[61B1-61B1];[61C1-61C1];
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.
61B1;61C1
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Lethal in combination with Df(3L)BSC121. Inferred to overlap with: Df(3L)BSC121.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Df(3L)ED201 mutants show beta lobe defects that cannot be rescued by expression of PtpmegUAS.cWa under the control of Scer\GAL4elav.PLu, suggesting that disruption of some other genes in this deficiency contribute to the beta lobe defects.
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 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}trh10512 and P{EP}EP3104EP3104