Entrez 60506 | Ensembl ENSG00000188937 | |
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Aliases NYX, CLRP, CSNB1, CSNB1A, CSNB4, NBM1, nyctalopin External IDs MGI: 2448607 HomoloGene: 11210 GeneCards: NYX |
Nyctalopin is a protein that in humans is encoded by the NYX gene. It is a leucine-rich proteoglycan which is expressed in the eye, spleen and brain in mice. Mutations in this gene cause congenital stationary night blindness in humans. A mouse strain called nob (no b-wave) carries a spontaneous mutation leading to a frameshift in this gene. These mice are used as an animal model for congenital stationary night blindness.
References
Nyctalopin Wikipedia(Text) CC BY-SA