[37E5-37E5];[38C6-38C6];
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.
37E5;38C6
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
No axonal lobe phenotypes are observed in the mushroom bodies of Df(2L)ED1303/+ mutants.
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
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}dntEP2158 and P{EP}EP623&P{PZ}spi01068 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG16798EP401&P{lacW}k07219 and P{lacW}k02501&P{lacW}k14810