Amino acid replacement: P392L.
C27251662T
P392L | pll-PA; P392L | pll-PB
P392L
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Shows brain tumours when heterozygous with the MBT chromosome.
Homozygotes and heterozygotes with Df(3R)R38.3 have a completely dorsalised phenotype and a stronger dorsalised phenotype when heterozygous with pll16. Heterozygotes produced some dorsalised phenotypes at 29oC when also heterozygous for Df(3R)XM3.
Strong pll allele.