======= TRIM8 ======= == Gene Information == * **Official Symbol**: TRIM8 * **Official Name**: tripartite motif containing 8 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=81603|81603]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9BZR9|Q9BZR9]] * **Interactions**: [[https://thebiogrid.org/search.php?search=TRIM8&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20TRIM8|Open PubMed]] * **OMIM**: [[https://omim.org/entry/606125|Open OMIM]] == Function Summary == * **Entrez Summary**: This gene encodes a member of the tripartite motif (TRIM) protein family. Based on similarities to other proteins, the encoded protein is suspected to be an E3 ubiquitin-protein ligase. Regulation of this gene may be altered in some cancers. Mutations resulting in a truncated protein product have been observed in early-onset epileptic encephalopathy (EOEE). [provided by RefSeq, Sep 2016]. * **UniProt Summary**: E3 ubiquitin-protein ligase which plays different roles in immune pathways. Participates in the activation of interferon- gamma signaling by promoting proteasomal degradation of the repressor SOCS1 (PubMed:12163497). Plays a positive role in the TNFalpha and IL-1beta signaling pathways. Mechanistically, induces the 'lys-63' polyubiquitination of MAP3K7/TAK1 component leading to the activation of NF-kappa-B (PubMed:22084099, PubMed:23152791). Modulates also STAT3 activity through negative regulation of PIAS3, either by degradation of PIAS3 through the ubiquitin-proteasome pathway or exclusion of PIAS3 from the nucleus (PubMed:20516148). {ECO:0000269|PubMed:12163497, ECO:0000269|PubMed:20516148, ECO:0000269|PubMed:22084099, ECO:0000269|PubMed:23152791}. |zf-C3HC4| |negative regulation of viral release from host cell| |negative regulation of viral entry into host cell| |negative regulation of viral transcription| |regulation of viral entry into host cell| |regulation of viral release from host cell| |transferase activity| |regulation of viral transcription| |interferon-gamma-mediated signaling pathway| |positive regulation of protein localization to nucleus| |negative regulation of viral life cycle| |negative regulation of viral process| |PML body| |regulation of protein localization to nucleus| |positive regulation of autophagy| |stem cell population maintenance| |maintenance of cell number| |regulation of viral life cycle| |positive regulation of NF-kappaB transcription factor activity| |cellular response to interferon-gamma| |response to interferon-gamma| |positive regulation of I-kappaB kinase/NF-kappaB signaling| |regulation of viral process| |negative regulation of multi-organism process| |regulation of symbiosis, encompassing mutualism through parasitism| |regulation of I-kappaB kinase/NF-kappaB signaling| |positive regulation of DNA-binding transcription factor activity| |negative regulation of locomotion| |positive regulation of cellular protein localization| |regulation of autophagy| |positive regulation of cellular catabolic process| |regulation of DNA-binding transcription factor activity| |positive regulation of catabolic process| |regulation of cellular protein localization| |cytokine-mediated signaling pathway| |protein ubiquitination| |innate immune response| |protein modification by small protein conjugation| |regulation of multi-organism process| |regulation of cellular catabolic process| |zinc ion binding| |protein homodimerization activity| |regulation of cellular localization| |defense response to other organism| |regulation of locomotion| |protein modification by small protein conjugation or removal| |regulation of catabolic process| |cellular response to cytokine stimulus| |positive regulation of intracellular signal transduction| |regulation of protein localization| |identical protein binding| |response to cytokine| |response to other organism| |response to external biotic stimulus| |response to biotic stimulus| |defense response| |positive regulation of signal transduction| |positive regulation of molecular function| |positive regulation of cell communication| |positive regulation of signaling| |regulation of intracellular signal transduction| |immune response| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp217|Mdivi-1 15μM R05 exp217]]|-1.91| |[[:results:exp59|UMK57 1μM R01 exp59]]|-1.72| No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 3/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|3/26| |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| == Essentiality in NALM6 == * **Essentiality Rank**: 7882 * **Expression level (log2 read counts)**: 5.59 {{:chemogenomics:nalm6 dist.png?nolink |}}