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XB-GENEPAGE-5786439
???displayGene.symbol???:
 slc52a1

???displayGene.name???: 
solute carrier family 52 (riboflavin transporter), member 1

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( Nomenclature history )

???displayGene.geneFunction???
electron transport

AI Protein Function :
slc52a1 encodes a plasma‑membrane riboflavin transporter that mediates vitamin B2 uptake and belongs to the solute carrier family; the protein is localized to the plasma membrane. Expression is reporte...[+]



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Diseases: 


MIM:
RIBOFLAVIN DEFICIENCY; RBFVD

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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