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Ask your administrator if you think this is wrong. ======= CCL5 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: CCL5 * **<color #00a2e8>Official Name</color>**: C-C motif chemokine ligand 5 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=6352|6352]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/P13501|P13501]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=CCL5&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20CCL5|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/187011|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: This gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, functions as a chemoattractant for blood monocytes, memory T helper cells and eosinophils. It causes the release of histamine from basophils and activates eosinophils. This cytokine is one of the major HIV-suppressive factors produced by CD8+ cells. It functions as one of the natural ligands for the chemokine receptor chemokine (C-C motif) receptor 5 (CCR5), and it suppresses in vitro replication of the R5 strains of HIV-1, which use CCR5 as a coreceptor. Alternative splicing results in multiple transcript variants that encode different isoforms. [provided by RefSeq, Jul 2013]. * **<color #00a2e8>UniProt Summary</color>**: Chemoattractant for blood monocytes, memory T-helper cells and eosinophils. Causes the release of histamine from basophils and activates eosinophils. May activate several chemokine receptors including CCR1, CCR3, CCR4 and CCR5. One of the major HIV-suppressive factors produced by CD8+ T-cells. Recombinant RANTES protein induces a dose-dependent inhibition of different strains of HIV-1, HIV-2, and simian immunodeficiency virus (SIV). The processed form RANTES(3-68) acts as a natural chemotaxis inhibitor and is a more potent inhibitor of HIV-1- infection. The second processed form RANTES(4-68) exhibits reduced chemotactic and HIV-suppressive activity compared with RANTES(1- 68) and RANTES(3-68) and is generated by an unidentified enzyme associated with monocytes and neutrophils (PubMed:16791620, PubMed:1380064, PubMed:8525373, PubMed:9516414, PubMed:15923218). May also be an agonist of the G protein-coupled receptor GPR75, stimulating inositol trisphosphate production and calcium mobilization through its activation. Together with GPR75, may play a role in neuron survival through activation of a downstream signaling pathway involving the PI3, Akt and MAP kinases. By activating GPR75 may also play a role in insulin secretion by islet cells (PubMed:23979485). {ECO:0000269|PubMed:1380064, ECO:0000269|PubMed:15923218, ECO:0000269|PubMed:16791620, ECO:0000269|PubMed:17001303, ECO:0000269|PubMed:23979485, ECO:0000269|PubMed:8525373, ECO:0000269|PubMed:9516414}. <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'> |IL8| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |chemokine receptor antagonist activity| |CCR4 chemokine receptor binding| |receptor signaling protein tyrosine kinase activator activity| |CCR1 chemokine receptor binding| |activation of phospholipase D activity| |positive regulation of natural killer cell chemotaxis| |positive regulation of homotypic cell-cell adhesion| |negative regulation of macrophage apoptotic process| |positive regulation of cell-cell adhesion mediated by integrin| |negative regulation of chemokine-mediated signaling pathway| |CCR5 chemokine receptor binding| |positive regulation of activation of Janus kinase activity| |phospholipase activator activity| |chemokine receptor binding| |regulation of natural killer cell chemotaxis| |regulation of activation of Janus kinase activity| |regulation of chronic inflammatory response| |regulation of chemokine-mediated signaling pathway| |regulation of macrophage apoptotic process| |regulation of cell-cell adhesion mediated by integrin| |positive regulation of T cell apoptotic process| |macrophage chemotaxis| |negative regulation by host of viral transcription| |positive regulation of macrophage chemotaxis| |positive regulation of T cell chemotaxis| |negative regulation of myeloid cell apoptotic process| |regulation of T cell chemotaxis| |positive regulation of monocyte chemotaxis| |positive regulation of lymphocyte apoptotic process| |negative regulation of T cell apoptotic process| |dendritic cell chemotaxis| |macrophage migration| |positive regulation of cell adhesion mediated by integrin| |positive regulation of macrophage migration| |eosinophil chemotaxis| |dendritic cell migration| |positive regulation of lymphocyte chemotaxis| |eosinophil migration| |positive regulation of mononuclear cell migration| |regulation of monocyte chemotaxis| |regulation of homotypic cell-cell adhesion| |regulation of lymphocyte chemotaxis| |negative regulation of viral transcription| |regulation of macrophage chemotaxis| |phosphatidylinositol phospholipase C activity| |positive regulation of leukocyte apoptotic process| |negative regulation of lymphocyte apoptotic process| |CCR chemokine receptor binding| |regulation of myeloid cell apoptotic process| |positive regulation of translational initiation| |positive regulation of T cell migration| |regulation of T cell apoptotic process| |lipopolysaccharide-mediated signaling pathway| |positive regulation of viral genome replication| |chemoattractant activity| |regulation of macrophage migration| |positive regulation of smooth muscle cell migration| |positive regulation of lymphocyte migration| |protein kinase B signaling| |monocyte chemotaxis| |regulation of granulocyte chemotaxis| |regulation of T cell migration| |negative regulation of leukocyte apoptotic process| |regulation of cell adhesion mediated by integrin| |regulation of mononuclear cell migration| |negative regulation of G protein-coupled receptor signaling pathway| |lymphocyte chemotaxis| |positive chemotaxis| |mononuclear cell migration| |chemokine activity| |leukocyte cell-cell adhesion| |regulation of lymphocyte apoptotic process| |positive regulation of protein tyrosine kinase activity| |protein self-association| |negative regulation of viral genome replication| |positive regulation of phospholipase activity| |regulation of smooth muscle cell migration| |negative regulation of cytokine-mediated signaling pathway| |positive regulation of viral life cycle| |regulation of lymphocyte migration| |regulation of viral transcription| |negative regulation of response to cytokine stimulus| |lymphocyte migration| |positive regulation of tyrosine phosphorylation of STAT protein| |regulation of phospholipase activity| |positive regulation of lipase activity| |modification by host of symbiont morphology or physiology| |interaction with symbiont| |regulation of tyrosine phosphorylation of STAT protein| |regulation of translational initiation| |chemokine-mediated signaling pathway| |negative regulation of viral life cycle| |regulation of leukocyte apoptotic process| |neutrophil chemotaxis| |positive regulation of receptor signaling pathway via JAK-STAT| |positive regulation of smooth muscle cell proliferation| |positive regulation of phosphatidylinositol 3-kinase signaling| |positive regulation of receptor signaling pathway via STAT| |positive regulation of leukocyte chemotaxis| |regulation of protein tyrosine kinase activity| |granulocyte chemotaxis| |response to chemokine| |cellular response to chemokine| |neutrophil migration| |regulation of viral genome replication| |positive regulation of T cell proliferation| |regulation of lipase activity| |negative regulation of viral process| |granulocyte migration| |positive regulation of viral process| |cellular response to fibroblast growth factor stimulus| |modification of morphology or physiology of other organism involved in symbiotic interaction| |regulation of leukocyte chemotaxis| |response to fibroblast growth factor| |regulation of phosphatidylinositol 3-kinase signaling| |positive regulation of calcium ion transport| |positive regulation of translation| |myeloid leukocyte migration| |positive regulation of leukocyte migration| |positive regulation of lymphocyte proliferation| |regulation of receptor signaling pathway via JAK-STAT| |positive regulation of mononuclear cell proliferation| |regulation of smooth muscle cell proliferation| |regulation of receptor signaling pathway via STAT| |positive regulation of chemotaxis| |positive regulation of leukocyte proliferation| |regulation of G protein-coupled receptor signaling pathway| |leukocyte chemotaxis| |regulation of viral life cycle| |protein tetramerization| |positive regulation of cellular amide metabolic process| |modification of morphology or physiology of other organism| |regulation of T cell proliferation| |cellular response to interferon-gamma| |regulation of cytokine-mediated signaling pathway| |cellular response to interleukin-1| |regulation of response to cytokine stimulus| |regulation of insulin secretion| |response to interferon-gamma| |cellular response to lipopolysaccharide| |positive regulation of epithelial cell proliferation| |positive regulation of peptidyl-tyrosine phosphorylation| |cellular response to molecule of bacterial origin| |regulation of leukocyte migration| |response to interleukin-1| |positive regulation of T cell activation| |regulation of viral process| |regulation of lymphocyte proliferation| |regulation of peptide hormone secretion| |cell chemotaxis| |regulation of mononuclear cell proliferation| |positive regulation of ERK1 and ERK2 cascade| |regulation of chemotaxis| |negative regulation of multi-organism process| |cellular response to biotic stimulus| |positive regulation of leukocyte cell-cell adhesion| |regulation of symbiosis, encompassing mutualism through parasitism| |regulation of leukocyte proliferation| |protein kinase activity| |cellular response to tumor necrosis factor| |regulation of calcium ion transport| |calcium ion transport| |regulation of peptidyl-tyrosine phosphorylation| |positive regulation of cell-cell adhesion| |response to tumor necrosis factor| |regulation of hormone secretion| |positive regulation of ion transport| |response to virus| |regulation of ERK1 and ERK2 cascade| |divalent metal ion transport| |regulation of leukocyte cell-cell adhesion| |divalent inorganic cation transport| |regulation of neuron death| |response to lipopolysaccharide| |regulation of T cell activation| |response to molecule of bacterial origin| |regulation of epithelial cell proliferation| |regulation of inflammatory response| |positive regulation of innate immune response| |regulation of translation| |positive regulation of lymphocyte activation| |positive regulation of response to biotic stimulus| |MAPK cascade| |leukocyte migration| |regulation of metal ion transport| |signal transduction by protein phosphorylation| |regulation of cell-cell adhesion| |positive regulation of leukocyte activation| |positive regulation of cell adhesion| |regulation of cellular amide metabolic process| |positive regulation of GTPase activity| |positive regulation of cell activation| |cellular calcium ion homeostasis| |calcium ion homeostasis| |regulation of innate immune response| |regulation of protein secretion| |cellular divalent inorganic cation homeostasis| |positive regulation of defense response| |regulation of GTPase activity| |divalent inorganic cation homeostasis| |regulation of peptide secretion| |inflammatory response| |positive regulation of cell migration| |cellular response to growth factor stimulus| |neutrophil activation| |cell-cell adhesion| |granulocyte activation| |response to toxic substance| |positive regulation of multi-organism process| |regulation of lymphocyte activation| |protein complex oligomerization| |cellular response to lipid| |regulation of response to biotic stimulus| |positive regulation of cell motility| |posttranscriptional regulation of gene expression| |response to growth factor| |regulation of hormone levels| |positive regulation of protein kinase activity| |positive regulation of cellular component movement| |cellular response to organic cyclic compound| |positive regulation of MAPK cascade| |chemotaxis| |taxis| |positive regulation of locomotion| |cellular metal ion homeostasis| |positive regulation of kinase activity| |myeloid leukocyte activation| |regulation of leukocyte activation| |positive regulation of response to external stimulus| |metal ion homeostasis| |cellular cation homeostasis| |metal ion transport| |regulation of cell activation| |positive regulation of apoptotic process| |cellular ion homeostasis| |positive regulation of programmed cell death| |positive regulation of transferase activity| |cytokine-mediated signaling pathway| |regulation of cell adhesion| |response to bacterium| |positive regulation of cell death| |regulation of ion transport| |regulation of protein transport| |cation homeostasis| |inorganic ion homeostasis| |regulation of peptide transport| |cellular chemical homeostasis| |regulation of establishment of protein localization| |regulation of secretion by cell| |regulation of MAPK cascade| |regulation of defense response| |innate immune response| |positive regulation of hydrolase activity| |regulation of multi-organism process| |symbiotic process| |ion homeostasis| |exocytosis| |regulation of protein kinase activity| |regulation of secretion| |interspecies interaction between organisms| |cation transport| |regulation of cell migration| |response to lipid| |positive regulation of immune response| |regulation of kinase activity| |protein homodimerization activity| |negative regulation of apoptotic process| |cellular homeostasis| |negative regulation of programmed cell death| |regulation of cell motility| |positive regulation of cell population proliferation| |response to organic cyclic compound| |leukocyte activation| |cell adhesion| |biological adhesion| |defense response to other organism| |cell migration| |protein phosphorylation| |regulation of transferase activity| |regulation of locomotion| |positive regulation of transport| |regulation of cellular component movement| |negative regulation of cell death| |secretion by cell| |cellular response to cytokine stimulus| |positive regulation of protein phosphorylation| |positive regulation of intracellular signal transduction| |regulation of protein localization| |export from cell| |cellular response to oxygen-containing compound| |positive regulation of phosphorylation| |identical protein binding| |cell activation| |cell motility| |localization of cell| |regulation of response to external stimulus| |response to cytokine| |chemical homeostasis| |cell-cell signaling| |secretion| |positive regulation of phosphate metabolic process| |positive regulation of phosphorus metabolic process| |regulation of immune response| |positive regulation of immune system process| |cellular response to endogenous stimulus| |positive regulation of protein modification process| |negative regulation of signal transduction| |regulation of hydrolase activity| |phosphorylation| |response to other organism| |response to external biotic stimulus| |locomotion| |G protein-coupled receptor signaling pathway| |response to biotic stimulus| |defense response| |negative regulation of cell communication| |negative regulation of signaling| |ion transport| |positive regulation of catalytic activity| |regulation of protein phosphorylation| |response to endogenous stimulus| |regulation of response to stress| |regulation of apoptotic process| |movement of cell or subcellular component| |response to oxygen-containing compound| |protein-containing complex assembly| |regulation of programmed cell death| |regulation of phosphorylation| |extracellular space| |positive regulation of cellular protein metabolic process| |regulation of cell population proliferation| |negative regulation of response to stimulus| |homeostatic process| |positive regulation of signal transduction| |regulation of immune system process| |regulation of cell death| |intracellular signal transduction| |positive regulation of protein metabolic process| |positive regulation of molecular function| |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| |protein-containing complex subunit organization| |regulation of transport| |immune response| |positive regulation of macromolecule biosynthetic process| |extracellular region| |vesicle-mediated transport| |positive regulation of cellular biosynthetic process| |positive regulation of gene expression| |positive regulation of biosynthetic process| </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:exp456|Benzoate 20000μM R08 exp456]]|-1.77| |[[:results:exp230|Epigallocatechin gallate 20μM R05 exp230]]|-1.77| |[[:results:exp225|Celastrol 0.12μM R05 exp225]]|-1.76| |[[:results:exp336|Asunaprenir 3μM R07 exp336]]|1.77| |[[:results:exp33|Rotenone 2μM R00 exp33]]|1.95| |[[:results:exp458|Bisphenol S 100μM R08 exp458]]|2.06| |[[:results:exp77|Prochlorperazine 5.2μM R02 exp77]]|2.09| </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>**: 11583 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 3.89 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='CCL5 Expression in NALM6 Cells: 3.89'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:36by 127.0.0.1