Amino acid replacement: Q789term.
Possible insertion of an unidentified mobile element.
C19892339T
Q789term | Su(Tpl)-PA; Q789term | Su(Tpl)-PB; Q789term | Su(Tpl)-PC
Q789term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
The hetero-allelic combination Su(Tpl)17/Su(Tpl)S-192 is embryonic lethal. Mutant cuticles display the following defects, with variable penetrance: abdominal segment 4 missing or fused to abdominal segment 3 or 5; abdominal segment 6 incomplete or fused to abdominal segment 5; incomplete head involution.
Site-specific increase in recombination frequency and premeiotic recombination in males.
Su(Tpl)[+]/Su(Tpl)17 is an enhancer of wing margin phenotype of Bx1
Su(Tpl)[+]/Su(Tpl)17 is an enhancer of wing margin phenotype of Nnd-1
Su(Tpl)[+]/Su(Tpl)17 is an enhancer of wing margin phenotype of ct53d
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.