The P{EP}RhoGEF64CEP3035 insertion present in the progenitor line is also still present.
Amino acid replacement: W295term.
G4765773A
W295term | RhoGEF64C-PA; W295term | RhoGEF64C-PB
W295term
G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. The point mutation was introduced onto a chromosome containing the P{EP}EP3035 insertion.
Expression of Gef64C29 under the control of Scer\GAL4elav.PLu (using the P{EP}Gef64CEP3035 insertion present on the Gef64C29 chromosome) does not result in a gain of function defective axon guidance phenotype.