1. Gene
  2. OLIG3 - oligodendrocyte transcription factor 3 Gene

OLIG3 - oligodendrocyte transcription factor 3 Gene

Homo sapiens

Also known as Bhlhb7; bHLHe20

Gene ID: 167826 | Gene type: protein coding

About OLIG3

Cytogenetic location: 6q23.3 Genomic coordinates (GRCh38): 6:137,492,199-137,494,394 (from NCBI)

This gene has 1 transcript (splice variant), 196 orthologues and 15 paralogues.

Summary

Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in neuron differentiation and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II; spinal cord motor neuron cell fate specification; and spinal cord motor neuron migration. Predicted to be part of chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

OLIG3 Products(1)

mRNA Protein Name
NM_175747.2 NP_786923.1 oligodendrocyte transcription factor 3
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

OLIG3 Protein Structure

HLH

HLH: Helix-loop-helix DNA-binding domain (85 - 137)

  • 0
  • 100
  • 200
  • 272 a.a.
Protein Preferred Names Protein Names

oligodendrocyte transcription factor 3

class B basic helix-loop-helix protein 7

OLIG3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
OLIG3 Q7RTU3 KRTAP10-8 Homo sapiens P60410 32296183
Intra
OLIG3 Q7RTU3 KRTAP10-8 Homo sapiens P60410 32296183
Intra
OLIG3 Q7RTU3 CADPS Homo sapiens A2RRN7 32296183
Intra
OLIG3 Q7RTU3 CADPS Homo sapiens A2RRN7 32296183
Intra
OLIG3 Q7RTU3 KRTAP19-5 Homo sapiens Q3LI72 32296183
Intra
OLIG3 Q7RTU3 KRTAP19-5 Homo sapiens Q3LI72 32296183
Intra
OLIG3 Q7RTU3 KRTAP11-1 Homo sapiens Q8IUC1 32296183
Intra
OLIG3 Q7RTU3 KRTAP11-1 Homo sapiens Q8IUC1 32296183
Intra
OLIG3 Q7RTU3 KRTAP11-1 Homo sapiens Q8IUC1 32296183
Intra
OLIG3 Q7RTU3 DMWD Homo sapiens G5E9A7 32814053
Intra
OLIG3 Q7RTU3 DMWD Homo sapiens G5E9A7 32814053
Intra
OLIG3 Q7RTU3 DMWD Homo sapiens G5E9A7 32814053
Intra
OLIG3 Q7RTU3 TLE5 Homo sapiens Q08117-2 32296183
Intra
OLIG3 Q7RTU3 TLE5 Homo sapiens Q08117-2 32296183
Intra
OLIG3 Q7RTU3 ATN1 Homo sapiens Q86V38 32296183
Intra
OLIG3 Q7RTU3 ATN1 Homo sapiens Q86V38 32296183
Intra
OLIG3 Q7RTU3 ATN1 Homo sapiens Q86V38 32296183
Intra
OLIG3 Q7RTU3 KRTAP9-8 Homo sapiens Q9BYQ0 32296183
Intra
OLIG3 Q7RTU3 KRTAP9-8 Homo sapiens Q9BYQ0 32296183
Intra
OLIG3 Q7RTU3 KRTAP9-8 Homo sapiens Q9BYQ0 32296183
Intra
OLIG3 Q7RTU3 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
OLIG3 Q7RTU3 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
OLIG3 Q7RTU3 KRTAP6-2 Homo sapiens Q3LI66 32296183
Intra
OLIG3 Q7RTU3 KRTAP6-2 Homo sapiens Q3LI66 32296183
Intra
OLIG3 Q7RTU3 RUNX1 Homo sapiens Q01196-8 32296183
Intra
OLIG3 Q7RTU3 RUNX1 Homo sapiens Q01196-8 32296183
Intra
OLIG3 Q7RTU3 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
OLIG3 Q7RTU3 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
OLIG3 Q7RTU3 WWOX Homo sapiens Q9NZC7-5 32296183
Intra
OLIG3 Q7RTU3 KRTAP6-1 Homo sapiens Q3LI64 32296183
Intra
OLIG3 Q7RTU3 KRTAP6-1 Homo sapiens Q3LI64 32296183
Intra
OLIG3 Q7RTU3 KRTAP19-2 Homo sapiens Q3LHN2 32296183
Intra
OLIG3 Q7RTU3 KRTAP19-2 Homo sapiens Q3LHN2 32296183
Intra
OLIG3 Q7RTU3 KRTAP6-3 Homo sapiens Q3LI67 32296183
Intra
OLIG3 Q7RTU3 KRTAP6-3 Homo sapiens Q3LI67 32296183
Intra
OLIG3 Q7RTU3 PLAGL2 Homo sapiens Q9UPG8 32296183
Intra
OLIG3 Q7RTU3 PLAGL2 Homo sapiens Q9UPG8 32296183
Intra
OLIG3 Q7RTU3 PLAGL2 Homo sapiens Q9UPG8 32296183
Intra
OLIG3 Q7RTU3 BYSL Homo sapiens Q13895 25416956
Intra
OLIG3 Q7RTU3 BYSL Homo sapiens Q13895 25416956
Intra
OLIG3 Q7RTU3 TRAF1 Homo sapiens Q13077 32296183
Intra
OLIG3 Q7RTU3 TRAF1 Homo sapiens Q13077 25416956
Intra
OLIG3 Q7RTU3 TRAF1 Homo sapiens Q13077 25416956
Intra
OLIG3 Q7RTU3 TRAF1 Homo sapiens Q13077 32296183
Intra
OLIG3 Q7RTU3 TRAF1 Homo sapiens Q13077 25416956
Intra
OLIG3 Q7RTU3 CARD10 Homo sapiens Q9BWT7 32296183
Intra
OLIG3 Q7RTU3 CARD10 Homo sapiens Q9BWT7 32296183
Intra
OLIG3 Q7RTU3 CARD10 Homo sapiens Q9BWT7 32296183
Intra
OLIG3 Q7RTU3 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
OLIG3 Q7RTU3 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
OLIG3 Q7RTU3 KRTAP3-3 Homo sapiens Q9BYR6 32296183
Intra
OLIG3 Q7RTU3 KRTAP3-3 Homo sapiens Q9BYR6 32296183
Intra
OLIG3 Q7RTU3 KRTAP3-3 Homo sapiens Q9BYR6 32296183
Intra
OLIG3 Q7RTU3 SPRED1 Homo sapiens Q7Z699 32814053
Intra
OLIG3 Q7RTU3 SPRED1 Homo sapiens Q7Z699 32814053
Intra
OLIG3 Q7RTU3 SPRED1 Homo sapiens Q7Z699 32814053
Intra
OLIG3 Q7RTU3 AP1M1 Homo sapiens Q9BXS5 32296183
Intra
OLIG3 Q7RTU3 MDFI Homo sapiens Q99750 32296183
Intra
OLIG3 Q7RTU3 MDFI Homo sapiens Q99750 32296183
Intra
OLIG3 Q7RTU3 MDFI Homo sapiens Q99750 25416956
Intra
OLIG3 Q7RTU3 MDFI Homo sapiens Q99750 32296183
Intra
OLIG3 Q7RTU3 HMG20A Homo sapiens Q9NP66 32296183
Intra
OLIG3 Q7RTU3 HMG20A Homo sapiens Q9NP66 32296183
Intra
OLIG3 Q7RTU3 HMG20A Homo sapiens Q9NP66 32296183
Intra
OLIG3 Q7RTU3 KRTAP3-2 Homo sapiens Q9BYR7 32296183
Intra
OLIG3 Q7RTU3 KRTAP3-2 Homo sapiens Q9BYR7 32296183
Intra
OLIG3 Q7RTU3 KRTAP3-2 Homo sapiens Q9BYR7 32296183
Intra
OLIG3 Q7RTU3 PROP1 Homo sapiens O75360 32296183
Intra
OLIG3 Q7RTU3 PROP1 Homo sapiens O75360 32296183
Intra
OLIG3 Q7RTU3 ARID5A Homo sapiens Q03989 32296183
Intra
OLIG3 Q7RTU3 ARID5A Homo sapiens Q03989 32296183
Intra
OLIG3 Q7RTU3 KRT86 Homo sapiens O43790 32296183
Intra
OLIG3 Q7RTU3 KRT86 Homo sapiens O43790 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Congenital Central Hypoventilation Syndrome

Cchs

Haddad Syndrome

Ondine Curse

Ondine Syndrome

Congenital Central Hypoventilation

Congenital Central Alveolar Hypoventilation Syndrome

Congenital Failure Of Autonomic Control

Ondine'S Curse

Primary Alveolar Hypoventilation

Ondine-Hirschsprung Disease

Central Congenital Hypoventilation Syndrome

Congenital Ondine Curse

Idiopathic Congenital Central Alveolar Hypoventilation

Congenital Central Alveolar Hypoventilation-Hirschsprung Disease Syndrome

Ondine-Hirschsprung Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus OLIG3 MGD MGI:2149955
Bos taurus OLIG3 VGNC VGNC:32426
Macaca mulatta OLIG3 VGNC VGNC:83439
Rattus norvegicus OLIG3 RGD RGD:1305997
Canis familiaris OLIG3 VGNC VGNC:44119
Felis catus OLIG3 VGNC VGNC:63966