ABCG5

GENERAL INFORMATION

? »

Gene name

ABCG5

Gene description

ATP-binding cassette, sub-family G (WHITE), member 5

Protein class

Disease related genes
Potential drug targets
Predicted membrane proteins
Transporters

Predicted localization

Membrane

Number of transcripts

2
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

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

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic and membranous expression in small intestine and liver.

ANTIBODY RELIABILITY

? »

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.
HPA016514
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

Lymph node

Liver

Duodenum

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

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

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (liver)

Organ

Expression



GENE INFORMATION

? »

Gene name

ABCG5 (HGNC Symbol)

Synonyms

STSL

Description

ATP-binding cassette, sub-family G (WHITE), member 5 (HGNC Symbol)

Entrez gene summary

The 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 White subfamily. The protein encoded by this gene functions as a half-transporter to limit intestinal absorption and promote biliary excretion of sterols. It is expressed in a tissue-specific manner in the liver, colon, and intestine. This gene is tandemly arrayed on chromosome 2, in a head-to-head orientation with family member ABCG8. Mutations in this gene may contribute to sterol accumulation and atheroschlerosis, and have been observed in patients with sitosterolemia. [provided by RefSeq, Jul 2008]

Chromosome

2

Cytoband

p21

Chromosome location (bp)

43812472 - 43838865

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000138075 (version 78.38)

Entrez gene

64240

UniProt

Q9H222 (UniProt - Evidence at protein level)

neXtProt

NX_Q9H222

Antibodypedia

ABCG5 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000260645
 
ENST00000405322
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ABCG5-001 ENSP00000260645
ENST00000260645
Q9H222
Show all »
Show » Show » 651 72.5 No 6
ABCG5-002 ENSP00000384513
ENST00000405322
E7EX35
Show all »
Show » Show » 480 53.4 No 6