Amino acid replacement: F290I. Mutation in the CR1 domain.
T2341753A
F247I | Raf-PA; F247I | Raf-PE
F290I
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Homozygotes are viable and morphologically normal. Embryos derived from phlSu3, Ras85DΔC40B double mutant germ cells die during embryogenesis with cuticles indistinguishable from those of Ras85DΔC40B mutants. Animals doubly mutant for phlSu3 and torrv66 are completely non-viable and resemble torrv66 mutants.
RafSu3, torrv66 has filzkorper phenotype
RafSu3, torrv66 has embryonic abdominal segment 8 phenotype
Relative suppressor ability: phlSu3 > phlSu8 > phlSu5 > phlSu2.