56F5;56F15
bk1 << mus209 << M(2)56F << bk2 << RpL30
Point mutation.
Flies heterozygous for the deletion show a Minute bristle phenotype.
The Df(2R)173 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).
Maternal effect lethal phenotype when heterozygous with alleles of plu.
Csik.
Not suppressed by RpL32+t3.3.
not suppressed by su(Hw)2 (E.B. Lewis in FBrf0020044)
Ref: Lindsley and Zimm, 1992
Cytologically invisible deletion. Deletion removes about 10kb of DNA.
A multilocus deficiency at 56F.
Cytologically invisible deletion.
Polytene chromosomes normal.
Limits of break 1 from polytene analysis (citation unavailable) Left limit of break 2 from polytene analysis (citation unavailable) Right limit of break 2 from non-inclusion of RpL30 (FBrf0067338)