Nucleotide substitution: G?A. Mutation is in the 3' splice site of intron 5, which is predicted to cause readthrough into intron 5, adding 28 nonspecific amino acids after E362 before a stop codon in exon 6.
G20351582A
G?A
G to A point mutation in the 3' splice site of the intron causes readthrough of the intron and early translation termination in the subsequent exon.
May be an antimorph.
eRF1U3/eRF1[+] is an enhancer of visible phenotype of Hsap\MAPTGMR.Ex.PJ
eRF1U3/eRF1[+] is an enhancer of eye phenotype of Hsap\MAPTGMR.Ex.PJ
One copy of eRF1U3 enhances the rough eye phenotype seen in flies expressing Hsap\MAPTGMR.Ex.PJ. Necrotic plaques are also seen.