Seroatlas · Human Serome Atlas

OLIG2

Oligodendrocyte transcription factor 2

Also known as: BHLHB1, bHLHe19, OLIG2_HUMAN, OLIGO2, PRKCBP2, RACK17

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q13516
Gene
OLIG2
Ensembl
ENSG00000205927
Chromosome
21
Canonical length
323 aa
Protein class
Cancer-related genes, Disease related genes, Predicted intracellular proteins, Transcription factors
Subcellular location
Nucleoplasm,Plasma membrane

OverviewNCBI Gene

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]

Canonical amino-acid sequenceUniProt

323 residues, UniProt reviewed canonical sequence.

>Q13516|OLIG2
     1  MDSDASLVSS RPSSPEPDDL FLPARSKGSS GSAFTGGTVS SSTPSDCPPE LSAELRGAMG
    61  SAGAHPGDKL GGSGFKSSSS STSSSTSSAA ASSTKKDKKQ MTEPELQQLR LKINSRERKR
   121  MHDLNIAMDG LREVMPYAHG PSVRKLSKIA TLLLARNYIL MLTNSLEEMK RLVSEIYGGH
   181  HAGFHPSACG GLAHSAPLPA ATAHPAAAAH AAHHPAVHHP ILPPAAAAAA AAAAAAAVSS
   241  ASLPGSGLPS VGSIRPPHGL LKSPSAAAAA PLGGGGGGSG ASGGFQHWGG MPCPCSMCQV
   301  PPPHHHVSAM GAGSLPRLTS DAK

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against OLIG2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.

Antibody reachability
Intracellular
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.65
Highest tissue expression
58 nTPM

Expression across tissuesHPA

Tissue

  • hippocampal formation: 58 nTPM
  • amygdala: 57 nTPM
  • cerebral cortex: 51 nTPM
  • midbrain: 50 nTPM
  • basal ganglia: 44 nTPM
  • spinal cord: 41 nTPM

Single-cell type

  • oligodendrocyte progenitor cells: 248 nCPM
  • oligodendrocytes: 70 nCPM
  • astrocytes: 5.7 nCPM
  • neutrophils: 2.1 nCPM
  • microglia: 1.8 nCPM
  • ependymal cells: 1.2 nCPM

Immune cell

  • eosinophil: 19 nTPM
  • basophil: 2.9 nTPM
  • classical monocyte: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM
  • MAIT T-cell: 0 nTPM

Brain region

  • white matter: 144 nTPM
  • medulla oblongata: 82 nTPM
  • basal ganglia: 81 nTPM
  • cerebral cortex: 76 nTPM
  • midbrain: 75 nTPM
  • cerebellum: 71 nTPM

Genetic constraint and essentialitygnomAD · DepMap

Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.

gnomAD LOEUF (loss-of-function intolerance)
1.31
gnomAD pLI
0.09
gnomAD missense Z
1.66
DepMap mean gene effect
-0.02
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of OLIG2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads OLIG2 as an antibody target. Whether an autoantibody or antibody against OLIG2 could matter depends on whether native OLIG2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

OLIG2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.

Annotation status

The present source text does not explicitly label OLIG2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/OLIG2. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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