Seroatlas · Human Serome Atlas

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 QP

LocalizationUniProt · 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

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.

Canonical record: https://seroatlas.com/gene/EXOSC6. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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