SLC22A12

GENERAL INFORMATION

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Gene name

SLC22A12

Gene description

Solute carrier family 22 (organic anion/urate transporter), member 12

Protein class

Disease related genes
Potential drug targets
Predicted membrane proteins
Transporters

Predicted localization

Membrane

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (kidney)
GTEx:Tissue enriched (kidney)

Protein evidence

Evidence at protein level

Protein localization

Distinct membranous expression in renal proximal tubules.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data. Presumed off target binding observed and disregarded.

Data reliability

Supportive based on 1 antibody.
HPA024575
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RNA AND PROTEIN EXPRESSION SUMMARY

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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

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enriched (kidney)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (kidney)

Organ

Expression



GENE INFORMATION

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Gene name

SLC22A12 (HGNC Symbol)

Synonyms

OAT4L, RST, URAT1

Description

Solute carrier family 22 (organic anion/urate transporter), member 12 (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is a member of the organic anion transporter (OAT) family, and it acts as a urate transporter to regulate urate levels in blood. This protein is an integral membrane protein primarily found in epithelial cells of the proximal tubule of the kidney. An elevated level of serum urate, hyperuricemia, is associated with increased incidences of gout, and mutations in this gene cause renal hypouricemia type 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]

Chromosome

11

Cytoband

q13.1

Chromosome location (bp)

64590641 - 64602353

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000197891 (version 78.38)

Entrez gene

116085

UniProt

Q96S37 (UniProt - Evidence at protein level)

neXtProt

NX_Q96S37

Antibodypedia

SLC22A12 antibodies


PROTEIN BROWSER

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ENST00000336464
 
ENST00000377567
 
ENST00000377572
 
ENST00000377574
 
ENST00000473690
 
 
 
 


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)

SLC22A12-001 ENSP00000366797
ENST00000377574
Q96S37
Show all »
Show » Show » 553 59.6 No >9
SLC22A12-002 ENSP00000366790
ENST00000377567
Q96S37
Show all »
Show » Show » 445 47.6 No 8
SLC22A12-004 ENSP00000438437
ENST00000473690
Q96S37
Show all »
Show » Show » 332 35.6 No 8
SLC22A12-005 ENSP00000336836
ENST00000336464
Q96S37
Show all »
Show » Show » 519 56.1 No >9
SLC22A12-201 ENSP00000366795
ENST00000377572
Q96S37
Show all »
Show » Show » 445 47.6 No 8