[76A1-76A1];[76B3-76B3];
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.
76A1;76B3
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
The distal half of the salivary gland turns but the proximal half does not in embryos homozygous for Df(3L)ED4799 by stage 14.
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 computationally determined from location of progenitor P insertion on genome sequence between P{EP}MESR6EP3142 and P{lacW}l(3)L3809L3809