======= CSNK1G2 ======= == Gene Information == * **Official Symbol**: CSNK1G2 * **Official Name**: casein kinase 1 gamma 2 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=1455|1455]] * **UniProt**: [[https://www.uniprot.org/uniprot/P78368|P78368]] * **Interactions**: [[https://thebiogrid.org/search.php?search=CSNK1G2&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20CSNK1G2|Open PubMed]] * **OMIM**: [[https://omim.org/entry/602214|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: Serine/threonine-protein kinase. Casein kinases are operationally defined by their preferential utilization of acidic proteins such as caseins as substrates. It can phosphorylate a large number of proteins. Participates in Wnt signaling. Phosphorylates COL4A3BP/CERT, MTA1 and SMAD3. Involved in brain development and vesicular trafficking and neurotransmitter releasing from small synaptic vesicles. Regulates fast synaptic transmission mediated by glutamate. SMAD3 phosphorylation promotes its ligand-dependent ubiquitination and subsequent proteasome degradation, thus inhibiting SMAD3-mediated TGF-beta responses. Hyperphosphorylation of the serine-repeat motif of COL4A3BP/CERT leads to its inactivation by dissociation from the Golgi complex, thus down-regulating ER-to-Golgi transport of ceramide and sphingomyelin synthesis. Triggers PER1 proteasomal degradation probably through phosphorylation. {ECO:0000269|PubMed:15077195, ECO:0000269|PubMed:15342122, ECO:0000269|PubMed:15917222, ECO:0000269|PubMed:18794808, ECO:0000269|PubMed:19005213}. |Pkinase| |Pkinase Tyr| |CK1gamma C| |peptidyl-threonine phosphorylation| |peptidyl-threonine modification| |sphingolipid biosynthetic process| |membrane lipid biosynthetic process| |positive regulation of canonical Wnt signaling pathway| |sphingolipid metabolic process| |peptidyl-serine phosphorylation| |positive regulation of Wnt signaling pathway| |protein autophosphorylation| |peptidyl-serine modification| |membrane lipid metabolic process| |regulation of canonical Wnt signaling pathway| |Wnt signaling pathway| |cell-cell signaling by wnt| |regulation of Wnt signaling pathway| |protein serine/threonine kinase activity| |cell surface receptor signaling pathway involved in cell-cell signaling| |endocytosis| |lipid biosynthetic process| |import into cell| |peptidyl-amino acid modification| |cellular lipid metabolic process| |protein phosphorylation| |cell-cell signaling| |lipid metabolic process| |phosphorylation| |organonitrogen compound biosynthetic process| |ATP binding| |positive regulation of signal transduction| |positive regulation of cell communication| |positive regulation of signaling| |vesicle-mediated transport| |membrane| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp147|Resveratrol 16μM R03 exp147]]|-1.89| |[[:results:exp434|Vemurafenib 6.6μM R08 exp434]]|1.71| 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**: 14488 * **Expression level (log2 read counts)**: 6.26 {{:chemogenomics:nalm6 dist.png?nolink |}}