87F12-87F14;88C2
87F12-87F14;88C1-88C3
87F15;88C1-88C3
87F12-87F14;88C1-88C2
87F2-87F14;88C1-88C3
l(3)02946 << bk1 << Dip-B << pr-set7 << bk2 << l(3)03471
Aberration fails to complement Df(3R)urd, Df(3R)293γ5, Df(3R)293γ7 and Df(3R)red-P52 and complements Df(3R)l26c.
No effect on In(1)wm4h position-effect variegation.
The Df(3R)red3l 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).
Strong enhancer of the eye pigment phenotype of wT81.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Homozygous embryos do not complete head involution, dorsal closure or tracheal formation.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Heterozygotes with wrl1 are fertile.
Heterozygotes sometimes have transformations typical of bithorax or postbithorax mutants.
Df(3R)red/+ progeny of Df(1)C128/+ females show a high frequency of homeotic transformations (Gans et al., 1980).
Separable from: tefured31
Ref: FBrf0028767.
Limits of break 1 from polytene analysis (FBrf0028767) Left limit of break 2 from inclusion of cv-c (FBrf0051995) Right limit of break 2 from polytene analysis (FBrf0086390)