70D2;70E8
70D2;70E8
70D3;70E3-70E8
70D;71F
70D1-70D2;70E7
Hsc70Cb << bk1 << D << shd << bk2 << gnu
Df(3L)fz-D21 Df(3L)fz2 embryos derived from fz23/Df(3L)fz-D21 Df(3L)fz2 females show a "denticle lawn" cuticle phenotype.
The Df(3L)fz-D21 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(3L)fz-D21 results in 1.1% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Double mutants of fz21, fz23 or Df(3L)fz-D21 with Df(3L)fz2 show variable embryonic segmentation defects ranging from a few extra denticles in the posterior part of some segments to complete replacement of naked cuticle with denticles. This phenotype is reminiscent of that for P{en1}wgen11 loss of function.
No effect on the eye pigment phenotype of wT81.
Shows no maternal enhancement of dpphr4.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Exhibit dominant suppression of Pc.
Adler.
"70D2;70E8" was stated as revision.
Left limit of break 1 from polytene analysis (FBrf0075380) Right limit of break 1 from inclusion of D (FBrf0075380) Limits of break 2 from polytene analysis (FBrf0075380)