XB-FEAT-12563712

summary from NCBI

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]

nomenclature changes

05.14.2018 Human symbol has changed for genepage ID: 12563712 From c2orf71 to pcare

Human symbol has changed for Entrez Gene: 388939. From C2orf71 to PCARE

Human name has changed for Entrez Gene: 388939. From chromosome 2 open reading frame 71 to photoreceptor cilium actin regulator