36A8-36A9;36F1
36A12-36A14;36E1-36E2
36A6-36A10;36E3-36F2
36A8-36A9;36E3-36E4
36A6-36A7;36F1-36F2
36A8-36A9;36E1-36E2
36A6-36A11;36E3-36F2
her << bk1 << l(2)k04206 << bk2 << Dox-A3
The 2L:16680054..16692000 release 6 coordinates of the left breakpoint are estimates based on figure 2 of FBrf0100594.
The 2L:18359026..18393441 release 6 coordinates of the right breakpoint are estimates based on FBrf0183166, which showed the breakpoint to map between the right end of Acp36DE and the right end of Fas3.
Breakpoint 1 was mapped to an EcoRI-HpaI restriction fragment. The position of the restriction fragment on the reference sequence was inferred by a FlyBase curator.
Df(2L)M36F-S6 is semi-lethal in combination with Df(2L)H20. Surviving males and females are fertile.
Inferred to overlap with: Df(2L)TW137.
Enhancer of In(1)wm4h position-effect variegation.
Df(2L)H20/Df(2L)TW119 lethal Df(2L)H20/Df(2L)M36F-S5 lethal Df(2L)H20/Df(2L)TW137 lethal Df(2L)H20/Df(2L)T317 lethal Df(2L)H20/Df(2L)TW201 lethal Df(2L)H20/Df(2L)203 lethal Df(2L)H20/Df(2L)330 lethal Df(2L)H20/Df(2L)VA18 lethal
Lysates from 4 hour old prepupae heterozygous for Df(2L)H20 show no reduction in caspase activation compared to wild type.
The Df(2L)H20 chromosome does not act as a dominant suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion).
Heterozygotes show no adult central brain defect.
Df(2L)H20 in combination with a pair of introgressions from D.simulans spanning 30F1-31E7 to 35D7-36A14 Dsim\Int(2L)S and 21A1 to 22D1--23A2 Dsim\Int(2L)D produces sterile male flies. These flies are female sterile.
Heterozygotes are flightless, but show normal muscle patterns, except for a reduced birefringence of the indirect flight muscles compared to those of wild type.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
Intermediate second site non-complementing phenotype with zipEbr and zipmhc-c6.1 : malformed phenotype penetrance 25-75%.
Shows no maternal enhancement of dpphr4.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Midgut development of mutant embryos is wild type.
Homozygous embryos have a truncated head and the stomodeum is shifted anteriorly.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Nonmotile germ cells.
C. Nusslein-Volhard.
Nusslein-Volhard.
Ref: Ashburner et al., 1990, Genetics 126: 679--694
Ref: FBrf0045239.
Limits of break 1 from polytene analysis (FBrf0044474) Left limit of break 2 from polytene analysis (FBrf0048188) Right limit of break 2 from polytene analysis (FBrf0044468)