[74D1-74D1];[75B11-75B11];
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.
74D1;75B11
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
No cardiac or bristle phenotypes are observed in heterozygous Df(3L)ED4710 mutant females.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS5}5-HA-1583 and P{RS3}UM-8103-3.
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}frc00073&P{PZ}frc02619 and P{lacW}l(3)j11B2j11B2 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(3)j11B2j11B2 and P{PZ}W05014