External Ids for C2orf71 Gene
Previous GeneCards Identifiers for C2orf71 Gene
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]
GeneCards Summary for C2orf71 Gene
UniProtKB/Swiss-Prot for C2orf71 Gene
May play an important role in the development of normal vision.