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SLC52A3

Official Full Name
solute carrier family 52 member 3
Organism
Homo sapiens
GeneID
113278
Background
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]
Synonyms
RFT2; BVVLS; RFVT3; hRFT2; BVVLS1; C20orf54; bA371L19.1;

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