PEX26

GENERAL INFORMATION

? »

Gene name

PEX26

Gene description

Peroxisomal biogenesis factor 26

Protein class

Disease related genes
Potential drug targets
Predicted intracellular proteins
Predicted membrane proteins
Transporters

Predicted localization

Intracellular,Membrane

Number of transcripts

5
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.

ANTIBODY RELIABILITY

? »

Data reliability
description

Antibody staining mainly consistent with RNA expression data.

Data reliability

Uncertain based on 1 antibody.
CAB070429
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

PEX26 (HGNC Symbol)

Synonyms

FLJ20695

Description

Peroxisomal biogenesis factor 26 (HGNC Symbol)

Entrez gene summary

This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Dec 2010]

Chromosome

22

Cytoband

q11.21

Chromosome location (bp)

18077920 - 18131138

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000215193 (version 78.38)

Entrez gene

55670

UniProt

Q7Z412 (UniProt - Evidence at protein level)

neXtProt

NX_Q7Z412

Antibodypedia

PEX26 antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000329627
 
ENST00000399744
 
ENST00000428061
 
ENST00000610387
 
ENST00000618979
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

PEX26-001 ENSP00000331106
ENST00000329627
Q7Z412
Show all »
Show » Show » 305 33.9 No 1
PEX26-002 ENSP00000382648
ENST00000399744
Q7Z412
Show all »
Show » Show » 305 33.9 No 1
PEX26-003 ENSP00000412441
ENST00000428061
Q7Z412
Show all »
Show » Show » 256 28.4 No 0
PEX26-201 ENSP00000482091
ENST00000610387
Q7Z412
Show all »
Show » Show » 256 28.4 No 0
PEX26-202 ENSP00000483492
ENST00000618979
Show » Show » 365 39.9 No 1