[29F5-29F5];[30B12-30B12];
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.
29F5;30B12
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Viable in combination with Dp(2;2)EDP9.
Weak over SM6a.
No cardiac or bristle phenotypes are observed in heterozygous Df(2L)ED678 mutant females.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k04003k04003 and P{PZ}tai01351 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}Oatp30BEP890 and P{EP}EP361&P{EP}peloEP2160