EXOSC6
Exosome complex component MTR3
Also known as: EAP4, EXOS6_HUMAN, hMtr3p, MTR3, Mtr3p, p11
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5RKV6
- Gene
- EXOSC6
- Ensembl
- ENSG00000223496
- Chromosome
- 16
- Canonical length
- 272 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene product constitutes one of the subunits of the multisubunit particle called exosome, which mediates mRNA degradation. The composition of human exosome is similar to its yeast counterpart. This protein is homologous to the yeast Mtr3 protein. Its exact function is not known, however, it has been shown using a cell-free RNA decay system that the exosome is required for rapid degradation of unstable mRNAs containing AU-rich elements (AREs), but not for poly(A) shortening. The exosome does not recognize ARE-containing mRNAs on its own, but requires ARE-binding proteins that could interact with the exosome and recruit it to unstable mRNAs, thereby promoting their rapid degradation. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
272 residues, UniProt reviewed canonical sequence.
>Q5RKV6|EXOSC6
1 MPGDHRRIRG PEESQPPQLY AADEEEAPGT RDPTRLRPVY ARAGLLSQAK GSAYLEAGGT
61 KVLCAVSGPR QAEGGERGGG PAGAGGEAPA ALRGRLLCDF RRAPFAGRRR RAPPGGCEER
121 ELALALQEAL EPAVRLGRYP RAQLEVSALL LEDGGSALAA ALTAAALALA DAGVEMYDLV
181 VGCGLSLAPG PAPTWLLDPT RLEEERAAAG LTVALMPVLN QVAGLLGSGE GGLTESWAEA
241 VRLGLEGCQR LYPVLQQSLV RAARRRGAAA QPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EXOSC6 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)
- 0.34
- Highest tissue expression
- 18 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 18 nTPM
- basal ganglia: 17 nTPM
- cerebral cortex: 16 nTPM
- hypothalamus: 13 nTPM
- amygdala: 11 nTPM
- bone marrow: 11 nTPM
Single-cell type
- hepatic stellate cells: 58 nCPM
- megakaryocyte progenitors: 48 nCPM
- retinal pigment epithelial cells: 47 nCPM
- erythrocyte progenitors: 46 nCPM
- fallopian secretory cells: 44 nCPM
- fallopian tube ciliated cells: 43 nCPM
Immune cell
- plasmacytoid DC: 6.1 nTPM
- basophil: 5 nTPM
- NK-cell: 4.8 nTPM
- naive CD4 T-cell: 4.5 nTPM
- naive B-cell: 4.2 nTPM
- naive CD8 T-cell: 4.2 nTPM
Brain region
- cerebellum: 64 nTPM
- pons: 64 nTPM
- basal ganglia: 64 nTPM
- thalamus: 64 nTPM
- amygdala: 64 nTPM
- cerebral cortex: 63 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)
- 1.28
- gnomAD pLI
- 0.52
- gnomAD missense Z
- -0.59
- DepMap mean gene effect
- -1.32
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- DNA deamination
- isotype switching
- nuclear mRNA surveillance
- poly(A)-dependent snoRNA 3'-end processing
- positive regulation of isotype switching
- RNA catabolic process
- RNA processing
- rRNA catabolic process
- rRNA processing
- U4 snRNA 3'-end processing
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EXOSC6 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 EXOSC6 as an antibody target. Whether an autoantibody or antibody against EXOSC6 could matter depends on whether native EXOSC6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EXOSC6 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 EXOSC6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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