CRX, cone-rod homeobox, 1406

N. diseases: 128; N. variants: 28
Disease: Rod-Cone Dystrophy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894673
rs104894673
Entrez Id: 1406
Gene Symbol: CRX
CRX
CUI: C4551714
Disease:
Rod-Cone Dystrophy 		0.010 GeneticVariation BEFREE R90W mice carry a substitution mutation in the CRX homeodomain, Arg90Trp, which is associated with dominant mild late-onset CoRD and recessive LCA. 24516401 2014