{"symbol":"SLC6A8","synonyms":["CCDS1","CRTR","CTR5"],"name":"solute carrier family 6 (neurotransmitter transporter), member 8","description":"The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]","ncbiEntrezGeneId":6535,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/6535","proteins":[{"symbol":"SC6A8_HUMAN","href":"/api/1.0/protein/SC6A8_HUMAN"}],"hgncRootFamilies":[{"name":"Solute carriers (SLC)","href":"/api/1.0/gene_family/Solute+carriers+%28SLC%29"}]}