SLC52A1

GENERAL INFORMATION

? »

Gene name

SLC52A1

Gene description

Solute carrier family 52 (riboflavin transporter), member 1

Protein class

Disease related genes
Potential drug targets
Predicted membrane proteins
Transporters

Predicted localization

Membrane

Number of transcripts

3
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Group enriched (duodenum, placenta, skin, small intestine)
GTEx:Tissue enhanced (skin, small intestine)

Protein evidence

Evidence at protein level

Protein localization

General cytoplasmic expression, most abundant in intestine.

ANTIBODY RELIABILITY

? »

Data reliability
description

Antibody staining not consistent with RNA expression data. Pending retesting.

Data reliability

Uncertain based on 1 antibody.
CAB011449
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Appendix

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Group enriched (duodenum, placenta, skin, small intestine)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (skin, small intestine)

Organ

Expression



GENE INFORMATION

? »

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)

5032600 - 5052009

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000132517 (version 78.38)

Entrez gene

55065

UniProt

Q9NWF4 (UniProt - Evidence at protein level)

neXtProt

NX_Q9NWF4

Antibodypedia

SLC52A1 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000254853
 
ENST00000424747
 
ENST00000512825
 
 
 
 


PROTEIN INFORMATION

? »

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