[<88A2];88C1--D1
88B1;88D3-88D4
88B1;88D2-88D3
bk1 << cash << bk2 << put
Homozygotes for Df(3R)red1 fail to hatch.
The Df(3R)red1 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)red1 results in 1.6% X chromosome nondisjunction and 0.6% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Midgut development of mutant embryos is wild type.
Heterozygosity for this deletion enhances the mutant ovarian phenotype of ovoD2.
Df(3R)red/+ progeny of Df(1)C128/+ females show a high frequency of homeotic transformations (Gans et al., 1980).
Right limit of break 1 from inclusion of ems (FBrf0049810) Left limit of break 2 from inclusion of l(3)06951 (FBrf0067338) Right limit of break 2 from non-inclusion of l(3)03719 (FBrf0067338)