SLC10A2

GENERAL INFORMATION

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Gene name

SLC10A2

Gene description

Solute carrier family 10 (sodium/bile acid cotransporter), member 2

Protein class

Disease related genes
Potential drug targets
Predicted membrane proteins
Transporters

Predicted localization

Membrane

Number of transcripts

1
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Group enriched (duodenum, kidney, small intestine)
GTEx:Tissue enriched (small intestine)

Protein evidence

Evidence at protein level

Protein localization

High membranous expression in small intestines.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly not consistent with RNA expression data. Presumed off target binding observed and disregarded.

Data reliability

Uncertain based on 1 antibody.
HPA004795
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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

Small intestine

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Group enriched (duodenum, kidney, small intestine)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (small intestine)

Organ

Expression



GENE INFORMATION

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Gene name

SLC10A2 (HGNC Symbol)

Synonyms

ASBT, ISBT

Description

Solute carrier family 10 (sodium/bile acid cotransporter), member 2 (HGNC Symbol)

Entrez gene summary

This gene encodes a sodium/bile acid cotransporter. This transporter is the primary mechanism for uptake of intestinal bile acids by apical cells in the distal ileum. Bile acids are the catabolic product of cholesterol metabolism, so this protein is also critical for cholesterol homeostasis. Mutations in this gene cause primary bile acid malabsorption (PBAM); muatations in this gene may also be associated with other diseases of the liver and intestines, such as familial hypertriglyceridemia (FHTG). [provided by RefSeq, Mar 2010]

Chromosome

13

Cytoband

q33.1

Chromosome location (bp)

103043998 - 103066846

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000125255 (version 78.38)

Entrez gene

6555

UniProt

Q12908 (UniProt - Evidence at protein level)

neXtProt

NX_Q12908

Antibodypedia

SLC10A2 antibodies


PROTEIN BROWSER

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ENST00000245312
 
 
 
 


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)

SLC10A2-001 ENSP00000245312
ENST00000245312
Q12908
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