Browse OLIG2

Summary
SymbolOLIG2
Nameoligodendrocyte lineage transcription factor 2
Aliases RACK17; OLIGO2; bHLHe19; oligodendrocyte-specific bHLH transcription factor 2; protein kinase C binding prot ......
Chromosomal Location21q22.11
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Basic function annotation.
> Subcellular Location, Domain and Function
> Gene Ontology
> KEGG and Reactome Pathway
> Subcellular Location, Domain and Function
 
Subcellular Location Nucleus Cytoplasm Note=The NLS contained in the bHLH domain could be masked in the native form and translocation to the nucleus could be mediated by interaction either with class E bHLH partner protein or with NKX2-2.
Domain PF00010 Helix-loop-helix DNA-binding domain
Function

Required for oligodendrocyte and motor neuron specification in the spinal cord, as well as for the development of somatic motor neurons in the hindbrain. Cooperates with OLIG1 to establish the pMN domain of the embryonic neural tube. Antagonist of V2 interneuron and of NKX2-2-induced V3 interneuron development (By similarity).

> Gene Ontology
 
Biological Process GO:0001708 cell fate specification
GO:0007272 ensheathment of neurons
GO:0008366 axon ensheathment
GO:0010001 glial cell differentiation
GO:0010720 positive regulation of cell development
GO:0010721 negative regulation of cell development
GO:0014013 regulation of gliogenesis
GO:0014015 positive regulation of gliogenesis
GO:0021510 spinal cord development
GO:0021515 cell differentiation in spinal cord
GO:0021517 ventral spinal cord development
GO:0021522 spinal cord motor neuron differentiation
GO:0021529 spinal cord oligodendrocyte cell differentiation
GO:0021530 spinal cord oligodendrocyte cell fate specification
GO:0021536 diencephalon development
GO:0021778 oligodendrocyte cell fate specification
GO:0021779 oligodendrocyte cell fate commitment
GO:0021780 glial cell fate specification
GO:0021781 glial cell fate commitment
GO:0021794 thalamus development
GO:0021953 central nervous system neuron differentiation
GO:0030900 forebrain development
GO:0042063 gliogenesis
GO:0042552 myelination
GO:0045165 cell fate commitment
GO:0045665 negative regulation of neuron differentiation
GO:0045685 regulation of glial cell differentiation
GO:0045687 positive regulation of glial cell differentiation
GO:0048663 neuron fate commitment
GO:0048709 oligodendrocyte differentiation
GO:0048713 regulation of oligodendrocyte differentiation
GO:0048714 positive regulation of oligodendrocyte differentiation
GO:0050768 negative regulation of neurogenesis
GO:0050769 positive regulation of neurogenesis
GO:0051961 negative regulation of nervous system development
GO:0051962 positive regulation of nervous system development
Molecular Function GO:0003705 transcription factor activity, RNA polymerase II distal enhancer sequence-specific binding
GO:0071837 HMG box domain binding
Cellular Component -
> KEGG and Reactome Pathway
 
KEGG -
Reactome -
Summary
SymbolOLIG2
Nameoligodendrocyte lineage transcription factor 2
Aliases RACK17; OLIGO2; bHLHe19; oligodendrocyte-specific bHLH transcription factor 2; protein kinase C binding prot ......
Chromosomal Location21q22.11
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between OLIG2 and anti-tumor immunity. The specific mechanism were also collected if the literature reports that a gene specifically promotes or inhibits the infiltration or function of T/NK cells.
> Text Mining
 

There is no record.

Summary
SymbolOLIG2
Nameoligodendrocyte lineage transcription factor 2
Aliases RACK17; OLIGO2; bHLHe19; oligodendrocyte-specific bHLH transcription factor 2; protein kinase C binding prot ......
Chromosomal Location21q22.11
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content High-throughput screening data (e.g. CRISPR-Cas9, shRNA and RNAi) for T cell-mediated killing. Genetic screen techniques can identify mechanisms of tumor cell resistance (e.g., PTPN2) and sensitivity (e.g., APLNR) to killing by cytotoxic T cells, the central effectors of anti-tumor immunity. After comprehensively searching, eight groups of screening data sets were collected in the current database. In this tab, users can check whether their selected genes cause resistance or increase sensitivity to T cell-mediated killing in various data sets.
> High-throughput Screening
  Statistical results of OLIG2 in screening data sets for detecting immune reponses.
PMID Screening System Cancer Type Cell Line Data Set Statistical Results Relation to immunity
29301958CRISPR-Cas9 melanomaB16F10Pmel-1 T cell NA/NSNA/NS
29301958CRISPR-Cas9 melanomaB16F10OT-1 T cell NA/NSNA/NS
28783722CRISPR-Cas9 melanomaMel6242CT-CRISPR NA/NSNA/NS
28723893CRISPR-Cas9 melanomaB16GVAX+Anti-PD1 NA/NSNA/NS
28723893CRISPR-Cas9 melanomaB16GVAX NA/NSNA/NS
25691366RNAiBreast cancerMCF7Luc-CTL assay NA/NSNA/NS
24476824shRNAmelanomaB16Primary screen NA/NSNA/NS
24476824shRNAmelanomaB16Secondary screen NA/NSNA/NS
Summary
SymbolOLIG2
Nameoligodendrocyte lineage transcription factor 2
Aliases RACK17; OLIGO2; bHLHe19; oligodendrocyte-specific bHLH transcription factor 2; protein kinase C binding prot ......
Chromosomal Location21q22.11
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Transcriptomic and genomic profiling of pre-treated tumor biopsies from responders and non-responders to immunotherapy. These data were used to identify signatures and mechanisms of response to checkpoint blockade (e.g., anti-PDL1 and anti-PD1). One example is that mutations in the gene PBRM1 benefit clinical survival of patients with clear cell renal cell carcinoma. After comprehensively searching, we collected 5 and 6 of transcriptomic and genomic data sets, respectively. In this tab, users can check whether their selected genes have significant difference of expression or mutation between responders and non-responders in various data sets.
> Expression difference between responders and non-responders
> Mutation difference between responders and non-responders
> Expression difference between responders and non-responders
 
Points in the above scatter plot represent the expression difference of OLIG2 in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)14121.5850.0152
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)651.0420.359
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)871.9850.03
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160.2540.765
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 59-0.2370.852
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470.8720.548
729033130MelanomaallAnti-PD-1 (nivolumab) 2623-0.2370.801
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 1511-0.9010.495
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 11120.90.585
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 4801
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 2801
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 682300.1840.155
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of OLIG2 in various data sets.
No PMID Cancer type Group Drug # Res # NRes % Mut/Res % Mut/NRes % Diff (R vs NR) Pval Anno
125765070Non-small cell lung cancer (NSCLC)allAnti-PD-1 (pembrolizumab) 14170001
225765070Non-small cell lung cancer (NSCLC)smokingAnti-PD-1 (pembrolizumab) 1030001
325765070Non-small cell lung cancer (NSCLC)non-smokingAnti-PD-1 (pembrolizumab) 4140001
426359337MelanomaallAnti-CTLA-4 (ipilimumab) 277301.4-1.41
526359337MelanomaBRAFiAnti-CTLA-4 (ipilimumab) 0140001
626359337Melanomanon-BRAFiAnti-CTLA-4 (ipilimumab) 275901.7-1.71
726997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)21170001
826997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)860001
926997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)13110001
1028552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160001
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590001
1228552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 470001
1329033130MelanomaallAnti-PD-1 (nivolumab) 38270001
1429033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 22130001
1529033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 16140001
1629301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 11130001
1729301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 610001
1829301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 5120001
Summary
SymbolOLIG2
Nameoligodendrocyte lineage transcription factor 2
Aliases RACK17; OLIGO2; bHLHe19; oligodendrocyte-specific bHLH transcription factor 2; protein kinase C binding prot ......
Chromosomal Location21q22.11
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of OLIG2. The immune-related signatures of 28 TIL types from Charoentong's study, which can be viewed in the download page. For each cancer type, the relative abundance of TILs were inferred by using gene set variation analysis (GSVA) based on gene expression profile. In this tab, users can examine which kinds of TILs might be regulated by the current gene.
> Lymphocyte
 
Summary
SymbolOLIG2
Nameoligodendrocyte lineage transcription factor 2
Aliases RACK17; OLIGO2; bHLHe19; oligodendrocyte-specific bHLH transcription factor 2; protein kinase C binding prot ......
Chromosomal Location21q22.11
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of OLIG2. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by OLIG2.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolOLIG2
Nameoligodendrocyte lineage transcription factor 2
Aliases RACK17; OLIGO2; bHLHe19; oligodendrocyte-specific bHLH transcription factor 2; protein kinase C binding prot ......
Chromosomal Location21q22.11
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of OLIG2. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolOLIG2
Nameoligodendrocyte lineage transcription factor 2
Aliases RACK17; OLIGO2; bHLHe19; oligodendrocyte-specific bHLH transcription factor 2; protein kinase C binding prot ......
Chromosomal Location21q22.11
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of OLIG2 expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolOLIG2
Nameoligodendrocyte lineage transcription factor 2
Aliases RACK17; OLIGO2; bHLHe19; oligodendrocyte-specific bHLH transcription factor 2; protein kinase C binding prot ......
Chromosomal Location21q22.11
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between OLIG2 and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolOLIG2
Nameoligodendrocyte lineage transcription factor 2
Aliases RACK17; OLIGO2; bHLHe19; oligodendrocyte-specific bHLH transcription factor 2; protein kinase C binding prot ......
Chromosomal Location21q22.11
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting OLIG2 collected from DrugBank database.
> Drugs from DrugBank database
 

There is no record.