embryonic/larval tracheal system
}
REF
{
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
REFM|FBrf0083714
|Meister and Braun
|1995.10
REFM|FBrf0102844
|Harvie et al.
|1998
REFM|FBrf0103143
|Jackle and Janning
|1998.8.10
}
ALESR
{
ASYM|FBal0137262==eyc04012b
REFDSR
{
RDID|FBrf0141505
|Sang and Ready
|2002
PHP|FBal0137262==eyc04012b homozygotes and
| FBal0137262==eyc04012b/FBab0002027==Df(2R)Px2 animals show
|disturbances in rhabdomere topology similar to the
| FBal0137261==eyc1 phenotype.
|FBal0137262==eyc04012b animals show mild fusion of the abdominal tergites.
PHM|(with Df(2R)Px2) rhabdomere
|rhabdomere
|abdominal tergite
}
REF
{
REFM|FBrf0141505
|Sang and Ready
|2002
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0019536 ICL 1 1360 SYM 1 1360{}17 ASTR 1 - CLOC 1 2B1-2B1 REF 1 2 DT 1 21 Aug 2003 RESZ 345
ID|FBti0019536
SYM|1360{}17
SYN|TE19536
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}17
CLOC|2B1-2B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003421.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019546 ICL 1 1360 SYM 1 1360{}27 ASTR 1 - CLOC 1 3B1-3B2 REF 1 2 DT 1 21 Aug 2003 RESZ 345
ID|FBti0019546
SYM|1360{}27
SYN|TE19546
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}27
CLOC|3B1-3B2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003425.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019595 ICL 1 1360 SYM 1 1360{}76 ASTR 1 - CLOC 1 6C12-6C12 REF 1 2 DT 1 21 Aug 2003 RESZ 347
ID|FBti0019595
SYM|1360{}76
SYN|TE19595
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}76
CLOC|6C12-6C12
LOCB|genomic location inferred from flanking sequence
DBAF|AE003438.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019613 ICL 1 1360 SYM 1 1360{}94 ASTR 1 - CLOC 1 9B1-9B1 REF 1 2 DT 1 21 Aug 2003 RESZ 345
ID|FBti0019613
SYM|1360{}94
SYN|TE19613
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}94
CLOC|9B1-9B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003449.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019634 ICL 1 1360 SYM 1 1360{}115 ASTR 1 - CLOC 1 11C1-11C1 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019634
SYM|1360{}115
SYN|TE19634
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}115
CLOC|11C1-11C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003490.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019637 ICL 1 1360 SYM 1 1360{}136 ASTR 1 - CLOC 1 13B4-13B4 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019637
SYM|1360{}136
SYN|TE19637
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}136
CLOC|13B4-13B4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003498.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019639 ICL 1 1360 SYM 1 1360{}154 ASTR 1 - CLOC 1 16F7-16F7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019639
SYM|1360{}154
SYN|TE19639
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}154
CLOC|16F7-16F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003507.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019662 ICL 1 1360 SYM 1 1360{}190 ASTR 1 - CLOC 1 19E7-19E7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019662
SYM|1360{}190
SYN|TE19662
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}190
CLOC|19E7-19E7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003569.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019709 ICL 1 1360 SYM 1 1360{}237 ASTR 1 - CLOC 1 20A5-20A5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019709
SYM|1360{}237
SYN|TE19709
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}237
CLOC|20A5-20A5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003122.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019717 ICL 1 1360 SYM 1 1360{}245 ASTR 1 - CLOC 1 20B1-20B1 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019717
SYM|1360{}245
SYN|TE19717
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}245
CLOC|20B1-20B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003574.5
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019770 ICL 1 1360 SYM 1 1360{}389 ASTR 1 - CLOC 1 35F1-35F1 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019770
SYM|1360{}389
SYN|TE19770
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}389
CLOC|35F1-35F1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003650.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019771 ICL 1 1360 SYM 1 1360{}396 ASTR 1 - CLOC 1 36C6-36C6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019771
SYM|1360{}396
SYN|TE19771
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}396
CLOC|36C6-36C6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003654.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019780 ICL 1 1360 SYM 1 1360{}420 ASTR 1 - CLOC 1 38A3-38A3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019780
SYM|1360{}420
SYN|TE19780
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}420
CLOC|38A3-38A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003664.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019799 ICL 1 1360 SYM 1 1360{}441 ASTR 1 - CLOC 1 38C2-38C2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019799
SYM|1360{}441
SYN|TE19799
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}441
CLOC|38C2-38C2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003666.5
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019825 ICL 1 1360 SYM 1 1360{}478 ASTR 1 - CLOC 1 38F4-38F4 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019825
SYM|1360{}478
SYN|TE19825
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}478
CLOC|38F4-38F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003668.5
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019828 ICL 1 1360 SYM 1 1360{}483 ASTR 1 - CLOC 1 39A5-39A5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019828
SYM|1360{}483
SYN|TE19828
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}483
CLOC|39A5-39A5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003669.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019831 ICL 1 1360 SYM 1 1360{}493 ASTR 1 - CLOC 1 39D5-39D5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019831
SYM|1360{}493
SYN|TE19831
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}493
CLOC|39D5-39D5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003670.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019839 ICL 1 1360 SYM 1 1360{}502 ASTR 1 - CLOC 1 39E2-39E2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019839
SYM|1360{}502
SYN|TE19839
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}502
CLOC|39E2-39E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019840 ICL 1 1360 SYM 1 1360{}503 ASTR 1 - CLOC 1 39E2-39E2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019840
SYM|1360{}503
SYN|TE19840
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}503
CLOC|39E2-39E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019841 ICL 1 1360 SYM 1 1360{}504 ASTR 1 - CLOC 1 39E2-39E2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019841
SYM|1360{}504
SYN|TE19841
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}504
CLOC|39E2-39E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019842 ICL 1 1360 SYM 1 1360{}505 ASTR 1 - CLOC 1 39E2-39E2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019842
SYM|1360{}505
SYN|TE19842
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}505
CLOC|39E2-39E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019847 ICL 1 1360 SYM 1 1360{}517 ASTR 1 - CLOC 1 39F3-39F3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019847
SYM|1360{}517
SYN|TE19847
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}517
CLOC|39F3-39F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019243 ICL 1 1360 SYM 1 1360{}528 ASTR 1 - CLOC 1 40E3-40E3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019243
SYM|1360{}528
SYN|TE19243
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}528
CLOC|40E3-40E3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003782.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019857 ICL 1 1360 SYM 1 1360{}542 ASTR 1 - CLOC 1 40F4-40F4 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019857
SYM|1360{}542
SYN|TE19857
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}542
CLOC|40F4-40F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003783.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019861 ICL 1 1360 SYM 1 1360{}548 ASTR 1 - CLOC 1 40F6-40F6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019861
SYM|1360{}548
SYN|TE19861
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}548
CLOC|40F6-40F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003783.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019864 ICL 1 1360 SYM 1 1360{}551 ASTR 1 - CLOC 1 40F7-40F7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019864
SYM|1360{}551
SYN|TE19864
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}551
CLOC|40F7-40F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003783.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019876 ICL 1 1360 SYM 1 1360{}569 ASTR 1 - CLOC 1 40F7-40F7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019876
SYM|1360{}569
SYN|TE19876
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}569
CLOC|40F7-40F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE002603.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019262 ICL 1 1360 SYM 1 1360{}573 ASTR 1 - CLOC 1 40F7-40F7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019262
SYM|1360{}573
SYN|TE19262
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}573
CLOC|40F7-40F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE002603.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019895 ICL 1 1360 SYM 1 1360{}608 ASTR 1 - CLOC 1 41E5-41E5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019895
SYM|1360{}608
SYN|TE19895
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}608
CLOC|41E5-41E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003788.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019896 ICL 1 1360 SYM 1 1360{}610 ASTR 1 - CLOC 1 41E5-41E5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019896
SYM|1360{}610
SYN|TE19896
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}610
CLOC|41E5-41E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003788.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019902 ICL 1 1360 SYM 1 1360{}636 ASTR 1 - CLOC 1 41F2-41F2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019902
SYM|1360{}636
SYN|TE19902
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}636
CLOC|41F2-41F2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019905 ICL 1 1360 SYM 1 1360{}644 ASTR 1 - CLOC 1 41F2-41F2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019905
SYM|1360{}644
SYN|TE19905
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}644
CLOC|41F2-41F2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019916 ICL 1 1360 SYM 1 1360{}661 ASTR 1 - CLOC 1 41F3-41F3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019916
SYM|1360{}661
SYN|TE19916
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}661
CLOC|41F3-41F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019917 ICL 1 1360 SYM 1 1360{}666 ASTR 1 - CLOC 1 41F3-41F3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019917
SYM|1360{}666
SYN|TE19917
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}666
CLOC|41F3-41F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019920 ICL 1 1360 SYM 1 1360{}676 ASTR 1 - CLOC 1 41F5-41F5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019920
SYM|1360{}676
SYN|TE19920
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}676
CLOC|41F5-41F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019922 ICL 1 1360 SYM 1 1360{}680 ASTR 1 - CLOC 1 41F5-41F5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019922
SYM|1360{}680
SYN|TE19922
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}680
CLOC|41F5-41F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019937 ICL 1 1360 SYM 1 1360{}700 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019937
SYM|1360{}700
SYN|TE19937
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}700
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019939 ICL 1 1360 SYM 1 1360{}702 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019939
SYM|1360{}702
SYN|TE19939
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}702
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019275 ICL 1 1360 SYM 1 1360{}709 ASTR 1 - CLOC 1 42A15-42A15 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0019275
SYM|1360{}709
SYN|TE19275
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}709
CLOC|42A15-42A15
LOCB|genomic location inferred from flanking sequence
DBAF|AE003789.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019969 ICL 1 1360 SYM 1 1360{}747 ASTR 1 - CLOC 1 42B1-42B2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019969
SYM|1360{}747
SYN|TE19969
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}747
CLOC|42B1-42B2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003789.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019978 ICL 1 1360 SYM 1 1360{}780 ASTR 1 - CLOC 1 44D3-44D3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019978
SYM|1360{}780
SYN|TE19978
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}780
CLOC|44D3-44D3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003836.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019279 ICL 1 1360 SYM 1 1360{}795 ASTR 1 - CLOC 1 46D1-46D2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019279
SYM|1360{}795
SYN|TE19279
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}795
CLOC|46D1-46D2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003831.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019992 ICL 1 1360 SYM 1 1360{}829 ASTR 1 - CLOC 1 51A4-51A4 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019992
SYM|1360{}829
SYN|TE19992
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}829
CLOC|51A4-51A4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003814.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019993 ICL 1 1360 SYM 1 1360{}835 ASTR 1 - CLOC 1 51F11-51F11 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0019993
SYM|1360{}835
SYN|TE19993
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}835
CLOC|51F11-51F11
LOCB|genomic location inferred from flanking sequence
DBAF|AE003811.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020017 ICL 1 1360 SYM 1 1360{}906 ASTR 1 - CLOC 1 62A2-62A2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0020017
SYM|1360{}906
SYN|TE20017
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}906
CLOC|62A2-62A2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003471.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020018 ICL 1 1360 SYM 1 1360{}907 ASTR 1 - CLOC 1 62A2-62A2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0020018
SYM|1360{}907
SYN|TE20018
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}907
CLOC|62A2-62A2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003471.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020116 ICL 1 1360 SYM 1 1360{}1005 ASTR 1 - CLOC 1 71B4-71B4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020116
SYM|1360{}1005
SYN|TE20116
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1005
CLOC|71B4-71B4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003532.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020143 ICL 1 1360 SYM 1 1360{}1032 ASTR 1 - CLOC 1 75A8-75A8 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020143
SYM|1360{}1032
SYN|TE20143
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1032
CLOC|75A8-75A8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003522.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020155 ICL 1 1360 SYM 1 1360{}1044 ASTR 1 - CLOC 1 75E1-75E2 REF 1 3 DT 1 21 Aug 2003 RESZ 464
ID|FBti0020155
SYM|1360{}1044
SYN|1360 1044
|TE20155
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1044
CLOC|75E1-75E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003519.3
}
REFDSR
{
RDID|FBrf0179132
|Bellen et al.
|2004
SYN|1360 1044
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0179132
|Bellen et al.
|2004
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020193 ICL 1 1360 SYM 1 1360{}1082 ASTR 1 - CLOC 1 78D4-78D4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020193
SYM|1360{}1082
SYN|TE20193
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1082
CLOC|78D4-78D4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003594.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020194 ICL 1 1360 SYM 1 1360{}1083 ASTR 1 - CLOC 1 78D4-78D4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020194
SYM|1360{}1083
SYN|TE20194
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1083
CLOC|78D4-78D4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003594.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020207 ICL 1 1360 SYM 1 1360{}1096 ASTR 1 - CLOC 1 80A1-80A1 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020207
SYM|1360{}1096
SYN|TE20207
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1096
CLOC|80A1-80A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003598.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020224 ICL 1 1360 SYM 1 1360{}1113 ASTR 1 - CLOC 1 80C5-80C5 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020224
SYM|1360{}1113
SYN|TE20224
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1113
CLOC|80C5-80C5
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020225 ICL 1 1360 SYM 1 1360{}1114 ASTR 1 - CLOC 1 80C5-80C5 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020225
SYM|1360{}1114
SYN|TE20225
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1114
CLOC|80C5-80C5
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020229 ICL 1 1360 SYM 1 1360{}1118 ASTR 1 - CLOC 1 80D1-80D1 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020229
SYM|1360{}1118
SYN|TE20229
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1118
CLOC|80D1-80D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020230 ICL 1 1360 SYM 1 1360{}1119 ASTR 1 - CLOC 1 80D1-80D1 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020230
SYM|1360{}1119
SYN|TE20230
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1119
CLOC|80D1-80D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020240 ICL 1 1360 SYM 1 1360{}1129 ASTR 1 - CLOC 1 80D3-80D3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020240
SYM|1360{}1129
SYN|TE20240
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1129
CLOC|80D3-80D3
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020243 ICL 1 1360 SYM 1 1360{}1132 ASTR 1 - CLOC 1 80D3-80D3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020243
SYM|1360{}1132
SYN|TE20243
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1132
CLOC|80D3-80D3
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020244 ICL 1 1360 SYM 1 1360{}1133 ASTR 1 - CLOC 1 80D3-80D3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020244
SYM|1360{}1133
SYN|TE20244
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1133
CLOC|80D3-80D3
LOCB|genomic location inferred from flanking sequence
DBAF|AE002656.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020249 ICL 1 1360 SYM 1 1360{}1138 ASTR 1 - CLOC 1 80D5-80D5 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020249
SYM|1360{}1138
SYN|TE20249
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1138
CLOC|80D5-80D5
LOCB|genomic location inferred from flanking sequence
DBAF|AE002656.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020271 ICL 1 1360 SYM 1 1360{}1160 ASTR 1 - CLOC 1 80E2-80E2 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020271
SYM|1360{}1160
SYN|TE20271
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1160
CLOC|80E2-80E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE002656.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020273 ICL 1 1360 SYM 1 1360{}1162 ASTR 1 - CLOC 1 80E3-80E3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020273
SYM|1360{}1162
SYN|TE20273
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1162
CLOC|80E3-80E3
LOCB|genomic location inferred from flanking sequence
DBAF|AE002656.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020282 ICL 1 1360 SYM 1 1360{}1171 ASTR 1 - CLOC 1 80F3-80F3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020282
SYM|1360{}1171
SYN|TE20282
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1171
CLOC|80F3-80F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE002665.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020291 ICL 1 1360 SYM 1 1360{}1180 ASTR 1 - CLOC 1 80F5-80F5 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020291
SYM|1360{}1180
SYN|TE20291
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1180
CLOC|80F5-80F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE002665.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020301 ICL 1 1360 SYM 1 1360{}1198 ASTR 1 - CLOC 1 82C2-82C2 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020301
SYM|1360{}1198
SYN|TE20301
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1198
CLOC|82C2-82C2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003606.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019290 ICL 1 1360 SYM 1 1360{}1201 ASTR 1 - CLOC 1 82C3-82C3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0019290
SYM|1360{}1201
SYN|TE19290
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1201
CLOC|82C3-82C3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003606.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020305 ICL 1 1360 SYM 1 1360{}1206 ASTR 1 - CLOC 1 82C4-82C4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020305
SYM|1360{}1206
SYN|TE20305
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1206
CLOC|82C4-82C4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003605.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019309 ICL 1 1360 SYM 1 1360{}1226 ASTR 1 - CLOC 1 83C4-83C4 REF 1 3 DT 1 21 Aug 2003 RESZ 450
ID|FBti0019309
SYM|1360{}1226
SYN|CR31553
|TE19309
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
SYN|CR31553
}
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1226
CLOC|83C4-83C4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003601.3
}
REF
{
REFM|FBrf0104946
|FlyBase
|1996-
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020322 ICL 1 1360 SYM 1 1360{}1257 ASTR 1 - CLOC 1 84E2-84E2 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020322
SYM|1360{}1257
SYN|TE20322
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1257
CLOC|84E2-84E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003676.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019330 ICL 1 1360 SYM 1 1360{}1258 ASTR 1 - CLOC 1 84E6-84E6 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0019330
SYM|1360{}1258
SYN|TE19330
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1258
CLOC|84E6-84E6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003677.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020323 ICL 1 1360 SYM 1 1360{}1270 ASTR 1 - CLOC 1 85B4-85B4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020323
SYM|1360{}1270
SYN|TE20323
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1270
CLOC|85B4-85B4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003680.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019361 ICL 1 1360 SYM 1 1360{}1299 ASTR 1 - CLOC 1 87B12-87B13 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019361
SYM|1360{}1299
SYN|TE19361
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1299
CLOC|87B12-87B13
LOCB|genomic location inferred from flanking sequence
DBAF|AE003696.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019418 ICL 1 1360 SYM 1 1360{}1408 ASTR 1 - CLOC 1 95A1-95A1 REF 1 3 DT 1 21 Aug 2003 RESZ 768
ID|FBti0019418
SYM|1360{}1408
SYN|CR31276
|TE19418
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
CLOC|95A1-95A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003743.3
}
REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
SYN|1360{}1408
CLOC|95A1-95A1
LOCB|genomic location inferred from flanking sequence
CC|"CR31276" was annotated as a "miscellaneous curator's observation" in
| release 3.1 of the genome annotation, but has been deleted in release 3.2
| as it corresponded to the FBti0019418==1360{}1408 insertion.
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019460 ICL 1 1360 SYM 1 1360{}1457 ASTR 1 - CLOC 1 99E3-99E3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0019460
SYM|1360{}1457
SYN|TE19460
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1457
CLOC|99E3-99E3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003773.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020393 ICL 1 1360 SYM 1 1360{}1463 ASTR 1 - CLOC 1 100A6-100A6 REF 1 3 DT 1 21 Aug 2003 RESZ 452
ID|FBti0020393
SYM|1360{}1463
SYN|CR31011
|TE20393
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
SYN|CR31011
}
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1463
CLOC|100A6-100A6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003775.2
}
REF
{
REFM|FBrf0104946
|FlyBase
|1996-
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020400 ICL 1 1360 SYM 1 1360{}1476 ASTR 1 - CLOC 1 102A1-102A1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020400
SYM|1360{}1476
SYN|TE20400
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1476
CLOC|102A1-102A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020403 ICL 1 1360 SYM 1 1360{}1479 ASTR 1 - CLOC 1 102A3-102A3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020403
SYM|1360{}1479
SYN|TE20403
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1479
CLOC|102A3-102A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020404 ICL 1 1360 SYM 1 1360{}1480 ASTR 1 - CLOC 1 102A3-102A3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020404
SYM|1360{}1480
SYN|TE20404
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1480
CLOC|102A3-102A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020405 ICL 1 1360 SYM 1 1360{}1481 ASTR 1 - CLOC 1 102A3-102A3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020405
SYM|1360{}1481
SYN|TE20405
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1481
CLOC|102A3-102A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019472 ICL 1 1360 SYM 1 1360{}1482 ASTR 1 - CLOC 1 102A4-102A4 REF 1 3 DT 1 21 Aug 2003 RESZ 439
ID|FBti0019472
SYM|1360{}1482
SYN|TE19472
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
CLOC|102A4-102A4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REFDSR
{
RDID|FBrf0179424
|Ryder et al.
|2004
SYN|1360{}1482
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0179424
|Ryder et al.
|2004
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019477 ICL 1 1360 SYM 1 1360{}1488 ASTR 1 - CLOC 1 102B1-102B1 REF 1 3 DT 1 21 Aug 2003 RESZ 439
ID|FBti0019477
SYM|1360{}1488
SYN|TE19477
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
CLOC|102B1-102B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REFDSR
{
RDID|FBrf0179424
|Ryder et al.
|2004
SYN|1360{}1488
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0179424
|Ryder et al.
|2004
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019479 ICL 1 1360 SYM 1 1360{}1491 ASTR 1 - CLOC 1 102B1-102B1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019479
SYM|1360{}1491
SYN|TE19479
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1491
CLOC|102B1-102B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019484 ICL 1 1360 SYM 1 1360{}1498 ASTR 1 - CLOC 1 102B5-102B5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019484
SYM|1360{}1498
SYN|TE19484
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1498
CLOC|102B5-102B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020414 ICL 1 1360 SYM 1 1360{}1502 ASTR 1 - CLOC 1 102B5-102B5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020414
SYM|1360{}1502
SYN|TE20414
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1502
CLOC|102B5-102B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020415 ICL 1 1360 SYM 1 1360{}1503 ASTR 1 - CLOC 1 102B5-102B5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020415
SYM|1360{}1503
SYN|TE20415
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1503
CLOC|102B5-102B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019485 ICL 1 1360 SYM 1 1360{}1504 ASTR 1 - CLOC 1 102B5-102B5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019485
SYM|1360{}1504
SYN|TE19485
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1504
CLOC|102B5-102B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020418 ICL 1 1360 SYM 1 1360{}1507 ASTR 1 - CLOC 1 102B6-102B7 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020418
SYM|1360{}1507
SYN|TE20418
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1507
CLOC|102B6-102B7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020419 ICL 1 1360 SYM 1 1360{}1508 ASTR 1 - CLOC 1 102B7-102B7 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020419
SYM|1360{}1508
SYN|TE20419
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1508
CLOC|102B7-102B7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019488 ICL 1 1360 SYM 1 1360{}1512 ASTR 1 - CLOC 1 102B8-102B8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019488
SYM|1360{}1512
SYN|TE19488
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1512
CLOC|102B8-102B8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020422 ICL 1 1360 SYM 1 1360{}1514 ASTR 1 - CLOC 1 102C1-102C1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020422
SYM|1360{}1514
SYN|TE20422
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1514
CLOC|102C1-102C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020423 ICL 1 1360 SYM 1 1360{}1515 ASTR 1 - CLOC 1 102C1-102C1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020423
SYM|1360{}1515
SYN|TE20423
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1515
CLOC|102C1-102C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019494 ICL 1 1360 SYM 1 1360{}1520 ASTR 1 - CLOC 1 102D1-102D1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019494
SYM|1360{}1520
SYN|TE19494
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1520
CLOC|102D1-102D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003843.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019496 ICL 1 1360 SYM 1 1360{}1525 ASTR 1 - CLOC 1 102D5-102D5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019496
SYM|1360{}1525
SYN|TE19496
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1525
CLOC|102D5-102D5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003843.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020432 ICL 1 1360 SYM 1 1360{}1530 ASTR 1 - CLOC 1 102E5-102E5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020432
SYM|1360{}1530
SYN|TE20432
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1530
CLOC|102E5-102E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003843.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020434 ICL 1 1360 SYM 1 1360{}1533 ASTR 1 - CLOC 1 102E5-102E5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020434
SYM|1360{}1533
SYN|TE20434
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1533
CLOC|102E5-102E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003843.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019500 ICL 1 1360 SYM 1 1360{}1536 ASTR 1 - CLOC 1 102F2-102F2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019500
SYM|1360{}1536
SYN|TE19500
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1536
CLOC|102F2-102F2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003847.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019502 ICL 1 1360 SYM 1 1360{}1539 ASTR 1 - CLOC 1 102F3-102F3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019502
SYM|1360{}1539
SYN|TE19502
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1539
CLOC|102F3-102F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019507 ICL 1 1360 SYM 1 1360{}1543 ASTR 1 - CLOC 1 102F4-102F4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019507
SYM|1360{}1543
SYN|TE19507
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1543
CLOC|102F4-102F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020437 ICL 1 1360 SYM 1 1360{}1545 ASTR 1 - CLOC 1 102F4-102F4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020437
SYM|1360{}1545
SYN|TE20437
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1545
CLOC|102F4-102F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020438 ICL 1 1360 SYM 1 1360{}1546 ASTR 1 - CLOC 1 102F4-102F4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020438
SYM|1360{}1546
SYN|TE20438
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1546
CLOC|102F4-102F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019516 ICL 1 1360 SYM 1 1360{}1558 ASTR 1 - CLOC 1 102F8-102F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019516
SYM|1360{}1558
SYN|TE19516
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1558
CLOC|102F8-102F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019518 ICL 1 1360 SYM 1 1360{}1561 ASTR 1 - CLOC 1 102F8-102F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019518
SYM|1360{}1561
SYN|TE19518
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1561
CLOC|102F8-102F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020446 ICL 1 1360 SYM 1 1360{}1565 ASTR 1 - CLOC 1 102F8-102F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020446
SYM|1360{}1565
SYN|TE20446
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1565
CLOC|102F8-102F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020451 ICL 1 1360 SYM 1 1360{}1570 ASTR 1 - CLOC 1 102F8-102F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020451
SYM|1360{}1570
SYN|TE20451
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1570
CLOC|102F8-102F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020452 ICL 1 1360 SYM 1 1360{}1571 ASTR 1 - CLOC 1 102F8-102F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020452
SYM|1360{}1571
SYN|TE20452
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1571
CLOC|102F8-102F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014399 ICL 1 ? SYM 1 1360{}da1 ASTR 1 - CLOC 1 31D11--E1 REF 1 5 DT 1 26 Mar 2002 RESZ 909
ID|FBti0014399
SYM|1360{}da1
SYN|?{}da1
ASTP|FBtp0011398==1360
DT|26 Mar 2002
|6 Jan 2000
ICL|?
ASGN|FBgn0000413==da
SK|FBst0000273
|da[1] pr[1] cn[1]/SM5
|Total=1
REFDSR
{
RDID|FBrf0055585
|Keyes et al.
|1992
PHC|lethal | maternal effect | conditional ts
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}da1
ASAL|FBal0002214==da1
MU|spontaneous
CLOC|31D11--E1
|Insertion site
LOCB|Proximity to gene: FBgn0000413==da
}
REFDSR
{
RDID|FBrf0068461
|Cummings and Cronmiller
|1994
PHC|(with da2) lethal
}
REFDSR
{
RDID|FBrf0138569
|Castanon et al.
|2001
PHC|lethal | conditional ts
}
REF
{
REFM|FBrf0055585
|Keyes et al.
|1992
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0068461
|Cummings and Cronmiller
|1994
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0138569
|Castanon et al.
|2001
}
ALESR
{
ASYM|FBal0002214==da1
REFDSR
{
RDID|FBrf0041411
|Uenoyama
|1984
PHP|FBal0016680==Sxlf1 heterozygous female progeny derived from
| heterozygous FBal0002214==da1
|mothers have reduced viability. The viability is increased if the
|FBal0016680==Sxlf1/+ progeny are also carrying
| FBal0012357==msl-31, and is decreased
|if the FBal0002214==da1/+ mothers are also carrying
| FBal0012357==msl-31. The frequency
|of sex transformation in FBal0016680==Sxlf1/+ female progeny
| derived from FBal0002214==da1/+
|mothers is increased if either the mothers or the progeny are homozygous
|for FBal0012357==msl-31. The frequency of morphological
| abnormalities seen
|... (see FBal0002214==da1 report)
}
REFDSR
{
RDID|FBrf0054060
|Bopp et al.
|1991
PHP|At the restrictive temperature (25oC) less than 1% of females derived
|from homozygous mothers eclose. At the permissive temperature (18oC)
|the viability of these females derived from homozygous mothers is 100%.
}
REFDSR
{
RDID|FBrf0078360
|Estes et al.
|1995
PHP|Homozygous females have no female offspring due to failure to properly
|regulate the FBgn0003659==Sxl gene in the zygote.
}
REFDSR
{
RDID|FBrf0094140
|Bell
|1954
PHP|Homozygous females when mated to any male produce normal sons but no
|daughters. Otherwise, FBgn0000413==da mutant cannot be distinguished from wild
|type.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|(=da); viable; temperature-sensitive hypomorph; strong
|daughterless maternal effect above 22oC; lethal
|with Df or amorphic alleles; lethal at 29oC
}
REFDSR
{
RDID|FBrf0106007
|Anand et al.
|1998
PHP|Does not interact with FBal0094602==Sxldlf,
| FBal0094543==fl(1)3535 or FBal0094542==fl(1)3546.
}
REFDSR
{
RDID|FBrf0138569
|Castanon et al.
|2001
PHP|Homozygotes survive at 18oC and die at 25oC.
|FBal0002214==da1 homozygous embryos lacking maternal and zygotic
| FBgn0000413==da have defects
|in mesodermal development. The mesoderm migrates properly, however,
|further mesodermal development is impaired. Somatic muscle development
|is severely suppressed, embryos have reduced numbers of aberrantly
|placed syncitial muscles. Heart development is also repressed.
PHM|embryonic/larval somatic muscle
|mesoderm
|embryonic/larval heart
}
REF
{
REFM|FBrf0041411
|Uenoyama
|1984
REFM|FBrf0054060
|Bopp et al.
|1991
REFM|FBrf0078360
|Estes et al.
|1995
REFM|FBrf0094140
|Bell
|1954
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0106007
|Anand et al.
|1998
REFM|FBrf0138569
|Castanon et al.
|2001
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0019679 ICL 1 1731 SYM 1 1731{}207 ASTR 1 - CLOC 1 20A1-20A1 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019679
SYM|1731{}207
SYN|TE19679
ASTP|FBtp0011400==1731
DT|21 Aug 2003
|21 Aug 2003
ICL|1731
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1731{}207
CLOC|20A1-20A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003568.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020325 ICL 1 1731 SYM 1 1731{}1272 ASTR 1 - CLOC 1 85B4-85B4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020325
SYM|1731{}1272
SYN|TE20325
ASTP|FBtp0011400==1731
DT|21 Aug 2003
|21 Aug 2003
ICL|1731
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1731{}1272
CLOC|85B4-85B4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003680.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015144 ICL 1 ? SYM 1 ?{}anon-4Caverzwickt ASTR 1 - CLOC 1 4C REF 1 2 DT 1 6 Jan 2000 RESZ 431
ID|FBti0015144
SYM|?{}anon-4Caverzwickt
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0014102==anon-4Ca
REFDSR
{
RDID|FBrf0064240
|Poeck et al.
|1991
SYN|?{}anon-4Caverzwickt
ASAL|FBal0065901==anon-4Caverzwickt
CLOC|4C
|Insertion site
LOCB|Proximity to gene: FBgn0014102==anon-4Ca
}
REF
{
REFM|FBrf0064240
|Poeck et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0002824 ICL 1 ? SYM 1 ?{}Antp72j ASTR 1 - CLOC 1 84A6--B2 REF 1 2 DT 1 5 Feb 1999 RESZ 630
ID|FBti0002824
SYM|?{}Antp72j
DT|5 Feb 1999
|24 Jun 1997
ICL|?
ASGN|FBgn0000095==Antp
SK|FBst0002162
|pb[6] pb[12] Antp[72j]/TM3, Sb[1]
|FBst0002255
|pb[6] FBal0000572==Antp[72j]
|Total=2
REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
ASAL|FBal0000572==Antp72j
MU|spontaneous
CLOC|84A6--B2
|Insertion site
LOCB|Proximity to gene: FBgn0000095==Antp
PHC|viable
CC|Insertion determined to be repetitive; approximately 8.3kb; not shown to
| coorelate with mutant phenotype.
}
REF
{
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0000572==Antp72j
REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
PHP|Antennae to leg transformations.
PHM|leg | ectopic
|antenna
}
REF
{
REFM|FBrf0039012
|Scott et al.
|1983
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0002825 ICL 1 ? SYM 1 ?{}AntpScx ASTR 1 - CLOC 1 84A6--B2 REF 1 5 DT 1 5 Feb 1999 RESZ 1379
ID|FBti0002825
SYM|?{}AntpScx
DT|5 Feb 1999
|24 Jun 1997
ICL|?
ASGN|FBgn0000095==Antp
|FBgn0003339==Scr
SK|FBst0002250
|ru[1] h[1] st[1] kni[ri-1] FBal0000617==Antp[Scx] p[p] e[s]/TM3, Sb[1]
|FBst0002257
|Antp[Scx] p[p] Sb[sbd-2] Ubx[bx-3] Ubx[pbx-1]/TM3, Sb[1]
|FBst0003407
|ru[1] h[1] st[1] cp[1] in[1] kni[ri-1] FBal0000617==Antp[Scx] p[p] cu[1] e[1]/TM3, Sb[1]
|Total=3
REFDSR
{
RDID|FBrf0027527
|Duncan and Kaufman
|1975
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0034841
|Kaufman et al.
|1980
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
ASAL|FBal0000617==AntpScx
MU|spontaneous
CLOC|84A6--B2
|Insertion site
LOCB|Proximity to gene: FBgn0000095==Antp
PHC|lethal | recessive
CC|Insertion determined to be repetitive; approximately 3kb; not shown to
| coorelate with mutant phenotype.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0149025
|Southworth and Kennison
|2002
ASAL|FBal0138396==ScrScx
PHC|(with Antp1) lethal
|(with Antp23) lethal
}
REF
{
REFM|FBrf0027527
|Duncan and Kaufman
|1975
REFM|FBrf0034841
|Kaufman et al.
|1980
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0149025
|Southworth and Kennison
|2002
}
ALESR
{
ASYM|FBal0138396==ScrScx
REFDSR
{
RDID|FBrf0149025
|Southworth and Kennison
|2002
PHP|Heterozygous males have an average of 2.7 ectopic sex comb teeth per
|second leg. The number of sex comb teeth on the first leg is normal.
|FBal0138396==ScrScx/FBal0015280==Scr4 males have the
| same average number of sex comb
|teeth per first leg as FBal0015280==Scr4/+ males.
|Heterozygous males have an average of 0.1 ectopic sex comb teeth per
|third leg.
|FBal0138396==ScrScx/FBal0015278==Scr2 males have an
| average of 1.3 ectopic sex comb teeth
|... (see FBal0138396==ScrScx report)
PHM|mesothoracic leg & sex comb | ectopic
|metathoracic leg & sex comb | ectopic
|(with Scr2) mesothoracic leg & sex comb | ectopic
|(with Scr4) mesothoracic leg & sex comb | ectopic
|(with Scr4) metathoracic leg & sex comb | ectopic
|(with Scr4, Dp(3;Y)77ab) mesothoracic leg & sex comb | ectopic
|(with Scr4, Dp(3;Y)77ab) metathoracic leg & sex comb | ectopic
|(with ScrTpl9) mesothoracic leg & sex comb | ectopic
|(with ScrTpl9) metathoracic leg & sex comb | ectopic
}
REF
{
REFM|FBrf0149025
|Southworth and Kennison
|2002
}
}
# EO ALESR
ALESR
{
ASYM|FBal0000617==AntpScx
REFDSR
{
RDID|FBrf0027527
|Duncan and Kaufman
|1975
PHP|Sex combs are present on all male legs.
PHM|sex comb | ectopic
}
REFDSR
{
RDID|FBrf0034841
|Kaufman et al.
|1980
PHP|Sex comb teeth are produced on the basitarsus of all six legs (transformation
|of meso- and metathoracic into prothoracic legs).
PHM|sex comb
|mesothoracic leg
|metathoracic leg
}
REFDSR
{
RDID|FBrf0034853
|Lewis et al.
|1980
PHP|Transformation of meso- and metathoracic legs to prothoracic leg identity.
PHM|mesothoracic leg
|metathoracic leg
}
REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
PHP|Partial transformation of second and third legs into first legs.
PHM|mesothoracic leg
|metathoracic leg
}
REFDSR
{
RDID|FBrf0043249
|Dura et al.
|1985
PHP|Enhanced by FBal0013723==ph-d2.
}
REFDSR
{
RDID|FBrf0046404
|Kennison and Russell
|1987
PHP|Suppressed by a duplication carrying FBgn0003042==Pc+.
}
REFDSR
{
RDID|FBrf0073734
|Lewis et al.
|1980
PHP|Transformation of meso- and metathoracic leg to prothoracic leg identity.
PHM|mesothoracic leg
|metathoracic leg
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Sex combs may be present on all six legs of male. At least
|one extra sex comb present in 75-90% of males. Third pair of
|legs less often affected than second.
|RK2.
PHM|sex comb
|mesothoracic leg
|metathoracic leg
}
REFDSR
{
RDID|FBrf0110811
|Sinclair et al.
|1984
PHP|Between 44.4% and 61.5% of heterozygous males have an extra sex combs
|phenotype.
PHM|leg
|sex comb | ectopic
}
REF
{
REFM|FBrf0027527
|Duncan and Kaufman
|1975
REFM|FBrf0034841
|Kaufman et al.
|1980
REFM|FBrf0034853
|Lewis et al.
|1980
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0043249
|Dura et al.
|1985
REFM|FBrf0046404
|Kennison and Russell
|1987
REFM|FBrf0073734
|Lewis et al.
|1980
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0110811
|Sinclair et al.
|1984
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014268 ICL 1 ? SYM 1 ?{}btl-a ASTR 1 - CLOC 1 102C2--3 REF 1 4 DT 1 6 Jan 2000 RESZ 762
ID|FBti0014268
SYM|?{}btl-a
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0005666==bt
REFDSR
{
RDID|FBrf0016176
|Hochman et al.
|1964
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0022724
|Hochman
|1971
PHC|lethal
}
REFDSR
{
RDID|FBrf0079869
|Ayme-Southgate et al.
|1995
SYN|?{}btl-a
ASAL|FBal0027983==btl-a
CLOC|102C2--3
|Insertion site
LOCB|Proximity to gene: FBgn0005666==bt
PHC|lethal | embryonic | recessive
|(with btD) lethal | embryonic
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | embryonic | recessive
}
REF
{
REFM|FBrf0016176
|Hochman et al.
|1964
REFM|FBrf0022724
|Hochman
|1971
REFM|FBrf0079869
|Ayme-Southgate et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0027983==btl-a
REFDSR
{
RDID|FBrf0079869
|Ayme-Southgate et al.
|1995
PHP|Homozygotes die as late embryos and do not have spontaneous muscle
|contractions. FBal0001328==btD/FBal0027983==btl-a
| transheterozygotes die as embryos.
}
REF
{
REFM|FBrf0079869
|Ayme-Southgate et al.
|1995
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014101 ICL 1 ? SYM 1 ?{}BxM ASTR 1 - CLOC 1 17C3--4 REF 1 2 DT 1 6 Jan 2000 RESZ 407
ID|FBti0014101
SYM|?{}BxM
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000242==Bx
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}BxM
ASAL|FBal0001443==BxM
MU|spontaneous
CLOC|17C3--4
|Insertion site
LOCB|Proximity to gene: FBgn0000242==Bx
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014994 ICL 1 P SYM 1 ?{}can8 ASTR 1 - CLOC 1 67D12 REF 1 3 DT 1 23 Jul 2001 RESZ 537
ID|FBti0014994
SYM|?{}can8
SYN|P{}can8
DT|23 Jul 2001
|6 Jan 2000
ICL|P
ASGN|FBgn0011569==can
REFDSR
{
RDID|FBrf0087570
|Lin et al.
|1996
SYN|P{}can8
ASAL|FBal0049380==can8
CLOC|67D12
|Insertion site
LOCB|Proximity to gene: FBgn0011569==can
PHC|male sterile | recessive
}
REFDSR
{
RDID|FBrf0135773
|Hiller et al.
|2001
PHC|male sterile
}
REF
{
REFM|FBrf0087570
|Lin et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135773
|Hiller et al.
|2001
}
ALESR
{
ASYM|FBal0049380==can8
REFDSR
{
RDID|FBrf0087570
|Lin et al.
|1996
PHP|Early stages of spermatogenesis up through mature primary spermatocytes
|are present and normal. Postmeiotic stages are completely absent.
|Mutant testes have an abundance of mature primary spermatocytes with
|large, round nuclei and prominent nucleoli.
|Spermatocytes arrest in the G2/M transition of meiosis I with partial
|chromosome condensation.
PHM|testis
|spermatocyte
}
REF
{
REFM|FBrf0087570
|Lin et al.
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014995 ICL 1 P SYM 1 ?{}can9 ASTR 1 - CLOC 1 67D12 REF 1 3 DT 1 23 Jul 2001 RESZ 537
ID|FBti0014995
SYM|?{}can9
SYN|P{}can9
DT|23 Jul 2001
|6 Jan 2000
ICL|P
ASGN|FBgn0011569==can
REFDSR
{
RDID|FBrf0087570
|Lin et al.
|1996
SYN|P{}can9
ASAL|FBal0049381==can9
CLOC|67D12
|Insertion site
LOCB|Proximity to gene: FBgn0011569==can
PHC|male sterile | recessive
}
REFDSR
{
RDID|FBrf0135773
|Hiller et al.
|2001
PHC|male sterile
}
REF
{
REFM|FBrf0087570
|Lin et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135773
|Hiller et al.
|2001
}
ALESR
{
ASYM|FBal0049381==can9
REFDSR
{
RDID|FBrf0087570
|Lin et al.
|1996
PHP|Early stages of spermatogenesis up through mature primary spermatocytes
|are present and normal. Postmeiotic stages are completely absent.
|Mutant testes have an abundance of mature primary spermatocytes with
|large, round nuclei and prominent nucleoli. Early stages of spermatogenesis
|up through mature primary spermatocytes are present and normal. Postmeiotic
|stages are completely absent. Mutant testes have an abundance of mature
|primary spermatocytes with large, round nuclei and prominent nucleoli.
|... (see FBal0049381==can9 report)
PHM|testis
|spermatocyte
}
REF
{
REFM|FBrf0087570
|Lin et al.
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016955 ICL 1 ? SYM 1 ?{}cg1 ASTR 1 - CLOC 1 50E1 REF 1 2 DT 1 25 Dec 2000 RESZ 602
ID|FBti0016955
SYM|?{}cg1
DT|25 Dec 2000
|25 Dec 2000
ICL|?
ASGN|FBgn0000289==cg
SK|FBst0000252
|cg[1] c[1]/SM5
|FBst0000253
|cg[1] c[1]/In(2LR)U, U[1]
|FBst0000292
|dw-24E[1] l(2)cg[1] cg[1]/SM5
|Total=3
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|female sterile | recessive
}
REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
SYN|?{}cg1
ASAL|FBal0001596==cg1
MU|spontaneous
CLOC|50E1
|Insertion site
LOCB|Proximity to gene: FBgn0000289==cg
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0130102
|Svendsen et al.
|2000
}
ALESR
{
ASYM|FBal0001596==cg1
REFDSR
{
RDID|FBrf0007527
|Beatty
|1949
PHP|Oogenesis highly irregular.
}
REFDSR
{
RDID|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
PHP|Terminal gaps in wing vein L4 and homozygotes have intercalary gaps in wing
| vein L5.
|Also abnormalities in legs and in oogenesis.
PHM|wing vein L4
|wing vein L5
|leg
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Sex combs of male extremely large. Number of sex comb teeth increased
|from 10 to 18; number of bractless bristles increased; width of distal
|portion of basitarsus increased 1.6 fold; total number of bristles on
|basitarsus increased in both sexes (FBrf0065640; FBrf0063395). Some
|distortion and shortening of legs. Wings show gap in vein L4 between
|posterior crossvein and margin. Wings slightly curved. Effects result from
|a combination of overgrowth and irregular folding of imaginal rudiments
|... (see FBal0001596==cg1 report)
PHM|sex comb
|wing vein L4
|wing
}
REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
PHP|Homozygous and FBal0001596==cg1/FBal0008129==cg07659
| flies have gaps in wing vein L4.
|Homozygous and FBal0001596==cg1/FBal0008129==cg07659
| males have extra sex comb teeth.
PHM|wing vein L4
|(with cg07659) wing vein L4
|sex comb | supernumerary
|(with cg07659) sex comb | supernumerary
}
REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
PHP|Homozygotes have phenotypes in the wing, leg and antenna.
|Approximately 10% of
| FBal0001596==cg1/FBal0008129==cg07659 and 50% of FBal0001596==cg1/FBal0119302==cg3
|animals eclose to adult stages, with most of the remaining animals
|dying as pharate adults.
|FBal0001596==cg1/FBal0001596==cg1,
| FBal0001596==cg1/FBal0008129==cg07659 and
| FBal0001596==cg1/FBal0119302==cg3 flies have
|defects in some combination of the posterior compartment longitudinal
|veins L4 and L5. Defects in vein L4, ranging from a slight thinning
|... (see FBal0001596==cg1 report)
PHM|wing
|leg
|antenna
|wing vein L4
|wing vein L5
|(with cg07659) wing vein L4
|(with cg07659) wing vein L5
|(with cg3) wing vein L4
|(with cg3) wing vein L5
|(with cg07659) wing vein L2
|wing margin | anterior
|(with cg3) wing margin | anterior
|(with cg07659) wing margin | anterior
|sex comb | supernumerary
|mesothoracic leg
|(with cg07659) ventral thoracic disc
|(with cg07659) sex comb | supernumerary
|(with cg07659) prothoracic tibial transverse bristle row | supernumerary
|(with cg3) wing | posterior compartment
|(with cg07659) wing | posterior compartment
}
REFDSR
{
RDID|FBrf0131401
|Song et al.
|2000
PHP|FBal0001596==cg1/FBal0125097==cgk11504
| transheterozygotes show pleiotropic defects in
|bristle number, wing venation and oogenesis.
PHM|(with cgk11504) wing vein
|(with cgk11504) macrochaeta
}
REF
{
REFM|FBrf0007527
|Beatty
|1949
REFM|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
REFM|FBrf0130102
|Svendsen et al.
|2000
REFM|FBrf0131401
|Song et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016968 ICL 1 ? SYM 1 ?{}cg3 ASTR 1 - CLOC 1 50E1 REF 1 2 DT 1 25 Dec 2000 RESZ 410
ID|FBti0016968
SYM|?{}cg3
DT|25 Dec 2000
|25 Dec 2000
ICL|?
ASGN|FBgn0000289==cg
REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
SYN|?{}cg3
ASAL|FBal0119302==cg3
CLOC|50E1
|Insertion site
LOCB|Proximity to gene: FBgn0000289==cg
PHC|lethal | recessive
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0130102
|Svendsen et al.
|2000
}
ALESR
{
ASYM|FBal0119302==cg3
REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
PHP|Most homozygotes survive until the pharate adult stage.
|Approximately 50% of FBal0001596==cg1/FBal0119302==cg3
| animals eclose to adult stages,
|with most of the remaining animals dying as pharate adults. FBal0001596==cg1/FBal0119302==cg3
|flies have defects in some combination of the posterior compartment
|longitudinal veins L4 and L5. Defects in vein L4, ranging from a slight
|thinning of the vein to gaps of increasing size are seen in 100% of
|wings. Defects in wing vein L5 are seen in less than 25% of flies.
|... (see FBal0119302==cg3 report)
PHM|(with cg1) wing vein L4
|(with cg1) wing vein L5
|(with cg1) wing margin | anterior
|(with cg07659) prothoracic tibial preapical bristle | supernumerary
|(with cg07659) sex comb | supernumerary
|(with cg1) wing | posterior compartment
|(with cg07659) wing | anterior compartment
|(with cg07659) ventral thoracic disc | anterior compartment
}
REF
{
REFM|FBrf0130102
|Svendsen et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014281 ICL 1 ? SYM 1 ?{}ci36 ASTR 1 - CLOC 1 102A1--3 REF 1 2 DT 1 6 Jan 2000 RESZ 443
ID|FBti0014281
SYM|?{}ci36
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004859==ci
SK|FBst0000643
|ci[36]
|Total=1
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}ci36
ASAL|FBal0001645==ci36
MU|spontaneous
CLOC|102A1--3
|Insertion site
LOCB|Proximity to gene: FBgn0004859==ci
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001645==ci36
REFDSR
{
RDID|FBrf0073755
|Locke and Tartof
|1994
PHP|Homozygous viable.
}
REFDSR
{
RDID|FBrf0092613
|Locke and Hanna
|1996
PHM|wing vein
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Less extreme than FBal0001644==ci1. Ranges from appearance of a plexus
|in L4 between crossveins to gaps in L4 and L5 posterior
|to crossveins.
|RK3.
}
REF
{
REFM|FBrf0073755
|Locke and Tartof
|1994
REFM|FBrf0092613
|Locke and Hanna
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016967 ICL 1 ? SYM 1 ?{}cin ASTR 1 - CLOC 1 102A1--3 REF 1 2 DT 1 25 Dec 2000 RESZ 481
ID|FBti0016967
SYM|?{}cin
DT|25 Dec 2000
|25 Dec 2000
ICL|?
ASGN|FBgn0004859==ci
REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
SYN|?{}cin
ASAL|FBal0119295==cin
CLOC|102A1--3
|Insertion site
LOCB|Proximity to gene: FBgn0004859==ci
PHC|(with ciD) lethal | pupal
|(with ci94) lethal | pupal
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
}
ALESR
{
ASYM|FBal0119295==cin
REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
PHP|A small percentage of flies have wing duplications and most flies have
|enlarged antennae.
|FBal0119295==cin/FBal0045443==ci94 imaginal discs show overgrowth.
PHM|wing
|antenna
|(with ci94) ventral thoracic disc
|(with ci94) dorsal mesothoracic disc
}
REF
{
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014283 ICL 1 ? SYM 1 ?{}ciW ASTR 1 - CLOC 1 102A1--3 REF 1 2 DT 1 6 Jan 2000 RESZ 439
ID|FBti0014283
SYM|?{}ciW
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004859==ci
SK|FBst0000646
|ci[W]
|Total=1
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}ciW
ASAL|FBal0001653==ciW
MU|spontaneous
CLOC|102A1--3
|Insertion site
LOCB|Proximity to gene: FBgn0004859==ci
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001653==ciW
REFDSR
{
RDID|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
PHP|Lack all longitudinal and transverse veins and affect morphogenesis
|of legs and eyes.
}
REFDSR
{
RDID|FBrf0073755
|Locke and Tartof
|1994
PHP|Homozygous viable.
}
REFDSR
{
RDID|FBrf0087686
|Sanchez-Herrero et al.
|1996
PHP|Homozygotes occasionally show overgrowth in the anterior compartment
|of the wing. FBal0001651==ciD/FBal0001653==ciW flies
| have abnormal legs.
PHM|wing | anterior compartment
|(with ciD) leg
}
REFDSR
{
RDID|FBrf0088080
|Dominguez et al.
|1996
PHP|Wings from homozygotes have, at low penetrance, a mirror symmetrical
|outgrowth composed of anterior wing material, resembling duplications
|caused by ectopic FBgn0000490==dpp expression.
PHM|wing
}
REFDSR
{
RDID|FBrf0092613
|Locke and Hanna
|1996
PHM|wing vein
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Homozygote is extreme ci type. Wings sometimes almost
|twice normal width, arclike, and virtually lack veins.
|Often present is a well-organized pattern of venation
|in which the posterior crossvein flows smoothly into
|L5. Legs lumpy, sex combs larger than normal, antennae
|enlarged, eyes smaller and extra bristles present.
|Heterozygote shows gap in L4 in 80% of flies. FBal0001653==ciW
|... (see FBal0001653==ciW report)
}
REFDSR
{
RDID|FBrf0108513
|Dominguez
|1999
PHP|When analyzed in large clones in the developing eye the packing in
|the ommatidial clusters is disrupted.
PHM|ommatidial cluster
}
REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
PHP|Heterozygotes show variable loss of vein L4 tissue.
PHM|wing vein L4
}
REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
PHP|Heterozygotes show wing vein L4 defects.
PHM|wing vein L4
}
REF
{
REFM|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
REFM|FBrf0073755
|Locke and Tartof
|1994
REFM|FBrf0087686
|Sanchez-Herrero et al.
|1996
REFM|FBrf0088080
|Dominguez et al.
|1996
REFM|FBrf0092613
|Locke and Hanna
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108513
|Dominguez
|1999
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
REFM|FBrf0130102
|Svendsen et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014284 ICL 1 ? SYM 1 ?{}cm1 ASTR 1 - CLOC 1 6E4 REF 1 2 DT 1 6 Jan 2000 RESZ 1330
ID|FBti0014284
SYM|?{}cm1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000330==cm
SK|FBst0000021
|cm[1]
|FBst0000022
|cm[1] ct[6]
|FBst0000175
|y[1] pn[1] w[1] FBal0001720==cm[1] ct[6] sn[3] oc[1] ras[2] v[1] dy[1] g[2] f[1] os[o] car[1] sw[1]/In(1)sc[S1], In(1)dl-49, y[c4] sc[S1] v[Of] B[1]
|FBst0001277
|cm[1] ct[6] v[1] m[74f]/C(1)M4, y[2]
|FBst0001282
|cm[1] m[74f] sd[1] os[s]
|FBst0001319
|Tp(1;2)w-ec, ec[64d] FBal0001720==cm[1] ct[6] sn[3]/C(1)DX, y[1] w[1] f[1]
|FBst0001570
|y[1] pn[1] w[1] FBal0001720==cm[1] ct[6] sn[3] oc[1] ras[2] v[1] dy[1] g[2] f[1] os[o]/FM6
|FBst0003169
|cm[1] ct[6] mys[ts1]
|FBst0003708
|y[1] FBal0001720==cm[1] Sxl[f1] v[1] f[1]/FM7a/Dp(1;2;Y)w[+]
|FBst0003719
|y[1] FBal0001720==cm[1] Sxl[M1] v[1] f[1]/FM7a/Dp(1;2;Y)w[+]
|FBst0004679
|cm[1] l(1)7Dd[4]/FM7a
|FBst0006027
|y[1] ac[1] sc[1] pn[1] w[1] rb[1] FBal0001720==cm[1] ct[1] sn[3] ras[4] v[1] m[1] g[1] f[1] car[1]/FM6
|Total=12
REFDSR
{
RDID|FBrf0112254
|Mullins et al.
|1999
SYN|?{}cm1
ASAL|FBal0001720==cm1
MU|spontaneous
CLOC|6E4
|Insertion site
LOCB|Proximity to gene: FBgn0000330==cm
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0112254
|Mullins et al.
|1999
}
ALESR
{
ASYM|FBal0001720==cm1
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: translucent dark ruby.
|Eye color: deep orange, with FBal0016127==st1.
|Eye color: lighter than FBal0001342==bw1, with FBal0001342==bw1.
|Malpighian tubule color: very pale yellow.
|RK1.
PHM|pigment cell
|Malpighian tubule
}
REFDSR
{
RDID|FBrf0112254
|Mullins et al.
|1999
PHP|Eye color: darker than wild type.
|Dramatic reduction in number of secondary and tertiary pigment granules
|surrounding the ommatidium. Outer rhabdomeres are also occasionally
|missing.
PHM|pigment cell
|secondary pigment cell pigment granule
|tertiary pigment cell pigment granule
|rhabdomere
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0112254
|Mullins et al.
|1999
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014285 ICL 1 ? SYM 1 ?{}cm4 ASTR 1 - CLOC 1 6E4 REF 1 2 DT 1 6 Jan 2000 RESZ 388
ID|FBti0014285
SYM|?{}cm4
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000330==cm
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}cm4
ASAL|FBal0001723==cm4
CLOC|6E4
|Insertion site
LOCB|Proximity to gene: FBgn0000330==cm
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001723==cm4
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|reverts spontaneously
|unstable
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014286 ICL 1 ? SYM 1 ?{}cosV1 ASTR 1 - CLOC 1 43B1--2 REF 1 2 DT 1 6 Jan 2000 RESZ 410
ID|FBti0014286
SYM|?{}cosV1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000352==cos
REFDSR
{
RDID|FBrf0096304
|Sisson et al.
|1997
SYN|?{}cosV1
ASAL|FBal0001778==cosV1
MU|spontaneous \?
CLOC|43B1--2
|Insertion site
LOCB|Proximity to gene: FBgn0000352==cos
}
REF
{
REFM|FBrf0096304
|Sisson et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001778==cosV1
REFDSR
{
RDID|FBrf0065539
|Preat et al.
|1993
PHP|Phenotypic interactions when in combination with FBgn0000352==cos.
}
REFDSR
{
RDID|FBrf0076434
|Capdevila and Guerrero
|1994
PHP|Viable mutation. Wing phenotype is similar to the phenotype resulting
|from ectopic expression of FBal0039403==hhScer\UAS.cCa, induction
| of overgrowth with
|a mirror image duplication of structures of the anterior and posterior
|compartments.
PHM|wing | posterior compartment
|wing | anterior compartment
}
REFDSR
{
RDID|FBrf0087686
|Sanchez-Herrero et al.
|1996
PHP|FBal0001784==Cos2
| FBal0001778==cosV1/FBal0001782==cosV5 flies have
| abnormal legs. FBal0031366==fuJ; FBal0001784==Cos2
|FBal0001778==cosV1/FBal0001782==cosV5 flies show a
| FBgn0000352==cos phenotype in the thorax and
|legs.
PHM|leg
}
REFDSR
{
RDID|FBrf0096304
|Sisson et al.
|1997
PHP|Displays adult pattern duplications in the presence of semidominant
|alleles of FBgn0000353==Cos.
}
REFDSR
{
RDID|FBrf0098968
|Sanchez et al.
|1997
PHP|FBal0001778==cosV1/FBal0001782==cosV5 females show
| duplication of the dorsal vaginal
|plate with an increment in the number of sensilla trichodea and loss
|of the ventral vaginal plate. The eighth tergite and vulva are reduced.
|Anal plates are abnormal.
|FBal0001778==cosV1/FBal0001782==cosV5 males show
| fusion of the lateral plates and the
|claspers. The hypandrium phragma is reduced.
PHM|female gonopod | dorsal
|female gonopod | ventral
|genital arch
|vulva
|epiproct
|hypoproct
|lateral plate
|clasper
|hypandrial process
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|class III allele
|FBal0001782==cosV5 >= FBal0001781==cosV4 =
| FBal0001778==cosV1 >= FBal0001779==cosV2 >= FBal0001780==cosV3
}
REF
{
REFM|FBrf0065539
|Preat et al.
|1993
REFM|FBrf0076434
|Capdevila and Guerrero
|1994
REFM|FBrf0087686
|Sanchez-Herrero et al.
|1996
REFM|FBrf0096304
|Sisson et al.
|1997
REFM|FBrf0098968
|Sanchez et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0024409 ICL 1 ? SYM 1 ?{}Cyp6g1PSU-R ASTR 1 - CLOC 1 48E7 REF 1 2 DT 1 3 Apr 2003 RESZ 373
ID|FBti0024409
SYM|?{}Cyp6g1PSU-R
DT|3 Apr 2003
|3 Apr 2003
ICL|?
ASGN|FBgn0025454==Cyp6g1
REFDSR
{
RDID|FBrf0155239
SYN|?{}Cyp6g1PSU-R
ASAL|FBal0141853==Cyp6g1PSU-R
CLOC|48E7
|Insertion site
LOCB|Proximity to gene: FBgn0025454==Cyp6g1
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155239
}
ALESR
{
ASYM|FBal0141853==Cyp6g1PSU-R
REFDSR
{
RDID|FBrf0155239
PHP|The "PSU-R" strain shows dominant complete resistance to DDT.
}
REF
{
REFM|FBrf0155239
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014881 ICL 1 ? SYM 1 ?{}Dfd1 ASTR 1 - CLOC 1 84A5 REF 1 2 DT 1 6 Jan 2000 RESZ 1881
ID|FBti0014881
SYM|?{}Dfd1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000439==Dfd
SK|FBst0000480
|Df(3R)ry27, FBal0002374==Dfd[1] cu[1] kar[1]/TM3, Sb[1]
|FBst0000487
|Dl[11]/In(3R)P, FBal0002374==Dfd[1] ca[1]
|FBst0000488
|Dl[12]/In(3R)P, FBal0002374==Dfd[1] ca[1]
|FBst0000495
|dwh[1]/In(3R)P, FBal0002374==Dfd[1] ca[1]
|FBst0000632
|wk[1]/In(3R)P, FBal0002374==Dfd[1] ca[1]
|FBst0000800
|Dfd[1] p[p]
|FBst0000857
|T(2;3)101, ru[1] h[1] e[4] ro[1] ca[1]/In(3R)P, FBal0002374==Dfd[1] ca[1]
|FBst0000859
|T(2;3)109, p[p]/In(3R)P, FBal0002374==Dfd[1] ca[1]
|FBst0000891
|T(3;4)c/In(3R)P, FBal0002374==Dfd[1] ca[1]
|FBst0000893
|T(3;4)e, h[1] th[1] st[1] cu[1] sr[1] e[s] ca[1]/In(3R)P, FBal0002374==Dfd[1] ca[1]
|FBst0000895
|Dp(4;3)f, h[1] th[1] st[1] cu[1] sr[1] e[s] ca[1]/In(3R)P, FBal0002374==Dfd[1]
|FBst0001714
|Df(3R)M86D, FBal0002374==Dfd[1] p[p]/TM3, Ser[1]
|FBst0002213
|ftz[6] FBal0002374==Dfd[1] p[p]/TM3, Sb[1]
|FBst0002341
|Dfd[1]/TM3, Sb[1]
|FBst0002439
|Dfd[1] Gld[n2] p[p]/TM3, Sb[1]
|FBst0004071
|T(3;4)Dubinin/In(3R)P, FBal0002374==Dfd[1]
|FBst0004342
|v[1] f[1]; Dp(1;3)126/In(3R)P, FBal0002374==Dfd[1] ca[1]
|FBst0004463
|In(3L)D, rho[ve-1] R[1] D[3] st[1] Ubx[1] e[4] Pr[1] ca[1]/In(3R)P, FBal0002374==Dfd[1] ca[1]
|FBst0004464
|M(3)40l30[1]/In(3L)P, In(3R)P, FBal0002374==Dfd[1] ca[1]
|Total=19
REFDSR
{
RDID|FBrf0051400
|McGinnis et al.
|1990
SYN|?{}Dfd1
ASAL|FBal0002374==Dfd1
MU|spontaneous
CLOC|84A5
|Insertion site
LOCB|Proximity to gene: FBgn0000439==Dfd
}
REF
{
REFM|FBrf0051400
|McGinnis et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0002374==Dfd1
REFDSR
{
RDID|FBrf0046135
|Regulski et al.
|1987
PHP|Adult head defects.
}
REFDSR
{
RDID|FBrf0051116
|McGinnis et al.
|1990
PHP|Adults have ventral eye and orbital tissue missing.
}
REFDSR
{
RDID|FBrf0051400
|McGinnis et al.
|1990
PHP|Loss of ventral eye and orbital regions in the adult head. Head defects
|phenocopied by FBal0038716==Dfdhs.PK constructs and heat-shock
| constructs of the
|human Hox4.2 in cells of the eye disc during third larval instar development.
PHM|ocellus | adult
}
REFDSR
{
RDID|FBrf0051503
|Chadwick et al.
|1990
PHP|Adult head deformations: lower eye and orbital structures are absent.
|Homozygotes have bulbous growths in the place of missing eye tissue,
|these may be duplications of the second antennal segment.
}
REFDSR
{
RDID|FBrf0103357
|Saget et al.
|1998
PHP|Heterozygous males have ectopic antero-ventral bristles on the head.
PHM|head bristle | ectopic
|adult head
|head bristle
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|dominant
|Eyes reduced ventrally and anteriorly, or furrowed. Vibrissae tufted.
|Extremely variable, often overlapping wild type, but usually
|excellent character with Ly or at 19oC. Classifiable in
|single dose in triploids (Schultz, 1934).
|Muller reported an occasional homozygote as extreme dwarf with flimsy wings.
|RK2.
}
REF
{
REFM|FBrf0046135
|Regulski et al.
|1987
REFM|FBrf0051116
|McGinnis et al.
|1990
REFM|FBrf0051400
|McGinnis et al.
|1990
REFM|FBrf0051503
|Chadwick et al.
|1990
REFM|FBrf0103357
|Saget et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014401 ICL 1 ? SYM 1 ?{}dlg12 ASTR 1 - CLOC 1 10B6--10 REF 1 5 DT 1 6 Jan 2000 RESZ 832
ID|FBti0014401
SYM|?{}dlg12
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001624==dlg1
REFDSR
{
RDID|FBrf0049482
|Woods and Bryant
|1989
SYN|?{}dlg12
ASAL|FBal0002671==dlg12
MU|X ray
CLOC|10B6--10
|Insertion site
LOCB|Proximity to gene: FBgn0001624==dlg1
PHC|lethal | recessive | conditional ts
}
REFDSR
{
RDID|FBrf0049894
|Perrimon et al.
|1989
PHC|lethal | conditional ts
}
REFDSR
{
RDID|FBrf0088171
|Guan et al.
|1996
PHC|lethal | recessive | conditional ts
}
REFDSR
{
RDID|FBrf0098920
|Goode and Perrimon
|1997
PHC|lethal | recessive | conditional ts
}
REF
{
REFM|FBrf0049482
|Woods and Bryant
|1989
REFM|FBrf0049894
|Perrimon et al.
|1989
REFM|FBrf0088171
|Guan et al.
|1996
REFM|FBrf0098920
|Goode and Perrimon
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0002671==dlg12
REFDSR
{
RDID|FBrf0049482
|Woods and Bryant
|1989
PHP|Completely lethal at 25oC, homozygotes show 75% viability at 18oC.
|Females exhibit a maternal-effect embryonic lethality when fertilized
|by FBal0002671==dlg12 sperm even at the permissive temperature.
| This lethality
|can be rescued by wild-type sperm.
}
REFDSR
{
RDID|FBrf0049894
|Perrimon et al.
|1989
PHP|Embryos exhibit defects associated with dorsal closure and head involution.
}
REFDSR
{
RDID|FBrf0088171
|Guan et al.
|1996
PHP|Temperature-sensitive allele. At the permissive temperature (18oC),
|hemizygotes show a hypomorphic phenotype, developing small imaginal
|disc tumors. Type I boutons appear similar to wild-type in these
|animals. At the restrictive temperature (29oC), hemizygotes show
|a similar phenotype to FBal0002675==dlg16 or
| FBal0002683==dlg114 hemizygotes, developing
|large tumors in the brain and imaginal discs. The subsynaptic reticulum
|at type I boutons is poorly developed in these animals.
|... (see FBal0002671==dlg12 report)
PHM|imaginal disc | conditional ts
|larval brain | conditional ts
|postsynaptic membrane
}
REFDSR
{
RDID|FBrf0098920
|Goode and Perrimon
|1997
PHP|FBal0002671==dlg12/FBal0002674==dlg15 animals are
| viable and have completely normal egg
|chambers at 18oC. After 6 hours at 25oC, follicle cells
| exit the
|follicular epithelium and intermingle with germ cells at the anterior
|and posterior poles of the egg chamber. Cells that remain in the epithelium
|retain their polarized characteristics, whereas those that have exited
|the epithelium have an apolar morphology. Nurse cells extend processes
|to meet the invasive follicle cells. Follicle cells at the anterior
|... (see FBal0002671==dlg12 report)
PHM|follicle cell | conditional ts
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Homozygotes fail to survive when raised at 25oC;
|when raised at 18oC however, 37% survival attained;
|hemizygous females show 65-70% survival at 18oC,
|but are also lethal at 25oC. Survival at 18oC
|nearly complete in heterozygotes with FBal0002674==dlg15 and
|FBal0002687==dlg118 and survival at 25oC is 4% and 95%
|respectively. Embryos produced by matings between
|... (see FBal0002671==dlg12 report)
}
REFDSR
{
RDID|FBrf0174574
|Szafranski and Goode
|2004
PHP|Delamination and migration of border follicle cells are both accelerated
|in FBal0002671==dlg12 heterozygotes.
|In FBal0002671==dlg12/FBal0002674==dlg15 flies the
| border follicle cells have much reduced
|polarity. Delamination of these cells is delayed, but their migration
|is accelerated.
PHM|border follicle cell
|(with dlg15) border follicle cell
}
REF
{
REFM|FBrf0049482
|Woods and Bryant
|1989
REFM|FBrf0049894
|Perrimon et al.
|1989
REFM|FBrf0088171
|Guan et al.
|1996
REFM|FBrf0098920
|Goode and Perrimon
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0174574
|Szafranski and Goode
|2004
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0002861 ICL 1 ? SYM 1 ?{}Dll10 ASTR 1 - CLOC 1 60E2 REF 1 2 DT 1 5 Feb 1999 RESZ 641
ID|FBti0002861
SYM|?{}Dll10
DT|5 Feb 1999
|24 Jun 1997
ICL|?
ASGN|FBgn0000157==Dll
REFDSR
{
RDID|FBrf0050642
|Cohen et al.
|1989
ASAL|FBal0001007==Dll10
MU|PM hybrid dysgenesis
CLOC|60E2
|Insertion site
LOCB|Proximity to gene: FBgn0000157==Dll
CC|8kb insertion, unidentified; within 13kb intron. See also FBti0002860==P{}60E.a, a
| P-element insertion also on the FBal0001007==Dll10 chromosome,
| 70kb 3' of the FBgn0000157==Dll transcript.
}
REF
{
REFM|FBrf0050642
|Cohen et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001007==Dll10
REFDSR
{
RDID|FBrf0050642
|Cohen et al.
|1989
PHP|Fails to develop limbs.
}
REF
{
REFM|FBrf0050642
|Cohen et al.
|1989
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015265 ICL 1 ? SYM 1 ?{}Dsim\lzL ASTR 1 - CLOC 1 - REF 1 2 DT 1 6 Jan 2000 RESZ 410
ID|FBti0015265
SYM|?{}Dsim\lzL
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0018267==Dsim\lz
REFDSR
{
RDID|FBrf0105876
|Loreto et al.
|1998
SYN|?{}Dsim\lzL
ASAL|FBal0095813==Dsim\lzL
LOCB|Proximity to gene: FBgn0018267==Dsim\lz
PHC|female sterile | recessive
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105876
|Loreto et al.
|1998
}
ALESR
{
ASYM|FBal0095813==Dsim\lzL
REFDSR
{
RDID|FBrf0105876
|Loreto et al.
|1998
PHP|The eyes are reduced in size in mutant flies and the surface of the
|eye has a glistening appearance and altered pigmentation. The tarsal
|claws are reduced. Homozygous females are sterile; the spermathecae
|and parovaria are absent.
|Eye color: brown.
PHM|eye
|tarsus
|spermathecal duct
|female accessory gland
}
REF
{
REFM|FBrf0105876
|Loreto et al.
|1998
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015255 ICL 1 ? SYM 1 ?{}Dsp11 ASTR 1 - CLOC 1 14B14--15 REF 1 2 DT 1 1 May 2001 RESZ 526
ID|FBti0015255
SYM|?{}Dsp11
SYN|?{}Dsp15101
|?{}bss5101
DT|1 May 2001
|6 Jan 2000
ICL|?
ASGN|FBgn0011764==Dsp1
REFDSR
{
RDID|FBrf0105889
|Mosrin-Huaman et al.
|1998
SYN|?{}bss5101
ASAL|FBal0094567==Dsp11
CLOC|14B14--15
|Insertion site
LOCB|Proximity to gene: FBgn0011764==Dsp1
PHC|lethal | recessive | partially
|sterile | recessive | partially
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105889
|Mosrin-Huaman et al.
|1998
}
ALESR
{
ASYM|FBal0094567==Dsp11
REFDSR
{
RDID|FBrf0105889
|Mosrin-Huaman et al.
|1998
PHP|Few hemizygous males survive to adulthood. They have severe morphological
|and physiological defects; they walk with difficulty, can hardly fly
|and have severely impaired fertility. These flies die prematurely
|(50% die within 5 days of eclosion).
|Few homozygous females survive to adulthood. They have the same phenotypical
|characteristics as hemizygous males. The females achieve complete
|oogenesis but lay few eggs. At 26oC these eggs do not hatch into
|... (see FBal0094567==Dsp11 report)
PHM|egg
|abdominal 5 ventral denticle belt
|abdominal 4 ventral denticle belt
|embryonic/first instar larval cuticle
}
REFDSR
{
RDID|FBrf0127514
|Decoville et al.
|2000
PHP|Homozygotes are poorly fertile and only 50% of eggs lead to viable
|larvae. Embryos which do not give rise to larvae stop development
|before the cellular blastoderm stage.
}
REFDSR
{
RDID|FBrf0132331
|Decoville et al.
|2001
PHP|Homozygous adults do not show paralysis after vibration of the culture
|vial.
|Homozygotes and hemizygotes die prematurely, show very low fertility
|and have various homeotic transformations.
|The first type of transformation corresponds to a T1 to T2 transformation;
|hemizygous males have reduced sex combs, with an average of 6 teeth
|(compared to the 11 seen in wild type). The size of the sex comb never
|... (see FBal0094567==Dsp11 report)
PHM|sex comb
|haltere
|wing | ectopic
|metathoracic laterotergite
|scutum | ectopic
|adult abdominal segment 6
|adult abdominal segment 5 | ectopic
|adult abdominal segment 4
|abdominal sternite bristle | ectopic
|metathoracic segment | anterior compartment
}
REF
{
REFM|FBrf0105889
|Mosrin-Huaman et al.
|1998
REFM|FBrf0127514
|Decoville et al.
|2000
REFM|FBrf0132331
|Decoville et al.
|2001
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014410 ICL 1 ? SYM 1 ?{}dsxT ASTR 1 - CLOC 1 84E5--6 REF 1 3 DT 1 6 Jan 2000 RESZ 454
ID|FBti0014410
SYM|?{}dsxT
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000504==dsx
REFDSR
{
RDID|FBrf0051864
|Nagoshi and Baker
|1990
SYN|?{}dsxT
ASAL|FBal0003205==dsxT
MU|spontaneous
CLOC|84E5--6
|Insertion site
LOCB|Proximity to gene: FBgn0000504==dsx
}
REF
{
REFM|FBrf0051864
|Nagoshi and Baker
|1990
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0003205==dsxT
REFDSR
{
RDID|FBrf0046300
|Nothiger et al.
|1987
PHP|Only affects XX flies: the terminalia of XX heterozygous flies carry
|abnormal male and female elements, with the female genitalia anterior
|to the male genitalia. The male genitalia are well developed, but
|the penis apparatus is reduced, the hypandrium is mostly absent and
|many bristles are abnormal. The female vaginal plate is always present,
|but is reduced in size with abnormal bristles. There is often a mass
|of yellow, chitinized material between the vaginal plates, which is
|... (see FBal0003205==dsxT report)
PHM|female terminalia
|female genitalia
|female gonopod
|prothoracic leg | female
|female analia
|anal plate | female
|genitalia
}
REFDSR
{
RDID|FBrf0076142
|Nagoshi et al.
|1995
PHP|No more than 26% of XX
| FBal0003205==dsxT/FBal0003154==dsx1 mutant
| pseudomales produce
|gonads with the most severe group 1 pseudotestes phenotype. The remaining
|pseudomales have a less severe phenotype, with viable germ cells.
|FBal0013357==otu10 and Df(1)otu-P&Dgr;1 cause an increase in
| severity of
|this phenotype: over 70% of the resulting gonads were of group 1.
PHM|germ cell
}
REF
{
REFM|FBrf0046300
|Nothiger et al.
|1987
REFM|FBrf0076142
|Nagoshi et al.
|1995
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014444 ICL 1 ? SYM 1 ?{}en1 ASTR 1 - CLOC 1 47F17--48A1 REF 1 3 DT 1 6 Jan 2000 RESZ 766
ID|FBti0014444
SYM|?{}en1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000577==en
SK|FBst0000256
|chl[1] en[1]/SM5
|FBst0000265
|cn[1] en[1]/SM5
|FBst0001146
|pwn[1] en[1]/SM5; mwh[1] jv[1]/TM1
|FBst0001424
|cn[1] FBal0003716==en[1] L[rm] nw[B] Bc[1] Pu[2] Pin[B]/SM5
|FBst0003065
|cn[1] en[1]/SM5; Dp(2;3)Su-en/TM1
|Total=5
REFDSR
{
RDID|FBrf0042028
|Poole et al.
|1985
PHC|lethal
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}en1
ASAL|FBal0003716==en1
MU|spontaneous
CLOC|47F17--48A1
|Insertion site
LOCB|Proximity to gene: FBgn0000577==en
}
REF
{
REFM|FBrf0042028
|Poole et al.
|1985
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0003716==en1
REFDSR
{
RDID|FBrf0005419
|Brasted
|1941
PHP|In males, extra sex comb often present smaller than normal and in
|mirror-image position in posterior compartment.
PHM|sex comb | ectopic
}
REFDSR
{
RDID|FBrf0013911
|Tokunaga
|1961
PHM|prothoracic tarsal segment | posterior compartment
}
REFDSR
{
RDID|FBrf0024005
|Garcia-Bellido and Santamaria
|1972
PHP|Duplications of transverse rows in female prothoracic leg, extra
|bristles in mesothoracic and metathoracic tarsi.
PHM|mesothoracic tibial transverse bristle row
|metathoracic tibial transverse bristle row
}
REFDSR
{
RDID|FBrf0027996
|Morata and Lawrence
|1975
PHP|Clones of FBal0003716==en1 cells of posterior compartment origin
| fail to
|respect anterior-posterior compartment border in wing disc as do
|FBal0012675==mwh1 clones in wing discs of
| FBal0003716==en1 homozygotes.
PHM|dorsal mesothoracic disc | posterior compartment | somatic clone
|dorsal mesothoracic disc | anterior/posterior compartment boundary | somatic clone
}
REFDSR
{
RDID|FBrf0028554
|Lawrence and Morata
|1976
PHP|Clones of FBal0003716==en1 cells of posterior compartment origin
| fail to
|respect anterior-posterior compartment border in wing disc as do
|FBal0012675==mwh1 clones in wing discs of
| FBal0003716==en1 homozygotes.
PHM|dorsal mesothoracic disc | posterior compartment | somatic clone
|dorsal mesothoracic disc | anterior/posterior compartment boundary | somatic clone
}
REFDSR
{
RDID|FBrf0033468
|Lawrence et al.
|1979
PHP|Duplications of transverse rows in female prothoracic leg, extra
|bristles in mesothoracic and metathoracic tarsi.
PHM|mesothoracic tibial transverse bristle row
|metathoracic tibial transverse bristle row
}
REFDSR
{
RDID|FBrf0037911
|Lawrence and Struhl
|1982
PHP|Homozygous clones in the wing are frequently lost in the posterior
|but not the anterior compartment.
PHM|wing | posterior compartment | somatic clone
}
REFDSR
{
RDID|FBrf0039205
|Morata et al.
|1983
PHP|At 29oC the third segment of the antenna is larger than wild-type
|in homozygous flies, and a bristle close to the border is often enlarged.
|This phenotype is enhanced by the FBgn0005562==M(3)65F mutation. FBal0003716==en1/FBal0003717==en2
|transheterozygotes have abnormal antennae, the phenotype increasing
|at higher temperatures (25 or 29oC). At 29oC the posterior compartment
|of the second segment is almost always abnormal, having extra anterior-like
|bristles which are often arranged in a mirror-image symmetry with respect
|... (see FBal0003716==en1 report)
PHM|antenna
|antennal segment 3
|(with en2) antennal segment 2 | posterior compartment
}
REFDSR
{
RDID|FBrf0039215
|Epper and Sanchez
|1983
PHP|Male FBal0003716==en1 homozygotes have abnormal genitalia, with a reduction
|in the number of clasper teeth, rudimentary dorsal parameres of the
|penis apparatus, and often incomplete rotation of the penis apparatus.
|Viable heteroallelic combinations with other FBgn0000577==en alleles show a more
|extreme phenotype, with a reduction in the genital arch process, hypandrium
|and hypandrial phragma as well. Extra genital arch and anal plate
|bristles are sometimes seen.
|... (see FBal0003716==en1 report)
PHM|hypandrium
|penis
|genital arch
|clasper
|female gonopod
}
REFDSR
{
RDID|FBrf0041008
|Eberlein
|1984
PHP|Shows wing to haltere transformation in FBal0003716==en1/FBal0003743==en28.
PHM|(with en28) wing
}
REFDSR
{
RDID|FBrf0042022
|Kuner et al.
|1985
PHP|Severe thoracic morphological defects.
}
REFDSR
{
RDID|FBrf0043525
|Gubb
|1985
PHP|The posterior wing is an abnormal shape in homozygous flies. The posterior
|wing veins have a variable disrupted pattern, with the anterior crossvein
|(ACV) often being absent or reduced and vein III often appearing slightly
|thickened. The campaniform sensillum associated with the ACV is often
|absent, while the campaniform sensilla of vein III may be increased
|in number. Campaniform sensilla are often found in the posterior wing,
|where they may or may not be associated with vein tissue. Many posterior
|... (see FBal0003716==en1 report)
PHM|wing | posterior
|anterior crossvein
|wing vein L3
|sensillum campaniformium of anterior crossvein
|sensillum campaniformium
|posterior hair
|alar lobe
|scutellum
|prothoracic leg
}
REFDSR
{
RDID|FBrf0046012
|Grau and Simpson
|1987
PHP|In FBal0001792==Cos10, FBal0003716==en1 double mutants
| the duplications characteristic
|of FBal0001792==Cos10 only occur in the original anterior
| compartment, and not
|in the transformed posterior compartment, indicating that the FBal0001792==Cos10
|duplications develop as a position response.
}
REFDSR
{
RDID|FBrf0049488
|Condie and Brower
|1989
PHP|Homozygous adults have abnormal wings, with a posterior to anterior
|transformation. The sex comb on the male prothoracic leg is partially
|duplicated posteriorly. The posterior wing is grossly disrupted in
|FBal0003716==en1/FBal0003717==en2 transheterozygotes,
| rarely having an organized fourth
|or fifth vein. The sex comb on the male prothoracic leg is duplicated
|posteriorly, more distal leg segments are fused and terminal claws
|are sometimes missing. The arista and other anterior elements of the
|... (see FBal0003716==en1 report)
PHM|wing
|wing vein L4
|wing vein L5
|sex comb
}
REFDSR
{
RDID|FBrf0051823
|Hama et al.
|1990
PHP|Heterozygotes with FBal0034516==enXho23 and
| FBal0034515==enSac27 display wing vein abnormalities.
}
REFDSR
{
RDID|FBrf0058044
|Held
|1993
PHP|Additional bristles in the second leg.
PHM|mesothoracic tarsal bristle longitudinal row 2
|mesothoracic tarsal bristle longitudinal row 2.5
}
REFDSR
{
RDID|FBrf0076129
|Felsenfeld and Kennison
|1995
PHP|Mutation has no effect on the FBal0005484==hhMrt phenotype.
}
REFDSR
{
RDID|FBrf0076146
|Sturtevant and Bier
|1995
PHP|Coordinate mutant.
}
REFDSR
{
RDID|FBrf0079370
|Schwartz et al.
|1995
PHP|Viable.
}
REFDSR
{
RDID|FBrf0079938
|Chase and Baker
|1995
PHP|Heterozygotes with FBal0016052==enspt display the FBgn0000577==en and
| spermatheca phenotypes
|at 25oC.
}
REFDSR
{
RDID|FBrf0080091
|Hidalgo
|1994
PHP|FBal0031487==hhbar3 in combination with
| FBab0022271==Df(2R)enE/FBal0003716==en1 causes a phenotype
|reminiscent of a weak FBgn0000490==dpp mutation is produced, narrowing of the
|space between wing veins 3 and 4. Posterior wing clones affect adjacent
|cells of the anterior compartment and cause an overall reduction in
|wing size.
}
REFDSR
{
RDID|FBrf0092613
|Locke and Hanna
|1996
PHP|Homozygotes exhibit a variety of wing vein alterations in the posterior
|compartment of the wing.
|Transheterozygotes with FBal0034506==enEnci have a posterior
| specific wing phenotype:
|bristles characteristic of the anterior wing margin are present on
|the posterior wing margin. Males have duplicated sex combs on the
|prothoracic legs.
PHM|wing & macrochaeta
|sex comb
|wing vein
|wing | posterior compartment
}
REFDSR
{
RDID|FBrf0103326
|Maschat et al.
|1998
PHP|2% of homozygotes and 5% of
| FBal0003716==en1/FBal0003769==en54 flies have a gap
| in the
|fourth wing vein at 25oC.
PHM|wing vein L4
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|viable
}
REF
{
REFM|FBrf0005419
|Brasted
|1941
REFM|FBrf0013911
|Tokunaga
|1961
REFM|FBrf0024005
|Garcia-Bellido and Santamaria
|1972
REFM|FBrf0027996
|Morata and Lawrence
|1975
REFM|FBrf0028554
|Lawrence and Morata
|1976
REFM|FBrf0033468
|Lawrence et al.
|1979
REFM|FBrf0037911
|Lawrence and Struhl
|1982
REFM|FBrf0039205
|Morata et al.
|1983
REFM|FBrf0039215
|Epper and Sanchez
|1983
REFM|FBrf0041008
|Eberlein
|1984
REFM|FBrf0042022
|Kuner et al.
|1985
REFM|FBrf0043525
|Gubb
|1985
REFM|FBrf0046012
|Grau and Simpson
|1987
REFM|FBrf0049488
|Condie and Brower
|1989
REFM|FBrf0051823
|Hama et al.
|1990
REFM|FBrf0058044
|Held
|1993
REFM|FBrf0076129
|Felsenfeld and Kennison
|1995
REFM|FBrf0076146
|Sturtevant and Bier
|1995
REFM|FBrf0079370
|Schwartz et al.
|1995
REFM|FBrf0079938
|Chase and Baker
|1995
REFM|FBrf0080091
|Hidalgo
|1994
REFM|FBrf0092613
|Locke and Hanna
|1996
REFM|FBrf0103326
|Maschat et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015054 ICL 1 ? SYM 1 ?{}Est-6unspecified ASTR 1 - CLOC 1 69A1 REF 1 2 DT 1 6 Jan 2000 RESZ 424
ID|FBti0015054
SYM|?{}Est-6unspecified
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000592==Est-6
REFDSR
{
RDID|FBrf0052539
|Brady et al.
|1990
SYN|?{}Est-6unspecified
ASAL|FBal0058970==Est-6unspecified
CLOC|69A1
|Insertion site
LOCB|Proximity to gene: FBgn0000592==Est-6
}
REF
{
REFM|FBrf0052539
|Brady et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014459 ICL 1 ? SYM 1 ?{}fliI2:19B ASTR 1 - CLOC 1 19F5 REF 1 3 DT 1 31 May 2000 RESZ 549
ID|FBti0014459
SYM|?{}fliI2:19B
SYN|?{}fliI2/19B
DT|31 May 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000709==fliI
REFDSR
{
RDID|FBrf0064390
|Campbell et al.
|1993
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0083951
|de Couet et al.
|1995
SYN|?{}fliI2/19B
ASAL|FBal0031278==fliI2:19B
CLOC|19F5
|Insertion site
LOCB|Proximity to gene: FBgn0000709==fliI
}
REF
{
REFM|FBrf0064390
|Campbell et al.
|1993
REFM|FBrf0083951
|de Couet et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0002826 ICL 1 ? SYM 1 ?{}ftz11 ASTR 1 - CLOC 1 84A6 REF 1 5 DT 1 5 Sep 2000 RESZ 1541
ID|FBti0002826
SYM|?{}ftz11
SYN|?{}ftzW20
|?{}ftzw20
DT|5 Sep 2000
|24 Jun 1997
ICL|?
ASGN|FBgn0001077==ftz
SK|FBst0001841
|y[1]; FBal0004816==ftz[11] red[1] e[1]/TM3, Sb[1]
|FBst0002027
|Ki[1] Dfd[12] FBal0004816==ftz[11] e[1]/TM3, Sb[1]
|FBst0002042
|zen[7] FBal0004816==ftz[11] e[1]/TM3, Sb[1]
|FBst0002224
|Ki[1] FBal0004816==ftz[11] p[p]/TM3, Sb[1]
|FBst0002225
|Df(3R)p25, Ki[1] FBal0004816==ftz[11] e[1]/TM3, Sb[1]
|Total=5
REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
SYN|?{}ftz11
ASAL|FBal0004816==ftz11
MU|ethyl methanesulfonate
CLOC|84A6
|Insertion site
LOCB|Proximity to gene: FBgn0001077==ftz
PHC|lethal | recessive
CC|Insertion determined to be repetitive; approximately 3kb; not shown to
| coorelate with mutant phenotype.
|Insertion determined to be repetitive element of appoximately 3kb;
| correlation with the mutant phenotype asssumed but not proven.
}
REFDSR
{
RDID|FBrf0040502
|Weiner et al.
|1984
ASAL|FBal0004816==ftz11
MU|ethyl methanesulfonate
PHC|lethal | embryonic | pair rule
}
REFDSR
{
RDID|FBrf0040715
|Wakimoto et al.
|1984
PHC|lethal | embryonic
}
REFDSR
{
RDID|FBrf0073734
|Lewis et al.
|1980
PHC|lethal | recessive
}
REF
{
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0040502
|Weiner et al.
|1984
REFM|FBrf0040715
|Wakimoto et al.
|1984
REFM|FBrf0073734
|Lewis et al.
|1980
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0004816==ftz11
REFDSR
{
RDID|FBrf0040502
|Weiner et al.
|1984
PHM|embryonic epidermis
|denticle belt
}
REFDSR
{
RDID|FBrf0040715
|Wakimoto et al.
|1984
PHP|FBal0004816==ftz11/FBab0002646==Df(3R)Scr show abnormal
| segmentation of the germ band,
|with at least half the segments missing. The segmentation of the ventral
|nerve cord is also affected. The labial lobe cannot be seen, and the
|H piece of the larval mouthparts is missing in late embryos. Dorsal
|closure is disrupted.
PHM|dorsal closure stage embryo
|central nervous system | embryonic
|hypostomal sclerite
}
REFDSR
{
RDID|FBrf0046027
|Bender et al.
|1987
PHM|epidermis | embryonic
|embryonic nervous system
}
REFDSR
{
RDID|FBrf0048119
|Jack et al.
|1988
PHP|Odd numbered denticle bands missing.
}
REFDSR
{
RDID|FBrf0049007
|Doe et al.
|1988
PHP|FBtp0005207==P{ftzK}; FBal0004816==ftz11/FBal0004818==ftz13
| individuals die as embryos or larvae.
|66% of FBtp0000074==P{ftzG};
| FBal0004816==ftz11/FBal0004818==ftz13 individuals
| survive to adulthood.
|FBtp0005207==P{ftzK}; FBal0004816==ftz11/FBal0004818==ftz13
| embryos are identified by weak segmentation
|defects in the CNS.
}
REFDSR
{
RDID|FBrf0049576
|Lawrence and Johnston
|1989
PHP|The eve stripes mature as wild-type.
}
REFDSR
{
RDID|FBrf0054059
|Parkhurst and Ish-Horowicz
|1991
PHP|Interacts with FBal0030148==RpII140wimp maternal effect.
}
REFDSR
{
RDID|FBrf0055876
|Panzer et al.
|1992
PHP|Parasegments 1 and 2 are fused and the salivary gland placodes occupy
|the posterior half of the fused parasegment in the FBgn0003339==Scr expression
|domain.
PHM|parasegment 1
|parasegment 2
}
REFDSR
{
RDID|FBrf0056133
|Tabata et al.
|1992
PHP|ftz embryos lack even-numbered hh stripes.
}
REFDSR
{
RDID|FBrf0084489
|Welte et al.
|1995
PHP|Heterozygotes with FBal0004823==ftzUal1 exhibit a higher
| frequency of heat shock
|induced transformation of abdominal segment 1 than those embryos carrying
|three wild type copies of FBgn0001077==ftz (FBab0003681==Dp(3;3)D1/+). An addition of another
|wild type FBgn0001077==ftz to these embryos results in another modest increase
|in frequency of transformation.
}
REFDSR
{
RDID|FBrf0086468
|Hyduk and Percival-Smith
|1996
PHP|Mutant embryos are deficient for cuticular structures derived from
|the even numbered parasegments.
PHM|parasegment 2
|parasegment 10
|parasegment 12
|parasegment 14
|parasegment 4
|parasegment 10
|parasegment 12
|parasegment 14
|parasegment 6
|parasegment 10
|parasegment 12
|parasegment 14
|parasegment 8
|parasegment 10
|parasegment 12
|parasegment 14
|epidermis | embryonic
}
REFDSR
{
RDID|FBrf0130058
|Rusch and Kaufman
|2000
PHP|The maxillary and labial lobes are fused in mutant embryos.
PHM|embryonic labial segment
|embryonic maxillary segment
}
REF
{
REFM|FBrf0040502
|Weiner et al.
|1984
REFM|FBrf0040715
|Wakimoto et al.
|1984
REFM|FBrf0046027
|Bender et al.
|1987
REFM|FBrf0048119
|Jack et al.
|1988
REFM|FBrf0049007
|Doe et al.
|1988
REFM|FBrf0049576
|Lawrence and Johnston
|1989
REFM|FBrf0054059
|Parkhurst and Ish-Horowicz
|1991
REFM|FBrf0055876
|Panzer et al.
|1992
REFM|FBrf0056133
|Tabata et al.
|1992
REFM|FBrf0084489
|Welte et al.
|1995
REFM|FBrf0086468
|Hyduk and Percival-Smith
|1996
REFM|FBrf0130058
|Rusch and Kaufman
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016757 ICL 1 ? SYM 1 ?{}ftz12 ASTR 1 - CLOC 1 - REF 1 3 DT 1 4 Dec 2000 RESZ 577
ID|FBti0016757
SYM|?{}ftz12
DT|4 Dec 2000
|16 Nov 2000
ICL|?
ASGN|FBgn0001077==ftz
SK|FBst0003311
|h[41] th[1] st[1] FBal0004817==ftz[12] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1]
|Total=1
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
ASAL|FBal0004817==ftz12
MU|ethyl methanesulfonate
CC|Unattributed statement that this allele is associated with a 5-kb insertion
| in the transcribed region.
}
REF
{
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014467 ICL 1 ? SYM 1 ?{}fw34e ASTR 1 - CLOC 1 11A1 REF 1 2 DT 1 6 Jan 2000 RESZ 526
ID|FBti0014467
SYM|?{}fw34e
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001083==fw
SK|FBst0000194
|y[2S] FBal0004903==fw[34e]
|Total=1
REFDSR
{
RDID|FBrf0091112
|Leshko-Lindsay and Corces
|1997
SYN|?{}fw34e
ASAL|FBal0004903==fw34e
CLOC|11A1
|Insertion site
LOCB|Proximity to gene: FBgn0001083==fw
PHC|lethal | partially
|lethal | female | pupal
}
REF
{
REFM|FBrf0091112
|Leshko-Lindsay and Corces
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0004903==fw34e
REFDSR
{
RDID|FBrf0091112
|Leshko-Lindsay and Corces
|1997
PHP|Mild defects in eye morphology. Defects in the development of the
|mechanosensory bristles including the macrochaetae, microchaetae and
|bristles surrounding the eye. Shortened head and scutellum.
|FBal0004903==fw34e/FBab0000482==Df(1)KA10 transheterozygotes do
| not produce any viable
|adult females, female lethal phase occurs in the pupal stages.
PHM|retina
|macrochaeta
|microchaeta
|eye & macrochaeta
|adult head
|scutellum
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Originally showed eye surface medium folded; bristles
|much gnarled. Schultz and Curry report that stock in
|1940 showed gnarled bristles and eye small but no
|vertical fold.
|RK2.
}
REF
{
REFM|FBrf0091112
|Leshko-Lindsay and Corces
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015044 ICL 1 ? SYM 1 ?{}fwU2 ASTR 1 - CLOC 1 11A1 REF 1 2 DT 1 6 Jan 2000 RESZ 431
ID|FBti0015044
SYM|?{}fwU2
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001083==fw
REFDSR
{
RDID|FBrf0091112
|Leshko-Lindsay and Corces
|1997
SYN|?{}fwU2
ASAL|FBal0057359==fwU2
CLOC|11A1
|Insertion site
LOCB|Proximity to gene: FBgn0001083==fw
PHC|lethal | partially
}
REF
{
REFM|FBrf0091112
|Leshko-Lindsay and Corces
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0057359==fwU2
REFDSR
{
RDID|FBrf0091112
|Leshko-Lindsay and Corces
|1997
PHP|Eyes are reduced in size and exhibit deep penetrating furrows in the
|retina that reach the basement membrane. Adjacent to the furrows the
|lamina has depressions. Ommatidial pattern is severely disorganized
|(appear as bent not straight columns and ommatidia are often missing
|in the retinal epithelium producing large gaps between the columns)
|and the ommatidia show altered morphology (lose hexagonal shape and
|appear flattened or rounded, number and spacing of photoreceptors is
|... (see FBal0057359==fwU2 report)
PHM|retina
|ommatidium
|lamina
|interommatidial bristle
|photoreceptor cell
|cone cell
|pigment cell
|macrochaeta
|microchaeta
|eye & macrochaeta
|adult head
|scutellum
}
REF
{
REFM|FBrf0091112
|Leshko-Lindsay and Corces
|1997
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015043 ICL 1 ? SYM 1 ?{}fwU3 ASTR 1 - CLOC 1 11A1 REF 1 2 DT 1 6 Jan 2000 RESZ 408
ID|FBti0015043
SYM|?{}fwU3
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001083==fw
REFDSR
{
RDID|FBrf0091112
|Leshko-Lindsay and Corces
|1997
SYN|?{}fwU3
ASAL|FBal0057358==fwU3
CLOC|11A1
|Insertion site
LOCB|Proximity to gene: FBgn0001083==fw
}
REF
{
REFM|FBrf0091112
|Leshko-Lindsay and Corces
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014468 ICL 1 ? SYM 1 ?{}fz28 ASTR 1 - CLOC 1 70D4--5 REF 1 2 DT 1 6 Jan 2000 RESZ 398
ID|FBti0014468
SYM|?{}fz28
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001085==fz
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
SYN|?{}fz28
ASAL|FBal0004944==fz28
MU|&ggr; ray
CLOC|70D4--5
|Insertion site
LOCB|Proximity to gene: FBgn0001085==fz
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0004944==fz28
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
PHP|Moderate phenotype.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Moderate thoracic bristle phenotype; moderate wing-hair disorientation.
PHM|macrochaeta & thorax | adult
|wing hair
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014996 ICL 1 ? SYM 1 ?{}fzGD4b ASTR 1 - CLOC 1 70D4--5 REF 1 2 DT 1 6 Jan 2000 RESZ 391
ID|FBti0014996
SYM|?{}fzGD4b
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001085==fz
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
SYN|?{}fzGD4b
ASAL|FBal0049583==fzGD4b
CLOC|70D4--5
|Insertion site
LOCB|Proximity to gene: FBgn0001085==fz
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0049583==fzGD4b
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
PHP|Moderate phenotype.
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014997 ICL 1 ? SYM 1 ?{}fzGL3a ASTR 1 - CLOC 1 70D4--5 REF 1 2 DT 1 6 Jan 2000 RESZ 391
ID|FBti0014997
SYM|?{}fzGL3a
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001085==fz
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
SYN|?{}fzGL3a
ASAL|FBal0049586==fzGL3a
CLOC|70D4--5
|Insertion site
LOCB|Proximity to gene: FBgn0001085==fz
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0049586==fzGL3a
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
PHP|Moderate phenotype.
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015598 ICL 1 ? SYM 1 ?{}g1 ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 1362
ID|FBti0015598
SYM|?{}g1
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
SK|FBst0000936
|Df(1)64c18, FBal0004957==g[1] sd[1]/Dp(1;2;Y)w[+]/C(1)DX, y[1] w[1] f[1]
|FBst0003958
|g[1]
|FBst0004306
|dec-1[2] sc[1] v[24] FBal0004957==g[1] f[1]/FM3
|FBst0004314
|fs(1)A1304[1] FBal0004957==g[1] f[1]/FM3
|FBst0004657
|l(1)2Cc[2] g[1]/FM7a
|FBst0004668
|l(1)3Da[5] sn[3] g[1]/FM7a
|FBst0004922
|Hk[1] FBal0004957==g[1] sd[1] l(1)15Bb[R31] f[1]/C(1)DX; Dp(1;4)r[+]/+
|FBst0004923
|Hk[1] FBal0004957==g[1] sd[1] l(1)15Dc[R3] f[1]/C(1)DX; Dp(1;4)r[+]/+
|FBst0004924
|Hk[1] FBal0004957==g[1] sd[1] l(1)15Dd[R12] f[1]/C(1)DX; Dp(1;4)r[+]/+
|FBst0006027
|y[1] ac[1] sc[1] pn[1] w[1] rb[1] cm[1] ct[1] sn[3] ras[4] v[1] m[1] FBal0004957==g[1] f[1] car[1]/FM6
|FBst0006888
|tsg[4] g[1]/FM7c
|FBst0200120
|g[1]
|FBst0200187
|g[1]; cn[1]; e[1]
|FBst0201169
|g[1]; cn[1]; e[1], skew[1]
|FBst0201170
|g[1]; cn[1]; e[1]; ey[1]
|FBst0201171
|g[1]
|Total=16
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}g1
ASAL|FBal0004957==g1
MU|spontaneous
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
ALESR
{
ASYM|FBal0004957==g1
REFDSR
{
RDID|FBrf0054090
|Tearle
|1991
PHP|Lightly pigmented eyes and some pigment deposition in the ocelli.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
PHP|Eye color: red pigments are reduced to 57 +/- 2% of wild-type levels,
|brown pigments are reduced to 25 +/- 3% of wild-type levels in females.
|Red pigments are reduced to 72 +/- 4% of wild-type levels, brown pigments
|are reduced to 66 +/- 1% of wild-type levels in males.
|Malpighian tubule color: colorless (wild-type color is orange).
|Testis color: pale yellow (wild-type color is bright yellow).
PHM|pigment cell
|Malpighian tubule
|testis sheath
}
REFDSR
{
RDID|FBrf0127175
|Kretzschmar et al.
|2000
PHP|Eye color: the drosopterin (red pigment) content of
| FBal0004957==g1 flies is
|reduced compared to wild type.
|Eye color: the drosopterin (red pigment) content of
| FBal0004957==g1 FBal0014434==rb1
|double mutant flies is reduced to 18% of wild type.
|Eye color: the xanthommatin (brown pigment) content of
| FBal0004957==g1 flies
|is reduced to 58% of wild type.
|Eye color: the xanthommatin (brown pigment) content of
| FBal0004957==g1 FBal0014434==rb1
|... (see FBal0004957==g1 report)
PHM|pigment cell
}
REF
{
REFM|FBrf0054090
|Tearle
|1991
REFM|FBrf0125153
|Lloyd et al.
|1999
REFM|FBrf0127175
|Kretzschmar et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015599 ICL 1 ? SYM 1 ?{}g3 ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 394
ID|FBti0015599
SYM|?{}g3
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}g3
ASAL|FBal0004960==g3
MU|spontaneous
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
ALESR
{
ASYM|FBal0004960==g3
REFDSR
{
RDID|FBrf0093727
|Simpson et al.
|1997
PHP|Eye color: dull brownish.
|Flies have reduced pigmentation throughout the body; pigment granules
|are still visible in the ommatidia but contain less pigment than
|wild-type.
PHM|pigment granule
}
REFDSR
{
RDID|FBrf0095986
|Ooi et al.
|1997
PHP|Eyes exhibit pigmentation defects and reduced number of pigment granules.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Like FBal0004957==g1, but gives lighter orange in combination with
|FBgn0003965==v. Has 21% normal red pigment and 47% normal brown pigment
|(Nolte, 1959). Malpighian tubes extremely
|pale yellow (Brehme and Demerec, 1942).
|RK1.
}
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
PHP|Eye color: red pigments are reduced to 45 +/- 1% of wild-type levels,
|brown pigments are reduced to 70 +/- 8% of wild-type levels in females.
|Red pigments are reduced to 50 +/- 3% of wild-type levels, brown pigments
|are reduced to 52 +/- 5% of wild-type levels in males.
|Malpighian tubule color: colorless (wild-type color is orange).
|Testis color: yellow (wild-type color is bright yellow).
PHM|pigment cell
|Malpighian tubule
|testis sheath
}
REFDSR
{
RDID|FBrf0129983
|Mullins et al.
|2000
PHP|In an assay for larval motility, FBal0004960==g3 mutants
| performed as well as
|wild-type larvae. In locomotor assays testing olfactory response to
|propionic acid, FBal0004960==g3 mutants perform significantly
| less well than
|wild-type larvae.
}
REF
{
REFM|FBrf0093727
|Simpson et al.
|1997
REFM|FBrf0095986
|Ooi et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
REFM|FBrf0129983
|Mullins et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015600 ICL 1 ? SYM 1 ?{}g4 ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 1241
ID|FBti0015600
SYM|?{}g4
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
SK|FBst0000009
|amx[1]/In(1)dl-49, m[2] FBal0004961==g[4]
|FBst0000243
|In(1)dl-49, In(1)Hw[2], y[1] ac[Hw-2] m[2] g[4]/C(1)RM, y[1] w[1] f[1]
|FBst0000793
|In(1)sc[7], In(1)AM, sc[7] ptg[4]/In(1)dl-49, y[1] ac[Hw-1] m[2] FBal0004961==g[4]
|FBst0001418
|In(1)sc[4], y[1] sc[4] wy[74i] f[1] fu[1] car[1] ABO-X[1]/In(1)dl-49, y[1] ac[Hw-1] m[2] FBal0004961==g[4]
|FBst0003963
|In(1)dl-49, Sxl[f1] v[Of] g[4]/R(YL)/C(1;YS)1, oc[1] ptg[1]
|FBst0003964
|In(1)dl-49, y[1] ac[Hw-1] m[2] FBal0004961==g[4] f[5]/R(1)2, In(1)w[vC]
|FBst0005393
|ras[1] v[1] l(1)10Bm[1]/In(1)dl-49, ac[Hw-1] m[2] FBal0004961==g[4]
|FBst0006019
|Df(1)w258-11, y[1]/In(1)dl-49, y[1] ac[Hw-1] m[2] FBal0004961==g[4]
|FBst1001484
|Df(1)sc[4]/ In(1)dl-49, y[1] Hw [1] m[2] g[4]/y[2]Y67g
|Total=9
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}g4
ASAL|FBal0004961==g4
MU|X ray
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
ALESR
{
ASYM|FBal0004961==g4
REFDSR
{
RDID|FBrf0005752
|Brehme and Demerec
|1942
PHP|Malpighian tubule color: extremely pale yellow.
PHM|Malpighian tubule
}
REFDSR
{
RDID|FBrf0012680
|Nolte
|1959
PHP|22% normal red pigment and 23% normal brown pigment.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: like FBal0004958==g2.
|RK1.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
PHP|Eye color: red pigments are reduced to 25 +/- 1% of wild-type levels,
|brown pigments are reduced to 28 +/- 5% of wild-type levels in females.
|Red pigments are reduced to 38 +/- 3% of wild-type levels, brown pigments
|are reduced to 37 +/- 3% of wild-type levels in males.
|Malpighian tubule color: very pale-clear (wild-type color is orange).
|Testis color: yellow (wild-type color is bright yellow).
PHM|pigment cell
|Malpighian tubule
|testis sheath
}
REF
{
REFM|FBrf0005752
|Brehme and Demerec
|1942
REFM|FBrf0012680
|Nolte
|1959
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015610 ICL 1 ? SYM 1 ?{}g61 ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 382
ID|FBti0015610
SYM|?{}g61
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}g61
ASAL|FBal0095411==g61
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015601 ICL 1 ? SYM 1 ?{}gEMS ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 385
ID|FBti0015601
SYM|?{}gEMS
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}gEMS
ASAL|FBal0004992==gEMS
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015602 ICL 1 ? SYM 1 ?{}gim ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 382
ID|FBti0015602
SYM|?{}gim
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}gim
ASAL|FBal0004994==gim
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0022289 ICL 1 ? SYM 1 ?{}gish1 ASTR 1 - CLOC 1 89B9--12 REF 1 2 DT 1 26 Mar 2002 RESZ 349
ID|FBti0022289
SYM|?{}gish1
DT|26 Mar 2002
|26 Mar 2002
ICL|?
ASGN|FBgn0011253==gish
REFDSR
{
RDID|FBrf0145174
|Hummel et al.
|2002
SYN|?{}gish1
CLOC|89B9--12
|Insertion site
LOCB|Proximity to gene: FBgn0011253==gish
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0145174
|Hummel et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014470 ICL 1 ? SYM 1 ?{}gro1 ASTR 1 - CLOC 1 96F10 REF 1 2 DT 1 6 Jan 2000 RESZ 442
ID|FBti0014470
SYM|?{}gro1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001139==gro
SK|FBst0000511
|gro[1]
|Total=1
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}gro1
ASAL|FBal0005217==gro1
MU|spontaneous
CLOC|96F10
|Insertion site
LOCB|Proximity to gene: FBgn0001139==gro
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0005217==gro1
REFDSR
{
RDID|FBrf0046015
|Knust et al.
|1987
PHP|Low penetrance bushes of bristles over compound eyes of homozygous
|flies. FBal0005217==gro1, FBgn0000591==E(spl)- transheterozygotes
| are viable and exhibit
|a large number of bristles on thorax, head and wings.
}
REFDSR
{
RDID|FBrf0055903
|Fischer-Vize et al.
|1992
PHP|FBal0045820==groBFP2/FBal0005217==gro1
| transheterozygotes have wild-type eyes.
}
REFDSR
{
RDID|FBrf0084542
|de Celis and Ruiz-Gomez
|1995
PHP|The wing phenotype of FBal0005217==gro1 heterozygous with
| deletions for FBgn0001139==gro
|is of overgrowth and pattern duplications in regions close to the D/V
|compartment boundary in the anterior compartment. Weak phenotypes
|include distal bifurcation of vein LIII and thickening of the proximal
|costa. Extreme phenotypes consist of overgrowth and pattern duplications
|in proximal or distal regions of the anterior wing margin, including
|duplication and triplication of LIII and loss of LII. Sensory elements
|... (see FBal0005217==gro1 report)
PHM|wing vein L1
|wing vein L2
|wing vein L3
|wing | anterior compartment
|wing | dorsal/ventral compartment boundary
|macrochaeta & head
|macrochaeta & thorax
|macrochaeta & abdominal tergite
|microchaeta & head
|microchaeta & thorax
|microchaeta & abdominal tergite
}
REFDSR
{
RDID|FBrf0099460
|Price et al.
|1997
PHP|FBal0082904==groC105/FBal0005217==gro1 mutants display
| enlarged and fused ocelli, and
|an increased number of fronto-orbital microchaetae.
PHM|ocellus
|microchaeta & head | adult
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Homozygotes have clumps of extra bristles above each
|eye which give impression of bushy eyebrows; also
|extra bristles on the humerus. Top of head tends to be
|malformed; ocelli often enlarged and run together. In
|selected stocks, penetrance approaches 100%, but is
|low in unselected stocks. Concluded to be an allele of
|E(spl) on the basis of the visible phenotype of
|... (see FBal0005217==gro1 report)
}
REF
{
REFM|FBrf0046015
|Knust et al.
|1987
REFM|FBrf0055903
|Fischer-Vize et al.
|1992
REFM|FBrf0084542
|de Celis and Ruiz-Gomez
|1995
REFM|FBrf0099460
|Price et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0025340 ICL 1 ? SYM 1 ?{}gt1a ASTR 1 - CLOC 1 3A3 REF 1 2 DT 1 7 Jul 2003 RESZ 685
ID|FBti0025340
SYM|?{}gt1a
SYN|?{}?{}gt1
DT|7 Jul 2003
|7 Jul 2003
ICL|?
ID2|FBti0014474
ASGN|FBgn0001150==gt
SK|FBst0000053
|gt[1] w[a]
|FBst0002113
|gt[1] w[a]; Ki[1] pb[4] p[p] ss[a40a]/TM2
|Total=2
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}gt1a
ASAL|FBal0005233==gt1
MU|spontaneous
CLOC|3A3
|Insertion site
LOCB|Proximity to gene: FBgn0001150==gt
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two insertions associated with this allele; see FBti0025341==?{}gt1b.
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0005233==gt1
REFDSR
{
RDID|FBrf0003150
|Bridges
|1935
PHP|Salivary gland chromosomes are double normal thickness in some cells.
PHM|larval salivary gland | embryonic & chromosome
}
REFDSR
{
RDID|FBrf0043261
|Narachi and Boyd
|1985
PHP|FBal0005252==gtQ292/FBal0005233==gt1 larvae show a
| reduction in the normal inhibition
|of DNA synthesis following treatment with N-acetoxy-2-acetylaminofluorene.
|FBal0005234==gt13z/FBal0005233==gt1 larvae do not have
| a defect in the repair of X-ray
|induced DNA breaks.
}
REFDSR
{
RDID|FBrf0049604
|Mohler et al.
|1989
PHP|Delayed pupariation and enlarged larvae, pupae and adults.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Larval development is 4 days longer than normal, resulting in giant
|larvae, pupae, and imagos. Adult weight is 1.7 times normal. Not all
|genetically FBgn0001150==gt flies show the giant character, the rest have normal
|size. The distribution is sharply bimodal. The percentage of
|phenotypically giant animals is greatest in well-fed cultures, and is
|also raised by the modifying action of FBal0001034==bb11.
|RK3.
}
REF
{
REFM|FBrf0003150
|Bridges
|1935
REFM|FBrf0043261
|Narachi and Boyd
|1985
REFM|FBrf0049604
|Mohler et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0025341 ICL 1 ? SYM 1 ?{}gt1b ASTR 1 - CLOC 1 3A3 REF 1 2 DT 1 7 Jul 2003 RESZ 685
ID|FBti0025341
SYM|?{}gt1b
SYN|?{}?{}gt1
DT|7 Jul 2003
|7 Jul 2003
ICL|?
ID2|FBti0014474
ASGN|FBgn0001150==gt
SK|FBst0000053
|gt[1] w[a]
|FBst0002113
|gt[1] w[a]; Ki[1] pb[4] p[p] ss[a40a]/TM2
|Total=2
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}gt1b
ASAL|FBal0005233==gt1
MU|spontaneous
CLOC|3A3
|Insertion site
LOCB|Proximity to gene: FBgn0001150==gt
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two insertions associated with this allele; see FBti0025340==?{}gt1a.
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0005233==gt1
REFDSR
{
RDID|FBrf0003150
|Bridges
|1935
PHP|Salivary gland chromosomes are double normal thickness in some cells.
PHM|larval salivary gland | embryonic & chromosome
}
REFDSR
{
RDID|FBrf0043261
|Narachi and Boyd
|1985
PHP|FBal0005252==gtQ292/FBal0005233==gt1 larvae show a
| reduction in the normal inhibition
|of DNA synthesis following treatment with N-acetoxy-2-acetylaminofluorene.
|FBal0005234==gt13z/FBal0005233==gt1 larvae do not have
| a defect in the repair of X-ray
|induced DNA breaks.
}
REFDSR
{
RDID|FBrf0049604
|Mohler et al.
|1989
PHP|Delayed pupariation and enlarged larvae, pupae and adults.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Larval development is 4 days longer than normal, resulting in giant
|larvae, pupae, and imagos. Adult weight is 1.7 times normal. Not all
|genetically FBgn0001150==gt flies show the giant character, the rest have normal
|size. The distribution is sharply bimodal. The percentage of
|phenotypically giant animals is greatest in well-fed cultures, and is
|also raised by the modifying action of FBal0001034==bb11.
|RK3.
}
REF
{
REFM|FBrf0003150
|Bridges
|1935
REFM|FBrf0043261
|Narachi and Boyd
|1985
REFM|FBrf0049604
|Mohler et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014520 ICL 1 ? SYM 1 ?{}Lim32 ASTR 1 - CLOC 1 37B13--C1 REF 1 3 DT 1 6 Jan 2000 RESZ 598
ID|FBti0014520
SYM|?{}Lim32
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002023==Lim3
SK|FBst0005386
|Lim3[2]/CyO
|Total=1
REFDSR
{
RDID|FBrf0046993
|Black et al.
|1987
PHC|lethal | larval | recessive
}
REFDSR
{
RDID|FBrf0084402
|Stathakis et al.
|1995
SYN|?{}Lim32
ASAL|FBal0008649==Lim32
MU|ethyl methanesulfonate + formaldehyde
CLOC|37B13--C1
|Insertion site
LOCB|Proximity to gene: FBgn0002023==Lim3
}
REF
{
REFM|FBrf0046993
|Black et al.
|1987
REFM|FBrf0084402
|Stathakis et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0008649==Lim32
REFDSR
{
RDID|FBrf0089206
|Wright
|1996
PHP|Most hemizygotes do not pupariate, remaining as second or third instar
|larvae up to 8 or 9 days after egg laying. A few hemizygotes do pupariate
|8 to 11 days after egg laying, and these pupae generally develop into
|pharate adults that do not eclose. These pharate adults show a complete
|lack of differentiated cuticle on the abdomen, and have reduced cuticle
|formation on the thorax and head.
PHM|cuticle & abdomen | pharate adult
|cuticle & thorax | pharate adult
|cuticle & head | pharate adult
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|strong allele in which second and third instar larvae
|persist until days eight and nine; few survive to
|pharate-adult stage with incomplete sclerotization.
}
REF
{
REFM|FBrf0089206
|Wright
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014535 ICL 1 ? SYM 1 ?{}lz34 ASTR 1 - CLOC 1 8D5--6 REF 1 2 DT 1 6 Jan 2000 RESZ 447
ID|FBti0014535
SYM|?{}lz34
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002576==lz
SK|FBst0000065
|lz[34]/C(1)DX, y[1] f[1]
|Total=1
REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
SYN|?{}lz34
ASAL|FBal0011773==lz34
MU|spontaneous
CLOC|8D5--6
|Insertion site
LOCB|Proximity to gene: FBgn0002576==lz
}
REF
{
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0011773==lz34
REFDSR
{
RDID|FBrf0011129
|Green and Green
|1956
PHP|Homozygotes have rough eyes which are reduced in size. Red eye pigment
|is distributed over the entire eye. The tarsal claws are reduced.
|The spermathecae and pars ovariae are absent in homozygous females.
PHM|eye
|spermathecum
|tarsus
|ovary
}
REFDSR
{
RDID|FBrf0068701
|Stocker et al.
|1993
PHP|The antennal funiculus is reduced in size in hemizygous males. All
|large and small basiconic sensilla on the antennal funiculus are missing,
|and the number of trichoid sensilla on the antennal funiculus is reduced.
|The number of coeloconic sensilla on the antennal funiculus is normal.
PHM|antennal segment 3
|sensillum basiconicum of antennal segment 3
|sensillum trichodeum of antennal segment 3
}
REFDSR
{
RDID|FBrf0083505
|Vosshall and Young
|1995
PHP|Displays locomotor activity rhythm with an approximately 24h period.
}
REFDSR
{
RDID|FBrf0086985
|Daga et al.
|1996
PHP|R7 cells are converted to outer receptor cells.
PHM|photoreceptor cell R7
}
REFDSR
{
RDID|FBrf0090446
|Batterham et al.
|1996
PHP|Homozygotes show disruption of the ommatidial array and fusion of ommatidia
|across the posterior half of the eye. Black pock marks are visible
|on the surface of the eye. The retina is moderately disorganized,
|particularly in the posterior region. The underlying lamina is also
|disorganized in the posterior region. The fenestrated membrane is
|abnormal. Rhabdomeric bundles are found in the cortex of the lamina.
|The number and type of photoreceptors in each ommatidium are sometimes
|... (see FBal0011773==lz34 report)
PHM|eye | posterior
|ommatidium
|eye
|lamina cortex
|retina
|lamina
}
REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
PHP|Rough eye phenotype. Some secondary pigment cells are absent. Photoreceptor
|neuron recruitment is perturbed. Some facets have only six cells,
|R7 appears to be transformed to R1-6-like photoreceptor cell. An R7-like
|cell is missing in some facets.
PHM|photoreceptor cell R7
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye phenotype intermediate between lz and FBal0011764==lz3.
|Surface of eye has large areas of fused facets with a
|few normal facets (Clayton, 1957);
|eye color dark red with small yellowish spots. Larval
|Malpighian tubes slightly lighter than normal;
|variable (Brehme and Demerec, 1942).
|Tarsal claws reduced. Spermathecae and parovaria
|... (see FBal0011773==lz34 report)
}
REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
PHP|FBal0011773==lz34 adults have a severe mutant eye phenotype.
| Ectopic cell
|death is seen in third larval instar eye discs.
PHM|eye
|eye disc
}
REF
{
REFM|FBrf0011129
|Green and Green
|1956
REFM|FBrf0068701
|Stocker et al.
|1993
REFM|FBrf0083505
|Vosshall and Young
|1995
REFM|FBrf0086985
|Daga et al.
|1996
REFM|FBrf0090446
|Batterham et al.
|1996
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0158867
|Siddall et al.
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014537 ICL 1 ? SYM 1 ?{}lzK ASTR 1 - CLOC 1 8D5--6 REF 1 2 DT 1 6 Jan 2000 RESZ 464
ID|FBti0014537
SYM|?{}lzK
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002576==lz
SK|FBst0002387
|lz[K]
|FBst0003657
|In(1)sc[260-14] lz[K]/C(1)DX, y[1] f[1]
|Total=2
REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
SYN|?{}lzK
ASAL|FBal0011825==lzK
CLOC|8D5--6
|Insertion site
LOCB|Proximity to gene: FBgn0002576==lz
}
REF
{
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0011825==lzK
REFDSR
{
RDID|FBrf0049495
|Renfranz and Benzer
|1989
PHP|A weak lz allele. Adult eye slightly rough, irregular facets shapes,
|eye disc appears normal.
}
REFDSR
{
RDID|FBrf0063599
|Krivshenko
|1956
PHP|Homozygous males have slightly narrow eyes, with uneven fused facets.
|Males are viable and fertile, homozygous females have not been obtained.
|Heterozygous females are phenotypically normal.
PHM|eye
|ommatidium
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|RK1.
|Tarsal claws normal. Spermathecae and parovaria present.
}
REFDSR
{
RDID|FBrf0068701
|Stocker et al.
|1993
PHP|The antennal funiculus is reduced in size in hemizygous males. The
|number of large and small basiconic sensilla is reduced. The density
|of the coeloconic sensilla on the antennal funiculus is increased and
|the density of the large basiconic sensilla on the antennal funiculus
|is decreased compared to wild-type.
PHM|antennal segment 3
|sensillum basiconicum of antennal segment 3
}
REFDSR
{
RDID|FBrf0086985
|Daga et al.
|1996
PHP|Some ommatidia have a supernumerary R7 photoreceptor cell, and some
|have extra outer photoreceptor cells.
PHM|photoreceptor cell
}
REFDSR
{
RDID|FBrf0090446
|Batterham et al.
|1996
PHP|Homozygous females have normal eyes. Hemizygous males have a mild
|rough eye phenotype, with disruption of the ommatidial array at the
|posterior rim of the eye. Black pock marks are visible on the surface
|of the eye.
PHM|eye | posterior
|ommatidium
|eye
}
REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
PHP|Mild eye phenotype. Defects in photoreceptor neuron recruitment.
|Some facets have seven cells with larger, R1 to R6 like rhabdomeres,
|an R7-like cell is absent. Facets may have a duplicated R7 cells.
|Other facets have normal looking R7 cells but incorrect numbers of
|outer photoreceptor cells.
PHM|photoreceptor cell R1
|photoreceptor cell R2
|photoreceptor cell R3
|photoreceptor cell R4
|photoreceptor cell R5
|photoreceptor cell R6
|photoreceptor cell R7
}
REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
PHP|FBal0011825==lzK adults have a mild mutant eye phenotype. Ectopic
| cell death
|is seen in third larval instar eye discs.
PHM|eye
|eye disc
}
REF
{
REFM|FBrf0049495
|Renfranz and Benzer
|1989
REFM|FBrf0063599
|Krivshenko
|1956
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0068701
|Stocker et al.
|1993
REFM|FBrf0086985
|Daga et al.
|1996
REFM|FBrf0090446
|Batterham et al.
|1996
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0158867
|Siddall et al.
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0037935 ICL 1 ? SYM 1 ?{}lzL ASTR 1 - CLOC 1 8D5--6 REF 1 2 DT 1 21 Oct 2003 RESZ 436
ID|FBti0037935
SYM|?{}lzL
DT|21 Oct 2003
|21 Oct 2003
ICL|?
ASGN|FBgn0002576==lz
SK|FBst0007366
|lz[L]/Dp(1;Y)lz[+]/FM7a
|Total=1
REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
SYN|?{}lzL
ASAL|FBal0061066==lzL
CLOC|8D5--6
|Insertion site
LOCB|Proximity to gene: FBgn0002576==lz
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0158867
|Siddall et al.
|2003
}
ALESR
{
ASYM|FBal0061066==lzL
REFDSR
{
RDID|FBrf0068701
|Stocker et al.
|1993
PHP|The antennal funiculus is reduced in size in hemizygous males. All
|large and small basiconic sensilla on the antennal funiculus are missing,
|and the number of trichoid sensilla on the antennal funiculus is reduced.
|The number of coeloconic sensilla on the antennal funiculus is normal.
|The density of the coeloconic sensilla on the antennal funiculus is
|increased and the density of the trichoid sensilla on the antennal
|funiculus is decreased compared to wild-type.
|... (see FBal0061066==lzL report)
PHM|antennal segment 3
|sensillum basiconicum of antennal segment 3
|sensillum trichodeum of antennal segment 3
|maxillary palp sensillum basiconicum
}
REFDSR
{
RDID|FBrf0090446
|Batterham et al.
|1996
PHP|Homozygotes have a total lack of ommatidial structure in the eye.
|Pigment is dispersed as a ring around the edge of the eye ("spectacle"
|phenotype). Few, if any lenses form, and the eye is covered by a cuticle
|scar. The 'retina' appears to lack pigment cells. Photoreceptor cell
|orientation is random, and the fenestrated membrane is absent.
PHM|eye
|ommatidium
|lens
|photoreceptor cell
|pigment cell
}
REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
PHP|15% of photoreceptor cell clusters are abnormal, cells R1 and R6 are
|not recruited properly. Uniform sheet of unorganized cone cells is
|found. The periphery of the retina contains cells in loosely organized
|clusters including cones as well as primary and secondary pigment cells,
|the darker pigment produces the 'spectacle' phenotype.
PHM|photoreceptor cell R1
|photoreceptor cell R6
|cone cell
}
REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
PHP|FBal0061066==lzL adults have a "spectacle" eye phenotype.
| Ommatidial clusters
|are rarely detectable in FBal0061066==lzL eyes. Ectopic cell
| death is seen
|in third larval instar eye discs, between rows 3 an 7 posterior to
|the morphogenetic furrow.
PHM|ommatidium
|eye disc
|eye
}
REF
{
REFM|FBrf0068701
|Stocker et al.
|1993
REFM|FBrf0090446
|Batterham et al.
|1996
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0158867
|Siddall et al.
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014543 ICL 1 ? SYM 1 ?{}mei-W681 ASTR 1 - CLOC 1 56D9 REF 1 2 DT 1 6 Jan 2000 RESZ 507
ID|FBti0014543
SYM|?{}mei-W681
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002716==mei-W68
ARGS|FBgn0002716
SK|FBst0004932
|y[1]/Dp(1;Y)y[+]; mei-W68[1]/CyO
|Total=1
REFDSR
{
RDID|FBrf0104768
|McKim and Hayashi-Hagihara
|1998
SYN|?{}mei-W681
ASAL|FBal0012191==mei-W681
CLOC|56D9
|Insertion site
LOCB|Proximity to gene: FBgn0002716==mei-W68
}
REF
{
REFM|FBrf0104768
|McKim and Hayashi-Hagihara
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012191==mei-W681
REFDSR
{
RDID|FBrf0059133
|McKim et al.
|1993
PHP|Metaphase arrest prevented.
}
REFDSR
{
RDID|FBrf0093814
|Carpenter
|1997.5.12
PHP|Ultrastructural studies of pachytene reveal synaptonemal complex that is
|normal in structure and length and which undergoes the same changes in
|length as is observed in wild type as the cells progress through
|pachytene; chromocentral organization and chromatin condensation are also
|normal. However, no late recombination nodules were observed in the nine
|nuclei reconstructed which were between the developmental landmarks which
|demark their presence in wild type.
}
REFDSR
{
RDID|FBrf0100602
|McKim et al.
|1998
PHP|Severe mutation.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Females homozygous for mei-W68 show a complete absence
|of meiotic recombination (Baker, unpublished data).
|A less severe allele (mei-W68L1-Lindsley) reduces
|exchange to approximately 60% of control levels and
|also alters the distribution of residual exchanges.
|Analysis of mitotic chromosome behavior (Baker et al.,
|1978) suggests that the FBgn0002716==mei-W68+ gene product is
|... (see FBal0012191==mei-W681 report)
}
REFDSR
{
RDID|FBrf0158977
|Carpenter
|2003
PHP|Crossing over is reduced in
| FBal0090228==mei-W68L1/FBal0012191==mei-W681 females.
|Homozygotes lack meiotic crossing over. Premeiotic exchanges occur
|in homozygous females.
|FBal0012191==mei-W681 is recessive to wild type when
| nondisjunction frequencies
|are examined but has dominant effects on crossing over.
|Homozygous and
| FBal0090228==mei-W68L1/FBal0012191==mei-W681 females
| show normal dynamics
|of germ-line mitotic divisions. The dynamics of entry into meiosis
|... (see FBal0012191==mei-W681 report)
PHM|late recombination nodule
|early recombination nodule
}
REF
{
REFM|FBrf0059133
|McKim et al.
|1993
REFM|FBrf0093814
|Carpenter
|1997.5.12
REFM|FBrf0100602
|McKim et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0158977
|Carpenter
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014164 ICL 1 ? SYM 1 ?{}N55e11 ASTR 1 - CLOC 1 3C7--9 REF 1 6 DT 1 6 Jan 2000 RESZ 911
ID|FBti0014164
SYM|?{}N55e11
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004647==N
SK|FBst0003015
|N[55e11] rb[1]/C(1)DX, y[1] w[1] f[1]; Dp(1;2)51b/+
|FBst1000218
|C(1)DX, y w f/ w[a] N[55e11]; Dp(1;2)51b/ +
|FBst1001512
|w[a] N[55e11]/FM7, lac-z
|Total=3
REFDSR
{
RDID|FBrf0040185
|Lehmann et al.
|1983
PHC|lethal | embryonic | neurogenic | recessive
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}N55e11
ASAL|FBal0012701==N55e11
MU|spontaneous
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REFDSR
{
RDID|FBrf0091115
|Long et al.
|1996
PHC|lethal | recessive
}
REF
{
REFM|FBrf0040185
|Lehmann et al.
|1983
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0091115
|Long et al.
|1996
REFM|FBrf0098202
|Brennan et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0112013
|Rauskolb et al.
|1999
}
ALESR
{
ASYM|FBal0012701==N55e11
REFDSR
{
RDID|FBrf0027480
|Shellenbarger and Mohler
|1975
PHP|Lethal in combination with FBal0012887==Nl1N-ts1 or
| FBal0012861==NAx-tsl at 29oC.
}
REFDSR
{
RDID|FBrf0038108
|Poulson and Lefevre
|1982
PHP|Male flies carrying FBab0003125==Dp(1;2)51bV76e show wing-notching and lateral
|incisions, leg defects and tarsal reductions, missing or multiple bristles,
|missing or fused ocelli and variegated or roughened eyes, at varying
|frequencies.
}
REFDSR
{
RDID|FBrf0040181
|Campos-Ortega
|1983
PHP|The presence of the FBal0012701==N55e11 did not affect the
| epidermal pattern in
|the thoracic and abdominal segments of hemizygotes derived from FBal0002643==dl1/FBal0002643==dl1
|hemizygotes. Double mutants FBal0012701==N55e11 and
| FBal0002644==dl2 had neuralization of
|additional ectodermal cells in the thoracic and abdominal segments.
|Double mutants FBal0012701==N55e11 and Tl had neuralization of
| the entire ectoderm,
|a huge CNS and no epidermis as it had been substituted for by neural
|tissue.
}
REFDSR
{
RDID|FBrf0040185
|Lehmann et al.
|1983
PHP|Extreme embryonic neurogenic phenotype.
PHM|epidermis | embryonic
}
REFDSR
{
RDID|FBrf0043047
|Vassin et al.
|1985
PHP|Notching of the tips and/or edges of the wing. Veins are frequently
|broadened at the marginal junctions, forming delta-like thickenings.
PHM|wing
|wing vein
}
REFDSR
{
RDID|FBrf0048995
|Brand and Campos-Ortega
|1988
PHP|The amount of maternally derived gene product does not modify the phenotype
|of double neurogenic mutants. FBal0012701==N55e11 expression was
| modified by
|the presence of ASC loss-of-function mutations. All embryonic cells
|initiate neural development but later in development some cells switch
|their fate either to epidermogenesis or cell death.
}
REFDSR
{
RDID|FBrf0051582
|Cabrera
|1990
PHP|Post-transcriptional control of AS-C expression is suppressed, all
|cells expressing RNA accumulate protein.
}
REFDSR
{
RDID|FBrf0053344
|Heitzler and Simpson
|1991
PHP|Neural hyperplasia of cells within a mutant clone. Mutant clones fail
|to form bristles.
}
REFDSR
{
RDID|FBrf0053362
|Corbin et al.
|1991
PHP|FBal0012701==N55e11 shows severe neural hypertrophy, a 6--9 fold
| increase in nau
|expressing cells per cluster relative to wild type. Embryos show a
|disrupted CNS pattern. When heterozygous with FBab0000974==Df(1)svr the CNS ladder
|structure is apparent, hypertrophy is seen in the nau expressing cells
|and the medial superclusters arise in a disrupted pattern compared
|to wildtype.
}
REFDSR
{
RDID|FBrf0053769
|Goriely et al.
|1991
PHP|Increase in SMCs per cluster in embryos lacking the maternal product.
}
REFDSR
{
RDID|FBrf0054994
|de Celis et al.
|1991
PHP|Homozygous clones produced during the last stages of the formation
|of the adult sensory organs develop into sensory organ mother cells
|when induced early, or its neural sublineage later.
}
REFDSR
{
RDID|FBrf0055911
|Skeath and Carroll
|1992
PHP|ac protein distribution in FBal0012701==N55e11 embryos show ac
| expression is not
|restricted to a single cell of an ectodermal cell cluster, instead
|most cells of the cluster retain ac expression at a high level, enlarge,
|delaminate and become neuroblasts.
}
REFDSR
{
RDID|FBrf0059323
|Bodmer et al.
|1993
PHP|Hyperplasia of replicating sensory precursors: due to an increased
|number of ectodermal cells being recruited as sensory precursor cells.
|Extra precursor cells are recruited beyond the normal time window
|for neurogenesis in the PNS.
PHM|ectoderm
}
REFDSR
{
RDID|FBrf0068598
|Menne and Klambt
|1994
PHP|Mutant embryos rarely form commissural or longitudinal connections.
|Although the first axons grow out at the same time as wild-type axons,
|they are never oriented towards the midline, and even fail to form
|connections on the ipsilateral side. Both anterior and middle pairs
|of midline glia are absent, and the posterior pair are duplicated but
|found at ectopic positions. There are 4-8 additional neuronal midline
|cells per segment.
PHM|central nervous system | embryonic
|midline glial cell
|midline glial cell | ectopic
}
REFDSR
{
RDID|FBrf0072582
|Bate et al.
|1993
PHP|Embryos exhibit few, if any, fused muscles. The unfused, birefringent
|fibers, have a random pattern of fine fibers apparently radiating out
|from small fragments of dorsal cuticle. The birefringent is clearly
|correlated with the expansion of the CNS and PNS, and the loss of epidermis
|and the degree to which myoblast fusion occurs. Where myoblast fusion
|fails conspicuous clusters of mesodermal cells are formed and if epidermal
|territories are expanded cells in these clusters may be recruited to
|... (see FBal0012701==N55e11 report)
PHM|embryonic/larval somatic muscle
|embryonic nervous system
|epidermis | embryonic
|myoblast | embryonic
}
REFDSR
{
RDID|FBrf0072959
|Diaz-Benjumea and Hafen
|1994
PHP|FBal0014587==rl1/FBab0002207==Df(2R)rl10a strongly enhances the
| wing phenotype of FBal0012701==N55e11/+.
}
REFDSR
{
RDID|FBrf0074921
|de Celis and Garcia-Bellido
|1994
PHP|Clones running along the veins differentiate broad stretches of cells
|with vein histotype, to differentiate cells must be within 10-15 normal
|cell diameters from the vein. Clones can also affect vein differentiation
|on the other wing surface. Clones can also reduce the intervein distance.
|Clones in the dorso-ventral compartment border can induce scalloping
|indicating non-autonomous effects in wing margin loss.
|Clonal behavior of FBgn0004647==N clones in the wing does not result from abnormal
|... (see FBal0012701==N55e11 report)
PHM|wing
|wing | dorsal/ventral compartment boundary
}
REFDSR
{
RDID|FBrf0074922
|de Celis et al.
|1991
PHP|Cause a complex pleiotropic syndrome including perturbations of the
|chaetae pattern.
}
REFDSR
{
RDID|FBrf0075100
|Hoch et al.
|1994
PHP|Embryos derived from germline clones show supernumerary Malpighian
|tubule tip cells segregating from the tubule primordial cells. The
|tubules of these embryos do not go on to secrete uric acid.
PHM|Malpighian tubule primordium | germ-line clone
|Malpighian tubule tip cell | germ-line clone
}
REFDSR
{
RDID|FBrf0076037
|Couso and Martinez Arias
|1994
PHP|FBal0012701==N55e11/FBal0012887==Nl1N-ts1 animals
| reared at 17oC and exposed to 29oC
|for 24 hrs in the second larval instar give rise to adults with duplicated
|(sometimes triplicated) legs, with ventral branch points, and reduced
|or absent wings with accompanying wing to notum transformation. This
|phenotype is identical to that produced by loss of FBgn0004009==wg during second
|and early third larval instar. Heterozygosity for
| FBal0012701==N55e11 reduces
|viability and increases penetrance of wing/haltere phenotypes of FBal0018482==wg1.
|... (see FBal0012701==N55e11 report)
}
REFDSR
{
RDID|FBrf0076146
|Sturtevant and Bier
|1995
PHP|Thickened vein mutant.
PHM|wing vein
}
REFDSR
{
RDID|FBrf0083156
|Gonzalez-Gaitan and Jaeckle
|1995
PHP|Instead of forming distinct invagination folds, the FBgn0004647==N mutant stomodeal
|nervous system anlage invaginates en masse.
PHM|stomatogastric nervous system primordium
}
REFDSR
{
RDID|FBrf0084329
|Rulifson and Blair
|1995
PHP|SMC differentiation and proneural activation in
| FBal0012701==N55e11 wing margin
|clones display dual phenotypes. Clones that do not substantially disrupt
|FBgn0004009==wg expression have neurogenic phenotypes and clones that disrupt
|FBgn0004009==wg expression have a mixture of antiproneural and neurogenic phenotypes.
}
REFDSR
{
RDID|FBrf0089977
|Guo et al.
|1996
PHP|Heterozygotes exhibit no obvious hair or socket abnormalities. Heterozygotes
|carrying one copy of FBtp0003391==P{hs-numb} in the absence of heat shock have
|double hairs without sockets at the anterior wing margin. This phenotype
|is enhanced with two copies of FBtp0003391==P{hs-numb}.
}
REFDSR
{
RDID|FBrf0090023
|de Celis et al.
|1996
PHP|Clones in the thorax produce patches of naked cuticle, due to the differentiation
|of the ectopic SOPs into neurons.
|Clones in the wing that reach the wing margin show a loss of margin
|and blade tissue due to the requirement for FBgn0004647==N at the D/V boundary.
|Wing veins also appear thicker.
PHM|sensory mother cell | ectopic
|macrochaeta
|wing
|dorsal double row
|ventral double row
|wing vein
}
REFDSR
{
RDID|FBrf0090425
|Abu-Issa and Cavicchi
|1996
PHP|Heterozygotes show thickening of the wing veins, occasional terminal
|nicking of the wing, and 1-4 ectopic bristles on the wing surface.
PHM|wing
|wing vein
|wing sensillum | ectopic
}
REFDSR
{
RDID|FBrf0090560
|Frise et al.
|1996
PHP|FBal0012701==N55e11/+ flies have a notched wing phenotype.
| Homozygous clones
|induced in the sensory organ precursor daughter IIa cells of the
|adult external sense organs, when FBal0058958==Scer\FLP1Scer\UAS.cBa
|expression is driven by FBal0052395==Scer\GAL4sca-109-68, produce
| a twinned
|hair phenotype.
PHM|wing
|external sensory organ | somatic clone
}
REFDSR
{
RDID|FBrf0091115
|Long et al.
|1996
PHP|Wing nicking phenotype.
}
REFDSR
{
RDID|FBrf0091127
|Murata et al.
|1996
PHP|Heterozygotes have a triangular expansion of the veins at the wing
|margin, and approximately 25% of flies have notched wings.
PHM|wing
|wing vein
}
REFDSR
{
RDID|FBrf0093461
|Giebel et al.
|1997
PHP|FBal0042573==Scer\GAL4da.G32-mediated coexpression of
| FBal0045936==l(1)scScer\UAS.cHa and FBal0061468==daScer\UAS.cGa
|cause increase of cells in the CNS: brain lobes are enlarged (protruding
|through the holes in the cephalic epidermis), the ventral cord shows
|regional enlargement and sensory organs contain a large number of neurons.
|Neural hyperplasia is also increased, epidermis, fore- and hindgut,
|tracheal tree and salivary glands are completely neuralized.
PHM|embryonic nervous system
|larval brain | embryonic
|ventral nerve cord
|epidermis
|larval foregut | embryonic
|larval hindgut | embryonic
|embryonic/larval tracheal system
|larval salivary gland | embryonic
}
REFDSR
{
RDID|FBrf0093711
|Seugnet et al.
|1997
PHP|Segregation of neuroblasts 5-2 and 7-4 is normal at early stages.
|Late embryos are strongly neuralized.
|Embryos derived from germline clones exhibit disturbed segmentation
|in some segments and some 5-2 equivalence groups are fused. Segregation
|of the 5-2 and 7-4 neuroblast occurs in an irregular manner at later
|stages.
PHM|neuroblast NB5-2 | germ-line clone
|neuroblast NB7-4 | germ-line clone
|central nervous system | larval | germ-line clone
|peripheral nervous system | larval | germ-line clone
}
REFDSR
{
RDID|FBrf0097687
|Vervoort et al.
|1997
PHP|Embryos exhibit supernumerary md neurons that derive from ASC precursors.
PHM|multidendritic neuron
}
REFDSR
{
RDID|FBrf0098202
|Brennan et al.
|1997
PHP|Hemizygous lethal. Heterozygotes have a neurogenic phenotype and have
|a marked increase in the number of bristles on the notum.
PHM|adult thoracic sensillum
}
REFDSR
{
RDID|FBrf0098359
|Stuttem and Campos-Ortega
|1997
PHP|Transplantation of single cells from FBal0012701==N55e11 embryos
| into the ventral
|neurogenic region of wild-type host embryos reveals non-autonomous
|behavior of these cells; the cells can give rise to both neural and
|epidermal offspring. Single cells from FBal0012701==N55e11
| embryos transplanted
|into the ventral neurogenic region of FBal0012701==N55e11 host
| embryos give
|rise to only neural cells. Single cells from FBal0012701==N55e11
| embryos transplanted
|into the procephalic neuroectoderm or the proctodeal anlage of wild-type
|... (see FBal0012701==N55e11 report)
}
REFDSR
{
RDID|FBrf0098813
|Jagla et al.
|1997
PHP|Homozygous embryos have an increased number of cardiac precursor cells.
PHM|embryonic/larval dorsal vessel | precursor
}
REFDSR
{
RDID|FBrf0099033
|Doherty et al.
|1997
PHM|epidermis | embryonic
}
REFDSR
{
RDID|FBrf0099460
|Price et al.
|1997
PHM|wing
}
REFDSR
{
RDID|FBrf0099884
|Sotillos et al.
|1997
PHP|Heterozygotes show scalloping of the wing margin and thickening of
|the wing veins.
PHM|wing
|wing vein
}
REFDSR
{
RDID|FBrf0101998
|Rottgen et al.
|1998
PHP|FBal0012701==N55e11/FBab0000579==Df(1)N-8 transheterozygotes
| exhibit ectopic bristles on
|the notum.
PHM|(with Df(1)N-8) scutum & macrochaeta | ectopic
}
REFDSR
{
RDID|FBrf0102423
|Zeng et al.
|1998
PHP|Homozygous clones on the central region of the adult scutum are devoid
|of any external bristle structures, such as shafts and sockets.
|Homozygous clones induced in the sensory organ lineage frequently have
|bristles with double shafts (approximately 39% of homozygous macrochaetae
|have double shafts).
PHM|socket & scutum | somatic clone
|macrochaeta & scutum | somatic clone
|macrochaeta | somatic clone
|sensory mother cell | somatic clone
}
REFDSR
{
RDID|FBrf0102699
|Martinez Arias
|1998
PHP|The cuticle of a
| FBal0012887==Nl1N-ts1/FBal0012701==N55e11 larva grown
| at 17oC until
|early stage 11 and then shifted to 30oC is shorter than wild-type
|and shows segment fusions.
PHM|embryonic/first instar larval cuticle
}
REFDSR
{
RDID|FBrf0102708
|Boube et al.
|1998
PHP|FBal0013509==pb5/FBal0013517==pb13 flies show a slight
| distal transformation of labium
|to antennal arista. If the flies are also heterozygous for FBal0012701==N55e11
|the number of pseudotracheal rows is reduced and a region of apparent
|ectoderm forms between the remaining pseudotracheal rows and the transformed
|antennal structures.
}
REFDSR
{
RDID|FBrf0102828
|Roch et al.
|1998
PHP|Wing veins are thickened.
PHM|wing vein
}
REFDSR
{
RDID|FBrf0104758
|Jagla et al.
|1998
PHP|The segmental border muscle progenitors do not segregate at all or
|do not divide properly.
PHM|segment border muscle | precursor
}
REFDSR
{
RDID|FBrf0104911
|Hoch and Jackle
|1998
PHP|Multiple Malpighian tubule tip cells develop in homozygous embryos.
PHM|Malpighian tubule tip cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|A weak Notch. Deltas on wing veins are most reliable
|character for classification. Lethal when heterozygous
|with FBal0012892==Nnd-3, FBal0012703==N60g11 and
| FBal0012759==NCo. In homozygotes and
|hemizygotes hyperplasia of central nervous system
|extreme; embryonic peripheral nervous system abnormal
|with sensilla undifferentiated (Hartenstein and
|Campos-Ortega, 1986).
}
REFDSR
{
RDID|FBrf0106041
|Rusconi and Corbin
|1998
PHP|The number of cells in the FBgn0002922==nau-expressing muscle precursor clusters
|is increased compared to wild-type in homozygous embryos. The number
|of cells in the FBgn0002922==nau-expressing muscle precursor clusters is increased
|to more than twice the number in homozygous embryos (lacking zygotic
|function) in homozygous embryos derived from homozygous female germline
|clones (lacking both maternal and zygotic function).
PHM|embryonic/larval somatic muscle
|embryonic/larval somatic muscle | germ-line clone
}
REFDSR
{
RDID|FBrf0107900
|Nagaraj et al.
|1999
PHP|FBal0012887==Nl1N-ts1/FBal0012701==N55e11 wing discs
| show a reduction in the size of
|the pouch.
|Heterozygotes show mild notching of the distal wing margin.
PHM|wing margin
|dorsal mesothoracic disc
}
REFDSR
{
RDID|FBrf0108514
|Llimargas
|1999
PHP|Mutants show a rudimentary tracheal tree, ectopic fusions between adjacent
|branches and absence of terminal branches. The number of tracheal cells
|is reduced, resulting in reduced branching. Temperature shifts of
|heterozygotes of
| FBal0012701==N55e11/FBal0012887==Nl1N-ts1 suggest
| that in addition to
|its early role in tracheal specification, FBgn0004647==N acts later in both fusion
|and terminal branching programs.
|Cell markers indicate a transformation of presumptive terminal or antifusion
|... (see FBal0012701==N55e11 report)
PHM|trachea | embryonic
}
REFDSR
{
RDID|FBrf0108607
|Bishop et al.
|1999
PHP|FBal0012887==Nl1N-ts1/FBal0012701==N55e11 flies
| exposed to the restrictive temperature
|during the third larval instar and pupal phases show a marked reduction
|in leg length with all areas of the leg segments (joint and interjoint
|tissue) being affected. Joints are completely lost, and also often
|apical bristles.
PHM|leg | conditional ts
|prothoracic tibial apical bristle | conditional ts
|mesothoracic tibial apical bristle | conditional ts
|metathoracic tibial apical bristle | conditional ts
}
REFDSR
{
RDID|FBrf0109019
|Rauskolb and Irvine
|1999
PHP|Homozygous clones in the leg form patches of naked cuticle. The clones
|fail to form joint structures in all regions of the leg (resulting
|in fusion of leg segments) and leg growth is reduced. Fusions are
|seen along the length of the tibia and femur, while end-to-end fusions
|are seen in other leg segments. In most cases, the failure to form
|joints is an autonomous property of the mutant cells in the clone,
|although occasionally joint formation is also inhibited in wild-type
|... (see FBal0012701==N55e11 report)
PHM|joint | somatic clone | cell autonomous
|joint | somatic clone | cell non-autonomous
|leg sensillum | somatic clone
|leg | somatic clone
|tibia | somatic clone
|femur | somatic clone
}
REFDSR
{
RDID|FBrf0109184
|zur Lage and Jarman
|1999
PHP|Leg discs of FBal0012887==Nl1N-ts1/FBal0012701==N55e11
| larvae reared at the restrictive
|temperature for 4-16 hours show a large, disorganized mass of sensory
|organ precursor cells below the epithelium where the SOP cells of the
|femoral chordotonal organ normally form.
PHM|ventral thoracic disc
}
REFDSR
{
RDID|FBrf0111977
|Micchelli and Blair
|1999
PHP|In somatic clones in the wing disc, the majority of
| FBal0012701==N55e11 clones
|that are in contact with the FBgn0000099==ap boundary, disrupt the Dorsal/ventral
|(D/V) lineage restriction. In the most extreme class, clones straddle
|or cross the normal site of the D/V boundary from either side, with
|most or all of the cells being in the wrong compartment. In some cases
|milder distortions lead to "bulging" clones and some clones do approximately
|respect the boundary. Disruptions are not always limited to the mutant
|... (see FBal0012701==N55e11 report)
PHM|dorsal mesothoracic disc | dorsal/ventral compartment boundary | somatic clone
}
REFDSR
{
RDID|FBrf0112013
|Rauskolb et al.
|1999
PHP|Homozygous mutant clones in the wing disc fail to respect the dorsal
|ventral boundary.
PHM|dorsal mesothoracic disc | somatic clone
}
REFDSR
{
RDID|FBrf0112024
|Rusconi and Corbin
|1999
PHP|The number of FBgn0001077==ftz expressing MP2 neurons increases compared to wild-type
|(About 30 on each side of the midline, as compared to 2 in wild-type)
|in homozygous embryos derived from homozygous female germ-line clones
|(lacking both maternal and zygotic function). The extra MP2 clusters
|extend further laterally than seen in FBgn0000463==Dl and FBgn0004837==Su(H). alleles. No
|segmentation defects are seen.
|In homozygous embryos derived from homozygous female germ-line clones
|... (see FBal0012701==N55e11 report)
PHM|dMP2 neuron | ectopic | germ-line clone
|vMP2 neuron | ectopic | germ-line clone
|RP2 neuron | ectopic | germ-line clone
}
REFDSR
{
RDID|FBrf0125167
|de Celis and Bray
|2000
PHP|Wing veins L3 and L5 are thicker than wild-type veins in heterozygous
|flies, and the thickened veins have smooth borders. The wings show
|moderate scalloping of the wing margin.
PHM|wing vein L3
|wing vein L5
|wing vein L3 | ectopic
|wing vein L5 | ectopic
|wing
}
REFDSR
{
RDID|FBrf0135724
|Udolph et al.
|2001
PHP|Glial cells in the central nervous system of embryos are not entirely
|absent.
|In clones of FBal0012701==N55e11 cells in a wild type background
| the pCC is
|transformed into aCC, SPGs are lost and neuronal cells are concomitantly
|gained within the NB1-1 lineage.
PHM|subperineurial glial cell | somatic clone
|neuron | supernumerary | somatic clone
|pCC neuron | somatic clone
|aCC neuron | supernumerary | somatic clone
}
REFDSR
{
RDID|FBrf0136942
|Lopez-Schier and St. Johnston
|2001
PHP|Homozygous somatic clones in the follicle cells do not differentiate
|as polar cells, but block the differentiation of epithelial follicle
|cells and causes them to remain as undifferentiated precursors. When
|a clone falls in a region where the follicle cells normally undergo
|morphogenetic movement, these movements do not occur. The stretched
|follicle cells fail to move over the nurse cells; the centripetal cells
|do not migrate between the oocyte and the nurse cells; and the more
|... (see FBal0012701==N55e11 report)
PHM|follicle cell | somatic clone
|centripetally migrating follicle cell | somatic clone
|interfollicle cell | somatic clone
|polar follicle cell | somatic clone
|mitotic cycle | somatic clone
}
REFDSR
{
RDID|FBrf0137222
|Grammont and Irvine
|2001
PHP|Follicles containing permanent somatic clones for
| FBal0012701==N55e11 are not
|recoverable. In egg chambers with transient somatic clones at either
|end of the follicle polar cells are absent. Where one of the polar-stalk
|precursors is mutant for FBal0012701==N55e11 long stalks (average
| 15 cells)
|develop.
PHM|egg chamber | somatic clone
|polar follicle cell | somatic clone | cell autonomous
|interfollicle cell | somatic clone | cell non-autonomous
}
REFDSR
{
RDID|FBrf0141471
|Lopez-Schier and St. Johnston
|2002
PHP|In mutant clones in the follicle cells the organization of the spectrin
|cytoskeleton is normal.
}
REFDSR
{
RDID|FBrf0141493
|Deng et al.
|2001
PHP|Cells in homozygous follicle cell clones have smaller nuclei than their
|wild-type neighbors (which probably indicates a lack of endocycles
|in the mutant cells). The mutant clones contain more cells than their
|wild-type twin spot sister clones, indicating additional mitoses.
|The mean ratio of the number of cells in the mutant clone/number of
|cells in the wild-type sister clone is 1.8 and the ratio does not change
|as a function of clone size. The DNA content is higher in wild-type
|... (see FBal0012701==N55e11 report)
PHM|follicle cell & nucleus | somatic clone
}
REFDSR
{
RDID|FBrf0144843
|Sudarsan et al.
|2002
PHP|FBgn0004647==N mutant embryos have about 89 cells in each Malpighian tubule cell
|(as opposed to about 125 in wild-type). The tubules are are shorter
|than wild-type which results from a dramatic reduction in cell division
|from Mitosis 17.
|FBgn0004647==N mutant embryos made as germ-line clones have about 89 cells in
|each Malpighian tubule cell (as opposed to about 125 in wild-type).
PHM|Malpighian tubule
|Malpighian tubule | germ-line clone
}
REFDSR
{
RDID|FBrf0146991
|Umesono et al.
|2002
PHP|At the earliest stage of the dorsal bipolar dendritic (dbd) sensory
|organ precursor (SOP) division excess FBgn0002970==nub-positive cells are located
|at the correct position in mutant embryos, suggesting that supernumerary
|dbd SOPs are produced. At stage 12, the dbd support glial cell (DBDG)
|is absent. Supernumerary PG3 glial cells and chordotonal organ ligament
|cells of the are present.
PHM|support cell of the dorsal bipolar dendritic cell
|peripheral glial cell 3 | supernumerary
|scolopidial ligament cell | supernumerary
}
REFDSR
{
RDID|FBrf0147142
|Iwaki and Lengyel
|2002
PHP|Mutant embryos completely lack hindgut boundary cell rows and rings.
PHM|embryonic hindgut
}
REFDSR
{
RDID|FBrf0150723
|Riede
|2001
PHP|Pupal lethal when heterozygous with the MBT chromosome.
}
REFDSR
{
RDID|FBrf0151253
|Glise et al.
|2002
PHP|Heterozygotes lack vein and sensory bristle tissue at the most distal
|tip of the wing.
PHM|wing | distal
|wing vein
|wing margin bristle
}
REFDSR
{
RDID|FBrf0151813
|Tsuda et al.
|2002
PHM|wing
}
REFDSR
{
RDID|FBrf0151928
|Orgogozo et al.
|2002
PHP|FBal0012701==N55e11/FBal0012887==Nl1N-ts1 flies form
| ectopic abdominal ventral multidendritic
|neurons and pI external sensory organ precursor cells, even when raised
|at 19oC.
PHM|(with Nl1N-ts1) abdominal ventral multidendritic neuron | ectopic
|(with Nl1N-ts1) external sensory organ precursor cell | ectopic
}
REFDSR
{
RDID|FBrf0155787
|Lebestky et al.
|2003
PHP|The number of crystal cell precursors seen in mutant lymph glands is
|significantly reduced.
PHM|procrystal cell
}
REFDSR
{
RDID|FBrf0160464
|Crozatier et al.
|2003
PHP|In heterozygous mutants, wing veins are wider than in wild-type, but
|selection of sensory organ precursors (SOP) is not affected. However,
|the campaniform sensillae are still overlapping the posterior-most
|L3 vein cells. The position of SOPs relative to the anterior posterior
|border is not changed in mutant discs, indicating that in the adult
|the position of L3 vein is shifted anteriorly by one or two rows of
|cells.
PHM|wing vein
|sensory mother cell
}
REFDSR
{
RDID|FBrf0167516
|Escudero et al.
|2003
PHP|Heterozygotes show a slight increase in the density of microchaetae
|on the notum.
}
REFDSR
{
RDID|FBrf0174561
|Fuss et al.
|2004
PHP|In FBal0012701==N55e11 homozygous embryos, the early steps of proventricular
|development including the formation of the ball-like evagination at
|the ectoderm/endoderm boundary occur normally. However, at stage 14,
|the anterior boundary cells of the keyhole region fail to invaginate
|into the endodermal cell layer, but arrest anteriorly and do not move
|inwards until the final stages of embryonic development (16 and 17).
|In addition, the posterior boundary cells of the endodermal component
|... (see FBal0012701==N55e11 report)
PHM|proventriculus inner layer primordium
|proventriculus intermediate layer primordium
|proventriculus outer layer primordium
|embryonic proventriculus
|keyhole structure
}
REFDSR
{
RDID|FBrf0174588
|Stute et al.
|2004
PHP|Marker expression and morphology suggest that numbers muscle founder
|cells are increased at the expense of fusion competent myoblasts in
|the visceral mesoderm of stage 11 FBal0012701==N55e11 mutant embryos.
PHM|fusion competent cell & visceral mesoderm
|muscle founder cell & visceral mesoderm
}
REFDSR
{
RDID|FBrf0179042
|Le Gall and Giniger
|2004
PHP|Mutant embryos show severe hyperplasia of the central and peripheral
|nervous systems.
PHM|embryonic central nervous system
|embryonic peripheral nervous system
}
REF
{
REFM|FBrf0027480
|Shellenbarger and Mohler
|1975
REFM|FBrf0038108
|Poulson and Lefevre
|1982
REFM|FBrf0040181
|Campos-Ortega
|1983
REFM|FBrf0040185
|Lehmann et al.
|1983
REFM|FBrf0043047
|Vassin et al.
|1985
REFM|FBrf0048995
|Brand and Campos-Ortega
|1988
REFM|FBrf0051582
|Cabrera
|1990
REFM|FBrf0053344
|Heitzler and Simpson
|1991
REFM|FBrf0053362
|Corbin et al.
|1991
REFM|FBrf0053769
|Goriely et al.
|1991
REFM|FBrf0054994
|de Celis et al.
|1991
REFM|FBrf0055911
|Skeath and Carroll
|1992
REFM|FBrf0059323
|Bodmer et al.
|1993
REFM|FBrf0068598
|Menne and Klambt
|1994
REFM|FBrf0072582
|Bate et al.
|1993
REFM|FBrf0072959
|Diaz-Benjumea and Hafen
|1994
REFM|FBrf0074921
|de Celis and Garcia-Bellido
|1994
REFM|FBrf0074922
|de Celis et al.
|1991
REFM|FBrf0075100
|Hoch et al.
|1994
REFM|FBrf0076037
|Couso and Martinez Arias
|1994
REFM|FBrf0076146
|Sturtevant and Bier
|1995
REFM|FBrf0083156
|Gonzalez-Gaitan and Jaeckle
|1995
REFM|FBrf0084329
|Rulifson and Blair
|1995
REFM|FBrf0089977
|Guo et al.
|1996
REFM|FBrf0090023
|de Celis et al.
|1996
REFM|FBrf0090425
|Abu-Issa and Cavicchi
|1996
REFM|FBrf0090560
|Frise et al.
|1996
REFM|FBrf0091115
|Long et al.
|1996
REFM|FBrf0091127
|Murata et al.
|1996
REFM|FBrf0093461
|Giebel et al.
|1997
REFM|FBrf0093711
|Seugnet et al.
|1997
REFM|FBrf0097687
|Vervoort et al.
|1997
REFM|FBrf0098202
|Brennan et al.
|1997
REFM|FBrf0098359
|Stuttem and Campos-Ortega
|1997
REFM|FBrf0098813
|Jagla et al.
|1997
REFM|FBrf0099033
|Doherty et al.
|1997
REFM|FBrf0099460
|Price et al.
|1997
REFM|FBrf0099884
|Sotillos et al.
|1997
REFM|FBrf0101998
|Rottgen et al.
|1998
REFM|FBrf0102423
|Zeng et al.
|1998
REFM|FBrf0102699
|Martinez Arias
|1998
REFM|FBrf0102708
|Boube et al.
|1998
REFM|FBrf0102828
|Roch et al.
|1998
REFM|FBrf0104758
|Jagla et al.
|1998
REFM|FBrf0104911
|Hoch and Jackle
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0106041
|Rusconi and Corbin
|1998
REFM|FBrf0107900
|Nagaraj et al.
|1999
REFM|FBrf0108514
|Llimargas
|1999
REFM|FBrf0108607
|Bishop et al.
|1999
REFM|FBrf0109019
|Rauskolb and Irvine
|1999
REFM|FBrf0109184
|zur Lage and Jarman
|1999
REFM|FBrf0111977
|Micchelli and Blair
|1999
REFM|FBrf0112013
|Rauskolb et al.
|1999
REFM|FBrf0112024
|Rusconi and Corbin
|1999
REFM|FBrf0125167
|de Celis and Bray
|2000
REFM|FBrf0135724
|Udolph et al.
|2001
REFM|FBrf0136942
|Lopez-Schier and St. Johnston
|2001
REFM|FBrf0137222
|Grammont and Irvine
|2001
REFM|FBrf0141471
|Lopez-Schier and St. Johnston
|2002
REFM|FBrf0141493
|Deng et al.
|2001
REFM|FBrf0144843
|Sudarsan et al.
|2002
REFM|FBrf0146991
|Umesono et al.
|2002
REFM|FBrf0147142
|Iwaki and Lengyel
|2002
REFM|FBrf0150723
|Riede
|2001
REFM|FBrf0151253
|Glise et al.
|2002
REFM|FBrf0151813
|Tsuda et al.
|2002
REFM|FBrf0151928
|Orgogozo et al.
|2002
REFM|FBrf0155787
|Lebestky et al.
|2003
REFM|FBrf0160464
|Crozatier et al.
|2003
REFM|FBrf0167516
|Escudero et al.
|2003
REFM|FBrf0174561
|Fuss et al.
|2004
REFM|FBrf0174588
|Stute et al.
|2004
REFM|FBrf0179042
|Le Gall and Giniger
|2004
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015595 ICL 1 ? SYM 1 ?{}N264-40 ASTR 1 - CLOC 1 3C7--9 REF 1 7 DT 1 31 May 2000 RESZ 1105
ID|FBti0015595
SYM|?{}N264-40
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0004647==N
SK|FBst0002212
|w[a] FBal0012749==N[264-40] rb[1]/C(1)DX, y[1] w[1] f[1]; Dp(1;2)72c21/+
|Total=1
REFDSR
{
RDID|FBrf0005044
|Demerec
|1940
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0024896
|Foster
|1973
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0027480
|Shellenbarger and Mohler
|1975
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0040185
|Lehmann et al.
|1983
PHC|lethal | embryonic | neurogenic | recessive
}
REFDSR
{
RDID|FBrf0046957
|Kelley et al.
|1987
SYN|?{}N264-40
ASAL|FBal0012749==N264-40
MU|X ray
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REFDSR
{
RDID|FBrf0051558
|Palka et al.
|1990
PHC|lethal | embryonic | recessive
}
REF
{
REFM|FBrf0005044
|Demerec
|1940
REFM|FBrf0024896
|Foster
|1973
REFM|FBrf0027480
|Shellenbarger and Mohler
|1975
REFM|FBrf0040185
|Lehmann et al.
|1983
REFM|FBrf0046957
|Kelley et al.
|1987
REFM|FBrf0051558
|Palka et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012749==N264-40
REFDSR
{
RDID|FBrf0005044
|Demerec
|1940
PHP|Lethality is not covered by FBab0009529==Dp(1;3)N264-58.
}
REFDSR
{
RDID|FBrf0024896
|Foster
|1973
PHP|Heterozygotes have a nicked wing phenotype.
|FBal0012852==NAx-16/FBal0012749==N264-40 females show
| temperature sensitive lethality.
|The temperature sensitive period for lethality is during the second
|larval instar stage.
PHM|wing
}
REFDSR
{
RDID|FBrf0027480
|Shellenbarger and Mohler
|1975
PHP|Lethal in combination with FBal0012887==Nl1N-ts1 or
| FBal0012861==NAx-tsl at 29oC.
|Homozygous lethal at 29oC.
}
REFDSR
{
RDID|FBrf0038108
|Poulson and Lefevre
|1982
PHP|Male flies carrying FBab0003125==Dp(1;2)51bV76e show wing-notching and lateral
|incisions, leg defects and tarsal reductions, missing or multiple bristles,
|missing or fused ocelli and variegated or roughened eyes, at varying
|frequencies.
}
REFDSR
{
RDID|FBrf0040185
|Lehmann et al.
|1983
PHP|Extreme embryonic neurogenic phenotype.
PHM|epidermis | embryonic
}
REFDSR
{
RDID|FBrf0051558
|Palka et al.
|1990
PHP|Heterozygotes have slightly elevated numbers of sensilla on the wing.
PHM|wing sensillum
}
REFDSR
{
RDID|FBrf0056217
|Jack and DeLotto
|1992
PHP|Homozygotes exhibit hypertrophy of the nervous system and a gap in
|the tip of the wing margin.
PHM|central nervous system
|wing
}
REFDSR
{
RDID|FBrf0104706
|Park et al.
|1998
PHP|FBgn0000606==eve-expressing pericardial cells fail to form in embryos derived
|from homozygous female germline clones.
PHM|embryonic/larval pericardial cell | germ-line clone
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Typical Notch. Male embryos show developmental
|abnormalities like those of FBab0000579==Df(1)N-8 (Poulson, 1939).
|Lethal with FBal0012892==Nnd-3.
}
REF
{
REFM|FBrf0005044
|Demerec
|1940
REFM|FBrf0024896
|Foster
|1973
REFM|FBrf0027480
|Shellenbarger and Mohler
|1975
REFM|FBrf0038108
|Poulson and Lefevre
|1982
REFM|FBrf0040185
|Lehmann et al.
|1983
REFM|FBrf0051558
|Palka et al.
|1990
REFM|FBrf0056217
|Jack and DeLotto
|1992
REFM|FBrf0104706
|Park et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015594 ICL 1 ? SYM 1 ?{}N264-109 ASTR 1 - CLOC 1 3C7--9 REF 1 2 DT 1 31 May 2000 RESZ 480
ID|FBti0015594
SYM|?{}N264-109
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0004647==N
REFDSR
{
RDID|FBrf0046957
|Kelley et al.
|1987
SYN|?{}N264-109
ASAL|FBal0012756==N264-109
MU|X ray
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|semi-lethal | recessive
}
REF
{
REFM|FBrf0046957
|Kelley et al.
|1987
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012756==N264-109
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Typical Notch except for semi-lethality with FBal0012892==Nnd-3.
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014176 ICL 1 ? SYM 1 ?{}Nfa-g88 ASTR 1 - CLOC 1 3C7--9 REF 1 2 DT 1 6 Jan 2000 RESZ 416
ID|FBti0014176
SYM|?{}Nfa-g88
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004647==N
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}Nfa-g88
ASAL|FBal0012871==Nfa-g88
MU|spontaneous
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012871==Nfa-g88
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Phenotype like FBal0012868==Nfa-g.
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014180 ICL 1 ? SYM 1 ?{}Nl1N-1 ASTR 1 - CLOC 1 3C7--9 REF 1 2 DT 1 6 Jan 2000 RESZ 481
ID|FBti0014180
SYM|?{}Nl1N-1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004647==N
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}Nl1N-1
ASAL|FBal0012876==Nl1N-1
MU|spontaneous
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012876==Nl1N-1
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|FBal0012876==Nl1N-1/+ females are wild type;
| FBal0012876==Nl1N-1/N females
|and FBal0012876==Nl1N-1/Y males are lethal; l(1)N/Y;FBab0009100==Dp(1;2)51b
|males are Co-like. Heterozygotes with recessive
|visibles at Notch are wild type. Developmental defects
|in FBal0012876==Nl1N-1/Y males are more limited than in N/Y males
|and the defects are confined to the anterior ectoderm
|(Poulson, 1967; Poulson, 1968). Like N mutants, FBal0012876==Nl1N-1
|... (see FBal0012876==Nl1N-1 report)
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014169 ICL 1 ? SYM 1 ?{}NS ASTR 1 - CLOC 1 3C7--9 REF 1 4 DT 1 6 Jan 2000 RESZ 613
ID|FBti0014169
SYM|?{}NS
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004647==N
REFDSR
{
RDID|FBrf0039985
|Kramers et al.
|1983
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0045066
|Schalet
|1986
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}NS
ASAL|FBal0012785==NS
MU|spontaneous
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REF
{
REFM|FBrf0039985
|Kramers et al.
|1983
REFM|FBrf0045066
|Schalet
|1986
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012785==NS
REFDSR
{
RDID|FBrf0045066
|Schalet
|1986
PHP|Heterozygotes display a weak notched wing phenotype.
PHM|wing
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Weak Notch. FBal0012785==NS/FBal0012860==NAx-S is lethal.
}
REF
{
REFM|FBrf0045066
|Schalet
|1986
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016277 ICL 1 ? SYM 1 ?{}ossisC-1 ASTR 1 - CLOC 1 17A5 REF 1 2 DT 1 17 Aug 2000 RESZ 347
ID|FBti0016277
SYM|?{}ossisC-1
DT|17 Aug 2000
|17 Aug 2000
ICL|?
ASGN|FBgn0004956==os
REFDSR
{
RDID|FBrf0128638
|Sefton et al.
|2000
SYN|?{}ossisC-1
CLOC|17A5
|Insertion site
LOCB|Proximity to gene: FBgn0004956==os
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0128638
|Sefton et al.
|2000
}
}
# EOR
TIR
{
RETE|ID 1 FBti0004662 ICL 1 ? SYM 1 ?{}ovoD1r38D ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 5 Feb 1999 RESZ 381
ID|FBti0004662
SYM|?{}ovoD1r38D
DT|5 Feb 1999
|29 Dec 1997
ICL|?
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
ASAL|FBal0050230==ovoD1r38D
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0050230==ovoD1r38D
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
PHP|Phenotypic category: ovo- svb-
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004663 ICL 1 ? SYM 1 ?{}ovoD1r47j ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 5 Feb 1999 RESZ 381
ID|FBti0004663
SYM|?{}ovoD1r47j
DT|5 Feb 1999
|29 Dec 1997
ICL|?
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
ASAL|FBal0050231==ovoD1r47j
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0050231==ovoD1r47j
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
PHP|Phenotypic category: ovo- svb-
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004664 ICL 1 ? SYM 1 ?{}ovoD1rOL ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 5 Feb 1999 RESZ 379
ID|FBti0004664
SYM|?{}ovoD1rOL
DT|5 Feb 1999
|29 Dec 1997
ICL|?
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
ASAL|FBal0050232==ovoD1rOL
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0050232==ovoD1rOL
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
PHP|Phenotypic category: ovo- svb-
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004661 ICL 1 ? SYM 1 ?{}ovoD1rP1 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 5 Feb 1999 RESZ 379
ID|FBti0004661
SYM|?{}ovoD1rP1
DT|5 Feb 1999
|29 Dec 1997
ICL|?
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
ASAL|FBal0050233==ovoD1rP1
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0050233==ovoD1rP1
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
PHP|Phenotypic category: ovo-, svb+ phenotype.
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014575 ICL 1 ? SYM 1 ?{}parahd9 ASTR 1 - CLOC 1 14D1--E1 REF 1 2 DT 1 6 Jan 2000 RESZ 409
ID|FBti0014575
SYM|?{}parahd9
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003036==para
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}parahd9
ASAL|FBal0013478==parahd9
CLOC|14D1--E1
|Insertion site
LOCB|Proximity to gene: FBgn0003036==para
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0013478==parahd9
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Temperature-sensitive.
|Hybrid dysgenesis gives no wild-type revertants.
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014577 ICL 1 ? SYM 1 ?{}parats115 ASTR 1 - CLOC 1 14D1--E1 REF 1 2 DT 1 6 Jan 2000 RESZ 415
ID|FBti0014577
SYM|?{}parats115
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003036==para
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}parats115
ASAL|FBal0013495==parats115
CLOC|14D1--E1
|Insertion site
LOCB|Proximity to gene: FBgn0003036==para
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0013495==parats115
REFDSR
{
RDID|FBrf0040979
|Ganetzky
|1984
PHP|Viability of double mutant males with FBal0023798==mlenap-ts1 is significantly
|reduced, even at permissive temperatures. Double mutant males at 25oC
|die at or near eclosion.
}
REFDSR
{
RDID|FBrf0099841
|Pittendrigh et al.
|1997
PHP|Homozygous flies do not show significant resistance to
|dichloro-diphenyl-trichloro ethane (DDT) compared to wild-type flies.
}
REF
{
REFM|FBrf0040979
|Ganetzky
|1984
REFM|FBrf0099841
|Pittendrigh et al.
|1997
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014581 ICL 1 ? SYM 1 ?{}pn3 ASTR 1 - CLOC 1 2E1 REF 1 3 DT 1 6 Jan 2000 RESZ 514
ID|FBti0014581
SYM|?{}pn3
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003116==pn
ARGS|FBgn0003116
SK|FBst0000099
|sc[1] FBal0013875==pn[3] g[2rv] Bx[2]
|Total=1
REFDSR
{
RDID|FBrf0054781
|Teng et al.
|1991
SYN|?{}pn3
ASAL|FBal0013875==pn3
CLOC|2E1
|Insertion site
LOCB|Proximity to gene: FBgn0003116==pn
}
REF
{
REFM|FBrf0054781
|Teng et al.
|1991
REFM|FBrf0091186
|Timmons and Shearn
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0013875==pn3
REFDSR
{
RDID|FBrf0054148
|Teng et al.
|1991
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Brownish-red eye.
|RK1.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0091186
|Timmons and Shearn
|1996
PHM|pigment cell
}
REF
{
REFM|FBrf0054148
|Teng et al.
|1991
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0091186
|Timmons and Shearn
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015556 ICL 1 ? SYM 1 ?{}Rab6D6E ASTR 1 - CLOC 1 33D1--2 REF 1 2 DT 1 4 Feb 2000 RESZ 457
ID|FBti0015556
SYM|?{}Rab6D6E
DT|4 Feb 2000
|4 Feb 2000
ICL|?
ASGN|FBgn0015797==Rab6
REFDSR
{
RDID|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
SYN|?{}Rab6D6E
ASAL|FBal0102875==Rab6D6E
CLOC|33D1--2
|Insertion site
LOCB|Proximity to gene: FBgn0015797==Rab6
PHC|lethal | recessive
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015560 ICL 1 ? SYM 1 ?{}Rab6D24A ASTR 1 - CLOC 1 33D1--2 REF 1 2 DT 1 4 Feb 2000 RESZ 460
ID|FBti0015560
SYM|?{}Rab6D24A
DT|4 Feb 2000
|4 Feb 2000
ICL|?
ASGN|FBgn0015797==Rab6
REFDSR
{
RDID|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
SYN|?{}Rab6D24A
ASAL|FBal0102896==Rab6D24A
CLOC|33D1--2
|Insertion site
LOCB|Proximity to gene: FBgn0015797==Rab6
PHC|lethal | recessive
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015559 ICL 1 ? SYM 1 ?{}Rab6D29D ASTR 1 - CLOC 1 33D1--2 REF 1 2 DT 1 4 Feb 2000 RESZ 460
ID|FBti0015559
SYM|?{}Rab6D29D
DT|4 Feb 2000
|4 Feb 2000
ICL|?
ASGN|FBgn0015797==Rab6
REFDSR
{
RDID|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
SYN|?{}Rab6D29D
ASAL|FBal0102892==Rab6D29D
CLOC|33D1--2
|Insertion site
LOCB|Proximity to gene: FBgn0015797==Rab6
PHC|lethal | recessive
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0016272 ICL 1 ? SYM 1 ?{}rb10 ASTR 1 - CLOC 1 4C7 REF 1 2 DT 1 17 Aug 2000 RESZ 395
ID|FBti0016272
SYM|?{}rb10
DT|17 Aug 2000
|17 Aug 2000
ICL|?
ASGN|FBgn0003210==rb
REFDSR
{
RDID|FBrf0127175
|Kretzschmar et al.
|2000
SYN|?{}rb10
ASAL|FBal0044308==rb10
CLOC|4C7
|Insertion site
LOCB|Proximity to gene: FBgn0003210==rb
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0127175
|Kretzschmar et al.
|2000
}
ALESR
{
ASYM|FBal0044308==rb10
REFDSR
{
RDID|FBrf0127175
|Kretzschmar et al.
|2000
PHP|FBal0044308==rb10/FBal0117392==rbS1 flies have a
| normal landing and optomotor response
|and respond normally to stationary visual stimulation. They show abnormal
|behavior in Buridan's paradigm, a test for alternating pattern fixation.
|FBab0000894==Df(1)rb1/FBal0044308==rb10 flies have a normal landing and
| optomotor response
|and respond normally to stationary visual stimulation. They show abnormal
|behavior in Buridan's paradigm, a test for alternating pattern fixation;
|fixation of visual landmarks is significantly impaired and there is
|... (see FBal0044308==rb10 report)
}
REF
{
REFM|FBrf0127175
|Kretzschmar et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015321 ICL 1 ? SYM 1 ?{}rod29D ASTR 1 - CLOC 1 100C6--7 REF 1 2 DT 1 6 Jan 2000 RESZ 398
ID|FBti0015321
SYM|?{}rod29D
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003268==rod
REFDSR
{
RDID|FBrf0112029
|Scaerou et al.
|1999
SYN|?{}rod29D
ASAL|FBal0101175==rod29D
CLOC|100C6--7
|Insertion site
LOCB|Proximity to gene: FBgn0003268==rod
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0112029
|Scaerou et al.
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015320 ICL 1 ? SYM 1 ?{}rodRP153 ASTR 1 - CLOC 1 100C6--7 REF 1 2 DT 1 6 Jan 2000 RESZ 404
ID|FBti0015320
SYM|?{}rodRP153
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003268==rod
REFDSR
{
RDID|FBrf0112029
|Scaerou et al.
|1999
SYN|?{}rodRP153
ASAL|FBal0101174==rodRP153
CLOC|100C6--7
|Insertion site
LOCB|Proximity to gene: FBgn0003268==rod
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0112029
|Scaerou et al.
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014609 ICL 1 ? SYM 1 ?{}rt2 ASTR 1 - CLOC 1 68C13 REF 1 2 DT 1 6 Jan 2000 RESZ 521
ID|FBti0014609
SYM|?{}rt2
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003292==rt
SK|FBst0000594
|se[1] FBal0014814==rt[2] th[1]/In(3L)P, Me[1]
|Total=1
REFDSR
{
RDID|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
SYN|?{}rt2
ASAL|FBal0014814==rt2
MU|spontaneous
CLOC|68C13
|Insertion site
LOCB|Proximity to gene: FBgn0003292==rt
}
REF
{
REFM|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0014814==rt2
REFDSR
{
RDID|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
PHP|The bodies of first instar larvae are rotated around the long axis,
|forcing the animals to move in a clockwise circle as they crawl. The
|larval cuticle presents a perfect segmental alignment of landmarks
|but the adult abdominal cuticle segments appear staggered relative
|to each other.
|Embryos show a variable but fully penetrant mutant phenotype. Common
|phenotypes include the lack of some muscles or the presence of very
|... (see FBal0014814==rt2 report)
PHM|cuticle | adult
|embryonic/larval somatic muscle
|embryonic/larval somatic muscle | lateral
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Abdomen twisted, as is rt. Viability erratic, usually
|about 50% wild type. Male fertile; female not tested.
|RK2.
}
REF
{
REFM|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014518 ICL 1 ? SYM 1 ?{}SamDCc ASTR 1 - CLOC 1 31D9 REF 1 3 DT 1 6 Jan 2000 RESZ 556
ID|FBti0014518
SYM|?{}SamDCc
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0019932==SamDC
ARGS|FBgn0019932
REFDSR
{
RDID|FBrf0058585
|Clegg et al.
|1993
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
SYN|?{}SamDCc
ASAL|FBal0034916==SamDCc
CLOC|31D9
|Insertion site
LOCB|Proximity to gene: FBgn0019932==SamDC
}
REF
{
REFM|FBrf0058585
|Clegg et al.
|1993
REFM|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0034916==SamDCc
REFDSR
{
RDID|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
PHP|Eclosion is delayed by 3 days in homozygous flies, and the adults have
|a Minute-like bristle phenotype.
|FBal0034916==SamDCc is lethal in combination with
| FBal0034918==SamDCe, if FBal0034918==SamDCe
|is maternally inherited.
| FBal0034916==SamDCc/FBal0034918==SamDCe flies in
| which FBal0034918==SamDCe
|is paternally inherited show a 3 day delay in eclosion and the adults
|have a Minute-like bristle phenotype.
|Homozygous, heterozygous,
| FBal0034916==SamDCc/FBal0034917==SamDCd, FBal0034916==SamDCc/FBal0034918==SamDCe
|... (see FBal0034916==SamDCc report)
PHM|macrochaeta
}
REF
{
REFM|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014618 ICL 1 ? SYM 1 ?{}sas796 ASTR 1 - CLOC 1 84C8--D1 REF 1 2 DT 1 6 Jan 2000 RESZ 469
ID|FBti0014618
SYM|?{}sas796
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002306==sas
ARGS|FBgn0002306
REFDSR
{
RDID|FBrf0055816
|Schonbaum et al.
|1992
SYN|?{}sas796
ASAL|FBal0015137==sas796
CLOC|84C8--D1
|Insertion site
LOCB|Proximity to gene: FBgn0002306==sas
PHC|lethal | larval | polyphasic | conditional cs
}
REF
{
REFM|FBrf0055816
|Schonbaum et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0015137==sas796
REFDSR
{
RDID|FBrf0055816
|Schonbaum et al.
|1992
PHP|Larval lethality is polyphasic, and occasionally viable, fertile adults
|are seen. The progeny of these adults have a variable phenotype ranging
|from severe FBgn0002306==sas defects, to normal, fertile flies. Abnormal tanned
|spots are found between the 4th and 5th, and 1st and 2nd rows of the
|setal belts in second instar larvae.
PHM|larval cuticle
}
REF
{
REFM|FBrf0055816
|Schonbaum et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014619 ICL 1 ? SYM 1 ?{}sas828 ASTR 1 - CLOC 1 84C8--D1 REF 1 2 DT 1 6 Jan 2000 RESZ 439
ID|FBti0014619
SYM|?{}sas828
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002306==sas
ARGS|FBgn0002306
REFDSR
{
RDID|FBrf0055816
|Schonbaum et al.
|1992
SYN|?{}sas828
ASAL|FBal0015138==sas828
CLOC|84C8--D1
|Insertion site
LOCB|Proximity to gene: FBgn0002306==sas
PHC|lethal | larval
}
REF
{
REFM|FBrf0055816
|Schonbaum et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0015138==sas828
REFDSR
{
RDID|FBrf0055816
|Schonbaum et al.
|1992
PHP|Larvae die during the first instar moult or as small second instar
|larvae.
}
REF
{
REFM|FBrf0055816
|Schonbaum et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014621 ICL 1 ? SYM 1 ?{}sc1744 ASTR 1 - CLOC 1 1A8 REF 1 3 DT 1 6 Jan 2000 RESZ 437
ID|FBti0014621
SYM|?{}sc1744
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004170==sc
REFDSR
{
RDID|FBrf0042024
|Campuzano et al.
|1985
SYN|?{}sc1744
ASAL|FBal0015224==sc1744
CLOC|1A8
|Insertion site
LOCB|Proximity to gene: FBgn0004170==sc
}
REF
{
REFM|FBrf0042024
|Campuzano et al.
|1985
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014622 ICL 1 ? SYM 1 ?{}scAc ASTR 1 - CLOC 1 1A8 REF 1 3 DT 1 6 Jan 2000 RESZ 431
ID|FBti0014622
SYM|?{}scAc
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004170==sc
REFDSR
{
RDID|FBrf0042024
|Campuzano et al.
|1985
SYN|?{}scAc
ASAL|FBal0015226==scAc
CLOC|1A8
|Insertion site
LOCB|Proximity to gene: FBgn0004170==sc
}
REF
{
REFM|FBrf0042024
|Campuzano et al.
|1985
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014205 ICL 1 ? SYM 1 ?{}Ser1 ASTR 1 - CLOC 1 97E6--8 REF 1 2 DT 1 6 Jan 2000 RESZ 235441
ID|FBti0014205
SYM|?{}Ser1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004197==Ser
SK|FBst0000076
|w[*]; Df(3R)107, e[*]/TM3, P{w[+mW.hs]=Thb8-lacZ}WD1, Sb[1] FBal0015427==Ser[1]
|FBst0000089
|y[1]; Df(3L)lxd6/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000120
|TM3, ry[RK] Sb[1] Ser[1]/TM6B, Tb[1]
|FBst0000207
|Su(Tpl)[10] kni[ri-1] Ki[1] p[p]/TM3, FBal0015427==Ser[1]
|FBst0000220
|bw[1]; Tcr[40] st[1]/TM3, FBal0015427==Ser[1]
|FBst0000383
|Df(3R)ea, kni[ri-1] p[p]/TM3, FBal0015427==Ser[1]
|FBst0000494
|l(3)DTS2[1] Sb[1]/TM3, FBal0015427==Ser[1]
|FBst0000500
|eg[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000504
|amd[21] Bl[1]/CyO; Gl[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000550
|Df(3R)ama, kni[ri-1] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000577
|ru[1] h[1] th[1] st[1] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000600
|Df(3L)Aprt-1, ru[1] h[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000635
|ry[506] P{ry[+t7.2]=PZ}heph[2]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0000669
|w[*]; Df(3R)Dr-rv1, ry[506]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0000695
|pr[1] cn[1]; su(pr)[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000756
|Df(3R)sbd105, p[p] Ubx[bx-1] sr[1] e[s]/TM3, FBal0015427==Ser[1]
|FBst0000809
|y[1]; Scr[W] Scr[4] p[p]/TM3, FBal0015427==Ser[1]
|FBst0000823
|Df(3R)D605/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000911
|w[1]; P{w[+mC]=UAS-Ubx.Ia.C}36.2/TM3, FBal0015427==Ser[1]
|FBst0000915
|ry[*] mus308[D5]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000916
|st[1] mus301[D1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000917
|st[1] mus301[D2]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000918
|st[1] mus301[D4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000920
|st[1] mus302[D2]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000921
|st[1] mus302[D3]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000922
|st[1] mus304[D1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000924
|st[1] mus305[D1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000925
|st[1] mus305[D2]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000926
|mwh[1] Fs(3)Hor[1] e[1]/T(1;3)OR60/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000928
|st[1] mus311[D1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000942
|y[1]; Dp(3;Y)Antp[+], y[+]; Scr[W] Scr[4] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0000992
|Me[65d] jv[1] se[1] by[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001026
|mwh[1] jv[1] hyl[1]/TM3, FBal0015427==Ser[1]
|FBst0001044
|Crn[1] in[1] kni[ri-1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001047
|rs[2] bul[D] Crn[1] in[1] kni[ri-1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001135
|ru[1] jv[1] trc[1] ca[1]/TM3, FBal0015427==Ser[1]
|FBst0001148
|P{ry[+t7.2]=ry11}ry2, mwh[1] aly[1] ry[506] e[1]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0001156
|y[1] w[a]; Doa[3]/TM3, FBal0015427==Ser[1]
|FBst0001254
|In(3L)C90, rs[2] th[1] st[1] cp[1] in[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001257
|ru[1] h[1] Dew[1]/TM3, FBal0015427==Ser[1]
|FBst0001268
|In(3R)251/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001325
|In(3L)gv[U], ru[1] h[1] gv[U] eyg[U] gl[2] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001403
|In(3LR)LD6, fz[1] st[1] cp[1] in[1] kni[ri-1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001408
|C(1)M4, y[2]; th[1] st[1] cp[1] in[1] kni[ri-1] Kg[V] Ki[1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001428
|In(3LR)bxd[194], p[p] Ubx[bxd-194]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001561
|w[*]; P{w[+mW.hs]=GAL4-arm.S}4a P{w[+mW.hs]=GAL4-arm.S}4b/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001614
|y[1] w[*]; TM3, y[+] Ser[1]/Sb[1]
|FBst0001615
|FM6, B[+]/?; SM5/Dp(?;2)bw[D], wg[Sp-1] bw[D]; TM3, y[+] Ser[1]/Sb[1]
|FBst0001640
|T(2;3)T4, CyO: st[1] Kg[V] red[1] Tb[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001674
|Ser[1]/In(3R)C, sprd[1] e[1] l(3)e[1]
|FBst0001678
|Ki[1] p[p] by[1] cu[1] red[1] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001683
|st[1] in[1] kni[ri-1] eg[2] Ki[1] p[p] e[s]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001692
|mwh[1] h[1] th[1] bld[1] e[s]/TM3, FBal0015427==Ser[1]
|FBst0001704
|CxD, ry[BW]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001714
|Df(3R)M86D, Dfd[1] p[p]/TM3, FBal0015427==Ser[1]
|FBst0001748
|In(3R)hb[bs23], hb[bs23] rsd[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001783
|ru[1] h[1] th[1] st[1] kni[1] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001789
|y[1]; TM2, p[p]/TM3, red[*] FBal0015427==Ser[1]
|FBst0001790
|CxD/TM3, red[*] FBal0015427==Ser[1]
|FBst0001791
|TM2, p[p]/TM3, red[*] FBal0015427==Ser[1]
|FBst0001806
|T(3;4)Antp[Ns-rv2], Antp[Ns-rv2]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001808
|TM3, ry[RK] Sb[1] FBal0015427==Ser[1] P{ry[+t7.2]=Delta2-3}99B/Df(3R)C7, ry[506]
|FBst0001823
|T(Y;3)Antp[Ns-rv19], Antp[Ns-rv19]/TM3, Sb[1] Ser[1]/T(2;3)ap[Xa], ap[Xa]
|FBst0001842
|Df(3R)Antp17/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001885
|Df(3R)Scr, red[1] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001909
|Df(3R)Tl-X, mwh[1] th[1] st[1] kni[ri-1] rn[roe-1] p[p] sr[1] e[1] ca[1]/TM3, FBal0015427==Ser[1]
|FBst0001910
|Df(3R)Tl-P, e[1] ca[1]/TM3, FBal0015427==Ser[1]
|FBst0001911
|Df(3R)Tl-I, e[1]/TM3, FBal0015427==Ser[1]
|FBst0001926
|sr[1] r-l[K2] cd[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001931
|Df(3R)by10, red[1] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001937
|Df(3R)GB104, red[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0001968
|Df(3R)p712, red[1] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002030
|In(1)w[m4h]; Df(3L)Ly, sens[Ly-1]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1] P{ry[+t7.2]=Delta2-3}99B
|FBst0002186
|In(3R)Scr[Msc], ru[1] Scr[Msc] pum[Msc] ss[1] e[s]/TM3, FBal0015427==Ser[1]
|FBst0002222
|ru[1] h[1] th[1] st[1] cu[1] sr[1] e[s] pnt[2] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002233
|In(3R)Antp[CB], Antp[CB]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002260
|zen[7] red[1] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002261
|zen[1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002287
|Antp[10] p[p]/TM3, FBal0015427==Ser[1]
|FBst0002362
|Df(3R)crb87-4, st[1] e[1]/TM3, FBal0015427==Ser[1]
|FBst0002363
|Df(3R)crb87-5, st[1] e[1]/TM3, FBal0015427==Ser[1]
|FBst0002371
|flr[3]/TM3, FBal0015427==Ser[1]
|FBst0002405
|In(3R)hb[D1], p[p] hb[D1] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002411
|Df(3R)Dl-KX23, e[*]/TM3, FBal0015427==Ser[1]
|FBst0002440
|w[1118]; Gld[n1] p[p] cu[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002461
|l(3)67Aa[2] kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002464
|Df(3R)R38.3, st[1] ry[506]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002485
|ru[1] h[1] th[1] st[1] cu[1] srp[3] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002500
|ru[1] h[1] th[1] st[1] cu[1] sr[1] e[s] stg[4] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002507
|ru[1] h[1] th[1] st[1] kni[ri-1] rn[roe-1] p[p] e[1] Tl[r4]/TM3, FBal0015427==Ser[1]
|FBst0002537
|w[*]; TM3, Sb[1] Ser[1]/TM6B, Tb[1]
|FBst0002553
|Df(3L)vin6, ru[1] h[1] gl[2] e[4] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002580
|l(3)84Ce[1] p[p] cu[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002585
|cn[1]; Df(3R)mbc-R1, ry[506]/TM3, ry[*] Sb[1] FBal0015427==Ser[1]
|FBst0002586
|Df(3R)23D1, ry[506]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002587
|Df(3L)2-30, kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002588
|Df(3L)9-56, kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002589
|Df(3L)2-66, kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002591
|Df(3L)8A-80, kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002592
|Df(3L)6-61, kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002593
|Df(3L)3-52, kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002596
|Df(3L)6B-29+Df(3R)6B-29, kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002597
|Df(3R)10-65, kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002598
|Df(3R)4-75, kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002609
|Df(3L)vin3, ru[1] h[1] gl[2] e[4] ca[1]/TM3, ry[*] Sb[1] FBal0015427==Ser[1]
|FBst0002610
|Df(3L)vin4, ru[1] h[1] gl[2] e[4] ca[1]/TM3, ry[*] Sb[1] FBal0015427==Ser[1]
|FBst0002611
|Df(3L)vin5, ru[1] h[1] gl[2] e[4] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002612
|Df(3L)vin7, h[1] gl[2] e[4] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002866
|Ubx[1] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002875
|l(3)85Ag[1] rsd[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002975
|ru[1] h[1] Ki[1] rn[roe-1] p[p] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002987
|th[1] st[1] kni[ri-1] rn[roe-1] osk[6] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002990
|Df(3L)Cat, kni[ri-1] Sb[sbd-1] e[*]/TM3, FBal0015427==Ser[1]
|FBst0002996
|Df(3L)st7, e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0002997
|Df(3L)st7P, In(3L)P/TM3, FBal0015427==Ser[1]
|FBst0003002
|Df(3L)Pc, kni[ri-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003007
|Df(3R)ry615/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003021
|In(3R)iab7[Spth], Abd-B[iab7-Spth]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003024
|Df(3L)h-i22, h[i22] Ki[1] rn[roe-1] p[p]/TM3, FBal0015427==Ser[1]
|FBst0003028
|Dfd[13] Scr[8] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003039
|y[1] w[1118]; P{w[+mW.hs]=GawB}pnr[MD237]/TM3, P{w[+mC]=UAS-y.C}MC2, FBal0015427==Ser[1]
|FBst0003043
|y[1] w[1118]; P{w[+mC]=UAS-y.C}MC1/TM3, P{UAS-y.C}MC2, FBal0015427==Ser[1]
|FBst0003050
|Df(3R)Sq219, e[*]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003053
|Df(3R)CA1/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003093
|ru[1] h[1] th[1] st[1] cu[1] yrt[2] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003094
|ru[1] h[1] th[1] st[1] hau[9G] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003095
|ru[1] h[1] th[1] st[1] nkd[2] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003097
|ru[1] h[1] th[1] st[1] knk[1] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003100
|st[1] put[135] e[1]/TM3, FBal0015427==Ser[1]
|FBst0003103
|ru[1] h[1] th[1] st[1] grn[7L] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003105
|ru[1] h[1] th[1] st[1] cu[1] sr[1] e[s] kay[1] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003106
|ru[1] h[1] th[1] st[1] cu[1] pnr[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003107
|ru[1] h[1] th[1] st[1] cno[2] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003128
|Df(3R)M-Kx1/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003222
|ru[1] h[1] th[1] st[1] opa[1] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003237
|ru[1] h[1] th[1] st[1] cu[1] sr[1] e[s] tld[9] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003251
|BicF[1]/TM3, Sb[1] Ser[1]; CyO, l(2)DTS513[1]/?
|FBst0003252
|st[1] bcd[7] p[p] osk[6]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003253
|th[1] st[1] kni[ri-1] rn[roe-1] p[p] osk[6] nos[L7] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003255
|th[1] st[1] kni[ri-1] bcd[6] rn[roe-1] p[p] e[1] tsl[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003257
|st[1] kni[ri-1] bcd[6] rn[roe-1] p[p] nos[L7] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003258
|st[1] pum[13] e[1] tsl[4] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003260
|st[1] pum[13]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003261
|st[1] kni[ri-1] bcd[6] pum[13]/TM3, FBal0015427==Ser[1]
|FBst0003282
|ru[1] h[1] th[1] st[1] hb[6] cu[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003290
|Dp(1;Y)B[S]; ru[1] st[1] e[1] Ets97D[tne-4] ca[1]/TM3, FBal0015427==Ser[1]
|FBst0003327
|ru[1] st[1] spn-E[1] e[1] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003332
|kni[9] pum[13]/TM3, FBal0015427==Ser[1]
|FBst0003334
|kni[9] tsl[4] e[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003340
|Df(3R)e-R1, Ki[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003349
|ru[1] h[1] th[1] st[1] cu[1] ems[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003354
|Df(3R)roe/TM3, FBal0015427==Ser[1]
|FBst0003355
|Df(3R)kar-Sz8/TM3, FBal0015427==Ser[1]
|FBst0003356
|Df(3R)ftzRARU, Df(3L)Pc, kni[ri-1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003360
|Df(3R)4SCB/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003369
|y[*]; Df(3R)awd-KRB, e[*] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003448
|ru[1] h[1] th[1] st[1] cu[1] sr[1] e[s] crb[2] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003639
|Df(3R)urd, ru[1] h[1] th[1] st[1] sr[1] e[s] ca[1]/TM3, Sb[1] FBal0015427==Ser[1] ca[*]
|FBst0003724
|st[1] mus310[D1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003725
|st[1] mus311[D2]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003742
|w[1118]; P{w[+mW.hs]=GawB}c768/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0003751
|w[1118]; P{w[+mW.hs]=GawB}c204/TM3, FBal0015427==Ser[1]
|FBst0003804
|v[1]; Df(3L)vin66, TM3, Sb[1] Ser[1]/Ubx[51]
|FBst0004014
|Cat[n1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004015
|Sod[n1] red[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004018
|Idh[F] Sod[F] Pgm[6tr] Ald[2]/TM3, Idh[S] Sod[S] Pgm[4tr] Sb[1] Ald[4] FBal0015427==Ser[1]
|FBst0004039
|Pgm[nGB1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004076
|y[2]; TM3, Sb[1] Ser[1]; T(3;4)bxd[101], ss[1] Ubx[bx-1] Ubx[bxd-101]
|FBst0004155
|w[*]; l(3)93Bc[1] e[LE1] cd[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004156
|l(3)93Bd[1] e[LE1] cd[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004157
|l(3)93Bg[1] e[LE1] cd[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004158
|Rab11[93Bi] e[LE1] cd[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004369
|P{ry[+t7.2]=lArB}neur[A101] ry[506]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004370
|Df(3L)Delta1AK, ru[1] h[1] ry[506] sr[1] e[s] ca[1]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004379
|Syx1A[Delta229] ry[506]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004404
|y[1]; ry[506] Pr[1] Bsb[1]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004432
|Df(3R)crb-F89-4, st[1] e[1]/TM3, FBal0015427==Ser[1]
|FBst0004504
|Df(3L)Ten-m-AL1/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004506
|Df(3L)Ten-m-AL29/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004534
|w[*]; Sb[1]/TM3, P{w[+mC]=ActGFP}JMR2, FBal0015427==Ser[1]
|FBst0004543
|y[1] w[67c23]; P{w[+mC]=lacW}bon[S048706]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004544
|y[1] w[67c23]; P{w[+mC]=lacW}gammaCop[S057302a], l(3)S057302b[S057302b]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004545
|y[1] w[67c23]; P{w[+mC]=lacW}Crc[S114307]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004546
|y[1] w[67c23]; P{w[+mC]=lacW}S136802, l(3)S136802[S136802]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004547
|y[1] w[67c23]; P{w[+mC]=lacW}melt[S144114]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004548
|y[1] w[67c23]; P{w[+mC]=lacW}aay[S042314]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004549
|y[1] w[67c23]; P{w[+mC]=lacW}S052908b, l(3)S052908a[S052908a]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004550
|y[1] w[67c23]; P{w[+mC]=lacW}trn[S064117]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004569
|cn[1]; tok[3]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004575
|fs(3)A1[1-320]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004588
|w[*]; P{w[+mC]=Cdk7[P140S]}SL1 Sb[1]/TM3, FBal0015427==Ser[1]
|FBst0004739
|mwh[1] jv[1] gig[109] red[1] ro[1]/TM3, FBal0015427==Ser[1]
|FBst0004787
|Df(3R)3-4, ru[1] th[1] st[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004857
|In(3R)82Fc[1], mwh[1] l(3)82Fc[1] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004858
|In(3R)82Fc[2], mwh[1] l(3)82Fc[2] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004859
|In(3)82Fe[1], mwh[1] l(3)82Fe[1] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004860
|l(3)70Da[1], mwh[1] red[1] e[4]/TM3, P{w[+mW.hs]=Thb8-lacZ}WD1, Sb[1] FBal0015427==Ser[1]
|FBst0004862
|mwh[1] ppl[2] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004863
|mwh[1] l(3)78Da[2] red[1] e[4]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004864
|mwh[1] l(3)82Fa[2] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004865
|mwh[1] l(3)82Fe[2] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004866
|mwh[1] l(3)82Ff[1] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004867
|mwh[1] l(3)82Fg[1] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004868
|mwh[1] kkv[82Fh-1] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004869
|mwh[1] l(3)82Fi[1] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004870
|mwh[1] l(3)82Fk[1] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004871
|sti[3] rn[roe-1] p[p]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004872
|T(2;3)82Fd[4], mwh[1] l(3)82Fd[4] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004873
|T(2;3)82Fh[2], mwh[1] kkv[82Fh-2] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004874
|T(2;3)82Fi[2], mwh[1] l(3)82Fi[2] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004875
|T(2;3)ME21, mwh[1] l(3)78Ae[1] red[1] e[4]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004876
|Df(3L)Pc-101, mwh[1] red[1] e[4]/TM3, ry[RK] red[2] Sb[1] FBal0015427==Ser[1]
|FBst0004883
|y[1] w[*]; In(3L)D[r8], mwh[1] D[r8] red[1] e[4]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004905
|Ab(3R;h)82Fj[1], mwh[1] l(3)82Fj[1] red[1] e[4]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004909
|cn[1]; T(3;4)11d, mwh[1] l(3)ry3[2] e[4] ry[506]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0004910
|cn[1]; mwh[1] P{ry[+t7.2]=ry11}l(3)ry3[1] ry[506]/TM3, In(3LR)D[6], D[6] ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004911
|CyO, P{ry[+t7.2]=ftz/lacB}E3/+; Hsc70Cb[1], mwh[1] red[1] e[4]/TM3, P{w[+mW.hs]=Thb8-lacZ}WD1, Sb[1] FBal0015427==Ser[1]
|FBst0004915
|mwh[1] l(3)78Da[1] red[1] e[1]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0004952
|st[1] e[1] mbc[D11.2]/TM3, FBal0015427==Ser[1]
|FBst0005121
|enc[R1] st[1] e[1] ca[1]/TM3, FBal0015427==Ser[1]
|FBst0005152
|w[1118]; P{w[+mF] ry[+t7.2]=wF}mas[P] ry[506]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0005352
|ms(3)K81[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0005370
|w[*]; htl[AB42]/TM3, P{ry[+t7.2]=ftz/lacC}SC1, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0005395
|srw[B18] p[p]/TM3, P{w[+mW.hs]=Thb8-lacZ}WD1, Sb[1] FBal0015427==Ser[1]
|FBst0005396
|tld[B4] p[p]/TM3, P{w[+mW.hs]=Thb8-lacZ}WD1, Sb[1] FBal0015427==Ser[1]
|FBst0005427
|ry[506] e[1] bam[Delta86]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0005437
|w[*]; TfIIA-S[E32]/TM3, P{w[+mW.hs]=Thb8-lacZ}WD1, Sb[1] FBal0015427==Ser[1]
|FBst0005441
|cn[1]; mwh[1] P{ry[+7.2]=ry11}l(3)ry3[1] e[1] ry[506]/TM3, Au[1] ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0005448
|w[*]; slug[3] ca[1]/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0005490
|cn[1] bw[1] Hsf[4]; P{w[+mC]=Hsf[+t8]}1/TM3, Sb[1] FBal0015427==Ser[1]
|FBst0005492
|w[*]; Df(3L)eyg[C1]/TM3, P{ry[+t7.2]=ftz/lacC}SC1, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0005575
|Df(3L)03844, P{ry[+t7.2]=PZ}sfl[03844] ry[506]/TM3, ry[RK] Sb[1] FBal0015427==Ser[1]
|FBst0005578
|y[1] w[1]; Klp64D[k1]/TM3, y[+] FBal0015427==Ser[1]
|FBst0005674
|y[1] w[1]; Klp64D[n123]/TM3, y[+] FBal0015427==Ser[1]
|FBst0005