NYX, nyctalopin, 60506

N. diseases: 36; N. variants: 20
Disease: Night Blindness, Congenital Stationary, Type 1A ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62637024
rs62637024
Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C3495587
Disease:
Night Blindness, Congenital Stationary, Type 1A 		0.700 GeneticVariation UNIPROT Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. 11062471 2000
dbSNP: rs62637024
rs62637024
Entrez Id: 60506
Gene Symbol: NYX
NYX
CUI: C3495587
Disease:
Night Blindness, Congenital Stationary, Type 1A 		0.700 GeneticVariation UNIPROT The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein. 11062472 2000