EPOP
Elongin BC and Polycomb repressive complex 2-associated protein
Also known as: C17orf96, EPOP_HUMAN, LOC100170841, PRR28
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NHQ4
- Gene
- EPOP
- Ensembl
- ENSG00000273604
- Chromosome
- 17
- Canonical length
- 379 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol,Cytoplasmic bodies
OverviewNCBI Gene
Predicted to enable chromatin binding activity. Predicted to be involved in neuron fate commitment; regulation of transcription by RNA polymerase II; and stem cell differentiation. Predicted to be located in chromosome and nucleus. Predicted to be part of ESC/E(Z) complex and elongin complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
379 residues, UniProt reviewed canonical sequence.
>A6NHQ4|EPOP
1 METLCPAPRL AVPASPRGSP CSPTPRKPCR GTQEFSPLCL RALAFCALAK PRASSLGPGP
61 GELAARSPVL RGPQAPLRPG GWAPDGLKHL WAPTGRPGVP NTAAGEDADV AACPRRGEEE
121 EGGGGFPHFG VRSCAPPGRC PAPPHPREST TSFASAPPRP APGLEPQRGP AASPPQEPSS
181 RPPSPPAGLS TEPAGPGTAP RPFLPGQPAE VDGNPPPAAP EAPAASPSTA SPAPAAPGDL
241 RQEHFDRLIR RSKLWCYAKG FALDTPSLRR GPERPPAKGP ARGAAKKRRL PAPPPRTAQP
301 RRPAPTLPTT STFSLLNCFP CPPALVVGED GDLKPASSLR LQGDSKPPPA HPLWRWQMGG
361 PAVPEPPGLK FWGINMDESLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EPOP 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)
- 0.7
- Highest tissue expression
- 14 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 14 nTPM
- testis: 11 nTPM
- amygdala: 5.8 nTPM
- parathyroid gland: 4.5 nTPM
- liver: 4.2 nTPM
- basal ganglia: 3.9 nTPM
Single-cell type
- brain inhibitory neurons: 2 nCPM
- brain excitatory neurons: 1.9 nCPM
- oligodendrocyte progenitor cells: 1.6 nCPM
- bergmann glia: 1.4 nCPM
- astrocytes: 1 nCPM
- renal collecting duct intercalated cells: 0.9 nCPM
Immune cell
- MAIT T-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebral cortex: 22 nTPM
- basal ganglia: 16 nTPM
- white matter: 12 nTPM
- amygdala: 6.7 nTPM
- hippocampal formation: 4.6 nTPM
- midbrain: 4.1 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)
- 1.24
- gnomAD pLI
- 0.28
- DepMap mean gene effect
- -0.54
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- neuron fate commitment
- regulation of transcription by RNA polymerase II
- stem cell differentiation
- transcription elongation-coupled chromatin remodeling
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EPOP 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 EPOP as an antibody target. Whether an autoantibody or antibody against EPOP could matter depends on whether native EPOP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EPOP 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 EPOP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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