9bp deletion, deleting amino acids 1065-1067.
Reported as a 9bp deletion that removes amino acid residues 1065-1067. Position of mutation on reference sequence inferred by FlyBase curator.
Homozygotes do not form pupae at either 18 or 25oC. Ptp69D7 embryos show motor axon defects; 57% of ISNb axons, 27% of ISN axons, 24% of SNa axons and 26% of SNc axons show defects. 25% of ISNb axons show a complete bypass phenotype and 15% show a partial bypass phenotype.
Ptp69D7 has abnormal neuroanatomy phenotype, suppressible by Ptp99A[+]/Ptp99A1
Ptp69D[+]/Ptp69D7 is a non-enhancer of abnormal neuroanatomy | embryonic stage phenotype of cknK.Δ324-331
Ptp69D[+]/Ptp69D7 is a non-suppressor of abnormal neuroanatomy | embryonic stage phenotype of cknK.Δ324-331
Ptp69D7 has larval intersegmental nerve phenotype, suppressible by Ptp99A[+]/Ptp99A1
Ptp69D[+]/Ptp69D7 is a non-enhancer of larval intersegmental nerve | embryonic stage phenotype of cknK.Δ324-331
Ptp69D[+]/Ptp69D7 is a non-enhancer of larval intersegmental nerve branch ISNb of A1-7 | embryonic stage phenotype of cknK.Δ324-331
Ptp69D[+]/Ptp69D7 is a non-suppressor of larval intersegmental nerve | embryonic stage phenotype of cknK.Δ324-331
Ptp69D[+]/Ptp69D7 is a non-suppressor of larval intersegmental nerve branch ISNb of A1-7 | embryonic stage phenotype of cknK.Δ324-331
A heterozygous or homozygous Ptp69D7 background fails to affect the penetrance of the ISNb bypass phenotype found in cknK.Δ324-331 heterozygotes or homozygotes.