27E;28C1-28C4
27D-27E;28C
27E;28C
27E1-27E3;28B1-28B3;26A6-26B1
eIF-4a << bk1 << wg << cuc << bk2 << l(2)rL220
Fails to complement Df(2L)TE29Aa-11.
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.
Homozygous embryos are very abnormal compared to wild-type and have no obvious segmentation. The hindgut is very short or absent, and the Malpighian tubules are either absent or show very short outbuddings.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
E.H. Grell.
The Df(2L)spd chromosome may 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), but the eye colour phenotype in the presence of Df(2L)spd overlaps the eye colour phenotype in a wild-type background so it cannot be unequivocally demonstrated that the deficiency chromosome uncovers a suppressor of telomeric silencing.
"27E1--3;28B1--3;26A6--B1" was stated as revision. "deficient_inversion ; SO:1000171" was stated as revision.
Left limit of break 1 from polytene analysis (FBrf0082073) Right limit of break 1 from polytene analysis (FBrf0076124) Left limit of break 2 from polytene analysis (FBrf0076124) Right limit of break 2 from non-inclusion of l(2)rL220 (FBrf0067338)