Amino acid replacement: A592G.
Amino acid replacement: W741term.
G11363838A
W741term | hop-PA
W741term
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). The mutation was annotated at the second base of the codon. The A592G substitution, also observed in the mutant strain, appears to be a polymorphism, since a G residue is present at this site in the reference sequence.
Paternal rescue of the maternal effect. Germline clone analysis demonstrates that embryos have one abdominal segment missing and A4 appears wider than wild type, and partial or complete fusion of T1 and T2.
larval/pupal lethal
Lefevre.
Fail to complement hop25.