======= IL36G ======= == Gene Information == * **Official Symbol**: IL36G * **Official Name**: interleukin 36 gamma * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=56300|56300]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9NZH8|Q9NZH8]] * **Interactions**: [[https://thebiogrid.org/search.php?search=IL36G&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20IL36G|Open PubMed]] * **OMIM**: [[https://omim.org/entry/605542|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: Cytokine that binds to and signals through the IL1RL2/IL-36R receptor which in turn activates NF-kappa-B and MAPK signaling pathways in target cells. Part of the IL-36 signaling system that is thought to be present in epithelial barriers and to take part in local inflammatory response; similar to the IL-1 system with which it shares the coreceptor IL1RAP. Seems to be involved in skin inflammatory response by acting on keratinocytes, dendritic cells and indirectly on T-cells to drive tissue infiltration, cell maturation and cell proliferation. In cultured keratinocytes induces the expression of macrophage, T-cell, and neutrophil chemokines, such as CCL3, CCL4, CCL5, CCL2, CCL17, CCL22, CL20, CCL5, CCL2, CCL17, CCL22, CXCL8, CCL20 and CXCL1; also stimulates its own expression and that of the prototypic cutaneous proinflammatory parameters TNF-alpha, S100A7/psoriasin and inducible NOS. May play a role in proinflammatory responses during particular neutrophilic airway inflammation: activates mitogen-activated protein kinases and NF-kappa B in primary lung fibroblasts, and stimulates the expression of IL-8 and CXCL3 and Th17 chemokine CCL20 in lung fibroblasts. May be involved in the innate immune response to fungal pathogens, such as Aspergillus fumigatus. {ECO:0000269|PubMed:11466363, ECO:0000269|PubMed:20870894, ECO:0000269|PubMed:21965679, ECO:0000269|PubMed:23095752, ECO:0000269|PubMed:23147407, ECO:0000269|PubMed:24829417}. |IL1| |interleukin-1 receptor binding| |neutrophil chemotaxis| |granulocyte chemotaxis| |neutrophil migration| |positive regulation of interleukin-6 production| |granulocyte migration| |myeloid leukocyte migration| |positive regulation of JNK cascade| |regulation of interleukin-6 production| |leukocyte chemotaxis| |positive regulation of stress-activated MAPK cascade| |positive regulation of stress-activated protein kinase signaling cascade| |cytokine activity| |positive regulation of I-kappaB kinase/NF-kappaB signaling| |cellular response to lipopolysaccharide| |regulation of JNK cascade| |cellular response to molecule of bacterial origin| |cell chemotaxis| |cellular response to biotic stimulus| |regulation of stress-activated MAPK cascade| |regulation of I-kappaB kinase/NF-kappaB signaling| |regulation of stress-activated protein kinase signaling cascade| |response to lipopolysaccharide| |response to molecule of bacterial origin| |leukocyte migration| |positive regulation of cytokine production| |inflammatory response| |cellular response to lipid| |positive regulation of MAPK cascade| |chemotaxis| |taxis| |cytokine-mediated signaling pathway| |response to bacterium| |regulation of cytokine production| |regulation of cellular response to stress| |regulation of MAPK cascade| |innate immune response| |response to lipid| |defense response to other organism| |cell migration| |cellular response to cytokine stimulus| |positive regulation of protein phosphorylation| |positive regulation of intracellular signal transduction| |cellular response to oxygen-containing compound| |positive regulation of phosphorylation| |localization of cell| |cell motility| |response to cytokine| |cell-cell signaling| |positive regulation of phosphate metabolic process| |positive regulation of phosphorus metabolic process| |positive regulation of protein modification process| |response to other organism| |response to external biotic stimulus| |locomotion| |response to biotic stimulus| |defense response| |regulation of protein phosphorylation| |regulation of response to stress| |movement of cell or subcellular component| |response to oxygen-containing compound| |regulation of phosphorylation| |extracellular space| |positive regulation of cellular protein metabolic process| |positive regulation of signal transduction| |positive regulation of protein metabolic process| |positive regulation of multicellular organismal process| |regulation of phosphate metabolic process| |regulation of phosphorus metabolic process| |positive regulation of cell communication| |positive regulation of signaling| |regulation of intracellular signal transduction| |regulation of protein modification process| |immune response| |extracellular region| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp108|Vinblastine 0.2μM R03 exp108]]|1.85| |[[:results:exp334|All-trans-Retinoic-Acid 40μM R07 exp334]]|2| No correlation found to any other genes in chemogenomics. 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| == Essentiality in NALM6 == * **Essentiality Rank**: 12636 * **Expression level (log2 read counts)**: -3.8 {{:chemogenomics:nalm6 dist.png?nolink |}}