[89E11-89E11];[89F1-89F1];
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.
89E11;89F1
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).
Df(3R)Exel6176 fails to complement Df(3R)ED5780.
Inferred to overlap with: Df(3R)ED5780.
Heterozygous Df(3R)Exel6176 flies that also carry Scer\GAL4GMR.PF display normal eye patterning.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Limits computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG5208EP562/P{EP}DadEP3196 and P{PZ}l(3)0788207882