-10
BMDD|Df(2R)71-81
BMDD|Df(2R)X3
BMDD|Df(2R)eve
BMDD|Df(2R)stan2
SYN|Complementation group K
|leonardo 14-3-3
}

REFDSR
{
RDID|FBrf0145821
|Acevedo and Skoulakis
|2002
SYN|leonardo
}

REFDSR
{
RDID|FBrf0147137
|Brody et al.
|2002
SYN|4-3-3 zeta
}

REFDSR
{
RDID|FBrf0151902
|Benton et al.
|2002
FNC|maintenance of oocyte identity (sensu Insecta) ; GO:0016350 | inferred from genetic interaction with FLYBASE:14-3-3&egr;; FB:FBgn0020238
|oocyte microtubule cytoskeleton polarization (sensu Insecta) ; GO:0048129 | inferred from genetic interaction with FLYBASE:14-3-3&egr;; FB:FBgn0020238
CEL|ring canal (sensu Insecta) ; GO:0045172 | inferred from direct assay
WTI|14-3-3&egr; (data from @14-3-3&zgr;<up>P1188</up>@)
SYN|leo
}

REFDSR
{
RDID|FBrf0151992
|Jauch et al.
|2002
SYN|leo
}

REFDSR
{
RDID|FBrf0155512
|Pellettieri and Seydoux
|2002
SYN|par-5
}

REFDSR
{
RDID|FBrf0158743
|Sathyanarayana et al.
|2003
SYN|leo
}

REFDSR
{
RDID|FBrf0158832
|Ahringer
|2003
SYN|leo
}

REFDSR
{
RDID|FBrf0158996
|Li and Li
|2003
WTI|tor (data from @14-3-3&zgr;<up>P1188</up>@)
SYN|leo
}

REFDSR
{
RDID|FBrf0159690
|Chen et al.
|2003
SYN|leo
}

REFDSR
{
RDID|FBrf0160472
|Davis et al.
|2003
SYN|leonardo
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
ENZ|transcription regulator activity ; GO:0030528 | inferred from electronic annotation
FNC|regulation of cell cycle ; GO:0000074 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
SYN|14-3-3zeta
}

REFDSR
{
RDID|FBrf0167337
|de Morais Guedes et al.
|2003
SYN|CG17870
}

REFDSR
{
RDID|FBrf0167437
|Brembs
|2003
SYN|leonardo
}

REFDSR
{
RDID|FBrf0173208
|Benton and St. Johnston
|2003
WTI|14-3-3&egr; (data from @14-3-3&zgr;<up>P1188</up>@, @14-3-3&zgr;<up>P1375</up>@)
SYN|leo
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|protein domain specific binding ; GO:0019904 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0174700
|Janody et al.
|2004
SYN|leonardo
}

REFDSR
{
RDID|FBrf0178744
|Goldstein
|2004.3.15
AM|Source for merge of: 14-3-3&zgr; l(2)46CFe
}

REFDSR
{
RDID|FBrf0178762
|Rana
|2004.7.8
AM|Source for merge of: 14-3-3&zgr; BEST:GH05075
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
SYN|leo
}

REFDSR
{
RDID|FBrf0179050
|Macara
|2004
SYN|14-3-3
|Par-5
}

REFDSR
{
RDID|FBrf0179255
|Huynh and St. Johnston
|2004
SYN|par-5
|14-3-3
}

REFDSR
{
RDID|FBrf0179660
|Jaramillo et al.
|2004
SYN|14-3-3
}

ALESR
{
ASYM|14-3-3&zgr;<up>07103</up>
SYN|l(2)-07103
|l(2)K07103
|l(2)k07103
|l(2)07103
|leo<up>07103</up>
|14-3-3<up>07103</up>
|l(2)07103<up>07103</up>
ID|FBal0008125
DBA|NA:Y12573
DIS|A. Spradling.
TRN|FBti0009122 == P{PZ}14-3-3&zgr;<up>07103</up>
|BDGP:l(2)07103
MU|P-element activity
REF|FBrf0067338
|FBrf0159690
|FBrf0145131
|FBrf0095439
|FBrf0093549
|FBrf0083714
|FBrf0093851
|FBrf0111489
|FBrf0107534
REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
OTH|Complements: @CCS<up>03221</up>@.
|Complements: @TER94<up>03775</up>@.
|Complements: @Pfk<up>06339</up>@.
|Complements: @l(2)k03610<up>k03610</up>@.
|Complements: @l(2)k03610<up>k03703</up>@.
|Complements: @l(2)k04308<up>k04308</up>@.
|Complements: @l(2)46Ed<up>k16104</up>@.
TRN|FBti0009122 == P{PZ}14-3-3&zgr;<up>07103</up>
|BDGP:l(2)07103
}

REFDSR
{
RDID|FBrf0093549
|Kockel et al.
|1997
AMSO|The lethality is rescued by @14-3-3&zgr;<up>arm.PK</up>@.
ARB|14-3-3&zgr;<up>arm.PK</up>
MD|@P{PZ}@ insertion into the first intron, 1633bp downstream of the splice
|donor site of exon I'.
TRN|FBti0009122 == P{PZ}14-3-3&zgr;<up>07103</up>
|BDGP:l(2)07103
MU|P-element activity
PHC|lethal | recessive
PHM|photoreceptor cell | somatic clone
ALC|hypomorph
PHI|Homozygous clones are recovered at low frequency and are small. Clones
|in the eye frequently lack some photoreceptor cells in the ommatidia.
SYN|l(2)-07103
}

REFDSR
{
RDID|FBrf0095439
|Kockel et al.
|1997
MD|@P{PZ}@ insertion in the 5' noncoding region.
OTH|Insertion is 2.8kb downstream of the @Jra@ transcription unit.
TRN|FBti0009122 == P{PZ}14-3-3&zgr;<up>07103</up>
|BDGP:l(2)07103
MU|P-element activity
}

REFDSR
{
RDID|FBrf0107534
|Zhang et al.
|1999
TRN|FBti0009122 == P{PZ}14-3-3&zgr;<up>07103</up>
|BDGP:l(2)07103
GIC|suppressor | dominant of @Src42A<up>Su(phl)1-1</up>@
GII|Dominantly suppresses the ability of @Src42A<up>Su(phl)1-1</up>@ to suppress
|the lethality of @phl<up>1</up>@/Y flies.
SYN|l(2)K07103
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
TRN|FBti0009122 == P{PZ}14-3-3&zgr;<up>07103</up>
|BDGP:l(2)07103
PHC|lethal | recessive
SYN|l(2)k07103
}

REFDSR
{
RDID|FBrf0145131
|Goldstein et al.
|2001
PHC|(with Df(2R)X1) lethal
SYN|l(2)07103
}

REFDSR
{
RDID|FBrf0159690
|Chen et al.
|2003
TRN|FBti0009122 == P{PZ}14-3-3&zgr;<up>07103</up>
|BDGP:l(2)07103
SYN|leo<up>07103</up>
}

SK|FBst0012335
|P{ry[+t7.2]=PZ}14-3-3zeta[07103] cn[1]/CyO; ry[506]
}

ALESR
{
ASYM|14-3-3&zgr;<up>12BL</up>
SYN|leo<up>12BL</up>
|14-3-3<up>12BL</up>
ID|FBal0065577
REF|FBrf0173208
|FBrf0098203
REFDSR
{
RDID|FBrf0098203
|Broadie et al.
|1997
MD|One partially deleted insertion in the first intron and the second
|partially deleted insertion resides in the original location.
PRG|14-3-3&zgr;<up>P1.3H</up>
MU|P-element activity
PHC|lethal | embryonic | recessive
|neurophysiology defective
PHM|epidermis | embryonic | lateral
|epidermis | embryonic | dorsal
ALC|loss of function
PHI|Homozygous embryos exhibit incomplete dorsal migration of the lateral
|epidermis and failure of dorsal epidermal closure. CNS and neuromusculature
|appear morphologically normal and the mutant embryos exhibit coordinated
|muscle movements similar to those observed in wild-type locomotion.
|Synaptogenesis at the neuromuscular junction (NMJ) is largely normal.
|Embryos also exhibit near normal physiological development and basal
|excitation-secretion function at the NMJ. The amplitude and frequency
|of endogenous excitatory junctional currents (EJCs) is reduced relative
|to wild type. This reduced function originates in a presynaptic defect,
|basal presynaptic function is mildly impaired. MEJC (miniature EJCs)
|amplitude is not altered. NMJ exhibits a transmission defect, the
|calcium dependence curve is shifted to the right indicating a higher
|level of external calcium is required to achieve the given level of
|secretion. Synaptic transmission fidelity and fatigue resistance properties
|are impaired. Short-term facilitation is strengthened but synaptic
|augmentation an potentiation are disrupted.
}

REFDSR
{
RDID|FBrf0173208
|Benton and St. Johnston
|2003
PHM|follicle cell | somatic clone
PHI|Homozygous follicle cell clones are recovered only at a low frequency,
|compared with sibling wild-type clones. Those mutant follicle cell
|clones that do survive have severe morphological defects.
SYN|leo<up>12BL</up>
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>2.3</up>
SYN|leo<up>2.3</up>
|leo<up>23</up>
|14-3-3<up>2.3</up>
ID|FBal0059634
REF|FBrf0093395
|FBrf0139731
|FBrf0090801
REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
MD|Deletion of the @P{lArB}@ insertion and portions of genomic sequence.
PRG|14-3-3&zgr;<up>P1375</up>
MU|&Dgr;2-3
PHC|(with 14-3-3&zgr;<up>P1375</up>) memory defective
|viable
|memory defective
PHI|Exhibits a decrement in the 3 to 240 minute memory performance. Transheterozygotes
|with @14-3-3&zgr;<up>P1375</up>@ show a highly significant reduction in 3 minute memory.
|Odor avoidance (octanol and benzaldehyde) is normal.
}

REFDSR
{
RDID|FBrf0093395
|Chang and Rubin
|1997
GIC2|visible | dominant with @14-3-3&egr;<up>j2B10</up>@/@14-3-3&egr;<up>j2B10</up>@
GIA2|ommatidium with @14-3-3&egr;<up>j2B10</up>@
|posterior crossvein with @14-3-3&egr;<up>j2B10</up>@
|eye with @14-3-3&egr;<up>j2B10</up>@
|photoreceptor cell with @14-3-3&egr;<up>j2B10</up>@
GII|@14-3-3&zgr;<up>2.3</up>@/+ @14-3-3&egr;<up>j2B10</up>@/@14-3-3&egr;<up>j2B10</up>@ flies have slightly
|roughened eyes, a low penetrance of missing photoreceptors and a gap
|in the posterior crossvein of the wings in more than 50% of cases.
SYN|leo<up>2.3</up>
}

REFDSR
{
RDID|FBrf0139731
|Philip et al.
|2001
ARB|14-3-3&zgr;<up>LI.15.hs</up>
|14-3-3&zgr;<up>LII.2.hs</up>
MD|Deletion in the intron between exons 1' and 2 of @14-3-3&zgr;@.
PHC|viable
|learning defective
|memory defective
PHI|No neuroanatomical aberrations are evident during development of the
|brain. Flies show reduced performance in a modified olfactory trap
|assay, using geraniol as the attractive odor, both immediately after
|training and 90 mins after training.
SYN|leo<up>23</up>
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>5-11</up>
SYN|5-11
|5.11
ID|FBal0157547
PHC|(with Df(2R)X1) lethal
REF|FBrf0145131
|FBrf0178744
REFDSR
{
RDID|FBrf0145131
|Goldstein et al.
|2001
MU|ethyl methanesulfonate \?
|diepoxybutane \?
|&ggr; ray \?
PHC|(with Df(2R)X1) lethal
SYN|5-11
}

REFDSR
{
RDID|FBrf0178744
|Goldstein
|2004.3.15
SYN|5.11
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>5.9</up>
SYN|14-3-3<up>5.9</up>
ID|FBal0059633
PHC|viable
|memory defective
PHI|Exhibits a decrement in the 3 minute memory performance.
|Odor avoidance (octanol and benzaldehyde) is normal.
REF|FBrf0090801
REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
MD|Deletion of the @P{lArB}@ insertion and portions of genomic sequence.
PRG|14-3-3&zgr;<up>P1375</up>
MU|&Dgr;2-3
PHC|viable
|memory defective
PHI|Exhibits a decrement in the 3 minute memory performance.
|Odor avoidance (octanol and benzaldehyde) is normal.
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>7B</up>
SYN|14-3-3<up>7B</up>
ID|FBal0059632
PHC|viable
|memory defective
PHI|Exhibits a decrement in the 3 minute memory performance.
|Odor avoidance (octanol and benzaldehyde) is normal.
REF|FBrf0090801
REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
MD|Deletion of a portion of the @P{lArB}@ insertion and genomic sequence.
PRG|14-3-3&zgr;<up>P1375</up>
TRN|FBti0012515 == P{?lArB}14-3-3&zgr;<up>7B</up>
MU|&Dgr;2-3
PHC|viable
|memory defective
PHI|Exhibits a decrement in the 3 minute memory performance.
|Odor avoidance (octanol and benzaldehyde) is normal.
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>7BL</up>
SYN|14-3-3<up>7BL</up>
ID|FBal0065576
PHC|lethal | embryonic | recessive
|neurophysiology defective
PHM|epidermis | embryonic | lateral
|epidermis | embryonic | dorsal
ALC|hypomorph
PHI|Homozygous embryos exhibit incomplete dorsal migration of the lateral
|epidermis and failure of dorsal epidermal closure. CNS and neuromusculature
|appear morphologically normal and the mutant embryos exhibit coordinated
|muscle movements similar to those observed in wild-type locomotion.
|Synaptogenesis at the neuromuscular junction (NMJ) is largely normal.
|Embryos also exhibit near normal physiological development and basal
|excitation-secretion function at the NMJ. The amplitude and frequency
|of endogenous excitatory junctional currents (EJCs) is reduced relative
|to wild type. This reduced function originates in a presynaptic defect,
|basal presynaptic function is mildly impaired. MEJC (miniature EJCs)
|amplitude is not altered. NMJ exhibits a transmission defect, the
|calcium dependence curve is shifted to the right indicating a higher
|level of external calcium is required to achieve the given level of
|secretion. Synaptic transmission fidelity and fatigue resistance properties
|are impaired. Short-term facilitation is strengthened but synaptic
|augmentation an potentiation are disrupted.
REF|FBrf0098203
REFDSR
{
RDID|FBrf0098203
|Broadie et al.
|1997
MD|Partially deleted insertion at the original location and a 500bp deletion
|in intron two.
PRG|14-3-3&zgr;<up>P1375</up>
MU|P-element activity
PHC|lethal | embryonic | recessive
|neurophysiology defective
PHM|epidermis | embryonic | lateral
|epidermis | embryonic | dorsal
ALC|hypomorph
PHI|Homozygous embryos exhibit incomplete dorsal migration of the lateral
|epidermis and failure of dorsal epidermal closure. CNS and neuromusculature
|appear morphologically normal and the mutant embryos exhibit coordinated
|muscle movements similar to those observed in wild-type locomotion.
|Synaptogenesis at the neuromuscular junction (NMJ) is largely normal.
|Embryos also exhibit near normal physiological development and basal
|excitation-secretion function at the NMJ. The amplitude and frequency
|of endogenous excitatory junctional currents (EJCs) is reduced relative
|to wild type. This reduced function originates in a presynaptic defect,
|basal presynaptic function is mildly impaired. MEJC (miniature EJCs)
|amplitude is not altered. NMJ exhibits a transmission defect, the
|calcium dependence curve is shifted to the right indicating a higher
|level of external calcium is required to achieve the given level of
|secretion. Synaptic transmission fidelity and fatigue resistance properties
|are impaired. Short-term facilitation is strengthened but synaptic
|augmentation an potentiation are disrupted.
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>9.8</up>
SYN|14-3-3<up>9.8</up>
ID|FBal0059631
PHC|viable
|memory defective
PHI|Exhibits a decrement in the 3 minute memory performance.
|Odor avoidance (octanol and benzaldehyde) is normal.
REF|FBrf0090801
REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
MD|Deletion of the @P{lArB}@ insertion and portions of genomic sequence.
PRG|14-3-3&zgr;<up>P1375</up>
MU|&Dgr;2-3
PHC|viable
|memory defective
PHI|Exhibits a decrement in the 3 minute memory performance.
|Odor avoidance (octanol and benzaldehyde) is normal.
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>E16</up>
SYN|E-16
|14-3-3<up>E16</up>
ID|FBal0060814
DBA|NA:Y12573
REF|FBrf0099843
|FBrf0093549
|FBrf0093851
REFDSR
{
RDID|FBrf0093549
|Kockel et al.
|1997
AMSO|The lethality is rescued by @14-3-3&zgr;<up>tKa</up>@ but not by @14-3-3&zgr;<up>arm.PK</up>@.
ANRB|14-3-3&zgr;<up>arm.PK</up>
ARB|14-3-3&zgr;<up>tKa</up>
ARG2|FBgn0004907.
MD|Imprecise excision of the @P{PZ}@ element, deleting 1957bp, including
|exons I and I'.
PRG|14-3-3&zgr;<up>07103</up>
MU|P-element activity
PHC|lethal | recessive
PHI|Homozygous clones are not recovered in a wild-type background or in
|flies carrying @Ras85D<up>V12.sev</up>@, but are recovered in flies carrying
|@phl::tor<up>12D.hs.sev</up>@.
SYN|E-16
}

REFDSR
{
RDID|FBrf0093851
|Mlodzik
|1997.5.10
PRG|14-3-3&zgr;<up>07103</up>
MU|P-element activity
}

REFDSR
{
RDID|FBrf0099843
|Isaksson et al.
|1997
GIA|suppressor | dominant of photoreceptor cell R1 | ectopic phenotype of @faf<up>BX4</up>@
|suppressor | dominant of photoreceptor cell R2 | ectopic phenotype of @faf<up>BX4</up>@
|suppressor | dominant of photoreceptor cell R3 | ectopic phenotype of @faf<up>BX4</up>@
|suppressor | dominant of photoreceptor cell R4 | ectopic phenotype of @faf<up>BX4</up>@
|suppressor | dominant of photoreceptor cell R5 | ectopic phenotype of @faf<up>BX4</up>@
|suppressor | dominant of photoreceptor cell R6 | ectopic phenotype of @faf<up>BX4</up>@
GII|The extra outer photoreceptor cell phenotype seen in @faf<up>BX4</up>@ homozygotes
|is dominantly suppressed by @14-3-3&zgr;<up>E16</up>@, with the average number
|of outer photoreceptor cells per ommatidium being reduced to 6.4.
PHC|lethal | recessive
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>E73</up>
SYN|14-3-3<up>E73</up>
ID|FBal0063650
REF|FBrf0095439
REFDSR
{
RDID|FBrf0095439
|Kockel et al.
|1997
MD|Deletion of the transcription start site and first exons.
PRG|14-3-3&zgr;<up>07103</up>
MU|&Dgr;2-3
ABA|FBab0027145 == Df(2R)E73
SYN|unnamed
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>EY03325</up>
ID|FBal0157546
REF|FBrf0104946
|FBrf0132177
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
AMIS|Separable from: @CG2269<up>EY03325</up>@.
TRN|FBti0038081 == P{EPgy2}14-3-3&zgr;<up>EY03325</up>
}

REFDSR
{
RDID|FBrf0132177
|Gene Disruption Project members
|2001-
TRN|FBti0038081 == P{EPgy2}14-3-3&zgr;<up>EY03325</up>
MU|P-element activity
}

SK|FBst0015902
|y[1] w[67c23]; P{w[+mC] y[+mDint2]=EPgy2}CG2269[EY03325] P{EPgy2}14-3-3zeta[EY03325]
}

ALESR
{
ASYM|14-3-3&zgr;<up>EY06147</up>
ID|FBal0162866
PHC|viable
|fertile
REF|FBrf0132177
REFDSR
{
RDID|FBrf0132177
|Gene Disruption Project members
|2001-
TRN|FBti0039931 == P{EPgy2}14-3-3&zgr;<up>EY06147</up>
PHC|viable
|fertile
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>KG02642</up>
ID|FBal0137676
REF|FBrf0132177
REFDSR
{
RDID|FBrf0132177
|Gene Disruption Project members
|2001-
TRN|FBti0023409 == P{SUPor-P}14-3-3&zgr;<up>KG02642</up>
|BDGP:KG02642
MU|P-element activity
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>P1188</up>
SYN|leo<up>P1188</up>
|P1188
|14-3-3<up>P1188</up>
ID|FBal0059629
REF|FBrf0173208
|FBrf0151902
|FBrf0098203
|FBrf0089671
|FBrf0158996
|FBrf0099365
|FBrf0129944
|FBrf0139731
|FBrf0090801
|FBrf0139721
REFDSR
{
RDID|FBrf0089671
|Han et al.
|1996
PRG|FBti0004638 == FBti0000841 == P{lArB}A4.1M2
TRN|FBti0009360 == P{lArB}14-3-3&zgr;<up>P1188</up>
MU|&Dgr;2-3
SYN|unnamed
}

REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
PRG|FBti0004638 == FBti0000841 == P{lArB}A4.1M2
TRN|FBti0009360 == P{lArB}14-3-3&zgr;<up>P1188</up>
MU|&Dgr;2-3
PHC|lethal | embryonic | recessive
PHI|Heterozygotes exhibit normal 3 minute memory performance.
|Odor avoidance (octanol and benzaldehyde) is normal.
SYN|unnamed
}

REFDSR
{
RDID|FBrf0098203
|Broadie et al.
|1997
MD|@P{lArB}@ insertion in the first intron.
TRN|FBti0009360 == P{lArB}14-3-3&zgr;<up>P1188</up>
PHC|lethal | recessive
|neurophysiology defective
ALC|hypomorph
PHI|Embryos do not exhibit a dorsal closure defect.
|The amplitude and frequency of endogenous excitatory junctional currents
|(EJCs) is reduced relative to wild type and the NMJ exhibits a transmission
|defect, the calcium dependence curve is shifted to the right indicating
|a higher level of external calcium is required to achieve the given
|level of secretion.
}

REFDSR
{
RDID|FBrf0099365
|Li et al.
|1997
PHM|embryonic/first instar larval cuticle | germ-line clone
|denticle belt | germ-line clone
|syncytial blastoderm embryo | germ-line clone
PHI|Embryos derived from homozygous female germline clones show a variable
|phenotype that is not significantly different whether or not the embryos
|contain a wild-type copy of @14-3-3&zgr;@ from the father. Approximately
|50% of the embryos do not develop cuticles, and the remainder develop
|cuticles with various segmentation defects including missing and/or
|fused denticle bands. The Filzkorper appear normal. Approximately
|50% of the embryos appear to stop development during the syncytial
|blastoderm stage, and contain many fewer nuclei compared to wild-type.
|Some of these nuclei appear fused.
|18% of embryos carrying @14-3-3&zgr;<up>hbNRE.RpII15</up>@ and derived from homozygous
|@14-3-3&zgr;<up>P1188</up>@ female germline clones have a wild-type anterior region
|but are missing all or part of the posterior region. 56% of these
|'anteriorly rescued' embryos have shortened Filzkorper.
SYN|leo<up>P1188</up>
}

REFDSR
{
RDID|FBrf0129944
|Li et al.
|2000
SYN|leo<up>P1188</up>
}

REFDSR
{
RDID|FBrf0139721
|Su et al.
|2001
TRN|FBti0009360 == P{lArB}14-3-3&zgr;<up>P1188</up>
PHC|mitotic | recessive | maternal effect
PHM|mitotic cycle | maternal effect
PHI|Homozygous embryos show no apparent defects in the timing of mitotic
|cycle 14 and show delayed mitosis after irradiation (as occurs in wild
|type).
|69 +/- 9% of mutant embryos derived from homozygous female germline
|clones fail to cellularize. 54/59 of the embryos have defects in cell
|division, including DNA bridges between telophase sister nuclei, asynchrony
|in division within a single embryo, free microtubule-organizing centers
|that are not associated with nuclei, loss of nuclei from the cortical
|monolayer of nuclei and larger than normal yolk DNA masses. Chromosome
|bridges interconnecting DNA masses are seen as early as telophase of
|the fourth embryonic mitosis. Mitotic spindles do appear to be formed
|in these embryos (as judged by the segregation of chromosome masses
|that are still linked by DNA bridges to opposite spindle poles), and
|attempts at the formation of mid-bodies are seen between segregating
|nuclei, despite the presence of chromosome bridges.
|Approximately 30% of embryos cellularize. These embryos have severe
|gastrulation defects.
SYN|P1188
}

REFDSR
{
RDID|FBrf0139731
|Philip et al.
|2001
ANRB|(with 14-3-3&zgr;<up>P1375</up>) 14-3-3&zgr;<up>LII.2.hs</up>
|(with 14-3-3&zgr;<up>P2335</up>) 14-3-3&zgr;<up>LII.2.hs</up>
|14-3-3&zgr;<up>LI.15.hs</up>
|14-3-3&zgr;<up>LII.2.hs</up>
APRB|(with 14-3-3&zgr;<up>P1375</up>) 14-3-3&zgr;<up>LI.15.hs</up>
|(with 14-3-3&zgr;<up>P2335</up>) 14-3-3&zgr;<up>LI.15.hs</up>
ARB|(with 14-3-3&zgr;<up>P1375</up>) 14-3-3&zgr;<up>LI.15.hs</up>
|(with 14-3-3&zgr;<up>P2335</up>) 14-3-3&zgr;<up>LI.15.hs</up>
MD|Insertion, in forward orientation, of @P{lArB}@ into the intron between
|exons 1' and 2 of @14-3-3&zgr;@.
TRN|FBti0009360 == P{lArB}14-3-3&zgr;<up>P1188</up>
PHC|lethal
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>P1375</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>P1375</up>) learning defective
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>, 14-3-3&zgr;<up>P1375</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>, 14-3-3&zgr;<up>P1375</up>) learning defective
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>P2335</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>P2335</up>) learning defective
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>, 14-3-3&zgr;<up>P2335</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>, 14-3-3&zgr;<up>P2335</up>) learning defective
PHI|Flies rescued from lethality by @14-3-3&zgr;<up>LI.15.hs</up>@ or @14-3-3&zgr;<up>LI.15.hs</up>@
|and @14-3-3&zgr;<up>LII.2.hs</up>@ show a 25-30% decrement in olfactory learning,
|comparable to that of (rescued) @14-3-3&zgr;<up>2.3</up>@. The restoration
|of learning by the transgenes decays back to mutant levels 60-70 hr
|later.
SYN|leo<up>P1188</up>
}

REFDSR
{
RDID|FBrf0151902
|Benton et al.
|2002
TRN|FBti0009360 == P{lArB}14-3-3&zgr;<up>P1188</up>
GIA2|oocyte | germ-line clone with @14-3-3&egr;<up>S-1259</up>@/+
|oocyte | germ-line clone with @14-3-3&egr;<up>j2B10</up>@/+
GIA|enhancer of nurse cell | ectopic | germ-line clone phenotype of @14-3-3&egr;<up>j2B10</up>@
|enhancer of oocyte | germ-line clone phenotype of @14-3-3&egr;<up>j2B10</up>@
GII|Many @14-3-3&zgr;<up>P1188</up>@ germ-line clones in @14-3-3&egr;<up>j2B10</up>@/+
|females have defects in oocyte specification and polarization.
|Many @14-3-3&zgr;<up>P1188</up>@ germ-line clones in @14-3-3&egr;<up>S-1259</up>@/+
|females have defects in oocyte specification.
|The penetrance of the oocyte to nurse cell transformation phenotype
|seen in @14-3-3&egr;<up>j2B10</up>@ germ-line clones (80% n=106) is dominantly
|enhanced to 100% by @14-3-3&zgr;<up>P1188</up>@.
PHC|lethal
PHI|Alleles or genotypes used: @14-3-3&zgr;<up>P1188</up>@ germ-line clones do not exhibit defects in oocyte specification or polarization.
SYN|leo<up>P1188</up>
}

REFDSR
{
RDID|FBrf0158996
|Li and Li
|2003
GIA|suppressor | maternal effect of embryonic/first instar larval cuticle | maternal effect phenotype of @tor<up>12D</up>@
SYN|leo<up>P1188</up>
}

REFDSR
{
RDID|FBrf0173208
|Benton and St. Johnston
|2003
GIA2|(with 14-3-3&zgr;<up>P1375</up>) follicle cell with @14-3-3&egr;<up>j2B10</up>@/+
GII|Follicular epithelium morphogenesis is normal in @14-3-3&zgr;<up>P1188</up>@/@14-3-3&zgr;<up>P1375</up>@
|; @14-3-3&egr;<up>j2B10</up>@/+ egg chambers up to stage 4, but the follicle
|cells subsequently lose their regular cuboidal shape.
PHM|follicle cell | somatic clone
PHI|Large homozygous follicle cell clones show dramatic defects in tissue
|organization, forming multilayers of morphologically abnormal cells
|that often fail to encapsulate germline cysts properly. Smaller homozygous
|follicle cell clones that arise after epithelium formation have milder
|and less penetrant defects in morphology and polarity.
SYN|leo<up>P1188</up>
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>P1375</up>
SYN|leo<up>P1375</up>
|14-3-3<up>P1375</up>
ID|FBal0059628
REF|FBrf0173208
|FBrf0098203
|FBrf0089671
|FBrf0139731
|FBrf0090801
REFDSR
{
RDID|FBrf0089671
|Han et al.
|1996
PRG|FBti0004638 == FBti0000841 == P{lArB}A4.1M2
TRN|FBti0009359 == P{lArB}14-3-3&zgr;<up>P1375</up>
MU|&Dgr;2-3
SYN|unnamed
}

REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
PRG|FBti0004638 == FBti0000841 == P{lArB}A4.1M2
TRN|FBti0009359 == P{lArB}14-3-3&zgr;<up>P1375</up>
MU|&Dgr;2-3
PHC|lethal | embryonic | recessive
|(with 14-3-3&zgr;<up>2.3</up>) memory defective
|(with 14-3-3&zgr;<up>X1</up>) memory defective
PHI|Heterozygotes exhibit normal 3 minute memory performance. Transheterozygotes
|with @14-3-3&zgr;<up>X1</up>@ or @14-3-3&zgr;<up>2.3</up>@ show a highly significant reduction in
|3 minute memory.
|Odor avoidance (octanol and benzaldehyde) is normal.
SYN|unnamed
}

REFDSR
{
RDID|FBrf0098203
|Broadie et al.
|1997
MD|@P{lArB}@ insertion in the first intron.
TRN|FBti0009359 == P{lArB}14-3-3&zgr;<up>P1375</up>
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0139731
|Philip et al.
|2001
ANRB|(with 14-3-3&zgr;<up>P1188</up>) 14-3-3&zgr;<up>LII.2.hs</up>
|(with 14-3-3&zgr;<up>P2335</up>) 14-3-3&zgr;<up>LII.2.hs</up>
APRB|(with 14-3-3&zgr;<up>P1188</up>) 14-3-3&zgr;<up>LI.15.hs</up>
|14-3-3&zgr;<up>LI.15.hs</up>
ARB|(with 14-3-3&zgr;<up>P1188</up>) 14-3-3&zgr;<up>LI.15.hs</up>
|(with 14-3-3&zgr;<up>P2335</up>) 14-3-3&zgr;<up>LI.15.hs</up>
|14-3-3&zgr;<up>LI.15.hs</up>
|14-3-3&zgr;<up>LII.2.hs</up>
MD|Insertion, in forward orientation, of @P{lArB}@ into the intron between
|exons 1' and 2 of @14-3-3&zgr;@.
TRN|FBti0009359 == P{lArB}14-3-3&zgr;<up>P1375</up>
PHC|lethal
|(with 14-3-3&zgr;<up>LI.15.hs</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>) learning defective
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>) learning defective
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>P1188</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>P1188</up>) learning defective
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>, 14-3-3&zgr;<up>P1188</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>, 14-3-3&zgr;<up>P1188</up>) learning defective
PHI|Flies rescued from lethality by @14-3-3&zgr;<up>LI.15.hs</up>@ or @14-3-3&zgr;<up>LI.15.hs</up>@
|and @14-3-3&zgr;<up>LII.2.hs</up>@ show a 25-30% decrement in olfactory learning,
|comparable to that of (rescued) @14-3-3&zgr;<up>2.3</up>@. The restoration
|of learning by the transgenes decays back to mutant levels 60-70 hr
|later.
SYN|leo<up>P1375</up>
}

REFDSR
{
RDID|FBrf0173208
|Benton and St. Johnston
|2003
GIA2|(with 14-3-3&zgr;<up>P1188</up>) follicle cell with @14-3-3&egr;<up>j2B10</up>@/+
GII|Follicular epithelium morphogenesis is normal in @14-3-3&zgr;<up>P1188</up>@/@14-3-3&zgr;<up>P1375</up>@
|; @14-3-3&egr;<up>j2B10</up>@/+ egg chambers up to stage 4, but the follicle
|cells subsequently lose their regular cuboidal shape.
SYN|leo<up>P1375</up>
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>P2335</up>
SYN|leo<up>P2335</up>
ID|FBal0134434
PHC|lethal
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>P1188</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>P1188</up>) learning defective
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>, 14-3-3&zgr;<up>P1188</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>, 14-3-3&zgr;<up>P1188</up>) learning defective
PHI|Flies rescued from lethality by @14-3-3&zgr;<up>LI.15.hs</up>@ or @14-3-3&zgr;<up>LI.15.hs</up>@
|and @14-3-3&zgr;<up>LII.2.hs</up>@ show a 25-30% decrement in olfactory learning,
|comparable to that of (rescued) @14-3-3&zgr;<up>2.3</up>@. The restoration
|of learning by the transgenes decays back to mutant levels 60-70 hr
|later.
REF|FBrf0139731
REFDSR
{
RDID|FBrf0139731
|Philip et al.
|2001
ANRB|(with 14-3-3&zgr;<up>P1188</up>) 14-3-3&zgr;<up>LII.2.hs</up>
|(with 14-3-3&zgr;<up>P1375</up>) 14-3-3&zgr;<up>LII.2.hs</up>
|14-3-3&zgr;<up>LI.15.hs</up>
|14-3-3&zgr;<up>LII.2.hs</up>
APRB|(with 14-3-3&zgr;<up>P1188</up>) 14-3-3&zgr;<up>LI.15.hs</up>
ARB|(with 14-3-3&zgr;<up>P1188</up>) 14-3-3&zgr;<up>LI.15.hs</up>
|(with 14-3-3&zgr;<up>P1375</up>) 14-3-3&zgr;<up>LI.15.hs</up>
MD|Insertion, in forward orientation, of @P{?}@ into the intron between
|exons 1' and 2 of @14-3-3&zgr;@.
TRN|FBti0023266 == P{?}14-3-3&zgr;<up>P2335</up>
MU|P-element activity
PHC|lethal
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>P1188</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>P1188</up>) learning defective
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>, 14-3-3&zgr;<up>P1188</up>) viable
|(with 14-3-3&zgr;<up>LI.15.hs</up>, 14-3-3&zgr;<up>LII.2.hs</up>, 14-3-3&zgr;<up>P1188</up>) learning defective
PHI|Flies rescued from lethality by @14-3-3&zgr;<up>LI.15.hs</up>@ or @14-3-3&zgr;<up>LI.15.hs</up>@
|and @14-3-3&zgr;<up>LII.2.hs</up>@ show a 25-30% decrement in olfactory learning,
|comparable to that of (rescued) @14-3-3&zgr;<up>2.3</up>@. The restoration
|of learning by the transgenes decays back to mutant levels 60-70 hr
|later.
SYN|leo<up>P2335</up>
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>P2355</up>
SYN|leo<up>P2355</up>
|14-3-3<up>P2355</up>
ID|FBal0062288
PHC|lethal | recessive
PHI|Heterozygosity for @14-3-3&zgr;<up>P2355</up>@ does not alter the @Ras85D<up>V12.sev</up>@
|phenotype.
REF|FBrf0093395
REFDSR
{
RDID|FBrf0093395
|Chang and Rubin
|1997
GIC2|lethal | dominant with @14-3-3&egr;<up>j2B10</up>@/@14-3-3&egr;<up>j2B10</up>@
PHC|lethal | recessive
PHI|Heterozygosity for @14-3-3&zgr;<up>P2355</up>@ does not alter the @Ras85D<up>V12.sev</up>@
|phenotype.
SYN|leo<up>P2355</up>
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>P1.3H</up>
SYN|14-3-3<up>P1.3H</up>
ID|FBal0059630
REF|FBrf0098203
|FBrf0090801
REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
MD|@P{lArB}@ insertion into the second intron.
OTH|Weak @14-3-3&zgr;@ mutation.
PRG|14-3-3&zgr;<up>P1375</up>
TRN|FBti0009381 == P{lArB}14-3-3&zgr;<up>P1.3H</up>
MU|&Dgr;2-3
PHC|viable
|memory defective
PHI|Exhibits a decrement in the 3 and 45 minute memory performance. Memory
|performance at 90 and 240 minutes is the same as controls.
|Odor avoidance (octanol and benzaldehyde) is normal.
}

REFDSR
{
RDID|FBrf0098203
|Broadie et al.
|1997
MD|Hop of the @P{lArB}@ insertion into intron 2.
PRG|14-3-3&zgr;<up>P1375</up>
TRN|FBti0009381 == P{lArB}14-3-3&zgr;<up>P1.3H</up>
MU|P-element activity
PHC|viable
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>R1</up>
SYN|14-3-3<up>R1</up>
ID|FBal0059627
PHC|viable
PHI|Normal memory performance over 3 to 240 minutes.
|Odor avoidance (octanol and benzaldehyde) is normal.
REF|FBrf0090801
REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
MD|Precise excision of the @P{lArB}@ insertion.
PRG|14-3-3&zgr;<up>P1375</up>
MU|&Dgr;2-3
PHC|viable
PHI|Normal memory performance over 3 to 240 minutes.
|Odor avoidance (octanol and benzaldehyde) is normal.
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>R2</up>
SYN|14-3-3<up>R2</up>
ID|FBal0059626
PHC|viable
PHI|Normal 3 minute memory performance.
|Odor avoidance (octanol and benzaldehyde) is normal.
REF|FBrf0090801
REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
MD|Precise excision of the @P{lArB}@ insertion.
PRG|14-3-3&zgr;<up>P1375</up>
MU|&Dgr;2-3
PHC|viable
PHI|Normal 3 minute memory performance.
|Odor avoidance (octanol and benzaldehyde) is normal.
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>unspecified</up>
ID|FBal0157545
REF|FBrf0179048
}

ALESR
{
ASYM|14-3-3&zgr;<up>X1</up>
SYN|leo<up>X.1</up>
|leo<up>X1</up>
|14-3-3<up>X1</up>
ID|FBal0059625
REF|FBrf0093395
|FBrf0139731
|FBrf0090801
REFDSR
{
RDID|FBrf0090801
|Skoulakis and Davis
|1996
MD|Deletion of the @P{lArB}@ insertion and portions of genomic sequence.
PRG|14-3-3&zgr;<up>P1375</up>
MU|&Dgr;2-3
PHC|(with 14-3-3&zgr;<up>P1375</up>) memory defective
|viable
|memory defective
PHI|Exhibits a decrement in the 3 minute memory performance. Transheterozygotes
|with @14-3-3&zgr;<up>P1375</up>@ show a highly significant reduction in 3 minute memory.
|Odor avoidance (octanol and benzaldehyde) is normal.
}

REFDSR
{
RDID|FBrf0093395
|Chang and Rubin
|1997
GIC2|visible | dominant with @14-3-3&egr;<up>j2B10</up>@/@14-3-3&egr;<up>j2B10</up>@
GIA2|ommatidium with @14-3-3&egr;<up>j2B10</up>@
|posterior crossvein with @14-3-3&egr;<up>j2B10</up>@
|eye with @14-3-3&egr;<up>j2B10</up>@
|photoreceptor cell with @14-3-3&egr;<up>j2B10</up>@
GII|@14-3-3&zgr;<up>X1</up>@/+ @14-3-3&egr;<up>j2B10</up>@/@14-3-3&egr;<up>j2B10</up>@ flies have slightly
|roughened eyes, a low penetrance of missing photoreceptors and a gap
|in the posterior crossvein of the wings in more than 50% of cases.
SYN|leo<up>X.1</up>
}

REFDSR
{
RDID|FBrf0139731
|Philip et al.
|2001
ARB|14-3-3&zgr;<up>LI.15.hs</up>
|14-3-3&zgr;<up>LII.2.hs</up>
MD|Deletion in the intron between exons 1' and 2 of @14-3-3&zgr;@.
PHC|viable
|learning defective
|memory defective
PHI|No neuroanatomical aberrations are evident during development of the
|brain. Flies show reduced performance in a modified olfactory trap
|assay, using geraniol as the attractive odor, both immediately after
|training and 90 mins after training.
SYN|leo<up>X1</up>
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>a.sev</up>
SYN|14-3-3<up>a.sev</up>
ID|FBal0062287
PHM|photoreceptor cell
PHI|Flies carrying @14-3-3&zgr;<up>a.sev</up>@ have a weakly penetrant loss of photoreceptor
|cell phenotype. The outer photoreceptor cells are more severely affected.
|Mode of assay: In transgenic Drosophila
REF|FBrf0093549
REFDSR
{
RDID|FBrf0093549
|Kockel et al.
|1997
NAM|antisense sevenless promoter construct
MD|Construct: A 1.0kb @14-3-3&zgr;@ cDNA fragment containing the complete open reading
|frame is expressed in the antisense orientation under the control of
|a @sev@ enhancer.
MU|in vitro construct | regulatory fusion
CNS|FBtp0008239 == P{sE.anti-14-3-3}
PHM|photoreceptor cell
PHI|Flies carrying @14-3-3&zgr;<up>a.sev</up>@ have a weakly penetrant loss of photoreceptor
|cell phenotype. The outer photoreceptor cells are more severely affected.
|Mode of assay: In transgenic Drosophila
SYN|unnamed
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>arm.PK</up>
SYN|14-3-3<up>arm.PK</up>
ID|FBal0062286
PHC|wild-type
PHI|Mode of assay: In transgenic Drosophila
REF|FBrf0093549
REFDSR
{
RDID|FBrf0093549
|Kockel et al.
|1997
NAM|armadillo promoter construct of Kockel
ARS|14-3-3&zgr;<up>07103</up>
AFS|14-3-3&zgr;<up>E16</up>
MD|Construct: A 1.0kb @14-3-3&zgr;@ cDNA fragment containing the complete open reading
|frame is expressed under the control of an @arm@ promoter.
MU|in vitro construct | regulatory fusion
CNS|FBtp0015025 == P{arm-14-3-3&zgr;.K}
PHC|wild-type
PHI|Mode of assay: In transgenic Drosophila
SYN|unnamed
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>hbNRE.RpII15</up>
SYN|14-3-3<up>hbNRE.RpII15</up>
ID|FBal0083670
PHM|embryo | posterior | germ-line clone
|filzkorper | germ-line clone
PHI|18% of embryos carrying @14-3-3&zgr;<up>hbNRE.RpII15</up>@ and derived from homozygous
|@14-3-3&zgr;<up>P1188</up>@ female germline clones have a wild-type anterior region
|but are missing all or part of the posterior region. 56% of these
|'anteriorly rescued' embryos have shortened Filzkorper.
|Mode of assay: In transgenic Drosophila
REF|FBrf0099365
REFDSR
{
RDID|FBrf0099365
|Li et al.
|1997
MD|Construct: A 1.4kb @RpII15@ promoter fragment drives expression of a 780bp @14-3-3&zgr;@
|cDNA which has a 150bp fragment from the @hb@ 3' untranslated region,
|containing a @nos@-response element (NRE), fused to its 3' end.
MU|in vitro construct | regulatory fusion
CNS|FBtp0009043 == P{RpII15-14-3-3.hbNRE}
PHM|embryo | posterior | germ-line clone
|filzkorper | germ-line clone
PHI|18% of embryos carrying @14-3-3&zgr;<up>hbNRE.RpII15</up>@ and derived from homozygous
|@14-3-3&zgr;<up>P1188</up>@ female germline clones have a wild-type anterior region
|but are missing all or part of the posterior region. 56% of these
|'anteriorly rescued' embryos have shortened Filzkorper.
|Mode of assay: In transgenic Drosophila
SYN|unnamed
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>hs.PL</up>
SYN|14-3-3<up>hs.PL</up>
ID|FBal0083669
PHM|denticle belt
PHI|Overexpression of @14-3-3&zgr;<up>hs.PL</up>@ in wild-type embryos results in deletion
|of denticle bands.
|Mode of assay: In transgenic Drosophila
REF|FBrf0099365
REFDSR
{
RDID|FBrf0099365
|Li et al.
|1997
NAM|heat shock construct of Li
MD|Construct: A 780bp @14-3-3&zgr;@ cDNA is expressed under the control of an Hsp70 promoter.
MU|in vitro construct | regulatory fusion
CNS|FBtp0009042 == P{hs-14-3-3.L}
GIA|suppressor | partially of embryonic/first instar larval cuticle phenotype of @tor<up>rv66</up>@
GII|Overexpression of @14-3-3&zgr;<up>hs.PL</up>@ partly rescues the cuticle of
|embryos derived from @tor<up>rv66</up>@ females.
PHM|denticle belt
PHI|Overexpression of @14-3-3&zgr;<up>hs.PL</up>@ in wild-type embryos results in deletion
|of denticle bands.
|Mode of assay: In transgenic Drosophila
SYN|unnamed
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>LI.15.hs</up>
ID|FBal0134436
PHC|(with 14-3-3&zgr;<up>P1375</up>) learning defective
|(with 14-3-3&zgr;<up>P1375</up>) viable
|wild-type
PHI|Mode of assay: In transgenic Drosophila
REF|FBrf0139731
REFDSR
{
RDID|FBrf0139731
|Philip et al.
|2001
AFS|14-3-3&zgr;<up>P1188</up>
|14-3-3&zgr;<up>P2335</up>
APR|(with 14-3-3&zgr;<up>LII.2.hs</up>) 14-3-3&zgr;<up>P1375</up>
|(with 14-3-3&zgr;<up>LII.2.hs</up>) 14-3-3&zgr;<up>P1375</up>/14-3-3&zgr;<up>P1188</up>
|(with 14-3-3&zgr;<up>LII.2.hs</up>) 14-3-3&zgr;<up>P1375</up>/14-3-3&zgr;<up>P2335</up>
|(with 14-3-3&zgr;<up>LII.2.hs</up>) 14-3-3&zgr;<up>P1188</up>/14-3-3&zgr;<up>P2335</up>
|14-3-3&zgr;<up>P1188</up>/14-3-3&zgr;<up>P2335</up>
|14-3-3&zgr;<up>P1375</up>
|14-3-3&zgr;<up>P1375</up>/14-3-3&zgr;<up>P1188</up>
ARS|14-3-3&zgr;<up>2.3</up>
|14-3-3&zgr;<up>P1188</up>/14-3-3&zgr;<up>P2335</up>
|14-3-3&zgr;<up>P1375</up>/14-3-3&zgr;<up>P1188</up>
|14-3-3&zgr;<up>P1375</up>/14-3-3&zgr;<up>P2335</up>
|14-3-3&zgr;<up>X1</up>
|14-3-3&zgr;<up>P1375</up>
AMSO|Induction with two 30 min heat shocks daily through embryonic, larval
|and pupal stages rescues the lethal phenotype of @14-3-3&zgr;<up>P1375</up>@.
|A single heat shock daily can also rescue to adulthood.
|Shows heat-shock specific rescue of the learning and memory defects
|of @14-3-3&zgr;<up>X1</up>@ and @14-3-3&zgr;<up>2.3</up>@.
|Flies rescued from lethality by @14-3-3&zgr;<up>LI.15.hs</up>@ or @14-3-3&zgr;<up>LI.15.hs</up>@
|and @14-3-3&zgr;<up>LII.2.hs</up>@ show a 25-30% decrement in olfactory learning,
|comparable to that of (rescued) @14-3-3&zgr;<up>2.3</up>@. The restoration
|of learning by the transgenes decays back to mutant levels 60-70 hr
|later.
MD|Construct: Expression of a @14-3-3&zgr;@ cDNA exons 1-6,7 is driven by a heat
|shock promoter.
MU|in vitro construct | regulatory fusion
CNS|FBtp0015596 == P{hs-14-3-3&zgr;.LI.15}
PHC|(with 14-3-3&zgr;<up>P1375</up>) learning defective
|(with 14-3-3&zgr;<up>P1375</up>) viable
|wild-type
PHI|Mode of assay: In transgenic Drosophila
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>LII.2.hs</up>
ID|FBal0134435
PHC|wild-type
PHI|Mode of assay: In transgenic Drosophila
REF|FBrf0139731
REFDSR
{
RDID|FBrf0139731
|Philip et al.
|2001
AFS|14-3-3&zgr;<up>P1188</up>
|14-3-3&zgr;<up>P1188</up>/14-3-3&zgr;<up>P2335</up>
|14-3-3&zgr;<up>P1375</up>/14-3-3&zgr;<up>P1188</up>
|14-3-3&zgr;<up>P1375</up>/14-3-3&zgr;<up>P2335</up>
|14-3-3&zgr;<up>P2335</up>
APR|(with 14-3-3&zgr;<up>LI.15.hs</up>) 14-3-3&zgr;<up>P1375</up>
|(with 14-3-3&zgr;<up>LI.15.hs</up>) 14-3-3&zgr;<up>P1375</up>/14-3-3&zgr;<up>P1188</up>
|(with 14-3-3&zgr;<up>LI.15.hs</up>) 14-3-3&zgr;<up>P1375</up>/14-3-3&zgr;<up>P2335</up>
|(with 14-3-3&zgr;<up>LI.15.hs</up>) 14-3-3&zgr;<up>P1188</up>/14-3-3&zgr;<up>P2335</up>
ARS|14-3-3&zgr;<up>2.3</up>
|14-3-3&zgr;<up>X1</up>
|14-3-3&zgr;<up>P1375</up>
AMSO|Induction with two 30 min heat shocks daily through embryonic, larval
|and pupal stages rescues the lethal phenotype of @14-3-3&zgr;<up>P1375</up>@.
|A single heat shock daily can also rescue to adulthood.
|Shows heat-shock specific rescue of the learning and memory defects
|of @14-3-3&zgr;<up>X1</up>@ and @14-3-3&zgr;<up>2.3</up>@.
|Flies rescued from lethality by @14-3-3&zgr;<up>LI.15.hs</up>@ and @14-3-3&zgr;<up>LII.2.hs</up>@
|show a 25-30% decrement in olfactory learning, comparable to that of
|(rescued) @14-3-3&zgr;<up>2.3</up>@. The restoration of learning by the transgenes
|decays back to mutant levels 60-70 hr later.
MD|Construct: Expression of a @14-3-3&zgr;@ cDNA exons 1-6',7 is driven by a heat
|shock promoter.
MU|in vitro construct | regulatory fusion
CNS|FBtp0015595 == P{hs-14-3-3&zgr;.LII.2}
PHC|wild-type
PHI|Mode of assay: In transgenic Drosophila
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>sev.PK</up>
SYN|14-3-3<up>sev.PK</up>
ID|FBal0062285
PHI|Flies carrying @14-3-3&zgr;<up>a.sev</up>@ appear wild-type.
|Mode of assay: In transgenic Drosophila
REF|FBrf0093549
REFDSR
{
RDID|FBrf0093549
|Kockel et al.
|1997
NAM|sevenless promoter construct of Kockel
MD|Construct: A 1.0kb @14-3-3&zgr;@ cDNA fragment containing the complete open reading
|frame is expressed in the sense orientation under the control of a
|@sev@ enhancer.
MU|in vitro construct | regulatory fusion
CNS|FBtp0008238 == P{sE.14-3-3}
PHI|Flies carrying @14-3-3&zgr;<up>a.sev</up>@ appear wild-type.
|Mode of assay: In transgenic Drosophila
SYN|unnamed
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>tKa</up>
SYN|14-3-3<up>tKa</up>
ID|FBal0062284
PHC|wild-type
PHI|Mode of assay: In transgenic Drosophila
REF|FBrf0093549
REFDSR
{
RDID|FBrf0093549
|Kockel et al.
|1997
ARS|14-3-3&zgr;<up>E16</up>
MD|Construct: 13.5kb genomic fragment containing the entire coding region and 1.7kb
|of upstream and downstream sequences.
MU|in vitro construct | genomic fragment
CNS|FBtp0008237 == P{14-3-3&zgr;<up>tKa</up>}
PHC|wild-type
PHI|Mode of assay: In transgenic Drosophila
SYN|unnamed
}

}

ALESR
{
ASYM|14-3-3&zgr;<up>+</up>
ID|FBal0066544
CLA|wild-type generic
REF|FBrf0105495
}

IFL|../torstoll/leonrd1.htm
SK|FBst0012335
|P{ry[+t7.2]=PZ}14-3-3zeta[07103] cn[1]/CyO; ry[506]
|FBst0015902
|y[1] w[67c23]; P{w[+mC] y[+mDint2]=EPgy2}CG2269[EY03325] P{EPgy2}14-3-3zeta[EY03325]
SKC|2
}
# EOR
GENR
{
RETE|ID 1 FBgn0010340	CLA 1 Gene	NAM 1 upstream of RpII140	GSYM 1 140up	DT 1 25 Dec 04	RESZ 6294	PDOM 1 INTERPRO:IPR003397 == Mitochondrial import inner membrane translocase, subunit Tim17	PTD 1	DBA 16	FNC 2 development	CEL 1 mitochondrial inner membrane	CLOC 1 88A9	ALESR 6	REF 12	
GSYM|140up
PTD
ARGS
DT|25 Dec 04
ID|FBgn0010340
UAB|Deficiency: Df(3R)red-P52
|Duplication: Dp(3;2)ry<up>+</up> (inferred from cytology)
SYN|CG9852
|DmRP140-upstream
|l(3)Z6
|DmRP140up
|l(3)88Ba
ID2|FBgn0004843
NAM|upstream of RpII140
CLOC|88A9
|Limits computationally determined from genome sequence between P{PZ}01949 and @P{lacW}trx<up>j14A6</up>@&@P{PZ}trx<up>00347</up>@
FNC|development ; GO:0007275
|protein transport ; GO:0015031
CEL|mitochondrial inner membrane ; GO:0005743
PDOM|IPR003397 == Mitochondrial import inner membrane translocase, subunit Tim17
GLOC|Maps to the right of RpII140: 0.02
GLC|@140up<up>Z6</up>@ maps 0.02cM from @RpII140<up>Z24</up>@, with @140up@ probably
|lying proximal to @RpII140@.
ENZ|protein transporter activity ; GO:0008565
|protein transporter activity ; GO:0008565 | inferred from electronic annotation
DBA|NA:AA941870
|BDGP-DGC:LD27182
|NA:AC007441
|BDGP:BACR10E03
|NA:AC007904
|BDGP:BACR01H04
|NA:AE003703
|PA:AAF55023
|NA:AW942742
|BDGP-DGC:LD27182
|NA:AY058577
|PA:AAL13806
|BDGP-DGC:LD27182
|NA:M62973
|NA:M62975
|PA:AAD40352
PAC|UniProt_Swiss_Prot:P81928
PHP|All known alleles are recessive lethals.
ASQ|FBan0009852
REF
{
REFM|FBrf0159398
|FlyBase Curators
|2002-
|9
REFM|FBrf0058600
|Hamilton et al.
|1993
|0
REFM|FBrf0120781
|Sitzler
|1999.8.31
|9
REFM|FBrf0126702
|Zheng
|1999.11
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0056267
|Mortin et al.
|1992
|0
REFM|FBrf0141598
|Wahlstrom et al.
|2001
|0
REFM|FBrf0058349
|Oldenburg et al.
|1993
|1
REFM|FBrf0179797
|Bloomington Drosophila Stock Center
|2004.11.6
|9
REFM|FBrf0054607
|Breen and Harte
|1991
|-1
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0054010
|Sitzler et al.
|1991
FNC|development ; GO:0007275 | inferred from mutant phenotype
SYN|DmRP140-upstream
}

REFDSR
{
RDID|FBrf0054607
|Breen and Harte
|1991
BMD|Df(3R)JY19
BMD|Df(3R)red-P52
BMDD|Df(3R)JY28
BMDD|Df(3R)red-P6
BMDD|Df(3R)red-P93
BMDD|Df(3R)red2l
BMDD|Df(3R)su(Hw)V
BMDD|Df(3R)trxE12
BMDD|T(Y;3)red<up>P4</up>
SYN|l(3)Z6
}

REFDSR
{
RDID|FBrf0056267
|Mortin et al.
|1992
BMD|Df(3R)red-P1
BMD|Df(3R)red-P52
BMDD|Df(3R)293&ggr;5
BMDD|Df(3R)red-P6
BMDD|Df(3R)red-P93
BMDD|Df(3R)su(Hw)V
}

REFDSR
{
RDID|FBrf0058600
|Hamilton et al.
|1993
GLOC|Maps to the right of RpII140: 0.02
GLC|@140up<up>Z6</up>@ maps 0.02cM from @RpII140<up>Z24</up>@, with @140up@ probably
|lying proximal to @RpII140@.
}

REFDSR
{
RDID|FBrf0092726
|Wiedemann et al.
|1997
PHP|Sequences important for the transcription of @RpII140@ are located
|in the untranslated leader of the divergently transcribed @140up@ gene.
SYN|DmRP140up
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
MD|Maps to clone: BACR01H04
|Maps to clone: BACR10E03
}

REFDSR
{
RDID|FBrf0120781
|Sitzler
|1999.8.31
SYN|unnamed
}

REFDSR
{
RDID|FBrf0120782
|Sitzler
|1999.8.31
MD|Gene order: Overall orientation not stated: 140up- RpII140+
SYN|DmRP140-upstream
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: LD27182 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0126702
|Zheng
|1999.11
AM|Source for identity of: 140up CG9852
}

REFDSR
{
RDID|FBrf0141598
|Wahlstrom et al.
|2001
MD|Gene order: Overall orientation not stated: Abi- twf+ 140up-
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|protein transporter activity ; GO:0008565 | inferred from electronic annotation
FNC|protein transport ; GO:0015031 | inferred from electronic annotation
CEL|mitochondrial inner membrane ; GO:0005743 | inferred from electronic annotation
}

ALESR
{
ASYM|140up<up>f07279</up>
ID|FBal0162865
REF|FBrf0179797
REFDSR
{
RDID|FBrf0179797
|Bloomington Drosophila Stock Center
|2004.11.6
TRN|FBti0042654 == PBac{WH}140up<up>f07279</up>
MU|piggyBac transposase
}

}

ALESR
{
ASYM|140up<up>M13</up>
ID|FBal0031933
PHC|lethal | recessive
REF|FBrf0056267
REFDSR
{
RDID|FBrf0056267
|Mortin et al.
|1992
MU|ethyl methanesulfonate
PHC|lethal | recessive
}

}

ALESR
{
ASYM|140up<up>Z6</up>
SYN|Z6
ID|FBal0031936
PHC|lethal | recessive
REF|FBrf0054607
|FBrf0058600
|FBrf0056267
REFDSR
{
RDID|FBrf0056267
|Mortin et al.
|1992
MU|ethyl methanesulfonate
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0058600
|Hamilton et al.
|1993
SYN|Z6
}

}

ALESR
{
ASYM|140up<up>Z29</up>
SYN|Z29
ID|FBal0031934
PHC|lethal | recessive
REF|FBrf0058600
|FBrf0056267
REFDSR
{
RDID|FBrf0056267
|Mortin et al.
|1992
MU|ethyl methanesulfonate
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0058600
|Hamilton et al.
|1993
SYN|Z29
}

}

ALESR
{
ASYM|140up<up>Z30</up>
SYN|Z30
ID|FBal0031935
PHC|lethal | recessive
REF|FBrf0058600
|FBrf0056267
REFDSR
{
RDID|FBrf0056267
|Mortin et al.
|1992
MU|ethyl methanesulfonate
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0058600
|Hamilton et al.
|1993
SYN|Z30
}

}

ALESR
{
ASYM|140up<up>+</up>
ID|FBal0066317
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067636	CLA 1 Gene	GSYM 1 146y	DT 1 25 Dec 04	RESZ 2191	ALESR 2	REF 1	
GSYM|146y
DT|25 Dec 04
ID|FBgn0067636
REF
{
REFM|FBrf0141372
|Ejima et al.
|2001
|0
}

ALESR
{
ASYM|146y<up>146y</up>
SYN|146y
ID|FBal0151007
PHC|viable
|fertile
|courtship defective | female
PHI|@146y<up>146y</up>@ virgin females show elevated ovulation; 30% of the virgin
|females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @146y<up>146y</up>@ virgin females are mated
|to wild-type males is lower than that seen when wild-type virgin females
|are mated to wild-type males, but is higher than that seen when wild-type
|mated females are mated to wild-type males. @146y<up>146y</up>@ mutant virgin
|females show ovipositor extrusion towards courting wild-type males
|(this extrusion behavior is normally observed in mated wild-type females
|but not in virgin wild-type females).
REF|FBrf0141372
REFDSR
{
RDID|FBrf0141372
|Ejima et al.
|2001
TRN|FBti0037976 == P{GawB}146y<up>146y</up>
MU|P-element activity
PHC|viable
|fertile
|courtship defective | female
PHI|@146y<up>146y</up>@ virgin females show elevated ovulation; 30% of the virgin
|females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @146y<up>146y</up>@ virgin females are mated
|to wild-type males is lower than that seen when wild-type virgin females
|are mated to wild-type males, but is higher than that seen when wild-type
|mated females are mated to wild-type males. @146y<up>146y</up>@ mutant virgin
|females show ovipositor extrusion towards courting wild-type males
|(this extrusion behavior is normally observed in mated wild-type females
|but not in virgin wild-type females).
SYN|146y
}

}

ALESR
{
ASYM|146y<up>+</up>
ID|FBal0151313
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004951	CLA 1 repetitive element	NAM 1 1.688 satellite-related 10Ea	GSYM 1 1688-10Ea	DT 1 25 Dec 04	RESZ 1081	DBA 3	WT 3 Euchromatic sequences of unknown function similar	CLOC 1 10E1--2	REF 3	
GSYM|1688-10Ea
DT|25 Dec 04
ID|FBgn0004951
CLA|repetitive_element
UAB|Deficiency: Df(1)HA85 (inferred from cytology)
|Duplication: Dp(1;2)v<up>+</up>65b (inferred from cytology)
SYN|1.688
|1688-10E<up>d</up>
NAM|1.688 satellite-related 10Ea
GLOC|1-[36]
CLOC|10E1--2
|Right limit from molecular mapping relative to 1688-10Eb (FBrf0057386)
WT|Euchromatic sequences of unknown function similar, in their sequence, to
|the 1.688 @satDNA@ repeat. It has been suggested (FBrf0057386) that they
|may be required for some sex chromosome specific function.
DBA|NA:X62938
|NA:Z50388
|dbSTS:24350
REF
{
REFM|FBrf0057386
|DiBartolomeis et al.
|1992
|0
REFM|FBrf0080225
|Madueno et al.
|1995
|0
REFM|FBrf0100592
|Law et al.
|1998
|0
}

REFDSR
{
RDID|FBrf0057386
|DiBartolomeis et al.
|1992
OTH|The X linked SR sequences may be required for sex chromosome specific functions.
}

REFDSR
{
RDID|FBrf0080225
|Madueno et al.
|1995
SYN|1.688
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004952	CLA 1 repetitive element	NAM 1 1.688 satellite-related 10Eb	GSYM 1 1688-10Eb	DT 1 25 Dec 04	RESZ 1274	DBA 3	WT 3 Euchromatic sequences of unknown function similar	CLOC 1 10E1--2	REF 4	
GSYM|1688-10Eb
DT|25 Dec 04
ID|FBgn0004952
CLA|repetitive_element
UAB|Deficiency: Df(1)HA85 (inferred from cytology)
|Duplication: Dp(1;2)v<up>+</up>65b (inferred from cytology)
SYN|1.688
|1688-10E<up>p</up>
NAM|1.688 satellite-related 10Eb
GLOC|1-[36]
CLOC|10E1--2
|Left limit from in situ hybridization (FBrf0057386)
|Right limit from in situ hybridization (FBrf0057386)
CYC|Experimentally determined: 10E1--2
WT|Euchromatic sequences of unknown function similar, in their sequence, to
|the 1.688 @satDNA@ repeat. It has been suggested (FBrf0057386) that they
|may be required for some sex chromosome specific function.
DBA|NA:X62937
|NA:Z32192
|dbSTS:4743
REF
{
REFM|FBrf0057386
|DiBartolomeis et al.
|1992
|0
REFM|FBrf0071734
|EDGP Project Members
|1994-
|9
REFM|FBrf0080225
|Madueno et al.
|1995
|0
REFM|FBrf0100592
|Law et al.
|1998
|0
}

REFDSR
{
RDID|FBrf0057386
|DiBartolomeis et al.
|1992
CLOC|10E1--2 (determined by in situ hybridization)
OTH|The X linked SR sequences may be required for sex chromosome specific functions.
}

REFDSR
{
RDID|FBrf0080225
|Madueno et al.
|1995
SYN|1.688
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004953	CLA 1 repetitive element	NAM 1 1.688 satellite-related 11EF	GSYM 1 1688-11EF	DT 1 25 Dec 04	RESZ 1034	WT 3 Euchromatic sequences of unknown function similar	CLOC 1 11E--F	REF 4	
GSYM|1688-11EF
DT|25 Dec 04
ID|FBgn0004953
CLA|repetitive_element
UAB|Deficiency: Df(1)C246 (inferred from cytology)
|Duplication: Dp(1;3)ras<up>v</up> (inferred from cytology)
SYN|1.688
NAM|1.688 satellite-related 11EF
GLOC|1-[41]
CLOC|11E--F
WT|Euchromatic sequences of unknown function similar, in their sequence, to
|the 1.688 @satDNA@ repeat. It has been suggested (FBrf0057386) that they
|may be required for some sex chromosome specific function.
REF
{
REFM|FBrf0057386
|DiBartolomeis et al.
|1992
|0
REFM|FBrf0047217
|Waring and Pollack
|1987
|0
REFM|FBrf0080225
|Madueno et al.
|1995
|0
REFM|FBrf0100592
|Law et al.
|1998
|0
}

REFDSR
{
RDID|FBrf0057386
|DiBartolomeis et al.
|1992
OTH|The X linked SR sequences may be required for sex chromosome specific functions.
}

REFDSR
{
RDID|FBrf0080225
|Madueno et al.
|1995
SYN|1.688
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0027098	CLA 1 repetitive element	GSYM 1 1688-2E	DT 1 25 Dec 04	RESZ 186	DBA 1	REF 1	
GSYM|1688-2E
DT|25 Dec 04
ID|FBgn0027098
CLA|repetitive_element
DBA|NA:AJ238704
REF
{
REFM|FBrf0107580
|Alatortsev et al.
|1998
|0
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004950	CLA 1 repetitive element	NAM 1 1.688 satellite-related 3C	GSYM 1 1688-3C	DT 1 25 Dec 04	RESZ 1236	DBA 3	WT 3 Euchromatic sequences of unknown function similar	CLOC 1 3C	REF 4	
GSYM|1688-3C
DT|25 Dec 04
ID|FBgn0004950
CLA|repetitive_element
UAB|Deficiency: T(1;3)143-3 (inferred from cytology)
|Duplication: Dp(1;Y)w<up>+</up>303 (inferred from cytology)
SYN|1.688
NAM|1.688 satellite-related 3C
GLOC|1-[1.5]
CLOC|3C
|Left limit from in situ hybridization (FBrf0057386)
|Right limit from in situ hybridization (FBrf0057386)
CYC|Experimentally determined: 3C
WT|Euchromatic sequences of unknown function similar, in their sequence, to
|the 1.688 @satDNA@ repeat. It has been suggested (FBrf0057386) that they
|may be required for some sex chromosome specific function.
DBA|NA:X62939
|NA:Z32250
|dbSTS:4802
REF
{
REFM|FBrf0057386
|DiBartolomeis et al.
|1992
|0
REFM|FBrf0071734
|EDGP Project Members
|1994-
|9
REFM|FBrf0080225
|Madueno et al.
|1995
|0
REFM|FBrf0100592
|Law et al.
|1998
|0
}

REFDSR
{
RDID|FBrf0057386
|DiBartolomeis et al.
|1992
CLOC|3C (determined by in situ hybridization)
OTH|The X linked SR sequences may be required for sex chromosome specific functions.
}

REFDSR
{
RDID|FBrf0080225
|Madueno et al.
|1995
SYN|1.688
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0000004	CLA 1 transposable element	NAM 1 17.6 element	GSYM 1 17.6	DT 1 25 Dec 04	RESZ 10027	DBA 29	WT 3 A retroviral-like transposable element	REF 78	
GSYM|17.6
DT|25 Dec 04
ID|FBgn0000004
CLA|transposable_element
SYN|17.6S
|176
|Dme176V
NAM|17.6 element
TE|element type: LTR retrotransposon
|terminal repeat length in bp: 512
|total length in bp: 7439
|target site duplication length in bp: 4
|number of copies in genome: 40 (FBrf0040123)
WT|A retroviral-like transposable element.  First described by Saigo et al.
|(FBrf0036029) as a sequence inserted into histone genes and hybridizing to
|@297@ elements.
DBA|NA:AL008791
|dbSTS:53385
|NA:L39084
|NA:M31561
|NA:M31562
|NA:M31563
|NA:M31564
|NA:M31565
|NA:M31566
|NA:M31567
|NA:M31569
|NA:M31570
|NA:M31571
|NA:M31573
|NA:M31574
|NA:V01517
|NA:V01518
|NA:X01472
|NA:X79394
|NA:Z31854
|dbSTS:4392
|NA:Z32251
|dbSTS:4803
|NA:Z32339
|dbSTS:4891
|NA:Z70850
|dbSTS:33719
|NA:Z71029
|dbSTS:33525
REV|FBrf0152077
|FBrf0100335
REF
{
REFM|FBrf0131051
|Marin and Llorens
|2000
|0
REFM|FBrf0057228
|Kulkosky et al.
|1992
|0
REFM|FBrf0116414
|Inouye
|1995.1.24
|9
REFM|FBrf0128568
|Maside et al.
|2000
|0
REFM|FBrf0055613
|de Frutos et al.
|1992
|0
REFM|FBrf0116412
|Inouye
|1995.1.24
|9
REFM|FBrf0116411
|Inouye
|1995.1.24
|9
REFM|FBrf0116410
|Inouye
|1995.1.24
|9
REFM|FBrf0056185
|von Sternberg et al.
|1992
|2
REFM|FBrf0040123
|Kugimiya et al.
|1983
|0
REFM|FBrf0111953
|Losada et al.
|1999
|0
REFM|FBrf0053865
|Arkhipova and Ilyin
|1991
|0
REFM|FBrf0151415
|Lerat et al.
|2002
|9
REFM|FBrf0116409
|Inouye
|1995.1.24
|9
REFM|FBrf0116408
|Inouye
|1995.1.24
|9
REFM|FBrf0116407
|Inouye
|1995.1.24
|9
REFM|FBrf0116406
|Inouye
|1995.1.24
|9
REFM|FBrf0116405
|Inouye
|1995.1.24
|9
REFM|FBrf0048585
|Huijser et al.
|1988
|0
REFM|FBrf0116404
|Inouye
|1995.1.24
|9
REFM|FBrf0167608
|Greil et al.
|2003
|0
REFM|FBrf0071734
|EDGP Project Members
|1994-
|9
REFM|FBrf0116403
|Inouye
|1995.1.24
|9
REFM|FBrf0116402
|Inouye
|1995.1.24
|9
REFM|FBrf0160656
|Kapitonov and Jurka
|2003
|0
REFM|FBrf0106414
|Desset et al.
|1999
|0
REFM|FBrf0144916
|Rizzon et al.
|2002
|0
REFM|FBrf0111944
|Lerat and Capy
|1999
|0
REFM|FBrf0051101
|Sandmeyer et al.
|1990
|2
REFM|FBrf0079059
|Mozer and Benzer
|1993
|1
REFM|FBrf0079058
|Mozer and Benzer
|1991
|1
REFM|FBrf0162162
|Lerat et al.
|2003
|0
REFM|FBrf0080225
|Madueno et al.
|1995
|0
REFM|FBrf0054202
|Kim and Belyaeva
|1991
|0
REFM|FBrf0059271
|Delpuech et al.
|1993
|0
REFM|FBrf0152077
|Pelisson et al.
|2002
|2
REFM|FBrf0079937
|Charlesworth et al.
|1994
|0
REFM|FBrf0099812
|Terzian et al.
|1997
|0
REFM|FBrf0041561
|Saigo et al.
|1984
|0
REFM|FBrf0054653
|McClure
|1991
|0
REFM|FBrf0079992
|Ding and Lipshitz
|1994
|0
REFM|FBrf0074490
|Sniegowski and Charlesworth
|1994
|0
REFM|FBrf0036029
|Saigo et al.
|1981
|0
REFM|FBrf0162058
|Aravin et al.
|2003
|0
REFM|FBrf0102359
|Makarova et al.
|1995
|0
REFM|FBrf0129733
|Biemont et al.
|1999
|2
REFM|FBrf0125337
|Boeke and Corces
|1989
|2
REFM|FBrf0073975
|Mozer and Benzer
|1994
|0
REFM|FBrf0138423
|Bowen and McDonald
|2001
|0
REFM|FBrf0052837
|Harada et al.
|1990
|0
REFM|FBrf0054937
|Jarrell and Meselson
|1991
|0
REFM|FBrf0125292
|Xiong and Eickbush
|1990
|0
REFM|FBrf0149117
|Syomin et al.
|2002
|0
REFM|FBrf0111330
|Biemont and Cizeron
|1999
|0
REFM|FBrf0041549
|Inouye et al.
|1984
|0
REFM|FBrf0134868
|Haoudi and Mason
|2000
|2
REFM|FBrf0078388
|Finnegan
|1992
|0
REFM|FBrf0127032
|Canizares et al.
|2000
|0
REFM|FBrf0083460
|Suh et al.
|1995
|0
REFM|FBrf0057833
|Kanda and Saigo
|1993
|0
REFM|FBrf0098551
|Suh et al.
|1994
|1
REFM|FBrf0100335
|Britten
|1997
|2
REFM|FBrf0105736
|Kanapin and Ivanov
|1998
|0
REFM|FBrf0127224
|Marsano et al.
|2000
|0
REFM|FBrf0149106
|Bartolome et al.
|2002
|0
REFM|FBrf0057534
|Waters et al.
|1992
|0
REFM|FBrf0149104
|Vieira et al.
|2002
|0
REFM|FBrf0051918
|Voelker et al.
|1990
|0
REFM|FBrf0111776
|Andrianov et al.
|1999
|0
REFM|FBrf0052879
|Scheinker et al.
|1990
|0
REFM|FBrf0111510
|Vieira et al.
|1999
|0
REFM|FBrf0130256
|Lerat et al.
|1999
|0
REFM|FBrf0045140
|Inouye et al.
|1986
|0
REFM|FBrf0109043
|Rutsov et al.
|1999
|0
REFM|FBrf0155828
|Kaminker et al.
|2002
|0
REFM|FBrf0054718
|Kim and Belyaeva
|1991
|0
REFM|FBrf0055481
|Arkhipova and Ilyin
|1992
|2
REFM|FBrf0108981
|Pantazidis et al.
|1999
|0
}

REFDSR
{
RDID|FBrf0052837
|Harada et al.
|1990
OTH|Transposition rates of mobile elements in lines AW and JH, in which
|spontaneous mutations have accumulated for about 400 generations, are
|studied. @412@ and @17.6@ elements rate of transposition is very low,
|@I-element@ and @hobo@ insertions occur much more frequently.
}

REFDSR
{
RDID|FBrf0059271
|Delpuech et al.
|1993
WT|Presence or absence of a long terminal repeat of 17.6 does not correlate
|with resistance or susceptibility to DDT in 31 strains of D.melanogaster
|and D.simulans from around the world.
}

REFDSR
{
RDID|FBrf0074490
|Sniegowski and Charlesworth
|1994
WT|Element copy numbers on inversion and standard chromosomes has been
|determined. The copy number is significantly higher within low frequency
|inversions than within the corresponding standard chromosome regions.
}

REFDSR
{
RDID|FBrf0079937
|Charlesworth et al.
|1994
WT|Estimating the genomic numbers of transposable elements demonstrates
|many families of element are over-represented in heterochromatin.
}

REFDSR
{
RDID|FBrf0079992
|Ding and Lipshitz
|1994
WT|The spatial and temporal expression patterns of fifteen families of
|retrotransposons are analyzed during embryogenesis and are found to
|be conserved. Results suggest that all families carry cis-acting elements
|that control their spatial and temporal expression patterns.
}

REFDSR
{
RDID|FBrf0083460
|Suh et al.
|1995
PHP|The chromosomal distribution of a number of retrotransposons in an
|isolated population of D.melanogaster (from Ishigaki Island, Okinawa,
|Japan) has been determined.
}

REFDSR
{
RDID|FBrf0099812
|Terzian et al.
|1997
OTH|Used in an investigation to address the relationship between retrotransposons
|and retroviruses and the coadaptation of these retroelements to their
|host genomes. Results indicate retrotransposons are heterogeneous
|in contrast to retroviruses, suggesting different modes of evolution
|by slippage-like mechanisms.
}

REFDSR
{
RDID|FBrf0116402
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116403
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116404
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116405
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116406
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116407
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116408
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116409
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116410
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116411
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116412
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0116414
|Inouye
|1995.1.24
SYN|17.6S
}

REFDSR
{
RDID|FBrf0151719
|Tulin et al.
|2002
SYN|176
}

REFDSR
{
RDID|FBrf0152077
|Pelisson et al.
|2002
SYN|Dme176V
}

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
TE|element type: LTR retrotransposon
|total length in bp: 7439
|number of copies in genome: 12 in euchromatin of Release 3 genome annotation, of which 7 are full length.
}

REFDSR
{
RDID|FBrf0162058
|Aravin et al.
|2003
}

REFDSR
{
RDID|FBrf0167608
|Greil et al.
|2003
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0027624	CLA 1 transposable element gene	GSYM 1 17.6\env	DT 1 25 Dec 04	RESZ 587	DBA 2	ALESR 1	REF 4	
GSYM|17.6\env
DT|25 Dec 04
ID|FBgn0027624
CLA|transposable_element_gene
AM|encoded by: @17.6@
DBA|NA:X01472
|PA:CAA25703
PAC|PIR:A03326
|UniProt_Swiss_Prot:P04283
REV|FBrf0152077
REF
{
REFM|FBrf0106414
|Desset et al.
|1999
|0
REFM|FBrf0152077
|Pelisson et al.
|2002
|2
REFM|FBrf0130256
|Lerat et al.
|1999
|0
REFM|FBrf0111944
|Lerat and Capy
|1999
|0
}

ALESR
{
ASYM|17.6\env<up>+</up>
ID|FBal0105454
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0044339	CLA 1 transposable element gene	GSYM 1 17.6\gag	DT 1 25 Dec 04	RESZ 249	DBA 2	ALESR 1	
GSYM|17.6\gag
DT|25 Dec 04
ID|FBgn0044339
CLA|transposable_element_gene
AM|encoded by: @17.6@
DBA|NA:X01472
|PA:CAA25701
PAC|PIR:A03325
|UniProt_Swiss_Prot:P04282
ALESR
{
ASYM|17.6\gag<up>+</up>
ID|FBal0122862
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0014453	CLA 1 transposable element gene	NAM 1 17.6 element transposase	GSYM 1 17.6\pol	DT 1 25 Dec 04	RESZ 812	DBA 2	WT 1 The transposase encoded by the @17.6@ element	ALESR 1	REF 2	
GSYM|17.6\pol
DT|25 Dec 04
ID|FBgn0014453
CLA|transposable_element_gene
SYN|17.6\T
|17.6 element transposase
AM|encoded by: @17.6@
WT|The transposase encoded by the @17.6@ element.
NAM|17.6 element transposase
DBA|NA:X01472
|PA:CAA25702
PAC|PIR:A03971
|UniProt_Swiss_Prot:P04323
REF
{
REFM|FBrf0106414
|Desset et al.
|1999
|0
REFM|FBrf0111944
|Lerat and Capy
|1999
|0
}

REFDSR
{
RDID|FBrf0073975
|Mozer and Benzer
|1994
NAM|17.6 element transposase
WT|The regulation of transcription of the @17.6@ retrotransposon provides
|a model for the study of innervation-dependent gene expression in postsynaptic
|cells during neurogenesis.
}

ALESR
{
ASYM|17.6\pol<up>+</up>
ID|FBal0105302
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0000007	CLA 1 transposable element	NAM 1 1731 element	GSYM 1 1731	DT 1 25 Dec 04	RESZ 11423	DBA 8	WT 5 A retroviral-like transposable element	REF 69	
GSYM|1731
DT|25 Dec 04
ID|FBgn0000007
CLA|transposable_element
SYN|17.31
|BcDNA:SD26211
ID2|FBgn0062845
NAM|1731 element
TE|element type: LTR retrotransposon
|terminal repeat length in bp: 336
|number of copies in genome: 10
|total length in bp: 4648 (FBrf0045155)
|target site duplication length in bp: 5 (FBrf0045155)
WT|A retroviral-like transposable element.  The first @1731@ element was
|identified because its transcription in tissue-culture cells is reduced in
|the presence of 20-hydroxyecdysone (FBrf0045155).  In cell lines the
|transcription of @1731@ is down-regulated by ecdysteroids (FBrf0053421;
|FBrf0054856).
DBA|NA:AJ564687
|NA:AY119276
|BDGP-DGC:SD26211
|NA:BI632431
|BDGP-DGC:SD26211
|NA:X04686
|NA:X04874
|NA:X07656
REF
{
REFM|FBrf0160656
|Kapitonov and Jurka
|2003
|0
REFM|FBrf0058493
|Kim et al.
|1993
|0
REFM|FBrf0134799
|van Steensel et al.
|2001
|9
REFM|FBrf0105935
|Slama-Schwok et al.
|1998
|0
REFM|FBrf0067697
|Fourcade-Peronnet et al.
|1994
|1
REFM|FBrf0057228
|Kulkosky et al.
|1992
|0
REFM|FBrf0155828
|Kaminker et al.
|2002
|0
REFM|FBrf0090548
|Faure et al.
|1996
|0
REFM|FBrf0056591
|Fourcade-Peronnet et al.
|1992
|0
REFM|FBrf0079108
|Nuzhdin and Mackay
|1995
|9
REFM|FBrf0064626
|Nahon et al.
|1993
|0
REFM|FBrf0055481
|Arkhipova and Ilyin
|1992
|2
REFM|FBrf0155500
|Maggert and Golic
|2002
|0
REFM|FBrf0144916
|Rizzon et al.
|2002
|0
REFM|FBrf0059024
|Montchamp-Moreau et al.
|1993
|0
REFM|FBrf0128568
|Maside et al.
|2000
|0
REFM|FBrf0054856
|Ziarczyk and Best-Belpomme
|1991
|0
REFM|FBrf0079937
|Charlesworth et al.
|1994
|0
REFM|FBrf0105736
|Kanapin and Ivanov
|1998
|0
REFM|FBrf0149015
|Yan et al.
|2002
|0
REFM|FBrf0053421
|Becker et al.
|1991
|0
REFM|FBrf0111510
|Vieira et al.
|1999
|0
REFM|FBrf0058488
|Codani-Simonart et al.
|1993
|0
REFM|FBrf0108387
|Dimitri and Junakovic
|1999
|2
REFM|FBrf0130256
|Lerat et al.
|1999
|0
REFM|FBrf0079992
|Ding and Lipshitz
|1994
|0
REFM|FBrf0086400
|Faure et al.
|1996
|0
REFM|FBrf0125292
|Xiong and Eickbush
|1990
|0
REFM|FBrf0098518
|Haoudi et al.
|1997
|0
REFM|FBrf0138423
|Bowen and McDonald
|2001
|0
REFM|FBrf0129733
|Biemont et al.
|1999
|2
REFM|FBrf0105955
|Whalen and Grigliatti
|1998
|0
REFM|FBrf0141542
|Maside et al.
|2001
|0
REFM|FBrf0149106
|Bartolome et al.
|2002
|0
REFM|FBrf0111953
|Losada et al.
|1999
|0
REFM|FBrf0149104
|Vieira et al.
|2002
|0
REFM|FBrf0099812
|Terzian et al.
|1997
|0
REFM|FBrf0056166
|di Franco et al.
|1992
|0
REFM|FBrf0167608
|Greil et al.
|2003
|0
REFM|FBrf0162058
|Aravin et al.
|2003
|0
REFM|FBrf0099810
|Flavell et al.
|1997
|0
REFM|FBrf0056194
|di Franco et al.
|1992
|0
REFM|FBrf0080187
|Lacoste and Fourcade-Peronnet
|1995
|0
REFM|FBrf0056004
|Champion et al.
|1992
|0
REFM|FBrf0050727
|Ziarczyk et al.
|1989
|0
REFM|FBrf0151629
|Flavell et al.
|1992
|0
REFM|FBrf0137949
|Alonso-Gonzalez et al.
|2001
|1
REFM|FBrf0129880
|Kalmykova et al.
|1999
|0
REFM|FBrf0049432
|di Franco et al.
|1989
|0
REFM|FBrf0045155
|Peronnet et al.
|1986
|0
REFM|FBrf0055722
|Ribaudo et al.
|1992
|0
REFM|FBrf0084234
|Nuzhdin
|1995
|0
REFM|FBrf0110995
|Vieira et al.
|1999
|1
REFM|FBrf0077988
|Arnault and Dufournel
|1994
|2
REFM|FBrf0058311
|Lacoste et al.
|1993
|1
REFM|FBrf0111944
|Lerat and Capy
|1999
|0
REFM|FBrf0076524
|Kim et al.
|1994
|0
REFM|FBrf0048831
|Fourcade-Peronnet et al.
|1988
|0
REFM|FBrf0085408
|Lacoste et al.
|1995
|0
REFM|FBrf0078389
|Finnegan
|1992
|0
REFM|FBrf0151719
|Tulin et al.
|2002
|0
REFM|FBrf0074490
|Sniegowski and Charlesworth
|1994
|0
REFM|FBrf0111330
|Biemont and Cizeron
|1999
|0
REFM|FBrf0052451
|Jakubczak et al.
|1990
|0
REFM|FBrf0129815
|Fortunati and Junakovic
|1999
|0
REFM|FBrf0134868
|Haoudi and Mason
|2000
|2
REFM|FBrf0085174
|Haoudi et al.
|1995
|0
REFM|FBrf0137199
|Aravin et al.
|2001
|0
REFM|FBrf0099793
|Alberola et al.
|1997
|0
}

REFDSR
{
RDID|FBrf0049432
|di Franco et al.
|1989
WT|The genomic distribution of transposable elements in somatic tissues and
|during development is homogeneous.
}

REFDSR
{
RDID|FBrf0054856
|Ziarczyk and Best-Belpomme
|1991
TE|element type: LTR retrotransposon
|total length in bp: 4648
|target site duplication length in bp: 5
|terminal repeat length in bp: 336
}

REFDSR
{
RDID|FBrf0056166
|di Franco et al.
|1992
WT|Stability of 11 transposable element families compared by Southern
|blotting among individuals of lines that had been subjected to 30
|generations of sister sib matings.  @412@, @roo@, @blood@, @297@, @1731@
|and @G-element@ all appear stable, whereas @copia@, @hobo@, @I-element@,
|@gypsy@ and @jockey@ elements show instability.
}

REFDSR
{
RDID|FBrf0056591
|Fourcade-Peronnet et al.
|1992
WTI|NssBF
}

REFDSR
{
RDID|FBrf0058488
|Codani-Simonart et al.
|1993
PHP|The behavior of the LTR is analyzed after transfer to human monocytes.
}

REFDSR
{
RDID|FBrf0059024
|Montchamp-Moreau et al.
|1993
WT|The distribution of @1731@ retrotransposon-hybridizing sequences reveals
|the sequences are widespread within both the Sophophora and Drosophila
|subgenera. The @1731@ retrotransposon family appears to have a long
|evolutionary history in the Drosophilidae genome.
}

REFDSR
{
RDID|FBrf0064626
|Nahon et al.
|1993
PHP|@Top2@ is involved in different functions of the @1731@ LTR.
}

REFDSR
{
RDID|FBrf0074490
|Sniegowski and Charlesworth
|1994
WT|Element copy numbers on inversion and standard chromosomes has been
|determined. The copy number is significantly higher within low frequency
|inversions than within the corresponding standard chromosome regions.
}

REFDSR
{
RDID|FBrf0076524
|Kim et al.
|1994
WT|The @1731@ promoter is active in Pleurodeles waltl oocytes suggesting
|in the case of horizontal transfer @1731@ can be expressed in vertebrate
|organisms.
}

REFDSR
{
RDID|FBrf0079108
|Nuzhdin and Mackay
|1995
PHP|The distribution of a number of transposable elements has been studied
|in 10 Harwich mutation accumulation lines.
}

REFDSR
{
RDID|FBrf0079937
|Charlesworth et al.
|1994
WT|Estimating the genomic numbers of transposable elements demonstrates
|many families of element are over-represented in heterochromatin.
}

REFDSR
{
RDID|FBrf0079992
|Ding and Lipshitz
|1994
WT|The spatial and temporal expression patterns of fifteen families of
|retrotransposons are analyzed during embryogenesis and are found to
|be conserved. Results suggest that all families carry cis-acting elements
|that control their spatial and temporal expression patterns.
}

REFDSR
{
RDID|FBrf0080187
|Lacoste and Fourcade-Peronnet
|1995
PHP|In vitro transcription of the @1731@ element promoter is repressed
|by @NssBF@ element binding protein(s).
}

REFDSR
{
RDID|FBrf0084234
|Nuzhdin
|1995
PPC|The distribution of transposable elements in D.simulans is similar
|to that found in D.melanogaster, though total copy number is lower.
}

REFDSR
{
RDID|FBrf0085408
|Lacoste et al.
|1995
WT|Overexpression of @Ssb-c31a@ in transfected cells represses the @1731@
|element promoter.
}

REFDSR
{
RDID|FBrf0090548
|Faure et al.
|1996
PHP|UVB-irradiation activation of @1731@-LTR requires a short sequence
|of the U3 region, the sequence is active in human or Schneider cell
|line. Sequence is similar to the binding sequence of members of the
|nuclear factor &kgr;B (NF-&kgr;B)/rel family.
}

REFDSR
{
RDID|FBrf0098518
|Haoudi et al.
|1997
OTH|Expression of @1731@ is regulated not only at the transcriptional level
|but also at the translational level, this regulation is different in
|the two sexes.
}

REFDSR
{
RDID|FBrf0099812
|Terzian et al.
|1997
OTH|Used in an investigation to address the relationship between retrotransposons
|and retroviruses and the coadaptation of these retroelements to their
|host genomes. Results indicate retrotransposons are heterogeneous
|in contrast to retroviruses, suggesting different modes of evolution
|by slippage-like mechanisms.
}

REFDSR
{
RDID|FBrf0129880
|Kalmykova et al.
|1999
TE|Two classes of @1731@ element are present in the genome. The first
|class uses conventional translational frameshifting to ensure expression
|of the @1731\RTase@ open reading frame. Most of the genomic copies
|are related to the second class where the frameshift is prevented as
|a result of a substitution of a rare codon recognizing a rare tRNA
|by a codon preferred by the host genome and the @1731\RTase@ ORF is
|restored by a downstream single nucleotide deletion.
}

REFDSR
{
RDID|FBrf0149104
|Vieira et al.
|2002
SYN|17.31
}

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
TE|element type: LTR retrotransposon
|total length in bp: 4648
|number of copies in genome: 2 in euchromatin of Release 3 genome annotation, of which 1 is full length.
|The single full length @1731@ element does not have a frameshift
|between the @1731\gag@ and @1731\RTase@ genes, so is expected to express
|a @1731\gag@-@1731\RTase@ fusion protein.
}

REFDSR
{
RDID|FBrf0162058
|Aravin et al.
|2003
}

REFDSR
{
RDID|FBrf0167608
|Greil et al.
|2003
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0020768	CLA 1 transposable element gene	NAM 1 1731 element gag	GSYM 1 1731\gag	DT 1 25 Dec 04	RESZ 2244	DBA 4	ALESR 3	REF 2	
GSYM|1731\gag
DT|25 Dec 04
ID|FBgn0020768
CLA|transposable_element_gene
SYN|ORF1
|1731 element gag
AM|encoded by: @1731@
NAM|1731 element gag
DBA|NA:AJ564687
|PA:CAD92840
|NA:X07656
|PA:CAA30502
PAC|PIR:S00953
REF
{
REFM|FBrf0129880
|Kalmykova et al.
|1999
|0
REFM|FBrf0058493
|Kim et al.
|1993
|0
}

REFDSR
{
RDID|FBrf0058493
|Kim et al.
|1993
WT|Translation of the gag protein is studied by transfection of the protein
|into cultured cells.
}

REFDSR
{
RDID|FBrf0085174
|Haoudi et al.
|1995
NAM|1731 element gag
WT|The largest @1731\gag@ polypeptides are present in the virus-like particles
|extracted from a D.melanogaster cell line, and a short @1731\gag@
|polypeptide is associated to the cell nucleus.
SYN|ORF1
}

REFDSR
{
RDID|FBrf0129880
|Kalmykova et al.
|1999
SYN|ORF1
}

ALESR
{
ASYM|1731\gag<up>a.T:Ecol\lacZ</up>
SYN|1731\gag<up>a.T:lacZ</up>
ID|FBal0062283
PHI|Mode of assay: Drosophila cell culture
REF|FBrf0058493
REFDSR
{
RDID|FBrf0058493
|Kim et al.
|1993
MD|Construct: An entire @1731@ harboring the first 9/10 of the ORF1 fused in frame
|with a KpnI-BamHI fragment of @Ecol\lacZ@ in antisense orientation.
OTH|Carried in plasmid pKM8-, expressed in S2 cells, D.virilis DV1 cels
|and D.hydei KUN-DH3 cells to study translation of the gag protein.
MU|in vitro construct | coding region fusion
PHI|Mode of assay: Drosophila cell culture
}

}

ALESR
{
ASYM|1731\gag<up>s.T:Ecol\lacZ</up>
SYN|1731\gag<up>s.T:lacZ</up>
ID|FBal0062282
PHI|Mode of assay: Drosophila cell culture
REF|FBrf0058493
REFDSR
{
RDID|FBrf0058493
|Kim et al.
|1993
MD|Construct: An entire @1731@ harboring the first 9/10 of the ORF1 fused in frame
|with a KpnI-BamHI fragment of @Ecol\lacZ@ in sense orientation.
OTH|Carried in plasmid pKM8+, expressed in S2 cells, D.virilis DV1 cels
|and D.hydei KUN-DH3 cells to study translation of the gag protein.
MU|in vitro construct | coding region fusion
PHI|Mode of assay: Drosophila cell culture
}

}

ALESR
{
ASYM|1731\gag<up>+</up>
ID|FBal0105349
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0044507	CLA 1 transposable element gene	GSYM 1 1731\LTR	DT 1 25 Dec 04	RESZ 225	DBA 4	ALESR 1	
GSYM|1731\LTR
DT|25 Dec 04
ID|FBgn0044507
CLA|transposable_element_gene
AM|encoded by: @1731@
DBA|NA:X04686
|PA:CAA28388
|NA:X04874
|PA:CAA28563
ALESR
{
ASYM|1731\LTR<up>+</up>
ID|FBal0123540
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0012032	CLA 1 transposable element gene	NAM 1 1731-repetitive-element reverse transcriptase	GSYM 1 1731\RTase	DT 1 25 Dec 04	RESZ 982	PTD 1	DBA 2	ALESR 1	REF 3	
GSYM|1731\RTase
PTD
DT|25 Dec 04
ID|FBgn0012032
CLA|transposable_element_gene
SYN|ORF2
|1731-repetitive-element reverse transcriptase
AM|encoded by: @1731@
NAM|1731-repetitive-element reverse transcriptase
DBA|NA:X07656
|PA:CAA30503
PAC|PIR:S00954
REF
{
REFM|FBrf0129880
|Kalmykova et al.
|1999
|0
REFM|FBrf0111944
|Lerat and Capy
|1999
|0
REFM|FBrf0085174
|Haoudi et al.
|1995
|0
}

REFDSR
{
RDID|FBrf0056004
|Champion et al.
|1992
NAM|1731-repetitive-element reverse transcriptase
PHP|The protein co-sediments
|with virus-like particles that exhibit reverse transcriptase activity.
}

REFDSR
{
RDID|FBrf0085174
|Haoudi et al.
|1995
SYN|ORF2
}

REFDSR
{
RDID|FBrf0129880
|Kalmykova et al.
|1999
SYN|ORF2
}

ALESR
{
ASYM|1731\RTase<up>+</up>
ID|FBal0105270
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067635	CLA 1 Gene	GSYM 1 188y	DT 1 25 Dec 04	RESZ 2191	ALESR 2	REF 1	
GSYM|188y
DT|25 Dec 04
ID|FBgn0067635
REF
{
REFM|FBrf0141372
|Ejima et al.
|2001
|0
}

ALESR
{
ASYM|188y<up>188y</up>
SYN|188y
ID|FBal0151006
PHC|viable
|fertile
|courtship defective | female
PHI|@188y<up>188y</up>@ virgin females show elevated ovulation; 15% of the virgin
|females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @188y<up>188y</up>@ virgin females are mated
|to wild-type males is lower than that seen when wild-type virgin females
|are mated to wild-type males, but is higher than that seen when wild-type
|mated females are mated to wild-type males. @188y<up>188y</up>@ mutant virgin
|females show ovipositor extrusion towards courting wild-type males
|(this extrusion behavior is normally observed in mated wild-type females
|but not in virgin wild-type females).
REF|FBrf0141372
REFDSR
{
RDID|FBrf0141372
|Ejima et al.
|2001
TRN|FBti0037975 == P{GawB}188y<up>188y</up>
MU|P-element activity
PHC|viable
|fertile
|courtship defective | female
PHI|@188y<up>188y</up>@ virgin females show elevated ovulation; 15% of the virgin
|females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @188y<up>188y</up>@ virgin females are mated
|to wild-type males is lower than that seen when wild-type virgin females
|are mated to wild-type males, but is higher than that seen when wild-type
|mated females are mated to wild-type males. @188y<up>188y</up>@ mutant virgin
|females show ovipositor extrusion towards courting wild-type males
|(this extrusion behavior is normally observed in mated wild-type females
|but not in virgin wild-type females).
SYN|188y
}

}

ALESR
{
ASYM|188y<up>+</up>
ID|FBal0151312
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0061475	CLA 1 multicopy cytosolic ribosomal RNA gene	GSYM 1 18SrRNA	DT 1 25 Dec 04	RESZ 5174	DBA 62	CEL 1 cytosolic small ribosomal subunit (sensu Eukaryota)	ALESR 2	REF 18	
GSYM|18SrRNA
DT|25 Dec 04
ID|FBgn0061475
CLA|multicopy_cytosolic_ribosomal_RNA_gene
SYN|18S rRNA
|18S rDNA
|18S RNA
|18S
|18s rRNA
|18SRNA
|BEST:GH11893
|BEST:GH15369
|BEST:LD10585
|BEST:LD33742
|BEST:LP07011
|BEST:SD07466
|NEST:bs01c01
ID2|FBgn0045764
|FBgn0045774
|FBgn0045784
|FBgn0045790
|FBgn0045822
|FBgn0045824
|FBgn0046105
AM|encoded by: @bb@, @Ybb@
|component genes: @18SrRNA:CR40456@
CEL|cytosolic small ribosomal subunit (sensu Eukaryota) ; GO:0005843
MD|Extrachromosomal circular DNA (eccDNA) is present throughout the fly's
|life cycle. The eccDNA population contains circular multimers of tandemly
|repeated genes, including @18SrRNA@.
DBA|NA:AA391571
|BDGP:LD10585.5prime
|NA:AI061668
|BDGP:LD33742.5prime
|NA:AI124285
|NA:AI134428
|BDGP:GH11893.5prime
|NA:AI292461
|BDGP:GH15369.5prime
|NA:AI293790
|BDGP:LP07011.5prime
|NA:AI534567
|BDGP:SD07466.5prime
|NA:AI944421
|NEST:bs01c01.y1
|NA:AI944431
|NEST:bs01c11.y1
|NA:AI944432
|NEST:bs01c12.y1
|NA:AI945228
|NEST:bs10d09.y1
|NA:AI945512
|NEST:bs13f12.y1
|NA:AI945622
|NEST:bs14h06.y1
|NA:AI945640
|NEST:bs15b02.y1
|NA:AI945661
|NEST:bs15c12.y1
|NA:AI945828
|NEST:bs17c11.y1
|NA:K01281
|NA:K01286
|NA:K01287
|NA:M20062
|NA:M20063
|NA:M20064
|NA:M21017
|NA:M26817
|NA:S80141
|NA:X15707
|NA:X97143
|NA:Z31795
|dbSTS:4332
|NA:Z31941
|dbSTS:4479
|NA:Z32130
|dbSTS:4682
|NA:Z32170
|dbSTS:4721
|NA:Z32171
|dbSTS:4722
|NA:Z32197
|dbSTS:4748
|NA:Z32373
|dbSTS:4935
|NA:Z32374
|dbSTS:4936
|NA:Z50228
|dbSTS:24192
|NA:Z50229
|dbSTS:24193
REF
{
REFM|FBrf0138565
|Giribet et al.
|2001
|0
REFM|FBrf0155623
|2
REFM|FBrf0094147
|Benevolenskaya et al.
|1997
|0
REFM|FBrf0125039
|Bejarano and Gonzalez
|1999
|0
REFM|FBrf0114952
|Field
|1988
|9
REFM|FBrf0120332
|Schlotterer
|1997.2.11
|9
REFM|FBrf0114951
|Field
|1988
|9
REFM|FBrf0111435
|Morel et al.
|1999
|0
REFM|FBrf0114950
|Field
|1988
|9
REFM|FBrf0159270
|Yuan et al.
|2003
|0
REFM|FBrf0132177
|Gene Disruption Project members
|2001-
|9
REFM|FBrf0094743
|Friedrich and Tautz
|1997
|0
REFM|FBrf0108854
|Krasnov et al.
|1999
|0
REFM|FBrf0158900
|Herold et al.
|2003
|0
REFM|FBrf0108186
|Giordano et al.
|1999
|0
REFM|FBrf0154285
|Ashburner
|2003.2.5
|9
REFM|FBrf0160455
|Cohen et al.
|2003
|0
REFM|FBrf0128400
|Bhadra et al.
|2000
|0
}

REFDSR
{
RDID|FBrf0055058
|Houck et al.
|1991
OTH|Samples of the semiparasitic mite Proctolaelaps regalis that have been
|in contact with D.melanogaster contain @bb@ sequences.
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0094147
|Benevolenskaya et al.
|1997
SYN|18S rDNA
}

REFDSR
{
RDID|FBrf0094743
|Friedrich and Tautz
|1997
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0108186
|Giordano et al.
|1999
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0108854
|Krasnov et al.
|1999
SYN|18S RNA
}

REFDSR
{
RDID|FBrf0111435
|Morel et al.
|1999
SYN|18S
}

REFDSR
{
RDID|FBrf0114950
|Field
|1988
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0114951
|Field
|1988
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0114952
|Field
|1988
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0120332
|Schlotterer
|1997.2.11
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0121292
|Tautz
|1990.3.15
CEL|cytosolic small ribosomal subunit (sensu Eukaryota) ; GO:0005843 | inferred from sequence similarity with EMBL:AF096450
|cytosolic small ribosomal subunit (sensu Eukaryota) ; GO:0005843 | inferred from sequence similarity with EMBL:AF187101
GPD|ribosomal-RNA-18S
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0125039
|Bejarano and Gonzalez
|1999
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0128400
|Bhadra et al.
|2000
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0138565
|Giribet et al.
|2001
SYN|18S
}

REFDSR
{
RDID|FBrf0151416
|Brogna et al.
|2002
SYN|18s rRNA
}

REFDSR
{
RDID|FBrf0158900
|Herold et al.
|2003
SYN|18S rRNA
}

REFDSR
{
RDID|FBrf0160455
|Cohen et al.
|2003
MD|Extrachromosomal circular DNA (eccDNA) is present throughout the fly's
|life cycle. The eccDNA population contains circular multimers of tandemly
|repeated genes, including @18SrRNA@.
}

ALESR
{
ASYM|18SrRNA<up>PL00621</up>
ID|FBal0162864
PHC|viable
|fertile
REF|FBrf0132177
REFDSR
{
RDID|FBrf0132177
|Gene Disruption Project members
|2001-
TRN|FBti0058304 == PBac{GAL4D,EYFP}18SrRNA<up>PL00621</up>
PHC|viable
|fertile
}

}

ALESR
{
ASYM|18SrRNA<up>+</up>
ID|FBal0142210
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0058456	CLA 1 Gene	GSYM 1 18SrRNA:CR40456	DT 1 25 Dec 04	RESZ 558	DBA 1	ALESR 1	REF 1	
GSYM|18SrRNA:CR40456
DT|25 Dec 04
ID|FBgn0058456
SYN|CR40456
AM|member gene of: @18SrRNA@
DBA|NA:AABU01001264
ASQ|FBan0040456
REF
{
REFM|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
|9
}

REFDSR
{
RDID|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
CYC|Heterochromatic, cytological location not yet determined. Maps to a
|region encoding rRNA genes; one of 20F, h29, h20.
}

ALESR
{
ASYM|18SrRNA:CR40456<up>+</up>
ID|FBal0143098
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004364	CLA 1 Gene	NAM 1 18 wheeler	GSYM 1 18w	DT 1 25 Dec 04	RESZ 25633	PDOM 6 INTERPRO:IPR000157 == TIR	PTD 1	DBA 17	FNC 11 antibacterial humoral response (sensu Protostomia)	CEL 4 cytoplasm	WT 1 @18w@ is a critical component of the humoral immune response	CLOC 1 56F8	ALESR 16	SK 2	REF 72	
GSYM|18w
PTD
ARGS
DT|25 Dec 04
ID|FBgn0004364
UAB|Deficiency: Df(2R)017
|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CG8896
|tlr
|18-wheeler
|wheeler
|18-Wheeler
|18W
|CT25100
|18 Wheeler
|toll
|l(2)00053
|Toll like receptor
NAM|18 wheeler
CLOC|56F8
|Limits computationally determined from genome sequence between @P{lacW}l(2)k08002<up>k08002</up>@ and @P{lacW}Ate1<up>k10809</up>@
CYC|Experimentally determined: 56F6--9, 56F8--12
FNC|antibacterial humoral response (sensu Protostomia) ; GO:0006961
|cell adhesion ; GO:0007155
|cytokine and chemokine mediated signaling pathway ; GO:0019221
|defense response ; GO:0006952
|defense response to bacteria ; GO:0042742
|development ; GO:0007275
|embryonic morphogenesis ; GO:0009795
|immune response ; GO:0006955
|macrophage activation ; GO:0042116
|morphogenesis ; GO:0009653
|signal transduction ; GO:0007165
CEL|cytoplasm ; GO:0005737
|integral to membrane ; GO:0016021
|membrane fraction ; GO:0005624
|plasma membrane ; GO:0005886
PDOM|IPR000157 == TIR
|IPR000372 == Cysteine-rich flanking region, N-terminal
|IPR000483 == Cysteine-rich flanking region, C-terminal
|IPR001611 == Leucine-rich repeat
|IPR003591 == Leucine-rich repeat, typical subtype
|IPR004075 == Interleukin-1 receptor, type I/Toll precursor
WT|@18w@ is a critical component of the humoral immune response.
ENZ|transmembrane receptor activity ; GO:0004888 | inferred from sequence similarity
|transmembrane receptor activity ; GO:0004888 | inferred from sequence similarity with FLYBASE:Tl; FB:FBgn0003717
|transmembrane receptor activity ; GO:0004888 | inferred from sequence similarity with FLYBASE:Toll-7; FB:FBgn0034476
|transmembrane receptor activity ; GO:0004888
DBA|NA:AC004428
|BDGP:DS08132
|NA:AC005286
|BDGP:DS08132
|NA:AE003793
|PA:AAF57509
|NA:AI403917
|BDGP-DGC:GH23463
|NA:AQ025714
|BDGP:l(2)k02701
|NA:AY051592
|PA:AAK93016
|BDGP-DGC:GH23463
|NA:L23171
|PA:AAA79208
|NA:S76155
|PA:AAB33383
PAC|PIR:T13852
|PIR:T13887
|UniProt_TrEMBL:Q24591
|UniProt_TrEMBL:Q961H0
|UniProt_TrEMBL:Q9V8Z5
ASQ|FBan0008896
REV|FBrf0123023
|FBrf0139665
|FBrf0156068
REF
{
REFM|FBrf0084996
|Eldon and Williams
|1996
|1
REFM|FBrf0100021
|Engstrom
|1998
|2
REFM|FBrf0068276
|Williams et al.
|1994
|1
REFM|FBrf0076940
|Chiang and Beachy
|1994
|-1
REFM|FBrf0100706
|Rock et al.
|1998
|2
REFM|FBrf0100705
|Medzhitov and Janeway
|1998
|2
REFM|FBrf0157223
|Kambris
|2002
|0
REFM|FBrf0128847
|Nappi and Ottaviani
|2000
|2
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
REFM|FBrf0101953
|Mathey-Prevot and Perrimon
|1998
|2
REFM|FBrf0151661
|Deal-Herr and Cook
|2002.9.10
|9
REFM|FBrf0101460
|Dushay et al.
|1998
|1
REFM|FBrf0108800
|Hoffmann et al.
|1999
|2
REFM|FBrf0155700
|Solano et al.
|2003
|0
REFM|FBrf0159908
|Janssens and Beyaert
|2002
|2
REFM|FBrf0114849
|Eldon
|1993
|9
REFM|FBrf0100558
|Dushay and Eldon
|1998
|2
REFM|FBrf0098089
|Mitcham et al.
|1996
|0
REFM|FBrf0174342
|Brennan and Anderson
|2004
|2
REFM|FBrf0141274
|Mi et al.
|2001.12.13
|9
REFM|FBrf0106857
|Liebermann and Hoffman
|1998
|2
REFM|FBrf0055359
|Eldon and Bellen
|1992
|1
REFM|FBrf0075393
|Eldon et al.
|1991
|1
REFM|FBrf0100747
|Wu and Anderson
|1998
|0
REFM|FBrf0129898
|Khush and Lemaitre
|2000
|2
REFM|FBrf0179348
|Moehring and Mackay
|2004
|0
REFM|FBrf0079825
|Eldon
|1995
|9
REFM|FBrf0106457
|Eldon et al.
|1999
|1
REFM|FBrf0126490
|Eldon et al.
|2000
|1
REFM|FBrf0088024
|Botas and Auwers
|1996
|0
REFM|FBrf0156068
|2
REFM|FBrf0079625
|Williams et al.
|1995
|1
REFM|FBrf0079624
|Williams et al.
|1994
|1
REFM|FBrf0174231
|Kiger et al.
|2003
|9
REFM|FBrf0073029
|Eldon et al.
|1994
|0
REFM|FBrf0127298
|Rubin et al.
|2000
|0
REFM|FBrf0125032
|Beaton
|1999.12.12
|9
REFM|FBrf0141068
|Kimbrell and Beutler
|2001
|2
REFM|FBrf0127230
|Meister et al.
|2000
|2
REFM|FBrf0126686
|Milshina
|1999.11
|9
REFM|FBrf0155844
|Lavine and Strand
|2002
|2
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
|9
REFM|FBrf0132111
|Hynes and Zhao
|2000
|9
REFM|FBrf0125817
|Janeway and Medzhitov
|1999
|2
REFM|FBrf0113821
|Chiang
|1995.7.26
|9
REFM|FBrf0098260
|Hoffmann and Reichhart
|1997
|2
REFM|FBrf0123023
|Govind
|1999
|2
REFM|FBrf0130108
|Tauszig et al.
|2000
|0
REFM|FBrf0161623
|Kurz and Ewbank
|2003
|2
REFM|FBrf0102791
|Syed et al.
|1998
|1
REFM|FBrf0111489
|Spradling et al.
|1999
|0
REFM|FBrf0099002
|Williams et al.
|1997
|0
REFM|FBrf0101333
|Williams et al.
|1998
|1
REFM|FBrf0075178
|Eldon and Bellen
|1992
|9
REFM|FBrf0174513
|Singh et al.
|2003
|2
REFM|FBrf0126670
|Gu
|1999.11
|9
REFM|FBrf0125476
|Luo and Zheng
|2000
|0
REFM|FBrf0141541
|Takeda and Akira
|2001
|2
REFM|FBrf0129777
|Cox et al.
|2000
|0
REFM|FBrf0139665
|Silverman and Maniatis
|2001
|2
REFM|FBrf0091791
|Williams et al.
|1997
|1
REFM|FBrf0131060
|Aderem and Ulevitch
|2000
|2
REFM|FBrf0111089
|Williams et al.
|1999
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0130159
|Wasserman
|2000
|2
REFM|FBrf0128867
|Syed and Eldon
|2000
|1
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0110608
|Qureshi et al.
|1999
|2
REFM|FBrf0178966
|Agaisse and Perrimon
|2004
|2
REFM|FBrf0132250
|Hedengren et al.
|2000
|0
REFM|FBrf0141597
|Mushegian and Medzhitov
|2001
|2
}

REFDSR
{
RDID|FBrf0055359
|Eldon and Bellen
|1992
CLOC|56F6--9 (determined by in situ hybridization)
}

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
CLOC|56F6--9
LOI|18w<up>00053</up>
|18w<up>k02701</up>
BMD|Df(2R)017
}

REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
ENZ|transmembrane receptor activity ; GO:0004888 | inferred from sequence similarity with FLYBASE:Tl; FB:FBgn0003717
FNC|cell adhesion ; GO:0007155 | inferred from direct assay
|morphogenesis ; GO:0009653 | inferred from mutant phenotype
CEL|membrane fraction ; GO:0005624 | inferred from direct assay
|plasma membrane ; GO:0005886 | inferred from sequence similarity with FLYBASE:Tl; FB:FBgn0003717
OTH|Etymology: named "18 wheeler" on basis of 18 stripes of expression
|during early gastrulation.
PHP|Molecular and phenotypic analysis suggests @18w@ participates in the
|developmental program specified by segmentation and homeotic genes
|as a cell adhesion or receptor molecule that facilitates cell movements.
}

REFDSR
{
RDID|FBrf0075178
|Eldon and Bellen
|1992
CLOC|56F8--12 (determined by in situ hybridization)
}

REFDSR
{
RDID|FBrf0075393
|Eldon et al.
|1991
PHP|@18w@ open reading frame encodes a protein with significant similarities
|to both @Tl@ and @chp@.
}

REFDSR
{
RDID|FBrf0076940
|Chiang and Beachy
|1994
PHP|@18w@ encodes a protein that contains multiple leucine rich motifs
|(LRR) in its presumed extracellular domain. @18w@ may be involved in
|cell-to-cell interactions.
SYN|tlr: Toll like receptor
}

REFDSR
{
RDID|FBrf0079625
|Williams et al.
|1995
PHP|The @18w@ protein functions as a receptor mediating intercellular communication
|during various developmental events, including pattern formation, imaginal
|cell determination and the larval immune response. Expression of @18w@
|protein in non-adhesive Schneider 2 cells promotes heterophilic cell
|aggregation as seen in similar experiments with @Tl@ and other receptor-ligand
|molecules.
}

REFDSR
{
RDID|FBrf0079825
|Eldon
|1995
PHP|@18w@ protein is 1389 amino aids in length.
}

REFDSR
{
RDID|FBrf0088024
|Botas and Auwers
|1996
SYN|18-wheeler
}

REFDSR
{
RDID|FBrf0099002
|Williams et al.
|1997
FNC|antibacterial humoral response (sensu Protostomia) ; GO:0006961 | inferred from mutant phenotype
|immune response ; GO:0006955 | inferred from expression pattern
CEL|cytoplasm ; GO:0005737 | inferred from direct assay
|plasma membrane ; GO:0005886 | inferred from direct assay
WT|@18w@ is a critical component of the humoral immune response.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
MD|Maps to clone: DS08132
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
CLOC|56F6--9 (determined by in situ hybridization)
BMD|Df(2R)017
}

REFDSR
{
RDID|FBrf0113821
|Chiang
|1995.7.26
SYN|tlr
}

REFDSR
{
RDID|FBrf0114849
|Eldon
|1993
SYN|wheeler
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: GH23463 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0125817
|Janeway and Medzhitov
|1999
SYN|18-Wheeler
}

REFDSR
{
RDID|FBrf0126686
|Milshina
|1999.11
AM|Source for identity of: 18w CG8896
}

REFDSR
{
RDID|FBrf0127230
|Meister et al.
|2000
FNC|defense response ; GO:0006952 | traceable author statement
|embryonic morphogenesis ; GO:0009795 | traceable author statement
}

REFDSR
{
RDID|FBrf0128847
|Nappi and Ottaviani
|2000
SYN|18-wheeler
}

REFDSR
{
RDID|FBrf0130108
|Tauszig et al.
|2000
SYN|18W
}

REFDSR
{
RDID|FBrf0130159
|Wasserman
|2000
SYN|18-wheeler
}

REFDSR
{
RDID|FBrf0132111
|Hynes and Zhao
|2000
SYN|CT25100
}

REFDSR
{
RDID|FBrf0133282
|Lemaitre
|2000.12.20
ENZ|transmembrane receptor activity ; GO:0004888 | inferred from sequence similarity
FNC|antibacterial humoral response (sensu Protostomia) ; GO:0006961 | non-traceable author statement
|signal transduction ; GO:0007165 | inferred from sequence similarity
CEL|integral to membrane ; GO:0016021 | inferred from sequence similarity
GPD|Toll receptor-like
SYN|18 Wheeler
}

REFDSR
{
RDID|FBrf0141068
|Kimbrell and Beutler
|2001
FNC|antibacterial humoral response (sensu Protostomia) ; GO:0006961 | traceable author statement
|development ; GO:0007275 | traceable author statement
}

REFDSR
{
RDID|FBrf0141274
|Mi et al.
|2001.12.13
ENZ|transmembrane receptor activity ; GO:0004888 | inferred from sequence similarity with FLYBASE:Toll-7; FB:FBgn0034476
}

REFDSR
{
RDID|FBrf0151661
|Deal-Herr and Cook
|2002.9.10
BMD|Df(2R)BSC22
}

REFDSR
{
RDID|FBrf0155700
|Solano et al.
|2003
SYN|18W
}

REFDSR
{
RDID|FBrf0159908
|Janssens and Beyaert
|2002
SYN|toll
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
FNC|cytokine and chemokine mediated signaling pathway ; GO:0019221 | inferred from electronic annotation
|defense response to bacteria ; GO:0042742 | inferred from electronic annotation
|macrophage activation ; GO:0042116 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0161623
|Kurz and Ewbank
|2003
}

REFDSR
{
RDID|FBrf0174231
|Kiger et al.
|2003
OTH|dsRNA made from templates generated with primers directed against
|this gene tested in RNAi screen for effects on Kc167 and S2R<up>+</up>
|cell morphology.
}

REFDSR
{
RDID|FBrf0179348
|Moehring and Mackay
|2004
PHP|Mutant allele fails to complement a QTL affecting male mating behavior.
}

ALESR
{
ASYM|18w<up>&Dgr;1-11</up>
ID|FBal0038075
PHC|lethal | recessive
ALC|loss of function
REF|FBrf0073029
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Internal excision within PZ element.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
PHC|lethal | recessive
ALC|loss of function
}

}

ALESR
{
ASYM|18w<up>&Dgr;1-14</up>
ID|FBal0038077
PHC|lethal | recessive
ALC|loss of function
PHI|Lethality is not complete. In uncrowded conditions 0.5% of the flies
|survive.
REF|FBrf0073029
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Excision plus possible additional defect.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
PHC|lethal | recessive
ALC|loss of function
PHI|Lethality is not complete. In uncrowded conditions 0.5% of the flies
|survive.
}

}

ALESR
{
ASYM|18w<up>&Dgr;1-15</up>
ID|FBal0038078
PHC|lethal | recessive
ALC|loss of function
PHI|Lethality is not complete. In uncrowded conditions 3% of the flies
|survive.
REF|FBrf0073029
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Internal excision within PZ element.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
PHC|lethal | recessive
ALC|loss of function
PHI|Lethality is not complete. In uncrowded conditions 3% of the flies
|survive.
}

}

ALESR
{
ASYM|18w<up>&Dgr;1-24</up>
ID|FBal0038079
PHC|lethal | recessive
ALC|loss of function
REF|FBrf0073029
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Internal excision within PZ element.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
PHC|lethal | recessive
ALC|loss of function
}

}

ALESR
{
ASYM|18w<up>&Dgr;1-82</up>
ID|FBal0038080
PHC|lethal | larval | recessive
PHM|leg
|antenna
|wing
|haltere
ALC|loss of function
PHI|Lethality is not complete. In uncrowded conditions 4% of the flies
|survive. Survivors eclose later than their sibs and die within a
|few days. Survivors typically show morphological defects in at least
|one appendage.
REF|FBrf0073029
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Deletion of PZ element and genomic DNA removing the transcription start
|site as well as most or all of the leader.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
PHC|lethal | larval | recessive
PHM|leg
|antenna
|wing
|haltere
ALC|loss of function
PHI|Lethality is not complete. In uncrowded conditions 4% of the flies
|survive. Survivors eclose later than their sibs and die within a
|few days. Survivors typically show morphological defects in at least
|one appendage.
}

}

ALESR
{
ASYM|18w<up>&Dgr;2-62</up>
ID|FBal0038081
PHC|lethal | recessive
ALC|loss of function
REF|FBrf0073029
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Internal excision within PZ element.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
PHC|lethal | recessive
ALC|loss of function
}

}

ALESR
{
ASYM|18w<up>&Dgr;2-63</up>
ID|FBal0038082
PHC|lethal | recessive
ALC|loss of function
REF|FBrf0073029
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Internal excision within PZ element.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
PHC|lethal | recessive
ALC|loss of function
}

}

ALESR
{
ASYM|18w<up>&Dgr;6-81</up>
ID|FBal0038083
PHC|lethal | recessive
ALC|loss of function
REF|FBrf0073029
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Internal excision within PZ element.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
PHC|lethal | recessive
ALC|loss of function
}

}

ALESR
{
ASYM|18w<up>&Dgr;7-35</up>
SYN|18w<up>7-35</up>
ID|FBal0033274
REF|FBrf0076940
|FBrf0151661
|FBrf0073029
|FBrf0132250
|FBrf0179348
|FBrf0099002
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Deletion of PZ element and 2.2kb of genomic DNA removing approximately
|2.2kb of open reading frame.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
PHC|lethal | larval | recessive
PHM|leg
|antenna
|wing
|haltere
ALC|loss of function
PHI|Lethality is not complete. In uncrowded conditions 0.5% of the flies
|survive. Survivors eclose later than their sibs and die within a few
|days. Survivors typically show morphological defects in at least one
|appendage.
}

REFDSR
{
RDID|FBrf0076940
|Chiang and Beachy
|1994
GII|In a @hh<up>bar3</up>@/@hh<up>6</up>@ background
|@18w<up>&Dgr;7-35</up>@ produces a dominant reduction in eye size
|resulting in a concave shape or nick at the anterior eye margin.
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0099002
|Williams et al.
|1997
MD|Imprecise excision of the @P{PZ}@ element present in @18w<up>00053</up>@,
|resulting in a 2.2kb deletion extending from the site of the @P{PZ}@
|insertion into the @18w@ open reading frame.
PRG|18w<up>00053</up>
MU|P-element activity
PHC|immune response defective | recessive
PHI|Only 56% of homozygous @18w<up>&Dgr;7-35</up>@ third instar larvae are still
|alive 24 hours after infection with either E.coli or E.cloacae,
|compared to 90% survival for @18w<up>&Dgr;7-35</up>@ heterozygotes,
|@18w<up>&Dgr;1-12</up>@ homozygotes or wild-type third instar larvae. Homozygous
|@18w<up>&Dgr;7-35</up>@ third instar larvae show 100% survival 24 hours after
|wounding with a sterile pyrogen-free needle.
SYN|18w<up>7-35</up>
}

REFDSR
{
RDID|FBrf0132250
|Hedengren et al.
|2000
SYN|18w<up>7-35</up>
}

SK|FBst0004372
|y[1] w[*]; 18w[Delta7-35]/CyO
}

ALESR
{
ASYM|18w<up>&Dgr;7-43</up>
ID|FBal0038084
PHC|lethal | recessive
ALC|loss of function
PHI|Lethality is not complete. In uncrowded conditions 2% of the flies
|survive.
REF|FBrf0073029
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Internal excision within PZ element.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
PHC|lethal | recessive
ALC|loss of function
PHI|Lethality is not complete. In uncrowded conditions 2% of the flies
|survive.
}

}

ALESR
{
ASYM|18w<up>00053</up>
SYN|l(2)00053
|l(2)00053<up>00053</up>
ID|FBal0007942
DIS|A. Spradling.
TRN|FBti0003351 == P{PZ}18w<up>00053</up>
|BDGP:l(2)00053
MU|P-element activity
REF|FBrf0067338
|FBrf0125032
|FBrf0073029
|FBrf0111489
|FBrf0099002
REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
ACM|18w<up>k02701</up>
AFC|18w<up>k02701</up>
OTH|Complements: @hts<up>01103</up>@.
|Complements: @mus209<up>02448</up>@.
|Complements: @mus209<up>02697</up>@.
|Complements: @5SrRNA<up>03068</up>@.
|Complements: @sm<up>05338</up>@.
|Complements: @mus209<up>06652</up>@.
|Complements: @l(2)k08002<up>k08002</up>@.
|Complements: @Ate1<up>k10809</up>@.
|Complements: @hts<up>k14523</up>@.
|Complements: @mus209<up>s1534</up>@.
|Complements: @l(2)s1866<up>s1866</up>@.
TRN|FBti0003351 == P{PZ}18w<up>00053</up>
|BDGP:l(2)00053
}

REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|P element insertion at 5' end of @18w@ transcription unit, 26bp from
|the predicted transcription start site, with the @Ecol\lacZ@ in the same transcriptional
|orientation as @18w@.
TRN|FBti0003351 == P{PZ}18w<up>00053</up>
|BDGP:l(2)00053
MU|P-element activity
PHC|lethal | recessive
ALC|hypomorph
PHI|Lethality is not complete. In uncrowded conditions 8-10% of the flies
|survive. Survivors are small, have morphological defects, are unable
|to fly or jump and have low fertility.
}

REFDSR
{
RDID|FBrf0099002
|Williams et al.
|1997
MD|Insertion of a @P{PZ}@ element approximately 400bp 5' of the @18w@
|open reading frame.
TRN|FBti0003351 == P{PZ}18w<up>00053</up>
|BDGP:l(2)00053
MU|P-element activity
SYN|l(2)00053
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
TRN|FBti0003351 == P{PZ}18w<up>00053</up>
|BDGP:l(2)00053
PHC|lethal | recessive
SYN|l(2)00053
}

}

ALESR
{
ASYM|18w<up>k02701</up>
SYN|l(2)k02701
ID|FBal0065575
REF|FBrf0067338
|FBrf0125032
|FBrf0111489
REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
ACM|18w<up>00053</up>
AFC|18w<up>00053</up>
DIS|I. Kiss.
OTH|Complements: @mus209<up>02448</up>@.
|Complements: @l(2)k08002<up>k08002</up>@.
|Complements: @Ate1<up>k10809</up>@.
|Complements: @hts<up>k14523</up>@.
|Complements: @l(2)s1866<up>s1866</up>@.
TRN|FBti0007254 == P{lacW}18w<up>k02701</up>
|BDGP:l(2)k02701
MU|P-element activity
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
TRN|FBti0007254 == P{lacW}18w<up>k02701</up>
|BDGP:l(2)k02701
PHC|lethal | recessive
SYN|l(2)k02701
}

SK|FBst0010518
|y[1] w[67c23]; P{w[+mC]=lacW}18w[k02701]/CyO
}

ALESR
{
ASYM|18w<up>unspecified</up>
ID|FBal0118616
REF|FBrf0129777
REFDSR
{
RDID|FBrf0129777
|Cox et al.
|2000
GIC|non-suppressor of @arm<up>3</up>@
}

}

ALESR
{
ASYM|18w<up>fl.cEa</up>
ID|FBal0038085
PHI|Schneider cells that express @18w@ show heterophilic cell adhesion
|properties.
|Mode of assay: Drosophila cell culture
REF|FBrf0073029
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
NAM|full length construct a of Eldon
MD|Construct: 5.2kb PvuI-SSpI fragment including @18w@ coding region, in pRmHa3 expression
|vector.
OTH|Carried in plasmid, used to transfect S2 cells.
MU|in vitro construct | other
PHI|Schneider cells that express @18w@ show heterophilic cell adhesion
|properties.
|Mode of assay: Drosophila cell culture
}

}

ALESR
{
ASYM|18w<up>&Dgr;1-12</up>
SYN|18w<up>1-12</up>
ID|FBal0038076
REF|FBrf0073029
|FBrf0099002
REFDSR
{
RDID|FBrf0073029
|Eldon et al.
|1994
MD|Precise or near precise excision of PZ element.
PRG|18w<up>00053</up>
MU|&Dgr;2-3
ALC|wild-type
PHI|No obvious morphological or behavioral defects.
}

REFDSR
{
RDID|FBrf0099002
|Williams et al.
|1997
MD|Precise excision of the @P{PZ}@ element.
AMIS|Revertant.
PRG|18w<up>00053</up>
MU|P-element activity
PHC|wild-type
|viable
PHI|90% of homozygous @18w<up>&Dgr;1-12</up>@ third instar larvae are still alive
|24 hours after infection with either E.coli or E.cloacae.
SYN|18w<up>1-12</up>
}

}

ALESR
{
ASYM|18w<up>+</up>
ID|FBal0066318
CLA|wild-type generic
REF|FBrf0105495
}

IFL|../dbzhnsky/eghtnw1.htm
SK|FBst0004372
|y[1] w[*]; 18w[Delta7-35]/CyO
|FBst0010518
|y[1] w[67c23]; P{w[+mC]=lacW}18w[k02701]/CyO
SKC|2
}
# EOR
GENR
{
RETE|ID 1 FBgn0043464	CLA 1 fusion gene	GSYM 1 18w::Tl	DT 1 25 Dec 04	RESZ 740	ALESR 1	REF 1	
GSYM|18w::Tl
DT|25 Dec 04
ID|FBgn0043464
CLA|fusion_gene
REF
{
REFM|FBrf0130108
|Tauszig et al.
|2000
|0
}

ALESR
{
ASYM|18w::Tl<up>&Dgr;LRR.T:Zzzz\FLAG</up>
ID|FBal0119723
PHI|Mode of assay: Drosophila cell culture
REF|FBrf0130108
REFDSR
{
RDID|FBrf0130108
|Tauszig et al.
|2000
MD|The truncated ectodomain from @Tl<up>&Dgr;LRR.T:Zzzz\FLAG</up>@ is fused to
|the transmembrane and intracytoplasmic domains of @18w@.
OTH|Carried in a plasmid and transfected into S2 cells.
MU|in vitro construct | coding region fusion
PHI|Mode of assay: Drosophila cell culture
}

}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070056	CLA 1 Gene	GSYM 1 19	DT 1 25 Dec 04	RESZ 302	ALESR 1	
GSYM|19
DT|25 Dec 04
ID|FBgn0070056
SYN|#19
REFDSR
{
RDID|FBrf0173481
|Pistillo et al.
|2004
OTH|Identification: In a screen for mutations affecting R7/R8 photoreceptor subtype specification.
SYN|#19
}

ALESR
{
ASYM|19<up>+</up>
ID|FBal0158437
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0069070	CLA 1 Gene	GSYM 1 194-26	DT 1 25 Dec 04	RESZ 1318	ALESR 2	REF 1	
GSYM|194-26
DT|25 Dec 04
ID|FBgn0069070
REF
{
REFM|FBrf0162144
|Morris et al.
|2003
|0
}

REFDSR
{
RDID|FBrf0162144
|Morris et al.
|2003
CYC|Maps to 3R by deficiency analysis (details unspecified).
}

ALESR
{
ASYM|194-26<up>194-26</up>
SYN|194-26
ID|FBal0152817
PHC|lethal | recessive
|female sterile | recessive | germ-line clone
PHI|Homozygous clones can be recovered in the eye.
|Females containing homozygous germ-line clones show defects in early
|oogenesis.
REF|FBrf0162144
REFDSR
{
RDID|FBrf0162144
|Morris et al.
|2003
AMIS|Selected as: a mutation that results in a failure to produce eggs when
|females carry homozygous germ-line clones.
|It is not certain whether the lethal mutation and the sterility map
|to the same lesion, since only a single allele of this complementation
|group has been recovered.
PHC|lethal | recessive
|female sterile | recessive | germ-line clone
PHI|Homozygous clones can be recovered in the eye.
|Females containing homozygous germ-line clones show defects in early
|oogenesis.
SYN|194-26
}

}

ALESR
{
ASYM|194-26<up>+</up>
ID|FBal0154332
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0022715	CLA 1 Gene	GSYM 1 19w	DT 1 25 Dec 04	RESZ 946	ALESR 2	REF 2	
GSYM|19w
DT|25 Dec 04
ID|FBgn0022715
REF
{
REFM|FBrf0098656
|Omelyanchuk and Lebedeva
|1997
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

ALESR
{
ASYM|19w<up>1</up>
ID|FBal0065574
PHC|mitotic
PHM|larval brain
|chromosome
PHI|Abnormal mitotic activity as assayed in the larval brain.
|Highly condensed chromsomes in metaphase.
REF|FBrf0098656
REFDSR
{
RDID|FBrf0098656
|Omelyanchuk and Lebedeva
|1997
TRN|FBti0007253 == P{lArB}19w<up>1</up>
MU|Js
PHC|mitotic
PHM|larval brain
|chromosome
PHI|Abnormal mitotic activity as assayed in the larval brain.
|Highly condensed chromsomes in metaphase.
}

}

ALESR
{
ASYM|19w<up>+</up>
ID|FBal0081522
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0015579	CLA 1 Gene	GSYM 1 2.1	DT 1 25 Dec 04	RESZ 654	WT 1 Isolated as an interactor with the @Pcl@ protein	ALESR 1	REF 4	
GSYM|2.1
DT|25 Dec 04
ID|FBgn0015579
WT|Isolated as an interactor with the @Pcl@ protein.
WTI|Pcl
REF
{
REFM|FBrf0091914
|Coulson et al.
|1997
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0101842
|Coulson et al.
|1998
|1
REFM|FBrf0084907
|Coulson et al.
|1996
|1
}

REFDSR
{
RDID|FBrf0084907
|Coulson et al.
|1996
WT|Isolated as an interactor with the @Pcl@ protein.
}

ALESR
{
ASYM|2.1<up>+</up>
ID|FBal0075461
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0069069	CLA 1 Gene	GSYM 1 20-51	DT 1 25 Dec 04	RESZ 1312	ALESR 2	REF 1	
GSYM|20-51
DT|25 Dec 04
ID|FBgn0069069
REF
{
REFM|FBrf0162144
|Morris et al.
|2003
|0
}

REFDSR
{
RDID|FBrf0162144
|Morris et al.
|2003
CYC|Maps to 3R by deficiency analysis (details unspecified).
}

ALESR
{
ASYM|20-51<up>20-51</up>
SYN|20-51
ID|FBal0152816
PHC|lethal | recessive
|female sterile | recessive | germ-line clone
PHI|Homozygous clones can be recovered in the eye.
|Females containing homozygous germ-line clones show defects in early
|oogenesis.
REF|FBrf0162144
REFDSR
{
RDID|FBrf0162144
|Morris et al.
|2003
AMIS|Selected as: a mutation that results in a failure to produce eggs when
|females carry homozygous germ-line clones.
|It is not certain whether the lethal mutation and the sterility map
|to the same lesion, since only a single allele of this complementation
|group has been recovered.
SYN|20-51
PHC|lethal | recessive
|female sterile | recessive | germ-line clone
PHI|Homozygous clones can be recovered in the eye.
|Females containing homozygous germ-line clones show defects in early
|oogenesis.
}

}

ALESR
{
ASYM|20-51<up>+</up>
ID|FBal0154331
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0043850	CLA 1 Gene	GSYM 1 2033	DT 1 25 Dec 04	RESZ 759	ALESR 2	REF 1	
GSYM|2033
DT|25 Dec 04
ID|FBgn0043850
REF
{
REFM|FBrf0131272
|Chanut et al.
|2000
|0
}

ALESR
{
ASYM|2033<up>2033</up>
ID|FBal0121019
PHC|visible | dominant
PHM|eye
|morphogenetic furrow
|ommatidium
PHI|Stop furrow mutant phenotype.
REF|FBrf0131272
REFDSR
{
RDID|FBrf0131272
|Chanut et al.
|2000
PHC|visible | dominant
PHM|eye
|morphogenetic furrow
|ommatidium
PHI|Stop furrow mutant phenotype.
}

}

ALESR
{
ASYM|2033<up>+</up>
ID|FBal0121460
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0022714	CLA 1 Gene	GSYM 1 22w	DT 1 25 Dec 04	RESZ 1962	CLOC 1 42A	ALESR 2	REF 5	
GSYM|22w
DT|25 Dec 04
ID|FBgn0022714
UAB|Deficiency: Df(2R)nap1 (inferred from cytology)
|Duplication: Dp(2;Y)cn<up>+</up> (inferred from cytology)
CLOC|42A
|Left limit from in situ hybridization (FBrf0098656)
|Right limit from in situ hybridization (FBrf0098656)
CYC|Experimentally determined: 42A
REF
{
REFM|FBrf0098656
|Omelyanchuk and Lebedeva
|1997
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0105088
|Omel'yanchuk et al.
|1997
|0
REFM|FBrf0102993
|Omel'ianchuk and Lebedeva
|1998
|0
REFM|FBrf0100614
|Omel'yanchuk et al.
|1997
|0
}

REFDSR
{
RDID|FBrf0098656
|Omelyanchuk and Lebedeva
|1997
CLOC|42A (determined by in situ hybridization)
LOI|22w<up>1</up>
}

REFDSR
{
RDID|FBrf0102993
|Omel'ianchuk and Lebedeva
|1998
PHP|Mutation in @22w@ blocks the cell cycle in metaphase.
}

ALESR
{
ASYM|22w<up>1</up>
SYN|22w
ID|FBal0065573
REF|FBrf0102993
|FBrf0098656
REFDSR
{
RDID|FBrf0098656
|Omelyanchuk and Lebedeva
|1997
TRN|FBti0007252 == P{lArB}22w<up>1</up>
MU|Js
PHC|mitotic
PHM|larval brain
|chromosome
PHI|Abnormal mitotic activity as assayed in the larval brain.
|Highly condensed chromosomes, increased metaphase index with rare anaphase.
}

REFDSR
{
RDID|FBrf0102993
|Omel'ianchuk and Lebedeva
|1998
TRN|FBti0007252 == P{lArB}22w<up>1</up>
PHM|chromosome
PHI|Flies show a block in metaphase (and rarely anaphase). The chromosomes
|have an abnormal morphology.
SYN|22w
}

}

ALESR
{
ASYM|22w<up>+</up>
ID|FBal0081521
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067634	CLA 1 Gene	GSYM 1 233y-a	DT 1 25 Dec 04	RESZ 2700	CLOC 1 87C1--3	ALESR 2	
GSYM|233y-a
DT|25 Dec 04
ID|FBgn0067634
UAB|Deficiency: Df(3R)ry615
SYN|233y
CYC|Experimentally determined: 87C1--3
CLOC|87C1--3 (determined by in situ hybridization)
REFDSR
{
RDID|FBrf0141372
|Ejima et al.
|2001
CLOC|87C1--3 (determined by in situ hybridization)
LOI|233y-a<up>233y-a</up>
BMD|Df(3R)ry615
SYN|233y
}

ALESR
{
ASYM|233y-a<up>233y-a</up>
SYN|233y
ID|FBal0151005
PHC|viable
|fertile
|courtship defective | female
PHI|@233y-a<up>233y-a</up>@ virgin females show elevated ovulation; 68% of the
|virgin females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @233y-a<up>233y-a</up>@ virgin females are
|mated to wild-type males is lower than that seen when wild-type virgin
|females are mated to wild-type males, but is higher than that seen
|when wild-type mated females are mated to wild-type males. @233y-a<up>233y-a</up>@
|mutant virgin females show ovipositor extrusion towards courting wild-type
|males (this extrusion behavior is normally observed in mated wild-type
|females but not in virgin wild-type females).
REF|FBrf0141372
REFDSR
{
RDID|FBrf0141372
|Ejima et al.
|2001
AMIS|Separable from: @P{GawB}233y-b@.
OTH|Excision of the @P{GawB}@ insertions in the "233y" line (which contains
|two insertions; @P{GawB}233y-a<up>233y-a</up>@ and @P{GawB}233y-b@) reverts
|the mutant phenotype.
TRN|FBti0037974 == P{GawB}233y-a<up>233y-a</up>
MU|P-element activity
PHC|viable
|fertile
|courtship defective | female
PHI|@233y-a<up>233y-a</up>@ virgin females show elevated ovulation; 68% of the
|virgin females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @233y-a<up>233y-a</up>@ virgin females are
|mated to wild-type males is lower than that seen when wild-type virgin
|females are mated to wild-type males, but is higher than that seen
|when wild-type mated females are mated to wild-type males. @233y-a<up>233y-a</up>@
|mutant virgin females show ovipositor extrusion towards courting wild-type
|males (this extrusion behavior is normally observed in mated wild-type
|females but not in virgin wild-type females).
SYN|233y
}

}

ALESR
{
ASYM|233y-a<up>+</up>
ID|FBal0151311
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0066319	CLA 1 Gene	GSYM 1 24D1	DT 1 25 Dec 04	RESZ 423	ALESR 1	REF 1	
GSYM|24D1
DT|25 Dec 04
ID|FBgn0066319
REF
{
REFM|FBrf0157136
|Jung and Bonini
|2003
|1
}

REFDSR
{
RDID|FBrf0157136
|Jung and Bonini
|2003
OTH|Identification: as a mutation that suppresses polyQ-induced neurodegeneration in Drosophila.
PHP|Mutations in @24D1@ are viable.
}

ALESR
{
ASYM|24D1<up>+</up>
ID|FBal0146587
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0028967	CLA 1 Gene	NAM 1 26-29kD-proteinase	GSYM 1 26-29-p	DT 1 25 Dec 04	RESZ 5409	PDOM 2 INTERPRO:IPR000169 == Peptidase, eukaryotic cysteine peptidase active site	DBA 11	FNC 1 proteolysis and peptidolysis	CLOC 1 70C10	ALESR 3	REF 12	
GSYM|26-29-p
DT|25 Dec 04
ID|FBgn0028967
UAB|Deficiency: Df(3L)fz-GF3b (inferred from cytology)
|Duplication: Dp(3;3)M71 (inferred from cytology)
SYN|CG8947
|l(3)s3635
|26,29kDa proteinase
|26-29kD-proteinase
|26/29kD-proteinase
ID2|FBgn0024586
CLOC|70C10
|Limits computationally determined from genome sequence between @P{EP}EP3561<up>EP3561</up>@ and @P{PZ}l(3)70Da<up>02402</up>@/@P{PZ}btl<up>00208</up>@
CYC|Experimentally determined: 70C, 70C4--6
FNC|proteolysis and peptidolysis ; GO:0006508
PDOM|IPR000169 == Peptidase, eukaryotic cysteine peptidase active site
|IPR000668 == Peptidase C1A, papain
NAM|26-29kD-proteinase
MD|Identified with: RE18380 (BDGP-DGC)
ENZ|cathepsin K activity ; GO:0004216 ; EC:3.4.22.38 | inferred from sequence similarity with EMBL:AJ006033; protein_id:CAA06825
|cathepsin K activity ; GO:0004216 ; EC:3.4.22.38
DBA|NA:AB011376
|PA:BAA86910
|NA:AE003536
|PA:AAF49777
|NA:AQ026395
|BDGP:l(3)s3635
|NA:AY122222
|PA:AAM52734
|BDGP-DGC:RE18380
|NA:BI213067
|BDGP-DGC:RE18380
PAC|UniProt_TrEMBL:Q9V3U6
ASQ|FBan0008947
REF
{
REFM|FBrf0111489
|Spradling et al.
|1999
|-1
REFM|FBrf0108756
|Fujimoto et al.
|1999
|0
REFM|FBrf0158900
|Herold et al.
|2003
|0
REFM|FBrf0126656
|Butler
|1999.11
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0157314
|Levis
|2003.4.25
|-1
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
}

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
CLOC|70C4--6
LOI|26-29-p<up>s3635</up>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ENZ|cathepsin K activity ; GO:0004216 ; EC:3.4.22.38 | inferred from sequence similarity with EMBL:AJ006033; protein_id:CAA06825
GPD|cathepsin K
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
CLOC|70C4--6 (determined by in situ hybridization)
LOI|26-29-p<up>s3635</up>
SYN|l(3)s3635
}

REFDSR
{
RDID|FBrf0115090
|Fujimoto
|1998.2.19
CLOC|70C
SYN|26,29kDa proteinase
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: RE18380 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0157314
|Levis
|2003.4.25
AM|Source for merge of: 26-29kD-proteinase l(3)s3635
SYN|26-29kD-proteinase
|26-29kD-proteinase
}

REFDSR
{
RDID|FBrf0158900
|Herold et al.
|2003
SYN|26/29kD-proteinase
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
FNC|proteolysis and peptidolysis ; GO:0006508 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
FNC|proteolysis and peptidolysis ; GO:0006508 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0179865
|Bloomington Drosophila Stock Center
|2004.9.23
NAM|26-29kD-proteinase
}

ALESR
{
ASYM|26-29-p<up>KG00154</up>
SYN|26-29kD-proteinase<up>KG00154</up>
ID|FBal0145254
PHC|viable
|fertile
REF|FBrf0157314
REFDSR
{
RDID|FBrf0157314
|Levis
|2003.4.25
MD|Insertion maps to position \+8 of the release 3 @26-29-p@ annotation.
OTH|Insertions in P{lacW}26-29-p<up>s3635</up> (lethal) and P{lacW}26-29-p<up>KG00154</up>
|(viable) map to identical positions, raising possibility that lethality
|of @26-29-p<up>s3635</up>@ maps to elsewhere in genome.
TRN|FBti0020878 == P{SUPor-P}26-29-p<up>KG00154</up>
MU|P-element activity
PHC|viable
|fertile
SYN|26-29kD-proteinase<up>KG00154</up>
}

}

ALESR
{
ASYM|26-29-p<up>s3635</up>
SYN|l(3)s3635<up>s3635</up>
|l(3)s3635
|26-29kD-proteinase<up>s3635</up>
ID|FBal0087042
REF|FBrf0067338
|FBrf0157314
|FBrf0111489
REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
OTH|Complements: @l(3)j2E11<up>j2E11</up>@.
TRN|FBti0009968 == P{lacW}26-29-p<up>s3635</up>
|BDGP:l(3)s3635
MU|P-element activity
PHC|lethal | recessive
SYN|l(3)s3635<up>s3635</up>
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
TRN|FBti0009968 == P{lacW}26-29-p<up>s3635</up>
|BDGP:l(3)s3635
PHC|lethal | recessive
SYN|l(3)s3635
}

REFDSR
{
RDID|FBrf0157314
|Levis
|2003.4.25
MD|Insertion maps to position \+8 of the release 3 @26-29-p@ annotation.
OTH|Insertions in P{lacW}26-29-p<up>s3635</up> (lethal) and P{lacW}26-29-p<up>KG00154</up>
|(viable) map to identical positions, raising possibility that lethality
|of @26-29-p<up>s3635</up>@ maps to elsewhere in genome.
TRN|FBti0009968 == P{lacW}26-29-p<up>s3635</up>
|BDGP:l(3)s3635
PHC|lethal
SYN|26-29kD-proteinase<up>s3635</up>
}

}

ALESR
{
ASYM|26-29-p<up>+</up>
ID|FBal0162888
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0066318	CLA 1 Gene	GSYM 1 26D19	DT 1 25 Dec 04	RESZ 1185	ALESR 2	REF 1	
GSYM|26D19
DT|25 Dec 04
ID|FBgn0066318
REF
{
REFM|FBrf0155698
|Reuter et al.
|2003
|0
}

REFDSR
{
RDID|FBrf0155698
|Reuter et al.
|2003
OTH|Identification: in a screen to isolate genes required for normal neuronal
|morphogenesis in larval mushroom body neurons.
}

ALESR
{
ASYM|26D19<up>26D19</up>
SYN|26D19
ID|FBal0145253
PHM|larval mushroom body | somatic clone
PHI|Distribution of a membrane marker in mushroom body neurons derived
|from mutant mushroom body neuroblast clones generated in newly hatched
|larvae and examined in the wandering third instar is abnormal.
REF|FBrf0155698
REFDSR
{
RDID|FBrf0155698
|Reuter et al.
|2003
MU|ethyl methanesulfonate
PHM|larval mushroom body | somatic clone
PHI|Distribution of a membrane marker in mushroom body neurons derived
|from mutant mushroom body neuroblast clones generated in newly hatched
|larvae and examined in the wandering third instar is abnormal.
SYN|26D19
}

}

ALESR
{
ASYM|26D19<up>+</up>
ID|FBal0146586
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0069068	CLA 1 Gene	GSYM 1 27-25	DT 1 25 Dec 04	RESZ 1312	ALESR 2	REF 1	
GSYM|27-25
DT|25 Dec 04
ID|FBgn0069068
REF
{
REFM|FBrf0162144
|Morris et al.
|2003
|0
}

REFDSR
{
RDID|FBrf0162144
|Morris et al.
|2003
CYC|Maps to 3R by deficiency analysis (details unspecified).
}

ALESR
{
ASYM|27-25<up>27-25</up>
SYN|27-25
ID|FBal0152815
PHC|lethal | recessive
|female sterile | recessive | germ-line clone
PHI|Homozygous clones can be recovered in the eye.
|Females containing homozygous germ-line clones show defects in early
|oogenesis.
REF|FBrf0162144
REFDSR
{
RDID|FBrf0162144
|Morris et al.
|2003
AMIS|Selected as: a mutation that results in a failure to produce eggs when
|females carry homozygous germ-line clones.
|It is not certain whether the lethal mutation and the sterility map
|to the same lesion, since only a single allele of this complementation
|group has been recovered.
PHC|lethal | recessive
|female sterile | recessive | germ-line clone
PHI|Homozygous clones can be recovered in the eye.
|Females containing homozygous germ-line clones show defects in early
|oogenesis.
SYN|27-25
}

}

ALESR
{
ASYM|27-25<up>+</up>
ID|FBal0154330
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0061474	CLA 1 multicopy cytosolic ribosomal RNA gene	GSYM 1 28SrRNA	DT 1 25 Dec 04	RESZ 6156	DBA 58	CEL 1 cytosolic large ribosomal subunit (sensu Eukaryota)	ALESR 1	REF 27	
GSYM|28SrRNA
DT|25 Dec 04
ID|FBgn0061474
CLA|multicopy_cytosolic_ribosomal_RNA_gene
SYN|28S rDNA
|28S RNA
|28S rRNA
|28S ribosomal RNA
|28S
|28s rRNA
|28SRNA
|BEST:LD41653
|BEST:HL02093
|BEST:HL02977
|BEST:HL03427
|NEST:bs10c09
|NEST:bs15g08
|NEST:bs17g11
|NEST:bs30g02
ID2|FBgn0045782
|FBgn0045792
|FBgn0045793
|FBgn0045794
|FBgn0045992
|FBgn0046040
|FBgn0046048
|FBgn0046072
AM|encoded by: @bb@, @Ybb@
|component genes: @28SrRNA:CR40459@
CEL|cytosolic large ribosomal subunit (sensu Eukaryota) ; GO:0005842
DBA|NA:AA567992
|BDGP:HL02093.5prime
|NA:AA697681
|BDGP:HL02977.5prime
|NA:AA697897
|BDGP:HL03427.5prime
|NA:AF059864
|NA:AF191294
|NA:AF191295
|NA:AI515941
|BDGP:LD41653.5prime
|NA:AI945047
|NEST:bs08d03.y1
|NA:AI945217
|NEST:bs10c09.y1
|NA:AI945697
|NEST:bs15g08.y1
|NA:AI945872
|NEST:bs17g11.y1
|NA:AI946059
|NEST:bs20c11.y1
|NA:AI946395
|NEST:bs25a05.y1
|NA:AI946792
|NEST:bs30g02.y1
|NA:AI946992
|NEST:bs33g11.y1
|NA:AI947151
|NEST:bs35f09.y1
|NA:AI947209
|NEST:bs36d01.y1
|NA:AY319386
|NA:K00467
|NA:K01574
|NA:K01575
|NA:K01576
|NA:K01577
|NA:K01578
|NA:K01579
|NA:K01580
|NA:K01581
|NA:K01582
|NA:K01583
|NA:K01584
|NA:K01585
|NA:K01586
|NA:K01587
|NA:K03138
|NA:K03139
|NA:K03140
|NA:K03141
|NA:M21017
|NA:V00232
|NA:V00245
|NA:X15707
|NA:X51922
|NA:X71158
|NA:X71159
REF
{
REFM|FBrf0152043
|Perez-Gonzalez and Eickbush
|2002
|0
REFM|FBrf0102893
|Belyaeva et al.
|1998
|0
REFM|FBrf0138565
|Giribet et al.
|2001
|0
REFM|FBrf0155623
|2
REFM|FBrf0104946
|FlyBase
|1996-
|9
REFM|FBrf0119344
|Rae
|1996.10.2
|9
REFM|FBrf0159270
|Yuan et al.
|2003
|0
REFM|FBrf0087464
|Jakubczak et al.
|1991
|0
REFM|FBrf0123212
|Talbert and Henikoff
|2000
|0
REFM|FBrf0173214
|Perez-Gonzalez
|2003
|0
REFM|FBrf0134799
|van Steensel et al.
|2001
|9
REFM|FBrf0117678
|Mandal
|1992.2.28
|9
REFM|FBrf0149108
|Ahmad and Henikoff
|2002
|0
REFM|FBrf0094743
|Friedrich and Tautz
|1997
|0
REFM|FBrf0111478
|Rodriguez-Trelles et al.
|1999
|0
REFM|FBrf0108186
|Giordano et al.
|1999
|0
REFM|FBrf0068470
|Ding and Lipshitz
|1993
|2
REFM|FBrf0119477
|Remsen
|1998.4.9
|9
REFM|FBrf0154285
|Ashburner
|2003.2.5
|9
REFM|FBrf0053438
|Smoller et al.
|1991
|0
REFM|FBrf0123005
|Eickbush et al.
|2000
|0
REFM|FBrf0123171
|Reim et al.
|1999
|0
REFM|FBrf0120864
|Solignac
|1993.2.2
|9
REFM|FBrf0120863
|Solignac
|1993.2.2
|9
REFM|FBrf0167625
|Sage and Csink
|2003
|0
REFM|FBrf0128400
|Bhadra et al.
|2000
|0
REFM|FBrf0155734
|Ye et al.
|2002
|0
}

REFDSR
{
RDID|FBrf0053438
|Smoller et al.
|1991
SYN|28S rDNA
}

REFDSR
{
RDID|FBrf0068470
|Ding and Lipshitz
|1993
SYN|28S RNA
}

REFDSR
{
RDID|FBrf0087464
|Jakubczak et al.
|1991
SYN|28S RNA
}

REFDSR
{
RDID|FBrf0094743
|Friedrich and Tautz
|1997
SYN|28S rRNA
}

REFDSR
{
RDID|FBrf0102893
|Belyaeva et al.
|1998
SYN|28S rRNA
}

REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
AM|Source for merge of: 28SrRNA BEST:HL02093 BEST:HL02977 BEST:HL03427
|Source for merge of: 28SrRNA NEST:bs10c09 NEST:bs15g08 NEST:bs17g11
|Source for merge of: 28SrRNA NEST:bs30g02 BEST:LD41653
}

REFDSR
{
RDID|FBrf0108186
|Giordano et al.
|1999
SYN|28S rRNA
}

REFDSR
{
RDID|FBrf0117678
|Mandal
|1992.2.28
SYN|28S rRNA
}

REFDSR
{
RDID|FBrf0119344
|Rae
|1996.10.2
SYN|28S rRNA
}

REFDSR
{
RDID|FBrf0119477
|Remsen
|1998.4.9
SYN|28S ribosomal RNA
}

REFDSR
{
RDID|FBrf0120863
|Solignac
|1993.2.2
SYN|28S ribosomal RNA
}

REFDSR
{
RDID|FBrf0120864
|Solignac
|1993.2.2
SYN|28S ribosomal RNA
}

REFDSR
{
RDID|FBrf0121292
|Tautz
|1990.3.15
CEL|cytosolic large ribosomal subunit (sensu Eukaryota) ; GO:0005842 | non-traceable author statement
GPD|ribosomal-RNA-28S
SYN|28S rRNA
}

REFDSR
{
RDID|FBrf0123005
|Eickbush et al.
|2000
SYN|28S
}

REFDSR
{
RDID|FBrf0123171
|Reim et al.
|1999
SYN|28S rRNA
}

REFDSR
{
RDID|FBrf0123212
|Talbert and Henikoff
|2000
SYN|28S rDNA
}

REFDSR
{
RDID|FBrf0128400
|Bhadra et al.
|2000
SYN|28S rRNA
}

REFDSR
{
RDID|FBrf0134799
|van Steensel et al.
|2001
SYN|28S
}

REFDSR
{
RDID|FBrf0137492
|Oliver
|2001.8.16
MD|Identified with: bs30g02.y1
|Identified with: bs17g11.y1
|Identified with: bs15g08.y1
|Identified with: bs10c09.y1
|Identified with: bs35f09.y1
|Identified with: bs36d01.y1
|Identified with: bs20c11.y1
|Identified with: bs33g11.y1
|Identified with: bs08d03.y1
|Identified with: bs25a05.y1
|Identified with: LD41653.5prime
|Identified with: HL03427.5prime
|Identified with: HL02977.5prime
|Identified with: HL02093.5prime
SYN|unnamed
}

REFDSR
{
RDID|FBrf0138565
|Giribet et al.
|2001
SYN|28S
}

REFDSR
{
RDID|FBrf0151416
|Brogna et al.
|2002
SYN|28s rRNA
}

REFDSR
{
RDID|FBrf0155734
|Ye et al.
|2002
SYN|28S rDNA
}

REFDSR
{
RDID|FBrf0160455
|Cohen et al.
|2003
MD|Extrachromosomal circular DNA (eccDNA) is present throughout the fly's
|life cycle. The eccDNA population contains circular multimers of tandemly
|repeated genes, including @28SrRNA@.
SYN|28S rDNA
}

REFDSR
{
RDID|FBrf0167625
|Sage and Csink
|2003
SYN|28S
}

ALESR
{
ASYM|28SrRNA<up>+</up>
ID|FBal0142209
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0058459	CLA 1 Gene	GSYM 1 28SrRNA:CR40459	DT 1 25 Dec 04	RESZ 558	DBA 1	ALESR 1	REF 1	
GSYM|28SrRNA:CR40459
DT|25 Dec 04
ID|FBgn0058459
SYN|CR40459
AM|member gene of: @28SrRNA@
DBA|NA:AABU01001264
ASQ|FBan0040459
REF
{
REFM|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
|9
}

REFDSR
{
RDID|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
CYC|Heterochromatic, cytological location not yet determined. Maps to a
|region encoding rRNA genes; one of 20F, h29, h20.
}

ALESR
{
ASYM|28SrRNA:CR40459<up>+</up>
ID|FBal0143097
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0000005	CLA 1 transposable element	NAM 1 297 element	GSYM 1 297	DT 1 25 Dec 04	RESZ 13638	DBA 23	REF 98	
GSYM|297
DT|25 Dec 04
ID|FBgn0000005
CLA|transposable_element
SYN|Dm297
|T1/T2
|BarA
|Dme297V
|EG:EG0007.2
|BcDNA:SD08734
ID2|FBgn0061365
NAM|297 element
TE|element type: LTR retrotransposon
|terminal repeat length in bp: 415
|total length in bp: 6995
|target site duplication length in bp: 4
|number of copies in genome: Approximately 30 (FBrf0032823)
|@297@ elements were first described by Potter et al. (FBrf0032823)
|but were originally identified by Wensink and Rubin as being
|complementary to abundant polyA RNA in tissue-culture cells.
MD|Identified with: SD08734 (BDGP-DGC)
DBA|NA:AB010261
|NA:AI542416
|BDGP-DGC:SD08734
|NA:AL033125
|NA:AW944568
|BDGP-DGC:SD08734
|NA:AY075583
|BDGP-DGC:SD08734
|NA:J01062
|NA:J01063
|NA:X03431
|NA:Z31754
|dbSTS:4290
|NA:Z31755
|dbSTS:4291
|NA:Z31802
|dbSTS:4339
|NA:Z32058
|dbSTS:4609
|NA:Z32434
|dbSTS:4220
|NA:Z50314
|dbSTS:24278
REV|FBrf0152077
REF
{
REFM|FBrf0137949
|Alonso-Gonzalez et al.
|2001
|1
REFM|FBrf0131051
|Marin and Llorens
|2000
|0
REFM|FBrf0108232
|Lukacsovich et al.
|1999
|0
REFM|FBrf0151719
|Tulin et al.
|2002
|0
REFM|FBrf0056287
|Pasyukova and Nuzhdin
|1992
|0
REFM|FBrf0128568
|Maside et al.
|2000
|0
REFM|FBrf0055613
|de Frutos et al.
|1992
|0
REFM|FBrf0079108
|Nuzhdin and Mackay
|1995
|9
REFM|FBrf0099793
|Alberola et al.
|1997
|0
REFM|FBrf0056185
|von Sternberg et al.
|1992
|2
REFM|FBrf0045130
|Inouye et al.
|1986
|0
REFM|FBrf0040123
|Kugimiya et al.
|1983
|0
REFM|FBrf0111953
|Losada et al.
|1999
|0
REFM|FBrf0053865
|Arkhipova and Ilyin
|1991
|0
REFM|FBrf0032823
|Potter et al.
|1979
|0
REFM|FBrf0151415
|Lerat et al.
|2002
|9
REFM|FBrf0038638
|Ikenaga and Saigo
|1982
|0
REFM|FBrf0074051
|Nuzhdin and Mackay
|1994
|0
REFM|FBrf0058967
|Kimura et al.
|1993
|0
REFM|FBrf0071734
|EDGP Project Members
|1994-
|9
REFM|FBrf0167608
|Greil et al.
|2003
|0
REFM|FBrf0044281
|Inouye et al.
|1986
|0
REFM|FBrf0160656
|Kapitonov and Jurka
|2003
|0
REFM|FBrf0106414
|Desset et al.
|1999
|0
REFM|FBrf0084234
|Nuzhdin
|1995
|0
REFM|FBrf0144916
|Rizzon et al.
|2002
|0
REFM|FBrf0111944
|Lerat and Capy
|1999
|0
REFM|FBrf0046121
|Baumann et al.
|1987
|0
REFM|FBrf0051101
|Sandmeyer et al.
|1990
|2
REFM|FBrf0162162
|Lerat et al.
|2003
|0
REFM|FBrf0080225
|Madueno et al.
|1995
|0
REFM|FBrf0054202
|Kim and Belyaeva
|1991
|0
REFM|FBrf0152077
|Pelisson et al.
|2002
|2
REFM|FBrf0167302
|Lukacsovich et al.
|2003
|0
REFM|FBrf0079937
|Charlesworth et al.
|1994
|0
REFM|FBrf0099812
|Terzian et al.
|1997
|0
REFM|FBrf0127056
|Dominguez and Albornoz
|1999
|0
REFM|FBrf0079992
|Ding and Lipshitz
|1994
|0
REFM|FBrf0056166
|di Franco et al.
|1992
|0
REFM|FBrf0074490
|Sniegowski and Charlesworth
|1994
|0
REFM|FBrf0057261
|Norris et al.
|1992
|0
REFM|FBrf0089687
|Hoogland and Biemont
|1996
|0
REFM|FBrf0076430
|Alexandrov and Alexandrova
|1994
|0
REFM|FBrf0085614
|Moriyama et al.
|1996
|1
REFM|FBrf0102359
|Makarova et al.
|1995
|0
REFM|FBrf0036022
|Rubin et al.
|1981
|0
REFM|FBrf0125337
|Boeke and Corces
|1989
|2
REFM|FBrf0129733
|Biemont et al.
|1999
|2
REFM|FBrf0104946
|FlyBase
|1996-
|9
REFM|FBrf0035709
|Spradling and Rubin
|1981
|2
REFM|FBrf0084471
|Vasil'eva et al.
|1995
|0
REFM|FBrf0078390
|Finnegan
|1992
|0
REFM|FBrf0138423
|Bowen and McDonald
|2001
|0
REFM|FBrf0054937
|Jarrell and Meselson
|1991
|0
REFM|FBrf0125292
|Xiong and Eickbush
|1990
|0
REFM|FBrf0149117
|Syomin et al.
|2002
|0
REFM|FBrf0111330
|Biemont and Cizeron
|1999
|0
REFM|FBrf0141652
|Carr et al.
|2001
|0
REFM|FBrf0080105
|Houle et al.
|1994
|0
REFM|FBrf0127290
|Reese et al.
|2000
|0
REFM|FBrf0149015
|Yan et al.
|2002
|0
REFM|FBrf0055733
|Aleksandrova and Alexandrov
|1992
|0
REFM|FBrf0127032
|Canizares et al.
|2000
|0
REFM|FBrf0083460
|Suh et al.
|1995
|0
REFM|FBrf0056148
|Charlesworth et al.
|1992
|0
REFM|FBrf0056146
|Charlesworth et al.
|1992
|0
REFM|FBrf0073800
|Mackay et al.
|1994
|0
REFM|FBrf0088079
|Dominguez and Albornoz
|1996
|0
REFM|FBrf0100592
|Law et al.
|1998
|0
REFM|FBrf0056140
|Higashijima et al.
|1992
|0
REFM|FBrf0098551
|Suh et al.
|1994
|1
REFM|FBrf0111326
|Ashburner et al.
|1999
|0
REFM|FBrf0105736
|Kanapin and Ivanov
|1998
|0
REFM|FBrf0127224
|Marsano et al.
|2000
|0
REFM|FBrf0127289
|Reese et al.
|2000
|0
REFM|FBrf0052039
|Leibovich
|1990
|0
REFM|FBrf0149106
|Bartolome et al.
|2002
|0
REFM|FBrf0149104
|Vieira et al.
|2002
|0
REFM|FBrf0125415
|Albornoz and Dominguez
|1999
|0
REFM|FBrf0111776
|Andrianov et al.
|1999
|0
REFM|FBrf0141542
|Maside et al.
|2001
|0
REFM|FBrf0056332
|Jiang and Gibson
|1992
|0
REFM|FBrf0057399
|Cuticchia et al.
|1992
|0
REFM|FBrf0111510
|Vieira et al.
|1999
|0
REFM|FBrf0052879
|Scheinker et al.
|1990
|0
REFM|FBrf0130256
|Lerat et al.
|1999
|0
REFM|FBrf0117580
|Lukacsovich
|1998.1.8
|9
REFM|FBrf0056195
|Biemont
|1992
|0
REFM|FBrf0056194
|di Franco et al.
|1992
|0
REFM|FBrf0056098
|Higashijima et al.
|1992
|0
REFM|FBrf0109043
|Rutsov et al.
|1999
|0
REFM|FBrf0155828
|Kaminker et al.
|2002
|0
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0054718
|Kim and Belyaeva
|1991
|0
REFM|FBrf0055481
|Arkhipova and Ilyin
|1992
|2
REFM|FBrf0051081
|Engels
|1989
|0
REFM|FBrf0108981
|Pantazidis et al.
|1999
|0
REFM|FBrf0146932
|Carr et al.
|2002
|0
}

REFDSR
{
RDID|FBrf0052039
|Leibovich
|1990
SYN|Dm297
}

REFDSR
{
RDID|FBrf0056098
|Higashijima et al.
|1992
SYN|T1/T2
}

REFDSR
{
RDID|FBrf0056140
|Higashijima et al.
|1992
SYN|T1/T2
}

REFDSR
{
RDID|FBrf0056146
|Charlesworth et al.
|1992
PPC|In a study of the distribution in the genome of 9 families of
|transposable element among chromosomes 2 and 3 of a natural population, it
|was found that the elements were distributed randomly in the distal section
|of chromosome arms, whereas some linkage disequilibrium was detected in
|proximal regions.  Different elements tend to occupy different sites.  The
|more proximal the site, the more likely the element was to show a
|non-random distribution.
}

REFDSR
{
RDID|FBrf0056148
|Charlesworth et al.
|1992
PHP|Distribution of 9 families of transposable elements in a natural
|population was studied and the hypothesis that transposable element
|abundance is regulated primarily by deleterious fitness consequences of
|ectopic meiotic exchange was supported.  Proximal euchromatin may only
|infrequently undergo exchange, and elements detected in population surveys
|of this kind tend to be inserted into sites where there is negligible
|effect on fitness.
}

REFDSR
{
RDID|FBrf0056166
|di Franco et al.
|1992
WT|Stability of 11 transposable element families compared by Southern
|blotting among individuals of lines that had been subjected to 30
|generations of sister sib matings.  @412@, @roo@, @blood@, @297@, @1731@
|and @G-element@ all appear stable, whereas @copia@, @hobo@, @I-element@,
|@gypsy@ and @jockey@ elements show instability.
}

REFDSR
{
RDID|FBrf0056287
|Pasyukova and Nuzhdin
|1992
WT|One substock of inbred lines shows considerable heterogeneity of
|insertion sites of @copia@ (frequency of insertions is 12% per haploid genome
|per generation) whereas @mdg1@, @mdg2@, @mdg3@, @gypsy@, @297@ and
|@HMS-Beagle@ were stable in all stocks examined.
}

REFDSR
{
RDID|FBrf0057261
|Norris et al.
|1992
SYN|BarA
}

REFDSR
{
RDID|FBrf0074051
|Nuzhdin and Mackay
|1994
OTH|Rates of transposition and excision of the @297@
|element have been determined.
}

REFDSR
{
RDID|FBrf0074490
|Sniegowski and Charlesworth
|1994
WT|Element copy numbers on inversion and standard chromosomes has been
|determined. The copy number is significantly higher within low frequency
|inversions than within the corresponding standard chromosome regions.
}

REFDSR
{
RDID|FBrf0079108
|Nuzhdin and Mackay
|1995
PHP|The distribution of a number of transposable elements has been studied
|in 10 Harwich mutation accumulation lines.
}

REFDSR
{
RDID|FBrf0079937
|Charlesworth et al.
|1994
WT|Estimating the genomic numbers of transposable elements demonstrates
|many families of element are over-represented in heterochromatin.
}

REFDSR
{
RDID|FBrf0079992
|Ding and Lipshitz
|1994
WT|The spatial and temporal expression patterns of fifteen families of
|retrotransposons are analyzed during embryogenesis and are found to
|be conserved. Results suggest that all families carry cis-acting elements
|that control their spatial and temporal expression patterns.
}

REFDSR
{
RDID|FBrf0083460
|Suh et al.
|1995
PHP|The chromosomal distribution of a number of retrotransposons in an
|isolated population of D.melanogaster (from Ishigaki Island, Okinawa,
|Japan) has been determined.
}

REFDSR
{
RDID|FBrf0084234
|Nuzhdin
|1995
PPC|The distribution of transposable elements in D.simulans is similar
|to that found in D.melanogaster, though total copy number is lower.
}

REFDSR
{
RDID|FBrf0089687
|Hoogland and Biemont
|1996
WT|Study of TE distribution (@P-element@, @hobo@, @I-element@, @copia@,
|@mdg1@, @mdg3@, @412@, @297@ and @roo@) along chromosome arms shows
|no global tendency for the TE site occupancy frequency to negatively
|follow the recombination rate, except for the 3L arm. The tendency
|for TE insertion number to increase from base to tip of some chromosome
|arms is simply explicable by a positive relationship with DNA content
|along the chromosomes. So for all TEs, except @hobo@, there is no
|relationship between distribution of TE insertion numbers weighted
|by DNA content and recombination rate. @hobo@ insertion site number
|is positively correlated with recombination rate.
}

REFDSR
{
RDID|FBrf0099812
|Terzian et al.
|1997
OTH|Used in an investigation to address the relationship between retrotransposons
|and retroviruses and the coadaptation of these retroelements to their
|host genomes. Results indicate retrotransposons are heterogeneous
|in contrast to retroviruses, suggesting different modes of evolution
|by slippage-like mechanisms.
}

REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
AM|Source for merge of: 297 BcDNA:SD08734
}

REFDSR
{
RDID|FBrf0117580
|Lukacsovich
|1998.1.8
SYN|unnamed
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: SD08734 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0152077
|Pelisson et al.
|2002
SYN|Dme297V
}

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
TE|element type: LTR retrotransposon
|total length in bp: 6995
|number of copies in genome: 57 in euchromatin of Release 3 genome annotation, of which 18 are full length.
}

REFDSR
{
RDID|FBrf0167608
|Greil et al.
|2003
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0027623	CLA 1 transposable element gene	GSYM 1 297\env	DT 1 25 Dec 04	RESZ 584	DBA 2	ALESR 1	REF 4	
GSYM|297\env
DT|25 Dec 04
ID|FBgn0027623
CLA|transposable_element_gene
AM|encoded by: @297@
DBA|NA:X03431
|PA:CAB57797
PAC|PIR:C24872
|UniProt_Swiss_Prot:P20829
REV|FBrf0152077
REF
{
REFM|FBrf0106414
|Desset et al.
|1999
|0
REFM|FBrf0152077
|Pelisson et al.
|2002
|2
REFM|FBrf0130256
|Lerat et al.
|1999
|0
REFM|FBrf0111944
|Lerat and Capy
|1999
|0
}

ALESR
{
ASYM|297\env<up>+</up>
ID|FBal0105453
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0044338	CLA 1 transposable element gene	GSYM 1 297\gag	DT 1 25 Dec 04	RESZ 246	DBA 2	ALESR 1	
GSYM|297\gag
DT|25 Dec 04
ID|FBgn0044338
CLA|transposable_element_gene
AM|encoded by: @297@
DBA|NA:X03431
|PA:CAA27159
PAC|PIR:A24872
|UniProt_Swiss_Prot:P20828
ALESR
{
ASYM|297\gag<up>+</up>
ID|FBal0122861
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0027622	CLA 1 transposable element gene	GSYM 1 297\pol	DT 1 25 Dec 04	RESZ 406	DBA 2	ALESR 1	REF 2	
GSYM|297\pol
DT|25 Dec 04
ID|FBgn0027622
CLA|transposable_element_gene
AM|encoded by: @297@
DBA|NA:X03431
|PA:CAB57796
PAC|PIR:B24872
|UniProt_Swiss_Prot:P20825
REF
{
REFM|FBrf0106414
|Desset et al.
|1999
|0
REFM|FBrf0111944
|Lerat and Capy
|1999
|0
}

ALESR
{
ASYM|297\pol<up>+</up>
ID|FBal0105452
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0066317	CLA 1 Gene	GSYM 1 29B70	DT 1 25 Dec 04	RESZ 1185	ALESR 2	REF 1	
GSYM|29B70
DT|25 Dec 04
ID|FBgn0066317
REF
{
REFM|FBrf0155698
|Reuter et al.
|2003
|0
}

REFDSR
{
RDID|FBrf0155698
|Reuter et al.
|2003
OTH|Identification: in a screen to isolate genes required for normal neuronal
|morphogenesis in larval mushroom body neurons.
}

ALESR
{
ASYM|29B70<up>29B70</up>
SYN|29B70
ID|FBal0145252
PHM|larval mushroom body | somatic clone
PHI|Distribution of a membrane marker in mushroom body neurons derived
|from mutant mushroom body neuroblast clones generated in newly hatched
|larvae and examined in the wandering third instar is abnormal.
REF|FBrf0155698
REFDSR
{
RDID|FBrf0155698
|Reuter et al.
|2003
MU|ethyl methanesulfonate
PHM|larval mushroom body | somatic clone
PHI|Distribution of a membrane marker in mushroom body neurons derived
|from mutant mushroom body neuroblast clones generated in newly hatched
|larvae and examined in the wandering third instar is abnormal.
SYN|29B70
}

}

ALESR
{
ASYM|29B70<up>+</up>
ID|FBal0146585
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0022713	CLA 1 Gene	GSYM 1 2Ab17	DT 1 25 Dec 04	RESZ 464	ALESR 1	REF 3	
GSYM|2Ab17
DT|25 Dec 04
ID|FBgn0022713
SYN|p2Ab17
REF
{
REFM|FBrf0065443
|Johansen et al.
|1993
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0078732
|Johansen et al.
|1994
|1
}

REFDSR
{
RDID|FBrf0065443
|Johansen et al.
|1993
SYN|p2Ab17
}

ALESR
{
ASYM|2Ab17<up>+</up>
ID|FBal0081520
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067331	CLA 1 Gene	GSYM 1 2D5	DT 1 25 Dec 04	RESZ 1400	GLOC 1 2-	ALESR 2	REF 2	
GSYM|2D5
DT|25 Dec 04
ID|FBgn0067331
GLOC|2-
GLC|Maps to 2L.
REF
{
REFM|FBrf0179903
|Crozatier et al.
|2004
|2
REFM|FBrf0158983
|Vegh and Basler
|2003
|0
}

REFDSR
{
RDID|FBrf0158983
|Vegh and Basler
|2003
GLOC|2-
GLC|Maps to 2L.
OTH|1 allele of @2D5@ been recovered in a screen for mutations with mutant
|phenotypes in clones in the wing.
}

ALESR
{
ASYM|2D5<up>2D5</up>
ID|FBal0148513
PHC|visible | somatic clone
|viable
PHM|wing vein | somatic clone
PHI|Homozygous clones in the wing induced by using @Scer\FLP1<up>Scer\UAS.cCa</up>@
|expressed under the control of @Scer\GAL4<up>vg.int2.1</up>@ can result in
|partial up to complete loss of all veins except L3.
REF|FBrf0158983
REFDSR
{
RDID|FBrf0158983
|Vegh and Basler
|2003
MU|ethyl methanesulfonate
PHC|visible | somatic clone
|viable
PHM|wing vein | somatic clone
PHI|Homozygous clones in the wing induced by using @Scer\FLP1<up>Scer\UAS.cCa</up>@
|expressed under the control of @Scer\GAL4<up>vg.int2.1</up>@ can result in
|partial up to complete loss of all veins except L3.
}

}

ALESR
{
ASYM|2D5<up>+</up>
ID|FBal0150111
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067330	CLA 1 Gene	GSYM 1 2F26	DT 1 25 Dec 04	RESZ 1556	GLOC 1 2-	ALESR 2	REF 2	
GSYM|2F26
DT|25 Dec 04
ID|FBgn0067330
GLOC|2-
GLC|Maps to 2L.
REF
{
REFM|FBrf0179903
|Crozatier et al.
|2004
|2
REFM|FBrf0158983
|Vegh and Basler
|2003
|0
}

REFDSR
{
RDID|FBrf0158983
|Vegh and Basler
|2003
GLOC|2-
GLC|Maps to 2L.
OTH|6 alleles of @2F26@ have been recovered in a screen for mutations with
|mutant phenotypes in clones in the wing.
}

ALESR
{
ASYM|2F26<up>unspecified</up>
ID|FBal0148512
PHC|visible | somatic clone
PHM|wing vein | ectopic | somatic clone
|wing | somatic clone
|wing vein L3 | somatic clone
PHI|Homozygous clones in the wing induced by using @Scer\FLP1<up>Scer\UAS.cCa</up>@
|expressed under the control of @Scer\GAL4<up>vg.int2.1</up>@ can result in
|massive ectopic veins between L3 and L4 or on L3.
REF|FBrf0158983
REFDSR
{
RDID|FBrf0158983
|Vegh and Basler
|2003
PHC|visible | somatic clone
PHM|wing vein | ectopic | somatic clone
|wing | somatic clone
|wing vein L3 | somatic clone
PHI|Homozygous clones in the wing induced by using @Scer\FLP1<up>Scer\UAS.cCa</up>@
|expressed under the control of @Scer\GAL4<up>vg.int2.1</up>@ can result in
|massive ectopic veins between L3 and L4 or on L3.
}

}

ALESR
{
ASYM|2F26<up>+</up>
ID|FBal0150110
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070055	CLA 1 Gene	GSYM 1 2L-144-32	DT 1 25 Dec 04	RESZ 1392	GLOC 1 2-	ALESR 2	REF 2	
GSYM|2L-144-32
DT|25 Dec 04
ID|FBgn0070055
GLOC|2-
GLC|Maps to 2L.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|2-
GLC|Maps to 2L.
}

ALESR
{
ASYM|2L-144-32<up>2L-144-32</up>
ID|FBal0157544
PHC|viable
|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones are
|U-shaped.
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHC|viable
|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones are
|U-shaped.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|2L-144-32<up>+</up>
ID|FBal0158436
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070054	CLA 1 Gene	GSYM 1 2L-250-35	DT 1 25 Dec 04	RESZ 1080	GLOC 1 2-	ALESR 2	REF 1	
GSYM|2L-250-35
DT|25 Dec 04
ID|FBgn0070054
GLOC|2-
GLC|Maps to 2L.
REF
{
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|2-
GLC|Maps to 2L.
}

ALESR
{
ASYM|2L-250-35<up>2L-250-35</up>
ID|FBal0157543
PHM|embryonic segment | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|segmentation defects.
REF|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHM|embryonic segment | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|segmentation defects.
}

}

ALESR
{
ASYM|2L-250-35<up>+</up>
ID|FBal0158435
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070053	CLA 1 Gene	GSYM 1 2L-311-30	DT 1 25 Dec 04	RESZ 1736	GLOC 1 2-	ALESR 2	REF 2	
GSYM|2L-311-30
DT|25 Dec 04
ID|FBgn0070053
GLOC|2-
GLC|Maps to 2L.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|2-
GLC|Maps to 2L.
}

ALESR
{
ASYM|2L-311-30<up>2L-311-30</up>
ID|FBal0157542
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHM|cephalopharyngeal skeleton | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|a short and strongly sclerotized head skeleton and a weak tail-up phenotype.
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
OTH|Complements: @Sos<up>unspecified</up>@.
|Complements: @trk<up>unspecified</up>@.
MU|ethyl methanesulfonate
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHM|cephalopharyngeal skeleton | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|a short and strongly sclerotized head skeleton and a weak tail-up phenotype.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|2L-311-30<up>+</up>
ID|FBal0158434
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070052	CLA 1 Gene	GSYM 1 2L-393-17	DT 1 25 Dec 04	RESZ 1550	GLOC 1 2-	ALESR 2	REF 2	
GSYM|2L-393-17
DT|25 Dec 04
ID|FBgn0070052
GLOC|2-
GLC|Maps to 2L.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|2-
GLC|Maps to 2L.
}

ALESR
{
ASYM|2L-393-17<up>2L-393-17</up>
ID|FBal0157541
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHM|dorsal closure stage embryo | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|a head involution defect.
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHM|dorsal closure stage embryo | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|a head involution defect.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|2L-393-17<up>+</up>
ID|FBal0158433
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0021755	CLA 1 Gene	GSYM 1 2R-F	DT 1 25 Dec 04	RESZ 2266	GLOC 1 2-	ALESR 2	SK 1	REF 3	
GSYM|2R-F
DT|25 Dec 04
ID|FBgn0021755
GLOC|2-
GLC|Located on 2R.
REF
{
REFM|FBrf0093664
|Prout et al.
|1997
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0099001
|Prout
|1997.3.19
|9
}

REFDSR
{
RDID|FBrf0093664
|Prout et al.
|1997
GLOC|2-
GLC|Located on 2R.
OTH|Identification: Genetic screen for autosomal mutations that produce
|blisters in somatic wing clones. 1 allele of @2R-F@ has been isolated.
WTI|mys (data from @2R-F<up>2R-22</up>@)
}

ALESR
{
ASYM|2R-F<up>2R-22</up>
ID|FBal0065570
REF|FBrf0093664
|FBrf0099001
REFDSR
{
RDID|FBrf0093664
|Prout et al.
|1997
MU|X ray
GIC|non-suppressor of @mys<up>b9</up>@
|enhancer | dominant of visible phenotype of @mys<up>8</up>@
|non-enhancer of @mys<up>b9</up>@
GIA|enhancer | dominant of wing phenotype of @mys<up>8</up>@
GII|Shows a weak genetic interaction with @mys<up>8</up>@; the frequency of
|wing blisters is increased from approximately 10% in @mys<up>8</up>@ single
|hemizygotes to approximately 20% in @mys<up>8</up>@ hemizygotes that are
|also heterozygous for @2R-F<up>2R-22</up>@.
PHC|viable
|visible | recessive
|visible | recessive | somatic clone
PHM|wing | somatic clone
|wing
PHI|Homozygous clones in the wing produce discrete, round blisters of variable
|size. These blisters can be located anywhere on the wing. Wing venation
|is normal. Homozygotes have fluid filled or collapsed wings.
SYN|unnamed
}

REFDSR
{
RDID|FBrf0099001
|Prout
|1997.3.19
PHC|viable
|visible | somatic clone
PHM|wing | somatic clone
PHI|Homozygous clones in the wing produce a blistered phenotype.
}

SK|FBst0002280
|y[1] w[1]; P{neoFRT}42D 2R-F[2R-22] P{w[+t*] ry[+t*]=white-un1}47A/CyO, P{w[+mC]=act-lacZ.B}CB1
}

ALESR
{
ASYM|2R-F<up>+</up>
ID|FBal0080607
CLA|wild-type generic
REF|FBrf0105495
}

SK|FBst0002280
|y[1] w[1]; P{neoFRT}42D 2R-F[2R-22] P{w[+t*] ry[+t*]=white-un1}47A/CyO, P{w[+mC]=act-lacZ.B}CB1
SKC|1
}
# EOR
GENR
{
RETE|ID 1 FBgn0021754	CLA 1 Gene	GSYM 1 2R-L	DT 1 25 Dec 04	RESZ 2122	GLOC 1 2-	ALESR 2	SK 1	REF 3	
GSYM|2R-L
DT|25 Dec 04
ID|FBgn0021754
GLOC|2-
GLC|Located on 2R.
REF
{
REFM|FBrf0093664
|Prout et al.
|1997
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0099001
|Prout
|1997.3.19
|9
}

REFDSR
{
RDID|FBrf0093664
|Prout et al.
|1997
GLOC|2-
GLC|Located on 2R.
OTH|Identification: Genetic screen for autosomal mutations that produce
|blisters in somatic wing clones. 1 allele of @2R-L@ has been isolated.
WTI|mys (data from @2R-L<up>84-2</up>@)
}

ALESR
{
ASYM|2R-L<up>84-2</up>
ID|FBal0065569
REF|FBrf0093664
|FBrf0099001
REFDSR
{
RDID|FBrf0093664
|Prout et al.
|1997
MU|X ray
GIC|non-suppressor of @mys<up>b9</up>@
|enhancer | dominant of visible phenotype of @mys<up>8</up>@
|non-enhancer of @mys<up>b9</up>@
GIA|enhancer | dominant of wing phenotype of @mys<up>8</up>@
GII|Shows a weak genetic interaction with @mys<up>8</up>@; the frequency
|of wing blisters is increased from approximately 10% in @mys<up>8</up>@ single
|hemizygotes to approximately 20% in @mys<up>8</up>@ hemizygotes that are also
|heterozygous for @2R-L<up>84-2</up>@.
PHC|lethal | larval | recessive
|visible | somatic clone
PHM|wing | somatic clone
PHI|Homozygous clones in the wing produce discrete, round blisters of variable
|size. These blisters can be located anywhere on the wing. Wing venation
|is normal.
SYN|unnamed
}

REFDSR
{
RDID|FBrf0099001
|Prout
|1997.3.19
PHC|visible | somatic clone
PHM|wing | somatic clone
PHI|Homozygous clones in the wing produce a blistered phenotype.
}

SK|FBst0002295
|y[1] w[1]; P{neoFRT}42D 2R-L[84-2] P{w[+t*] ry[+t*]=white-un1}47A/CyO, P{w[+mC]=act-lacZ.B}CB1
}

ALESR
{
ASYM|2R-L<up>+</up>
ID|FBal0080606
CLA|wild-type generic
REF|FBrf0105495
}

SK|FBst0002295
|y[1] w[1]; P{neoFRT}42D 2R-L[84-2] P{w[+t*] ry[+t*]=white-un1}47A/CyO, P{w[+mC]=act-lacZ.B}CB1
SKC|1
}
# EOR
GENR
{
RETE|ID 1 FBgn0065042	CLA 1 multicopy cytosolic ribosomal RNA gene	GSYM 1 2SrRNA	DT 1 25 Dec 04	RESZ 1190	DBA 4	CEL 1 cytosolic large ribosomal subunit (sensu Eukaryota)	ALESR 1	REF 6	
GSYM|2SrRNA
DT|25 Dec 04
ID|FBgn0065042
CLA|multicopy_cytosolic_ribosomal_RNA_gene
SYN|5.8S and 2S ribosomal rRNA
|2S rRNA
|2SRNA
AM|encoded by: @bb@, @Ybb@
|component genes: @2SrRNA:CR40455@, @2SrRNA:CR40458@
CEL|cytosolic large ribosomal subunit (sensu Eukaryota) ; GO:0005842
DBA|NA:AF083522
|NA:M21017
|NA:U20145
|NA:V00236
REF
{
REFM|FBrf0154285
|Ashburner
|2003.2.5
|9
REFM|FBrf0127122
|Hori et al.
|2000
|0
REFM|FBrf0030092
|Jordan and Glover
|1977
|0
REFM|FBrf0029053
|Jordan et al.
|1976
|0
REFM|FBrf0115021
|Fox
|1995.1.20
|9
REFM|FBrf0026290
|Jordan
|1974
|0
}

REFDSR
{
RDID|FBrf0115021
|Fox
|1995.1.20
SYN|5.8S and 2S ribosomal rRNA
}

REFDSR
{
RDID|FBrf0121292
|Tautz
|1990.3.15
CEL|cytosolic large ribosomal subunit (sensu Eukaryota) ; GO:0005842 | non-traceable author statement
GPD|ribosomal-RNA-2S
SYN|2S rRNA
}

REFDSR
{
RDID|FBrf0127122
|Hori et al.
|2000
SYN|2S rRNA
}

ALESR
{
ASYM|2SrRNA<up>+</up>
ID|FBal0143096
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0058455	CLA 1 Gene	GSYM 1 2SrRNA:CR40455	DT 1 25 Dec 04	RESZ 555	DBA 1	ALESR 1	REF 1	
GSYM|2SrRNA:CR40455
DT|25 Dec 04
ID|FBgn0058455
SYN|CR40455
AM|member gene of: @2SrRNA@
DBA|NA:AABU01001264
ASQ|FBan0040455
REF
{
REFM|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
|9
}

REFDSR
{
RDID|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
CYC|Heterochromatic, cytological location not yet determined. Maps to a
|region encoding rRNA genes; one of 20F, h29, h20.
}

ALESR
{
ASYM|2SrRNA:CR40455<up>+</up>
ID|FBal0143095
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0058458	CLA 1 Gene	GSYM 1 2SrRNA:CR40458	DT 1 25 Dec 04	RESZ 555	DBA 1	ALESR 1	REF 1	
GSYM|2SrRNA:CR40458
DT|25 Dec 04
ID|FBgn0058458
SYN|CR40458
AM|member gene of: @2SrRNA@
DBA|NA:AABU01001264
ASQ|FBan0040458
REF
{
REFM|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
|9
}

REFDSR
{
RDID|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
CYC|Heterochromatic, cytological location not yet determined. Maps to a
|region encoding rRNA genes; one of 20F, h29, h20.
}

ALESR
{
ASYM|2SrRNA:CR40458<up>+</up>
ID|FBal0143094
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0069067	CLA 1 Gene	GSYM 1 30-1	DT 1 25 Dec 04	RESZ 1862	CLOC 1 91C7--D1	ALESR 2	REF 1	
GSYM|30-1
DT|25 Dec 04
ID|FBgn0069067
CYC|Experimentally determined: 91C7--D1
CLOC|91C7--D1 (determined by in situ hybridization)
REF
{
REFM|FBrf0162144
|Morris et al.
|2003
|0
}

REFDSR
{
RDID|FBrf0162144
|Morris et al.
|2003
CLOC|91C7--D1 (determined by in situ hybridization)
CYC|Mapping based on deficiency analysis (details unspecified).
AM|The relationship between "soft-boiled" and "30-1" is unclear; @30-1<up>30-1</up>@
|("30-1") fails to complement the lethality of @soft-boiled<up>6-57</up>@,
|but many normal homozygous @30-1<up>30-1</up>@ germ-line clones can be recovered
|in females, so it is unclear whether @30-1<up>30-1</up>@ and @soft-boiled<up>6-57</up>@
|are allelic or whether they share a second site lethal mutation that
|maps to the 91C7--91D1 interval.
}

ALESR
{
ASYM|30-1<up>30-1</up>
SYN|30-1
ID|FBal0152814
PHC|lethal | recessive
PHI|Homozygous clones can be recovered in the eye.
|Many normal homozygous germ-line clones can be recovered in females.
REF|FBrf0162144
REFDSR
{
RDID|FBrf0162144
|Morris et al.
|2003
AMIS|@30-1<up>30-1</up>@ fails to complement the lethality of @soft-boiled<up>6-57</up>@,
|but many normal homozygous @30-1<up>30-1</up>@ germ-line clones can be recovered
|in females, so it is unclear whether @30-1<up>30-1</up>@ and @soft-boiled<up>6-57</up>@
|are allelic or whether they share a second site lethal mutation that
|maps to the 91C7--91D1 interval.
OTH|Fails to complement: @soft-boiled<up>6-57</up>@.
PHC|lethal | recessive
PHI|Homozygous clones can be recovered in the eye.
|Many normal homozygous germ-line clones can be recovered in females.
SYN|30-1
}

}

ALESR
{
ASYM|30-1<up>+</up>
ID|FBal0154329
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0029514	CLA 1 Gene	GSYM 1 312	DT 1 25 Dec 04	RESZ 2068	PTD 1	DBA 13	CLOC 1 61F7	ALESR 2	SK 1	REF 6	
GSYM|312
PTD
DT|25 Dec 04
ID|FBgn0029514
UAB|Deficiency: Df(3L)Ar14-8 (inferred from cytology)
SYN|CG9166
|BEST:CK01660
ID2|FBgn0035214
|FBgn0046312
CLOC|61F7
|Limits computationally determined from genome sequence between @P{PZ}l(3)02640<up>02640</up>@ and @P{EP}rho<up>EP3704</up>@&@P{PZ}l(3)06226<up>06226</up>@
DBA|NA:AA141383
|BDGP:CK01660.3prime
|NA:AE003471
|PA:AAF47489
|NA:AF209778
|PA:AAF23489
|NA:AI386522
|BDGP-DGC:GH16625
|NA:AW941820
|BDGP-DGC:GH16625
|NA:AY060311
|PA:AAL25350
|BDGP-DGC:GH16625
PAC|UniProt_TrEMBL:Q9U3Y9
|UniProt_TrEMBL:Q9W0F9
ASQ|FBan0009166
REF
{
REFM|FBrf0137492
|Oliver
|2001.8.16
|9
REFM|FBrf0104946
|FlyBase
|1996-
|9
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0178762
|Rana
|2004.7.8
|9
REFM|FBrf0129568
|Bayraktaroglu
|2000.8.7
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: GH16625 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0129568
|Bayraktaroglu
|2000.8.7
AM|Source for merge of: 312 CG9166
}

REFDSR
{
RDID|FBrf0137492
|Oliver
|2001.8.16
MD|Identified with: CK01660.3prime
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

REFDSR
{
RDID|FBrf0178762
|Rana
|2004.7.8
AM|Source for merge of: 312 BEST:CK01660
}

ALESR
{
ASYM|312<up>EP826</up>
ID|FBal0157540
REF|FBrf0104946
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
MD|The @P{EP}312<up>EP826</up>@ insertion maps within both @312@
|and @Ptp61F@ (nested genes on opposite strands).
AMIS|Associated with: @Ptp61F<up>EP826</up>@.
TRN|FBti0016497 == P{EP}312<up>EP826</up>
MU|P-element activity
}

SK|FBst0102266
|P{EP}312[EP826]
}

ALESR
{
ASYM|312<up>+</up>
ID|FBal0103396
CLA|wild-type generic
}

SK|FBst0102266
|P{EP}312[EP826]
SKC|1
}
# EOR
GENR
{
RETE|ID 1 FBgn0027097	CLA 1 Gene	GSYM 1 31B8	DT 1 25 Dec 04	RESZ 1117	GLOC 1 2-	ALESR 2	REF 1	
GSYM|31B8
DT|25 Dec 04
ID|FBgn0027097
GLOC|2-
REF
{
REFM|FBrf0108422
|Liu and Montell
|1999
|0
}

REFDSR
{
RDID|FBrf0108422
|Liu and Montell
|1999
GLOC|2-
}

ALESR
{
ASYM|31B8<up>31B8</up>
SYN|31B8
ID|FBal0097443
PHM|border follicle cell
PHI|Heterozygotes show defects in border cell migration; the border cells
|fail to initiate migration and remain at or near the anterior tip of
|the egg chamber even in stage 10.
REF|FBrf0108422
REFDSR
{
RDID|FBrf0108422
|Liu and Montell
|1999
AMIS|Selected as: a mutation that causes defects in border cell migration
|when homozygous clones are induced in the follicle cells.
MU|ethyl methanesulfonate
PHM|border follicle cell
PHI|Heterozygotes show defects in border cell migration; the border cells
|fail to initiate migration and remain at or near the anterior tip of
|the egg chamber even in stage 10.
SYN|31B8
}

}

ALESR
{
ASYM|31B8<up>+</up>
ID|FBal0097825
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0024507	CLA 1 Gene	GSYM 1 33-13	DT 1 25 Dec 04	RESZ 1073	CEL 1 nucleus	CLOC 1 65A1--6	ALESR 1	REF 3	
GSYM|33-13
DT|25 Dec 04
ID|FBgn0024507
UAB|Deficiency: Df(3L)XAS96 (inferred from cytology)
|Duplication: Dp(3;3)M67C<up>+</up>1 (inferred from cytology)
CLOC|65A1--6
|Left limit from (method unavailable) (FBrf0101248)
|Right limit from (method unavailable) (FBrf0101248)
CYC|Experimentally determined: 65A1--6
CEL|nucleus ; GO:0005634
ENZ|DNA binding ; GO:0003677
|DNA binding ; GO:0003677 | inferred from direct assay
REF
{
REFM|FBrf0138231
|Anholt and Mackay
|2001
|0
REFM|FBrf0106419
|Dietrich and Krause
|1999
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0101248
|Dietrich and Krause
|1998
ENZ|DNA binding ; GO:0003677 | inferred from direct assay
CLOC|65A1--6
CEL|nucleus ; GO:0005634 | inferred from direct assay
OTH|Identification: Yeast two hybrid screen for proteins that interact
|with @ftz@.
SYN|unnamed
}

ALESR
{
ASYM|33-13<up>+</up>
ID|FBal0088441
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0061473	CLA 1 Gene	GSYM 1 34-20	DT 1 25 Dec 04	RESZ 401	ALESR 1	REF 1	
GSYM|34-20
DT|25 Dec 04
ID|FBgn0061473
REF
{
REFM|FBrf0144706
|Ward and Desai
|2001
|1
}

REFDSR
{
RDID|FBrf0144706
|Ward and Desai
|2001
OTH|Identification: In a screen for dominant phenotypic modifiers of
|a @Ptp69D@ phenotype.
WTI|Ptp69D
}

ALESR
{
ASYM|34-20<up>+</up>
ID|FBal0133952
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0022951	CLA 1 Gene	GSYM 1 36w	DT 1 25 Dec 04	RESZ 1100	CLOC 1 28A--B	ALESR 2	REF 2	
GSYM|36w
DT|25 Dec 04
ID|FBgn0022951
UAB|Deficiency: Df(2L)spd (inferred from cytology)
|Duplication: Dp(2;2)C619 (inferred from cytology)
CLOC|28A--B
|Left limit from in situ hybridization (FBrf0099036)
|Right limit from in situ hybridization (FBrf0099036)
CYC|Experimentally determined: 28A--B
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0099036
|Omelyanchuk
|1997.10.10
|9
}

REFDSR
{
RDID|FBrf0099036
|Omelyanchuk
|1997.10.10
CLOC|28A--B (determined by in situ hybridization)
LOI|36w<up>1</up>
}

ALESR
{
ASYM|36w<up>1</up>
ID|FBal0066287
PHC|female sterile | partially
REF|FBrf0099036
REFDSR
{
RDID|FBrf0099036
|Omelyanchuk
|1997.10.10
TRN|FBti0007275 == P{lArB}36w<up>1</up>
MU|P-element activity
PHC|female sterile | partially
}

}

ALESR
{
ASYM|36w<up>+</up>
ID|FBal0081720
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070051	CLA 1 Gene	GSYM 1 37	DT 1 25 Dec 04	RESZ 302	ALESR 1	
GSYM|37
DT|25 Dec 04
ID|FBgn0070051
SYN|#37
REFDSR
{
RDID|FBrf0173481
|Pistillo et al.
|2004
OTH|Identification: In a screen for mutations affecting R7/R8 photoreceptor subtype specification.
SYN|#37
}

ALESR
{
ASYM|37<up>+</up>
ID|FBal0158432
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0028551	CLA 1 Gene	GSYM 1 3Cy(2)2	DT 1 25 Dec 04	RESZ 1086	CLOC 1 38E--F	ALESR 2	REF 1	
GSYM|3Cy(2)2
DT|25 Dec 04
ID|FBgn0028551
UAB|Deficiency: Df(2L)pr-A14 (inferred from cytology)
|Duplication: Dp(2;f)Bl (inferred from cytology)
CLOC|38E--F
|Left limit from (method unavailable) (FBrf0110768)
|Right limit from (method unavailable) (FBrf0110768)
CYC|Experimentally determined: 38E--F
REF
{
REFM|FBrf0110768
|Senger et al.
|1999
|1
}

REFDSR
{
RDID|FBrf0110768
|Senger et al.
|1999
CLOC|38E--F
LOI|3Cy(2)2<up>1</up>
}

ALESR
{
ASYM|3Cy(2)2<up>1</up>
SYN|3Cy(2)2
ID|FBal0100469
PHC|lethal | embryonic | recessive
PHI|Homozygotes die during late embryogenesis.
REF|FBrf0110768
REFDSR
{
RDID|FBrf0110768
|Senger et al.
|1999
TRN|FBti0013981 == P{lacZ}3Cy(2)2<up>1</up>
MU|P-element activity
PHC|lethal | embryonic | recessive
PHI|Homozygotes die during late embryogenesis.
SYN|3Cy(2)2
}

}

ALESR
{
ASYM|3Cy(2)2<up>+</up>
ID|FBal0101098
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067329	CLA 1 Gene	GSYM 1 3F43	DT 1 25 Dec 04	RESZ 1204	GLOC 1 3-	ALESR 2	REF 1	
GSYM|3F43
DT|25 Dec 04
ID|FBgn0067329
GLOC|3-
REF
{
REFM|FBrf0158983
|Vegh and Basler
|2003
|0
}

REFDSR
{
RDID|FBrf0158983
|Vegh and Basler
|2003
GLOC|3-
OTH|2 alleles of @3F43@ been recovered in a screen for mutations with mutant
|phenotypes in clones in the wing.
}

ALESR
{
ASYM|3F43<up>unspecified</up>
ID|FBal0148511
PHC|visible | somatic clone
PHM|wing sensillum | ectopic | somatic clone
PHI|Homozygous clones in the wing induced by using @Scer\FLP1<up>Scer\UAS.cCa</up>@
|expressed under the control of @Scer\GAL4<up>vg.int2.1</up>@ can result in
|ectopic bristles in the wing.
REF|FBrf0158983
REFDSR
{
RDID|FBrf0158983
|Vegh and Basler
|2003
PHC|visible | somatic clone
PHM|wing sensillum | ectopic | somatic clone
PHI|Homozygous clones in the wing induced by using @Scer\FLP1<up>Scer\UAS.cCa</up>@
|expressed under the control of @Scer\GAL4<up>vg.int2.1</up>@ can result in
|ectopic bristles in the wing.
}

}

ALESR
{
ASYM|3F43<up>+</up>
ID|FBal0150109
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070050	CLA 1 Gene	GSYM 1 3L-114-20	DT 1 25 Dec 04	RESZ 1196	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3L-114-20
DT|25 Dec 04
ID|FBgn0070050
GLOC|3-
GLC|Maps to 3L.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3L.
}

ALESR
{
ASYM|3L-114-20<up>3L-114-20</up>
ID|FBal0157539
PHI|Embryos derived from females carrying homozygous germ line clones have
|a partially penetrant tail-up phenotype.
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHI|Embryos derived from females carrying homozygous germ line clones have
|a partially penetrant tail-up phenotype.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|3L-114-20<up>+</up>
ID|FBal0158431
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070049	CLA 1 Gene	GSYM 1 3L-200-14	DT 1 25 Dec 04	RESZ 1564	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3L-200-14
DT|25 Dec 04
ID|FBgn0070049
GLOC|3-
GLC|Maps to 3L.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3L.
}

ALESR
{
ASYM|3L-200-14<up>3L-200-14</up>
ID|FBal0157538
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHM|embryonic segment | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|strong segmentation defects and are short.
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHM|embryonic segment | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|strong segmentation defects and are short.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|3L-200-14<up>+</up>
ID|FBal0158430
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070048	CLA 1 Gene	GSYM 1 3L-211-27	DT 1 25 Dec 04	RESZ 1732	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3L-211-27
DT|25 Dec 04
ID|FBgn0070048
GLOC|3-
GLC|Maps to 3L.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3L.
}

ALESR
{
ASYM|3L-211-27<up>3L-211-27</up>
ID|FBal0157537
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHM|embryonic head | maternal effect | germ-line clone
|embryonic segment | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|segmentation and head defects. Few embryos hatch.
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHM|embryonic head | maternal effect | germ-line clone
|embryonic segment | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|segmentation and head defects. Few embryos hatch.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|3L-211-27<up>+</up>
ID|FBal0158429
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070047	CLA 1 Gene	GSYM 1 3L-215-13	DT 1 25 Dec 04	RESZ 1516	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3L-215-13
DT|25 Dec 04
ID|FBgn0070047
GLOC|3-
GLC|Maps to 3L.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3L.
}

ALESR
{
ASYM|3L-215-13<up>3L-215-13</up>
SYN|3L-215-13
ID|FBal0157536
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHM|egg | non-rescuable maternal effect | germ-line clone
|dorsal appendage | non-rescuable maternal effect | germ-line clone
PHI|Females carrying homozygous germ line clones produce undeveloped eggs
|with fused dorsal appendages.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHM|egg | maternal effect | germ-line clone
|dorsal appendage | maternal effect | germ-line clone
PHI|Females carrying homozygous germ line clones produce ventralized eggs
|with fused dorsal appendages.
SYN|3L-215-13
}

}

ALESR
{
ASYM|3L-215-13<up>+</up>
ID|FBal0158428
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070046	CLA 1 Gene	GSYM 1 3L-61-3	DT 1 25 Dec 04	RESZ 1514	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3L-61-3
DT|25 Dec 04
ID|FBgn0070046
GLOC|3-
GLC|Maps to 3L.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3L.
}

ALESR
{
ASYM|3L-61-3<up>3L-61-3</up>
ID|FBal0157535
PHM|embryonic abdominal segment | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones show
|variable deletions of mid-abdominal segments. Some brownish embryos
|with holes are seen.
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
OTH|Complements: @Rpd3<up>unspecified</up>@.
MU|ethyl methanesulfonate
PHM|embryonic abdominal segment | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones show
|variable deletions of mid-abdominal segments. Some brownish embryos
|with holes are seen.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|3L-61-3<up>+</up>
ID|FBal0158427
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0021753	CLA 1 Gene	GSYM 1 3L-B	DT 1 25 Dec 04	RESZ 1604	GLOC 1 3-	ALESR 2	SK 1	REF 3	
GSYM|3L-B
DT|25 Dec 04
ID|FBgn0021753
GLOC|3-
REF
{
REFM|FBrf0093664
|Prout et al.
|1997
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0099001
|Prout
|1997.3.19
|9
}

REFDSR
{
RDID|FBrf0093664
|Prout et al.
|1997
GLOC|3-
OTH|Identification: Genetic screen for autosomal mutations that produce
|blisters in somatic wing clones. 1 allele of @3L-B@ has been isolated.
}

ALESR
{
ASYM|3L-B<up>3L-27</up>
ID|FBal0065568
REF|FBrf0093664
|FBrf0099001
REFDSR
{
RDID|FBrf0093664
|Prout et al.
|1997
MU|X ray
GII|Shows no interaction with @mys<up>b9</up>@ or @mys<up>8</up>@.
GIC|non-enhancer of @mys<up>8</up>@
|non-enhancer of @mys<up>b9</up>@
|non-suppressor of @mys<up>8</up>@
|non-suppressor of @mys<up>b9</up>@
PHC|viable
|visible | dominant
PHM|wing
PHI|Heterozygotes and homozygotes have small wings with blisters.
SYN|unnamed
}

REFDSR
{
RDID|FBrf0099001
|Prout
|1997.3.19
PHC|viable
|visible | dominant
PHM|wing
PHI|Heterozygotes have a wing blister phenotype.
}

SK|FBst0002300
|y[1] w[1]; 3L-B[3L-27] P{neoFRT}80B/TM6B, P{w[+mC]=iab-2(1.7)lacZ}6B, Tb[1]
}

ALESR
{
ASYM|3L-B<up>+</up>
ID|FBal0080605
CLA|wild-type generic
REF|FBrf0105495
}

SK|FBst0002300
|y[1] w[1]; 3L-B[3L-27] P{neoFRT}80B/TM6B, P{w[+mC]=iab-2(1.7)lacZ}6B, Tb[1]
SKC|1
}
# EOR
GENR
{
RETE|ID 1 FBgn0067328	CLA 1 Gene	GSYM 1 3N5	DT 1 25 Dec 04	RESZ 1249	GLOC 1 3-	ALESR 2	REF 1	
GSYM|3N5
DT|25 Dec 04
ID|FBgn0067328
GLOC|3-
REF
{
REFM|FBrf0158983
|Vegh and Basler
|2003
|0
}

REFDSR
{
RDID|FBrf0158983
|Vegh and Basler
|2003
GLOC|3-
OTH|1 allele of @3N5@ been recovered in a screen for mutations with mutant
|phenotypes in clones in the wing.
}

ALESR
{
ASYM|3N5<up>3N5</up>
ID|FBal0148510
PHC|visible | somatic clone
PHM|wing | posterior compartment | somatic clone
PHI|Homozygous clones in the wing induced by using @Scer\FLP1<up>Scer\UAS.cCa</up>@
|expressed under the control of @Scer\GAL4<up>vg.int2.1</up>@ can result in
|partial loss of the posterior compartment of the wing.
REF|FBrf0158983
REFDSR
{
RDID|FBrf0158983
|Vegh and Basler
|2003
PHC|visible | somatic clone
PHM|wing | posterior compartment | somatic clone
PHI|Homozygous clones in the wing induced by using @Scer\FLP1<up>Scer\UAS.cCa</up>@
|expressed under the control of @Scer\GAL4<up>vg.int2.1</up>@ can result in
|partial loss of the posterior compartment of the wing.
}

}

ALESR
{
ASYM|3N5<up>+</up>
ID|FBal0150108
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070045	CLA 1 Gene	GSYM 1 3R-168-17	DT 1 25 Dec 04	RESZ 1572	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3R-168-17
DT|25 Dec 04
ID|FBgn0070045
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|3R-168-17<up>3R-168-17</up>
ID|FBal0157534
PHM|embryonic segment | maternal effect | germ-line clone
|embryonic/first instar larval cuticle | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|variable segmentation defects or little cuticle.
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHM|embryonic segment | maternal effect | germ-line clone
|embryonic/first instar larval cuticle | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|variable segmentation defects or little cuticle.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|3R-168-17<up>+</up>
ID|FBal0158426
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070044	CLA 1 Gene	GSYM 1 3R-196-22	DT 1 25 Dec 04	RESZ 1768	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3R-196-22
DT|25 Dec 04
ID|FBgn0070044
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|3R-196-22<up>3R-196-22</up>
ID|FBal0157533
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHM|embryonic segment | maternal effect | germ-line clone
|denticle belt | terminal | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|segmentation defects (fusions of ventral denticle belts).
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHM|embryonic segment | maternal effect | germ-line clone
|denticle belt | terminal | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|segmentation defects (fusions of ventral denticle belts).
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|3R-196-22<up>+</up>
ID|FBal0158425
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070043	CLA 1 Gene	GSYM 1 3R-259-18	DT 1 25 Dec 04	RESZ 1465	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3R-259-18
DT|25 Dec 04
ID|FBgn0070043
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|3R-259-18<up>3R-259-18</up>
SYN|3R-259-18
ID|FBal0157532
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHM|dorsal appendage | non-rescuable maternal effect | germ-line clone
PHI|Females carrying homozygous germ line clones produce eggs which have
|fused dorsal appendages. No developed embryos are produced.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHM|egg | maternal effect | germ-line clone
|dorsal appendage | maternal effect | germ-line clone
PHI|Females carrying homozygous germ line clones produce ventralized eggs
|with fused dorsal appendages.
SYN|3R-259-18
}

}

ALESR
{
ASYM|3R-259-18<up>+</up>
ID|FBal0158424
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070042	CLA 1 Gene	GSYM 1 3R-31-22	DT 1 25 Dec 04	RESZ 1384	GLOC 1 3-	ALESR 2	REF 1	
GSYM|3R-31-22
DT|25 Dec 04
ID|FBgn0070042
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|3R-31-22<up>3R-31-22</up>
ID|FBal0157531
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
|viable
PHM|embryonic/first instar larval cuticle | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|undifferentiated cuticle.
REF|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
|viable
PHM|embryonic/first instar larval cuticle | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones have
|undifferentiated cuticle.
}

}

ALESR
{
ASYM|3R-31-22<up>+</up>
ID|FBal0158423
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070041	CLA 1 Gene	GSYM 1 3R-35-29	DT 1 25 Dec 04	RESZ 1724	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3R-35-29
DT|25 Dec 04
ID|FBgn0070041
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|3R-35-29<up>3R-35-29</up>
ID|FBal0157530
PHC|lethal | embryonic | maternal effect | recessive | germ-line clone
PHM|embryonic head | maternal effect | germ-line clone
|embryonic segment | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones show
|variable segment fusions and head defects. Few embryos hatch.
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHC|lethal | embryonic | maternal effect | recessive | germ-line clone
PHM|embryonic head | maternal effect | germ-line clone
|embryonic segment | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones show
|variable segment fusions and head defects. Few embryos hatch.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|3R-35-29<up>+</up>
ID|FBal0158422
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070040	CLA 1 Gene	GSYM 1 3R-40-7	DT 1 25 Dec 04	RESZ 1434	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3R-40-7
DT|25 Dec 04
ID|FBgn0070040
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|3R-40-7<up>3R-40-7</up>
ID|FBal0157529
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
OTH|Complements: @scrib<up>unspecified</up>@.
MU|ethyl methanesulfonate
PHM|embryonic/first instar larval cuticle | maternal effect | germ-line clone
|egg | maternal effect | germ-line clone
PHI|Females carrying homozygous germ line clones produce short eggs which
|develop into brownish embryos with undifferentiated cuticle.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHM|egg | maternal effect | germ-line clone
PHI|Females carrying homozygous germ line clones produce small eggs.
}

}

ALESR
{
ASYM|3R-40-7<up>+</up>
ID|FBal0158421
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070039	CLA 1 Gene	GSYM 1 3R-64-22	DT 1 25 Dec 04	RESZ 1450	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3R-64-22
DT|25 Dec 04
ID|FBgn0070039
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|3R-64-22<up>3R-64-22</up>
ID|FBal0157528
PHC|viable
|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones are
|brownish or undifferentiated or twisted.
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHC|viable
|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones are
|brownish or undifferentiated or twisted.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
}

}

ALESR
{
ASYM|3R-64-22<up>+</up>
ID|FBal0158420
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070038	CLA 1 Gene	GSYM 1 3R-64-33	DT 1 25 Dec 04	RESZ 1128	GLOC 1 3-	ALESR 2	REF 1	
GSYM|3R-64-33
DT|25 Dec 04
ID|FBgn0070038
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|3R-64-33<up>3R-64-33</up>
ID|FBal0157527
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones look
|normal but fail to hatch.
REF|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones look
|normal but fail to hatch.
}

}

ALESR
{
ASYM|3R-64-33<up>+</up>
ID|FBal0158419
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070037	CLA 1 Gene	GSYM 1 3R-66-38	DT 1 25 Dec 04	RESZ 1618	GLOC 1 3-	ALESR 2	REF 1	
GSYM|3R-66-38
DT|25 Dec 04
ID|FBgn0070037
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|3R-66-38<up>3R-66-38</up>
ID|FBal0157526
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
|viable
PHM|filzkorper | maternal effect | germ-line clone
|embryonic head | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones are
|short. Filzkorper are sometimes short and the head may be open. Many
|eggs are undeveloped.
REF|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHC|lethal | embryonic | non-rescuable maternal effect | recessive | germ-line clone
|viable
PHM|filzkorper | maternal effect | germ-line clone
|embryonic head | maternal effect | germ-line clone
PHI|Embryos derived from females carrying homozygous germ line clones are
|short. Filzkorper are sometimes short and the head may be open. Many
|eggs are undeveloped.
}

}

ALESR
{
ASYM|3R-66-38<up>+</up>
ID|FBal0158418
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070036	CLA 1 Gene	GSYM 1 3R-69-15	DT 1 25 Dec 04	RESZ 1457	GLOC 1 3-	ALESR 2	REF 2	
GSYM|3R-69-15
DT|25 Dec 04
ID|FBgn0070036
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0179049
|Luschnig et al.
|2004
|0
REFM|FBrf0179048
|Luschnig et al.
|2004
|9
}

REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|3R-69-15<up>3R-69-15</up>
SYN|3R-69-15
ID|FBal0157525
REF|FBrf0179049
|FBrf0179048
REFDSR
{
RDID|FBrf0179048
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHM|dorsal appendage | non-rescuable maternal effect | germ-line clone
PHI|Females carrying homozygous germ line clones produce eggs which have
|fused dorsal appendages. Some spindle-like eggs are seen.
}

REFDSR
{
RDID|FBrf0179049
|Luschnig et al.
|2004
MU|ethyl methanesulfonate
PHM|egg | maternal effect | germ-line clone
|dorsal appendage | maternal effect | germ-line clone
PHI|Females carrying homozygous germ line clones produce ventralized eggs
|with fused dorsal appendages.
SYN|3R-69-15
}

}

ALESR
{
ASYM|3R-69-15<up>+</up>
ID|FBal0158417
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0021751	CLA 1 Gene	GSYM 1 3R-C	DT 1 25 Dec 04	RESZ 1920	GLOC 1 3-	ALESR 2	SK 1	REF 4	
GSYM|3R-C
DT|25 Dec 04
ID|FBgn0021751
GLOC|3-
GLC|Located on 3R.
REF
{
REFM|FBrf0104793
|Walsh and Brown
|1998
|0
REFM|FBrf0093664
|Prout et al.
|1997
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0099001
|Prout
|1997.3.19
|9
}

REFDSR
{
RDID|FBrf0093664
|Prout et al.
|1997
GLOC|3-
GLC|Located on 3R.
OTH|Identification: Genetic screen for autosomal mutations that produce
|blisters in somatic wing clones. 1 allele of @3R-C@ has been isolated.
}

ALESR
{
ASYM|3R-C<up>3R-11</up>
ID|FBal0065566
REF|FBrf0093664
|FBrf0099001
REFDSR
{
RDID|FBrf0093664
|Prout et al.
|1997
MU|X ray
GII|Shows no interaction with @mys<up>b9</up>@ or @mys<up>8</up>@.
GIC|non-enhancer of @mys<up>8</up>@
|non-enhancer of @mys<up>b9</up>@
|non-suppressor of @mys<up>8</up>@
|non-suppressor of @mys<up>b9</up>@
PHC|lethal | pupal | recessive
|visible | somatic clone
PHM|wing | somatic clone
|wing vein
PHI|Homozygous clones in the wing produce discrete, round blisters of variable
|size. These blisters can be located anywhere on the wing and are associated
|with abnormalities in venation.
SYN|unnamed
}

REFDSR
{
RDID|FBrf0099001
|Prout
|1997.3.19
PHC|visible | somatic clone
PHM|wing | somatic clone
PHI|Homozygous clones in the wing produce a blistered phenotype.
}

SK|FBst0002306
|P{neoFRT}82B 3R-C[3R-11] P{w[+t*] ry[+t*]=white-un1}90E/TM6B, P{w[+mC]=iab-2(1.7)lacZ}6B, Tb[1]
}

ALESR
{
ASYM|3R-C<up>+</up>
ID|FBal0080603
CLA|wild-type generic
REF|FBrf0105495
}

SK|FBst0002306
|P{neoFRT}82B 3R-C[3R-11] P{w[+t*] ry[+t*]=white-un1}90E/TM6B, P{w[+mC]=iab-2(1.7)lacZ}6B, Tb[1]
SKC|1
}
# EOR
GENR
{
RETE|ID 1 FBgn0061472	CLA 1 Gene	GSYM 1 3R-I256	DT 1 25 Dec 04	RESZ 1183	GLOC 1 3-	ALESR 2	REF 1	
GSYM|3R-I256
DT|25 Dec 04
ID|FBgn0061472
GLOC|3-
GLC|Maps to 3R. Mutation maps to a 307kb interval between SNP markers
|3R121 and 3R125.
REF
{
REFM|FBrf0141677
|Berger et al.
|2001
|0
}

REFDSR
{
RDID|FBrf0141677
|Berger et al.
|2001
GLOC|3-
GLC|Maps to 3R. Mutation maps to a 307kb interval between SNP markers
|3R121 and 3R125.
OTH|Identification: mutation isolated in a mosaic screen for abnormal patterns
|of neuronal connectivity in the adult visual system.
}

ALESR
{
ASYM|3R-I256<up>3R-I256</up>
SYN|3R-I256
ID|FBal0131823
PHM|neuron | somatic clone
PHI|Mosaics show visual system connectivity defects.
REF|FBrf0141677
REFDSR
{
RDID|FBrf0141677
|Berger et al.
|2001
AMIS|Selected as: a mutation that shows abnormal patterns of neuronal connectivity
|in the adult visual system in a mosaic screen.
MU|chemical mutagenesis
PHM|neuron | somatic clone
PHI|Mosaics show visual system connectivity defects.
SYN|3R-I256
}

}

ALESR
{
ASYM|3R-I256<up>+</up>
ID|FBal0133951
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0005384	CLA 1 transposable element	NAM 1 3S18 element	GSYM 1 3S18	DT 1 25 Dec 04	RESZ 5744	DBA 10	WT 8 A retroviral-like transposable element	REF 28	
GSYM|3S18
DT|25 Dec 04
ID|FBgn0005384
CLA|transposable_element
SYN|BEL: BEL element
|bel
|Bel
|Belshazar/3S18
|Motu 4
|BcDNA:SD27140
|BEL
|BEL element
ID2|FBgn0000172
|FBgn0062843
NAM|3S18 element
TE|element type: LTR retrotransposon
|total length in bp: 6126 (FBrf0081893)
|terminal repeat length in bp: 361 (FBrf0081893)
|target site duplication length in bp: 5 (FBrf0041384)
|number of copies in genome: Approximately 15 (FBrf0043377) or approximately 25 (FBrf0040134)
WT|A retroviral-like transposable element.  Described as an insertion
|associated with the @w<up>a4</up>@ mutation by Goldberg et al.
|(FBrf0040134) (as BEL), and as an insertion within the non-transcribed
|spacer of an rDNA repeat by Bell et al. (FBrf0043377) and Fabijanski and
|Pellegrini (FBrf0038558). In situ hybridization experiments indicate that
|@3S18@ elements are located at about twenty-five sites throughout the
|genome and that their distribution differs from one strain to another. The
|ends of this element hybridize to each other.
MD|Identified with: SD27140 (BDGP-DGC)
DBA|NA:AY119280
|BDGP-DGC:SD27140
|NA:AY183921
|NA:BI633144
|BDGP-DGC:SD27140
|NA:U23420
|NA:Z50268
|dbSTS:24232
|NA:Z83532
|dbSTS:47480
REF
{
REFM|FBrf0043377
|Bell et al.
|1985
|0
REFM|FBrf0051920
|Zhang and Hawley
|1990
|0
REFM|FBrf0155828
|Kaminker et al.
|2002
|0
REFM|FBrf0134631
|Frame et al.
|2001
|0
REFM|FBrf0041384
|O'Hare et al.
|1984
|0
REFM|FBrf0104946
|FlyBase
|1996-
|9
REFM|FBrf0111510
|Vieira et al.
|1999
|0
REFM|FBrf0138423
|Bowen and McDonald
|2001
|0
REFM|FBrf0078393
|Finnegan
|1992
|0
REFM|FBrf0078391
|Finnegan
|1992
|0
REFM|FBrf0100260
|Sun et al.
|1997
|0
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0038558
|Fabijanski and Pellegrini
|1982
|0
REFM|FBrf0149106
|Bartolome et al.
|2002
|0
REFM|FBrf0144916
|Rizzon et al.
|2002
|0
REFM|FBrf0041457
|Mattox and Davidson
|1984
|0
REFM|FBrf0055613
|de Frutos et al.
|1992
|0
REFM|FBrf0114405
|Davis
|1995.3.24
|9
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
|0
REFM|FBrf0136848
|Mozer
|2001
|0
REFM|FBrf0157045
|9
REFM|FBrf0129733
|Biemont et al.
|1999
|2
REFM|FBrf0051351
|Zhang et al.
|1990
|0
REFM|FBrf0111330
|Biemont and Cizeron
|1999
|0
REFM|FBrf0162058
|Aravin et al.
|2003
|0
REFM|FBrf0079992
|Ding and Lipshitz
|1994
|0
REFM|FBrf0162162
|Lerat et al.
|2003
|0
REFM|FBrf0160656
|Kapitonov and Jurka
|2003
|0
}

REFDSR
{
RDID|FBrf0040134
|Goldberg et al.
|1983
PHP|Sequences homologous to @3S18@ are present about 25 times in the Drosophila
|genome.
SYN|BEL
}

REFDSR
{
RDID|FBrf0049635
|Rabinow and Birchler
|1989
TE|number of copies in genome: Approximately 25
SYN|BEL
}

REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
SYN|BEL
}

REFDSR
{
RDID|FBrf0073744
|Lim and Simmons
|1994
WT|Progeny derived from @w<up>a</up>@/@w<up>a4</up>@ heterozygotes demonstrate that
|ectopic recombination between paired @3S18@ elements produces duplications and
|deficiencies.
SYN|BEL
}

REFDSR
{
RDID|FBrf0079992
|Ding and Lipshitz
|1994
WT|The spatial and temporal expression patterns of fifteen families of
|retrotransposons are analyzed during embryogenesis and are found to
|be conserved. Results suggest that all families carry cis-acting elements
|that control their spatial and temporal expression patterns.
}

REFDSR
{
RDID|FBrf0081893
|Davis and Judd
|1995
TE|number of copies in genome: Approximately 15-25
|total length in bp: 6126
|terminal repeat length in bp: 361
SYN|BEL
}

REFDSR
{
RDID|FBrf0100260
|Sun et al.
|1997
SYN|BEL
}

REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
AM|Source for merge of: 3S18 BcDNA:SD27140
}

REFDSR
{
RDID|FBrf0111510
|Vieira et al.
|1999
SYN|BEL
}

REFDSR
{
RDID|FBrf0114405
|Davis
|1995.3.24
SYN|BEL
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: SD27140 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0129733
|Biemont et al.
|1999
SYN|bel
}

REFDSR
{
RDID|FBrf0134631
|Frame et al.
|2001
SYN|BEL
}

REFDSR
{
RDID|FBrf0138423
|Bowen and McDonald
|2001
SYN|BEL
}

REFDSR
{
RDID|FBrf0144916
|Rizzon et al.
|2002
SYN|Bel
}

REFDSR
{
RDID|FBrf0149106
|Bartolome et al.
|2002
SYN|BEL
}

REFDSR
{
RDID|FBrf0155821
|Sun et al.
|2003
SYN|Belshazar/3S18
|Bel
|Motu 4
}

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
TE|element type: LTR retrotransposon
|total length in bp: 6126
|number of copies in genome: 6 in euchromatin of Release 3 genome annotation, of which 4 are full length.
}

REFDSR
{
RDID|FBrf0157045
SYN|Bel
}

REFDSR
{
RDID|FBrf0160656
|Kapitonov and Jurka
|2003
SYN|Bel
}

REFDSR
{
RDID|FBrf0162058
|Aravin et al.
|2003
}

REFDSR
{
RDID|FBrf0162162
|Lerat et al.
|2003
SYN|bel
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0044337	CLA 1 transposable element gene	GSYM 1 3S18\ORF	DT 1 25 Dec 04	RESZ 219	DBA 2	ALESR 1	
GSYM|3S18\ORF
DT|25 Dec 04
ID|FBgn0044337
CLA|transposable_element_gene
AM|encoded by: @3S18@
DBA|NA:U23420
|PA:AAB03640
PAC|PIR:T13250
ALESR
{
ASYM|3S18\ORF<up>+</up>
ID|FBal0122860
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0015580	CLA 1 Gene	NAM 1 4.1	GSYM 1 4.1	DT 1 25 Dec 04	RESZ 323	DBA 1	ALESR 1	REF 2	
GSYM|4.1
DT|25 Dec 04
ID|FBgn0015580
NAM|4.1
DBA|NA:AC003923
REF
{
REFM|FBrf0065526
|Parra et al.
|1993
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

ALESR
{
ASYM|4.1<up>+</up>
ID|FBal0075462
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0000001	CLA 1 nuclear untranslated RNA gene	NAM 1 4.5SRNA	GSYM 1 4.5SRNA	DT 1 25 Dec 04	RESZ 827	CLOC 1 65A	ALESR 1	REF 2	
GSYM|4.5SRNA
DT|25 Dec 04
ID|FBgn0000001
CLA|nuclear_untranslated_RNA_gene
UAB|Deficiency: Df(3L)XAS96 (inferred from cytology)
|Duplication: Dp(3;3)M67C<up>+</up>1 (inferred from cytology)
NAM|4.5SRNA
GLOC|3-[21]
CLOC|65A
|Left limit from in situ hybridization (FBrf0042734)
|Right limit from in situ hybridization (FBrf0042734)
CYC|Experimentally determined: 65A
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0042734
|Steffensen et al.
|1985
|1
}

REFDSR
{
RDID|FBrf0042734
|Steffensen et al.
|1985
CLOC|65A (determined by in situ hybridization)
GPD|RNA-4.5S
OTH|A function for the 4.5S RNA is still in the realm of speculation.
}

ALESR
{
ASYM|4.5SRNA<up>+</up>
ID|FBal0066319
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0022712	CLA 1 Gene	GSYM 1 406	DT 1 25 Dec 04	RESZ 497	WT 1 @406@ is required for continued renewal of the male germ line	ALESR 1	REF 2	
GSYM|406
DT|25 Dec 04
ID|FBgn0022712
WT|@406@ is required for continued renewal of the male germ line.
REF
{
REFM|FBrf0078655
|Hime et al.
|1994
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0078655
|Hime et al.
|1994
WT|@406@ is required for continued renewal of the male germ line.
}

ALESR
{
ASYM|406<up>+</up>
ID|FBal0081519
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0000006	CLA 1 transposable element	NAM 1 412 element	GSYM 1 412	DT 1 25 Dec 04	RESZ 24173	DBA 27	REF 166	
GSYM|412
DT|25 Dec 04
ID|FBgn0000006
CLA|transposable_element
SYN|mdg2
|mdg-2
|MDG2
|Dm412
|MDG412
|EG:BACR37P7.4
|Motu 3
|Ubx-t72
|BcDNA:GM07634
|mdg2 element
ID2|FBgn0010159
|FBgn0062487
NAM|412 element
TE|element type: LTR retrotransposon
|terminal repeat length in bp: 481 or 571 (FBrf0036946)
|total length in bp: 7.6kb (FBrf0041380)
|target site duplication length in bp: 4 (FBrf0036946)
|number of copies in genome: 40 (FBrf0036946)
DBA|NA:AL008801
|dbSTS:53384
|NA:AL050231
|NA:AY183920
|EPD:17018
|NA:M30371
|NA:M30372
|NA:M30373
|NA:M54873
|NA:M54874
|NA:V00195
|NA:V00196
|NA:X04132
|NA:X52763
|NA:X52764
|NA:Z31757
|dbSTS:4293
|NA:Z31842
|dbSTS:4382
|NA:Z32198
|dbSTS:4749
|NA:Z70811
|dbSTS:33579
|NA:Z70825
|dbSTS:33682
|NA:Z83387
|dbSTS:47388
PAC|UniProt_TrEMBL:Q8T3I3
REV|FBrf0129733
|FBrf0098575
REF
{
REFM|FBrf0141542
|Maside et al.
|2001
|0
REFM|FBrf0149117
|Syomin et al.
|2002
|0
REFM|FBrf0151273
|Stein et al.
|2002
|0
REFM|FBrf0129815
|Fortunati and Junakovic
|1999
|0
REFM|FBrf0078392
|Finnegan
|1992
|0
REFM|FBrf0091382
|Furman and Bukharina
|1996
|0
REFM|FBrf0093473
|Graba et al.
|1997
|2
REFM|FBrf0151504
|Veraksa et al.
|2002
|0
REFM|FBrf0053528
|Leibovich
|1991
|0
REFM|FBrf0105736
|Kanapin and Ivanov
|1998
|0
REFM|FBrf0055613
|de Frutos et al.
|1992
|0
REFM|FBrf0036946
|Will et al.
|1981
|0
REFM|FBrf0049432
|di Franco et al.
|1989
|0
REFM|FBrf0080225
|Madueno et al.
|1995
|0
REFM|FBrf0149106
|Bartolome et al.
|2002
|0
REFM|FBrf0149104
|Vieira et al.
|2002
|0
REFM|FBrf0111510
|Vieira et al.
|1999
|0
REFM|FBrf0082311
|Maksimiv et al.
|1995
|0
REFM|FBrf0089219
|Zhang et al.
|1996
|0
REFM|FBrf0162058
|Aravin et al.
|2003
|0
REFM|FBrf0146932
|Carr et al.
|2002
|0
REFM|FBrf0083530
|Zabanov et al.
|1995
|0
REFM|FBrf0138461
|Costas et al.
|2001
|0
REFM|FBrf0056195
|Biemont
|1992
|0
REFM|FBrf0056194
|di Franco et al.
|1992
|0
REFM|FBrf0052641
|Gould et al.
|1990
|0
REFM|FBrf0086648
|Tan et al.
|1996
|0
REFM|FBrf0130134
|Vasil'eva et al.
|2000
|0
REFM|FBrf0079992
|Ding and Lipshitz
|1994
|0
REFM|FBrf0053865
|Arkhipova and Ilyin
|1991
|0
REFM|FBrf0155828
|Kaminker et al.
|2002
|0
REFM|FBrf0085614
|Moriyama et al.
|1996
|1
REFM|FBrf0155823
|Celniker et al.
|2002
|0
REFM|FBrf0052837
|Harada et al.
|1990
|0
REFM|FBrf0155821
|Sun et al.
|2003
|0
REFM|FBrf0134868
|Haoudi and Mason
|2000
|2
REFM|FBrf0056189
|Purugganan and Wessler
|1992
|0
REFM|FBrf0152071
|Borie et al.
|2002
|0
REFM|FBrf0081987
|Feinstein et al.
|1995
|0
REFM|FBrf0107409
|Vasil'eva et al.
|1998
|0
REFM|FBrf0136953
|Robert et al.
|2001
|0
REFM|FBrf0056185
|von Sternberg et al.
|1992
|2
REFM|FBrf0102359
|Makarova et al.
|1995
|0
REFM|FBrf0052594
|Kim et al.
|1990
|0
REFM|FBrf0141114
|Benos
|1999.12.13
|9
REFM|FBrf0049963
|Kim et al.
|1989
|0
REFM|FBrf0100260
|Sun et al.
|1997
|0
REFM|FBrf0052039
|Leibovich
|1990
|0
REFM|FBrf0068432
|Buff et al.
|1993
|0
REFM|FBrf0108981
|Pantazidis et al.
|1999
|0
REFM|FBrf0091151
|Ratner and Vasil'eva
|1996
|0
REFM|FBrf0102948
|Junakovic et al.
|1998
|0
REFM|FBrf0052034
|Gerasimova et al.
|1990
|0
REFM|FBrf0054124
|Pret and Searles
|1991
|0
REFM|FBrf0044554
|Dzhumagaliev et al.
|1986
|0
REFM|FBrf0083473
|Terrinoni et al.
|1995
|1
REFM|FBrf0054718
|Kim and Belyaeva
|1991
|0
REFM|FBrf0057399
|Cuticchia et al.
|1992
|0
REFM|FBrf0129733
|Biemont et al.
|1999
|2
REFM|FBrf0068424
|Botas
|1993
|2
REFM|FBrf0036313
|Baev et al.
|1981
|0
REFM|FBrf0158886
|Van Doren et al.
|2003
|0
REFM|FBrf0104396
|Akhmanova and Hennig
|1998
|0
REFM|FBrf0052022
|Avedisov et al.
|1990
|0
REFM|FBrf0045017
|Chang et al.
|1986
|0
REFM|FBrf0083460
|Suh et al.
|1995
|0
REFM|FBrf0064793
|Bate
|1993
|2
REFM|FBrf0056166
|di Franco et al.
|1992
|0
REFM|FBrf0141652
|Carr et al.
|2001
|0
REFM|FBrf0088079
|Dominguez and Albornoz
|1996
|0
REFM|FBrf0057228
|Kulkosky et al.
|1992
|0
REFM|FBrf0137200
|Kirby et al.
|2001
|0
REFM|FBrf0072501
|Anikeeva et al.
|1994
|0
REFM|FBrf0041380
|Shepherd and Finnegan
|1984
|0
REFM|FBrf0102924
|Furman et al.
|1998
|0
REFM|FBrf0138423
|Bowen and McDonald
|2001
|0
REFM|FBrf0134638
|Borie et al.
|2000
|0
REFM|FBrf0134799
|van Steensel et al.
|2001
|9
REFM|FBrf0127032
|Canizares et al.
|2000
|0
REFM|FBrf0053397
|Mahoney et al.
|1991
|0
REFM|FBrf0089687
|Hoogland and Biemont
|1996
|0
REFM|FBrf0130255
|Nuzhdin
|1999
|2
REFM|FBrf0055481
|Arkhipova and Ilyin
|1992
|2
REFM|FBrf0125337
|Boeke and Corces
|1989
|2
REFM|FBrf0162162
|Lerat et al.
|2003
|0
REFM|FBrf0137949
|Alonso-Gonzalez et al.
|2001
|1
REFM|FBrf0084471
|Vasil'eva et al.
|1995
|0
REFM|FBrf0052005
|Zabanov et al.
|1990
|0
REFM|FBrf0152038
|Coffman et al.
|2002
|0
REFM|FBrf0127224
|Marsano et al.
|2000
|0
REFM|FBrf0064615
|Morata
|1993
|2
REFM|FBrf0125292
|Xiong and Eickbush
|1990
|0
REFM|FBrf0053585
|Rodin et al.
|1991
|0
REFM|FBrf0056148
|Charlesworth et al.
|1992
|0
REFM|FBrf0053421
|Becker et al.
|1991
|0
REFM|FBrf0105793
|Cizeron et al.
|1998
|0
REFM|FBrf0056146
|Charlesworth et al.
|1992
|0
REFM|FBrf0076430
|Alexandrov and Alexandrova
|1994
|0
REFM|FBrf0090845
|Vieira and Biemont
|1996
|0
REFM|FBrf0162159
|Vasil'eva et al.
|2003
|0
REFM|FBrf0098575
|Nikitin and Shmookler Reis
|1997
|2
REFM|FBrf0044280
|Yuki et al.
|1986
|0
REFM|FBrf0160656
|Kapitonov and Jurka
|2003
|0
REFM|FBrf0056332
|Jiang and Gibson
|1992
|0
REFM|FBrf0054836
|Haynes et al.
|1991
|0
REFM|FBrf0100771
|Moore et al.
|1998
|0
REFM|FBrf0074490
|Sniegowski and Charlesworth
|1994
|0
REFM|FBrf0056294
|Ratner et al.
|1992
|0
REFM|FBrf0079937
|Charlesworth et al.
|1994
|0
REFM|FBrf0072994
|Driver and Vogrig
|1994
|0
REFM|FBrf0123225
|Vasilyeva et al.
|1999
|0
REFM|FBrf0051081
|Engels
|1989
|0
REFM|FBrf0101991
|Riechmann et al.
|1998
|0
REFM|FBrf0054198
|Goryachkovskaya and Vasilyeva
|1991
|0
REFM|FBrf0111953
|Losada et al.
|1999
|0
REFM|FBrf0099583
|Vasil'eva et al.
|1997
|0
REFM|FBrf0100563
|Furman and Bukharina
|1997
|0
REFM|FBrf0131051
|Marin and Llorens
|2000
|0
REFM|FBrf0083977
|Greig and Akam
|1995
|0
REFM|FBrf0134564
|Hayes et al.
|2001
|0
REFM|FBrf0058967
|Kimura et al.
|1993
|0
REFM|FBrf0098551
|Suh et al.
|1994
|1
REFM|FBrf0078101
|Boyle and DiNardo
|1995
|0
REFM|FBrf0031217
|Finnegan et al.
|1978
|0
REFM|FBrf0135823
|Benos et al.
|2001
|0
REFM|FBrf0051664
|Castelli-Gair and Garcia-Bellido
|1990
|0
REFM|FBrf0045129
|Yuki et al.
|1986
|0
REFM|FBrf0055845
|Brookman et al.
|1992
|0
REFM|FBrf0082744
|Vasil'eva et al.
|1995
|0
REFM|FBrf0092473
|Boyle et al.
|1997
|0
REFM|FBrf0036022
|Rubin et al.
|1981
|0
REFM|FBrf0100750
|Broihier et al.
|1998
|0
REFM|FBrf0077988
|Arnault and Dufournel
|1994
|2
REFM|FBrf0056275
|Ratner and Vasil'eva
|1992
|0
REFM|FBrf0145151
|Vasilyeva et al.
|2001
|1
REFM|FBrf0098744
|Arnault et al.
|1997
|0
REFM|FBrf0057537
|Ratner et al.
|1992
|0
REFM|FBrf0083015
|Aulard et al.
|1995
|0
REFM|FBrf0083014
|Aulard et al.
|1995
|1
REFM|FBrf0099808
|Nuzhdin et al.
|1997
|0
REFM|FBrf0144916
|Rizzon et al.
|2002
|0
REFM|FBrf0051854
|Fridell et al.
|1990
|0
REFM|FBrf0099807
|Biemont et al.
|1997
|0
REFM|FBrf0144915
|Bubenshchikova et al.
|2002
|0
REFM|FBrf0112805
|Baev
|1994.12.13
|9
REFM|FBrf0112804
|Baev
|1994.12.13
|9
REFM|FBrf0084234
|Nuzhdin
|1995
|0
REFM|FBrf0105955
|Whalen and Grigliatti
|1998
|0
REFM|FBrf0105952
|Vasil'eva et al.
|1998
|0
REFM|FBrf0104490
|Nabirochkin et al.
|1998
|0
REFM|FBrf0052879
|Scheinker et al.
|1990
|0
REFM|FBrf0108673
|Cizeron and Biemont
|1999
|0
REFM|FBrf0048823
|Micard et al.
|1988
|0
REFM|FBrf0167683
|Vasil'eva and Ratner
|2003
|0
REFM|FBrf0128568
|Maside et al.
|2000
|0
REFM|FBrf0151719
|Tulin et al.
|2002
|0
REFM|FBrf0111330
|Biemont and Cizeron
|1999
|0
REFM|FBrf0054206
|Kolesnikova et al.
|1991
|0
REFM|FBrf0071734
|EDGP Project Members
|1994-
|9
REFM|FBrf0054202
|Kim and Belyaeva
|1991
|0
REFM|FBrf0079108
|Nuzhdin and Mackay
|1995
|9
REFM|FBrf0029352
|Rubin et al.
|1976
|0
REFM|FBrf0167513
|Artero et al.
|2003
|0
REFM|FBrf0109131
|Vasil'eva et al.
|1998
|0
REFM|FBrf0055781
|Kim et al.
|1992
|0
REFM|FBrf0167670
|Ratner et al.
|2001
|0
}

REFDSR
{
RDID|FBrf0049432
|di Franco et al.
|1989
TE|The genomic distribution of transposable elements in somatic tissues and
|during development is homogeneous.
}

REFDSR
{
RDID|FBrf0049963
|Kim et al.
|1989
SYN|mdg2
}

REFDSR
{
RDID|FBrf0052005
|Zabanov et al.
|1990
SYN|mdg-2
}

REFDSR
{
RDID|FBrf0052022
|Avedisov et al.
|1990
TE|The @mdg1@ element shows considerable homology with the @412@ element.
}

REFDSR
{
RDID|FBrf0052034
|Gerasimova et al.
|1990
SYN|mdg2
}

REFDSR
{
RDID|FBrf0052594
|Kim et al.
|1990
TE|The distribution of a number of transposable elements, including @412@
|elements, in a D.melanogaster laboratory strain with a high
|frequency of spontaneous mutations and its derivatives, has been studied.
}

REFDSR
{
RDID|FBrf0052837
|Harada et al.
|1990
TE|Transposition rates of mobile elements in lines AW and JH, in which
|spontaneous mutations have accumulated for about 400 generations, are
|studied. @412@ and @17.6@ elements rate of transposition is very low,
|@I-element@ and @hobo@ insertions occur much more frequently.
}

REFDSR
{
RDID|FBrf0053397
|Mahoney et al.
|1991
TE|The @412@ transposon inserted into @ft@ differs from previously
|described @412@ insertions: the 5' LTR contains an additional 33bp of which 29
|are a direct repeat of the LTR sequence, there is a 3bp insertion between
|@ft@ and the 5' LTR, 11bp of @ft@ DNA at site of insertion is lost.
}

REFDSR
{
RDID|FBrf0053528
|Leibovich
|1991
SYN|MDG2
}

REFDSR
{
RDID|FBrf0053585
|Rodin et al.
|1991
SYN|mdg2
}

REFDSR
{
RDID|FBrf0053865
|Arkhipova and Ilyin
|1991
SYN|mdg2
}

REFDSR
{
RDID|FBrf0054198
|Goryachkovskaya and Vasilyeva
|1991
SYN|Dm412
}

REFDSR
{
RDID|FBrf0054206
|Kolesnikova et al.
|1991
SYN|Dm412
}

REFDSR
{
RDID|FBrf0055733
|Aleksandrova and Alexandrov
|1992
PHP|Polymorphism of transposable elements in inbred lines has been examined:
|@P-element@, @gypsy@, @jockey@, @I-element@, @mdg1@, @412@, @mdg3@
|and @297@ sites are largely stable, whereas @roo@ and @copia@ sites
|are polymorphic.
SYN|mdg2
}

REFDSR
{
RDID|FBrf0055781
|Kim et al.
|1992
TE|During the course of experiments with genetically unstable MS strains
|gypsy elements were observed to transpose whereas @mdg1@ and @412@ sites in
|the X chromosome were unchanged.
}

REFDSR
{
RDID|FBrf0055845
|Brookman et al.
|1992
MD|Expression of the @412@ element provides a useful early marker for the
|development of the gonadal mesoderm. This high level of expression
|does not depend on contact with germ cells, but does depend on @abd-A@
|and @Abd-B@.
}

REFDSR
{
RDID|FBrf0056146
|Charlesworth et al.
|1992
PPC|In a study of the distribution in the genome of 9 families of
|transposable element among chromosomes 2 and 3 of a natural population, it
|was found that the elements were distributed randomly in the distal section
|of chromosome arms, whereas some linkage disequilibrium was detected in
|proximal regions.  Different elements tend to occupy different sites.  The
|more proximal the site, the more likely the element was to show a
|non-random distribution.
}

REFDSR
{
RDID|FBrf0056148
|Charlesworth et al.
|1992
PPC|Distribution of 9 families of transposable elements in a natural
|population was studied and the hypothesis that transposable element
|abundance is regulated primarily by deleterious fitness consequences of
|ectopic meiotic exchange was supported.
}

REFDSR
{
RDID|FBrf0056166
|di Franco et al.
|1992
TE|Stability of 11 transposable element families compared by Southern
|blotting among individuals of lines that had been subjected to 30
|generations of sister sib matings.  @412@, @roo@, @blood@, @297@, @1731@
|and @G-element@ all appear stable, whereas @copia@, @hobo@, @I-element@,
|@gypsy@ and @jockey@ elements show instability.
}

REFDSR
{
RDID|FBrf0056275
|Ratner and Vasil'eva
|1992
PPC|Mobile genetic elements participate directly in the expression,
|variability, selection and evolution of different quantitative characters.
}

REFDSR
{
RDID|FBrf0056287
|Pasyukova and Nuzhdin
|1992
PHP|One substock of inbred lines shows considerable heterogeneity of
|insertion sites of @copia@ (frequency of insertions is 12% per haploid genome
|per generation) whereas @mdg1@, @mdg2@, @mdg3@, @gypsy@, @297@ and
|@HMS-Beagle@ were stable in all stocks examined.
SYN|mdg2
}

REFDSR
{
RDID|FBrf0056294
|Ratner et al.
|1992
TE|Increase in transposition of @412@ by heavy heat shock treatment is
|statistically significant.
}

REFDSR
{
RDID|FBrf0057537
|Ratner et al.
|1992
TE|Multiple transpositions of @copia@-like @412@ occur in the next generation
|after heat shock treatment.
}

REFDSR
{
RDID|FBrf0058967
|Kimura et al.
|1993
SYN|mdg-2
}

REFDSR
{
RDID|FBrf0068432
|Buff et al.
|1993
SYN|mdg2
}

REFDSR
{
RDID|FBrf0072501
|Anikeeva et al.
|1994
SYN|Dm412
}

REFDSR
{
RDID|FBrf0072994
|Driver and Vogrig
|1994
TE|The @copia@ and @412@ transposable elements increase in copy number in
|aged adult tissue due to the activation of reverse transcriptase.
}

REFDSR
{
RDID|FBrf0074490
|Sniegowski and Charlesworth
|1994
TE|Element copy numbers on inversion and standard chromosomes has been
|determined. The copy number is significantly higher within low frequency
|inversions than within the corresponding standard chromosome regions.
}

REFDSR
{
RDID|FBrf0079937
|Charlesworth et al.
|1994
TE|Estimating the genomic numbers of transposable elements demonstrates
|many families of element are over-represented in heterochromatin.
}

REFDSR
{
RDID|FBrf0079992
|Ding and Lipshitz
|1994
TE|The spatial and temporal expression patterns of fifteen families of
|retrotransposons during embryogenesis suggest that all families carry
|cis-acting elements that control their spatial and temporal expression
|patterns.
}

REFDSR
{
RDID|FBrf0082240
|Kozhemiakina and Furman
|1995
TE|Spontaneous insertions and excisions of @mdg1@, @copia@, @412@ and
|@roo@ have been monitored over 65 generations of mass mating. Excisions
|are outnumbered by insertions. Their contribution to variation for
|transposable element location is not great.
SYN|Dm412
}

REFDSR
{
RDID|FBrf0082311
|Maksimiv et al.
|1995
SYN|mdg2
}

REFDSR
{
RDID|FBrf0082744
|Vasil'eva et al.
|1995
SYN|Dm412
}

REFDSR
{
RDID|FBrf0084234
|Nuzhdin
|1995
TE|The distribution of transposable elements in D.simulans is similar
|to that found in D.melanogaster, though total copy number is lower.
}

REFDSR
{
RDID|FBrf0084471
|Vasil'eva et al.
|1995
SYN|MDG2
}

REFDSR
{
RDID|FBrf0086648
|Tan et al.
|1996
MD|@412@ is expressed in a cell-specific manner during embryogenesis.
|At stage 11 transcripts are present in bilateral clusters of cells
|within the mesoderm. The posterior clusters of cells become associated
|with the gonads at stage 13. Results demonstrate development of the
|visceral muscle or fat body do not affect the expression of @412@ during
|embryogenesis.
}

REFDSR
{
RDID|FBrf0089687
|Hoogland and Biemont
|1996
TE|Study of TE distribution (@P-element@, @hobo@, @I-element@, @copia@,
|@mdg1@, @mdg3@, @412@, @297@ and @roo@) along chromosome arms shows
|no global tendency for the TE site occupancy frequency to negatively
|follow the recombination rate, except for the 3L arm.
}

REFDSR
{
RDID|FBrf0090845
|Vieira and Biemont
|1996
PPC|Insertion site numbers are determined in various natural populations.
|@Dsim\412@ exhibits a lower insertion number than @412@ due to a lower
|proportion of insertions on the X chromosome. Results suggest that
|selection is a major mechanism explaining @412@ and @Dsim\412@ copy
|number (selection being stronger in D.simulans than in D.melanogaster).
PPS|sampled from: France
|Portugal
|Arabia
}

REFDSR
{
RDID|FBrf0091151
|Ratner and Vasil'eva
|1996
SYN|Dm412
}

REFDSR
{
RDID|FBrf0091152
|Ratner and Amikishiev
|1996
TE|Functional site motifs are distributed within the @412@ element.
SYN|Dm412
|MDG2
}

REFDSR
{
RDID|FBrf0091153
|Ratner and Amikishiev
|1996
TE|Analysis of motifs of functional sites reveals these motifs ensure
|the basic molecular functions of @412@, expression of its open reading
|frame, transcription, induction of transposition and modification of
|adjacent genes and polygenes.
SYN|Dm412
|MDG2
}

REFDSR
{
RDID|FBrf0091382
|Furman and Bukharina
|1996
SYN|Dm412
}

REFDSR
{
RDID|FBrf0098744
|Arnault et al.
|1997
TE|No transposition was detected in progeny after heat shock of parents.
}

REFDSR
{
RDID|FBrf0099583
|Vasil'eva et al.
|1997
SYN|Dm412
}

REFDSR
{
RDID|FBrf0099807
|Biemont et al.
|1997
PPC|A lower proportion of @copia@, @mdg1@ and @412@ element insertion
|sites on the X chromosome in comparison with autosomes (in
|D.melanogaster and D.simulans populations) suggests that selection
|against the detrimental effects of TE insertions in the major force
|containing TE copies in populations.
}

REFDSR
{
RDID|FBrf0099808
|Nuzhdin et al.
|1997
TE|Correlations between the rate of transposition and TE copy number are
|determined for @412@ and @roo@ and are found to be zero.
}

REFDSR
{
RDID|FBrf0100563
|Furman and Bukharina
|1997
SYN|Dm412
}

REFDSR
{
RDID|FBrf0102924
|Furman et al.
|1998
SYN|Dm412
}

REFDSR
{
RDID|FBrf0105435
|Furman and Bukharina
|1998
OTH|Transposable elements can be used to reveal cross-over events.
SYN|Dm412
}

REFDSR
{
RDID|FBrf0105952
|Vasil'eva et al.
|1998
SYN|Dm412
}

REFDSR
{
RDID|FBrf0108673
|Cizeron and Biemont
|1999
PPC|More rearranged copies of the 412 element are found in D.simulans
|(@Dsim\412@) than in D.melanogaster (@412@).
}

REFDSR
{
RDID|FBrf0112804
|Baev
|1994.12.13
SYN|MDG412
}

REFDSR
{
RDID|FBrf0112805
|Baev
|1994.12.13
SYN|MDG412
}

REFDSR
{
RDID|FBrf0134638
|Borie et al.
|2000
TE|The expression of @412@ varies greatly between populations.
}

REFDSR
{
RDID|FBrf0141114
|Benos
|1999.12.13
SYN|EG:BACR37P7.4
}

REFDSR
{
RDID|FBrf0152071
|Borie et al.
|2002
}

REFDSR
{
RDID|FBrf0155821
|Sun et al.
|2003
SYN|Motu 3
}

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
TE|element type: LTR retrotransposon
|total length in bp: 7566
|number of copies in genome: 31 in euchromatin of Release 3 genome annotation, of which 24 are full length.
}

REFDSR
{
RDID|FBrf0162058
|Aravin et al.
|2003
}

REFDSR
{
RDID|FBrf0167513
|Artero et al.
|2003
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0043849	CLA 1 transposable element gene	GSYM 1 412\ORF1	DT 1 25 Dec 04	RESZ 300	DBA 2	ALESR 1	REF 1	
GSYM|412\ORF1
DT|25 Dec 04
ID|FBgn0043849
CLA|transposable_element_gene
AM|encoded by: @412@
DBA|NA:X04132
|PA:CAA27747
PAC|PIR:A29349
REF
{
REFM|FBrf0138461
|Costas et al.
|2001
|0
}

ALESR
{
ASYM|412\ORF1<up>+</up>
ID|FBal0121459
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0043848	CLA 1 transposable element gene	GSYM 1 412\ORF2	DT 1 25 Dec 04	RESZ 300	DBA 2	ALESR 1	REF 1	
GSYM|412\ORF2
DT|25 Dec 04
ID|FBgn0043848
CLA|transposable_element_gene
AM|encoded by: @412@
DBA|NA:X04132
|PA:CAA27749
PAC|PIR:B29349
REF
{
REFM|FBrf0138461
|Costas et al.
|2001
|0
}

ALESR
{
ASYM|412\ORF2<up>+</up>
ID|FBal0121458
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0043847	CLA 1 transposable element gene	GSYM 1 412\ORF3	DT 1 25 Dec 04	RESZ 274	DBA 2	ALESR 1	
GSYM|412\ORF3
DT|25 Dec 04
ID|FBgn0043847
CLA|transposable_element_gene
AM|encoded by: @412@
DBA|NA:X04132
|PA:CAA27750
PAC|PIR:C29349
|UniProt_Swiss_Prot:P10394
|UniProt_TrEMBL:Q8T3I3
ALESR
{
ASYM|412\ORF3<up>+</up>
ID|FBal0121457
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0043846	CLA 1 transposable element gene	GSYM 1 412\ORF4	DT 1 25 Dec 04	RESZ 218	DBA 2	ALESR 1	
GSYM|412\ORF4
DT|25 Dec 04
ID|FBgn0043846
CLA|transposable_element_gene
AM|encoded by: @412@
DBA|NA:X04132
|PA:CAA27748
PAC|PIR:D29349
ALESR
{
ASYM|412\ORF4<up>+</up>
ID|FBal0121456
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0046319	CLA 1 transposable element gene	GSYM 1 412\sORF2	DT 1 25 Dec 04	RESZ 337	ALESR 1	REF 1	
GSYM|412\sORF2
DT|25 Dec 04
ID|FBgn0046319
CLA|transposable_element_gene
REF
{
REFM|FBrf0138461
|Costas et al.
|2001
|0
}

REFDSR
{
RDID|FBrf0138461
|Costas et al.
|2001
AM|encoded by: @412@
}

ALESR
{
ASYM|412\sORF2<up>+</up>
ID|FBal0127164
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0015002	CLA 1 transposable element	NAM 1 422 element	GSYM 1 422	DT 1 25 Dec 04	RESZ 410	WT 1 A transposable element that remains to be fully characterized	REF 1	
GSYM|422
DT|25 Dec 04
ID|FBgn0015002
CLA|transposable_element
NAM|422 element
WT|A transposable element that remains to be fully characterized.
REF
{
REFM|FBrf0067208
|Frolov et al.
|1994
|0
}

REFDSR
{
RDID|FBrf0067208
|Frolov et al.
|1994
WT|The @422@ element was identified during the molecular analysis of the
|@pn@ locus.
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0069066	CLA 1 Gene	GSYM 1 4B7-11	DT 1 25 Dec 04	RESZ 886	GLOC 1 3-	ALESR 2	REF 1	
GSYM|4B7-11
DT|25 Dec 04
ID|FBgn0069066
GLOC|3-
GLC|Maps to 3R.
REF
{
REFM|FBrf0160777
|Martin et al.
|2003
|0
}

REFDSR
{
RDID|FBrf0160777
|Martin et al.
|2003
GLOC|3-
GLC|Maps to 3R.
}

ALESR
{
ASYM|4B7-11<up>4B7-11</up>
SYN|4B7-11
ID|FBal0152813
PHM|egg chamber | germ-line clone
PHI|The egg chamber contains more than 16 germ cells in females containing
|homozygous germline clones.
REF|FBrf0160777
REFDSR
{
RDID|FBrf0160777
|Martin et al.
|2003
MU|ethyl methanesulfonate
PHM|egg chamber | germ-line clone
PHI|The egg chamber contains more than 16 germ cells in females containing
|homozygous germline clones.
SYN|4B7-11
}

}

ALESR
{
ASYM|4B7-11<up>+</up>
ID|FBal0154328
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0039258	CLA 1 Gene	NAM 1 &bgr;-4-galactosyltransferase 7	GSYM 1 &bgr;4GalT7	DT 1 25 Dec 04	RESZ 12639	PDOM 1 INTERPRO:IPR003859 == Metazoa galactosyltransferase	PTD 1	DBA 11	FNC 6 chondroitin sulfate biosynthesis	CEL 2 Golgi apparatus	CLOC 1 96B16	ALESR 5	REF 11	
GSYM|&bgr;4GalT7
PTD
DT|25 Dec 04
ID|FBgn0039258
UAB|Deficiency: Df(3R)XTA1 (inferred from cytology)
|Duplication: Dp(3;3)Su<up>8</up> (inferred from cytology)
SYN|CG11780
|CG11780
|CG11780
|CG11780
|CG11780
|D&bgr;4GalT7
|d&bgr;4GalTI
|&bgr;-4-galactosyltransferase 7
CLOC|96B16
|Limits computationally determined from genome sequence between @P{PZ}ssh<up>01207</up>@ and @P{lacW}OstStt3<up>j2D9</up>@
FNC|chondroitin sulfate biosynthesis ; GO:0030206
|glycosaminoglycan biosynthesis ; GO:0006024
|heparan sulfate proteoglycan biosynthesis ; GO:0015012
|polysaccharide metabolism ; GO:0005976
|protein amino acid glycosylation ; GO:0006486
|proteoglycan biosynthesis ; GO:0030166
CEL|Golgi apparatus ; GO:0005794
|integral to membrane ; GO:0016021
PDOM|IPR003859 == Metazoa galactosyltransferase
NAM|&bgr;-4-galactosyltransferase 7
ENZ|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.- | non-traceable author statement
|xylosylprotein 4-beta-galactosyltransferase activity ; GO:0046525 ; EC:2.4.1.133 | inferred from direct assay
|xylosylprotein 4-beta-galactosyltransferase activity ; GO:0046525 ; EC:2.4.1.133 | inferred from sequence similarity with HUGO:B4GALT7; OMIM:604327
|xylosylprotein 4-beta-galactosyltransferase activity ; GO:0046525 ; EC:2.4.1.133 | inferred from sequence similarity with WB:sqv-3; WP:CE00306
|xylosylprotein 4-beta-galactosyltransferase activity ; GO:0046525 ; EC:2.4.1.133 | non-traceable author statement
|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.- | inferred from direct assay
|metal ion binding ; GO:0046872
|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.-
|xylosylprotein 4-beta-galactosyltransferase activity ; GO:0046525 ; EC:2.4.1.133
|metal ion binding ; GO:0046872 | inferred from sequence similarity with HUGO:B4GALT1; OMIM:137060
DBA|NA:AA142310
|BDGP:CK02622
|NA:AB091099
|PA:BAC22695
|NA:AE003750
|PA:AAF56377
|NA:AY094665
|PA:AAM11018
|BDGP-DGC:AT28119
|NA:BF491385
|BDGP-DGC:AT28119
PAC|UniProt_TrEMBL:Q8I6J0
|UniProt_TrEMBL:Q8T3P3
|UniProt_TrEMBL:Q9VBZ9
ASQ|FBan0011780
REF
{
REFM|FBrf0159024
|Takemae et al.
|2003
|-1
REFM|FBrf0174714
|Inlow and Restifo
|2004
|0
REFM|FBrf0152785
|Furukawa
|2002.8.30
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0126651
|Ashburner
|1999.11
|9
REFM|FBrf0152109
|Nakamura et al.
|2002
|-1
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
REFM|FBrf0151720
|Vadaie et al.
|2002
|-1
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0104946
|FlyBase
|1996-
|9
}

REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
AM|Source for identity of: &bgr;4GalT7 CG11780
|Source for identity of &bgr;4GalT7 CG11780 was sequence comparison
|(date:021108).
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: AT28119 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0151720
|Vadaie et al.
|2002
ENZ|xylosylprotein 4-beta-galactosyltransferase activity ; GO:0046525 ; EC:2.4.1.133 | inferred from direct assay
|xylosylprotein 4-beta-galactosyltransferase activity ; GO:0046525 ; EC:2.4.1.133 | inferred from sequence similarity with HUGO:B4GALT7; OMIM:604327
|xylosylprotein 4-beta-galactosyltransferase activity ; GO:0046525 ; EC:2.4.1.133 | inferred from sequence similarity with WB:sqv-3; WP:CE00306
NAM|&bgr;-4-galactosyltransferase 7
FNC|proteoglycan biosynthesis ; GO:0030166 | inferred from sequence similarity with HUGO:B4GALT7; OMIM:604327
MD|Identified with: CK02622
AM|Source for identity of: &bgr;4GalT7 CG11780
CEL|Golgi apparatus ; GO:0005794 | inferred from direct assay
GPD|beta-4-galactosyltransferase VII
SYN|CG11780
}

REFDSR
{
RDID|FBrf0152109
|Nakamura et al.
|2002
ENZ|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.- | inferred from direct assay
MD|Identified with: CK02622
SYN|D&bgr;4GalT7
}

REFDSR
{
RDID|FBrf0152785
|Furukawa
|2002.8.30
ENZ|xylosylprotein 4-beta-galactosyltransferase activity ; GO:0046525 ; EC:2.4.1.133 | non-traceable author statement
FNC|glycosaminoglycan biosynthesis ; GO:0006024 | non-traceable author statement
}

REFDSR
{
RDID|FBrf0155642
|Wilson
|2002
ENZ|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.- | non-traceable author statement
FNC|chondroitin sulfate biosynthesis ; GO:0030206 | non-traceable author statement
|heparan sulfate proteoglycan biosynthesis ; GO:0015012 | non-traceable author statement
SYN|CG11780
}

REFDSR
{
RDID|FBrf0159024
|Takemae et al.
|2003
ENZ|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.- | inferred from direct assay
|metal ion binding ; GO:0046872 | inferred from sequence similarity with HUGO:B4GALT1; OMIM:137060
FNC|proteoglycan biosynthesis ; GO:0030166 | inferred from sequence similarity with HUGO:B4GALT1; OMIM:137060
MD|Identified with: CK02622
CEL|integral to membrane ; GO:0016021 | inferred from sequence similarity
GPD|proteoglycan UDP-galactose:&bgr;-xylose &bgr;1,4-galactosyltransferase I
SYN|d&bgr;4GalTI
|CG11780
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
FNC|polysaccharide metabolism ; GO:0005976 | inferred from electronic annotation
|protein amino acid glycosylation ; GO:0006486 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0174714
|Inlow and Restifo
|2004
SYN|CG11780
}

ALESR
{
ASYM|&bgr;4GalT7<up>Act5C.T:Avic\GFP</up>
ID|FBal0138598
PHI|Mode of assay: Drosophila cell culture
REF|FBrf0151720
REFDSR
{
RDID|FBrf0151720
|Vadaie et al.
|2002
MD|Construct: An @Act5C@ promoter drives expression of @&bgr;4GalT7@ tagged at the
|C-terminal end with @T:Avic\GFP@.
OTH|Carried in plasmid pAc5.1DmGalT-VII-GFP and transfected into S2 cells
|to study the subcellular localization of the protein produced.
MU|in vitro construct | regulatory fusion
|in vitro construct | coding region fusion
PHI|Mode of assay: Drosophila cell culture
}

}

ALESR
{
ASYM|&bgr;4GalT7<up>dsRNA.C.Scer\UAS</up>
ID|FBal0148522
PHC|lethal with @Scer\GAL4<up>Act5C.PHb</up>@
PHI|Mode of assay: In transgenic Drosophila
REF|FBrf0159024
REFDSR
{
RDID|FBrf0159024
|Takemae et al.
|2003
MD|Construct: @Scer\UAS@ regulatory sequences drive expression of an inverted repeat
|(in head-to-head orientation) of the C-terminal region of @&bgr;4GalT7@
|(amino acids 209-322).
MU|in vitro construct | RNAi
CNS|FBtp0017456 == P{UAS-&bgr;4GalT7.dsRNA.C}
PHC|lethal with @Scer\GAL4<up>Act5C.PHb</up>@
PHI|Mode of assay: In transgenic Drosophila
}

}

ALESR
{
ASYM|&bgr;4GalT7<up>dsRNA.N.Scer\UAS</up>
ID|FBal0148521
PHC|lethal with @Scer\GAL4<up>Act5C.PHb</up>@
PHI|Mode of assay: In transgenic Drosophila
REF|FBrf0159024
REFDSR
{
RDID|FBrf0159024
|Takemae et al.
|2003
MD|Construct: @Scer\UAS@ regulatory sequences drive expression of an inverted repeat
|(in head-to-head orientation) of the N-terminal region of @&bgr;4GalT7@
|(amino acids 1-167).
MU|in vitro construct | RNAi
CNS|FBtp0017455 == P{UAS-&bgr;4GalT7.dsRNA.N}
PHC|lethal with @Scer\GAL4<up>Act5C.PHb</up>@
PHI|Mode of assay: In transgenic Drosophila
}

}

ALESR
{
ASYM|&bgr;4GalT7<up>dsRNA.Scer\UAS</up>
ID|FBal0148520
PHC|visible with @Scer\GAL4<up>ptc-559.1</up>@
|visible with @Scer\GAL4<up>sd-SG29.1</up>@
|visible with @Scer\GAL4<up>ap-md544</up>@
|visible with @Scer\GAL4<up>en-e16E</up>@
|visible with @Scer\GAL4<up>Dll-md23</up>@
|visible with @Scer\GAL4<up>da.G32</up>@
PHM|wing with @Scer\GAL4<up>ptc-559.1</up>@
|wing with @Scer\GAL4<up>sd-SG29.1</up>@
|wing | dorsal compartment with @Scer\GAL4<up>ap-md544</up>@
|wing vein L2 with @Scer\GAL4<up>ap-md544</up>@
|wing | posterior compartment with @Scer\GAL4<up>en-e16E</up>@
|leg | distal with @Scer\GAL4<up>Dll-md23</up>@
|leg | distal with @Scer\GAL4<up>da.G32</up>@
PHI|The distance between wing veins 3 and 4 is significantly reduced compared
|to wild type in flies expressing @&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@ under
|the control of @Scer\GAL4<up>ptc-559.1</up>@.
|The distance between wing veins 3 and 4 is weakly reduced compared
|to wild type in flies expressing @&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@ under
|the control of @Scer\GAL4<up>sd-SG29.1</up>@.
|The dorsal compartment of the wing is reduced in size in flies expressing
|@&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@ under the control of @Scer\GAL4<up>ap-md544</up>@.
|The loss of tissue is more pronounced toward the edges of the wing,
|and wing vein 2 is completely lost from the dorsal surface of the wing.
|The posterior compartment of the wing is reduced in size in flies expressing
|@&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@ under the control of @Scer\GAL4<up>en-e16E</up>@.
|The loss of tissue is most pronounced between the posterior edge of
|the wing and wing vein 5.
|The legs are truncated distally in flies expressing @&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@
|under the control of @Scer\GAL4<up>Dll-md23</up>@.
|Distal truncations are seen in about 15% of legs in flies expressing
|@&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@ under the control of @Scer\GAL4<up>da.G32</up>@.
|Mode of assay: In transgenic Drosophila
REF|FBrf0152109
REFDSR
{
RDID|FBrf0152109
|Nakamura et al.
|2002
MD|Construct: @Scer\UAS@ regulatory sequences drive expression of two copies of @&bgr;4GalT7@
|exon 2 in an inverted repeat, separated by @&bgr;4GalT7@ intron 2 and
|22bp of vector sequences.
MU|in vitro construct | regulatory fusion
|in vitro construct | RNAi
CNS|FBtp0017454 == P{UAS-&bgr;4GalT7.dsRNA}
PHC|visible with @Scer\GAL4<up>ptc-559.1</up>@
|visible with @Scer\GAL4<up>sd-SG29.1</up>@
|visible with @Scer\GAL4<up>ap-md544</up>@
|visible with @Scer\GAL4<up>en-e16E</up>@
|visible with @Scer\GAL4<up>Dll-md23</up>@
|visible with @Scer\GAL4<up>da.G32</up>@
PHM|wing with @Scer\GAL4<up>ptc-559.1</up>@
|wing with @Scer\GAL4<up>sd-SG29.1</up>@
|wing | dorsal compartment with @Scer\GAL4<up>ap-md544</up>@
|wing vein L2 with @Scer\GAL4<up>ap-md544</up>@
|wing | posterior compartment with @Scer\GAL4<up>en-e16E</up>@
|leg | distal with @Scer\GAL4<up>Dll-md23</up>@
|leg | distal with @Scer\GAL4<up>da.G32</up>@
PHI|The distance between wing veins 3 and 4 is significantly reduced compared
|to wild type in flies expressing @&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@ under
|the control of @Scer\GAL4<up>ptc-559.1</up>@.
|The distance between wing veins 3 and 4 is weakly reduced compared
|to wild type in flies expressing @&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@ under
|the control of @Scer\GAL4<up>sd-SG29.1</up>@.
|The dorsal compartment of the wing is reduced in size in flies expressing
|@&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@ under the control of @Scer\GAL4<up>ap-md544</up>@.
|The loss of tissue is more pronounced toward the edges of the wing,
|and wing vein 2 is completely lost from the dorsal surface of the wing.
|The posterior compartment of the wing is reduced in size in flies expressing
|@&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@ under the control of @Scer\GAL4<up>en-e16E</up>@.
|The loss of tissue is most pronounced between the posterior edge of
|the wing and wing vein 5.
|The legs are truncated distally in flies expressing @&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@
|under the control of @Scer\GAL4<up>Dll-md23</up>@.
|Distal truncations are seen in about 15% of legs in flies expressing
|@&bgr;4GalT7<up>dsRNA.Scer\UAS</up>@ under the control of @Scer\GAL4<up>da.G32</up>@.
|Mode of assay: In transgenic Drosophila
}

}

ALESR
{
ASYM|&bgr;4GalT7<up>+</up>
ID|FBal0138678
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0027538	CLA 1 Gene	GSYM 1 &bgr;4GalTA	DT 1 25 Dec 04	RESZ 3065	PDOM 2 INTERPRO:IPR001998 == Xylose isomerase	PTD 1	DBA 13	FNC 3 polysaccharide metabolism	CLOC 1 50E6	ALESR 2	SK 1	REF 9	
GSYM|&bgr;4GalTA
PTD
DT|25 Dec 04
ID|FBgn0027538
UAB|Deficiency: Df(2R)L7 (inferred from cytology)
|Duplication: Dp(2;2)SMG45 (inferred from cytology)
SYN|CG8536
|CG8536
|CG8536
|CG8536
|d&bgr;4GalTA
|BcDNA:GH13356
CLOC|50E6
|Limits computationally determined from genome sequence between @P{lacW}l(2)s3475<up>s3475</up>@/@P{lacW}Hsc70-5<up>k04907</up>@ and @P{PZ}Tfb1<up>06949</up>@/@P{PZ}l(2)03563<up>03563</up>@
FNC|polysaccharide metabolism ; GO:0005976
|protein amino acid glycosylation ; GO:0006486
|sperm individualization ; GO:0007291
PDOM|IPR001998 == Xylose isomerase
|IPR003859 == Metazoa galactosyltransferase
MD|Identified with: GH13356 (BDGP-DGC)
|Identified with: RE56531 (BDGP-DGC)
ENZ|xylose isomerase activity ; GO:0009045 ; EC:5.3.1.5
|xylose isomerase activity ; GO:0009045 ; EC:5.3.1.5 | inferred from electronic annotation
DBA|NA:AE003815
|PA:AAF58268
|NA:AF132158
|PA:AAD34746
|NA:AI135553
|BDGP-DGC:GH13356
|NA:AI513247
|BDGP-DGC:GH13356
|NA:AY095531
|PA:AAM12262
|BDGP-DGC:RE56531
|NA:BI370121
|BDGP-DGC:RE56531
PAC|UniProt_TrEMBL:Q9XZ05
ASQ|FBan0008536
REF
{
REFM|FBrf0174714
|Inlow and Restifo
|2004
|0
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0126651
|Ashburner
|1999.11
|9
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|FBrf0104946
|FlyBase
|1996-
|9
REFM|FBrf0147072
|Kim et al.
|2002
|0
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: GH13356 (BDGP-DGC)
|Identified with: RE56531 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0147072
|Kim et al.
|2002
SYN|CG8536
}

REFDSR
{
RDID|FBrf0159024
|Takemae et al.
|2003
SYN|CG8536
|d&bgr;4GalTA
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
FNC|polysaccharide metabolism ; GO:0005976 | inferred from electronic annotation
|protein amino acid glycosylation ; GO:0006486 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0173722
|Haines and Irvine
|2004
FNC|sperm individualization ; GO:0007291 | inferred from mutant phenotype
SYN|CG8536
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|xylose isomerase activity ; GO:0009045 ; EC:5.3.1.5 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0174714
|Inlow and Restifo
|2004
SYN|BcDNA:GH13356
}

ALESR
{
ASYM|&bgr;4GalTA<up>EP2551</up>
ID|FBal0157553
REF|FBrf0104946
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
TRN|FBti0016425 == P{EP}&bgr;4GalTA<up>EP2551</up>
MU|P-element activity
}

SK|FBst0102765
|P{EP}beta4GalTA[EP2551]
}

ALESR
{
ASYM|&bgr;4GalTA<up>+</up>
ID|FBal0148674
CLA|wild-type generic
}

SK|FBst0102765
|P{EP}beta4GalTA[EP2551]
SKC|1
}
# EOR
GENR
{
RETE|ID 1 FBgn0039625	CLA 1 Gene	GSYM 1 &bgr;4GalTB	DT 1 25 Dec 04	RESZ 2104	PDOM 1 INTERPRO:IPR003859 == Metazoa galactosyltransferase	PTD 1	DBA 6	FNC 2 polysaccharide metabolism	CLOC 1 98F5	ALESR 2	REF 6	
GSYM|&bgr;4GalTB
PTD
DT|25 Dec 04
ID|FBgn0039625
UAB|Deficiency: Df(3R)3450 (inferred from cytology)
|Duplication: Dp(3;3)501 (inferred from cytology)
SYN|CG14517
|CG14517
|d&bgr;4GalTB
CLOC|98F5
|Limits computationally determined from genome sequence between @P{PZ}l(3)06487<up>06487</up>@ and @P{EP}EP3390<up>EP3390</up>@
FNC|polysaccharide metabolism ; GO:0005976
|protein amino acid glycosylation ; GO:0006486
PDOM|IPR003859 == Metazoa galactosyltransferase
MD|Identified with: RE31995 (BDGP-DGC)
DBA|NA:AE003768
|PA:AAF56843
|NA:BI236014
|BDGP-DGC:RE31995
|NA:BT003627
|PA:AAO39631
PAC|UniProt_TrEMBL:Q86NU9
|UniProt_TrEMBL:Q9VAQ8
ASQ|FBan0014517
REF
{
REFM|FBrf0179797
|Bloomington Drosophila Stock Center
|2004.11.6
|9
REFM|FBrf0126651
|Ashburner
|1999.11
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: RE31995 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0159024
|Takemae et al.
|2003
SYN|CG14517
|d&bgr;4GalTB
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
FNC|polysaccharide metabolism ; GO:0005976 | inferred from electronic annotation
|protein amino acid glycosylation ; GO:0006486 | inferred from electronic annotation
}

ALESR
{
ASYM|&bgr;4GalTB<up>f00376</up>
ID|FBal0162871
REF|FBrf0179797
REFDSR
{
RDID|FBrf0179797
|Bloomington Drosophila Stock Center
|2004.11.6
TRN|FBti0041888 == PBac{WH}&bgr;4GalTB<up>f00376</up>
MU|piggyBac transposase
}

}

ALESR
{
ASYM|&bgr;4GalTB<up>+</up>
ID|FBal0149038
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0031491	CLA 1 Gene	GSYM 1 &agr;4GT1	DT 1 25 Dec 04	RESZ 4415	PDOM 2 INTERPRO:IPR007577 == Glycosyltransferase sugar-binding region containing DXD motif	DBA 17	FNC 4 carbohydrate metabolism	CEL 1 Golgi stack	CLOC 1 23C4	ALESR 4	SK 3	REF 5	
GSYM|&agr;4GT1
DT|25 Dec 04
ID|FBgn0031491
UAB|Deficiency: Df(2L)JS17 (inferred from cytology)
|Duplication: Dp(2;1)JS13 (inferred from cytology)
SYN|CG17223
|CG17223
CLOC|23C4
|Limits computationally determined from genome sequence between @P{PZ}lilli<up>00632</up>@ and @P{PZ}toc<up>01361</up>@
FNC|carbohydrate metabolism ; GO:0005975
|glycolipid biosynthesis ; GO:0009247
|glycolipid metabolism ; GO:0006664
|lipid metabolism ; GO:0006629
CEL|Golgi stack ; GO:0005795
PDOM|IPR007577 == Glycosyltransferase sugar-binding region containing DXD motif
|IPR007652 == Alpha 1,4-glycosyltransferase conserved region
MD|Identified with: GH17972 (BDGP-DGC)
ENZ|transferase activity, transferring glycosyl groups ; GO:0016757 ; EC:2.4.-.- | inferred from electronic annotation
|transferase activity ; GO:0016740 ; EC:2.-.-.- | inferred from electronic annotation
|transferase activity ; GO:0016740 ; EC:2.-.-.-
|transferase activity, transferring glycosyl groups ; GO:0016757 ; EC:2.4.-.-
|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.-
|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.- | inferred from electronic annotation
|alpha-1,4-N-acetylgalactosaminyltransferase activity ; GO:0035248
|alpha-1,4-N-acetylgalactosaminyltransferase activity ; GO:0035248 | inferred from direct assay
|alpha-1,4-N-acetylgalactosaminyltransferase activity ; GO:0035248 | non-traceable author statement
DBA|NA:AE003581
|PA:AAF51162
|NA:AI387443
|BDGP-DGC:GH17972
|NA:AJ621420
|PA:CAF18556
|NA:AQ072899
|BDGP:EP(2)2097
|NA:AQ073576
|BDGP:EP(2)2426
|NA:AW940684
|BDGP-DGC:GH17972
|NA:AY051524
|PA:AAK92948
|BDGP-DGC:GH17972
|NA:BZ286380
|BDGP:EY00269
PAC|UniProt_TrEMBL:Q9VQK4
ASQ|FBan0017223
REF
{
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|FBrf0182462
|Wilson
|2004.1.21
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0132177
|Gene Disruption Project members
|2001-
|9
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: GH17972 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
ENZ|transferase activity ; GO:0016740 ; EC:2.-.-.- | inferred from electronic annotation
|transferase activity, transferring glycosyl groups ; GO:0016757 ; EC:2.4.-.- | inferred from electronic annotation
FNC|carbohydrate metabolism ; GO:0005975 | inferred from electronic annotation
|lipid metabolism ; GO:0006629 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.- | inferred from electronic annotation
CEL|Golgi stack ; GO:0005795 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0179897
|Mucha et al.
|2004
ENZ|alpha-1,4-N-acetylgalactosaminyltransferase activity ; GO:0035248 | inferred from direct assay
FNC|glycolipid biosynthesis ; GO:0009247 | inferred from direct assay
AM|Source for identity of: &agr;4GT1 CG17223
SYN|CG17223
}

REFDSR
{
RDID|FBrf0182462
|Wilson
|2004.1.21
ENZ|alpha-1,4-N-acetylgalactosaminyltransferase activity ; GO:0035248 | non-traceable author statement
FNC|glycolipid metabolism ; GO:0006664 | non-traceable author statement
GPD|alpha-1,4-N-acetylgalactosaminyltransferase
}

ALESR
{
ASYM|&agr;4GT1<up>EP2097</up>
SYN|CG17223<up>EP2097</up>
ID|FBal0131575
REF|FBrf0132177
REFDSR
{
RDID|FBrf0132177
|Gene Disruption Project members
|2001-
TRN|FBti0010845 == P{EP}&agr;4GT1<up>EP2097</up>
|BDGP:EP(2)2097
MU|P-element activity
}

SK|FBst0103233
|P{EP}CG17223[EP2097]
}

ALESR
{
ASYM|&agr;4GT1<up>EP2426</up>
SYN|CG17223<up>EP2426</up>
ID|FBal0131574
REF|FBrf0132177
REFDSR
{
RDID|FBrf0132177
|Gene Disruption Project members
|2001-
TRN|FBti0011121 == P{EP}&agr;4GT1<up>EP2426</up>
|BDGP:EP(2)2426
MU|P-element activity
}

SK|FBst0103306
|P{EP}CG17223[EP2426]
}

ALESR
{
ASYM|&agr;4GT1<up>EY00269</up>
SYN|CG17223<up>EY00269</up>
ID|FBal0148288
REF|FBrf0132177
REFDSR
{
RDID|FBrf0132177
|Gene Disruption Project members
|2001-
TRN|FBti0024088 == P{EPgy2}&agr;4GT1<up>EY00269</up>
|BDGP:EY00269
MU|P-element activity
}

SK|FBst0014824
|y[1] w[67c23]; P{w[+mC] y[+mDint2]=EPgy2}CG17223[EY00269]
}

ALESR
{
ASYM|&agr;4GT1<up>+</up>
ID|FBal0162894
CLA|wild-type generic
}

SK|FBst0103233
|P{EP}CG17223[EP2097]
|FBst0103306
|P{EP}CG17223[EP2426]
|FBst0014824
|y[1] w[67c23]; P{w[+mC] y[+mDint2]=EPgy2}CG17223[EY00269]
SKC|3
}
# EOR
GENR
{
RETE|ID 1 FBgn0039378	CLA 1 Gene	GSYM 1 &agr;4GT2	DT 1 25 Dec 04	RESZ 2088	PDOM 1 INTERPRO:IPR007652 == Alpha 1,4-glycosyltransferase conserved region	DBA 2	FNC 2 carbohydrate metabolism	CEL 1 Golgi stack	CLOC 1 96F3	ALESR 1	REF 2	
GSYM|&agr;4GT2
DT|25 Dec 04
ID|FBgn0039378
UAB|Deficiency: Df(3R)boss9 (inferred from cytology)
|Duplication: Dp(3;3)Su<up>8</up> (inferred from cytology)
SYN|CG5878
|CG5878
CLOC|96F3
|Limits computationally determined from genome sequence between @P{PZ}l(3)rQ197<up>rQ197</up>@ and @P{lacW}scrib<up>j7B3</up>@
FNC|carbohydrate metabolism ; GO:0005975
|lipid metabolism ; GO:0006629
CEL|Golgi stack ; GO:0005795
PDOM|IPR007652 == Alpha 1,4-glycosyltransferase conserved region
ENZ|transferase activity, transferring glycosyl groups ; GO:0016757 ; EC:2.4.-.- | inferred from electronic annotation
|transferase activity ; GO:0016740 ; EC:2.-.-.- | inferred from electronic annotation
|transferase activity ; GO:0016740 ; EC:2.-.-.-
|transferase activity, transferring glycosyl groups ; GO:0016757 ; EC:2.4.-.-
|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.-
|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.- | inferred from electronic annotation
DBA|NA:AE003753
|PA:AAF56516
PAC|UniProt_TrEMBL:Q9VBL5
ASQ|FBan0005878
REF
{
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
ENZ|transferase activity ; GO:0016740 ; EC:2.-.-.- | inferred from electronic annotation
|transferase activity, transferring glycosyl groups ; GO:0016757 ; EC:2.4.-.- | inferred from electronic annotation
FNC|carbohydrate metabolism ; GO:0005975 | inferred from electronic annotation
|lipid metabolism ; GO:0006629 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|galactosyltransferase activity ; GO:0008378 ; EC:2.4.1.- | inferred from electronic annotation
CEL|Golgi stack ; GO:0005795 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0179897
|Mucha et al.
|2004
AM|Source for identity of: &agr;4GT2 CG5878
SYN|CG5878
}

ALESR
{
ASYM|&agr;4GT2<up>+</up>
ID|FBal0162937
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0044336	CLA 1 Gene	GSYM 1 5-68	DT 1 25 Dec 04	RESZ 913	ALESR 2	REF 1	
GSYM|5-68
DT|25 Dec 04
ID|FBgn0044336
REF
{
REFM|FBrf0129796
|Eberl et al.
|2000
|0
}

ALESR
{
ASYM|5-68<up>5-68</up>
ID|FBal0122335
PHC|behavioral | recessive
|locomotor behavior defective | recessive
|uncoordinated | recessive
PHI|Mutants are uncoordinated. Sound-evoked potential recorded from the
|antennal nerve are normal.
REF|FBrf0129796
REFDSR
{
RDID|FBrf0129796
|Eberl et al.
|2000
PHC|behavioral | recessive
|locomotor behavior defective | recessive
|uncoordinated | recessive
PHI|Mutants are uncoordinated. Sound-evoked potential recorded from the
|antennal nerve are normal.
SYN|unnamed
}

}

ALESR
{
ASYM|5-68<up>+</up>
ID|FBal0122859
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004168	CLA 1 Gene	NAM 1 Serotonin receptor 1A	GSYM 1 5-HT1A	DT 1 25 Dec 04	RESZ 7908	PDOM 1 INTERPRO:IPR000276 == Rhodopsin-like GPCR superfamily	PTD 1	DBA 9	FNC 4 serotonin receptor signaling pathway	CEL 2 integral to membrane	WT 2 One of several known Drosophila serotonin receptor encoding genes	CLOC 1 56B2--5	ALESR 1	REF 24	
GSYM|5-HT1A
PTD
ARGS
DT|25 Dec 04
ID|FBgn0004168
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CG16720
|5HT-dro2A
|5HT-drp<down>2A</down>
|5HT1A
|5-HT1ADro
|5htdro2a
|DRO2A
|5-HT-dro2A
|5-HT<down>1ADro</down>
|Dm5HTdro2A
|5HT-R2A: Serotonin receptor 2A
|Serotonin receptor 2A
|serotonin-receptor-2A
NAM|Serotonin receptor 1A
CLOC|56B2--5
|Limits computationally determined from genome sequence between @P{lacW}prod<up>k08810</up>@ and @P{PZ}ena<up>02029</up>@/@P{lacW}cora<up>k08713</up>@
CYC|Experimentally determined: 56A--B
FNC|serotonin receptor signaling pathway ; GO:0007210
|serotonin receptor, adenylate cyclase inhibiting pathway ; GO:0007198
|serotonin receptor, phospholipase C activating pathway ; GO:0007208
|transmission of nerve impulse ; GO:0019226
CEL|integral to membrane ; GO:0016021
|integral to plasma membrane ; GO:0005887
WT|One of several known Drosophila serotonin receptor encoding genes.
|Presumed to be a recent duplication of @5-HT1B@ gene.
PDOM|IPR000276 == Rhodopsin-like GPCR superfamily
ENZ|amine receptor activity ; GO:0008227 | inferred from sequence similarity
|G-protein coupled serotonin receptor activity ; GO:0016609 | non-traceable author statement
|G-protein coupled serotonin receptor activity ; GO:0016609 | inferred from sequence similarity
|serotonin receptor activity ; GO:0004993 | traceable author statement
|serotonin receptor activity ; GO:0004993 | inferred from sequence similarity with MGD:Htr1a; MGI:MGI:96273
|5-HT1 receptor activity ; GO:0001586 | non-traceable author statement
|amine receptor activity ; GO:0008227
|G-protein coupled serotonin receptor activity ; GO:0016609
|serotonin receptor activity ; GO:0004993
|5-HT1 receptor activity ; GO:0001586
DBA|NA:AC007839
|BDGP:BACR01N09
|NA:AE003797
|PA:AAF57603
|PA:AAM68432
|NA:BI370929
|BDGP-DGC:RE57708
|NA:Z11489
|PA:CAA77570
PAC|GCR:0254
|PIR:S18153
|PIR:S19155
|UniProt_Swiss_Prot:P28285
|UniProt_TrEMBL:Q9V8Q9
ASQ|FBan0016720
REV|FBrf0138226
REF
{
REFM|FBrf0138226
|Blenau and Baumann
|2001
|2
REFM|FBrf0141499
|Shim et al.
|2001
|0
REFM|FBrf0129744
|Brody and Cravchik
|2000
|0
REFM|FBrf0128759
|Lai
|1999.11
|9
REFM|FBrf0080576
|Maroteaux
|1995.5.31
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0154602
|1
REFM|FBrf0126659
|Cravchik
|1999.11
|9
REFM|FBrf0123896
|Swiss-Prot Project Members
|1992.12.1
|9
REFM|FBrf0058170
|Hen
|1993
|0
REFM|FBrf0064857
|Boschert et al.
|1991
|1
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0152099
|Radford et al.
|2002
|0
REFM|FBrf0108201
|Hita et al.
|1999
|9
REFM|FBrf0054500
|Buchner
|1991
|2
REFM|FBrf0104704
|Pebusque et al.
|1998
|0
REFM|FBrf0088108
|Feng et al.
|1996
|0
REFM|FBrf0110590
|Prokop
|1999
|2
REFM|FBrf0141689
|Claridge-Chang et al.
|2001
|0
REFM|FBrf0102326
|Han et al.
|1998
|0
REFM|FBrf0064277
|Witz et al.
|1991
|1
REFM|FBrf0055969
|Saudou et al.
|1992
|0
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
}

REFDSR
{
RDID|FBrf0054500
|Buchner
|1991
SYN|5HT-dro2A
}

REFDSR
{
RDID|FBrf0055969
|Saudou et al.
|1992
CLOC|56A--B (determined by in situ hybridization)
FNC|serotonin receptor, adenylate cyclase inhibiting pathway ; GO:0007198 | inferred from direct assay
|serotonin receptor, phospholipase C activating pathway ; GO:0007208 | inferred from direct assay
WT|@5-HT1A@ receptor inhibits adenylate cyclase and activates phospholipase
|C. Expression starts in late embryos predominantly in midline motor
|neurones, suggesting a role in motor control. @5-HT1A@ and @5-HT1B@
|have a common chromosomal location and high sequence homology suggesting
|they are the result of a recent duplication event.
}

REFDSR
{
RDID|FBrf0058170
|Hen
|1993
SYN|5HT-drp<down>2A</down>
}

REFDSR
{
RDID|FBrf0064277
|Witz et al.
|1991
SYN|5HT1A
}

REFDSR
{
RDID|FBrf0064857
|Boschert et al.
|1991
SYN|5HT-dro2A
}

REFDSR
{
RDID|FBrf0066373
|Boschert et al.
|1991
SYN|5HT-dro2A: serotonin-receptor-2A
}

REFDSR
{
RDID|FBrf0080576
|Maroteaux
|1995.5.31
SYN|5-HT1ADro
}

REFDSR
{
RDID|FBrf0088108
|Feng et al.
|1996
SYN|5htdro2a
}

REFDSR
{
RDID|FBrf0102326
|Han et al.
|1998
SYN|DRO2A
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ENZ|serotonin receptor activity ; GO:0004993 | inferred from sequence similarity with MGD:Htr1a; MGI:MGI:96273
FNC|serotonin receptor signaling pathway ; GO:0007210 | inferred by curator from GO:0004993
MD|Maps to clone: BACR01N09
CEL|integral to membrane ; GO:0016021 | inferred from sequence similarity with MGD:Htr1a; MGI:MGI:96273
GPD|serotonin-receptor
}

REFDSR
{
RDID|FBrf0108201
|Hita et al.
|1999
MD|Maps to clone: DS07626
}

REFDSR
{
RDID|FBrf0123896
|Swiss-Prot Project Members
|1992.12.1
ENZ|G-protein coupled serotonin receptor activity ; GO:0016609 | non-traceable author statement
FNC|serotonin receptor, adenylate cyclase inhibiting pathway ; GO:0007198 | non-traceable author statement
CEL|integral to plasma membrane ; GO:0005887 | non-traceable author statement
GPD|5-hydroxytryptamine receptor 2A
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: RE57708 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0128759
|Lai
|1999.11
AM|Source for identity of: 5-HT1A CG16720
}

REFDSR
{
RDID|FBrf0129744
|Brody and Cravchik
|2000
ENZ|G-protein coupled serotonin receptor activity ; GO:0016609 | inferred from sequence similarity
FNC|serotonin receptor signaling pathway ; GO:0007210 | inferred from sequence similarity
CEL|integral to membrane ; GO:0016021 | inferred from sequence similarity
GPD|serotonin receptor
}

REFDSR
{
RDID|FBrf0135704
|Tierney
|2001
SYN|5-HT-dro2A
|5-HT<down>1ADro</down>
|5HT-dro2A
ENZ|5-HT1 receptor activity ; GO:0001586 | non-traceable author statement
|serotonin receptor activity ; GO:0004993 | traceable author statement
FNC|serotonin receptor, adenylate cyclase inhibiting pathway ; GO:0007198 | traceable author statement
|serotonin receptor, phospholipase C activating pathway ; GO:0007208 | traceable author statement
}

REFDSR
{
RDID|FBrf0138226
|Blenau and Baumann
|2001
SYN|Dm5HTdro2A
}

REFDSR
{
RDID|FBrf0141689
|Claridge-Chang et al.
|2001
MD|Shows particularly robust cycling of transcription in adult heads,
|as assessed by expression analysis using high density oligonucleotide
|arrays with probe generated during three 12-point time course experiments
|over the course of 6 days.
}

REFDSR
{
RDID|FBrf0152099
|Radford et al.
|2002
ENZ|amine receptor activity ; GO:0008227 | inferred from sequence similarity
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
FNC|transmission of nerve impulse ; GO:0019226 | inferred from electronic annotation
}

ALESR
{
ASYM|5-HT1A<up>+</up>
ID|FBal0071518
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004572	CLA 1 Gene	NAM 1 Serotonin receptor 1B	GSYM 1 5-HT1B	DT 1 25 Dec 04	RESZ 6980	PDOM 1 INTERPRO:IPR000276 == Rhodopsin-like GPCR superfamily	PTD 1	DBA 4	FNC 4 serotonin receptor signaling pathway	CEL 2 integral to membrane	WT 2 One of several known Drosophila serotonin receptor encoding genes	CLOC 1 56B1	ALESR 1	REF 21	
GSYM|5-HT1B
PTD
MMP
DT|25 Dec 04
ID|FBgn0004572
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CG15113
|5HT-dro2B
|5HT-dro<down>2B</down>
|5-HT1BDro
|5-HT<down>dro2B</down>
|5htdro2b
|DRO2B
|5-HT-dro2B
|5-HT<down>1BDro</down>
|Dm5HTdro2B
|5HT-R2B: Serotonin receptor 2B
|Serotonin receptor 2B
NAM|Serotonin receptor 1B
CLOC|56B1
|Limits computationally determined from genome sequence between @P{lacW}prod<up>k08810</up>@ and @P{PZ}ena<up>02029</up>@/@P{lacW}cora<up>k08713</up>@
CYC|Experimentally determined: 56A--B
FNC|serotonin receptor signaling pathway ; GO:0007210
|serotonin receptor, adenylate cyclase inhibiting pathway ; GO:0007198
|serotonin receptor, phospholipase C activating pathway ; GO:0007208
|transmission of nerve impulse ; GO:0019226
CEL|integral to membrane ; GO:0016021
|integral to plasma membrane ; GO:0005887
WT|One of several known Drosophila serotonin receptor encoding genes.
|Presumed to be a recent duplication of @5-HT1A@ gene.
PDOM|IPR000276 == Rhodopsin-like GPCR superfamily
ENZ|amine receptor activity ; GO:0008227 | inferred from sequence similarity
|G-protein coupled serotonin receptor activity ; GO:0016609 | non-traceable author statement
|G-protein coupled serotonin receptor activity ; GO:0016609 | inferred from sequence similarity
|serotonin receptor activity ; GO:0004993 | traceable author statement
|serotonin receptor activity ; GO:0004993 | inferred from sequence similarity with MGD:Htr1a; MGI:MGI:96273
|5-HT1 receptor activity ; GO:0001586 | non-traceable author statement
|amine receptor activity ; GO:0008227
|G-protein coupled serotonin receptor activity ; GO:0016609
|serotonin receptor activity ; GO:0004993
|5-HT1 receptor activity ; GO:0001586
DBA|NA:AE003797
|PA:AAF57610
|NA:Z11490
|PA:CAA77571
PAC|GCR:0255
|PIR:S18154
|PIR:S19156
|UniProt_Swiss_Prot:P28286
|UniProt_TrEMBL:Q9V8Q3
ASQ|FBan0015113
REV|FBrf0138226
REF
{
REFM|FBrf0138226
|Blenau and Baumann
|2001
|2
REFM|FBrf0129744
|Brody and Cravchik
|2000
|0
REFM|FBrf0080576
|Maroteaux
|1995.5.31
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0154602
|1
REFM|FBrf0126659
|Cravchik
|1999.11
|9
REFM|FBrf0123897
|Swiss-Prot Project Members
|1992.12.1
|9
REFM|FBrf0058170
|Hen
|1993
|0
REFM|FBrf0064857
|Boschert et al.
|1991
|1
REFM|FBrf0152099
|Radford et al.
|2002
|0
REFM|FBrf0108201
|Hita et al.
|1999
|9
REFM|FBrf0054500
|Buchner
|1991
|2
REFM|FBrf0104704
|Pebusque et al.
|1998
|0
REFM|FBrf0088108
|Feng et al.
|1996
|0
REFM|FBrf0110590
|Prokop
|1999
|2
REFM|FBrf0066373
|Boschert et al.
|1991
|1
REFM|FBrf0086561
|Obosi et al.
|1996
|0
REFM|FBrf0102326
|Han et al.
|1998
|0
REFM|FBrf0055969
|Saudou et al.
|1992
|0
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
}

REFDSR
{
RDID|FBrf0054500
|Buchner
|1991
SYN|5HT-dro2B
}

REFDSR
{
RDID|FBrf0055969
|Saudou et al.
|1992
CLOC|56A--B (determined by in situ hybridization)
FNC|serotonin receptor, adenylate cyclase inhibiting pathway ; GO:0007198 | inferred from direct assay
|serotonin receptor, phospholipase C activating pathway ; GO:0007208 | inferred from direct assay
WT|@5-HT1B@ receptor inhibits adenylate cyclase and activates phospholipase
|C. Expression starts in late embryos and is restricted to distinct
|populations in the CNS. @5-HT1A@ and @5-HT1B@ have a common chromosomal
|location and high sequence homology suggesting they are the result
|of a recent duplication event.
}

REFDSR
{
RDID|FBrf0058170
|Hen
|1993
SYN|5HT-dro<down>2B</down>
}

REFDSR
{
RDID|FBrf0064857
|Boschert et al.
|1991
SYN|5HT-dro2B
}

REFDSR
{
RDID|FBrf0066373
|Boschert et al.
|1991
SYN|5HT-dro2B
}

REFDSR
{
RDID|FBrf0080576
|Maroteaux
|1995.5.31
SYN|5-HT1BDro
}

REFDSR
{
RDID|FBrf0086561
|Obosi et al.
|1996
SYN|5-HT<down>dro2B</down>
}

REFDSR
{
RDID|FBrf0088108
|Feng et al.
|1996
SYN|5htdro2b
}

REFDSR
{
RDID|FBrf0102326
|Han et al.
|1998
SYN|DRO2B
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ENZ|serotonin receptor activity ; GO:0004993 | inferred from sequence similarity with MGD:Htr1a; MGI:MGI:96273
FNC|serotonin receptor signaling pathway ; GO:0007210 | inferred by curator from GO:0004993
CEL|integral to membrane ; GO:0016021 | inferred from sequence similarity with MGD:Htr1a; MGI:MGI:96273
GPD|serotonin-receptor
}

REFDSR
{
RDID|FBrf0123897
|Swiss-Prot Project Members
|1992.12.1
ENZ|G-protein coupled serotonin receptor activity ; GO:0016609 | non-traceable author statement
FNC|serotonin receptor, adenylate cyclase inhibiting pathway ; GO:0007198 | non-traceable author statement
CEL|integral to plasma membrane ; GO:0005887 | non-traceable author statement
GPD|5-hydroxytryptamine receptor 2B
}

REFDSR
{
RDID|FBrf0129744
|Brody and Cravchik
|2000
ENZ|G-protein coupled serotonin receptor activity ; GO:0016609 | inferred from sequence similarity
FNC|serotonin receptor signaling pathway ; GO:0007210 | inferred from sequence similarity
CEL|integral to membrane ; GO:0016021 | inferred from sequence similarity
GPD|serotonin receptor
}

REFDSR
{
RDID|FBrf0135704
|Tierney
|2001
ENZ|5-HT1 receptor activity ; GO:0001586 | non-traceable author statement
|serotonin receptor activity ; GO:0004993 | traceable author statement
FNC|serotonin receptor, adenylate cyclase inhibiting pathway ; GO:0007198 | traceable author statement
|serotonin receptor, phospholipase C activating pathway ; GO:0007208 | traceable author statement
SYN|5-HT-dro2B
|5-HT<down>1BDro</down>
|5HT-dro2B
}

REFDSR
{
RDID|FBrf0138226
|Blenau and Baumann
|2001
SYN|Dm5HTdro2B
}

REFDSR
{
RDID|FBrf0152099
|Radford et al.
|2002
ENZ|amine receptor activity ; GO:0008227 | inferred from sequence similarity
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
FNC|transmission of nerve impulse ; GO:0019226 | inferred from electronic annotation
}

ALESR
{
ASYM|5-HT1B<up>+</up>
ID|FBal0071519
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0013743	CLA 1 Gene	NAM 1 Serotonin receptor 2	GSYM 1 5-HT2	DT 1 25 Dec 04	RESZ 13365	PDOM 1 INTERPRO:IPR000276 == Rhodopsin-like GPCR superfamily	PTD 1	DBA 13	FNC 3 germ-band extension	CEL 2 integral to membrane	CLOC 1 82C3--4	ALESR 6	REF 27	
GSYM|5-HT2
PTD
DT|25 Dec 04
ID|FBgn0013743
UAB|Deficiency: Df(3R)110
|Duplication: Dp(3;3)81-83 (inferred from cytology)
SYN|CG1056
|5HT-dro<down>1</down>
|5-HT2Dro
|5-HT<down>2</down>
|5HT2Dro
|5-ht2Dro
|5HT<down>2Dro</down>
|5-HT<down>2Dro</down>
|5HT2-Dro
|Dm5HT2
|5HT-R82A
NAM|Serotonin receptor 2
GLOC|3-
CLOC|82C3--4
|Limits computationally determined from genome sequence between @P{PZ}l(3)02733<up>02733</up>@ and @P{EP}EP974@
CYC|Experimentally determined: 82C, 82C--D, 82C--E
FNC|germ-band extension ; GO:0007377
|serotonin receptor signaling pathway ; GO:0007210
|transmission of nerve impulse ; GO:0019226
CEL|integral to membrane ; GO:0016021
|plasma membrane ; GO:0005886
PDOM|IPR000276 == Rhodopsin-like GPCR superfamily
ENZ|amine receptor activity ; GO:0008227 | inferred from sequence similarity
|G-protein coupled serotonin receptor activity ; GO:0016609 | inferred from sequence similarity
|serotonin receptor activity ; GO:0004993 | traceable author statement
|serotonin receptor activity ; GO:0004993 | non-traceable author statement
|5-HT2 receptor activity ; GO:0001587 | non-traceable author statement
|amine receptor activity ; GO:0008227
|G-protein coupled serotonin receptor activity ; GO:0016609
|serotonin receptor activity ; GO:0004993
|5-HT2 receptor activity ; GO:0001587
DBA|NA:AA699149
|BDGP-DGC:HL07802
|NA:AE003605
|PA:AAN13284
|PA:AAF52113
|NA:AW942018
|BDGP-DGC:HL07802
|NA:AY061039
|PA:AAL28587
|BDGP-DGC:HL07802
|NA:X81835
|PA:CAA57429
|NA:X85407
PAC|UniProt_TrEMBL:Q24511
|UniProt_TrEMBL:Q8IPN2
|UniProt_TrEMBL:Q95RY6
|UniProt_TrEMBL:Q9VN38
ASQ|FBan0001056
REV|FBrf0138226
|FBrf0138225
REF
{
REFM|FBrf0111346
|Colas et al.
|1999
|-1
REFM|FBrf0131362
|Miller et al.
|2000
|0
REFM|FBrf0101089
|Maroteaux et al.
|1998
|1
REFM|FBrf0138226
|Blenau and Baumann
|2001
|2
REFM|FBrf0138225
|Vanden Broeck
|2001
|2
REFM|FBrf0129744
|Brody and Cravchik
|2000
|0
REFM|FBrf0109520
|Colas et al.
|1999
|1
REFM|FBrf0117712
|Maroteaux
|1995.3.14
|9
REFM|FBrf0117711
|Maroteaux
|1994.9.19
|9
REFM|FBrf0083085
|Colas et al.
|1995
|1
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0132177
|Gene Disruption Project members
|2001-
|9
REFM|FBrf0154602
|1
REFM|FBrf0083842
|Colas et al.
|1995
|1
REFM|FBrf0058170
|Hen
|1993
|0
REFM|FBrf0106916
|Maroteaux et al.
|1999
|1
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0092338
|Colas et al.
|1997
|1
REFM|FBrf0152099
|Radford et al.
|2002
|0
REFM|FBrf0086363
|Colas et al.
|1996
|1
REFM|FBrf0104704
|Pebusque et al.
|1998
|0
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0141689
|Claridge-Chang et al.
|2001
|0
REFM|FBrf0078230
|Colas et al.
|1995
|1
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
REFM|FBrf0173702
|Schaerlinger et al.
|2004
|1
}

REFDSR
{
RDID|FBrf0058170
|Hen
|1993
SYN|5HT-dro<down>1</down>
}

REFDSR
{
RDID|FBrf0078230
|Colas et al.
|1995
WT|Identified in a screen for genes encoding G-protein coupled receptors.
}

REFDSR
{
RDID|FBrf0080576
|Maroteaux
|1995.5.31
CLOC|82C--D (determined by in situ hybridization)
WT|This serotonin receptor displays a sequence, gene organization and pharmacology
|typical of the mammalian serotonin 5-HT2 receptor type (5-HT2B subtype)
|acting on phospholipase C.
SYN|5-HT2Dro
}

REFDSR
{
RDID|FBrf0081644
|Colas et al.
|1995
CEL|plasma membrane ; GO:0005886 | inferred from direct assay
|plasma membrane ; GO:0005886 | inferred from sequence similarity
WT|Characterization of @5-HT2@ reveals it is expressed in the central
|nervous system during larval and adult stages and the receptor is expressed
|at the blastoderm stage in a pattern similar to that of @ftz@.
BMD|Df(3R)110
BMDD|Df(3R)6-7
SYN|5-HT<down>2</down>
}

REFDSR
{
RDID|FBrf0083085
|Colas et al.
|1995
SYN|5-HT2Dro
}

REFDSR
{
RDID|FBrf0083842
|Colas et al.
|1995
SYN|5-HT2Dro
}

REFDSR
{
RDID|FBrf0086363
|Colas et al.
|1996
SYN|5-HT2Dro
}

REFDSR
{
RDID|FBrf0092338
|Colas et al.
|1997
SYN|5HT2Dro
}

REFDSR
{
RDID|FBrf0101089
|Maroteaux et al.
|1998
SYN|5-HT2Dro
}

REFDSR
{
RDID|FBrf0106916
|Maroteaux et al.
|1999
SYN|5-ht2Dro
}

REFDSR
{
RDID|FBrf0109520
|Colas et al.
|1999
SYN|5-ht2Dro
}

REFDSR
{
RDID|FBrf0111346
|Colas et al.
|1999
FNC|germ-band extension ; GO:0007377 | inferred from mutant phenotype
MD|Peaks of @5-HT2@ expression and serotonin synthesis coincide precisely
|with the onset of convergent extension of the ectoderm.
|Maps to clone: DS04152
|Maps to clone: 56E12
|Maps to clone: 78C10
BMD|Df(3R)110
BMD|Df(3R)HTRE
BMD|Df(3R)HTRI
BMDD|Df(3R)HTR6
PHP|Mutants do not extend the germband properly, and ectodermal movements
|become asynchronous with the morphogenetic movements in the endoderm
|and mesoderm. Adherens junctions in the ectoderm show altered subcellular
|distribution at the onset of the asynchronicity.
SYN|5HT<down>2Dro</down>
}

REFDSR
{
RDID|FBrf0111347
|Colas et al.
|1999
CLOC|82C--E
WT|Serotinin, acting through the @5-HT2@ gene product, is necessary for
|proper gastrulation.
BMD|Df(3R)HTRI
BMDD|Df(3R)HTR6
PHP|Deletion
|of @5-HT2@ is associated with a specific, double-line cuticular
|phenotype.
SYN|5HT<down>2Dro</down>
}

REFDSR
{
RDID|FBrf0117711
|Maroteaux
|1994.9.19
SYN|5-HT2Dro
}

REFDSR
{
RDID|FBrf0117712
|Maroteaux
|1995.3.14
ENZ|serotonin receptor activity ; GO:0004993 | non-traceable author statement
GLOC|3-
CLOC|82C
FNC|serotonin receptor signaling pathway ; GO:0007210 | non-traceable author statement
CEL|plasma membrane ; GO:0005886 | non-traceable author statement
GPD|serotonin-receptor
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: HL07802 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0129744
|Brody and Cravchik
|2000
ENZ|G-protein coupled serotonin receptor activity ; GO:0016609 | inferred from sequence similarity
FNC|serotonin receptor signaling pathway ; GO:0007210 | inferred from sequence similarity
CEL|integral to membrane ; GO:0016021 | inferred from sequence similarity
GPD|serotonin receptor
}

REFDSR
{
RDID|FBrf0135704
|Tierney
|2001
ENZ|5-HT2 receptor activity ; GO:0001587 | non-traceable author statement
|serotonin receptor activity ; GO:0004993 | traceable author statement
FNC|serotonin receptor signaling pathway ; GO:0007210 | traceable author statement
SYN|5-HT<down>2Dro</down>
}

REFDSR
{
RDID|FBrf0138225
|Vanden Broeck
|2001
SYN|5HT2-Dro
}

REFDSR
{
RDID|FBrf0138226
|Blenau and Baumann
|2001
SYN|Dm5HT2
}

REFDSR
{
RDID|FBrf0141689
|Claridge-Chang et al.
|2001
MD|Shows particularly robust cycling of transcription in adult heads,
|as assessed by expression analysis using high density oligonucleotide
|arrays with probe generated during three 12-point time course experiments
|over the course of 6 days.
}

REFDSR
{
RDID|FBrf0152099
|Radford et al.
|2002
ENZ|amine receptor activity ; GO:0008227 | inferred from sequence similarity
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
FNC|transmission of nerve impulse ; GO:0019226 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

REFDSR
{
RDID|FBrf0173702
|Schaerlinger et al.
|2004
SYN|5-HT2Dro
}

ALESR
{
ASYM|5-HT2<up>M51</up>
ID|FBal0157524
PHC|lethal | embryonic | recessive
REF|FBrf0173702
REFDSR
{
RDID|FBrf0173702
|Schaerlinger et al.
|2004
PHC|lethal | embryonic | recessive
}

}

ALESR
{
ASYM|5-HT2<up>PL00052</up>
ID|FBal0162863
PHC|viable
|fertile
REF|FBrf0132177
REFDSR
{
RDID|FBrf0132177
|Gene Disruption Project members
|2001-
TRN|FBti0058212 == PBac{GAL4D,EYFP}5-HT2<up>PL00052</up>
PHC|viable
|fertile
}

}

ALESR
{
ASYM|5-HT2<up>a.Y32.hs</up>
ID|FBal0101837
PHC|lethal | conditional ts
PHM|extended germ band embryo embryo
|pole cell
|ventral midline
PHI|Mutant embryos show abnormal germband extension movements. There is
|a desynchronization between germband extension and mesodermal and endodermal
|invaginations, and a premature termination of movements. The ventral
|midline closure is often incomplete, and pole cells abnormally positioned.
|Mode of assay: In transgenic Drosophila
REF|FBrf0111346
REFDSR
{
RDID|FBrf0111346
|Colas et al.
|1999
NAM|antisense Y32 heat shock construct
MD|Construct: Expression of @5-HT2@ cDNA including the N-terminus, the extracellular
|region and the first transmembrane region in the antisense orientation
|is driven by a heat shock promoter.
MU|in vitro construct | regulatory fusion
CNS|FBtp0011635 == P{hs-5-HT2.Y32.a}
PHC|lethal | conditional ts
PHM|extended germ band embryo embryo
|pole cell
|ventral midline
PHI|Mutant embryos show abnormal germband extension movements. There is
|a desynchronization between germband extension and mesodermal and endodermal
|invaginations, and a premature termination of movements. The ventral
|midline closure is often incomplete, and pole cells abnormally positioned.
|Mode of assay: In transgenic Drosophila
}

}

ALESR
{
ASYM|5-HT2<up>hs.PC</up>
ID|FBal0101836
PHC|lethal | dominant | conditional ts
PHM|epidermis | embryonic
PHI|Even after a heat shock of only 8 minutes the ectodermal layer elongation
|is disturbed, and lethality results.
|Mode of assay: In transgenic Drosophila
REF|FBrf0111346
REFDSR
{
RDID|FBrf0111346
|Colas et al.
|1999
NAM|heat shock construct of Colas
MD|Construct: Expression of full length @5-HT2@ cDNA is driven by a heat shock promoter.
MU|in vitro construct | regulatory fusion
CNS|FBtp0011634 == P{hs-5-HT2.C}
PHC|lethal | dominant | conditional ts
PHM|epidermis | embryonic
PHI|Even after a heat shock of only 8 minutes the ectodermal layer elongation
|is disturbed, and lethality results.
|Mode of assay: In transgenic Drosophila
}

}

ALESR
{
ASYM|5-HT2<up>Scer\UAS.cCa</up>
ID|FBal0101838
PHC|viable with @Scer\GAL4<up>Kr.PM</up>@
|viable | poor | conditional ts with @Scer\GAL4<up>Kr.PM</up>@
PHM|gastrula stage embryo with @Scer\GAL4<up>Kr.PM</up>@
PHI|When expression is driven by @Scer\GAL4<up>Kr.PM</up>@ there are initially
|significant perturbations at the beginning of gastrulation, due to
|a mistiming in morphogenetic movements, which is compensated later
|in embryogenesis by an increase in rate of cell movement. Heat shocking
|increases the lethality.
|Mode of assay: In transgenic Drosophila
REF|FBrf0111346
REFDSR
{
RDID|FBrf0111346
|Colas et al.
|1999
NAM|Saccharomyces cerevisiae UAS construct a of Colas
MD|Construct: Expression of full length @5-HT2@ cDNA is governed by @Scer\UAS@ regulatory
|sequences.
MU|in vitro construct | regulatory fusion
CNS|FBtp0011636 == P{UAS-5-HT2.C}
PHC|viable with @Scer\GAL4<up>Kr.PM</up>@
|viable | poor | conditional ts with @Scer\GAL4<up>Kr.PM</up>@
PHM|gastrula stage embryo with @Scer\GAL4<up>Kr.PM</up>@
PHI|When expression is driven by @Scer\GAL4<up>Kr.PM</up>@ there are initially
|significant perturbations at the beginning of gastrulation, due to
|a mistiming in morphogenetic movements, which is compensated later
|in embryogenesis by an increase in rate of cell movement. Heat shocking
|increases the lethality.
|Mode of assay: In transgenic Drosophila
}

}

ALESR
{
ASYM|5-HT2<up>+</up>
ID|FBal0066320
CLA|wild-type generic
REF|FBrf0105495
}

IFL|../hjmuller/serotr1.htm
}
# EOR
GENR
{
RETE|ID 1 FBgn0004573	CLA 1 Gene	NAM 1 Serotonin receptor 7	GSYM 1 5-HT7	DT 1 25 Dec 04	RESZ 7766	PDOM 3 INTERPRO:IPR000276 == Rhodopsin-like GPCR superfamily	PTD 1	DBA 11	FNC 3 nerve-nerve synaptic transmission	CEL 3 integral to membrane	WT 3 @5-HT7@ receptor stimulates adenylate cyclase	CLOC 1 100B1	ALESR 2	REF 22	
GSYM|5-HT7
PTD
DT|25 Dec 04
ID|FBgn0004573
UAB|Deficiency: Df(3R)tll-e (inferred from cytology)
|Duplication: Dp(3;3)516 (inferred from cytology)
SYN|CG12073
|5HT-dro
|5HT-dro1
|5-HT7Dro
|5-HT<down>dro1</down>
|5htdror
|DRO1
|5-HT-dro1
|5-HT<down>7Dro</down>
|5-HT-dro
|5-HTdro1
|5-HT<down>7</down>
|Dm5HTdro1
|5HT-R1: Serotonin receptor 1
|Serotonin receptor 1
NAM|Serotonin receptor 7
CLOC|100B1
|Limits computationally determined from genome sequence between @P{lacW}l(3)s2500<up>s2500</up>@ and @P{PZ}Aph-4<up>07028</up>@&@P{PZ}dco<up>rK215</up>@
CYC|Experimentally determined: 100A, 99F--100A
FNC|nerve-nerve synaptic transmission ; GO:0007270
|serotonin receptor signaling pathway ; GO:0007210
|serotonin receptor, adenylate cyclase activating pathway ; GO:0007192
CEL|integral to membrane ; GO:0016021
|integral to plasma membrane ; GO:0005887
|plasma membrane ; GO:0005886
PDOM|IPR000276 == Rhodopsin-like GPCR superfamily
|IPR000929 == Dopamine receptor
|IPR007455 == Serglycin
WT|@5-HT7@ receptor stimulates adenylate cyclase. Expression starts in
|late embryos and is restricted to distinct cell populations in the
|CNS.
ENZ|amine receptor activity ; GO:0008227 | inferred from sequence similarity
|G-protein coupled serotonin receptor activity ; GO:0016609 | non-traceable author statement
|G-protein coupled serotonin receptor activity ; GO:0016609 | inferred from sequence similarity
|serotonin receptor activity ; GO:0004993 | traceable author statement
|amine receptor activity ; GO:0008227
|dopamine receptor activity ; GO:0004952
|G-protein coupled serotonin receptor activity ; GO:0016609
|serotonin receptor activity ; GO:0004993
|serotonin receptor activity ; GO:0004993 | inferred from sequence similarity with UniProt:Q64264
|dopamine receptor activity ; GO:0004952 | inferred from electronic annotation
DBA|NA:AA201540
|BDGP-DGC:LD04507
|NA:AE003776
|PA:AAF57104
|NA:AW941548
|BDGP-DGC:LD04507
|NA:AY118491
|PA:AAM49860
|BDGP-DGC:LD04507
|NA:M55533
|PA:AAA28305
PAC|GCR:0023
|PIR:A38271
|UniProt_Swiss_Prot:P20905
ASQ|FBan0012073
REV|FBrf0138226
REF
{
REFM|FBrf0075179
|Boschert et al.
|1991
|9
REFM|FBrf0138226
|Blenau and Baumann
|2001
|2
REFM|FBrf0129744
|Brody and Cravchik
|2000
|0
REFM|FBrf0123747
|Swiss-Prot Project Members
|1991.2.1
|9
REFM|FBrf0080576
|Maroteaux
|1995.5.31
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0126659
|Cravchik
|1999.11
|9
REFM|FBrf0052872
|Witz et al.
|1990
|0
REFM|FBrf0051655
|Saudou et al.
|1990
|0
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|FBrf0152099
|Radford et al.
|2002
|0
REFM|FBrf0104704
|Pebusque et al.
|1998
|0
REFM|FBrf0088108
|Feng et al.
|1996
|0
REFM|FBrf0179797
|Bloomington Drosophila Stock Center
|2004.11.6
|9
REFM|FBrf0066373
|Boschert et al.
|1991
|1
REFM|FBrf0086561
|Obosi et al.
|1996
|0
REFM|FBrf0102326
|Han et al.
|1998
|0
REFM|FBrf0055969
|Saudou et al.
|1992
|0
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
}

REFDSR
{
RDID|FBrf0051655
|Saudou et al.
|1990
SYN|5HT-dro
}

REFDSR
{
RDID|FBrf0052872
|Witz et al.
|1990
CLOC|99F--100A (determined by in situ hybridization)
}

REFDSR
{
RDID|FBrf0055969
|Saudou et al.
|1992
CLOC|100A (determined by in situ hybridization)
WT|@5-HT7@ receptor stimulates adenylate cyclase. Expression starts in
|late embryos and is restricted to distinct cell populations in the
|CNS.
}

REFDSR
{
RDID|FBrf0064857
|Boschert et al.
|1991
CLOC|100A (determined by in situ hybridization)
SYN|5HT-dro1
}

REFDSR
{
RDID|FBrf0066373
|Boschert et al.
|1991
SYN|5HT-dro1
}

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
MD|Identified with: D1183
}

REFDSR
{
RDID|FBrf0075179
|Boschert et al.
|1991
CLOC|100A (determined by in situ hybridization)
}

REFDSR
{
RDID|FBrf0080576
|Maroteaux
|1995.5.31
SYN|5-HT7Dro
}

REFDSR
{
RDID|FBrf0086561
|Obosi et al.
|1996
SYN|5-HT<down>dro1</down>
}

REFDSR
{
RDID|FBrf0088108
|Feng et al.
|1996
SYN|5htdror
}

REFDSR
{
RDID|FBrf0102326
|Han et al.
|1998
SYN|DRO1
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ENZ|serotonin receptor activity ; GO:0004993 | inferred from sequence similarity with UniProt:Q64264
FNC|serotonin receptor signaling pathway ; GO:0007210 | inferred from sequence similarity with UniProt:Q64264
CEL|plasma membrane ; GO:0005886 | inferred from sequence similarity with MGD:Htr2c; MGI:MGI:96281
GPD|serotonin-receptor
}

REFDSR
{
RDID|FBrf0123747
|Swiss-Prot Project Members
|1991.2.1
ENZ|G-protein coupled serotonin receptor activity ; GO:0016609 | non-traceable author statement
FNC|serotonin receptor, adenylate cyclase activating pathway ; GO:0007192 | non-traceable author statement
CEL|integral to plasma membrane ; GO:0005887 | non-traceable author statement
GPD|5-hydroxytryptamine receptor 1
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: LD04507 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0129744
|Brody and Cravchik
|2000
ENZ|G-protein coupled serotonin receptor activity ; GO:0016609 | inferred from sequence similarity
FNC|serotonin receptor signaling pathway ; GO:0007210 | inferred from sequence similarity
CEL|integral to membrane ; GO:0016021 | inferred from sequence similarity
GPD|serotonin receptor
}

REFDSR
{
RDID|FBrf0135704
|Tierney
|2001
ENZ|serotonin receptor activity ; GO:0004993 | traceable author statement
FNC|serotonin receptor, adenylate cyclase activating pathway ; GO:0007192 | traceable author statement
SYN|5-HT-dro1
|5-HT<down>7Dro</down>
|5-HT-dro
|5-HTdro1
|5HT-dro1
|5-HT<down>7</down>
}

REFDSR
{
RDID|FBrf0138226
|Blenau and Baumann
|2001
SYN|Dm5HTdro1
}

REFDSR
{
RDID|FBrf0152099
|Radford et al.
|2002
ENZ|amine receptor activity ; GO:0008227 | inferred from sequence similarity
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
FNC|nerve-nerve synaptic transmission ; GO:0007270 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|dopamine receptor activity ; GO:0004952 | inferred from electronic annotation
}

ALESR
{
ASYM|5-HT7<up>f05214</up>
ID|FBal0162862
PHC|viable
|fertile
REF|FBrf0179797
REFDSR
{
RDID|FBrf0179797
|Bloomington Drosophila Stock Center
|2004.11.6
TRN|FBti0042434 == PBac{WH}5-HT7<up>f05214</up>
MU|piggyBac transposase
PHC|viable
|fertile
}

}

ALESR
{
ASYM|5-HT7<up>+</up>
ID|FBal0071517
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0025466	CLA 1 existence-uncertain gene	NAM 1 5-Hydroxy Tryptophan decarboxylase	GSYM 1 5-HTdc	DT 1 25 Dec 04	RESZ 749	ALESR 1	REF 1	
GSYM|5-HTdc
DT|25 Dec 04
ID|FBgn0025466
CLA|existence-uncertain gene
SYN|5-Hydroxy Tryptophan decarboxylase
NAM|5-Hydroxy Tryptophan decarboxylase
ENZ|aromatic-L-amino-acid decarboxylase activity ; GO:0004058 ; EC:4.1.1.28 | inferred from direct assay
|aromatic-L-amino-acid decarboxylase activity ; GO:0004058 ; EC:4.1.1.28
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0040032
|Livingstone and Tempel
|1983
ENZ|aromatic-L-amino-acid decarboxylase activity ; GO:0004058 ; EC:4.1.1.28 | inferred from direct assay
NAM|5-Hydroxy Tryptophan decarboxylase
GPD|aromatic-L-amino-acid decarboxylase
}

ALESR
{
ASYM|5-HTdc<up>+</up>
ID|FBal0092394
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0061471	CLA 1 multicopy cytosolic ribosomal RNA gene	GSYM 1 5.8SrRNA	DT 1 25 Dec 04	RESZ 1073	DBA 6	ALESR 1	REF 5	
GSYM|5.8SrRNA
DT|25 Dec 04
ID|FBgn0061471
CLA|multicopy_cytosolic_ribosomal_RNA_gene
SYN|5.8S and 2S ribosomal rRNA
|5.8S DNA and IGS
|5.8S rRNA
|5.8SRNA
AM|encoded by: @bb@, @Ybb@
|component genes: @5.8SrRNA:CR40454@, @5.8SrRNA:CR40457@
DBA|NA:AF083522
|NA:M21017
|NA:U20145
|NA:V00236
|NA:X15707
|NA:X68958
REF
{
REFM|FBrf0117968
|McKee
|1993.7.12
|9
REFM|FBrf0154285
|Ashburner
|2003.2.5
|9
REFM|FBrf0127122
|Hori et al.
|2000
|0
REFM|FBrf0115021
|Fox
|1995.1.20
|9
REFM|FBrf0121292
|Tautz
|1990.3.15
|9
}

REFDSR
{
RDID|FBrf0115021
|Fox
|1995.1.20
SYN|5.8S and 2S ribosomal rRNA
}

REFDSR
{
RDID|FBrf0117968
|McKee
|1993.7.12
SYN|5.8S DNA and IGS
}

REFDSR
{
RDID|FBrf0121292
|Tautz
|1990.3.15
SYN|5.8S rRNA
}

REFDSR
{
RDID|FBrf0127122
|Hori et al.
|2000
SYN|5.8S rRNA
}

ALESR
{
ASYM|5.8SrRNA<up>+</up>
ID|FBal0142208
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0058454	CLA 1 Gene	GSYM 1 5.8SrRNA:CR40454	DT 1 25 Dec 04	RESZ 561	DBA 1	ALESR 1	REF 1	
GSYM|5.8SrRNA:CR40454
DT|25 Dec 04
ID|FBgn0058454
SYN|CR40454
AM|member gene of: @5.8SrRNA@
DBA|NA:AABU01001264
ASQ|FBan0040454
REF
{
REFM|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
|9
}

REFDSR
{
RDID|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
CYC|Heterochromatic, cytological location not yet determined. Maps to a
|region encoding rRNA genes; one of 20F, h29, h20.
}

ALESR
{
ASYM|5.8SrRNA:CR40454<up>+</up>
ID|FBal0143092
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0058457	CLA 1 Gene	GSYM 1 5.8SrRNA:CR40457	DT 1 25 Dec 04	RESZ 561	DBA 1	ALESR 1	REF 1	
GSYM|5.8SrRNA:CR40457
DT|25 Dec 04
ID|FBgn0058457
SYN|CR40457
AM|member gene of: @5.8SrRNA@
DBA|NA:AABU01001264
ASQ|FBan0040457
REF
{
REFM|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
|9
}

REFDSR
{
RDID|FBrf0173307
|Drosophila Heterochromatin Genome Project
|2004
CYC|Heterochromatic, cytological location not yet determined. Maps to a
|region encoding rRNA genes; one of 20F, h29, h20.
}

ALESR
{
ASYM|5.8SrRNA:CR40457<up>+</up>
ID|FBal0143091
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0051107	CLA 1 Gene	GSYM 1 5PtaseI	DT 1 25 Dec 04	RESZ 2590	DBA 2	FNC 1 inositol phosphate dephosphorylation	CLOC 1 96B17	ALESR 2	REF 5	
GSYM|5PtaseI
DT|25 Dec 04
ID|FBgn0051107
UAB|Deficiency: Df(3R)XTA1 (inferred from cytology)
|Duplication: Dp(3;3)Su<up>8</up> (inferred from cytology)
SYN|CG31107
|CG7613
|CG31107
|dm5PtaseI
ID2|FBgn0039263
CLOC|96B17
|Limits computationally determined from genome sequence between @P{PZ}ssh<up>01207</up>@ and @P{lacW}OstStt3<up>j2D9</up>@
FNC|inositol phosphate dephosphorylation ; GO:0046855
ENZ|inositol-polyphosphate 5-phosphatase activity ; GO:0004445 ; EC:3.1.3.56
|inositol-polyphosphate 5-phosphatase activity ; GO:0004445 ; EC:3.1.3.56 | inferred from mutant phenotype
DBA|NA:AE003750
|PA:AAF56383
PAC|UniProt_TrEMBL:Q9VBZ3
ASQ|FBan0031107
REF
{
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0148886
|FlyBase Genome Annotators
|2002-2003
|9
REFM|FBrf0174231
|Kiger et al.
|2003
|9
REFM|FBrf0126682
|Li
|1999.11
|9
REFM|FBrf0179834
|Seeds
|2004
|-1
}

REFDSR
{
RDID|FBrf0148886
|FlyBase Genome Annotators
|2002-2003
AM|Source for split of: CG7613
|Annotation CG7613 split into CG31110 and CG31107 in release 3 of the
|genome annotation.
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

REFDSR
{
RDID|FBrf0174231
|Kiger et al.
|2003
OTH|dsRNA made from templates generated with primers directed against
|this gene tested in RNAi screen for effects on Kc167 and S2R<up>+</up>
|cell morphology.
}

REFDSR
{
RDID|FBrf0179834
|Seeds
|2004
ENZ|inositol-polyphosphate 5-phosphatase activity ; GO:0004445 ; EC:3.1.3.56 | inferred from mutant phenotype
FNC|inositol phosphate dephosphorylation ; GO:0046855 | inferred from mutant phenotype
AM|Source for identity of: 5PtaseI CG31107
GPD|inositol (1,4,5)-triphosphate 5-phosphatase
SYN|CG31107
|dm5PtaseI
}

ALESR
{
ASYM|5PtaseI<up>dsRNA.cSa</up>
ID|FBal0162861
PHI|Mode of assay: Drosophila cell culture
REF|FBrf0179834
REFDSR
{
RDID|FBrf0179834
|Seeds
|2004
MD|Construct: Template corresponding to @5PtaseI@ sequences.
OTH|dsRNA has been synthesized from the template and used to treat S2 cells
|to study the phenotypic consequences of dsRNA interference (RNAi) of
|the @5PtaseI@ gene.
MU|in vitro construct | RNAi
PHI|Mode of assay: Drosophila cell culture
}

}

ALESR
{
ASYM|5PtaseI<up>+</up>
ID|FBal0162965
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0000002	CLA 1 multicopy cytosolic ribosomal RNA gene	NAM 1 5S ribosomal RNA	GSYM 1 5SrRNA	DT 1 25 Dec 04	RESZ 14250	DBA 11	CEL 1 cytosolic large ribosomal subunit (sensu Eukaryota)	WT 2 The locus encoding the genes for 5S RNA	CLOC 1 56F1--2	ALESR 5	SK 1	REF 40	
GSYM|5SrRNA
DT|25 Dec 04
ID|FBgn0000002
CLA|multicopy_cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|5SRNA
|5S
|l(2)03068
|Dm5S
|RNA X
|PZ03068
|5S rRNA
|2S rRNA
|5S rDNA
|5S-rDNA
|5SrDNA
ID2|FBgn0010528
NAM|5S ribosomal RNA
GLOC|2-[90]
CLOC|56F1--2
|Left limit from in situ hybridization (FBrf0067338)
|Right limit from in situ hybridization (FBrf0067338)
CYC|Experimentally determined: 56E--F, 56F, 56F1--2, 56F1--7
AM|component genes: @5SrRNA:CR33353@, @5SrRNA:CR33354@, @5SrRNA:CR33355@,
|component genes: @5SrRNA:CR33357@, @5SrRNA:CR33358@, @5SrRNA:CR33359@,
|component genes: @5SrRNA:CR33360@, @5SrRNA:CR33361@, @5SrRNA:CR33362@,
|component genes: @5SrRNA:CR33364@, @5SrRNA:CR33365@, @5SrRNA:CR33366@,
|component genes: @5SrRNA:CR33367@, @5SrRNA:CR33368@, @5SrRNA:CR33369@,
|component genes: @5SrRNA:CR33370@, @5SrRNA:CR33372@, @5SrRNA:CR33373@,
|component genes: @5SrRNA:CR33374@, @5SrRNA:CR33375@, @5SrRNA:CR33376@,
|component genes: @5SrRNA:CR33377@, @5SrRNA:CR33378@, @5SrRNA:CR33379@,
|component genes: @5SrRNA:CR33380@, @5SrRNA:CR33381@, @5SrRNA:CR33382@,
|component genes: @5SrRNA:CR33383@, @5SrRNA:CR33384@, @5SrRNA:CR33385@,
|component genes: @5SrRNA:CR33386@, @5SrRNA:CR33387@, @5SrRNA:CR33388@,
|component genes: @5SrRNA:CR33389@, @5SrRNA:CR33390@, @5SrRNA:CR33391@,
|component genes: @5SrRNA:CR33392@, @5SrRNA:CR33393@, @5SrRNA:CR33394@,
|component genes: @5SrRNA:CR33395@, @5SrRNA:CR33396@, @5SrRNA:CR33397@,
|component genes: @5SrRNA:CR33398@, @5SrRNA:CR33399@, @5SrRNA:CR33400@,
|component genes: @5SrRNA:CR33401@, @5SrRNA:CR33402@, @5SrRNA:CR33403@,
|component genes: @5SrRNA:CR33404@, @5SrRNA:CR33405@, @5SrRNA:CR33406@,
|component genes: @5SrRNA:CR33407@, @5SrRNA:CR33408@, @5SrRNA:CR33409@,
|component genes: @5SrRNA:CR33410@, @5SrRNA:CR33411@, @5SrRNA:CR33412@,
|component genes: @5SrRNA:CR33413@, @5SrRNA:CR33414@, @5SrRNA:CR33415@,
|component genes: @5SrRNA:CR33417@, @5SrRNA:CR33418@, @5SrRNA:CR33419@,
|component genes: @5SrRNA:CR33420@, @5SrRNA:CR33421@, @5SrRNA:CR33422@,
|component genes: @5SrRNA:CR33423@, @5SrRNA:CR33424@, @5SrRNA:CR33425@,
|component genes: @5SrRNA:CR33426@, @5SrRNA:CR33427@, @5SrRNA:CR33428@,
|component genes: @5SrRNA:CR33429@, @5SrRNA:CR33430@, @5SrRNA:CR33431@,
|component genes: @5SrRNA:CR33432@, @5SrRNA:CR33433@, @5SrRNA:CR33434@,
|component genes: @5SrRNA:CR33435@, @5SrRNA:CR33436@, @5SrRNA:CR33437@,
|component genes: @5SrRNA:CR33438@, @5SrRNA:CR33439@, @5SrRNA:CR33440@,
|component genes: @5SrRNA:CR33441@, @5SrRNA:CR33442@, @5SrRNA:CR33443@,
|component genes: @5SrRNA:CR33444@, @5SrRNA:CR33445@, @5SrRNA:CR33446@,
|component genes: @5SrRNA:CR33447@, @5SrRNA:CR33448@, @5SrRNA:CR33449@,
|component genes: @5SrRNA:CR33450@, @5SrRNA:CR33451@, @5SrRNA:CR33452@
CEL|cytosolic large ribosomal subunit (sensu Eukaryota) ; GO:0005842
WT|The locus encoding the genes for 5S RNA.  Ordinarily, the haploid
|complement carries approximately 165 copies of 5S genes.
DBA|NA:AQ025605
|BDGP:l(2)03068
|NA:J01122
|NA:J01854
|NA:M11034
|NA:M25016
|NA:M25181
|NA:X01082
|NA:X06937
|NA:X06938
|NA:X87880
PHP|Heterozygous deficiency for the region is normal in phenotype.
REF
{
REFM|FBrf0111489
|Spradling et al.
|1999
|0
REFM|FBrf0134799
|van Steensel et al.
|2001
|9
REFM|FBrf0084251
|Paques et al.
|1995
|0
REFM|FBrf0128662
|Takada et al.
|2000
|0
REFM|FBrf0054341
|Preiser and Levinger
|1991
|0
REFM|FBrf0086568
|Paques et al.
|1996
|0
REFM|FBrf0037913
|Tschudi et al.
|1982
|0
REFM|FBrf0048240
|Samson and Wegnez
|1988
|0
REFM|FBrf0058810
|Matunis et al.
|1993
|0
REFM|FBrf0027507
|Procunier and Tartof
|1975
|0
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|2
REFM|FBrf0041596
|Sharp et al.
|1984
|0
REFM|FBrf0122003
|Wegnez
|1995.6.6
|9
REFM|FBrf0098998
|Hansen et al.
|1997
|0
REFM|FBrf0035460
|Tschudi and Pirrotta
|1980
|0
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
|-1
REFM|FBrf0083714
|Meister and Braun
|1995.10
|9
REFM|FBrf0083745
|Arkhipova
|1995
|0
REFM|FBrf0152006
|Ishizuka et al.
|2002
|0
REFM|FBrf0051101
|Sandmeyer et al.
|1990
|2
REFM|FBrf0100595
|Liu and Restifo
|1998
|0
REFM|FBrf0029713
|Hershey et al.
|1977
|0
REFM|FBrf0161558
|Saunders
|2003
|0
REFM|FBrf0028698
|Benhamou and Jordan
|1976
|0
REFM|FBrf0035459
|Junakovic
|1980
|0
REFM|FBrf0127122
|Hori et al.
|2000
|0
REFM|FBrf0027234
|Rubin and Hogness
|1975
|0
REFM|FBrf0048648
|Sharp and Garcia
|1988
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
REFM|FBrf0089555
|Deshpande et al.
|1996
|0
REFM|FBrf0054354
|Preiser and Levinger
|1991
|0
REFM|FBrf0036942
|Thompson et al.
|1981
|0
REFM|FBrf0104768
|McKim and Hayashi-Hagihara
|1998
|0
REFM|FBrf0161514
|Dominski
|2003
|0
REFM|FBrf0167625
|Sage and Csink
|2003
|0
REFM|FBrf0131150
|Berk
|2000
|2
REFM|FBrf0129876
|Jones and Kadonaga
|2000
|0
REFM|FBrf0029697
|Artavanis-Tsakonas et al.
|1977
|0
REFM|FBrf0031166
|Procunier and Dunn
|1978
|0
}

REFDSR
{
RDID|FBrf0021974
|Wimber and Steffensen
|1970
CLOC|56E--F (determined by in situ hybridization)
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0035460
|Tschudi and Pirrotta
|1980
CLOC|56F (determined by in situ hybridization)
}

REFDSR
{
RDID|FBrf0037913
|Tschudi et al.
|1982
WT|The Oregon R Yale stock contains various arrangements of the 5SrRNA
|cluster, one variant is due to the insertion of a @roo@ element. Others,
|that lack the @roo@ insertion, have a variety of deletions removing 0--60%
|of the genes at the insertion site. The Oregon R Heidelberg stock
|studied has no @roo@ element so has no heterogeneity in cluster arrangement.
|D.melanogaster shows a large redundancy of 5SrRNA genes as there is
|no visible phenotype when homozygous or heterozygous against a total
|deletion of the cluster.
}

REFDSR
{
RDID|FBrf0038450
|DeLotto et al.
|1982
CLOC|56F (determined by in situ hybridization)
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0041596
|Sharp et al.
|1984
MD|In vitro transcription of isolated repeat units of @5SrRNA@ in a KcO
|cell extract reveals three @5SrRNA@ variants.  The "5SI" variant is
|transcribed with a relatively high efficiency in vitro.  The "5SII"
|variant is identical to "5SI", except for a two-nucleotide deletion
|at positions 28 and 29, and is transcribed in vitro at an efficiency
|of approximately 40% compared to the "5SI" variant.  The "5SIII"
|variant has the same sequence as "5SI" except for a single G to A
|transition at position 86, but is not transcribed in vitro.
}

REFDSR
{
RDID|FBrf0048240
|Samson and Wegnez
|1988
CLOC|56F (determined by in situ hybridization)
}

REFDSR
{
RDID|FBrf0051101
|Sandmeyer et al.
|1990
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0054341
|Preiser and Levinger
|1991
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0054354
|Preiser and Levinger
|1991
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0056422
|Levinger et al.
|1992
OTH|The effects of stem I and loop A transversions, transitions, selected
|additions and deletions on @5SrRNA@ processing are studied.
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0058769
|Preiser et al.
|1993
PHP|@La@ binds to the 3' terminus of the @5SrRNA@ primary transcript, inhibiting
|a 3' exonuclease activity.
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0058810
|Matunis et al.
|1993
SYN|5S
}

REFDSR
{
RDID|FBrf0063869
|Shimada
|1992
PHP|The distribution of split 5.8S rRNA was studied in Diptera and Siphonaptera
|to learn the origin of 5.8S rRNA. Four species of mosquitoes and a
|flea have a single 5.8S rRNA. A crane fly, a midge, a robber fly,
|a house fly and D.melanogaster have split 5.8S rRNA.
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0063901
|Szabo
|1974
CLOC|56F1--7 (determined by in situ hybridization)
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
CLOC|56F1--2
LOI|5SrRNA<up>03068</up>
BMDD|Df(2R)017
SYN|l(2)03068
}

REFDSR
{
RDID|FBrf0074691
|Vasisht et al.
|1994
PHP|Point mutations introduced in vitro into pre-@5SrRNA@ have been used
|to determine which regions of the pre-RNA are required for processing.
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0083714
|Meister and Braun
|1995.10
SYN|l(2)03068
}

REFDSR
{
RDID|FBrf0083745
|Arkhipova
|1995
SYN|Dm5S
}

REFDSR
{
RDID|FBrf0086568
|Paques et al.
|1996
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0089555
|Deshpande et al.
|1996
SYN|5S
}

REFDSR
{
RDID|FBrf0098238
|Fox
|1997
OTH|@5SrRNA@ was discovered while studying heat-induced alterations of the
|ribosome.
SYN|RNA X
}

REFDSR
{
RDID|FBrf0098998
|Hansen et al.
|1997
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0100595
|Liu and Restifo
|1998
SYN|PZ03068
}

REFDSR
{
RDID|FBrf0104768
|McKim and Hayashi-Hagihara
|1998
SYN|l(2)03068
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
CLOC|56F1--2 (determined by in situ hybridization)
LOI|5SrRNA<up>03068</up>
AM|Source for merge of: 5SRNA l(2)03068
CEL|cytosolic large ribosomal subunit (sensu Eukaryota) ; GO:0005842 | non-traceable author statement
GPD|ribosomal-RNA-5S
BMDD|Df(2R)017
}

REFDSR
{
RDID|FBrf0122003
|Wegnez
|1995.6.6
SYN|5S rRNA
}

REFDSR
{
RDID|FBrf0127122
|Hori et al.
|2000
SYN|2S rRNA
}

REFDSR
{
RDID|FBrf0128662
|Takada et al.
|2000
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0129876
|Jones and Kadonaga
|2000
SYN|5S
}

REFDSR
{
RDID|FBrf0131150
|Berk
|2000
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0134799
|van Steensel et al.
|2001
SYN|5S
}

REFDSR
{
RDID|FBrf0160455
|Cohen et al.
|2003
MD|Extrachromosomal circular DNA (eccDNA) is present throughout the fly's
|life cycle. The eccDNA population contains circular multimers of tandemly
|repeated genes, including @5SrRNA@.
SYN|5S rDNA
}

REFDSR
{
RDID|FBrf0161514
|Dominski
|2003
SYN|5SRNA
}

REFDSR
{
RDID|FBrf0161558
|Saunders
|2003
SYN|5S-rDNA
}

REFDSR
{
RDID|FBrf0167625
|Sage and Csink
|2003
SYN|5SrDNA
}

ALESR
{
ASYM|5SrRNA<up>03068</up>
SYN|l(2)03068<up>03068</up>
|PZ03068
|l(2)03068
|5SRNA<up>03068</up>
ID|FBal0008014
DIS|A. Spradling.
TRN|FBti0004438 == P{PZ}5SrRNA<up>03068</up>
|BDGP:l(2)03068
MU|P-element activity
PHC|semi-lethal
REF|FBrf0067338
|FBrf0166453
|FBrf0100595
|FBrf0083714
|FBrf0111489
REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
OTH|Complements: @18w<up>00053</up>@.
|Complements: @mus209<up>02448</up>@.
|Complements: @mus209<up>02697</up>@.
|Complements: @mus209<up>06652</up>@.
|Complements: @l(2)k08002<up>k08002</up>@.
|Complements: @RpL30<up>k09918</up>@.
|Complements: @hts<up>k14523</up>@.
|Complements: @l(2)k16210<up>k16210</up>@.
|Complements: @mus209<up>s1534</up>@.
TRN|FBti0004438 == P{PZ}5SrRNA<up>03068</up>
|BDGP:l(2)03068
SYN|l(2)03068<up>03068</up>
}

REFDSR
{
RDID|FBrf0083714
|Meister and Braun
|1995.10
SYN|l(2)03068<up>03068</up>
}

REFDSR
{
RDID|FBrf0100595
|Liu and Restifo
|1998
OTH|@H217<up>H217</up>@ complements @5SrRNA<up>03068</up>@.
TRN|FBti0004438 == P{PZ}5SrRNA<up>03068</up>
|BDGP:l(2)03068
PHC|semi-lethal | recessive
SYN|PZ03068
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
TRN|FBti0004438 == P{PZ}5SrRNA<up>03068</up>
|BDGP:l(2)03068
PHC|lethal | recessive
SYN|l(2)03068
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
}

SK|FBst0011265
|cn[1] P{ry[+t7.2]=PZ}5SrRNA[03068]/CyO; ry[506]
}

ALESR
{
ASYM|5SrRNA<up>L62</up>
SYN|5SRNA<up>L62</up>
ID|FBal0027937
DIS|L. Sandler.
OTH|@T(Y;2)L62@ breakpoint splits the 5SrRNA gene cluster.
MU|X ray
ABA|FBab0008617 == T(Y;2)L62
}

ALESR
{
ASYM|5SrRNA<up>216</up>
SYN|5SRNA<up>216</up>
ID|FBal0047967
PHI|Mode of assay: In transgenic Drosophila
REF|FBrf0086568
REFDSR
{
RDID|FBrf0086568
|Paques et al.
|1996
MD|Construct: Truncated @5SrRNA@ unit, 216bp.
MU|in vitro construct | other
CNS|FBtp0005757 == P{CAR1}
|FBtp0011305 == P{CAR2}
|FBtp0011306 == P{CAR3}
|FBtp0011307 == P{E22}
PHI|Mode of assay: In transgenic Drosophila
SYN|unnamed
}

}

ALESR
{
ASYM|5SrRNA<up>376</up>
SYN|5SRNA<up>376</up>
ID|FBal0047968
PHI|Mode of assay: In transgenic Drosophila
REF|FBrf0086568
REFDSR
{
RDID|FBrf0086568
|Paques et al.
|1996
MD|Construct: Complete @5SrRNA@ unit, 376bp.
MU|in vitro construct | other
CNS|FBtp0005757 == P{CAR1}
|FBtp0011305 == P{CAR2}
|FBtp0011306 == P{CAR3}
|FBtp0011307 == P{E22}
PHI|Mode of assay: In transgenic Drosophila
SYN|unnamed
}

}

ALESR
{
ASYM|5SrRNA<up>+</up>
ID|FBal0141974
CLA|wild-type generic
}

SK|FBst0011265
|cn[1] P{ry[+t7.2]=PZ}5SrRNA[03068]/CyO; ry[506]
SKC|1
}
# EOR
GENR
{
RETE|ID 1 FBgn0069065	CLA 1 multicopy cytosolic ribosomal RNA pseudogene	NAM 1 5S ribosomal RNA pseudogene	GSYM 1 5SrRNA-&PSgr;	DT 1 25 Dec 04	RESZ 264	
GSYM|5SrRNA-&PSgr;
DT|25 Dec 04
ID|FBgn0069065
CLA|multicopy_cytosolic_ribosomal_RNA_pseudogene
NAM|5S ribosomal RNA pseudogene
AM|component genes: @5SrRNA-&PSgr;:CR33356@, @5SrRNA-&PSgr;:CR33363@, @5SrRNA-&PSgr;:CR33416@, @5SrRNA-&PSgr;:CR33371@
}
# EOR
GENR
{
RETE|ID 1 FBgn0053356	CLA 1 cytosolic ribosomal RNA pseudogene	GSYM 1 5SrRNA-&PSgr;:CR33356	DT 1 25 Dec 04	RESZ 661	DBA 1	CLOC 1 56E2	REF 1	
GSYM|5SrRNA-&PSgr;:CR33356
DT|25 Dec 04
ID|FBgn0053356
CLA|cytosolic_ribosomal_RNA_pseudogene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33356
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA-&PSgr;@
DBA|NA:AE003794
ASQ|FBan0033356
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33356) in release 3.2 of the genome annotation.
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053363	CLA 1 cytosolic ribosomal RNA pseudogene	GSYM 1 5SrRNA-&PSgr;:CR33363	DT 1 25 Dec 04	RESZ 661	DBA 1	CLOC 1 56E2	REF 1	
GSYM|5SrRNA-&PSgr;:CR33363
DT|25 Dec 04
ID|FBgn0053363
CLA|cytosolic_ribosomal_RNA_pseudogene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33363
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA-&PSgr;@
DBA|NA:AE003794
ASQ|FBan0033363
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33363) in release 3.2 of the genome annotation.
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053371	CLA 1 cytosolic ribosomal RNA pseudogene	GSYM 1 5SrRNA-&PSgr;:CR33371	DT 1 25 Dec 04	RESZ 661	DBA 1	CLOC 1 56E2	REF 1	
GSYM|5SrRNA-&PSgr;:CR33371
DT|25 Dec 04
ID|FBgn0053371
CLA|cytosolic_ribosomal_RNA_pseudogene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33371
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA-&PSgr;@
DBA|NA:AE003794
ASQ|FBan0033371
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33371) in release 3.2 of the genome annotation.
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053416	CLA 1 cytosolic ribosomal RNA pseudogene	GSYM 1 5SrRNA-&PSgr;:CR33416	DT 1 25 Dec 04	RESZ 661	DBA 1	CLOC 1 56E2	REF 1	
GSYM|5SrRNA-&PSgr;:CR33416
DT|25 Dec 04
ID|FBgn0053416
CLA|cytosolic_ribosomal_RNA_pseudogene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33416
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA-&PSgr;@
DBA|NA:AE003794
ASQ|FBan0033416
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33416) in release 3.2 of the genome annotation.
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053353	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33353	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33353
DT|25 Dec 04
ID|FBgn0053353
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33353
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033353
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33353) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33353<up>+</up>
ID|FBal0154327
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053354	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33354	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33354
DT|25 Dec 04
ID|FBgn0053354
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33354
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033354
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33354) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33354<up>+</up>
ID|FBal0154326
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053355	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33355	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33355
DT|25 Dec 04
ID|FBgn0053355
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33355
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033355
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33355) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33355<up>+</up>
ID|FBal0154325
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053357	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33357	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33357
DT|25 Dec 04
ID|FBgn0053357
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33357
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033357
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33357) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33357<up>+</up>
ID|FBal0154324
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053358	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33358	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33358
DT|25 Dec 04
ID|FBgn0053358
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33358
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033358
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33358) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33358<up>+</up>
ID|FBal0154323
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053359	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33359	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33359
DT|25 Dec 04
ID|FBgn0053359
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33359
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033359
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33359) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33359<up>+</up>
ID|FBal0154322
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053360	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33360	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33360
DT|25 Dec 04
ID|FBgn0053360
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33360
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033360
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33360) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33360<up>+</up>
ID|FBal0154321
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053361	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33361	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33361
DT|25 Dec 04
ID|FBgn0053361
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33361
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033361
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33361) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33361<up>+</up>
ID|FBal0154320
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053362	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33362	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33362
DT|25 Dec 04
ID|FBgn0053362
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33362
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033362
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33362) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33362<up>+</up>
ID|FBal0154319
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053364	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33364	DT 1 25 Dec 04	RESZ 914	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33364
DT|25 Dec 04
ID|FBgn0053364
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33364
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
DBA|NA:AE003794
ASQ|FBan0033364
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
OTH|New annotation (CR33364) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33364<up>+</up>
ID|FBal0154318
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053365	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33365	DT 1 25 Dec 04	RESZ 914	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33365
DT|25 Dec 04
ID|FBgn0053365
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33365
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
DBA|NA:AE003794
ASQ|FBan0033365
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
OTH|New annotation (CR33365) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33365<up>+</up>
ID|FBal0154317
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053366	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33366	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33366
DT|25 Dec 04
ID|FBgn0053366
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33366
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|Variant; single nucleotide change at position 82.
DBA|NA:AE003794
ASQ|FBan0033366
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant; single nucleotide change at position 82.
OTH|New annotation (CR33366) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33366<up>+</up>
ID|FBal0154316
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053367	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33367	DT 1 25 Dec 04	RESZ 832	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33367
DT|25 Dec 04
ID|FBgn0053367
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33367
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|Variant with two nucleotide changes; may be inactive.
DBA|NA:AE003794
ASQ|FBan0033367
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant with two nucleotide changes; may be inactive.
OTH|New annotation (CR33367) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33367<up>+</up>
ID|FBal0154315
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053368	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33368	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33368
DT|25 Dec 04
ID|FBgn0053368
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33368
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033368
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33368) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33368<up>+</up>
ID|FBal0154314
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053369	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33369	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33369
DT|25 Dec 04
ID|FBgn0053369
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33369
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033369
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33369) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33369<up>+</up>
ID|FBal0154313
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053370	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33370	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33370
DT|25 Dec 04
ID|FBgn0053370
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33370
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033370
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33370) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33370<up>+</up>
ID|FBal0154312
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053372	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33372	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33372
DT|25 Dec 04
ID|FBgn0053372
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33372
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033372
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33372) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33372<up>+</up>
ID|FBal0154311
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053373	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33373	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33373
DT|25 Dec 04
ID|FBgn0053373
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33373
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033373
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33373) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33373<up>+</up>
ID|FBal0154310
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053374	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33374	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33374
DT|25 Dec 04
ID|FBgn0053374
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33374
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033374
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33374) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33374<up>+</up>
ID|FBal0154309
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053375	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33375	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33375
DT|25 Dec 04
ID|FBgn0053375
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33375
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033375
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33375) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33375<up>+</up>
ID|FBal0154308
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053376	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33376	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33376
DT|25 Dec 04
ID|FBgn0053376
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33376
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033376
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33376) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33376<up>+</up>
ID|FBal0154307
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053377	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33377	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33377
DT|25 Dec 04
ID|FBgn0053377
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33377
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033377
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33377) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33377<up>+</up>
ID|FBal0154306
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053378	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33378	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33378
DT|25 Dec 04
ID|FBgn0053378
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33378
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033378
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33378) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33378<up>+</up>
ID|FBal0154305
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053379	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33379	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33379
DT|25 Dec 04
ID|FBgn0053379
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33379
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033379
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33379) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33379<up>+</up>
ID|FBal0154304
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053380	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33380	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33380
DT|25 Dec 04
ID|FBgn0053380
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33380
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033380
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33380) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33380<up>+</up>
ID|FBal0154303
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053381	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33381	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33381
DT|25 Dec 04
ID|FBgn0053381
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33381
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033381
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33381) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33381<up>+</up>
ID|FBal0154302
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053382	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33382	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33382
DT|25 Dec 04
ID|FBgn0053382
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33382
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033382
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33382) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33382<up>+</up>
ID|FBal0154301
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053383	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33383	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33383
DT|25 Dec 04
ID|FBgn0053383
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33383
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033383
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33383) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33383<up>+</up>
ID|FBal0154300
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053384	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33384	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33384
DT|25 Dec 04
ID|FBgn0053384
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33384
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033384
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33384) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33384<up>+</up>
ID|FBal0154299
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053385	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33385	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33385
DT|25 Dec 04
ID|FBgn0053385
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33385
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033385
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33385) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33385<up>+</up>
ID|FBal0154298
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053386	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33386	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33386
DT|25 Dec 04
ID|FBgn0053386
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33386
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033386
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33386) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33386<up>+</up>
ID|FBal0154297
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053387	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33387	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33387
DT|25 Dec 04
ID|FBgn0053387
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33387
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033387
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33387) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33387<up>+</up>
ID|FBal0154296
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053388	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33388	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33388
DT|25 Dec 04
ID|FBgn0053388
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33388
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033388
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33388) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33388<up>+</up>
ID|FBal0154295
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053389	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33389	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33389
DT|25 Dec 04
ID|FBgn0053389
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33389
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033389
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33389) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33389<up>+</up>
ID|FBal0154294
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053390	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33390	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33390
DT|25 Dec 04
ID|FBgn0053390
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33390
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033390
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33390) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33390<up>+</up>
ID|FBal0154293
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053391	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33391	DT 1 25 Dec 04	RESZ 812	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33391
DT|25 Dec 04
ID|FBgn0053391
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33391
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
MD|Variant: single base change at position 17.
DBA|NA:AE003794
ASQ|FBan0033391
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single base change at position 17.
OTH|New annotation (CR33391) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33391<up>+</up>
ID|FBal0154292
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053392	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33392	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33392
DT|25 Dec 04
ID|FBgn0053392
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33392
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033392
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33392) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33392<up>+</up>
ID|FBal0154291
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053393	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33393	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33393
DT|25 Dec 04
ID|FBgn0053393
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33393
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033393
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33393) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33393<up>+</up>
ID|FBal0154290
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053394	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33394	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33394
DT|25 Dec 04
ID|FBgn0053394
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33394
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033394
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33394) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33394<up>+</up>
ID|FBal0154289
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053395	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33395	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33395
DT|25 Dec 04
ID|FBgn0053395
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33395
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033395
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33395) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33395<up>+</up>
ID|FBal0154288
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053396	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33396	DT 1 25 Dec 04	RESZ 721	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33396
DT|25 Dec 04
ID|FBgn0053396
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33396
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1--2
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033396
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33396) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33396<up>+</up>
ID|FBal0154287
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053397	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33397	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33397
DT|25 Dec 04
ID|FBgn0053397
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33397
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033397
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33397) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33397<up>+</up>
ID|FBal0154286
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053398	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33398	DT 1 25 Dec 04	RESZ 914	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33398
DT|25 Dec 04
ID|FBgn0053398
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33398
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
DBA|NA:AE003794
ASQ|FBan0033398
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
OTH|New annotation (CR33398) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33398<up>+</up>
ID|FBal0154285
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053399	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33399	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33399
DT|25 Dec 04
ID|FBgn0053399
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33399
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033399
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33399) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33399<up>+</up>
ID|FBal0154284
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053400	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33400	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33400
DT|25 Dec 04
ID|FBgn0053400
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33400
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide change at position 54.
DBA|NA:AE003794
ASQ|FBan0033400
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide change at position 54.
OTH|New annotation (CR33400) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33400<up>+</up>
ID|FBal0154283
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053401	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33401	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33401
DT|25 Dec 04
ID|FBgn0053401
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33401
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide change at position 54.
DBA|NA:AE003794
ASQ|FBan0033401
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide change at position 54.
OTH|New annotation (CR33401) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33401<up>+</up>
ID|FBal0154282
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053402	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33402	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33402
DT|25 Dec 04
ID|FBgn0053402
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33402
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide change at position 54.
DBA|NA:AE003794
ASQ|FBan0033402
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide change at position 54.
OTH|New annotation (CR33402) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33402<up>+</up>
ID|FBal0154281
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053403	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33403	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33403
DT|25 Dec 04
ID|FBgn0053403
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33403
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033403
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33403) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33403<up>+</up>
ID|FBal0154280
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053404	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33404	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33404
DT|25 Dec 04
ID|FBgn0053404
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33404
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033404
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33404) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33404<up>+</up>
ID|FBal0154279
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053405	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33405	DT 1 25 Dec 04	RESZ 952	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33405
DT|25 Dec 04
ID|FBgn0053405
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33405
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide substitution at position 54, plus
|additional single base deletion; may be inactive.
DBA|NA:AE003794
ASQ|FBan0033405
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide substitution at position 54, plus
|additional single base deletion; may be inactive.
OTH|New annotation (CR33405) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33405<up>+</up>
ID|FBal0154278
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053406	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33406	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33406
DT|25 Dec 04
ID|FBgn0053406
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33406
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033406
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33406) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33406<up>+</up>
ID|FBal0154277
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053407	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33407	DT 1 25 Dec 04	RESZ 846	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33407
DT|25 Dec 04
ID|FBgn0053407
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33407
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Similar to 5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033407
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Similar to 5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33407) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33407<up>+</up>
ID|FBal0154276
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053408	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33408	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33408
DT|25 Dec 04
ID|FBgn0053408
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33408
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033408
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33408) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33408<up>+</up>
ID|FBal0154275
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053409	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33409	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33409
DT|25 Dec 04
ID|FBgn0053409
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33409
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033409
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33409) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33409<up>+</up>
ID|FBal0154274
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053410	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33410	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33410
DT|25 Dec 04
ID|FBgn0053410
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33410
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033410
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33410) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33410<up>+</up>
ID|FBal0154273
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053411	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33411	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33411
DT|25 Dec 04
ID|FBgn0053411
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33411
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033411
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33411) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33411<up>+</up>
ID|FBal0154272
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053412	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33412	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33412
DT|25 Dec 04
ID|FBgn0053412
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33412
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033412
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33412) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33412<up>+</up>
ID|FBal0154271
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053413	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33413	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33413
DT|25 Dec 04
ID|FBgn0053413
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33413
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033413
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33413) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33413<up>+</up>
ID|FBal0154270
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053414	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33414	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33414
DT|25 Dec 04
ID|FBgn0053414
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33414
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033414
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33414) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33414<up>+</up>
ID|FBal0154269
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053415	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33415	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33415
DT|25 Dec 04
ID|FBgn0053415
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33415
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033415
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33415) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33415<up>+</up>
ID|FBal0154268
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053417	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33417	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33417
DT|25 Dec 04
ID|FBgn0053417
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33417
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033417
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33417) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33417<up>+</up>
ID|FBal0154267
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053418	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33418	DT 1 25 Dec 04	RESZ 914	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33418
DT|25 Dec 04
ID|FBgn0053418
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33418
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
DBA|NA:AE003794
ASQ|FBan0033418
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
OTH|New annotation (CR33418) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33418<up>+</up>
ID|FBal0154266
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053419	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33419	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33419
DT|25 Dec 04
ID|FBgn0053419
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33419
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide change at position 54.
DBA|NA:AE003794
ASQ|FBan0033419
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide change at position 54.
OTH|New annotation (CR33419) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33419<up>+</up>
ID|FBal0154265
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053420	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33420	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33420
DT|25 Dec 04
ID|FBgn0053420
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33420
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide change at position 54.
DBA|NA:AE003794
ASQ|FBan0033420
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide change at position 54.
OTH|New annotation (CR33420) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33420<up>+</up>
ID|FBal0154264
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053421	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33421	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33421
DT|25 Dec 04
ID|FBgn0053421
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33421
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033421
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33421) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33421<up>+</up>
ID|FBal0154263
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053422	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33422	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33422
DT|25 Dec 04
ID|FBgn0053422
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33422
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033422
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33422) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33422<up>+</up>
ID|FBal0154262
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053423	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33423	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33423
DT|25 Dec 04
ID|FBgn0053423
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33423
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide change at position 82.
DBA|NA:AE003794
ASQ|FBan0033423
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide change at position 82.
OTH|New annotation (CR33423) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33423<up>+</up>
ID|FBal0154261
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053424	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33424	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33424
DT|25 Dec 04
ID|FBgn0053424
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33424
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033424
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33424) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33424<up>+</up>
ID|FBal0154260
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053425	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33425	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33425
DT|25 Dec 04
ID|FBgn0053425
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33425
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033425
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33425) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33425<up>+</up>
ID|FBal0154259
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053426	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33426	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33426
DT|25 Dec 04
ID|FBgn0053426
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33426
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033426
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33426) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33426<up>+</up>
ID|FBal0154258
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053427	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33427	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33427
DT|25 Dec 04
ID|FBgn0053427
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33427
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033427
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33427) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33427<up>+</up>
ID|FBal0154257
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053428	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33428	DT 1 25 Dec 04	RESZ 914	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33428
DT|25 Dec 04
ID|FBgn0053428
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33428
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
DBA|NA:AE003794
ASQ|FBan0033428
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
OTH|New annotation (CR33428) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33428<up>+</up>
ID|FBal0154256
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053429	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33429	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33429
DT|25 Dec 04
ID|FBgn0053429
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33429
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033429
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33429) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33429<up>+</up>
ID|FBal0154255
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053430	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33430	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33430
DT|25 Dec 04
ID|FBgn0053430
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33430
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033430
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33430) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33430<up>+</up>
ID|FBal0154254
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053431	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33431	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33431
DT|25 Dec 04
ID|FBgn0053431
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33431
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033431
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33431) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33431<up>+</up>
ID|FBal0154253
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053432	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33432	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33432
DT|25 Dec 04
ID|FBgn0053432
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33432
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033432
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33432) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33432<up>+</up>
ID|FBal0154252
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053433	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33433	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33433
DT|25 Dec 04
ID|FBgn0053433
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33433
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033433
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33433) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33433<up>+</up>
ID|FBal0154251
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053434	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33434	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33434
DT|25 Dec 04
ID|FBgn0053434
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33434
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033434
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33434) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33434<up>+</up>
ID|FBal0154250
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053435	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33435	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33435
DT|25 Dec 04
ID|FBgn0053435
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33435
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033435
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33435) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33435<up>+</up>
ID|FBal0154249
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053436	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33436	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33436
DT|25 Dec 04
ID|FBgn0053436
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33436
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033436
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33436) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33436<up>+</up>
ID|FBal0154248
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053437	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33437	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33437
DT|25 Dec 04
ID|FBgn0053437
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33437
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033437
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33437) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33437<up>+</up>
ID|FBal0154247
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053438	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33438	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33438
DT|25 Dec 04
ID|FBgn0053438
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33438
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033438
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33438) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33438<up>+</up>
ID|FBal0154246
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053439	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33439	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33439
DT|25 Dec 04
ID|FBgn0053439
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33439
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide change at position 54.
DBA|NA:AE003794
ASQ|FBan0033439
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide change at position 54.
OTH|New annotation (CR33439) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33439<up>+</up>
ID|FBal0154245
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053440	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33440	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33440
DT|25 Dec 04
ID|FBgn0053440
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33440
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033440
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33440) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33440<up>+</up>
ID|FBal0154244
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053441	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33441	DT 1 25 Dec 04	RESZ 938	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33441
DT|25 Dec 04
ID|FBgn0053441
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33441
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide change at same position as 5SIII variant
|(see FBrf0041596), may be inactive.
DBA|NA:AE003794
ASQ|FBan0033441
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide change at same position as 5SIII variant
|(see FBrf0041596), may be inactive.
OTH|New annotation (CR33441) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33441<up>+</up>
ID|FBal0154243
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053442	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33442	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33442
DT|25 Dec 04
ID|FBgn0053442
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33442
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide change at position 54.
DBA|NA:AE003794
ASQ|FBan0033442
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide change at position 54.
OTH|New annotation (CR33442) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33442<up>+</up>
ID|FBal0154242
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053443	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33443	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33443
DT|25 Dec 04
ID|FBgn0053443
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33443
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|Variant: single nucleotide change at position 82.
DBA|NA:AE003794
ASQ|FBan0033443
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|Variant: single nucleotide change at position 82.
OTH|New annotation (CR33443) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33443<up>+</up>
ID|FBal0154241
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053444	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33444	DT 1 25 Dec 04	RESZ 914	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33444
DT|25 Dec 04
ID|FBgn0053444
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33444
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
DBA|NA:AE003794
ASQ|FBan0033444
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
OTH|New annotation (CR33444) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33444<up>+</up>
ID|FBal0154240
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053445	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33445	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33445
DT|25 Dec 04
ID|FBgn0053445
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33445
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033445
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33445) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33445<up>+</up>
ID|FBal0154239
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053446	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33446	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33446
DT|25 Dec 04
ID|FBgn0053446
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33446
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033446
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33446) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33446<up>+</up>
ID|FBal0154238
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053447	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33447	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33447
DT|25 Dec 04
ID|FBgn0053447
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33447
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033447
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33447) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33447<up>+</up>
ID|FBal0154237
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053448	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33448	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33448
DT|25 Dec 04
ID|FBgn0053448
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33448
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033448
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33448) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33448<up>+</up>
ID|FBal0154236
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053449	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33449	DT 1 25 Dec 04	RESZ 914	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33449
DT|25 Dec 04
ID|FBgn0053449
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33449
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
DBA|NA:AE003794
ASQ|FBan0033449
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596), plus additional single nucleotide
|change; may be inactive.
OTH|New annotation (CR33449) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33449<up>+</up>
ID|FBal0154235
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053450	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33450	DT 1 25 Dec 04	RESZ 824	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33450
DT|25 Dec 04
ID|FBgn0053450
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33450
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (see FBrf0041596); may be inactive.
DBA|NA:AE003794
ASQ|FBan0033450
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (see FBrf0041596); may be inactive.
OTH|New annotation (CR33450) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33450<up>+</up>
ID|FBal0154234
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053451	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33451	DT 1 25 Dec 04	RESZ 718	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33451
DT|25 Dec 04
ID|FBgn0053451
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33451
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
DBA|NA:AE003794
ASQ|FBan0033451
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
OTH|New annotation (CR33451) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33451<up>+</up>
ID|FBal0154233
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0053452	CLA 1 cytosolic ribosomal RNA gene	GSYM 1 5SrRNA:CR33452	DT 1 25 Dec 04	RESZ 906	DBA 1	CLOC 1 56E2	ALESR 1	REF 1	
GSYM|5SrRNA:CR33452
DT|25 Dec 04
ID|FBgn0053452
CLA|cytosolic_ribosomal_RNA_gene
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
SYN|CR33452
CLOC|56E2
|Limits computationally determined from genome sequence between @P{PZ}sm<up>05338</up>@/@P{PZ}emm<up>1</up>@ and @P{lacW}l(2)k08002<up>k08002</up>@
|56F1
AM|member gene of: @5SrRNA@
MD|5SIII variant (FBrf0041596), plus additional single nucleotide
|change; may be inactive.
DBA|NA:AE003794
ASQ|FBan0033452
REF
{
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
|9
}

REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
MD|5SIII variant (FBrf0041596), plus additional single nucleotide
|change; may be inactive.
OTH|New annotation (CR33452) in release 3.2 of the genome annotation.
}

ALESR
{
ASYM|5SrRNA:CR33452<up>+</up>
ID|FBal0154232
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0022711	CLA 1 Gene	GSYM 1 61bis	DT 1 25 Dec 04	RESZ 698	CLOC 1 68C	ALESR 1	REF 2	
GSYM|61bis
DT|25 Dec 04
ID|FBgn0022711
UAB|Deficiency: Df(3L)vin66 (inferred from cytology)
|Duplication: Dp(3;3)M67C<up>+</up>4 (inferred from cytology)
CLOC|68C
|Left limit from in situ hybridization (FBrf0098649)
|Right limit from in situ hybridization (FBrf0098649)
CYC|Experimentally determined: 68C
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0098649
|Aragnol et al.
|1997
|1
}

REFDSR
{
RDID|FBrf0098649
|Aragnol et al.
|1997
CLOC|68C (determined by in situ hybridization)
}

ALESR
{
ASYM|61bis<up>+</up>
ID|FBal0081518
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0012033	CLA 1 Gene	GSYM 1 65F	DT 1 25 Dec 04	RESZ 798	ALESR 1	REF 6	
GSYM|65F
DT|25 Dec 04
ID|FBgn0012033
DIS|H. Ruohola-Baker and T.A. Jongens.
MD|Encodes an oocyte-specific mRNA.
REF
{
REFM|FBrf0076114
|Mahajan-Miklos and Cooley
|1994
|0
REFM|FBrf0065590
|Theurkauf et al.
|1993
|1
REFM|FBrf0065589
|Theurkauf et al.
|1993
|0
REFM|FBrf0075028
|Knowles and Cooley
|1994
|2
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0076115
|Theurkauf
|1994
|0
}

REFDSR
{
RDID|FBrf0065589
|Theurkauf et al.
|1993
MD|Encodes an oocyte-specific mRNA.
}

ALESR
{
ASYM|65F<up>+</up>
ID|FBal0066322
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0008639	CLA 1 Gene	NAM 1 66Dem	GSYM 1 66Dem	DT 1 25 Dec 04	RESZ 775	WT 1 An incompletely characterized homeodomain sequence	CLOC 1 66B	ALESR 1	REF 2	
GSYM|66Dem
DT|25 Dec 04
ID|FBgn0008639
UAB|Deficiency: Df(3L)Mg27 (inferred from cytology)
|Duplication: Dp(3;3)M67C<up>+</up>2 (inferred from cytology)
NAM|66Dem
GLOC|3-[25]
CLOC|66B
|Left limit from in situ hybridization (FBrf0065373)
|Right limit from in situ hybridization (FBrf0065373)
CYC|Experimentally determined: 66B
WT|An incompletely characterized homeodomain sequence.
REF
{
REFM|FBrf0065373
|Dessain and McGinnis
|1993
|2
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0065373
|Dessain and McGinnis
|1993
CLOC|66B (determined by in situ hybridization)
}

ALESR
{
ASYM|66Dem<up>+</up>
ID|FBal0071521
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0044335	CLA 1 Gene	GSYM 1 674	DT 1 25 Dec 04	RESZ 340	ALESR 1	REF 1	
GSYM|674
DT|25 Dec 04
ID|FBgn0044335
REF
{
REFM|FBrf0133992
|Myat and Andrew
|2001
|1
}

REFDSR
{
RDID|FBrf0133992
|Myat and Andrew
|2001
PHP|In mutants the salivary gland is branched rather than a linear tube.
}

ALESR
{
ASYM|674<up>+</up>
ID|FBal0122858
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0044334	CLA 1 Gene	GSYM 1 682	DT 1 25 Dec 04	RESZ 460	ALESR 1	
GSYM|682
DT|25 Dec 04
ID|FBgn0044334
SYN|Line 682
REFDSR
{
RDID|FBrf0134185
|Guo and Zinsmaier
|2001
PHP|Mutants show normal EJP amplitudes at low stimulation frequency,
|while at a high stimulation frequency EJPs completely fail within 20
|seconds. Simultaneously, the frequency of spontaneously occurring
|mEJPs increases dramatically.
SYN|Line 682
}

ALESR
{
ASYM|682<up>+</up>
ID|FBal0122857
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0065040	CLA 1 Gene	GSYM 1 6BP	DT 1 25 Dec 04	RESZ 391	ALESR 1	
GSYM|6BP
DT|25 Dec 04
ID|FBgn0065040
SYN|D6BP
|Drosophila INT6 binding protein
REFDSR
{
RDID|FBrf0145005
|Traicoff and Callahan
|2000
OTH|Identification: as a protein that specifically binds @Int6@ protein
|in a yeast two hybrid assay.
SYN|D6BP: Drosophila INT6 binding protein
}

ALESR
{
ASYM|6BP<up>+</up>
ID|FBal0143090
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067633	CLA 1 Gene	GSYM 1 70	DT 1 25 Dec 04	RESZ 2550	CLOC 1 92A1--3	ALESR 2	REF 1	
GSYM|70
DT|25 Dec 04
ID|FBgn0067633
UAB|Deficiency: Df(3R)Dl-BX12
CYC|Experimentally determined: 92A1--3
CLOC|92A1--3 (determined by in situ hybridization)
REF
{
REFM|FBrf0141372
|Ejima et al.
|2001
|0
}

REFDSR
{
RDID|FBrf0141372
|Ejima et al.
|2001
CLOC|92A1--3 (determined by in situ hybridization)
LOI|70<up>70</up>
BMD|Df(3R)Dl-BX12
}

ALESR
{
ASYM|70<up>70</up>
SYN|70
ID|FBal0151004
PHC|viable
|fertile
|courtship defective | female
PHI|@70<up>70</up>@ virgin females show elevated ovulation; 50% of the virgin
|females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @70<up>70</up>@ virgin females are mated
|to wild-type males is lower than that seen when wild-type virgin females
|are mated to wild-type males, but is higher than that seen when wild-type
|mated females are mated to wild-type males. @70<up>70</up>@ mutant virgin
|females show ovipositor extrusion towards courting wild-type males
|(this extrusion behavior is normally observed in mated wild-type females
|but not in virgin wild-type females).
REF|FBrf0141372
REFDSR
{
RDID|FBrf0141372
|Ejima et al.
|2001
OTH|Excision of the @P{GawB}70<up>70</up>@ insertion reverts the mutant phenotype.
TRN|FBti0037973 == P{GawB}70<up>70</up>
MU|P-element activity
PHC|viable
|fertile
|courtship defective | female
PHI|@70<up>70</up>@ virgin females show elevated ovulation; 50% of the virgin
|females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @70<up>70</up>@ virgin females are mated
|to wild-type males is lower than that seen when wild-type virgin females
|are mated to wild-type males, but is higher than that seen when wild-type
|mated females are mated to wild-type males. @70<up>70</up>@ mutant virgin
|females show ovipositor extrusion towards courting wild-type males
|(this extrusion behavior is normally observed in mated wild-type females
|but not in virgin wild-type females).
SYN|70
}

}

ALESR
{
ASYM|70<up>+</up>
ID|FBal0151310
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0062518	CLA 1 Gene	GSYM 1 752	DT 1 25 Dec 04	RESZ 924	FNC 1 transforming growth factor beta receptor signaling pathway	CEL 1 cellular_component unknown	WT 1 Involved in @dpp@ signaling in the developing wing	ALESR 1	REF 1	
GSYM|752
DT|25 Dec 04
ID|FBgn0062518
SYN|#752
FNC|transforming growth factor beta receptor signaling pathway ; GO:0007179
CEL|cellular_component unknown ; GO:0008372
WT|Involved in @dpp@ signaling in the developing wing.
ENZ|molecular_function unknown ; GO:0005554
|molecular_function unknown ; GO:0005554 | no biological data available
REF
{
REFM|FBrf0159398
|FlyBase Curators
|2002-
|9
}

REFDSR
{
RDID|FBrf0146151
|Jung et al.
|2002
FNC|transforming growth factor beta receptor signaling pathway ; GO:0007179 | inferred from mutant phenotype
WT|Involved in @dpp@ signaling in the developing wing.
SYN|#752
}

REFDSR
{
RDID|FBrf0159398
|FlyBase Curators
|2002-
ENZ|molecular_function unknown ; GO:0005554 | no biological data available
CEL|cellular_component unknown ; GO:0008372 | no biological data available
}

ALESR
{
ASYM|752<up>+</up>
ID|FBal0135552
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0041707	CLA 1 Gene	GSYM 1 7B2	DT 1 25 Dec 04	RESZ 3877	PDOM 1 INTERPRO:IPR007945 == Neuroendocrine 7B2 precursor	PTD 1	DBA 11	FNC 4 neuropeptide signaling pathway	CEL 1 secretory granule	CLOC 1 83A1	ALESR 2	REF 9	
GSYM|7B2
PTD
DT|25 Dec 04
ID|FBgn0041707
UAB|Duplication: Dp(3;3)Tpl-T34 (inferred from cytology)
SYN|CG1168
|CG1168
|d7B2
|FBgn0040073
ID2|FBgn0037318
CLOC|83A1
|Limits computationally determined from genome sequence between @P{PZ}l(3)02733<up>02733</up>@ and @P{EP}EP974@
FNC|neuropeptide signaling pathway ; GO:0007218
|peptide hormone processing ; GO:0016486
|signal transduction ; GO:0007165
|transmission of nerve impulse ; GO:0019226
CEL|secretory granule ; GO:0030141
PDOM|IPR007945 == Neuroendocrine 7B2 precursor
ENZ|proprotein convertase 2 activator activity ; GO:0016484 | inferred from sequence similarity with EMBL:U72709
|neuropeptide hormone activity ; GO:0005184 | inferred from electronic annotation
|neuropeptide hormone activity ; GO:0005184
|proprotein convertase 2 activator activity ; GO:0016484
DBA|NA:AE003603
|PA:AAF52036
|NA:AI062015
|BDGP-DGC:GH01053.5prime
|NA:AJ271974
|PA:CAB72934
|NA:AW941705
|BDGP-DGC:GH01053
|NA:AY119453
|PA:AAM50107
|BDGP-DGC:GH01053
PAC|UniProt_TrEMBL:Q9N9Z7
|UniProt_TrEMBL:Q9VNB0
ASQ|FBan0001168
REF
{
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0126678
|Kodira
|1999.11
|9
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
REFM|FBrf0125653
|Hwang
|2000.2.8
|9
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0128499
|Hwang et al.
|2000
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ENZ|proprotein convertase 2 activator activity ; GO:0016484 | inferred from sequence similarity with EMBL:U72709
FNC|peptide hormone processing ; GO:0016486 | inferred from sequence similarity with EMBL:U72709
}

REFDSR
{
RDID|FBrf0123056
|Hwang et al.
|1999
SYN|d7B2
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: GH01053 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0125653
|Hwang
|2000.2.8
GPD|secretory granule neuroendocrine protein
}

REFDSR
{
RDID|FBrf0129037
|Taghert
|2000.5.2
MD|Identified with: GH01053.5prime
AM|Source for merge of: 7B2 CG1168
SYN|CG1168
|d7B2
}

REFDSR
{
RDID|FBrf0130241
|Tellam et al.
|2000
MD|Gene order: Overall orientation not stated: tRNA:R:83AB- kkv+ 7B2-
SYN|unnamed
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
ENZ|neuropeptide hormone activity ; GO:0005184 | inferred from electronic annotation
FNC|signal transduction ; GO:0007165 | inferred from electronic annotation
|transmission of nerve impulse ; GO:0019226 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
FNC|neuropeptide signaling pathway ; GO:0007218 | inferred from electronic annotation
CEL|secretory granule ; GO:0030141 | inferred from electronic annotation
}

ALESR
{
ASYM|7B2<up>cHa</up>
ID|FBal0117934
PHI|Mode of assay: Drosophila cell culture
REF|FBrf0128499
REFDSR
{
RDID|FBrf0128499
|Hwang et al.
|2000
NAM|construct a of Hwang
MD|Construct: Contains @7B2@ coding sequences.
OTH|Carried in a plasmid, transfected into S2 cells and used to study the
|activation of @amon@ by @7B2@.
MU|in vitro construct | other
PHI|Mode of assay: Drosophila cell culture
}

}

ALESR
{
ASYM|7B2<up>+</up>
ID|FBal0116908
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0000003	CLA 1 nuclear untranslated RNA gene	NAM 1 RNA 7SL	GSYM 1 7SLRNA	DT 1 25 Dec 04	RESZ 1396	DBA 3	FNC 1 SRP-dependent cotranslational protein-membrane targeting	CEL 1 signal recognition particle (sensu Eukaryota)	CLOC 1 84A5	ALESR 1	REF 4	
GSYM|7SLRNA
DT|25 Dec 04
ID|FBgn0000003
CLA|nuclear_untranslated_RNA_gene
UAB|Deficiency: Df(3R)BD5 (inferred from cytology)
|Duplication: Dp(3;Y)77ab (inferred from cytology)
SYN|CR32864
NAM|RNA 7SL
CLOC|84A5
|Limits computationally determined from genome sequence between @P{PZ}pb<up>04498</up>@ and @P{lacW}l(3)L2100<up>L2100</up>@
FNC|SRP-dependent cotranslational protein-membrane targeting ; GO:0006614
CEL|signal recognition particle (sensu Eukaryota) ; GO:0005786
DBA|NA:AE003673
|NA:X00952
|NA:X01056
ASQ|FBan0032864
REF
{
REFM|FBrf0040773
|Gundelfinger et al.
|1984
|0
REFM|FBrf0148886
|FlyBase Genome Annotators
|2002-2003
|9
REFM|FBrf0155827
|Misra et al.
|2002
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0040773
|Gundelfinger et al.
|1984
FNC|SRP-dependent cotranslational protein-membrane targeting ; GO:0006614 | inferred from sequence similarity
CEL|signal recognition particle (sensu Eukaryota) ; GO:0005786 | inferred from sequence similarity
GPD|RNA-7SL
}

REFDSR
{
RDID|FBrf0148886
|FlyBase Genome Annotators
|2002-2003
OTH|New annotation (CR32864) in release 3 of the genome annotation.
}

ALESR
{
ASYM|7SLRNA<up>+</up>
ID|FBal0066323
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0052208	CLA 1 Gene	GSYM 1 825-Oak	DT 1 25 Dec 04	RESZ 1531	PTD 1	DBA 2	FNC 1 biological_process unknown	CEL 1 cellular_component unknown	CLOC 1 76B3	ALESR 1	REF 3	
GSYM|825-Oak
PTD
DT|25 Dec 04
ID|FBgn0052208
SYN|CG32208
CLOC|76B3
|Limits computationally determined from genome sequence between @P{EP}MESR6<up>EP3142</up>@ and @P{lacW}l(3)L3809<up>L3809</up>@
FNC|biological_process unknown ; GO:0000004
CEL|cellular_component unknown ; GO:0008372
ENZ|molecular_function unknown ; GO:0005554
|molecular_function unknown ; GO:0005554 | no biological data available
DBA|NA:AE003516
|PA:AAN11647
PAC|UniProt_TrEMBL:Q8IQU7
ASQ|FBan0032208
REF
{
REFM|FBrf0148886
|FlyBase Genome Annotators
|2002-2003
|9
REFM|FBrf0151675
|Prochnik
|2002.10.14
|9
REFM|FBrf0159398
|FlyBase Curators
|2002-
|9
}

REFDSR
{
RDID|FBrf0148886
|FlyBase Genome Annotators
|2002-2003
OTH|New annotation (CG32208) in release 3 of the genome annotation.
}

REFDSR
{
RDID|FBrf0151675
|Prochnik
|2002.10.14
AM|Source for identity of: 825-Oak CG32208
OTH|Etymology: unrevealed!
|Name "825-Oak" chosen by Simon Prochnik to mark his contribution to
|the FlyBase Release 3 annotation project.
}

REFDSR
{
RDID|FBrf0159398
|FlyBase Curators
|2002-
ENZ|molecular_function unknown ; GO:0005554 | no biological data available
FNC|biological_process unknown ; GO:0000004 | no biological data available
CEL|cellular_component unknown ; GO:0008372 | no biological data available
}

ALESR
{
ASYM|825-Oak<up>+</up>
ID|FBal0140827
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0023418	CLA 1 Gene	GSYM 1 8H11	DT 1 25 Dec 04	RESZ 1452	FNC 1 axon guidance	CEL 1 cellular_component unknown	WT 2 @8H11@ has an important role in the process by which axons navigate	ALESR 1	REF 4	
GSYM|8H11
DT|25 Dec 04
ID|FBgn0023418
FNC|axon guidance ; GO:0007411
CEL|cellular_component unknown ; GO:0008372
WT|@8H11@ has an important role in the process by which axons navigate
|across the ventral midline.
ENZ|molecular_function unknown ; GO:0005554
|molecular_function unknown ; GO:0005554 | no biological data available
REF
{
REFM|FBrf0159398
|FlyBase Curators
|2002-
|9
REFM|FBrf0101103
|Noordermeer et al.
|1998
|1
REFM|FBrf0099424
|Noordermeer et al.
|1997
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0099424
|Noordermeer et al.
|1997
FNC|axon guidance ; GO:0007411 | non-traceable author statement
WT|@8H11@ has an important role in the process by which axons navigate
|across the ventral midline.
OTH|Defined by a reverse genetic approach designed to identify novel
|extracellular molecules that are involved in axon guidance.
PHP|Loss of function and ectopic expression experiments indicate a
|significant role for @8H11@ in the establishment of the anterior and
|posterior commissures.
}

REFDSR
{
RDID|FBrf0159398
|FlyBase Curators
|2002-
ENZ|molecular_function unknown ; GO:0005554 | no biological data available
CEL|cellular_component unknown ; GO:0008372 | no biological data available
}

ALESR
{
ASYM|8H11<up>+</up>
ID|FBal0087454
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0044332	CLA 1 Gene	GSYM 1 9.35	DT 1 25 Dec 04	RESZ 1258	FNC 1 germ cell migration	CEL 1 cellular_component unknown	GLOC 1 2L	ALESR 1	REF 3	
GSYM|9.35
DT|25 Dec 04
ID|FBgn0044332
FNC|germ cell migration ; GO:0008354
CEL|cellular_component unknown ; GO:0008372
GLOC|2L
|Maps to the right of dp
|Maps to the left of b
ENZ|molecular_function unknown ; GO:0005554
|molecular_function unknown ; GO:0005554 | no biological data available
REF
{
REFM|FBrf0135351
|Lehmann
|2001.3.15
|9
REFM|FBrf0159398
|FlyBase Curators
|2002-
|9
REFM|FBrf0133952
|Stein et al.
|2001
|1
}

REFDSR
{
RDID|FBrf0133952
|Stein et al.
|2001
FNC|germ cell migration ; GO:0008354 | inferred from genetic interaction with FLYBASE:Hmgcr; FB:FBgn0001205
WTI|Hmgcr
PHP|Mutants disrupt germ cell migration - germ cells are lost in the
|posterior of the embryo and on top of the midgut.
}

REFDSR
{
RDID|FBrf0135351
|Lehmann
|2001.3.15
GLOC|2L
|Maps to the right of dp
|Maps to the left of b
}

REFDSR
{
RDID|FBrf0159398
|FlyBase Curators
|2002-
ENZ|molecular_function unknown ; GO:0005554 | no biological data available
CEL|cellular_component unknown ; GO:0008372 | no biological data available
}

ALESR
{
ASYM|9.35<up>+</up>
ID|FBal0122855
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0043016	CLA 1 Gene	GSYM 1 91R	DT 1 25 Dec 04	RESZ 1226	GLOC 1 3-	ALESR 2	REF 2	
GSYM|91R
DT|25 Dec 04
ID|FBgn0043016
GLOC|3-
REF
{
REFM|FBrf0127214
|Maitra et al.
|2000
|0
REFM|FBrf0151345
|Maitra et al.
|2002
|0
}

REFDSR
{
RDID|FBrf0127214
|Maitra et al.
|2000
GLOC|3-
}

ALESR
{
ASYM|91R<up>91R</up>
SYN|91R
ID|FBal0118615
REF|FBrf0127214
|FBrf0151345
REFDSR
{
RDID|FBrf0127214
|Maitra et al.
|2000
OTH|A factor (or factors) on the third chromosome of D.melanogaster (@91R@)
|affects the levels of @Cyp6a2@ and @Cyp6a8@ RNA expression. It is
|suggested that in the "91-R" strain there is a mutation in this 3rd
|chromosome factor (@91R<up>91R</up>@) allowing high levels of @Cyp6a2@ and
|@Cyp6a8@ expression. It is not clear whether or not the @Cyp6a2@ and
|@Cyp6a8@ genes are also mutated in this strain or whether the high
|level of expression is due solely to the mutation in the @91R@ factor.
SYN|91R
}

REFDSR
{
RDID|FBrf0151345
|Maitra et al.
|2002
SYN|91R
}

}

ALESR
{
ASYM|91R<up>+</up>
ID|FBal0119080
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067632	CLA 1 Gene	GSYM 1 91Y	DT 1 25 Dec 04	RESZ 2257	ALESR 2	SK 1	REF 1	
GSYM|91Y
DT|25 Dec 04
ID|FBgn0067632
SYN|091y
REF
{
REFM|FBrf0141372
|Ejima et al.
|2001
|0
}

REFDSR
{
RDID|FBrf0141372
|Ejima et al.
|2001
SYN|091y
}

ALESR
{
ASYM|91Y<up>91Y</up>
SYN|091y
ID|FBal0151003
PHC|viable
|fertile
|courtship defective | female
PHI|@91Y<up>91Y</up>@ virgin females show elevated ovulation; 19% of the virgin
|females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @91Y<up>91Y</up>@ virgin females are mated
|to wild-type males is lower than that seen when wild-type virgin females
|are mated to wild-type males, but is higher than that seen when wild-type
|mated females are mated to wild-type males. @91Y<up>91Y</up>@ mutant virgin
|females show ovipositor extrusion towards courting wild-type males
|(this extrusion behavior is normally observed in mated wild-type females
|but not in virgin wild-type females).
REF|FBrf0141372
REFDSR
{
RDID|FBrf0141372
|Ejima et al.
|2001
TRN|FBti0004588 == P{GawB}91Y<up>91Y</up>
MU|P-element activity
PHC|viable
|fertile
|courtship defective | female
PHI|@91Y<up>91Y</up>@ virgin females show elevated ovulation; 19% of the virgin
|females show ovulation (compared to 0% of virgin Oregon-R females).
|The flies show no obvious defects in viability, fertility, morphology
|or locomotor activity.
|The courtship index observed when @91Y<up>91Y</up>@ virgin females are mated
|to wild-type males is lower than that seen when wild-type virgin females
|are mated to wild-type males, but is higher than that seen when wild-type
|mated females are mated to wild-type males. @91Y<up>91Y</up>@ mutant virgin
|females show ovipositor extrusion towards courting wild-type males
|(this extrusion behavior is normally observed in mated wild-type females
|but not in virgin wild-type females).
SYN|091y
}

SK|FBst0003737
|w[*]; P{w[+mW.hs]=GawB}91Y[91Y]
}

ALESR
{
ASYM|91Y<up>+</up>
ID|FBal0151309
CLA|wild-type generic
}

SK|FBst0003737
|w[*]; P{w[+mW.hs]=GawB}91Y[91Y]
SKC|1
}
# EOR
GENR
{
RETE|ID 1 FBgn0044331	CLA 1 Gene	GSYM 1 936	DT 1 25 Dec 04	RESZ 519	ALESR 1	REF 1	
GSYM|936
DT|25 Dec 04
ID|FBgn0044331
REF
{
REFM|FBrf0134185
|Guo and Zinsmaier
|2001
|1
}

REFDSR
{
RDID|FBrf0134185
|Guo and Zinsmaier
|2001
PHP|EJP amplitudes are reduced by about 60% in mutants. During high
|frequency stimulation at 10 Hz, EJP amplitudes significantly
|facilitate to 135% of the original response in mutants, while EJPs
|in controls become depressed to 80%.
}

ALESR
{
ASYM|936<up>+</up>
ID|FBal0122854
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0008641	CLA 1 Gene	NAM 1 94Che	GSYM 1 94Che	DT 1 25 Dec 04	RESZ 774	WT 1 An incompletely characterized homeodomain sequence	CLOC 1 94B	ALESR 1	REF 2	
GSYM|94Che
DT|25 Dec 04
ID|FBgn0008641
UAB|Deficiency: Df(3R)hh (inferred from cytology)
|Duplication: Dp(3;3)M95A<up>+</up>13 (inferred from cytology)
NAM|94Che
GLOC|3-[76]
CLOC|94B
|Left limit from in situ hybridization (FBrf0065373)
|Right limit from in situ hybridization (FBrf0065373)
CYC|Experimentally determined: 94B
WT|An incompletely characterized homeodomain sequence.
REF
{
REFM|FBrf0065373
|Dessain and McGinnis
|1993
|2
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0065373
|Dessain and McGinnis
|1993
CLOC|94B (determined by in situ hybridization)
}

ALESR
{
ASYM|94Che<up>+</up>
ID|FBal0071522
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0070035	CLA 1 Gene	GSYM 1 966	DT 1 25 Dec 04	RESZ 544	ALESR 1	REF 1	
GSYM|966
DT|25 Dec 04
ID|FBgn0070035
REF
{
REFM|FBrf0173506
|Song and Wharton
|2004
|1
}

REFDSR
{
RDID|FBrf0173506
|Song and Wharton
|2004
OTH|Identification: genetic screen in a sensitized background for mutants that
|affect @nos@-dependent abdominal segmentation in the embryos.
PHP|In @966@ heterozygous mutants, a modified @nos@ mRNA is
|inefficiently localized and little @nos@ activity accumulates.
}

ALESR
{
ASYM|966<up>+</up>
ID|FBal0158416
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0000009	CLA 1 Gene	NAM 1 Abnormal abdomen	GSYM 1 A	DT 1 25 Dec 04	RESZ 4533	WT 4 Defined by incompletely characterized mutations that show an 'abnormal	CLOC 1 3A5	ALESR 4	REF 14	
GSYM|A
DT|25 Dec 04
ID|FBgn0000009
UAB|Deficiency: Df(1)TEM7 (inferred from cytology)
|Duplication: Dp(1;Y)w<up>+</up>303 (inferred from cytology)
SYN|Abnormal
NAM|Abnormal abdomen
GLOC|1-4.5
CLOC|3A5
DIS|Morgan, July 1911.
GLC|1-[1.0]
CYC|Cytology from deficiency analysis of @A<up>53g</up>@ (Hillman, in
|FBrf0066905); however this is at variance with the genetic position of @A<up>1</up>@.
WT|Defined by incompletely characterized mutations that show an 'abnormal
|abdomen' phenotype. Expressivity and penetrance very sensitive to
|environmental conditions. Stocks accumulate modifiers, resulting in
|apparent reversion (FBrf0006100).
PHP|Very variable mutant phenotype affecting abdominal tergites and sternites.
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|2
REFM|FBrf0025024
|Hillman
|1973
|0
REFM|FBrf0025023
|Rose and Hillman
|1973
|0
REFM|FBrf0025022
|Hillman et al.
|1973
|0
REFM|FBrf0000823
|Morgan and Bridges
|1916
|0
REFM|FBrf0026596
|Shafer and Hillman
|1974
|0
REFM|FBrf0015469
|Hillman and Barbour
|1963
|1
REFM|FBrf0063471
|Gooskov
|1971
|0
REFM|FBrf0065663
|Hillman
|1953
|0
REFM|FBrf0000764
|Morgan
|1915
|0
REFM|FBrf0063908
|Thalmann
|1974
|0
REFM|FBrf0029533
|Hillman
|1977
|0
REFM|FBrf0020251
|Rose and Hillman
|1969
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0063908
|Thalmann
|1974
WTI|E(A<up>53g</up>) (data from @A<up>53g</up>@)
}

ALESR
{
ASYM|A<up>1</up>
ID|FBal0000037
OTH|Highly variable, wild phenotype in old dry cultures. Heterozygotes less
|extreme than homozygotes or hemizygous and males.
|Lost by reversion to wild type.
PHC|visible | semidominant
|viable | female
|female fertile
PHM|abdominal tergite
|abdominal sternite
|cuticle
|microchaeta
|abdomen
|macrochaeta
|abdomen
PHI|Tergites and sternites raggedly incomplete, exposing a thin crinkled
|cuticle; bristles and hairs on abdomen correspondingly eliminated.
|RK2 in well-fed cultures.
REF|FBrf0000823
}

ALESR
{
ASYM|A<up>70</up>
ID|FBal0000038
AMSO|Allelism conjectural.
REF|FBrf0063471
}

ALESR
{
ASYM|A<up>53g</up>
SYN|A53g
ID|FBal0000039
AMSO|May not be allelic to @A<up>1</up>@.
DIS|Hillman, July 1953.
OTH|Supernatents from homogenates of @A<up>53g</up>@-bearing adults stimulate amino
|acid incorporation and aminoacylation of tRNA more than those from wild
|type (FBrf0020251). Mutant late pupae and adults show increased
|concentrations of soluble protein.
|Expression in @A<up>53g</up>@/@A<up>53g</up>@ females > @A<up>53g</up>@/Y males >
|@A<up>53g</up>@/+ females.
|Expression maternally influenced (FBrf0026596). Highly variable;
|sensitive to modifiers on X, 2 and 3, including @E(A<up>53g</up>)@ on 2L. Sensitive
|to culture conditions; expression reduced in old cultures and under
|conditions of crowding, low temperature (TSP in late second and early third
|instar) and low humidity.  Also reduced by agents that inhibit RNA or
|protein synthesis or oxidative phosphorylation (FBrf0025022).
|Expression of biochemical phenotype correlated with that of visible
|phenotype (FBrf0025023).
MU|spontaneous
PHC|visible | semidominant
PHM|abdominal tergite
PHI|Epidermal foldings of abdomen abnormal. Tergite formation incomplete,
|ranging from loss of tergites 2-8 in extreme cases to loss of lateral part
|of tergite in one or more segments.
|RK2 in young cultures.
REF|FBrf0015469
|FBrf0065663
|FBrf0025024
|FBrf0029533
|FBrf0063908
REFDSR
{
RDID|FBrf0063908
|Thalmann
|1974
GIC2|enhanceable by @E(A<up>53g</up>)<up>1</up>@
}

}

ALESR
{
ASYM|A<up>+</up>
ID|FBal0071523
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0000008	CLA 1 Gene	NAM 1 arc	GSYM 1 a	DT 1 24 Dec 04	RESZ 26937	PDOM 1 INTERPRO:IPR001478 == PDZ/DHR/GLGF	PTD 1	DBA 16	FNC 1 eye morphogenesis (sensu Endopterygota)	CEL 2 adherens junction	WT 2 @a@ may affect eye development by modulating adherens junctions of	CLOC 1 58C1--5	ALESR 27	SK 8	REF 33	
GSYM|a
PTD
DT|24 Dec 04
ID|FBgn0000008
UAB|Deficiency: Df(2R)Egfr5 (inferred from cytology)
|Duplication: Dp(2;2)l-32 (inferred from cytology)
SYN|CG6741
|CG13505
|CG6741
|CG13505
|CG13505
|CG6741
|bran: broad angular
|Arc
|broad angular
|bran
ID2|FBgn0034701
|FBgn0034702
NAM|arc
GLOC|2-99.2
CLOC|58C1--5
|Limits computationally determined from genome sequence between @P{EP}CG6393<up>EP2457</up>@ and @P{PZ}ari-2<up>07768</up>@
DIS|Bridges, 24th May 1912.
CYC|Experimentally determined: 58C--D
FNC|eye morphogenesis (sensu Endopterygota) ; GO:0007456
CEL|adherens junction ; GO:0005912
|apical plasma membrane ; GO:0016324
PDOM|IPR001478 == PDZ/DHR/GLGF
WT|@a@ may affect eye development by modulating adherens junctions of
|the developing ommatidia.
ENZ|protein binding ; GO:0005515
|protein binding ; GO:0005515 | inferred from electronic annotation
DBA|NA:AE003456
|PA:AAF46810
|PA:AAF46809
|NA:AF188473
|PA:AAF37816
|NA:AF188474
|PA:AAF37817
|NA:AF188475
|PA:AAF37818
|NA:AI389852
|BDGP-DGC:GH21134
|NA:AW940815
|BDGP-DGC:GH21134
|NA:AY058433
|PA:AAL13662
|BDGP-DGC:GH21134
PAC|UniProt_TrEMBL:Q9W283
WTI|svr
ASQ|FBan0006741
REV|FBrf0141282
REF
{
REFM|FBrf0160992
|Szuplewski et al.
|2003
|0
REFM|FBrf0094738
|Fradkin
|1957
|0
REFM|-2114620305
|Lewis
|Cited in Lindsley and Grell
|-1
|1968
REFM|FBrf0003308
|Goldschmidt
|1935
|0
REFM|FBrf0139846
|Lengyel
|2001.1.4
|9
REFM|FBrf0001379
|Morgan et al.
|1925
|2
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0094793
|Goldschmidt
|1944
|0
REFM|FBrf0131066
|Lengyel
|2000.8.1
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0003816
|Bridges
|1937
|0
REFM|FBrf0003920
|Dunn and Mossige
|1937
|0
REFM|FBrf0006430
|Goldschmidt
|1945
|0
REFM|FBrf0101731
|Liu et al.
|1998
|1
REFM|FBrf0000979
|Bridges and Morgan
|1919
|0
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
|9
REFM|FBrf0006895
|Goldschmidt
|1947
|0
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|-2114621701
|Lewis
|Cited in Lindsley and Grell
|0
|1968
REFM|FBrf0127206
|Liu and Lengyel
|2000
|0
REFM|FBrf0003299
|Goldschmidt
|1935
|0
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|2
REFM|FBrf0063692
|Meyer
|1963
|0
REFM|FBrf0020044
|Lindsley and Grell
|1968
|2
REFM|FBrf0141282
|Tepass et al.
|2001
|2
REFM|FBrf0129141
|Millburn
|2000.5.31
|9
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0127946
|Liu
|1999.9.21
|9
REFM|FBrf0129140
|Lengyel
|2000.3.26
|9
REFM|FBrf0167841
|Mueller and Bossinger
|2003
|2
REFM|FBrf0100133
|Liu and Lengyel
|1997
|1
REFM|FBrf0138539
|Bilder
|2001
|2
}

REFDSR
{
RDID|FBrf0003816
|Bridges
|1937
BMD|Df(2R)M58F
BMDD|Df(2R)P
}

REFDSR
{
RDID|FBrf0003920
|Dunn and Mossige
|1937
BMD|Df(2R)M58F
}

REFDSR
{
RDID|FBrf0006430
|Goldschmidt
|1945
BMD|Df(2R)a-ba2
}

REFDSR
{
RDID|FBrf0020044
|Lindsley and Grell
|1968
PHP|Defined by recessive mutations that result in a broad, often bent, wing.
}

REFDSR
{
RDID|FBrf0063692
|Meyer
|1963
GLOC|2-99.2
BMD|In(2LR)a<up>M60</up>
}

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
BMDD|Df(2R)E3578
BMDD|Df(2R)ST1
BMDD|Df(2R)XE-916
BMDD|Df(2R)nap16
}

REFDSR
{
RDID|FBrf0094793
|Goldschmidt
|1944
GLOC|2-
BMD|Df(2R)a-ba2
SYN|bran: broad angular
}

REFDSR
{
RDID|FBrf0100133
|Liu and Lengyel
|1997
NAM|arc
SYN|Arc
}

REFDSR
{
RDID|FBrf0101731
|Liu et al.
|1998
NAM|arc
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: GH21134 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0127206
|Liu and Lengyel
|2000
FNC|eye morphogenesis (sensu Endopterygota) ; GO:0007456 | inferred from mutant phenotype
MD|Gene order: In direction of increasing cytology: mei-S332+ a+ ari-2+ dve+
CEL|adherens junction ; GO:0005912 | inferred from direct assay
|apical plasma membrane ; GO:0016324 | inferred from direct assay
WT|@a@ may affect eye development by modulating adherens junctions of
|the developing ommatidia.
BMD|Df(2R)a<up>7</up>
BMD|Df(2R)a<up>EX1</up>
BMD|Df(2R)a<up>EX2</up>
}

REFDSR
{
RDID|FBrf0127946
|Liu
|1999.9.21
CLOC|58C--D
CEL|adherens junction ; GO:0005912 | non-traceable author statement
}

REFDSR
{
RDID|FBrf0129140
|Lengyel
|2000.3.26
AM|Source for merge of: a CG6741
SYN|CG6741
}

REFDSR
{
RDID|FBrf0129141
|Millburn
|2000.5.31
AM|Source for merge of: a CG13505
SYN|CG13505
}

REFDSR
{
RDID|FBrf0131066
|Lengyel
|2000.8.1
AM|Source for merge of: a CG13505 CG6741
SYN|CG13505
|CG6741
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

REFDSR
{
RDID|FBrf0167841
|Mueller and Bossinger
|2003
SYN|Arc
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|protein binding ; GO:0005515 | inferred from electronic annotation
}

ALESR
{
ASYM|a<up>1</up>
ID|FBal0000040
MU|spontaneous
PHC|visible | recessive
PHM|wing
|crossvein
PHI|Wings broader; bent downward in slight, even arc;
|edges drawn down to diamond shape. Sometimes in stock,
|wings are bent upward instead of downward. Crossveins
|closer together.
|RK2.
REF|FBrf0006430
|FBrf0020044
|FBrf0127206
|-2114620305
|FBrf0160992
REFDSR
{
RDID|-2114620305
|Lewis
|Cited in Lindsley and Grell
GIC2|non-suppressible by @su(Hw)<up>2</up>@
}

REFDSR
{
RDID|FBrf0127206
|Liu and Lengyel
|2000
OTH|Allelic series of mutations: @Df(2R)a<up>EX1</up>@ = @Df(2R)a<up>EX2</up>@ > a<up>EM50</up>
|>= @a<up>k11011b</up>@ > @a<up>EM1</up>@ >= @a<up>EM27</up>@ > @a<up>1</up>@ > @a<up>EM15</up>@.
}

REFDSR
{
RDID|FBrf0160992
|Szuplewski et al.
|2003
GII|@a<up>1</up>@ does not show a significant interaction with @vri<up>unspecified</up>@
|in double heterozygous combination.
}

SK|FBst0001554
|a[1] px[1] or[1]
|FBst0003301
|al[1] dp[ov1] b[1] pr[1] cn[1] vg[1] c[1] a[1] px[1] bw[1] mi[1] sp[1]/SM1
|FBst0006525
|dp[ov1] cn[1] l(2)57Da[1] a[1] px[1] sp[1]/SM1
|FBst0000312
|hy[1] a[1] px[1] sp[1]/SM1
}

ALESR
{
ASYM|a<up>7</up>
ID|FBal0117621
ABA|FBab0029357 == Df(2R)a<up>7</up>
PHM|(with Df(2R)a<up>EX1</up>) eye
|(with Df(2R)a<up>EX1</up>) ommatidium
PHI|@a<up>7</up>@/@Df(2R)a<up>EX1</up>@ flies have eyes that are significantly smaller
|than wild-type, and those eyes have rhomboidal ommatidia. The arrangement
|of photoreceptors within each ommatidium appears wild-type. @a<up>7</up>@/@Df(2R)a<up>EX1</up>@
|have no detectable phenotype in epithelial development.
REF|FBrf0127206
REFDSR
{
RDID|FBrf0127206
|Liu and Lengyel
|2000
MD|Breakpoint is just before exon 4.
PRG|a<up>k11011b</up>
MU|X ray
ABA|FBab0029357 == Df(2R)a<up>7</up>
GIA2|(with Df(2R)a<up>EX1</up>) eye, non-enhanceable by @nmo<up>P1</up>@/@nmo<up>P1</up>@
GIC2|(with Df(2R)a<up>EX1</up>) non-enhanceable by @Df(3L)MY10@/+
|(with Df(2R)a<up>EX1</up>) non-enhanceable by @arm<up>1</up>@/+
|(with Df(2R)a<up>EX1</up>) non-enhanceable by @cno<up>mis1</up>@/@cno<up>mis1</up>@
|(with Df(2R)a<up>EX1</up>) non-suppressible by @Df(3L)MY10@/+
|(with Df(2R)a<up>EX1</up>) non-suppressible by @arm<up>1</up>@/+
|(with Df(2R)a<up>EX1</up>) non-suppressible by @cno<up>mis1</up>@/@cno<up>mis1</up>@
GIC|(with Df(2R)a<up>EX1</up>) non-enhancer of @pyd<up>tam</up>@
GIA|(with Df(2R)a<up>EX1</up>) non-enhancer of eye phenotype of @nmo<up>P1</up>@
GIC|(with Df(2R)a<up>EX1</up>) non-suppressor of @pyd<up>tam</up>@
GIA|(with Df(2R)a<up>EX1</up>) non-suppressor of eye phenotype of @nmo<up>P1</up>@
GIC|(with Df(2R)a<up>EX1</up>) non-enhancer of @cno<up>mis1</up>@
|(with Df(2R)a<up>EX1</up>) non-suppressor of @cno<up>mis1</up>@
GIA2|(with Df(2R)a<up>EX1</up>) eye, non-suppressible by @nmo<up>P1</up>@/@nmo<up>P1</up>@
GII|The addition of @pyd<up>tam</up>@/+, @nmo<up>P1</up>@/@nmo<up>P1</up>@, @cno<up>mis1</up>@/@cno<up>mis1</up>@
|or @arm<up>1</up>@/+ has no effect on @a<up>7</up>@/@Df(2R)a<up>EX1</up>@ flies.
PHM|(with Df(2R)a<up>EX1</up>) eye
|(with Df(2R)a<up>EX1</up>) ommatidium
PHI|@a<up>7</up>@/@Df(2R)a<up>EX1</up>@ flies have eyes that are significantly smaller
|than wild-type, and those eyes have rhomboidal ommatidia. The arrangement
|of photoreceptors within each ommatidium appears wild-type. @a<up>7</up>@/@Df(2R)a<up>EX1</up>@
|have no detectable phenotype in epithelial development.
}

SK|FBst0007100
|w[*]; Df(2R)a[7]/CyO
}

ALESR
{
ASYM|a<up>57e14</up>
ID|FBal0063000
REF|FBrf0094738
REFDSR
{
RDID|FBrf0094738
|Fradkin
|1957
DIS|Fradkin, 1957.
MU|spontaneous
}

}

ALESR
{
ASYM|a<up>Ba</up>
SYN|Bran
ID|FBal0000048
NAM|Broad angular Dominant
DIS|Goldschmidt.
PRG|a<up>ba</up>
MU|spontaneous
PHC|visible | dominant
PHM|wing
|posterior scutellar bristle
|macrochaeta
PHI|Wings broader and shorter than wild type, blunt at the
|tip; frequently shows upturned posterior scutellar bristles.
|@a<up>Ba</up>@/@a<up>ba</up>@ shows Minute-like bristles.
|RK2.
REF|FBrf0006430
|FBrf0020044
}

ALESR
{
ASYM|a<up>ba</up>
SYN|bran
ID|FBal0000055
NAM|broad angular
DIS|Goldschmidt, 1934.
OTH|Claimed to recur repeatedly in certain lines (FBrf0006430).
CYA|Polytene chromosomes normal (Kodani).
MU|spontaneous
GIA2|wing with @svr<up>poi</up>@
PHC|visible | recessive
PHM|wing
|posterior scutellar bristle
PHI|Wings broader and shorter than wild type, blunt at the
|tip. Frequently shows upturned posterior scutellar
|bristles. In combination with @svr<up>poi</up>@, produces soft
|blistered wing. Other interactions described by
|Goldschmidt (FBrf0006430: table 74). Wing grows in pupal stage
|to full length and then retracts, possibly with
|histolysis (FBrf0003308).
|RK2.
REF|FBrf0003308
|FBrf0094793
|FBrf0006430
REFDSR
{
RDID|FBrf0094793
|Goldschmidt
|1944
DIS|R.B. Goldschmidt.
CYA|Polytene chromosomes normal.
PHC|visible
PHM|wing
PHI|RK2.
|Wings are broad and short or broad and blunt at the tip.
SYN|bran
}

}

ALESR
{
ASYM|a<up>ba1</up>
SYN|bran<up>1</up>
ID|FBal0000041
DIS|Goldschmidt.
CYA|Polytene chromosomes normal (Kodani).
MU|spontaneous
PHI|Nearly normal; distinguished by its interaction with certain
|@svr@ alleles (see FBrf0006430: table 74).
|RK3.
REF|FBrf0094793
|FBrf0006430
|FBrf0020044
REFDSR
{
RDID|FBrf0094793
|Goldschmidt
|1944
DIS|R.B. Goldschmidt.
CYA|Polytene chromosomes normal.
PHC|visible
PHM|wing
PHI|RK3
|Almost normal wings.
SYN|bran<up>1</up>
}

}

ALESR
{
ASYM|a<up>ba2</up>
SYN|bran<up>2</up>
ID|FBal0000042
DIS|Goldschmidt.
CYA|Polytene chromosomes normal (Kodani).
MU|spontaneous
ABA|FBab0002062 == Df(2R)a-ba2
PHC|wild-type
PHI|Normal; distinguished by its interaction with certain
|@svr@ alleles (see FBrf0006430: table 74).
|RK3.
REF|FBrf0094793
|FBrf0006430
|FBrf0020044
REFDSR
{
RDID|FBrf0094793
|Goldschmidt
|1944
DIS|R.B. Goldschmidt.
ABA|FBab0002062 == Df(2R)a-ba2
PHC|visible
PHM|wing
PHI|RK2.
|Wings are broad and short or broad and blunt at the tip. Small basal
|blisters appear.
SYN|bran<up>2</up>
}

}

ALESR
{
ASYM|a<up>ba3</up>
SYN|bran<up>3</up>
ID|FBal0000043
DIS|Goldschmidt.
CYA|Polytene chromosomes normal (Kodani).
MU|spontaneous
PHC|wild-type
PHI|Normal; distinguished by its interaction with certain
|@svr@ alleles (see FBrf0006430: table 74).
|RK3.
REF|FBrf0006430
|FBrf0020044
}

ALESR
{
ASYM|a<up>ba4</up>
SYN|bran<up>4</up>
ID|FBal0000044
DIS|Goldschmidt.
CYA|Polytene chromosomes normal (Kodani).
PRG|a<up>ba3</up> \?
MU|spontaneous
PHC|visible | recessive
PHM|wing
|posterior scutellar bristle
PHI|Wings broader and shorter than wild type, blunt at the
|tip. Frequently shows upturned posterior scutellar
|bristles.
|Distinguished from @a<up>ba</up>@ by its interaction with
|certain @svr@ alleles (see FBrf0006430: table 74).
|RK2.
REF|FBrf0094793
|FBrf0006430
|FBrf0020044
REFDSR
{
RDID|FBrf0094793
|Goldschmidt
|1944
DIS|R.B. Goldschmidt.
PHC|visible
PHM|wing
PHI|RK5
|Wings are broad and short or broad and blunt at the tip.
SYN|bran<up>4</up>
}

}

ALESR
{
ASYM|a<up>BaC</up>
SYN|Bran<up>Ca</up>
ID|FBal0000049
NAM|Broad angular in Canton-S
DIS|Goldschmidt.
CYA|Polytene chromosomes normal (Hannah-Alava).
MU|spontaneous
GIA2|wing with @svr<up>unspecified</up>@
GIC2|visible | dominant with @svr<up>unspecified</up>@
PHC|visible | recessive
PHM|wing
PHI|@a<up>BaC</up>@/+ is normal; @a<up>BaC</up>@/@a<up>ba</up>@ has broad
|angular wing, but overlaps wild type. @a<up>BaC</up>@ is dominant
|in its interaction with certain @svr@ alleles.
|RK3.
REF|FBrf0006430
|FBrf0006895
|FBrf0020044
}

ALESR
{
ASYM|a<up>badb</up>
ID|FBal0027938
NAM|broad angular dumpy blistered
DIS|Goldschmidt.
CYA|Polytene chromosomes normal (Kodani).
MU|spontaneous
PHC|visible | recessive
PHM|wing
|posterior scutellar bristle
PHI|Wings broader and shorter than wild type, blunt at the
|tip. Frequently shows upturned posterior scutellar
|bristles.
|Distinguished from @a<up>ba</up>@ by its interaction with
|certain @svr@ alleles (see FBrf0006430: table 74).
|RK2.
REF|FBrf0094793
|FBrf0006430
|FBrf0020044
REFDSR
{
RDID|FBrf0094793
|Goldschmidt
|1944
DIS|R.B. Goldschmidt.
CYA|Polytene chromosomes normal.
PHC|visible
PHM|wing
PHI|RK3
|Wings are broad and short or broad and blunt at the tip.
SYN|bran<up>db</up>
}

}

ALESR
{
ASYM|a<up>badp</up>
SYN|bran<up>dp</up>
ID|FBal0000046
NAM|broad angular dumpy
DIS|Goldschmidt.
OTH|Claimed by Goldschmidt to recur repeatedly in certain lines.
CYA|Polytene chromosomes normal (Kodani).
MU|spontaneous
PHC|wild-type
PHI|Normal; distinguished by its interaction with certain
|@svr@ alleles (see FBrf0006430: table 74).
|RK3.
REF|FBrf0094793
|FBrf0006430
|FBrf0020044
REFDSR
{
RDID|FBrf0094793
|Goldschmidt
|1944
DIS|R.B. Goldschmidt.
CYA|Polytene chromosomes normal.
PHI|RK4.
SYN|bran<up>dp</up>
}

}

ALESR
{
ASYM|a<up>Bap1</up>
ID|FBal0000050
NAM|Broad angular in silver-pointed
MU|spontaneous
REF|FBrf0006430
|FBrf0020044
}

ALESR
{
ASYM|a<up>Bap2</up>
SYN|Bran<up>poi47-2</up>
ID|FBal0000051
DIS|Goldschmidt, 1947.
CYA|Polytene chromosomes normal (Hannah-Alava).
MU|spontaneous
GIC2|visible | dominant with @svr<up>unspecified</up>@
PHC|lethal | recessive
PHI|Phenotype normal in combination with @a<up>ba</up>@ and @a@<up>+</up>.
|RK2 as lethal.
REF|FBrf0006430
|FBrf0006895
|FBrf0020044
}

ALESR
{
ASYM|a<up>Bapl</up>
SYN|Bran<up>poi47-1</up>
ID|FBal0039120
DIS|Goldschmidt, 1947.
CYA|Polytene chromosomes normal (Hannah-Alava).
MU|spontaneous
PHC|visible | dominant
PHM|wing
|posterior scutellar bristle
PHI|Wings broader and shorter than wild type, blunt at the
|tip; frequently shows upturned posterior scutellar bristles.
|RK2.
REF|FBrf0006895
}

ALESR
{
ASYM|a<up>bar</up>
SYN|bran<up>r</up>
ID|FBal0000047
NAM|broad angular rudimentary
DIS|Goldschmidt.
PRG|a<up>badp</up>
MU|spontaneous
PHC|visible | recessive
PHM|wing
PHI|Wings broad, round and @dp@-like. Interacts with certain
|@svr@ alleles (see FBrf0006430: table 74).
|RK2.
REF|FBrf0094793
|FBrf0006430
|FBrf0020044
REFDSR
{
RDID|FBrf0094793
|Goldschmidt
|1944
DIS|R.B. Goldschmidt.
CYA|Polytene chromosomes normal.
PHC|visible
PHM|wing
PHI|RK4
|Broad and truncated wings.
SYN|bran<up>r</up>
}

}

ALESR
{
ASYM|a<up>BaX</up>
SYN|bran<up>X</up>
|Bran<up>x</up>
|a<up>baX</up>
ID|FBal0000052
NAM|Broad angular from X irradiation
DIS|Goldschmidt.
MU|X ray
NAF|Discarded.
PHC|visible | dominant
|lethal | recessive \?
PHM|wing
PHI|Resembles @a<up>ba2</up>@ and @a<up>badb</up>@ but more or
|less dominant. Homozygote never obtained. Interactions
|listed by Goldschmidt (FBrf0006430: table 153).
|RK2.
REF|FBrf0094793
|FBrf0006430
|FBrf0020044
REFDSR
{
RDID|FBrf0094793
|Goldschmidt
|1944
DIS|R.B. Goldschmidt.
MU|X ray
NAF|Discarded.
SYN|bran<up>X</up>
}

}

ALESR
{
ASYM|a<up>Bay</up>
SYN|Bran<up>y px b1</up>
ID|FBal0000053
DIS|Goldschmidt.
CYA|Polytene chromosomes normal (Hannah-Alava).
MU|spontaneous
GIA2|wing with @svr<up>poi</up>@
PHC|visible | dominant
|lethal | recessive
|sterile | recessive
PHM|wing
PHI|Heterozygote shows broad-angular phenotype with occasional truncate-like
|wings. In combination with @svr<up>poi</up>@, resembles @r@ and @bs@.
|RK2 as lethal.
REF|FBrf0006430
|FBrf0006895
|FBrf0020044
}

ALESR
{
ASYM|a<up>EM1</up>
ID|FBal0117619
PHC|viable
REF|FBrf0127206
REFDSR
{
RDID|FBrf0127206
|Liu and Lengyel
|2000
OTH|Allelic series of mutations: @Df(2R)a<up>EX1</up>@ = @Df(2R)a<up>EX2</up>@ > a<up>EM50</up>
|>= @a<up>k11011b</up>@ > @a<up>EM1</up>@ >= @a<up>EM27</up>@ > @a<up>1</up>@ > @a<up>EM15</up>@.
MU|ethyl methanesulfonate
PHC|viable
}

SK|FBst0007150
|cn[1] a[EM1] bw[1] sp[1]/SM6b
}

ALESR
{
ASYM|a<up>EM15</up>
ID|FBal0117620
PHC|viable
REF|FBrf0127206
REFDSR
{
RDID|FBrf0127206
|Liu and Lengyel
|2000
OTH|Allelic series of mutations: @Df(2R)a<up>EX1</up>@ = @Df(2R)a<up>EX2</up>@ > a<up>EM50</up>
|>= @a<up>k11011b</up>@ > @a<up>EM1</up>@ >= @a<up>EM27</up>@ > @a<up>1</up>@ > @a<up>EM15</up>@.
MU|ethyl methanesulfonate
PHC|viable
}

}

ALESR
{
ASYM|a<up>EM27</up>
ID|FBal0117618
PHC|viable
REF|FBrf0127206
REFDSR
{
RDID|FBrf0127206
|Liu and Lengyel
|2000
OTH|Allelic series of mutations: @Df(2R)a<up>EX1</up>@ = @Df(2R)a<up>EX2</up>@ > a<up>EM50</up>
|>= @a<up>k11011b</up>@ > @a<up>EM1</up>@ >= @a<up>EM27</up>@ > @a<up>1</up>@ > @a<up>EM15</up>@.
MU|ethyl methanesulfonate
PHC|viable
}

}

ALESR
{
ASYM|a<up>EM50</up>
ID|FBal0117617
PHC|viable
REF|FBrf0127206
REFDSR
{
RDID|FBrf0127206
|Liu and Lengyel
|2000
MU|ethyl methanesulfonate
PHC|viable
}

}

ALESR
{
ASYM|a<up>EX3</up>
ID|FBal0117616
PHC|lethal | recessive
REF|FBrf0127206
REFDSR
{
RDID|FBrf0127206
|Liu and Lengyel
|2000
PRG|a<up>k11011b</up>
MU|P-element activity
PHC|lethal | recessive
}

}

ALESR
{
ASYM|a<up>k11011b</up>
SYN|a<up>P</up>
ID|FBal0117614
PHM|wing
|eye
ALC|hypomorph
PHI|Homozygotes develop broad and downwardly bent wings. The also have
|slightly smaller, but otherwise normal looking eyes.
REF|FBrf0127206
REFDSR
{
RDID|FBrf0127206
|Liu and Lengyel
|2000
MD|The insertion is 11bp after the transcription start.
OTH|Allelic series of mutations: @Df(2R)a<up>EX1</up>@ = @Df(2R)a<up>EX2</up>@ > a<up>EM50</up>
|>= @a<up>k11011b</up>@ > @a<up>EM1</up>@ >= @a<up>EM27</up>@ > @a<up>1</up>@ > @a<up>EM15</up>@.
TRN|FBti0012078 == P{lacW}a<up>k11011b</up>
MU|P-element activity
PHM|wing
|eye
ALC|hypomorph
PHI|Homozygotes develop broad and downwardly bent wings. The also have
|slightly smaller, but otherwise normal looking eyes.
SYN|a<up>P</up>
}

SK|FBst0007075
|w[*]; P{w[+mc]=lacW}a[k11011b]
}

ALESR
{
ASYM|a<up>M60</up>
ID|FBal0000054
NAM|of Meyer
DIS|Meyer, June 1960.
MU|X ray
ABA|FBab0004848 == In(2LR)a<up>M60</up>
PHC|visible | dominant
|lethal | recessive
PHI|RK3A.
REF|FBrf0063692
REFDSR
{
RDID|FBrf0063692
|Meyer
|1963
DIS|Meyer.
MU|X ray
ABA|FBab0004848 == In(2LR)a<up>M60</up>
PHC|lethal | recessive
}

}

ALESR
{
ASYM|a<up>yUAS</up>
SYN|a<up>UAS</up>
|a<up>Scer\UAS.cLa</up>
ID|FBal0117615
PHC|lethal with @Scer\GAL4<up>Act5C.PI</up>@
PHM|eye with @Scer\GAL4<up>Act5C.PI</up>@
|ommatidium with @Scer\GAL4<up>Act5C.PI</up>@
|eye with @Scer\GAL4<up>GMR.PF</up>@
PHI|@a<up>yUAS</up>@ homozygotes develop normal wings and eyes.
|@a<up>yUAS</up>@ driven by @Scer\GAL4<up>en-e16E</up>@ produces no phenotype.
|@a<up>yUAS</up>@ driven by @Scer\GAL4<up>Act5C.PI</up>@ leads to pupal lethality,
|these pupae have rough eye with fused ommatidia, but otherwise appear
|morphologically normal. @a<up>yUAS</up>@ driven by @Scer\GAL4<up>GMR.PF</up>@
|produces flies with a rough eye phenotype with eyes larger than seen
|in wild-type or with @Scer\GAL4<up>GMR.PF</up>@ alone.
REF|FBrf0139846
|FBrf0127206
REFDSR
{
RDID|FBrf0127206
|Liu and Lengyel
|2000
MD|A @P{yUAS}@ element (containing five copies of the @Scer\UAS@
|regulatory sequence fused upstream of a basal Hsp70 promoter) is
|inserted upstream of @a@ by @P-element@ replacement.
TRN|FBti0020936 == P{Mae-UAS.6.11}a<up>yUAS</up>
PHC|lethal with @Scer\GAL4<up>Act5C.PI</up>@
PHM|eye with @Scer\GAL4<up>Act5C.PI</up>@
|ommatidium with @Scer\GAL4<up>Act5C.PI</up>@
|eye with @Scer\GAL4<up>GMR.PF</up>@
PHI|@a<up>yUAS</up>@ homozygotes develop normal wings and eyes.
|@a<up>yUAS</up>@ driven by @Scer\GAL4<up>en-e16E</up>@ produces no phenotype.
|@a<up>yUAS</up>@ driven by @Scer\GAL4<up>Act5C.PI</up>@ leads to pupal lethality,
|these pupae have rough eye with fused ommatidia, but otherwise appear
|morphologically normal. @a<up>yUAS</up>@ driven by @Scer\GAL4<up>GMR.PF</up>@
|produces flies with a rough eye phenotype with eyes larger than seen
|in wild-type or with @Scer\GAL4<up>GMR.PF</up>@ alone.
SYN|a<up>UAS</up>
}

REFDSR
{
RDID|FBrf0139846
|Lengyel
|2001.1.4
MD|Replacement of the @P{lacW}@ element in @a<up>k11011b</up>@ with a @P{yUAS}@
|element.
PRG|P{lacW}a<up>k11011b</up>
TRN|FBti0020936 == P{Mae-UAS.6.11}a<up>yUAS</up>
MU|gene conversion
|P-element activity
SYN|a<up>UAS</up>
}

SK|FBst0007071
|y[1] w[*]; P{y[+t7.7]=Mae-UAS.6.11}a[yUAS]
}

ALESR
{
ASYM|a<up>+</up>
ID|FBal0068527
CLA|wild-type generic
REF|FBrf0105495
}

IFL|../dbzhnsky/arc1.htm
SK|FBst0001554
|a[1] px[1] or[1]
|FBst0003301
|al[1] dp[ov1] b[1] pr[1] cn[1] vg[1] c[1] a[1] px[1] bw[1] mi[1] sp[1]/SM1
|FBst0007150
|cn[1] a[EM1] bw[1] sp[1]/SM6b
|FBst0006525
|dp[ov1] cn[1] l(2)57Da[1] a[1] px[1] sp[1]/SM1
|FBst0000312
|hy[1] a[1] px[1] sp[1]/SM1
|FBst0007100
|w[*]; Df(2R)a[7]/CyO
|FBst0007075
|w[*]; P{w[+mc]=lacW}a[k11011b]
|FBst0007071
|y[1] w[*]; P{y[+t7.7]=Mae-UAS.6.11}a[yUAS]
SKC|8
}
# EOR
GENR
{
RETE|ID 1 FBgn0004930	CLA 1 Gene	NAM 1 abnormal abdomen (1) 48	GSYM 1 a(1)48	DT 1 24 Dec 04	RESZ 4070	WT 1 Defined by incompletely characterized mutations that show an 'abnormal abdomen' phenotype	GLOC 1 1-	ALESR 4	REF 5	
GSYM|a(1)48
DT|24 Dec 04
ID|FBgn0004930
NAM|abnormal abdomen (1) 48
GLOC|1-
DIS|Zimmermann, 1948.
AM|Genetic relations not worked out.
WT|Defined by incompletely characterized mutations that show an 'abnormal abdomen' phenotype.
WTI|a(2)48
|a(3)48
PHP|Used to describe three X chromosomes with little or no
|effect of their own but which increase the incidence
|of abdominal malformations in crosses with a(2) and
|a(3).
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|2
REFM|FBrf0009915
|Zimmermann
|1954
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0020044
|Lindsley and Grell
|1968
|2
REFM|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
|0
}

REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
WTI|a(2)48 (data from @a(1)48<up>48</up>@, @a(1)48<up>50</up>@)
|a(3)48 (data from @a(1)48<up>48</up>@, @a(1)48<up>50</up>@)
}

ALESR
{
ASYM|a(1)48<up>48</up>
SYN|a(1)48
ID|FBal0000056
MU|spontaneous
PHC|visible | recessive
|viable | good
|fertile | good
PHM|abdomen
PHI|RK3.
REF|FBrf0020044
|FBrf0063299
REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
MU|spontaneous
GII|Increases the penetrance of @a(2)48<up>48</up>@ and @a(3)48<up>1</up>@.
GIC|enhancer of @a(2)48<up>48</up>@
|enhancer of @a(3)48<up>1</up>@
PHC|viable
|fertile
SYN|a(1)48
}

}

ALESR
{
ASYM|a(1)48<up>50</up>
SYN|a(1)50
ID|FBal0000057
DIS|Zimmerman, 1950.
MU|spontaneous
GIC|enhancer of @a(2)48<up>50</up>@
|enhancer of @a(3)48<up>1</up>@
PHC|visible | recessive
|viable | good
|fertile | good
PHM|abdomen | adult
PHI|RK3.
|Irregularities in abdomen most frequently involving the
|anterior segments. Penetrance 1%. Enhances maternal
|effects of @a(2)48<up>50</up>@ and @a(3)48<up>1</up>@.
REF|FBrf0020044
|FBrf0009915
|FBrf0063299
REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
MU|spontaneous
GII|Increases the penetrance of @a(2)48<up>48</up>@ and @a(3)48<up>1</up>@.
GIC|enhancer of @a(2)48<up>48</up>@
|enhancer of @a(3)48<up>1</up>@
PHC|viable
|fertile
SYN|a(1)50
}

}

ALESR
{
ASYM|a(1)48<up>51</up>
SYN|a(1)51
ID|FBal0000058
DIS|Zimmerman, 1951.
MU|spontaneous
PHC|visible | recessive | maternal effect
|viable | good
|fertile | good
PHM|abdomen | adult
PHI|RK3.
|Shows maternal effect only, with 2% of progeny
|affected. Abnormalities more anterior than those of
|@a(2)48<up>50</up>@ and @a(1)48<up>50</up>@.
REF|FBrf0020044
|FBrf0009915
|FBrf0063299
REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
MU|spontaneous
PHC|viable
|fertile
SYN|a(1)51
}

}

ALESR
{
ASYM|a(1)48<up>+</up>
ID|FBal0071524
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004931	CLA 1 Gene	NAM 1 abnormal abdomen HM26	GSYM 1 a(1)HM26	DT 1 24 Dec 04	RESZ 1532	WT 1 Defined by incompletely characterized mutations that show an 'abnormal abdomen' phenotype	CLOC 1 [1B1--5C2]	ALESR 2	REF 3	
GSYM|a(1)HM26
DT|24 Dec 04
ID|FBgn0004931
SYN|l(1)HM26
NAM|abnormal abdomen HM26
GLOC|Maps to the right of y
|Maps to the left of cv
CLOC|[1B1--5C2]
|Left limit from recombination mapping relative to y (FBrf0024658)
|Right limit from recombination mapping relative to cv (FBrf0024658)
WT|Defined by incompletely characterized mutations that show an 'abnormal abdomen' phenotype.
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|2
REFM|FBrf0024658
|Mayoh and Suzuki
|1973
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0024658
|Mayoh and Suzuki
|1973
GLOC|Maps to the right of y
|Maps to the left of cv
}

ALESR
{
ASYM|a(1)HM26<up>1</up>
ID|FBal0000059
MU|ethyl methanesulfonate
PHC|visible | recessive | conditional cs
PHM|abdominal tergite
|abdominal sternite
PHI|Missing or reduced sternites; missing or angled
|tergites; black specks on ventral surface of abdomen
|in about one-third of males at 22<up>o</up>C and more than
|half of males at 17<up>o</up>C. Viability reduced at 17<up>o</up>C
|relative to that at 22<up>o</up>C.
REF|FBrf0066905
|FBrf0024658
}

ALESR
{
ASYM|a(1)HM26<up>+</up>
ID|FBal0068528
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004932	CLA 1 existence-uncertain gene	NAM 1 abnormal abdomen HM27	GSYM 1 a(1)HM27	DT 1 24 Dec 04	RESZ 1197	WT 1 Defined by incompletely characterized mutations that show an 'abnormal abdomen' phenotype	GLOC 1 1-	ALESR 2	REF 3	
GSYM|a(1)HM27
DT|24 Dec 04
ID|FBgn0004932
CLA|existence-uncertain gene
SYN|l(1)HM27
NAM|abnormal abdomen HM27
GLOC|1-
GLC|Maps near @y@.
WT|Defined by incompletely characterized mutations that show an 'abnormal abdomen' phenotype.
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|2
REFM|FBrf0024658
|Mayoh and Suzuki
|1973
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

ALESR
{
ASYM|a(1)HM27<up>1</up>
ID|FBal0000060
MU|ethyl methanesulfonate
PHC|visible | recessive | conditional cs
PHM|abdominal tergite
|abdominal sternite
PHI|Missing or reduced sternites; missing or angled
|tergites; black specks on ventral surface of abdomen; more severe at
|17<up>o</up>C than at 22<up>o</up>C. Viability slightly reduced at
|17<up>o</up>C relative to that at 22<up>o</up>C.
REF|FBrf0066905
|FBrf0024658
}

ALESR
{
ASYM|a(1)HM27<up>+</up>
ID|FBal0068529
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004933	CLA 1 Gene	NAM 1 abnormal abdomen (2) 48	GSYM 1 a(2)48	DT 1 24 Dec 04	RESZ 4094	WT 1 Defined by incompletely characterized mutations that show an 'abnormal abdomen' phenotype	GLOC 1 2-	ALESR 5	REF 5	
GSYM|a(2)48
DT|24 Dec 04
ID|FBgn0004933
NAM|abnormal abdomen (2) 48
GLOC|2-
DIS|Zimmermann, 1948.
AM|Genetic relations not worked out.
PEVR|T(1;2)N<up>264-9</up>
WT|Defined by incompletely characterized mutations that show an 'abnormal abdomen' phenotype.
WTI|a(1)48
|a(3)48
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|2
REFM|FBrf0009915
|Zimmermann
|1954
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0020044
|Lindsley and Grell
|1968
|2
REFM|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
|0
}

REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
WTI|a(1)48 (data from @a(2)48<up>48</up>@)
|a(3)48 (data from @a(2)48<up>A51</up>@)
}

ALESR
{
ASYM|a(2)48<up>48</up>
SYN|a(2)48
ID|FBal0057944
OTH|Penetrance 7%. Also shows maternal effect.
PHC|visible | recessive
|viable | good
|fertile | good
PHM|abdominal tergite
|abdominal sternite
PHI|Abdominal irregularities most frequently involve
|anterior segments.
|RK3.
REF|FBrf0020044
|FBrf0066905
|FBrf0063299
REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
AFC|a(2)48<up>A51</up>
MU|spontaneous
GIC2|enhanceable by @a(1)48<up>48</up>@
|enhanceable by @a(1)48<up>50</up>@
PHC|viable
|fertile
SYN|a(2)48
}

}

ALESR
{
ASYM|a(2)48<up>50</up>
SYN|a(2)50
ID|FBal0000061
DIS|Zimmerman, 1950.
OTH|Penetrance 7%.
MU|spontaneous
GIC2|enhanceable by @a(1)48<up>50</up>@
NAF|Stated to be lost.
PHC|viable | good
|fertile | good
|visible | recessive
|visible | recessive | maternal effect
PHM|abdomen | adult
PHI|Abdominal irregularities most frequently involve
|anterior segments.
|RK3.
REF|FBrf0009915
|FBrf0063299
REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
MU|spontaneous
NAF|Stated to be lost.
SYN|a(2)50
}

}

ALESR
{
ASYM|a(2)48<up>51</up>
SYN|a(2)51
ID|FBal0000062
DIS|Zimmerman, 1951.
MU|spontaneous
NAF|Stated to be lost.
PHC|visible | recessive | maternal effect
PHI|Penetrance 50%.
|RK3.
REF|FBrf0009915
|FBrf0063299
REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
MU|spontaneous
NAF|Stated to be lost.
SYN|a(2)51
}

}

ALESR
{
ASYM|a(2)48<up>A51</up>
SYN|A(2)51
|A(2)48<up>51</up>
ID|FBal0000063
DIS|Zimmerman, 1951.
MU|spontaneous
GIC|enhancer | dominant of @a(3)48<up>1</up>@
PHC|wild-type
PHI|RK3.
REF|FBrf0009915
|FBrf0063299
REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
AFC|a(2)48<up>48</up>
MU|spontaneous
GIC|enhancer of @a(3)48<up>1</up>@
GII|Increases the penetrance of @a(2)48<up>48</up>@ and @a(3)48<up>1</up>@.
SYN|A(2)51
}

}

ALESR
{
ASYM|a(2)48<up>+</up>
ID|FBal0071525
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004934	CLA 1 Gene	NAM 1 abnormal abdomen (3) 48	GSYM 1 a(3)48	DT 1 24 Dec 04	RESZ 2174	WT 1 Defined by incompletely characterized mutations that show an 'abnormal abdomen' phenotype	GLOC 1 3-	ALESR 2	REF 4	
GSYM|a(3)48
DT|24 Dec 04
ID|FBgn0004934
NAM|abnormal abdomen (3) 48
GLOC|3-
DIS|Zimmermann, 1948.
WT|Defined by incompletely characterized mutations that show an 'abnormal abdomen' phenotype.
WTI|a(1)48
|a(2)48
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|2
REFM|FBrf0009915
|Zimmermann
|1954
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
|0
}

REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
WTI|a(1)48 (data from @a(3)48<up>1</up>@)
|a(2)48 (data from @a(3)48<up>1</up>@)
}

ALESR
{
ASYM|a(3)48<up>1</up>
SYN|a(3)48
ID|FBal0000064
MU|spontaneous
GIC2|enhanceable by @a(1)48<up>50</up>@
|enhanceable by @a(2)48<up>A51</up>@
PHC|visible | recessive | maternal effect
|viable | good
|fertile | good
PHM|abdominal tergite
|abdominal sternite
PHI|Incompletely penetrant.  Affects only 2.5% of progeny.
|Irregularities most frequently involve posterior
|segments of abdomen.
|RK3.
REF|FBrf0066905
|FBrf0009915
|FBrf0063299
REFDSR
{
RDID|FBrf0063299
|Zoologisches Institut der Universitat Gottingen
|1952
MU|spontaneous
GIC2|enhanceable by @a(1)48<up>48</up>@
|enhanceable by @a(1)48<up>50</up>@
|enhanceable by @a(2)48<up>A51</up>@
PHC|viable
|fertile
SYN|a(3)48
}

}

ALESR
{
ASYM|a(3)48<up>+</up>
ID|FBal0068530
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0004929	CLA 1 existence-uncertain gene	NAM 1 Abnormal abdomen polygenic	GSYM 1 A-p	DT 1 25 Dec 04	RESZ 1135	ALESR 1	REF 7	
GSYM|A-p
DT|25 Dec 04
ID|FBgn0004929
CLA|existence-uncertain gene
SYN|AA
|Asy: Asymmetric
|Asymmetric
NAM|Abnormal abdomen polygenic
DIS|Sobels, Sep. 1949.
GLC|Polygenic.
PHP|Incomplete mediodorsal fusion and onesided reduction
|of tergites. When more than one tergite is abnormal,
|spiral segmentation types are most frequent.
|Expression strongly dependent on environment.
|Penetrance and expressivity correlated (Bezem and
|Sobels, 1953). In strains selected for penetrance
|of @A-p@, mediodorsal fusion or asymmetrical reduction
|of head and thorax also occur.
REF
{
REFM|FBrf0008552
|Sobels
|1952
|0
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|2
REFM|FBrf0008585
|Sobels
|1952
|0
REFM|FBrf0063879
|Sobels et al.
|1951
|0
REFM|FBrf0063880
|Sobels
|1950
|0
REFM|FBrf0009221
|Bezem and Sobels
|1953
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

ALESR
{
ASYM|A-p<up>+</up>
ID|FBal0071526
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0011293	CLA 1 Gene	NAM 1 antennal protein 10	GSYM 1 a10	DT 1 24 Dec 04	RESZ 3972	PDOM 1 INTERPRO:IPR005055 == Insect pheromone-binding protein A10/OS-D	PTD 1	DBA 6	FNC 1 sensory perception of chemical stimulus	CLOC 1 73E4	ALESR 1	REF 13	
GSYM|a10
PTD
DT|24 Dec 04
ID|FBgn0011293
UAB|Deficiency: Df(3L)st7 (inferred from cytology)
|Duplication: Dp(3;3)st<up>+</up>g18 (inferred from cytology)
SYN|CG6642
|OS-D
|A10
|Phk-1
|OS-D/A10
|Pherokine 1
|Os-D
ID2|FBgn0010402
NAM|antennal protein 10
CLOC|73E4
|Limits computationally determined from genome sequence between @P{PZ}Baldspot<up>02281</up>@ and @P{PZ}blot<up>01658</up>@
CYC|Experimentally determined: 73F, 83C--D
FNC|sensory perception of chemical stimulus ; GO:0007606
PDOM|IPR005055 == Insect pheromone-binding protein A10/OS-D
ENZ|odorant binding ; GO:0005549
|pheromone binding ; GO:0005550
|odorant binding ; GO:0005549 | non-traceable author statement
|pheromone binding ; GO:0005550 | non-traceable author statement
|carrier activity ; GO:0005386 | inferred from electronic annotation
|carrier activity ; GO:0005386
DBA|NA:AE003525
|PA:AAF49381
|NA:U02546
|PA:AAA21358
|NA:U05244
|PA:AAC46473
PAC|UniProt_Swiss_Prot:Q27377
ASQ|FBan0006642
REF
{
REFM|FBrf0075175
|Hekmat-Scafe
|1995
|9
REFM|FBrf0117975
|McKenna
|1993.10.15
|9
REFM|FBrf0126686
|Milshina
|1999.11
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0073868
|McKenna et al.
|1994
|0
REFM|FBrf0161599
|Sabatier et al.
|2003
|0
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0124368
|Swiss-Prot Project Members
|1997.2.1
|9
REFM|FBrf0127265
|Park et al.
|2000
|0
REFM|FBrf0118974
|Pikielny
|1994.1.18
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0066935
|Pikielny et al.
|1994
|0
}

REFDSR
{
RDID|FBrf0066935
|Pikielny et al.
|1994
WT|@a10@ is one of seven clones that have been identified from subtracted
|cDNA libraries, containing antennal cDNA from which head cDNAs have
|been subtracted. The protein is expressed in
|subsets of olfactory hairs and have a putative signal peptide at the
|amino terminus.
}

REFDSR
{
RDID|FBrf0073868
|McKenna et al.
|1994
CLOC|73F (determined by in situ hybridization)
OTH|Isolated from a subtracted antennal cDNA library enriched for cDNAs
|expressed in the antennae but not the rest of the head or body of adult
|flies.
PHP|An @a10@ cDNA has been cloned and sequenced.
SYN|OS-D
}

REFDSR
{
RDID|FBrf0075175
|Hekmat-Scafe
|1995
CLOC|73F (stated as revision)
WT|Encodes a putative olfactant binding protein.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
FNC|sensory perception of chemical stimulus ; GO:0007606 | inferred from sequence similarity with EMBL:AF070961
}

REFDSR
{
RDID|FBrf0117975
|McKenna
|1993.10.15
ENZ|pheromone binding ; GO:0005550 | non-traceable author statement
CLOC|83C--D
SYN|OS-D
}

REFDSR
{
RDID|FBrf0118974
|Pikielny
|1994.1.18
CLOC|73F
}

REFDSR
{
RDID|FBrf0124368
|Swiss-Prot Project Members
|1997.2.1
ENZ|odorant binding ; GO:0005549 | non-traceable author statement
GPD|odorant binding protein A10
}

REFDSR
{
RDID|FBrf0127265
|Park et al.
|2000
SYN|A10
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
ENZ|carrier activity ; GO:0005386 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0161599
|Sabatier et al.
|2003
SYN|Phk-1
|OS-D/A10
|Pherokine 1
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

ALESR
{
ASYM|a10<up>+</up>
ID|FBal0071527
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0025723	CLA 1 Gene	GSYM 1 A122	DT 1 25 Dec 04	RESZ 2070	CLOC 1 [38E3--43E14]	ALESR 2	REF 2	
GSYM|A122
DT|25 Dec 04
ID|FBgn0025723
CLOC|[38E3--43E14]
|Left limit from recombination mapping relative to Bl (FBrf0104442)
|Right limit from recombination mapping relative to cn (FBrf0104442)
GLOC|2-?
|Maps to the right of b
|Maps to the right of Bl
|Maps to the left of cn
|Maps to the left of L
GLC|Maps close to @cn@, and closer to @Bl@ than to @L@.
REF
{
REFM|FBrf0104442
|Go and Artavanis-Tsakonas
|1998
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0104442
|Go and Artavanis-Tsakonas
|1998
GLOC|2-?
|Maps to the right of b
|Maps to the right of Bl
|Maps to the left of cn
|Maps to the left of L
GLC|Maps close to @cn@, and closer to @Bl@ than to @L@.
OTH|Identification: Screen for genetic modifiers of @N<up>Ax-16</up>@.
WTI|N (data from @A122<up>A122</up>@)
}

ALESR
{
ASYM|A122<up>A122</up>
SYN|A122
ID|FBal0093527
PHC|lethal | larval | recessive
REF|FBrf0104442
REFDSR
{
RDID|FBrf0104442
|Go and Artavanis-Tsakonas
|1998
MU|ethyl methanesulfonate
GIC|suppressor of visible phenotype of @N<up>Ax-16</up>@
|suppressor of visible phenotype of @N<up>Ax-9</up>@
GIA|suppressor of wing vein phenotype of @N<up>Ax-16</up>@
|suppressor of macrochaeta phenotype of @N<up>Ax-16</up>@
|suppressor of microchaeta phenotype of @N<up>Ax-16</up>@
|suppressor of macrochaeta phenotype of @N<up>Ax-9</up>@
GII|Suppresses the bristle and wing vein phenotypes of @N<up>Ax-16</up>@ and the
|'fewer bristle' phenotype of @N<up>Ax-9</up>@.
PHC|lethal | larval | recessive
SYN|A122
}

}

ALESR
{
ASYM|A122<up>+</up>
ID|FBal0093737
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0028965	CLA 1 Gene	GSYM 1 A16	DT 1 25 Dec 04	RESZ 2693	PTD 1	DBA 16	CLOC 1 34A4	ALESR 3	REF 5	
GSYM|A16
PTD
DT|25 Dec 04
ID|FBgn0028965
UAB|Duplication: Dp(2;2)GYL (inferred from cytology)
SYN|CG9933
|CG9933
ID2|FBgn0032468
CLOC|34A4
|Limits computationally determined from genome sequence between @P{lacW}l(2)k07015<up>k07015</up>@/@P{PZ}l(2)rK639<up>rK639</up>@ and @P{lacW}l(2)k11328<up>k11328</up>@/@P{lacW}l(2)k10105<up>k10105</up>@
CYC|Experimentally determined: 34A
DBA|NA:AA391464
|BDGP-DGC:LD10135
|NA:AA941120
|BDGP:LD25087.5prime
|NA:AC010214
|BDGP:BACR27F17
|NA:AE003638
|PA:AAF53239
|NA:AI109007
|BDGP:GH07495.3prime
|NA:AI109028
|BDGP:GH07525.3prime
|NA:AY122156
|PA:AAM52668
|BDGP-DGC:LD10135
|NA:CL868617
PAC|UniProt_TrEMBL:Q9VK43
ASQ|FBan0009933
REF
{
REFM|FBrf0112243
|Greig and O'Kane
|1999.10.21
|9
REFM|FBrf0104946
|FlyBase
|1996-
|9
REFM|FBrf0179797
|Bloomington Drosophila Stock Center
|2004.11.6
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0132177
|Gene Disruption Project members
|2001-
|9
}

REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
AM|Source for merge of: A16 CG9933
|Source for merge of A16 CG9933 was shared cDNA (LD25087.5prime) (date:030604).
}

REFDSR
{
RDID|FBrf0112243
|Greig and O'Kane
|1999.10.21
CLOC|34A (determined by in situ hybridization)
MD|Maps to clone: BACR27F17
|Identified with: GH07495.3prime
|Identified with: GH07525.3prime
|Identified with: LD25087.5prime
OTH|Identification: interacts with @G-i&agr;65A@ in a yeast two hybrid
|screen.
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: LD10135 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
SYN|CG9933
}

ALESR
{
ASYM|A16<up>e00533</up>
ID|FBal0162859
PHC|viable
|fertile
REF|FBrf0179797
REFDSR
{
RDID|FBrf0179797
|Bloomington Drosophila Stock Center
|2004.11.6
TRN|FBti0041406 == PBac{RB}A16<up>e00533</up>
MU|piggyBac transposase
PHC|viable
|fertile
}

}

ALESR
{
ASYM|A16<up>EY14223</up>
ID|FBal0162860
PHC|viable
|fertile
REF|FBrf0132177
REFDSR
{
RDID|FBrf0132177
|Gene Disruption Project members
|2001-
TRN|FBti0057765 == P{EPgy2}A16<up>EY14223</up>
PHC|viable
|fertile
}

}

ALESR
{
ASYM|A16<up>+</up>
ID|FBal0102311
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067327	CLA 1 Gene	GSYM 1 A23	DT 1 25 Dec 04	RESZ 1387	ALESR 2	REF 1	
GSYM|A23
DT|25 Dec 04
ID|FBgn0067327
REF
{
REFM|FBrf0150728
|Akieda and Merriam
|2001
|0
}

ALESR
{
ASYM|A23<up>A23</up>
SYN|A23
ID|FBal0148509
PHC|lethal with @Scer\GAL4<up>Act5C.PI</up>@
|eye color defective with @Scer\GAL4<up>GMR.PF</up>@
PHM|pigment cell with @Scer\GAL4<up>GMR.PF</up>@
PHI|Postmitotic adult bristles are normal in animals expressing @A23<up>A23</up>@
|under the control of @Scer\GAL4<up>B11</up>@.
|Eyes show partial pigment loss in animals expressing @A23<up>A23</up>@ under
|the control of @Scer\GAL4<up>GMR.PF</up>@.
REF|FBrf0150728
REFDSR
{
RDID|FBrf0150728
|Akieda and Merriam
|2001
TRN|FBti0027613 == P{Mae-UAS.6.11}A23<up>A23</up>
MU|P-element activity
PHC|lethal with @Scer\GAL4<up>Act5C.PI</up>@
|eye color defective with @Scer\GAL4<up>GMR.PF</up>@
PHM|pigment cell with @Scer\GAL4<up>GMR.PF</up>@
PHI|Postmitotic adult bristles are normal in animals expressing @A23<up>A23</up>@
|under the control of @Scer\GAL4<up>B11</up>@.
|Eyes show partial pigment loss in animals expressing @A23<up>A23</up>@ under
|the control of @Scer\GAL4<up>GMR.PF</up>@.
SYN|A23
}

}

ALESR
{
ASYM|A23<up>+</up>
ID|FBal0150107
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0020515	CLA 1 Gene	GSYM 1 A3	DT 1 25 Dec 04	RESZ 1954	PTD 1	FNC 1 asymmetric protein localization	CEL 1 plasma membrane	WT 3 The expression pattern	CLOC 1 92B2--C3	ALESR 1	REF 5	
GSYM|A3
PTD
DT|25 Dec 04
ID|FBgn0020515
UAB|Deficiency: Df(3R)I9
|Deficiency: Df(3R)Dl-BX12 (inferred from cytology)
|Duplication: Dp(3;3)C123.3 (inferred from cytology)
CLOC|92B2--C3
|Left limit from inclusion within Df(3R)ora<up>I9</up> (FBrf0093828)
|Right limit from inclusion within Df(3R)ora<up>I9</up> (FBrf0093828)
FNC|asymmetric protein localization ; GO:0008105
CEL|plasma membrane ; GO:0005886
WT|The expression pattern, cellular localization and loss of function
|phenotype of @A3@ strongly suggests @A3@ plays an important role in the
|asymmetric localization of @pros@ during mitosis.
ENZ|molecular_function unknown ; GO:0005554
|molecular_function unknown ; GO:0005554 | no biological data available
REF
{
REFM|FBrf0093828
|Shen
|1997.4.19
|9
REFM|FBrf0159398
|FlyBase Curators
|2002-
|9
REFM|FBrf0100478
|Jan
|1997
|1
REFM|FBrf0091690
|Shen et al.
|1997
|1
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0091690
|Shen et al.
|1997
FNC|asymmetric protein localization ; GO:0008105 | non-traceable author statement
CEL|plasma membrane ; GO:0005886 | non-traceable author statement
WT|The expression pattern, cellular localization and loss of function
|phenotype of @A3@ strongly suggests @A3@ plays an important role in the
|asymmetric localization of @pros@ during mitosis.
OTH|Identification: Yeast two hybrid screen for proteins that interact
|directly with @numb@ and @pros@.
}

REFDSR
{
RDID|FBrf0093828
|Shen
|1997.4.19
BMD|Df(3R)I9
}

REFDSR
{
RDID|FBrf0159398
|FlyBase Curators
|2002-
ENZ|molecular_function unknown ; GO:0005554 | no biological data available
}

ALESR
{
ASYM|A3<up>+</up>
ID|FBal0079507
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0028550	CLA 1 Gene	GSYM 1 A3-3	DT 1 25 Dec 04	RESZ 5258	PDOM 4 INTERPRO:IPR000837 == Fos transforming protein	PTD 1	DBA 13	FNC 1 regulation of transcription, DNA-dependent	CEL 1 nucleus	CLOC 1 1E5	ALESR 4	SK 2	REF 10	
GSYM|A3-3
PTD
DT|25 Dec 04
ID|FBgn0028550
UAB|Deficiency: Df(1)S39 (inferred from cytology)
|Duplication: Dp(1;3)sta (inferred from cytology)
SYN|CG11405
|CG11405
|EG:33C11.1
ID2|FBgn0026877
CLOC|1E5
|Limits computationally determined from genome sequence between @P{EP}EP1615@&@P{EP}EP964@ and P{EP}EG:114D9.1<up>EP1542</up>
CYC|Experimentally determined: 1F
FNC|regulation of transcription, DNA-dependent ; GO:0006355
CEL|nucleus ; GO:0005634
PDOM|IPR000837 == Fos transforming protein
|IPR004827 == Basic-leucine zipper (bZIP) transcription factor
|IPR008917 == Eukaryotic transcription factor, DNA-binding
|IPR011616 == bZIP transcription factor, bZIP_1
ENZ|DNA binding ; GO:0003677
|protein dimerization activity ; GO:0046983 | inferred from sequence similarity
|protein dimerization activity ; GO:0046983
|DNA binding ; GO:0003677 | inferred from electronic annotation
DBA|NA:AE003420
|PA:AAF45599
|NA:AI404815
|BDGP-DGC:GH24653
|NA:AL035331
|PA:CAA22962
|NA:AL121806
|PA:CAB65887
|NA:AW940950
|BDGP-DGC:GH24653
|NA:AY121628
|PA:AAM51955
|BDGP-DGC:GH24653
PAC|UniProt_TrEMBL:Q8MRE5
|UniProt_TrEMBL:Q9XZS8
ASQ|FBan0011405
REF
{
REFM|FBrf0125090
|Gatt and Ashburner
|2000.2.3
|9
REFM|FBrf0111592
|Heitzeberg
|1999.9.15
|9
REFM|FBrf0132177
|Gene Disruption Project members
|2001-
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0152056
|Fassler et al.
|2002
|0
REFM|FBrf0174218
|Boutros et al.
|2004
|9
REFM|FBrf0109889
|Heitzeberg et al.
|1999
|1
REFM|FBrf0174215
|FlyBase Curators et al.
|2004-
|9
REFM|FBrf0104946
|FlyBase
|1996-
|9
}

REFDSR
{
RDID|FBrf0109889
|Heitzeberg et al.
|1999
}

REFDSR
{
RDID|FBrf0111592
|Heitzeberg
|1999.9.15
CLOC|1F
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: GH24653 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0125090
|Gatt and Ashburner
|2000.2.3
AM|Source for merge of: A3-3 EG:33C11.1
}

REFDSR
{
RDID|FBrf0133222
|Benos
|2000.12.13
SYN|CG11405
|EG:33C11.1
}

REFDSR
{
RDID|FBrf0135823
|Benos et al.
|2001
MD|Identified with: GH24653
SYN|EG:33C11.1
}

REFDSR
{
RDID|FBrf0141117
|Benos
|1999.12.28
MD|Gene order: In direction of increasing cytology: CG14628+ CG32859- CG11378+ CG11384-
|Gene order: CG11379+ CG14627+ CG14626+ CG11380+
|Gene order: CG14625+ CG14624+ CG11382+ CG11398-
|Gene order: CG3638- CG11403- A3-3-
SYN|EG:33C11.1
}

REFDSR
{
RDID|FBrf0152056
|Fassler et al.
|2002
ENZ|protein dimerization activity ; GO:0046983 | inferred from sequence similarity
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

REFDSR
{
RDID|FBrf0174215
|FlyBase Curators et al.
|2004-
ENZ|DNA binding ; GO:0003677 | inferred from electronic annotation
FNC|regulation of transcription, DNA-dependent ; GO:0006355 | inferred from electronic annotation
CEL|nucleus ; GO:0005634 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0174218
|Boutros et al.
|2004
PHP|RNAi generated by PCR using primers directed to this gene causes a
|cell growth and viability phenotype when assayed in Kc167 and S2R<up>+</up>
|cells.
}

ALESR
{
ASYM|A3-3<up>1</up>
ID|FBal0100468
PHC|lethal | larval | partially | recessive
|female fertile | reduced
PHI|Homozygotes show reduced viability during larval development.
|Mutant females mated to wild-type males lay eggs, but most of them
|do not show any development.  The percentage of defective eggs
|increases with the age of the female flies.
REF|FBrf0109889
REFDSR
{
RDID|FBrf0109889
|Heitzeberg et al.
|1999
MD|@P{lArB}@ insertion in an intron.
TRN|FBti0013984 == P{lArB}A3-3<up>1</up>
MU|P-element activity
PHC|lethal | larval | partially | recessive
|female fertile | reduced
PHI|Homozygotes show reduced viability during larval development.
|Mutant females mated to wild-type males lay eggs, but most of them
|do not show any development.  The percentage of defective eggs
|increases with the age of the female flies.
SYN|unnamed
}

}

ALESR
{
ASYM|A3-3<up>BG02445</up>
ID|FBal0157523
REF|FBrf0104946
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
TRN|FBti0017722 == P{GT1}A3-3<up>BG02445</up>
MU|P-element activity
}

SK|FBst0012687
|P{w[+mGT]=GT1}A3-3[BG02445] w[1118]
}

ALESR
{
ASYM|A3-3<up>EY02562</up>
ID|FBal0157522
REF|FBrf0132177
REFDSR
{
RDID|FBrf0132177
|Gene Disruption Project members
|2001-
TRN|FBti0033171 == P{EPgy2}A3-3<up>EY02562</up>
MU|P-element activity
}

SK|FBst0015872
|y[1] P{w[+mC] y[+mDint2]=EPgy2}A3-3[EY02562] w[67c23]/FM7c
}

ALESR
{
ASYM|A3-3<up>+</up>
ID|FBal0101097
CLA|wild-type generic
}

SK|FBst0012687
|P{w[+mGT]=GT1}A3-3[BG02445] w[1118]
|FBst0015872
|y[1] P{w[+mC] y[+mDint2]=EPgy2}A3-3[EY02562] w[67c23]/FM7c
SKC|2
}
# EOR
GENR
{
RETE|ID 1 FBgn0020514	CLA 1 Gene	GSYM 1 A35	DT 1 25 Dec 04	RESZ 786	CLOC 1 54D4--E7	ALESR 1	REF 3	
GSYM|A35
DT|25 Dec 04
ID|FBgn0020514
UAB|Duplication: Dp(2;Y)53D;57C (inferred from cytology)
CLOC|54D4--E7
|Left limit from in situ hybridization (FBrf0093842)
|Right limit from in situ hybridization (FBrf0093842)
CYC|Experimentally determined: 54D4--E7
REF
{
REFM|FBrf0093842
|Foss
|1997.4.18
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0091815
|Foss et al.
|1997
|1
}

REFDSR
{
RDID|FBrf0091815
|Foss et al.
|1997
SYN|unnamed
}

REFDSR
{
RDID|FBrf0093842
|Foss
|1997.4.18
CLOC|54D4--E7 (determined by in situ hybridization)
}

ALESR
{
ASYM|A35<up>+</up>
ID|FBal0079506
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0024506	CLA 1 Gene	GSYM 1 A359	DT 1 25 Dec 04	RESZ 768	ALESR 1	REF 5	
GSYM|A359
DT|25 Dec 04
ID|FBgn0024506
REV|FBrf0128450
REF
{
REFM|FBrf0101072
|Dobens and Raftery
|1998
|1
REFM|FBrf0106423
|Dobens et al.
|1999
|1
REFM|FBrf0102087
|Dobens
|1998.3.17
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0128450
|Dobens and Raftery
|2000
|2
}

REFDSR
{
RDID|FBrf0101072
|Dobens and Raftery
|1998
OTH|@dpp@ target gene.
}

REFDSR
{
RDID|FBrf0102087
|Dobens
|1998.3.17
LOI|P{lArB}A359.1M3
}

ALESR
{
ASYM|A359<up>+</up>
ID|FBal0088440
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0067326	CLA 1 Gene	GSYM 1 A43	DT 1 25 Dec 04	RESZ 1785	ALESR 2	REF 1	
GSYM|A43
DT|25 Dec 04
ID|FBgn0067326
REF
{
REFM|FBrf0150728
|Akieda and Merriam
|2001
|0
}

ALESR
{
ASYM|A43<up>A43</up>
SYN|A43
ID|FBal0148508
PHC|lethal with @Scer\GAL4<up>Act5C.PI</up>@
|viable with @Scer\GAL4<up>byn-Gal4</up>@
|visible with @Scer\GAL4<up>GMR.PF</up>@
|eye color defective with @Scer\GAL4<up>GMR.PF</up>@
PHM|eye with @Scer\GAL4<up>GMR.PF</up>@
|pigment cell with @Scer\GAL4<up>GMR.PF</up>@
PHI|Postmitotic adult bristles are normal in animals expressing @A43<up>A43</up>@
|under the control of @Scer\GAL4<up>B11</up>@.
|Eyes are small and show partial pigment loss in animals expressing
|@A43<up>A43</up>@ under the control of @Scer\GAL4<up>GMR.PF</up>@.
REF|FBrf0150728
REFDSR
{
RDID|FBrf0150728
|Akieda and Merriam
|2001
TRN|FBti0027612 == P{Mae-UAS.6.11}A43<up>A43</up>
MU|P-element activity
PHC|lethal with @Scer\GAL4<up>Act5C.PI</up>@
|viable with @Scer\GAL4<up>byn-Gal4</up>@
|visible with @Scer\GAL4<up>GMR.PF</up>@
|eye color defective with @Scer\GAL4<up>GMR.PF</up>@
PHM|eye with @Scer\GAL4<up>GMR.PF</up>@
|pigment cell with @Scer\GAL4<up>GMR.PF</up>@
PHI|Postmitotic adult bristles are normal in animals expressing @A43<up>A43</up>@
|under the control of @Scer\GAL4<up>B11</up>@.
|Eyes are small and show partial pigment loss in animals expressing
|@A43<up>A43</up>@ under the control of @Scer\GAL4<up>GMR.PF</up>@.
SYN|A43
}

}

ALESR
{
ASYM|A43<up>+</up>
ID|FBal0150106
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0027096	CLA 1 Gene	GSYM 1 A45	DT 1 25 Dec 04	RESZ 195	ALESR 1	REF 1	
GSYM|A45
DT|25 Dec 04
ID|FBgn0027096
REF
{
REFM|FBrf0108059
|Vosshall et al.
|1999
|0
}

ALESR
{
ASYM|A45<up>+</up>
ID|FBal0097824
CLA|wild-type generic
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0011294	CLA 1 Gene	NAM 1 antennal protein 5	GSYM 1 a5	DT 1 24 Dec 04	RESZ 3559	PDOM 2 INTERPRO:IPR001858 == Phosphatidylethanolamine-binding protein	PTD 1	DBA 8	FNC 1 signal transduction	CLOC 1 22A1	ALESR 1	REF 10	
GSYM|a5
PTD
ARGS
DT|24 Dec 04
ID|FBgn0011294
UAB|Deficiency: Df(2L)frtz17 (inferred from cytology)
|Duplication: Dp(2;2)M<up>+</up>Su<up>24+</up>-1 (inferred from cytology)
SYN|CG5430
|A5
NAM|antennal protein 5
CLOC|22A1
|Limits computationally determined from genome sequence between @P{PZ}l(2)10685<up>10685</up>@&@P{lacW}l(2)k00619<up>k00619</up>@ and @P{lacW}RFeSP<up>k11704</up>@
CYC|Experimentally determined: 22A--B
FNC|signal transduction ; GO:0007165
PDOM|IPR001858 == Phosphatidylethanolamine-binding protein
|IPR008914 == PEBP
MD|Maps to clone: DS08613
|Maps to clone: BACR16D07
ENZ|phosphatidylethanolamine binding ; GO:0008429 | non-traceable author statement
|kinase inhibitor activity ; GO:0019210 | inferred from electronic annotation
|kinase inhibitor activity ; GO:0019210
|phosphatidylethanolamine binding ; GO:0008429
|phosphatidylethanolamine binding ; GO:0008429 | inferred from sequence similarity with UniProt:P31044
DBA|NA:AC004439
|BDGP:DS08613
|NA:AC092221
|BDGP:BACR16D07
|NA:AE003586
|PA:AAF51385
|NA:U05243
|PA:AAC46472
PAC|UniProt_Swiss_Prot:P54185
ASQ|FBan0005430
REF
{
REFM|FBrf0126686
|Milshina
|1999.11
|9
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0126682
|Li
|1999.11
|9
REFM|FBrf0141153
|Swiss-Prot Project Members
|1996.10.1
|9
REFM|FBrf0161459
|Mi et al.
|2003.9.9
|9
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0118975
|Pikielny
|1994.1.18
|9
REFM|FBrf0127265
|Park et al.
|2000
|0
REFM|FBrf0105495
|FlyBase
|1992-
|9
REFM|FBrf0066935
|Pikielny et al.
|1994
|0
}

REFDSR
{
RDID|FBrf0066935
|Pikielny et al.
|1994
PHP|@a5@ is one of seven clones that have been identified from subtracted
|cDNA libraries, containing antennal cDNA from which head cDNAs have
|been subtracted. The protein is expressed in
|subsets of olfactory hairs and have a putative signal peptide at the
|amino terminus. @a5@ protein is highly similar both to vertebrate
|brain proteins that bind hydrophobic ligands and to yeast and nematode
|proteins.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ENZ|phosphatidylethanolamine binding ; GO:0008429 | inferred from sequence similarity with UniProt:P31044
MD|Maps to clone: DS08613
|Maps to clone: BACR16D07
}

REFDSR
{
RDID|FBrf0118975
|Pikielny
|1994.1.18
CLOC|22A--B
}

REFDSR
{
RDID|FBrf0126682
|Li
|1999.11
AM|Source for identity of: a5 CG5430
}

REFDSR
{
RDID|FBrf0127265
|Park et al.
|2000
SYN|A5
}

REFDSR
{
RDID|FBrf0141153
|Swiss-Prot Project Members
|1996.10.1
ENZ|phosphatidylethanolamine binding ; GO:0008429 | non-traceable author statement
GPD|odorant binding protein A5
}

REFDSR
{
RDID|FBrf0161459
|Mi et al.
|2003.9.9
ENZ|kinase inhibitor activity ; GO:0019210 | inferred from electronic annotation
FNC|signal transduction ; GO:0007165 | inferred from electronic annotation
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

ALESR
{
ASYM|a5<up>+</up>
ID|FBal0068531
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0023130	CLA 1 Gene	GSYM 1 a6	DT 1 24 Dec 04	RESZ 3660	PTD 1	DBA 16	FNC 1 embryonic development (sensu Insecta)	CEL 1 cellular_component unknown	CLOC 1 2B7	ALESR 2	REF 14	
GSYM|a6
PTD
ARGS
DT|24 Dec 04
ID|FBgn0023130
UAB|Deficiency: Df(1)A94 (inferred from cytology)
|Duplication: Dp(1;Y)2E (inferred from cytology)
SYN|CG3771
|CG3771
|CG3771
|EG:9D2.3
CLOC|2B7
|Limits computationally determined from genome sequence between @P{EP}br<up>EP1515</up>@ and @P{EP}EP1444@/@P{EP}CG14818<up>EP1190</up>@
CYC|Experimentally determined: 2B6--8
FNC|embryonic development (sensu Insecta) ; GO:0001700
CEL|cellular_component unknown ; GO:0008372
ENZ|odorant binding ; GO:0005549
|odorant binding ; GO:0005549 | non-traceable author statement
DBA|NA:AA439160
|BDGP-DGC:LD13641
|NA:AE003421
|PA:AAF45661
|NA:AL031025
|PA:CAA19836
|EDGP:9D2
|NA:AW942280
|BDGP-DGC:LD13641
|NA:AY069426
|PA:AAL39571
|BDGP-DGC:LD13641
|NA:Y16065
|PA:CAA76017
|NA:Y16066
|PA:CAA76018
PAC|UniProt_Swiss_Prot:O46341
ASQ|FBan0003771
REF
{
REFM|FBrf0135823
|Benos et al.
|2001
|0
REFM|FBrf0159398
|FlyBase Curators
|2002-
|9
REFM|FBrf0126686
|Milshina
|1999.11
|9
REFM|FBrf0123119
|Makunin et al.
|1999
|0
REFM|FBrf0179438
|Schwartz et al.
|2004
|0
REFM|FBrf0126705
|FamiliarityBreedsContempt
|1999.11
|9
REFM|FBrf0133223
|Benos
|2000.12.13
|9
REFM|FBrf0133222
|Benos
|2000.12.13
|9
REFM|FBrf0125078
|BDGP Project Members
|2000-
|9
REFM|FBrf0127005
|Benos et al.
|2000
|2
REFM|FBrf0166452
|Giot
|2003
|9
REFM|FBrf0173176
|Peter
|2002
|9
REFM|FBrf0117663
|Makunin
|1997.12.30
|9
REFM|FBrf0105495
|FlyBase
|1992-
|9
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ENZ|odorant binding ; GO:0005549 | non-traceable author statement
MD|Maps to clone: 9D2
}

REFDSR
{
RDID|FBrf0117663
|Makunin
|1997.12.30
CLOC|2B6--8
}

REFDSR
{
RDID|FBrf0123119
|Makunin et al.
|1999
FNC|embryonic development (sensu Insecta) ; GO:0001700 | inferred from expression pattern
}

REFDSR
{
RDID|FBrf0125078
|BDGP Project Members
|2000-
MD|Identified with: LD13641 (BDGP-DGC)
}

REFDSR
{
RDID|FBrf0133222
|Benos
|2000.12.13
SYN|CG3771
|EG:9D2.3
}

REFDSR
{
RDID|FBrf0133223
|Benos
|2000.12.13
SYN|EG:9D2.3
}

REFDSR
{
RDID|FBrf0135823
|Benos et al.
|2001
MD|Identified with: LD13641
SYN|EG:9D2.3
}

REFDSR
{
RDID|FBrf0159398
|FlyBase Curators
|2002-
CEL|cellular_component unknown ; GO:0008372 | no biological data available
}

REFDSR
{
RDID|FBrf0166452
|Giot
|2003
}

REFDSR
{
RDID|FBrf0179438
|Schwartz et al.
|2004
SYN|CG3771
}

ALESR
{
ASYM|a6<up>t5581</up>
ID|FBal0159528
PHI|Mode of assay: In transgenic Drosophila
REF|FBrf0179438
REFDSR
{
RDID|FBrf0179438
|Schwartz et al.
|2004
MD|Construct: 30kb genomic clone containing the @CG3795@, @a6@, @CG14798@ and @b6@
|transcription units and part of the @CG32809@ transcription unit.
MU|in vitro construct | genomic fragment
CNS|FBtp0019009 == P{5581}
PHI|Mode of assay: In transgenic Drosophila
}

}

ALESR
{
ASYM|a6<up>+</up>
ID|FBal0087232
CLA|wild-type generic
REF|FBrf0105495
}

}
# EOR
GENR
{
RETE|ID 1 FBgn0026612	CLA 1 Gene	GSYM 1 A69	DT 1 25 Dec 04	RESZ 356	ALESR 1	REF 1	
GSYM|A69
DT|