[96F10-96F10];[97D2-97D2];
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.
96F10;97D2
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Df(3R)ED6232/Df(3R)E(spl)δ-6 mutant embryos display a significant increase in the number of Ap neurons, as compared with controls.
Df(3R)ED6232/Df(3R)grob32.2, in combination with gro+t10.4, mutant embryos do not display any significant change in the number of Ap neurons, as compared with controls.
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.
Confirmed by PCR (using the 3-step process described on http://www.drosdel.org.uk/del_confirm.php).
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}l(3)rQ197rQ197 and P{lacW}scribj7B3 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}scribj7B3 and P{lacW}His2AvL1602