Browse MAF

Summary
SymbolMAF
Namev-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
Aliases c-MAF; AYGRP; CCA4; CTRCT21; Avian musculoaponeurotic fibrosarcoma (MAF) protooncogene; T lymphocyte c-maf l ......
Chromosomal Location16q22-q23
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
Domain PF03131 bZIP Maf transcription factor
PF08383 Maf N-terminal region
Function

Acts as a transcriptional activator or repressor. Involved in embryonic lens fiber cell development. Recruits the transcriptional coactivators CREBBP and/or EP300 to crystallin promoters leading to up-regulation of crystallin gene during lens fiber cell differentiation. Activates the expression of IL4 in T helper 2 (Th2) cells. Increases T-cell susceptibility to apoptosis by interacting with MYB and decreasing BCL2 expression. Together with PAX6, transactivates strongly the glucagon gene promoter through the G1 element. Activates transcription of the CD13 proximal promoter in endothelial cells. Represses transcription of the CD13 promoter in early stages of myelopoiesis by affecting the ETS1 and MYB cooperative interaction. Involved in the initial chondrocyte terminal differentiation and the disappearance of hypertrophic chondrocytes during endochondral bone development. Binds to the sequence 5'-[GT]G[GC]N[GT]NCTCAGNN-3' in the L7 promoter. Binds to the T-MARE (Maf response element) sites of lens-specific alpha- and beta-crystallin gene promoters. Binds element G1 on the glucagon promoter. Binds an AT-rich region adjacent to the TGC motif (atypical Maf response element) in the CD13 proximal promoter in endothelial cells (By similarity). When overexpressed, represses anti-oxidant response element (ARE)-mediated transcription. Involved either as an oncogene or as a tumor suppressor, depending on the cell context. Binds to the ARE sites of detoxifying enzyme gene promoters.

> Gene Ontology
 
Biological Process GO:0001501 skeletal system development
GO:0001654 eye development
GO:0002062 chondrocyte differentiation
GO:0002088 lens development in camera-type eye
GO:0007423 sensory organ development
GO:0032330 regulation of chondrocyte differentiation
GO:0043010 camera-type eye development
GO:0043583 ear development
GO:0048839 inner ear development
GO:0051216 cartilage development
GO:0061035 regulation of cartilage development
GO:0061448 connective tissue development
GO:0070306 lens fiber cell differentiation
Molecular Function GO:0001228 transcriptional activator activity, RNA polymerase II transcription regulatory region sequence-specific binding
Cellular Component GO:0000785 chromatin
> KEGG and Reactome Pathway
 
KEGG -
Reactome -
Summary
SymbolMAF
Namev-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
Aliases c-MAF; AYGRP; CCA4; CTRCT21; Avian musculoaponeurotic fibrosarcoma (MAF) protooncogene; T lymphocyte c-maf l ......
Chromosomal Location16q22-q23
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Literatures that report relations between MAF 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
 
  Literatures describing the relation between MAF and anti-tumor immunity in human cancer.
PMID Cancer type Relation to immunity Evidence sentences
26139534MelanomaInhibit immunity (T cell function)Therefore, the melanoma microenvironment contributes to skewing of CD8 T cell differentiation programs, in part by TGFβ/IL-6-mediated induction of Maf.
Summary
SymbolMAF
Namev-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
Aliases c-MAF; AYGRP; CCA4; CTRCT21; Avian musculoaponeurotic fibrosarcoma (MAF) protooncogene; T lymphocyte c-maf l ......
Chromosomal Location16q22-q23
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 MAF 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
SymbolMAF
Namev-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
Aliases c-MAF; AYGRP; CCA4; CTRCT21; Avian musculoaponeurotic fibrosarcoma (MAF) protooncogene; T lymphocyte c-maf l ......
Chromosomal Location16q22-q23
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 MAF in various data sets.
No PMID Cancer type Group Drug # Res # NRes Log2 (Fold Change) P value Anno
126997480MelanomaallAnti-PD-1 (pembrolizumab and nivolumab)1412-0.1980.424
226997480MelanomaMAPKiAnti-PD-1 (pembrolizumab and nivolumab)65-0.2440.891
326997480Melanomanon-MAPKiAnti-PD-1 (pembrolizumab and nivolumab)87-0.1610.898
428552987Urothelial cancerallAnti-PD-L1 (atezolizumab) 9160.0690.838
528552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590.1260.96
628552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 47-0.0040.999
729033130MelanomaallAnti-PD-1 (nivolumab) 26230.1020.819
829033130MelanomaNIV3-PROGAnti-PD-1 (nivolumab) 15110.2470.891
929033130MelanomaNIV3-NAIVEAnti-PD-1 (nivolumab) 1112-0.0340.986
1029301960Clear cell renal cell carcinoma (ccRCC)allAnti-PD-1 (nivolumab) 480.1750.899
1129301960Clear cell renal cell carcinoma (ccRCC)VEGFRiAnti-PD-1 (nivolumab) 2001
1229301960Clear cell renal cell carcinoma (ccRCC)non-VEGFRiAnti-PD-1 (nivolumab) 280.6320.762
1329443960Urothelial cancerallAnti-PD-L1 (atezolizumab) 68230-0.4620.00156
> Mutation difference between responders and non-responders
 
Points in the above scatter plot represent the mutation difference of MAF 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) 14177.107.10.452
225765070Non-small cell lung cancer (NSCLC)smokingAnti-PD-1 (pembrolizumab) 1030001
325765070Non-small cell lung cancer (NSCLC)non-smokingAnti-PD-1 (pembrolizumab) 414250250.222
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) 91606.2-6.21
1128552987Urothelial cancersmokingAnti-PD-L1 (atezolizumab) 590001
1228552987Urothelial cancernon-smokingAnti-PD-L1 (atezolizumab) 47014.3-14.31
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
SymbolMAF
Namev-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
Aliases c-MAF; AYGRP; CCA4; CTRCT21; Avian musculoaponeurotic fibrosarcoma (MAF) protooncogene; T lymphocyte c-maf l ......
Chromosomal Location16q22-q23
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of MAF. 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
SymbolMAF
Namev-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
Aliases c-MAF; AYGRP; CCA4; CTRCT21; Avian musculoaponeurotic fibrosarcoma (MAF) protooncogene; T lymphocyte c-maf l ......
Chromosomal Location16q22-q23
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of MAF. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by MAF.
> Immunoinhibitor
> Immunostimulator
> MHC molecule
> Immunoinhibitor
 
> Immunostimulator
 
> MHC molecule
 
Summary
SymbolMAF
Namev-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
Aliases c-MAF; AYGRP; CCA4; CTRCT21; Avian musculoaponeurotic fibrosarcoma (MAF) protooncogene; T lymphocyte c-maf l ......
Chromosomal Location16q22-q23
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of MAF. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene.
> Chemokine
> Receptor
> Chemokine
 
> Receptor
 
Summary
SymbolMAF
Namev-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
Aliases c-MAF; AYGRP; CCA4; CTRCT21; Avian musculoaponeurotic fibrosarcoma (MAF) protooncogene; T lymphocyte c-maf l ......
Chromosomal Location16q22-q23
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Distribution of MAF expression across immune and molecular subtypes.
> Immune subtype
> Molecular subtype
> Immune subtype
 
> Molecular subtype
 
Summary
SymbolMAF
Namev-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
Aliases c-MAF; AYGRP; CCA4; CTRCT21; Avian musculoaponeurotic fibrosarcoma (MAF) protooncogene; T lymphocyte c-maf l ......
Chromosomal Location16q22-q23
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Associations between MAF and clinical features.
> Overall survival analysis
> Cancer stage
> Tumor grade
> Overall survival
 
> Stage
 
> Grade
 
Summary
SymbolMAF
Namev-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
Aliases c-MAF; AYGRP; CCA4; CTRCT21; Avian musculoaponeurotic fibrosarcoma (MAF) protooncogene; T lymphocyte c-maf l ......
Chromosomal Location16q22-q23
External Links HGNC, NCBI, Ensembl, Uniprot, GeneCards
Content Drugs targeting MAF collected from DrugBank database.
> Drugs from DrugBank database
 

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