1Lt - 5E3 | 17C - 6B | 17C - 1Rt
bk1 << swa << vs << bk2
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Flies heterozygous for the deletion show a Minute bristle phenotype.
Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.
Weak second site non-complementing phenotype with zipmhc-c6.1 (not zipEbr): malformed phenotype penetrance 10-24%.
Shows no maternal enhancement of dpphr4.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Midgut development of mutant embryos is wild type.
Homozygous embryos are very abnormal compared to wild-type.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
5E3-5E8;6B
Deficient for 5E3-5E8;6B.
5E3-5E8;6B;17C