Harman Patil (Editor)

CRX (gene)

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

Entrez
  
1406

Human
  
Mouse

Ensembl
  
ENSG00000105392

CRX (gene)

Aliases
  
CRX, CORD2, CRD, LCA7, OTX3, cone-rod homeobox

External IDs
  
MGI: 1194883 HomoloGene: 467 GeneCards: CRX

Cone-rod homeobox protein is a protein that in humans is encoded by the CRX gene.

Function

The protein encoded by this gene is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined.

References

CRX (gene) Wikipedia