[94A1-94A1];[94C1-94C1];
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.
94A1;94C1
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Inferred to overlap with: Df(3R)BSC804.
Inferred to overlap with: Df(3R)BSC637.
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 of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}tsl00617 and P{lacW}howj5B5&P{EP}EP738 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}GclmL0580 and P{EP}hhEP3521