Amino acid replacement: W271term.
G1299655A
W271term | scf-PA; W134term | scf-PB
W271term
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). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Heterozygous adults do not show significant anterior transformations.
scf1/scf[+] is an enhancer of adult abdominal segment 6 | male phenotype of trxB11
scf1/scf[+] is an enhancer of adult abdominal segment 5 | ectopic | male phenotype of trxB11
scf1/scf[+] is an enhancer of adult abdominal segment 6 | male phenotype of Polr2BZ43
scf1/scf[+] is an enhancer of adult abdominal segment 5 | ectopic | male phenotype of Polr2BZ43
scf1/scf[+] is a suppressor of adult abdominal segment 4 | male phenotype of Pc3
scf1/scf[+] is a suppressor of adult abdominal segment 5 | ectopic | male phenotype of Pc3
scf1/scf[+] is a suppressor of abdominal tergite 4 | male phenotype of Pc3
The penetrance of the ectopic pigmentation phenotype seen in the A4 tergite of Pc3/+ males is reduced from 59.2% to 30.6% if they are also heterozygous for scf1.
scf1/+ significantly enhances the penetrance of the A6 to A5 transformation phenotype that is seen in trxB11/+ and in RpII140Z43/+ males.