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10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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OLIG3
oligodendrocyte transcription factor 3
Chromosome 6 · 6q23.3
NCBI Gene: 167826Ensembl: ENSG00000177468.7HGNC: HGNC:18003UniProt: Q7RTU3
28PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transcription Factor
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
sequence-specific double-stranded DNA bindingprotein bindingDNA-binding transcription factor activity, RNA polymerase II-specificE-box bindingneurodegenerative diseaserheumatoid arthritisulcerative colitistesticular hydrocele
✦AI Summary

OLIG3 (oligodendrocyte transcription factor 3) is a basic helix-loop-helix transcription factor that functions in neural cell specification and CNS development 1. In the spinal cord, OLIG3 participates in determining distinct specification programs for neuronal classes and regulating glial and neuronal cell differentiation during development and neural regeneration 2. OLIG3 expression is regulated by multiple signaling pathways including nodal, FGF, retinoic acid, BMP, and hedgehog signals along the dorsoventral axis of the embryonic CNS 1. During human thalamic development, OLIG3 marks the extent and boundaries of the thalamic proliferative zone, serving as a structural marker in the emerging thalamic protomap 3. Disease relevance: OLIG3 variants have been associated with multiple pathological conditions. A missense variant (p.Arg210Gly) in OLIG3 co-segregated with osteoarthritis in a Finnish family and was predicted pathogenic, suggesting a role in cartilage and bone physiology 4. OLIG3 at the 6q23 locus is a confirmed rheumatoid arthritis susceptibility gene 5, with the OLIG3/TNFAIP3 locus showing significant association with RA particularly in autoantibody-positive patients 6. GWAS studies identified OLIG3 association with tau neuropathology in progressive supranuclear palsy 7. These findings underscore OLIG3's broader role in immune-inflammatory and neurodegenerative disease susceptibility.

Sources cited
1
OLIG3 is a bHLH transcription factor involved in neural cell type specification, regulated by nodal, FGF, RA, BMP, and hedgehog signaling
PMID: 19425111
2
OLIG3 regulates glial and neuronal cell differentiation in developing spinal cord and injured neural tissue
PMID: 34228233
3
OLIG3 marks the extent of thalamic ventricular zone and boundaries in human fetal thalamic development
PMID: 39990522
4
OLIG3 missense variant (p.Arg210Gly) co-segregated with osteoarthritis and was predicted pathogenic
PMID: 30157244
5
OLIG3 at 6q23 locus is associated with rheumatoid arthritis susceptibility
PMID: 17982455
6
OLIG3/TNFAIP3 locus associated with RA susceptibility, particularly in autoantibody-positive patients
PMID: 20353580
7
OLIG3 associated with tau neuropathology in progressive supranuclear palsy GWAS
PMID: 33635380
Disease Associationsⓘ20
neurodegenerative diseaseOpen Targets
0.46Moderate
rheumatoid arthritisOpen Targets
0.38Weak
ulcerative colitisOpen Targets
0.29Weak
testicular hydroceleOpen Targets
0.27Weak
inflammatory bowel diseaseOpen Targets
0.27Weak
Crohn's diseaseOpen Targets
0.27Weak
COVID-19Open Targets
0.26Weak
thyroid diseaseOpen Targets
0.26Weak
celiac diseaseOpen Targets
0.25Weak
asthmaOpen Targets
0.22Weak
autoimmune diseaseOpen Targets
0.22Weak
obesityOpen Targets
0.20Weak
enteritisOpen Targets
0.19Weak
colitisOpen Targets
0.19Weak
Oral ulcerOpen Targets
0.19Weak
multiple sclerosisOpen Targets
0.19Weak
ACPA-positive rheumatoid arthritisOpen Targets
0.19Weak
septic shockOpen Targets
0.18Weak
Tietze syndromeOpen Targets
0.17Weak
Abnormality of the integumentOpen Targets
0.16Weak
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
BHLHE22Shared pathway100%BHLHE23Shared pathway100%TNFAIP3Protein interaction80%NEUROD6Shared pathway67%NEUROG2Shared pathway67%OLIG1Shared pathway67%
Tissue Expression6 tissues
Liver
0%
Lung
0%
Brain
0%
Heart
0%
Bone Marrow
0%
Ovary
0%
Gene Interaction Network
Click a node to explore
OLIG3BHLHE22BHLHE23TNFAIP3NEUROD6NEUROG2OLIG1
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q7RTU3
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.40LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.86 [0.55–1.40]
RankingsWhere OLIG3 stands among ~20K protein-coding genes
  • #12,404of 20,598
    Most Researched28
  • #14,486of 17,882
    Most Constrained (LOEUF)1.40
Genes detectedOLIG3
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Studying associations between variants in TRAF1-C5 and TNFAIP3-OLIG3 and the progression of joint destruction in rheumatoid arthritis in multiple cohorts.
PMID: 22586175
Ann Rheum Dis · 2012
1.00
2
Development of the early fetal human thalamus: from a protomap to emergent thalamic nuclei.
PMID: 39990522
Front Neuroanat · 2025
0.90
3
Whole exome sequencing in Finnish families identifies new candidate genes for osteoarthritis.
PMID: 30157244
PLoS One · 2018
0.80
4
The Effects of the Olig Family on the Regulation of Spinal Cord Development and Regeneration.
PMID: 34228233
Neurochem Res · 2021
0.70
5
Evaluation of the rheumatoid arthritis susceptibility loci HLA-DRB1, PTPN22, OLIG3/TNFAIP3, STAT4 and TRAF1/C5 in an inception cohort.
PMID: 20353580
Arthritis Res Ther · 2010
0.60