86C1;87B5
86C1;87B1-87B5
86C1;87B5
86C1;85B1-85B5
hth << bk1 << TfIIFβ << svp << bk2 << Pp1-87B
Inferred to overlap with: Df(3R)Exel8154.
Dominant suppressor of In(1)wm4h variegation.
The size of the tracheal lumen is different to wild type in Df(3R)M-Kx1 embryos.
The Df(3R)M-Kx1 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).
Heterozygosity for Df(3R)M-Kx1 results in 2.3% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Heterozygous males differ significantly from control males in their homo- and heterosexual courtship. These males do not discriminate between male and female target flies.
Dominantly suppresses the KrIf-1/+ eye phenotype.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Shows no maternal enhancement of dpphr4.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Homozygous embryos have holes in the epidermis and dorsal closure is abnormal. Midgut constrictions are variable and the hindgut is contorted and bloated.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Vassin.
The left Df(3R)M-Kx1 breakpoint lies in CG4596 or Sodh-2 or in the region between them, and lies in the range 3R:6699495..6703853 (R5) (predicted cytology: 86C7).
The right breakpoint of Df(3R)M-Kx1 lies within CG10013 or CG10038 or in the region between them, and lies in the range 3R:8150560..8176137 (R5) (predicted cytology: 87B6-7).
Limits of break 1 from polytene analysis (FBrf0047003) Left limit of break 2 from polytene analysis (FBrf0076124) Right limit of break 2 from polytene analysis (FBrf0047003)