An indel mutation, resulting in a nom protein that is four amino acids longer than the wild-type protein, but lacks the first zinc finger domain entirely and part of the second zinc finger domain with an in-frame inappropriate amino acid stretch.
A 171 bp deletion that removes 104 bp from the 3' end of exon two and 67
bp from the 5' end of intron two. This causes a read-through of intron sequences and the addition of 41 novel amino acids to the protein. The first zinc finger domain is completely removed as well as the first cysteine of the second zinc finger domain.
nom557/nom557 and nom557/Df(3R)BSC197 individuals arrest development at the second instar larval stage, with the larvae being larger than controls.
nom557 has lethal - all die before end of second instar larval stage phenotype, suppressible by nvdUAS.cUa/Scer\GAL4phtm.PO
nom557/nom60 has lethal - all die before end of second instar larval stage phenotype, suppressible by nvdUAS.cUa/Scer\GAL4phtm.PO
nom557/nom33 has lethal - all die before end of second instar larval stage phenotype, suppressible by nvdUAS.cUa/Scer\GAL4phtm.PO
Scer\GAL4phtm.PO, nom557, nvdUAS.cUa has viable phenotype