88B1;88C2
88A10-88B1;88C2-88C3
88A10;88C2-88C3
140up << bk1 << l(3)88Bb << spn-B << bk2 << cv-c
Breakpoint(s) molecularly mapped
Heterozygosity for In(3R)UbxP18 Df(3R)red-P93 results in 1.1% X chromosome nondisjunction and 0.7% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
The Df(3R)red-P93 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).
Homozygous embryos show abnormal dorsal closure.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Flies heterozygous for Df(3R)red-P93 show no detectable transformation of halteres to wings or third legs to second legs. Flies heterozygous for both Df(3R)red-P93 and ash16 express partial transformation of halteres to wings or third legs to second legs, there is also evidence of a maternal as well as zygotic component to the interaction.
Df(3R)red/+ progeny of Df(1)C128/+ females show a high frequency of homeotic transformations (Gans et al., 1980).
Jurgens.
Left limit of break 1 from non-inclusion of 140up (FBrf0054607) Right limit of break 1 from inclusion of l(3)88Bb (FBrf0054607) Left limit of break 2 from polytene analysis (FBrf0041709) Right limit of break 2 from non-inclusion of cv-c (FBrf0054607)