{"symbol":"CABP4","synonyms":["CSNB2B","CRSD"],"name":"calcium binding protein 4","description":"This gene encodes a member of the CABP family of calcium binding protein characterized by four EF-hand motifs. Mutations in this gene are associated with congenital stationary night blindness type 2B. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]","ncbiEntrezGeneId":57010,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/57010","proteins":[{"symbol":"CABP4_HUMAN","href":"/api/1.0/protein/CABP4_HUMAN"}],"hgncRootFamilies":[{"name":"EF-hand domain containing","href":"/api/1.0/gene_family/EF-hand+domain+containing"}]}