[86D8-86D8];[86E13-86E13];
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.
86D8;86E13
This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).
Viable in combination with Df(3R)MS32.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Does not show a Minute phenotype: analysis aimed at identification of M(3)86D.
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 of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP3340EP3340 and P{PZ}tho1&P{PZ}l(3)0462905275 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}tho1&P{PZ}l(3)0462905275 and P{EP}Lk6EP886