65F3;66B9
65F3;66B10
65F3;66B3-66B9
qm << bk1 << mus301 << lqf << bk2 << Nmt
Fails to complement Df(3L)ZP1.
The size of the tracheal lumen is different to wild type in Df(3L)pbl-X1 embryos.
The Df(3L)pbl-X1 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(3L)pbl-X1 results in 1.3% X chromosome nondisjunction and 0.4% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.
Dominant suppressor of dshhs.sev.B mutant polarity phenotype.
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.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Used in D.melanogaster/D.simulans hybrids to map at least four non-overlapping regions on the D.simulans 3R that have effects on the species difference of cuticular hydrocarbon profile.
The left Df(3L)pbl-X1 breakpoint lies within CTCF or pst or in the region between them, and lies in the range 3L:7349161..7350625 (R5) (predicted cytology: 65F6-65F6).
The right Df(3L)pbl-X1 breakpoint lies within CG7504 or mus301 or in the region between them, and lies in the range 3L:8125230..8134144 (R5) (predicted cytology: 66B7-66B8).
Limits of break 1 from polytene analysis (FBrf0055848) Limits of break 2 from polytene analysis (FBrf0086978)