[85A5-85A5];[85D1-85D1];
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 core set of 209 isogenic deletions provides ~60% euchromatic genome coverage.
85A5;85D1
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
No cardiac or bristle phenotypes are observed in heterozygous Df(3R)ED5330 mutant females.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.
Limits computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(3)L4740L4740 and P{EP}D1EP473