Amino acid replacement: W699term.
Amino acid alteration. In addition, the P{GSV6}Nedd4GS13178 insertion is still present on the chromosome.
G17544485A
W485term | Nedd4-PE; W648term | Nedd4-PF; W623term | Nedd4-PG; W686term | Nedd4-PH; W675term | Nedd4-PI; W699term | Nedd4-PJ; W526term | Nedd4-PK; W697term | Nedd4-PL; W691term | Nedd4-PM
W699term
G to A nucleotide change at the second or third position of the wild type Trp codon leads to a nonsense mutation. (exact site of mutation unspecified). The mutation was annotated at the second base of the codon. The P{GSV6}Nedd4GS13178 insertion is still present on the chromosome.
viable, with Scer\GAL4da.G32
Selected as: a revertant of the larval lethality caused by expression of Nedd4GS13178 under the control of Scer\GAL4da.G32.