| Name |
|---|
C2ORF71 Genechromosome 2 open reading frame 71 The protein encoded by this gene is highly expressed in photoreceptors and may associate with the primary cilium of the outer segment. The encoded protein appears to undergo post-translational lipid modification. Nonsense and missense variants of this gene appear to cause a recessive form of retinitis pigmentosa. [provided by RefSeq, Jun 2010] |
c2orf71 Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term c2orf71 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Retinal protein C2orf71 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal protein C2orf71 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |