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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].
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: ct054; hRFT2; RFT2; Riboflavin transporter 2; solute carrier family 52 (riboflavin transporter), member 3; Solute carrier family 52, riboflavin transporter, member 3
基因别名: 2310046K01Rik; bA371L19.1; BVVLS; BVVLS1; C20orf54; hRFT2; RFT2; RFVT3; SLC52A3
UniProt ID: (Human) Q9NQ40, (Mouse) Q9D6X5
Entrez Gene ID: (Human) 113278, (Mouse) 69698