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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...[+]



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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
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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