[62E8-62E8];[62F5-62F5];
A set of isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Initial set of 519 isogenic deletions provides 56% genome coverage.
The current Exelixis collection at the Bloomington Stock Center differs from the original described in FBrf0175003 : a significant number were shown not to carry a deletion and have been removed from the collection; a number of stocks have been lost; a number of additional deletions are included that were generated after publication.
62E8;62F5
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Inferred to overlap with: Df(3L)BSC412.
No cardiac or bristle phenotypes are observed in heterozygous Df(3L)Exel6091 mutant females.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.