OLIG2

GENERAL INFORMATION

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Gene name

OLIG2

Gene description

Oligodendrocyte lineage transcription factor 2

Protein class

Cancer-related genes
Disease related genes
Predicted intracellular proteins
Transcription factors

Predicted localization

Intracellular

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (cerebral cortex)
GTEx:Tissue enhanced (cerebral cortex, hippocampus)

Protein evidence

Evidence at protein level

Protein localization

Selective nuclear expression in subsets of glial cells.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining consistent with RNA expression data.

Data reliability

Supportive based on 2 antibodies.
HPA003254 , CAB019381
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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
Nasopharynx
N/A
N/A
Bronchus
N/A
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lateral ventricle

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 (cerebral cortex)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (cerebral cortex, hippocampus)

Organ

Expression



GENE INFORMATION

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Gene name

OLIG2 (HGNC Symbol)

Synonyms

BHLHB1, bHLHe19, OLIGO2, PRKCBP2, RACK17

Description

Oligodendrocyte lineage transcription factor 2 (HGNC Symbol)

Entrez gene summary

This gene encodes a basic helix-loop-helix transcription factor which is expressed in oligodendroglial tumors of the brain. The protein is an essential regulator of ventral neuroectodermal progenitor cell fate. The gene is involved in a chromosomal translocation t(14;21)(q11.2;q22) associated with T-cell acute lymphoblastic leukemia. Its chromosomal location is within a region of chromosome 21 which has been suggested to play a role in learning deficits associated with Down syndrome. [provided by RefSeq, Jul 2008]

Chromosome

21

Cytoband

q22.11

Chromosome location (bp)

33025845 - 33029196

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000205927 (version 78.38)

Entrez gene

10215

UniProt

Q13516 (UniProt - Evidence at protein level)

neXtProt

NX_Q13516

Antibodypedia

OLIG2 antibodies


PROTEIN BROWSER

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ENST00000333337
 
ENST00000382357
 
ENST00000430860
 
 
 
 


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)

OLIG2-001 ENSP00000371794
ENST00000382357
Q13516
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Show » Show » 323 32.4 No 0
OLIG2-002 ENSP00000331040
ENST00000333337
Q13516
Show all »
Show » Show » 323 32.4 No 0
OLIG2-003 ENSP00000391183
ENST00000430860
C9J444
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Show » 62 6.1 No 0