[70F4-70F4];[71E1-71E1];
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.
70F4;71E1
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Inferred to overlap with: Df(3L)BSC558.
No cardiac or bristle phenotypes are observed in heterozygous Df(3L)ED217 mutant females.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}Mpcp00564 and P{PZ}l(3)rO220rO220 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}Tfb2EP572 and P{lacW}thj5C8&P{PZ}Mbs03802