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Nat Genet. 1992 Jul;1(4):251-6.

Defective colour vision associated with a missense mutation in the human green visual pigment gene.

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1
Department of Medicine, University of Washington, Seattle 98195.

Abstract

All red/green colour vision defects described so far have been associated with gross rearrangements within the red/green opsin gene array (Xq28). We now describe a male with severe deuteranomaly without such a rearrangement. A substitution of a highly conserved cysteine by arginine at position 203 in the green opsins presumably accounted for his colour vision defect. Surprisingly, this mutation was fairly common (2%) in the population but apparently was not always expressed. In analogy with nonexpression of some 5'green-red hybrid genes in persons with normal colour vision, we suggest that failure of manifestation occurs when the mutant gene is located at a distal (3') position among several green opsin genes. This mutation might also predispose to certain X-linked retinal dystrophies.

PMID:
1302020
DOI:
10.1038/ng0792-251
[Indexed for MEDLINE]

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