PDCD2
Programmed cell death protein 2
Also known as: PDCD2_HUMAN, RP8, ZMYND7
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q16342
- Gene
- PDCD2
- Ensembl
- ENSG00000071994
- Chromosome
- 6
- Canonical length
- 344 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytokinetic bridge
OverviewNCBI Gene
This gene encodes a nuclear protein expressed in a variety of tissues. Expression of this gene has been shown to be repressed by B-cell CLL/lymphoma 6 (BCL6), a transcriptional repressor required for lymph node germinal center development, suggesting that BCL6 regulates apoptosis by its effects on this protein. Alternative splicing results in multiple transcript variants and pseudogenes have been identified on chromosomes 9 and 12. [provided by RefSeq, Dec 2010]
Canonical amino-acid sequenceUniProt
344 residues, UniProt reviewed canonical sequence.
>Q16342|PDCD2
1 MAAAGARPVE LGFAESAPAW RLRSEQFPSK VGGRPAWLGA AGLPGPQALA CELCGRPLSF
61 LLQVYAPLPG RPDAFHRCIF LFCCREQPCC AGLRVFRNQL PRKNDFYSYE PPSENPPPET
121 GESVCLQLKS GAHLCRVCGC LGPKTCSRCH KAYYCSKEHQ TLDWRLGHKQ ACAQPDHLDH
181 IIPDHNFLFP EFEIVIETED EIMPEVVEKE DYSEIIGSMG EALEEELDSM AKHESREDKI
241 FQKFKTQIAL EPEQILRYGR GIAPIWISGE NIPQEKDIPD CPCGAKRILE FQVMPQLLNY
301 LKADRLGKSI DWGILAVFTC AESCSLGTGY TEEFVWKQDV TDTPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PDCD2 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)
- 0.32
- Highest tissue expression
- 47 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 47 nTPM
- pancreas: 43 nTPM
- lymph node: 40 nTPM
- breast: 40 nTPM
- thymus: 39 nTPM
- epididymis: 38 nTPM
Single-cell type
- esophageal basal cells: 138 nCPM
- esophageal suprabasal cells: 133 nCPM
- esophageal apical cells: 113 nCPM
- gastric progenitor cells: 101 nCPM
- differentiating spermatogonia: 101 nCPM
- breast lactating cells: 90 nCPM
Immune cell
- T-reg: 20 nTPM
- NK-cell: 19 nTPM
- myeloid DC: 17 nTPM
- MAIT T-cell: 17 nTPM
- memory CD4 T-cell: 16 nTPM
- plasmacytoid DC: 16 nTPM
Brain region
- cerebellum: 17 nTPM
- hypothalamus: 17 nTPM
- midbrain: 17 nTPM
- cerebral cortex: 16 nTPM
- medulla oblongata: 16 nTPM
- pons: 16 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)
- 1.37
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.05
- DepMap mean gene effect
- -1.21
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic process
- regulation of hematopoietic progenitor cell differentiation
- ribosomal small subunit biogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PDCD2 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 PDCD2 as an antibody target. Whether an autoantibody or antibody against PDCD2 could matter depends on whether native PDCD2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PDCD2 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 PDCD2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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