{"symbol":"C2ORF71","synonyms":["PCARE","RP54","C2orf71"],"name":"chromosome 2 open reading frame 71","description":"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]","ncbiEntrezGeneId":388939,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/388939","proteins":[{"symbol":"CB071_HUMAN","href":"/api/1.0/protein/CB071_HUMAN"}],"hgncRootFamilies":[]}