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.