Coordinates according to accession number AF395904. Mutation in the "roe" specific exon of rn.
Nucleotide substitution: C629T.
Amino acid replacement: Q191term.
C7276851T
C629T
Q190term | rn-PC
Q191term
rnroe-3 shows "roe" phenotypes.
Homozygotes exhibit a small rough eye phenotype.
Rough eye: irregular facets. Acts in dosage sensitive manner.
Rough eye phenotype.
Grigliatti.