C3196462T
C1964T
S655F | Hsp83-PA; S655F | Hsp83-PB
S655F
Amino acid replacement: S655F. Nucleotide substitution: C1964T.
Nucleotide substitution: C1964T. Amino acid replacement: S655F.
Viable in transheterozygous combination with Hsp839J1; males are sterile and females are weakly fertile. Hsp839J1/Hsp83e4A males show some defects during spermatogenesis. The number and shape of spermatocytes within 16-cell cysts are mostly normal (5-10% are abnormal). The nuclei and nebenkern within spermatids are mostly normal (5-10% are abnormal). Individualised sperm are present, but are not motile. Hsp8308445/Hsp83e4A males show defects during spermatogenesis. Excessive numbers of primary spermatocytes are seen in many developing cysts. Spermatids with variable number, size and shape of nuclei and nebenkern are seen. Individualised sperm are present but they are not motile and are fragile.
Mutation fails to genetically interact with sevS11.T:Hsap\MYC, 'sev351', phl12 or phl::tor12D.hs.sev.