Amino acid replacement: S?L.
C12625171T
C?T
S377L | Vha55-PA; S377L | Vha55-PB; S377L | Vha55-PC
S?L
Reported as a missense mutation in the third coding exon of Vha55 in the Ser of the string LPSLS from TCG to TTG.
Mutants have less opaque Malpighian tubules than controls (when examined by birefringence).
Vha55[+]/Vha5512 is an enhancer of visible | heat sensitive phenotype of Ivir\M2UAS.cAa, Scer\GAL4GMR.PU
Vha55[+]/Vha5512 is an enhancer of eye | heat sensitive phenotype of Ivir\M2UAS.cAa, Scer\GAL4GMR.PU