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Immunogen sequence: MSRLPTYYL TTFFVGEGLS GLLPALVALA QGSGLTTCVN VTEISDSVPS PVPTRETDIA QGVPRALVSA LPGMEAPLSH LESRYLPAHF SPLVFFLLLS IMMACCLVAF FVLQRQPRCW EASVEDLLND QVTLHSIRLR EENDLGPAGM VDSSQGQGYL EEKAAPCCPA HLAFV (130-303 aa encoded by BC009750)
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].
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: ct054; hRFT2; RFT2; Riboflavin transporter 2; solute carrier family 52 (riboflavin transporter), member 3; Solute carrier family 52, riboflavin transporter, member 3
Gene Aliases: 2310046K01Rik; bA371L19.1; BVVLS; BVVLS1; C20orf54; hRFT2; RFT2; RFVT3; SLC52A3
UniProt ID: (Human) Q9NQ40, (Mouse) Q9D6X5
Entrez Gene ID: (Human) 113278, (Mouse) 69698
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