EAPP
E2F-associated phosphoprotein
Also known as: BM036, C14orf11, EAPP_HUMAN, FLJ20578
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q56P03
- Gene
- EAPP
- Ensembl
- ENSG00000129518
- Chromosome
- 14
- Canonical length
- 285 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear speckles
OverviewNCBI Gene
This gene encodes a phosphoprotein that interacts with several members of the E2F family of proteins. The protein localizes to the nucleus, and is present throughout the cell cycle except during mitosis. It functions to modulate E2F-regulated transcription and stimulate proliferation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Canonical amino-acid sequenceUniProt
285 residues, UniProt reviewed canonical sequence.
>Q56P03|EAPP
1 MNRLPDDYDP YAVEEPSDEE PALSSSEDEV DVLLHGTPDQ KRKLIRECLT GESESSSEDE
61 FEKEMEAELN STMKTMEDKL SSLGTGSSSG NGKVATAPTR YYDDIYFDSD SEDEDRAVQV
121 TKKKKKKQHK IPTNDELLYD PEKDNRDQAW VDAQRRGYHG LGPQRSRQQQ PVPNSDAVLN
181 CPACMTTLCL DCQRHESYKT QYRAMFVMNC SINKEEVLRY KASENRKKRR VHKKMRSNRE
241 DAAEKAETDV EEIYHPVMCT ECSTEVAVYD KDEVFHFFNV LASHSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EAPP 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)
- 0.49
- Highest tissue expression
- 84 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 84 nTPM
- parathyroid gland: 50 nTPM
- ovary: 49 nTPM
- rectum: 48 nTPM
- breast: 47 nTPM
- colon: 47 nTPM
Single-cell type
- syncytiotrophoblasts: 267 nCPM
- neutrophils: 233 nCPM
- ovarian stromal cells: 209 nCPM
- migrating cytotrophoblasts: 187 nCPM
- enterocytes: 177 nCPM
- cytotrophoblasts: 169 nCPM
Immune cell
- neutrophil: 135 nTPM
- basophil: 134 nTPM
- eosinophil: 130 nTPM
- T-reg: 117 nTPM
- memory B-cell: 99 nTPM
- NK-cell: 97 nTPM
Brain region
- white matter: 28 nTPM
- cerebellum: 28 nTPM
- hypothalamus: 26 nTPM
- spinal cord: 25 nTPM
- cerebral cortex: 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)
- 1.51
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.03
- DepMap mean gene effect
- -0.68
- 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
- negative regulation of transcription elongation by RNA polymerase II
- positive regulation of cell population proliferation
- positive regulation of transcription elongation by RNA polymerase II
Cellular components
Protein domainsUniProt · Pfam · InterPro
- E2F-associated phosphoprotein
- E2F-associated phosphoprotein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EAPP 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 EAPP as an antibody target. Whether an autoantibody or antibody against EAPP could matter depends on whether native EAPP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EAPP 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 EAPP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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