{"symbol":"ZNF513","synonyms":["HMFT0656"],"name":"zinc finger protein 513","description":"The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]","ncbiEntrezGeneId":130557,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/130557","proteins":[{"symbol":"ZN513_HUMAN","href":"/api/1.0/protein/ZN513_HUMAN"}],"hgncRootFamilies":[{"name":"Zinc fingers","href":"/api/1.0/gene_family/Zinc+fingers"}]}