{"symbol":"SLC52A3","synonyms":["HRFT2","BVVLS1","C20ORF54","BVVLS","RFT2","RFVT3","BA371L19.1"],"name":"solute carrier family 52 (riboflavin transporter), member 3","description":"This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. [provided by RefSeq, Mar 2012]","ncbiEntrezGeneId":113278,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/113278","proteins":[{"symbol":"S52A3_HUMAN","href":"/api/1.0/protein/S52A3_HUMAN"}],"hgncRootFamilies":[{"name":"Solute carriers (SLC)","href":"/api/1.0/gene_family/Solute+carriers+%28SLC%29"}]}