PDCD7
Programmed cell death protein 7
Also known as: 59K, ES18, HES18, PDCD7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N8D1
- Gene
- PDCD7
- Ensembl
- ENSG00000090470
- Chromosome
- 15
- Canonical length
- 485 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli,Plasma membrane
OverviewNCBI Gene
This gene encodes a 59 kDa protein that is associated with the U11 small nuclear ribonucleoprotein (snRNP), which is a component of the minor U12-type spliceosome responsible for catalyzing pre-mRNA splicing of U12-type introns. [provided by RefSeq, Dec 2010]
Canonical amino-acid sequenceUniProt
485 residues, UniProt reviewed canonical sequence.
>Q8N8D1|PDCD7
1 MALPPFFGQG RPGPPPPQPP PPAPFGCPPP PLPSPAFPPP LPQRPGPFPG ASAPFLQPPL
61 ALQPRASAEA SRGGGGAGAF YPVPPPPLPP PPPQCRPFPG TDAGERPRPP PPGPGPPWSP
121 RWPEAPPPPA DVLGDAALQR LRDRQWLEAV FGTPRRAGCP VPQRTHAGPS LGEVRARLLR
181 ALRLVRRLRG LSQALREAEA DGAAWVLLYS QTAPLRAELA ERLQPLTQAA YVGEARRRLE
241 RVRRRRLRLR ERAREREAER EAEAARAVER EQEIDRWRVK CVQEVEEKKR EQELKAAADG
301 VLSEVRKKQA DTKRMVDILR ALEKLRKLRK EAAARKGVCP PASADETFTH HLQRLRKLIK
361 KRSELYEAEE RALRVMLEGE QEEERKRELE KKQRKEKEKI LLQKREIESK LFGDPDEFPL
421 AHLLEPFRQY YLQAEHSLPA LIQIRHDWDQ YLVPSDHPKG NFVPQGWVLP PLPSNDIWAT
481 AVKLHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PDCD7 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)
- 0.53
- Highest tissue expression
- 18 nTPM
Expression across tissuesHPA
Tissue
- testis: 18 nTPM
- esophagus: 17 nTPM
- ovary: 17 nTPM
- endometrium: 16 nTPM
- cervix: 15 nTPM
- colon: 15 nTPM
Single-cell type
- early primary spermatocytes: 191 nCPM
- retinal bipolar cells: 123 nCPM
- esophageal apical cells: 104 nCPM
- rod photoreceptor cells: 97 nCPM
- cone photoreceptor cells: 93 nCPM
- undifferentiated spermatogonia: 91 nCPM
Immune cell
- NK-cell: 3.3 nTPM
- naive B-cell: 2.4 nTPM
- memory B-cell: 2.3 nTPM
- basophil: 2.1 nTPM
- gdT-cell: 2 nTPM
- naive CD4 T-cell: 2 nTPM
Brain region
- cerebellum: 39 nTPM
- cerebral cortex: 36 nTPM
- white matter: 36 nTPM
- pons: 32 nTPM
- medulla oblongata: 32 nTPM
- thalamus: 31 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about PDCD7.
Disease | ImmuneIEDB
Conditions an epitope on PDCD7 was assayed in.
- hepatocellular carcinoma T cell
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)
- 1.12
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.75
- DepMap mean gene effect
- -0.88
- 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
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Programmed cell death protein 7
- Apoptosis-promoting protein
- Programmed cell death protein 7
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PDCD7 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
- RBM40
- RNPC3
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PDCD7 as an antibody target. Whether an autoantibody or antibody against PDCD7 could matter depends on whether native PDCD7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PDCD7 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 PDCD7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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