Entrez 1406 | Ensembl ENSG00000105392 | |
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Aliases CRX, CORD2, CRD, LCA7, OTX3, cone-rod homeobox External IDs MGI: 1194883 HomoloGene: 467 GeneCards: CRX |
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(Text) CC BY-SA