======= CNOT11 ======= == Gene Information == * **Official Symbol**: CNOT11 * **Official Name**: CCR4-NOT transcription complex subunit 11 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=55571|55571]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9UKZ1|Q9UKZ1]] * **Interactions**: [[https://thebiogrid.org/search.php?search=CNOT11&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20CNOT11|Open PubMed]] * **OMIM**: [[https://omim.org/entry/620509|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: Component of the CCR4-NOT complex which is one of the major cellular mRNA deadenylases and is linked to various cellular processes including bulk mRNA degradation, miRNA-mediated repression, translational repression during translational initiation and general transcription regulation. Additional complex functions may be a consequence of its influence on mRNA expression. Is required for the association of CNOT10 with the CCR4-NOT complex. Seems not to be required for complex deadenylase function. |DUF2363| |CCR4-NOT complex| |nuclear-transcribed mRNA poly(A) tail shortening| |DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest| |intracellular signal transduction involved in G1 DNA damage checkpoint| |signal transduction involved in mitotic DNA integrity checkpoint| |signal transduction involved in mitotic DNA damage checkpoint| |signal transduction involved in mitotic cell cycle checkpoint| |signal transduction involved in mitotic G1 DNA damage checkpoint| |nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay| |mitotic G1 DNA damage checkpoint| |mitotic G1/S transition checkpoint| |G1 DNA damage checkpoint| |signal transduction involved in DNA damage checkpoint| |signal transduction involved in DNA integrity checkpoint| |signal transduction involved in cell cycle checkpoint| |DNA damage response, signal transduction by p53 class mediator| |positive regulation of cell cycle arrest| |gene silencing by RNA| |mitotic DNA damage checkpoint| |negative regulation of G1/S transition of mitotic cell cycle| |mitotic DNA integrity checkpoint| |signal transduction in response to DNA damage| |negative regulation of cell cycle G1/S phase transition| |regulation of cell cycle arrest| |signal transduction by p53 class mediator| |DNA damage checkpoint| |DNA integrity checkpoint| |regulation of G1/S transition of mitotic cell cycle| |gene silencing| |mitotic cell cycle checkpoint| |regulation of cell cycle G1/S phase transition| |cell cycle checkpoint| |nuclear-transcribed mRNA catabolic process| |negative regulation of mitotic cell cycle phase transition| |mRNA catabolic process| |negative regulation of cell cycle phase transition| |RNA catabolic process| |positive regulation of cell cycle process| |negative regulation of mitotic cell cycle| |negative regulation of cell cycle process| |regulation of translation| |nucleobase-containing compound catabolic process| |positive regulation of cell cycle| |regulation of cellular amide metabolic process| |regulation of mitotic cell cycle phase transition| |heterocycle catabolic process| |cellular nitrogen compound catabolic process| |aromatic compound catabolic process| |regulation of cell cycle phase transition| |organic cyclic compound catabolic process| |posttranscriptional regulation of gene expression| |cell population proliferation| |negative regulation of cell cycle| |mitotic cell cycle process| |regulation of mitotic cell cycle| |mitotic cell cycle| |mRNA metabolic process| |regulation of cell cycle process| |molecular function| |cellular response to DNA damage stimulus| |cellular macromolecule catabolic process| |cell cycle process| |macromolecule catabolic process| |regulation of cell cycle| |cell cycle| |RNA metabolic process| |intracellular signal transduction| |cellular response to stress| |negative regulation of gene expression| |organic substance catabolic process| |cellular catabolic process| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp458|Bisphenol S 100μM R08 exp458]]|-2.02| 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**: 7233 * **Expression level (log2 read counts)**: 6.17 {{:chemogenomics:nalm6 dist.png?nolink |}}