Single base pair deletion within codon Q648, resulting in a frameshift. The resulting truncated protein is predicated to contain 648 amino acids from wild-type p followed by 39 additional amino acids. Also contains a silent base change in the P62 codon and a nucleotide change in the p upstream region (POU sequence CAAAT is changed to CCAAT).
The deletion of a single base (A) in codon Q648 causes a frameshift and early translation termination 39 aa downstream.
Eye colour: abnormal with reduced levels of red and brown pigment (25 and 20% of wild-type levels respectively).
Malpighian tubule colour: somewhat lighter than normal.
Eye colour: dull ruby with purplish tone. 40% normal red and 33% normal brown pigment.
psnb has visible phenotype, enhanceable by Rab32ltd-1
psnb has abnormal eye color phenotype, enhanceable by Rab32ltd-1
psnb has pigment cell phenotype, enhanceable by Rab32ltd-1
Dobzhansky.
Polytene chromosomes show no evidence of a deletion.
The p1, pp and psnb alleles have been found to have identical changes in sequence, despite being reported to have arisen independently. It seems more likely that stock contamination, mislabelling, or loss occurred some time during past handling of stocks, rather than the same lesions having occurred independently three times.