11D1-11D2;11F1-11F2
11D1-11D2;11F1-11F2
11D1-11D2;11F7-11F8
bk1 << hep << mew << bk2 << s
This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).
Transmission rate of Dp(1;f)J21A through females to progeny is 28%, Df(1)N12 has no effect on transmission.
Flies heterozygous for the deletion show a Minute bristle 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.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
No significant change in female lethality when in combination with Sxlf1.
Hemizygous embryos were examined with polarised light microscopy and antibody staining: muscle pattern incomplete due to muscle absences and detachments.
Lefevre.
Left limit of break 1 from polytene analysis (FBrf0023568) Right limit of break 1 from inclusion of hep (FBrf0083963) Limits of break 2 from polytene analysis (FBrf0023568)