SLC52A1

GENE INFORMATION

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Gene name

SLC52A1 (HGNC Symbol)

Synonyms

FLJ10060, GPCR42, GPR172B, hRFT1, PAR2, RFVT1

Description

Solute carrier family 52 (riboflavin transporter), member 1 (HGNC Symbol)

Entrez gene summary

Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents. This gene encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2013]

Chromosome

17

Cytoband

p13.2

Chromosome location (bp)

4935895 - 4955304

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000132517 (version 75.37)

Entrez gene

55065

UniProt

Q9NWF4 (UniProt - Evidence at protein level)

neXtProt

NX_Q9NWF4

Antibodypedia

SLC52A1 antibodies
 

PROTEIN VIEW

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SLC52A1-001
 
SLC52A1-002
 
SLC52A1-201
 
 
 
 
 

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)

SLC52A1-001 ENSP00000254853
ENST00000254853
Q9NWF4
Show all »
Show » Show » 448 46.3 Yes >9
SLC52A1-002 ENSP00000443026
ENST00000512825
F5H5Y1
Show all »
Show » 350 36.5 Yes 7
SLC52A1-201 ENSP00000399979
ENST00000424747
Q9NWF4
Show all »
Show » Show » 448 46.3 Yes >9