EID2
EP300-interacting inhibitor of differentiation 2
Also known as: CRI2, EID-2, EID2_HUMAN, MGC20452
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N6I1
- Gene
- EID2
- Ensembl
- ENSG00000176396
- Chromosome
- 19
- Canonical length
- 236 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables SMAD binding activity. Involved in several processes, including negative regulation of transcription by RNA polymerase II; negative regulation of transmembrane receptor protein serine/threonine kinase signaling pathway; and transforming growth factor beta receptor complex assembly. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
236 residues, UniProt reviewed canonical sequence.
>Q8N6I1|EID2
1 MSKLPADSSV PQTGAANGDR DVPQAEVGRG RREPAPAQPE EAGEGAMAAA RGGPVPAARE
61 GRMAAARAAP AAAARGAPVA AAALARAAAA GRESPAAAAA REARMAEVAR LLGEPVDEEG
121 PEGRPRSRHG NGGLAALPYL RLRHPLSVLG INYQQFLRHY LENYPIAPGR IQELEERRRR
181 FVEACRAREA AFDAEYQRNP HRVDLDILTF TIALTASEVI NPLIEELGCD KFINRELocalizationUniProt · AlphaFold · HPA
Whether an antibody against EID2 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)
- 0.61
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 26 nTPM
- hypothalamus: 22 nTPM
- adrenal gland: 19 nTPM
- basal ganglia: 19 nTPM
- amygdala: 18 nTPM
- hippocampal formation: 18 nTPM
Single-cell type
- cytotrophoblasts: 58 nCPM
- migrating cytotrophoblasts: 40 nCPM
- fallopian tube ciliated cells: 27 nCPM
- pancreatic islet cells: 25 nCPM
- respiratory ciliated cells: 24 nCPM
- müller glia: 24 nCPM
Immune cell
- naive CD8 T-cell: 1.4 nTPM
- memory CD4 T-cell: 1 nTPM
- memory CD8 T-cell: 1 nTPM
- naive CD4 T-cell: 1 nTPM
- gdT-cell: 0.8 nTPM
- MAIT T-cell: 0.8 nTPM
Brain region
- cerebral cortex: 33 nTPM
- hypothalamus: 26 nTPM
- basal ganglia: 23 nTPM
- pons: 22 nTPM
- medulla oblongata: 21 nTPM
- cerebellum: 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)
- 1.19
- gnomAD pLI
- 0.3
- gnomAD missense Z
- 0.8
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 10% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell differentiation
- muscle organ development
- negative regulation of DNA-templated transcription
- negative regulation of SMAD protein signal transduction
- negative regulation of transcription by RNA polymerase II
- negative regulation of transforming growth factor beta receptor signaling pathway
- regulation of cell population proliferation
- transforming growth factor beta receptor complex assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of EID2 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 EID2 as an antibody target. Whether an autoantibody or antibody against EID2 could matter depends on whether native EID2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EID2 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 EID2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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