ABCD3

GENERAL INFORMATION

? »

Gene name

ABCD3

Gene description

ATP-binding cassette, sub-family D (ALD), member 3

Protein class

Predicted membrane proteins
Transporters

Predicted localization

Membrane

Number of transcripts

2
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

General cytoplasmic expression with a granular pattern.

ANTIBODY RELIABILITY

? »

Data reliability
description

Antibody staining consistent with RNA expression data.

Data reliability

Supportive based on 4 antibodies.
HPA032026 , HPA032027 , CAB032516 , CAB075749
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

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

? »

Gene name

ABCD3 (HGNC Symbol)

Synonyms

PMP70, PXMP1, ZWS2

Description

ATP-binding cassette, sub-family D (ALD), member 3 (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 ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein likely plays an important role in peroxisome biogenesis. Mutations have been associated with some forms of Zellweger syndrome, a heterogeneous group of peroxisome assembly disorders. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]

Chromosome

1

Cytoband

p21.3

Chromosome location (bp)

94418455 - 94518666

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000117528 (version 78.38)

Entrez gene

5825

UniProt

P28288 (UniProt - Evidence at protein level)

neXtProt

NX_P28288

Antibodypedia

ABCD3 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000315713
 
ENST00000370214
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ABCD3-001 ENSP00000359233
ENST00000370214
P28288
Show all »
Show » Show » 659 75.5 No 5
ABCD3-002 ENSP00000326880
ENST00000315713
P28288
Show all »
Show » Show » 236 27.1 No 3