FB2026_02 , released June 18, 2026
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Cook, K. (2014.5.2). Verifying the lethality of the P{lacW}CG5385[SH0834] insertion. 
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FBrf0224934
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Personal communication to FlyBase
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In crosses here, I showed that the P element-bearing chromosome in stock
29486      w*; P{w+mC=lacW}CG5385SH0834 P{ry+t7.2=neoFRT}40A, l(2)SH0834SH0834/CyO 
is lethal in combination with Df(2L)BSC207 and Df(2L)ED729. The overlap of these deletions defines a ~6 gene interval containing the P{lacW}CG5385SH0834 insertion. Consequently, it is highly likely that l(2)SH0834SH0834 maps to the P{lacW}CG5385SH0834 insertion site. The gene entries for CG5385 and l(2)SH0834 should be merged. Likewise the allele entries for CG5385SH0834 and l(2)SH0834SH0834 should be merged. 
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    English
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    Aberrations (2)
    Alleles (1)
    Genes (1)
    Insertions (1)