EXOSC4
Exosome complex component RRP41
Also known as: EXOS4_HUMAN, FLJ20591, hRrp41p, p12A, RRP41, RRP41A, Rrp41p, SKI6, Ski6p
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NPD3
- Gene
- EXOSC4
- Ensembl
- ENSG00000178896
- Chromosome
- 8
- Canonical length
- 245 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles,Cytosol
OverviewNCBI Gene
Enables mRNA 3'-UTR AU-rich region binding activity. Involved in several processes, including DNA deamination; maturation of 5.8S rRNA; and nuclear-transcribed mRNA catabolic process. Acts upstream of or within defense response to virus. Located in cytosol; euchromatin; and nuclear lumen. Part of exosome (RNase complex). [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
245 residues, UniProt reviewed canonical sequence.
>Q9NPD3|EXOSC4
1 MAGLELLSDQ GYRVDGRRAG ELRKIQARMG VFAQADGSAY IEQGNTKALA VVYGPHEIRG
61 SRARALPDRA LVNCQYSSAT FSTGERKRRP HGDRKSCEMG LQLRQTFEAA ILTQLHPRSQ
121 IDIYVQVLQA DGGTYAACVN AATLAVLDAG IPMRDFVCAC SAGFVDGTAL ADLSHVEEAA
181 GGPQLALALL PASGQIALLE MDARLHEDHL ERVLEAAAQA ARDVHTLLDR VVRQHVREAS
241 ILLGDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EXOSC4 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)
- 0.28
- Highest tissue expression
- 94 nTPM
Expression across tissuesHPA
Tissue
- testis: 94 nTPM
- liver: 36 nTPM
- adrenal gland: 31 nTPM
- esophagus: 28 nTPM
- choroid plexus: 27 nTPM
- basal ganglia: 26 nTPM
Single-cell type
- other brain neurons: 7.9 nCPM
- oligodendrocytes: 6 nCPM
- brain excitatory neurons: 5.7 nCPM
- brain inhibitory neurons: 5.4 nCPM
- oligodendrocyte progenitor cells: 4.4 nCPM
- astrocytes: 4 nCPM
Immune cell
- plasmacytoid DC: 91 nTPM
- classical monocyte: 77 nTPM
- intermediate monocyte: 75 nTPM
- myeloid DC: 74 nTPM
- naive B-cell: 57 nTPM
- memory B-cell: 55 nTPM
Brain region
- cerebral cortex: 35 nTPM
- basal ganglia: 24 nTPM
- cerebellum: 24 nTPM
- medulla oblongata: 24 nTPM
- thalamus: 24 nTPM
- choroid plexus: 23 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)
- 0.98
- gnomAD pLI
- 0.07
- gnomAD missense Z
- 0.56
- DepMap mean gene effect
- -1.25
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 11% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- defense response to virus
- DNA deamination
- histone mRNA catabolic process
- maturation of 5.8S rRNA
- nuclear mRNA surveillance
- nuclear-transcribed mRNA catabolic process
- poly(A)-dependent snoRNA 3'-end processing
- positive regulation of cell growth
- 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 EXOSC4 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 EXOSC4 as an antibody target. Whether an autoantibody or antibody against EXOSC4 could matter depends on whether native EXOSC4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EXOSC4 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 EXOSC4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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