CNOT8
CCR4-NOT transcription complex subunit 8
Also known as: CAF1, CALIF, CNOT8_HUMAN, hCAF1, POP2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UFF9
- Gene
- CNOT8
- Ensembl
- ENSG00000155508
- Chromosome
- 5
- Canonical length
- 292 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
Enables poly(A)-specific ribonuclease activity. Involved in miRNA-mediated gene silencing by mRNA destabilization and positive regulation of cell population proliferation. Located in nucleus. Part of CCR4-NOT complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
292 residues, UniProt reviewed canonical sequence.
>Q9UFF9|CNOT8
1 MPAALVENSQ VICEVWASNL EEEMRKIREI VLSYSYIAMD TEFPGVVVRP IGEFRSSIDY
61 QYQLLRCNVD LLKIIQLGLT FTNEKGEYPS GINTWQFNFK FNLTEDMYSQ DSIDLLANSG
121 LQFQKHEEEG IDTLHFAELL MTSGVVLCDN VKWLSFHSGY DFGYMVKLLT DSRLPEEEHE
181 FFHILNLFFP SIYDVKYLMK SCKNLKGGLQ EVADQLDLQR IGRQHQAGSD SLLTGMAFFR
241 MKELFFEDSI DDAKYCGRLY GLGTGVAQKQ NEDVDSAQEK MSILAIINNM QQLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CNOT8 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 112 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 112 nTPM
- thymus: 65 nTPM
- adipose tissue: 61 nTPM
- lymph node: 55 nTPM
- blood vessel: 53 nTPM
- tonsil: 50 nTPM
Single-cell type
- early spermatids: 130 nCPM
- neutrophils: 125 nCPM
- decidual stromal cells: 113 nCPM
- late primary spermatocytes: 94 nCPM
- alveolar cells type 2: 92 nCPM
- neutrophil progenitors: 88 nCPM
Immune cell
- basophil: 278 nTPM
- eosinophil: 270 nTPM
- total PBMC: 170 nTPM
- myeloid DC: 133 nTPM
- classical monocyte: 128 nTPM
- neutrophil: 127 nTPM
Brain region
- choroid plexus: 61 nTPM
- thalamus: 45 nTPM
- white matter: 45 nTPM
- spinal cord: 44 nTPM
- medulla oblongata: 42 nTPM
- pons: 41 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.58
- gnomAD pLI
- 0.22
- gnomAD missense Z
- 2.16
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- miRNA-mediated gene silencing by mRNA destabilization
- nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay
- nuclear-transcribed mRNA poly(A) tail shortening
- positive regulation of cell population proliferation
- positive regulation of mRNA catabolic process
- regulation of translation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CNOT8 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CNOT8 as an antibody target. Whether an autoantibody or antibody against CNOT8 could matter depends on whether native CNOT8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CNOT8 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CNOT8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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