XB-GENEPAGE-6032790
???displayGene.symbol???:
slc52a3
???displayGene.name???:
solute carrier family 52 (riboflavin transporter), member 3
???displayGene.synonyms???
(
Nomenclature history )
???displayGene.geneFunction???
Uncharacterized conserved protein
AI Protein Function
:
slc52a3 encodes a plasma‑membrane solute carrier transporter that mediates riboflavin (vitamin B2) uptake; the protein is classified as a membrane‑bound transporter and is localized to the cell surface...[+]
InterPro
:
???displayGene.geneInteractants???
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Diseases:
Disease Ontology:
Brown-Vialetto-Van Laere syndrome
MIM:
BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1
External Links:
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| ???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
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