SCUBA

CNOT2 — CCR4-NOT transcription complex subunit 2

CNOT2 belongs to a gene co-expression module in 4 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

CNOT2's module in each cell type

Cell typeModuleShares the module with
CD19⁺ B cellsB cell activation
BCR/AP1/NFKb pathway
ADGRG5, BCAR3, CD86, CLIP2, CTSH, FAS, GABARAPL2, GPR137B +7 moreView in SCUBA
Gamma-delta T cellsT Cell Exhaustion
Exhaustion
ACADVL, ACSS1, ADSS2, B4GALT3, CDK11A, CHP1, CNOT8, CRELD2 +20 more
Innate lymphoid cellsInnate Immune Activation
Inflammation
ANKRD11, ATP10D, COA4, DOCK10, IKZF2, NIFK, PRKDC, PSMD11 +13 moreView in SCUBA
MacrophagesNF-κB Activation
Inflammatory
BCL3, BLOC1S6, CD83, CFLAR, CHMP1B, CSRNP1, CYLD, DNAJB6 +33 moreView in SCUBA

About the gene

SynonymsCDC36, NOT2, NOT2H
Chromosome12: 70243002-70354993
Predicted locationIntracellular
Essential geneYes
Protein classDisease related genes, Essential proteins, Human disease related genes, Predicted intracellular proteins
Molecular functionDevelopmental protein, Repressor
Biological processRNA-mediated gene silencing, Transcription, Transcription regulation, Translation regulation

Function

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. Required for the CCR4- NOT complex structural integrity. Can repress transcription and may link the CCR4-NOT complex to transcriptional regulation; the repressive function may specifically involve the N-Cor repressor complex containing HDAC3, NCOR1 and NCOR2. Involved in the maintenance of embryonic stem (ES) cell identity.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.