P{XP} insertion lines from Exelixis were remapped and assessed for inclusion in the Gene Disruption Project collection; flanking sequence data were submitted to GenBank.
A set of transgenic insertion stocks derived by TE mobilization using the P-element construct P{XP}. The P{XP} construct carries the w+mC mini-white marker, long (199-bp) Scer\FRT sites, and is designed to allow flexible use of Scer\UAS sites for Scer\GAL4-driven misexpression of adjacent genes. FRT sites allow Scer\FLP-mediated recombination between other FRT-containing elements, and thus can be used to generate molecularly defined deletions.
Exelixis, Inc. determined the insertion site of P{XP}d10684 to be at Release 3 genomic coordinate 11434362 on chromosome arm 2L. The Gene Disruption project determined the insertion site of P{XP}d10684 to be at Release 3 genomic coordinate 11434604 on arm 2L. This corresponds to 32F2 on both the Release 3 and Release 4 maps.
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d10684