Amino acid replacement: W436term.
possibly insertion of unidentified mobile element.
G19893397A
W436term | Su(Tpl)-PA; W436term | Su(Tpl)-PB; W436term | Su(Tpl)-PC
W436term
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 hetero-allelic combination Su(Tpl)10/Su(Tpl)S-192 is embryonic lethal. Mutant cuticles display the following defects, with variable penetrance: Mutant cuticles display the following defects, with variable penetrance: abdominal segment 2 missing, incomplete or fused to abdominal segment 3; abdominal segment 4 incomplete or fused to abdominal segment 3 or 5; metathoracic segment missing, incomplete or fused to abdominal segment 1; incomplete head involution.
site-specific increase in recombination frequency and in premeiotic recombination in males.
Su(Tpl)[+]/Su(Tpl)10 is an enhancer of wing margin phenotype of Nnd-1
Su(Tpl)[+]/Su(Tpl)10 is an enhancer of wing margin phenotype of ct53d
Su(Tpl)10 is a suppressor of phenotype of Tplunspecified
Su(Tpl)10 entirely eliminates the abnormalities and death caused by Tpl trisomy (such as Dp(3;3)Tpl or Dp(3;3)TplJE19 flies), and results in viable, fertile adults.
Suppresses the triplo-lethal effect of Tpl.
Su(Tpl)XS-706/Su(Tpl)10 is partially rescued by Su(Tpl)Chi.Tag:polyHis,Tag:Xpress
Su(Tpl)s1/Su(Tpl)10 is partially rescued by Su(Tpl)Chi.Tag:polyHis,Tag:Xpress
This mutation was previously reported to be an allele of Tpl (FBrf0051978). However, the effect on Tpl has been found not to map to the Tpl locus itself at 83E, but instead maps to a separate locus called Su(Tpl) at 76B-76D.