SLC52A3

GENE INFORMATION

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Gene name

SLC52A3 (HGNC Symbol)

Synonyms

bA371L19.1, C20orf54, hRFT2, RFVT3

Description

solute carrier family 52 (riboflavin transporter), member 3 (HGNC Symbol)

Entrez gene summary

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]

Chromosome

20 (Chromosome progress)

Cytoband

p13

Chromosome location (bp)

740724 - 749131

Ensembl

ENSG00000101276 (version 73.37)

Entrez gene

113278

UniProt

Q9NQ40 (UniProt - Evidence at protein level)

neXtProt

NX_Q9NQ40

Antibodypedia

SLC52A3 antibodies
 

PROTEIN VIEW

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SLC52A3-001
 
SLC52A3-004
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

SLC52A3-001 ENSP00000217254
ENST00000217254
Q9NQ40
Show all »
Show » Show » 469 50.8 Yes >9
SLC52A3-004 ENSP00000371370
ENST00000381944
Q9NQ40
Show all »
Show » Show » 415 45 Yes 8