Entity Details

Primary name CNOT2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9NZN8
EntryNameCNOT2_HUMAN
FullNameCCR4-NOT transcription complex subunit 2
TaxID9606
Evidenceevidence at protein level
Length540
SequenceStatuscomplete
DateCreated2004-04-13
DateModified2021-06-02

Ontological Relatives

GenesCNOT2

GO terms

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GOName
GO:0000122 negative regulation of transcription by RNA polymerase II
GO:0000289 nuclear-transcribed mRNA poly(A) tail shortening
GO:0000932 P-body
GO:0001829 trophectodermal cell differentiation
GO:0003712 transcription coregulator activity
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0006357 regulation of transcription by RNA polymerase II
GO:0006417 regulation of translation
GO:0006977 DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest
GO:0010606 positive regulation of cytoplasmic mRNA processing body assembly
GO:0016020 membrane
GO:0030014 CCR4-NOT complex
GO:0030015 CCR4-NOT core complex
GO:0031047 gene silencing by RNA
GO:0033147 negative regulation of intracellular estrogen receptor signaling pathway
GO:0090503 RNA phosphodiester bond hydrolysis, exonucleolytic
GO:2000036 regulation of stem cell population maintenance

Subcellular Location

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Subcellular Location
Cytoplasm
Nucleus

Domains

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DomainNameCategoryType
IPR007282 NOT2/NOT3/NOT5, C-terminalDomainDomain
IPR038635 CCR4-NOT complex subunit 2/3/5, N-terminal domain superfamilyFamilyHomologous superfamily
IPR040168 Not2/Not3/Not5FamilyFamily

Diseases

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Disease IDSourceNameDescription
618608 OMIMIntellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies (IDNADFS)An autosomal dominant disorder characterized by delayed development, speech delay with nasal speech, and characteristic facial features including upslanted palpebral fissures, anteverted nares, a thin upper lip, and micrognathia. Some patients may have skeletal anomalies, such as brachydactyly, toe syndactyly and flat feet. The disease is caused by variants affecting the gene represented in this entry.

Interactions

70 interactions

InteractorPartnerSourcesPublicationsLink
CNOT2_HUMANCNOT3_HUMANBioGRID, DIP, HPRD, IntAct, MINT16189514 16778766 20211142 21984185 26344197 26496610 29395067 31515488 32296183 details
CNOT2_HUMANCNOT1_HUMANBioGRID, HPRD, IntAct, MINT, UniProt10637334 16778766 26496610 27173435 29395067 unassigned1312 details
CNOT2_HUMANGPS2_HUMANBioGRID, UniProt16712523 details
CNOT2_HUMANRACK1_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANHSF2B_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANCT085_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANCSN1_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANZFHX3_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANPSB4_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANBEX1_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANTBX2_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANCSTF2_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANBCL6_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANPRR35_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANTEKT3_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANCCHCR_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANARMC5_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANGCSAM_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANMFR1L_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANCK001_HUMANBioGRID, IntAct32296183 details
CNOT2_HUMANDDB1_HUMANBioGRID, IntAct20211142 details
CNOT2_HUMANNCOR2_HUMANBioGRID16712523 details
CNOT2_HUMANNCOR1_HUMANBioGRID16712523 details
CNOT2_HUMANCNOT4_HUMANBioGRID29395067 30692204 details
CNOT2_HUMANGLT10_HUMANBioGRID32296183 details
CNOT2_HUMANCNOT8_HUMANBioGRID, HPRD, IntAct, MINT16778766 26496610 29395067 details
CNOT2_HUMANTOB1_HUMANBioGRID, IntAct, UniProt18377426 28514442 details
CNOT2_HUMANCNO6L_HUMANBioGRID, IntAct, UniProt17452450 26496610 27173435 29395067 unassigned1312 details
CNOT2_HUMANCNOT6_HUMANIntAct, UniProt17452450 unassigned1312 details
CNOT2_HUMANSSXT_HUMANIntAct20195357 details
CNOT2_HUMANTNR6C_HUMANBioGRID, DIP, UniProt21981923 21984185 29395067 details
CNOT2_HUMANAGO2_HUMANBioGRID, UniProt21981923 29395067 details
CNOT2_HUMANTNR6B_HUMANBioGRID, UniProt21981923 29395067 details
CNOT2_HUMANTNR6A_HUMANBioGRID, UniProt21981923 29395067 details
CNOT2_HUMANHDAC3_HUMANBioGRID, UniProt16712523 details
CNOT2_HUMANTB182_HUMANBioGRID, IntAct26496610 27173435 29395067 unassigned1312 details
CNOT2_HUMANCNO10_HUMANBioGRID, IntAct26496610 27173435 29395067 unassigned1312 details
CNOT2_HUMANCNO11_HUMANBioGRID, IntAct26496610 27173435 28514442 29395067 unassigned1312 details
CNOT2_HUMANCNOT9_HUMANBioGRID, IntAct26496610 27173435 29395067 unassigned1312 details
CNOT2_HUMANNFKB1_HUMANBioGRID, IntAct27173435 unassigned1312 details
CNOT2_HUMANAGAL_HUMANBioGRID, IntAct27173435 unassigned1312 details
CNOT2_HUMANCNOT7_HUMANBioGRID, IntAct26186194 27173435 28514442 29395067 unassigned1312 details
CNOT2_HUMANGPBL1_HUMANBioGRID, IntAct28514442 29395067 details
CNOT2_HUMANDISC1_HUMANIntAct31413325 details
CNOT2_HUMANOBI1_HUMANBioGRID24778252 29395067 details
CNOT2_HUMANRC3H1_HUMANBioGRID26170170 29395067 30209976 details
CNOT2_HUMANSQSTM_HUMANBioGRID28537904 details
CNOT2_HUMANZ3H7A_HUMANBioGRID29395067 30995489 details
CNOT2_HUMANPATL1_HUMANBioGRID29395067 details
CNOT2_HUMANPUM1_HUMANBioGRID29395067 details
CNOT2_HUMANRBMS1_HUMANBioGRID29395067 details
CNOT2_HUMANSMG7_HUMANBioGRID29395067 details
CNOT2_HUMANUBP2L_HUMANBioGRID29395067 details
CNOT2_HUMANYTHD1_HUMANBioGRID29395067 details
CNOT2_HUMANYTHD2_HUMANBioGRID29395067 details
CNOT2_HUMANYTHD3_HUMANBioGRID29395067 details
CNOT2_HUMANMEX3B_HUMANBioGRID29395067 details
CNOT2_HUMANPRC2A_HUMANBioGRID29395067 details
CNOT2_HUMANRN214_HUMANBioGRID29395067 details
CNOT2_HUMANSMAG2_HUMANBioGRID29395067 details
CNOT2_HUMANUNK_HUMANBioGRID29395067 details
CNOT2_HUMANTTP_HUMANBioGRID29395067 details
CNOT2_HUMANALMS1_HUMANBioGRID29395067 details
CNOT2_HUMANIF4E2_HUMANBioGRID29395067 details
CNOT2_HUMANWDCP_HUMANBioGRID29395067 details
CNOT2_HUMANFXR2_HUMANBioGRID29395067 details
CNOT2_HUMANLS14A_HUMANBioGRID29395067 details
CNOT2_HUMANENTR1_HUMANBioGRID29395067 details
CNOT2_HUMANG3BP1_HUMANBioGRID29395067 details
CNOT2_HUMANR3HD2_HUMANBioGRID29395067 details