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Ask your administrator if you think this is wrong. ======= IFIH1 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: IFIH1 * **<color #00a2e8>Official Name</color>**: interferon induced with helicase C domain 1 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=64135|64135]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q9BYX4|Q9BYX4]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=IFIH1&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20IFIH1|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/606951|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein that is upregulated in response to treatment with beta-interferon and a protein kinase C-activating compound, mezerein. Irreversible reprogramming of melanomas can be achieved by treatment with both these agents; treatment with either agent alone only achieves reversible differentiation. Genetic variation in this gene is associated with diabetes mellitus insulin-dependent type 19. [provided by RefSeq, Jul 2012]. * **<color #00a2e8>UniProt Summary</color>**: Innate immune receptor which acts as a cytoplasmic sensor of viral nucleic acids and plays a major role in sensing viral infection and in the activation of a cascade of antiviral responses including the induction of type I interferons and proinflammatory cytokines. Its ligands include mRNA lacking 2'-O- methylation at their 5' cap and long-dsRNA (>1 kb in length). Upon ligand binding it associates with mitochondria antiviral signaling protein (MAVS/IPS1) which activates the IKK-related kinases: TBK1 and IKBKE which phosphorylate interferon regulatory factors: IRF3 and IRF7 which in turn activate transcription of antiviral immunological genes, including interferons (IFNs); IFN-alpha and IFN-beta. Responsible for detecting the Picornaviridae family members such as encephalomyocarditis virus (EMCV) and mengo encephalomyocarditis virus (ENMG). Can also detect other viruses such as dengue virus (DENV), west Nile virus (WNV), and reovirus. Also involved in antiviral signaling in response to viruses containing a dsDNA genome, such as vaccinia virus. Plays an important role in amplifying innate immune signaling through recognition of RNA metabolites that are produced during virus infection by ribonuclease L (RNase L). May play an important role in enhancing natural killer cell function and may be involved in growth inhibition and apoptosis in several tumor cell lines. {ECO:0000269|PubMed:14645903, ECO:0000269|PubMed:19211564, ECO:0000269|PubMed:19656871, ECO:0000269|PubMed:21217758, ECO:0000269|PubMed:21742966}. <button type='primary' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> |CARD| |ResIII| |DEAD| |Helicase C| |RIG-I C-RD| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |regulation of type III interferon production| |MDA-5 signaling pathway| |positive regulation of interferon-beta secretion| |regulation of interferon-beta secretion| |cytoplasmic pattern recognition receptor signaling pathway in response to virus| |detection of virus| |positive regulation of interferon-alpha secretion| |regulation of interferon-alpha secretion| |cellular response to exogenous dsRNA| |positive regulation of tumor necrosis factor secretion| |cellular response to dsRNA| |multi-organism cellular process| |positive regulation of interferon-alpha production| |regulation of tumor necrosis factor secretion| |regulation of interferon-alpha production| |positive regulation of interferon-beta production| |positive regulation of interleukin-6 secretion| |ribonucleoprotein complex binding| |cellular response to virus| |cytoplasmic pattern recognition receptor signaling pathway| |response to exogenous dsRNA| |negative regulation of type I interferon production| |single-stranded RNA binding| |regulation of interferon-beta production| |response to dsRNA| |positive regulation of response to cytokine stimulus| |RNA helicase activity| |protein sumoylation| |double-stranded RNA binding| |positive regulation of type I interferon production| |positive regulation of tumor necrosis factor production| |positive regulation of tumor necrosis factor superfamily cytokine production| |positive regulation of interleukin-6 production| |regulation of type I interferon production| |pattern recognition receptor signaling pathway| |positive regulation of cytokine secretion| |regulation of interleukin-6 production| |regulation of tumor necrosis factor production| |regulation of tumor necrosis factor superfamily cytokine production| |intracellular receptor signaling pathway| |regulation of response to cytokine stimulus| |defense response to virus| |regulation of cytokine secretion| |innate immune response-activating signal transduction| |activation of innate immune response| |positive regulation of protein secretion| |negative regulation of cytokine production| |response to virus| |protein deubiquitination| |positive regulation of peptide secretion| |protein modification by small protein removal| |peptidyl-lysine modification| |positive regulation of innate immune response| |positive regulation of response to biotic stimulus| |positive regulation of secretion by cell| |positive regulation of protein transport| |positive regulation of secretion| |positive regulation of cytokine production| |regulation of innate immune response| |positive regulation of establishment of protein localization| |regulation of protein secretion| |positive regulation of defense response| |regulation of peptide secretion| |positive regulation of multi-organism process| |regulation of response to biotic stimulus| |cellular response to organic cyclic compound| |immune response-activating signal transduction| |immune response-regulating signaling pathway| |positive regulation of response to external stimulus| |activation of immune response| |cellular response to nitrogen compound| |regulation of cytokine production| |viral process| |regulation of protein transport| |regulation of peptide transport| |regulation of establishment of protein localization| |regulation of secretion by cell| |regulation of defense response| |innate immune response| |protein modification by small protein conjugation| |regulation of multi-organism process| |symbiotic process| |regulation of secretion| |interspecies interaction between organisms| |zinc ion binding| |positive regulation of immune response| |peptidyl-amino acid modification| |response to organic cyclic compound| |defense response to other organism| |protein modification by small protein conjugation or removal| |positive regulation of transport| |regulation of protein localization| |identical protein binding| |response to nitrogen compound| |immune effector process| |regulation of response to external stimulus| |positive regulation of immune system process| |regulation of immune response| |negative regulation of multicellular organismal process| |proteolysis| |response to other organism| |response to external biotic stimulus| |response to biotic stimulus| |defense response| |DNA binding| |regulation of response to stress| |ATP binding| |regulation of immune system process| |intracellular signal transduction| |positive regulation of multicellular organismal process| |regulation of transport| |immune response| </modal> \\ === CRISPR Data === <button type='primary' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> ^Screen^Score^ |[[:results:exp363|GSK-J4 1-1.25μM to day4 R07 exp363]]|-1.8| </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 15324 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 3.62 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='IFIH1 Expression in NALM6 Cells: 3.62'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2025/12/10 20:19by 127.0.0.1