[68C13-68C13];[69B4-69B4];
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.
68C13;69B4;[68C13-68C13];[69B4-69B4];
68C13;69B4
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Df(3L)ED4475/Df(3R)ED10556 or Df(3L)ED4475/Df(3R)ED5660 flies (which are hemizygous for RpL10Aa and RpL10Ab) do not show Minute phenotypes.
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}l(3)0123901239&P{lacW}l(3)01239j9B4 and P{PZ}CycA02461&P{PZ}CycA03946 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}l(3)0508805088 and P{PZ}l(3)0692406924