EPC1
Enhancer of polycomb homolog 1
Also known as: EPC1_HUMAN, Epl1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H2F5
- Gene
- EPC1
- Ensembl
- ENSG00000120616
- Chromosome
- 10
- Canonical length
- 836 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Nuclear bodies
OverviewNCBI Gene
This gene encodes a member of the polycomb group (PcG) family. The encoded protein is a component of the NuA4 histone acetyltransferase complex and can act as both a transcriptional activator and repressor. The encoded protein has been linked to apoptosis, DNA repair, skeletal muscle differentiation, gene silencing, and adult T-cell leukemia/lymphoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
Canonical amino-acid sequenceUniProt
836 residues, UniProt reviewed canonical sequence.
>Q9H2F5|EPC1
1 MSKLSFRARA LDASKPLPVF RCEDLPDLHE YASINRAVPQ MPTGMEKEEE SEHHLQRAIS
61 AQQVYGEKRD NMVIPVPEAE SNIAYYESIY PGEFKMPKQL IHIQPFSLDA EQPDYDLDSE
121 DEVFVNKLKK KMDICPLQFE EMIDRLEKGS GQQPVSLQEA KLLLKEDDEL IREVYEYWIK
181 KRKNCRGPSL IPSVKQEKRD GSSTNDPYVA FRRRTEKMQT RKNRKNDEAS YEKMLKLRRD
241 LSRAVTILEM IKRREKSKRE LLHLTLEIME KRYNLGDYNG EIMSEVMAQR QPMKPTYAIP
301 IIPITNSSQF KHQEAMDVKE FKVNKQDKAD LIRPKRKYEK KPKVLPSSAA ATPQQTSPAA
361 LPVFNAKDLN QYDFPSSDEE PLSQVLSGSS EAEEDNDPDG PFAFRRKAGC QYYAPHLDQT
421 GNWPWTSPKD GGLGDVRYRY CLTTLTVPQR CIGFARRRVG RGGRVLLDRA HSDYDSVFHH
481 LDLEMLSSPQ HSPVNQFANT SETNTSDKSF SKDLSQILVN IKSCRWRHFR PRTPSLHDSD
541 NDELSCRKLY RSINRTGTAQ PGTQTCSTST QSKSSSGSAH FAFTAEQYQQ HQQQLALMQK
601 QQLAQIQQQQ ANSNSSTNTS QNLASNQQKS GFRLNIQGLE RTLQGFVSKT LDSASAQFAA
661 SALVTSEQLM GFKMKDDVVL GIGVNGVLPA SGVYKGLHLS STTPTALVHT SPSTAGSALL
721 QPSNITQTSS SHSALSHQVT AANSATTQVL IGNNIRLTVP SSVATVNSIA PINARHIPRT
781 LSAVPSSALK LAAAANCQVS KVPSSSSVDS VPRENHESEK PALNNIADNT VAMEVTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EPC1 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)
- 0.6
- Highest tissue expression
- 141 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 141 nTPM
- thymus: 30 nTPM
- skeletal muscle: 29 nTPM
- tongue: 22 nTPM
- cerebellum: 21 nTPM
- lymph node: 20 nTPM
Single-cell type
- myonuclei: 586 nCPM
- t-cells: 400 nCPM
- innate lymphoid cells: 358 nCPM
- nk-cells: 354 nCPM
- lactotrophs: 321 nCPM
- thyrotrophs: 309 nCPM
Immune cell
- basophil: 66 nTPM
- neutrophil: 47 nTPM
- eosinophil: 36 nTPM
- naive B-cell: 31 nTPM
- memory B-cell: 28 nTPM
- plasmacytoid DC: 27 nTPM
Brain region
- cerebellum: 38 nTPM
- white matter: 27 nTPM
- basal ganglia: 22 nTPM
- cerebral cortex: 22 nTPM
- medulla oblongata: 21 nTPM
- midbrain: 21 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)
- 0.13
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.67
- DepMap mean gene effect
- -0.29
- 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
- DNA-templated transcription
- double-strand break repair via homologous recombination
- negative regulation of DNA-templated transcription
- negative regulation of gene expression, epigenetic
- negative regulation of transcription by RNA polymerase II
- positive regulation of DNA-templated transcription
- positive regulation of double-strand break repair via homologous recombination
- positive regulation of transcription by RNA polymerase II
- regulation of apoptotic process
- regulation of cell cycle
- regulation of double-strand break repair
- regulation of transcription by RNA polymerase II
- sperm DNA condensation
- spermatid development
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EPC1 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 EPC1 as an antibody target. Whether an autoantibody or antibody against EPC1 could matter depends on whether native EPC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EPC1 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 EPC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...