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FB2026_01
,
released March 12, 2026
[102B7-102B7];[102D5-102D5];
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.
102B7;102D5
Df(4)ED6380 mutant embryos show defects in the frontal ganglion and in the esophageal ganglia, as compared to controls.
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{SUPor-P}KG02769 and P{SUPor-P}AsatorKG05051&P{SUPor-P}KG01424 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{SUPor-P}AsatorKG05051&P{SUPor-P}KG01424 and PBac{3HPy+}C024