JUN

Gene Information
 
Gene Symbol
JUN
 
Aliases
AP-1, AP1, c-Jun, cJUN, p39
 
Entrez Gene ID
 
Gene Name
Jun proto-oncogene, AP-1 transcription factor subunit
 
Chromosomal Location
1p32.1
 
HGNC ID
 
Summary
This gene is the putative transforming gene of avian sarcoma virus 17. It encodes a protein which is highly similar to the viral protein, and which interacts directly with specific target DNA sequences to regulate gene expression. This gene is intronless and is mapped to 1p32-p31, a chromosomal region involved in both translocations and deletions in human malignancies. [provided by RefSeq, Jul 2008]
 
RefSeq DNA
 
RefSeq mRNA
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0000122 Biological process Negative regulation of transcription by RNA polymerase II IBA 21873635
GO:0007179 Biological process Transforming growth factor beta receptor signaling pathway IDA 9732876
GO:0007265 Biological process Ras protein signal transduction IDA 24623306
GO:0009314 Biological process Response to radiation IBA 21873635
GO:0009612 Biological process Response to mechanical stimulus IBA 21873635
Protein Information
 
Protein Name
Transcription factor AP-1, Jun activation domain binding protein, activator protein 1, enhancer-binding protein AP1, jun oncogene, proto-oncogene c-Jun, proto-oncogene cJun, v-jun avian sarcoma virus 17 oncogene homolog, v-jun sarcoma virus 17 oncogene homolog
 
Function
 
Refseq Proteins
 
UniProt
 
PDB
 
Pfam
Pfam Accession Pfam ID
PF00170 bZIP_1
PF03957 Jun
Pathways
 
KEGG
 
Reactome
 

Endocrine resistance
MAPK signaling pathway
ErbB signaling pathway
cAMP signaling pathway
Mitophagy - animal
Apoptosis
Wnt signaling pathway
Osteoclast differentiation
Focal adhesion
Tight junction
Toll-like receptor signaling pathway
NOD-like receptor signaling pathway
C-type lectin receptor signaling pathway
IL-17 signaling pathway
Th1 and Th2 cell differentiation
Th17 cell differentiation
T cell receptor signaling pathway
B cell receptor signaling pathway
TNF signaling pathway
Neurotrophin signaling pathway
GnRH signaling pathway
Estrogen signaling pathway
Oxytocin signaling pathway
Relaxin signaling pathway
Non-alcoholic fatty liver disease (NAFLD)
AGE-RAGE signaling pathway in diabetic complications
Cocaine addiction
Amphetamine addiction
Epithelial cell signaling in Helicobacter pylori infection
Salmonella infection
Pertussis
Yersinia infection
Leishmaniasis
Chagas disease (American trypanosomiasis)
Hepatitis B
Measles
Human T-cell leukemia virus 1 infection
Kaposi sarcoma-associated herpesvirus infection
Epstein-Barr virus infection
Human immunodeficiency virus 1 infection
Pathways in cancer
Viral carcinogenesis
Colorectal cancer
Renal cell carcinoma
Breast cancer
Choline metabolism in cancer
PD-L1 expression and PD-1 checkpoint pathway in cancer
Inflammatory bowel disease (IBD)
Rheumatoid arthritis
Fluid shear stress and atherosclerosis

 

Pre-NOTCH Transcription and Translation
Oxidative Stress Induced Senescence
Senescence-Associated Secretory Phenotype (SASP)
FCERI mediated MAPK activation
Activation of the AP-1 family of transcription factors
MAPK6/MAPK4 signaling
TP53 Regulates Transcription of DNA Repair Genes
Regulation of PTEN gene transcription
Estrogen-dependent gene expression
WNT5:FZD7-mediated leishmania damping

Interactions
 
STRING MINT IntAct
ENSP00000312652 P41159
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Cardiovascular Diseases
Hypertensive disease
Digestive System Diseases
Cholestasis
Endocrine System Diseases
PCOS
Immune System Diseases
Juvenile arthritis
Still Disease
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
AP-1,EGR-1,TF 
chronic low-grade inflammation 
 
Rotterdam criteria 
Related 
PCOS (8 lean, 8 obese) and 16 weight-matched controls 
Lean women with PCOS exhibited greater AP-1 activation and MMP2 protein content after glucose ingestion and higher plasma MMP9 and CRP levels than lean controls 

| © 2019, Biomedical Informatics Centre, NIRRH |
National Institute for Research in Reproductive Health, Jehangir Merwanji Street, Parel, Mumbai-400 012
Tel: 91-22-24192104, Fax No: 91-22-24139412