[91A5-91A5];[91F1-91F1];
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.
91A5;91F1
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Inferred to overlap with: Df(3R)BSC473.
Inferred to overlap with: Df(3R)BSC474.
Inferred to overlap with: Df(3R)Cha9.
Lethal in combination with Df(3R)Cha9.
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 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}cdi07013&P{lacW}nosj3B6 and P{PZ}l(3)0334603346