Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3661
Gene name Gene Name - the full gene name approved by the HGNC.
Interferon regulatory factor 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
IRF3
Synonyms (NCBI Gene) Gene synonyms aliases
IIAE7
Disease Acronyms (UniProt) Disease acronyms from UniProt database
IIAE7
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.33
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the interferon regulatory transcription factor (IRF) family. The encoded protein is found in an inactive cytoplasmic form that upon serine/threonine phosphorylation forms a complex with CREBBP. This complex translocates to th
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs143769046 C>T Likely-benign, risk-factor Missense variant, non coding transcript variant, intron variant, coding sequence variant
rs750526659 C>G,T Risk-factor Coding sequence variant, non coding transcript variant, intron variant, missense variant
Transcription factors
Transcription factor Regulation Reference
E2F1 Repression 21225257;22464952
IRF4 Repression 19955181
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0000785 Component Chromatin ISA
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA 21873635
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA 8524823
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IMP 17560375
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603734 6118 ENSG00000126456
Protein
UniProt ID Q14653
Protein name Interferon regulatory factor 3 (IRF-3)
Protein function Key transcriptional regulator of type I interferon (IFN)-dependent immune responses which plays a critical role in the innate immune response against DNA and RNA viruses (PubMed:22394562, PubMed:24049179, PubMed:25636800, PubMed:27302953, PubMed
PDB 1J2F , 1QWT , 1T2K , 1ZOQ , 2O61 , 2O6G , 2PI0 , 3A77 , 3QU6 , 5JEJ , 5JEK , 5JEL , 5JEM , 5JEO , 5JER , 6SIV , 6SJA , 7JFL
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00605 IRF 7 110 Interferon regulatory factor transcription factor Domain
PF10401 IRF-3 201 380 Interferon-regulatory factor 3 Family
Tissue specificity TISSUE SPECIFICITY: Expressed constitutively in a variety of tissues. {ECO:0000269|PubMed:8524823}.
Sequence
Sequence length 427
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Toll-like receptor signaling pathway
NOD-like receptor signaling pathway
RIG-I-like receptor signaling pathway
Cytosolic DNA-sensing pathway
Alcoholic liver disease
Shigellosis
Pertussis
Yersinia infection
Hepatitis C
Hepatitis B
Measles
Human cytomegalovirus infection
Influenza A
Human papillomavirus infection
Kaposi sarcoma-associated herpesvirus infection
Herpes simplex virus 1 infection
Epstein-Barr virus infection
Human immunodeficiency virus 1 infection
Coronavirus disease - COVID-19
Viral carcinogenesis
Lipid and atherosclerosis
  ISG15 antiviral mechanism
IRF3 mediated activation of type 1 IFN
LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production
Regulation of innate immune responses to cytosolic DNA
IRF3-mediated induction of type I IFN
Interferon gamma signaling
TICAM1-dependent activation of IRF3/IRF7
Interferon alpha/beta signaling
TRAF3-dependent IRF activation pathway
TRAF6 mediated IRF7 activation
Negative regulators of DDX58/IFIH1 signaling
Activation of IRF3/IRF7 mediated by TBK1/IKK epsilon
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Melanoma Cutaneous Melanoma rs121913315, rs121913323, rs137853080, rs137853081, rs121909232, rs121913388, rs104894094, rs104894095, rs104894097, rs104894098, rs104894099, rs104894109, rs137854599, rs11547328, rs104894340
View all (64 more)
26619011
Unknown
Disease term Disease name Evidence References Source
Vitiligo Vitiligo GWAS
Schizophrenia Schizophrenia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Acute On Chronic Liver Failure Associate 26173605
Adenocarcinoma of Lung Associate 28566697
Alzheimer Disease Stimulate 30076830
Alzheimer Disease Associate 39753133
Asthma Associate 24475887
Atherosclerosis Associate 20154210
Autoimmune Diseases Associate 26794091
Biliary Atresia Associate 29070776
Breast Neoplasms Associate 31287789
Carcinogenesis Associate 23449805, 28566697