ABCB11

GENERAL INFORMATION

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Gene name

ABCB11

Gene description

ATP-binding cassette, sub-family B (MDR/TAP), member 11

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:Tissue enriched (liver)
GTEx:Tissue enhanced (liver, testis)

Protein evidence

Evidence at protein level

Protein localization

Distinct expression in liver bile canaliculi.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining consistent with RNA expression data.

Data reliability

Supportive based on 1 antibody.
HPA019035
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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 (liver)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (liver, testis)

Organ

Expression



GENE INFORMATION

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Gene name

ABCB11 (HGNC Symbol)

Synonyms

ABC16, BSEP, PFIC-2, PFIC2, PGY4, SPGP

Description

ATP-binding cassette, sub-family B (MDR/TAP), member 11 (HGNC Symbol)

Entrez gene summary

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is the major canalicular bile salt export pump in man. Mutations in this gene cause a form of progressive familial intrahepatic cholestases which are a group of inherited disorders with severe cholestatic liver disease from early infancy. [provided by RefSeq, Jul 2008]

Chromosome

2

Cytoband

q31.1

Chromosome location (bp)

168922938 - 169031322

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000073734 (version 78.38)

Entrez gene

8647

UniProt

O95342 (UniProt - Evidence at protein level)

neXtProt

NX_O95342

Antibodypedia

ABCB11 antibodies


PROTEIN BROWSER

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ENST00000263817
 
 
 
 


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)

ABCB11-001 ENSP00000263817
ENST00000263817
O95342
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