Trisha Shetty (Editor)

Nyctalopin

Updated on
Edit
Like
Comment
Share on FacebookTweet on TwitterShare on LinkedInShare on Reddit
Species
  
Human

Entrez
  
60506

Human
  
Mouse

Ensembl
  
ENSG00000188937

Nyctalopin

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