loss of function allele
Q931term | Ptp69D-PA; Q930term | Ptp69D-PB
Amino acid replacement: Q931term.
Mutation is predicted to result in a protein truncated shortly after the transmembrane domain (before the catalytic domain).
Nucleotide substitution: C?T.
lethal (with Df(3L)8ex34)
lethal (with Ptp69D1)
lethal (with Ptp69D4)
lethal (with Ptp69D8ex25)
photoreceptor cell & axon | somatic clone
Photoreceptor fates are correctly specified, but their axons project abnormally into the optic lobes in homozygous clones in the eye.