POP4
Ribonuclease P protein subunit p29
Also known as: RPP29, RPP29_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95707
- Gene
- POP4
- Ensembl
- ENSG00000105171
- Chromosome
- 19
- Canonical length
- 220 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli
OverviewNCBI Gene
This gene encodes one of the protein subunits of the small nucleolar ribonucleoprotein complexes: the endoribonuclease for mitochondrial RNA processing complex and the ribonuclease P complex. The encoded protein is localized to the nucleus and associates directly with the RNA component of these complexes. This protein is involved in processing of precursor RNAs. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]
Canonical amino-acid sequenceUniProt
220 residues, UniProt reviewed canonical sequence.
>O95707|POP4
1 MKSVIYHALS QKEANDSDVQ PSGAQRAEAF VRAFLKRSTP RMSPQAREDQ LQRKAVVLEY
61 FTRHKRKEKK KKAKGLSARQ RRELRLFDIK PEQQRYSLFL PLHELWKQYI RDLCSGLKPD
121 TQPQMIQAKL LKADLHGAII SVTKSKCPSY VGITGILLQE TKHIFKIITK EDRLKVIPKL
181 NCVFTVETDG FISYIYGSKF QLRSSERSAK KFKAKGTIDLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against POP4 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)
- 0.42
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 13 nTPM
- kidney: 11 nTPM
- blood vessel: 10 nTPM
- heart muscle: 10 nTPM
- adrenal gland: 10 nTPM
- adipose tissue: 9.8 nTPM
Single-cell type
- gastric progenitor cells: 147 nCPM
- late primary spermatocytes: 122 nCPM
- oocytes: 97 nCPM
- esophageal apical cells: 86 nCPM
- esophageal suprabasal cells: 80 nCPM
- hofbauer cells: 78 nCPM
Immune cell
- basophil: 73 nTPM
- T-reg: 53 nTPM
- intermediate monocyte: 52 nTPM
- memory B-cell: 48 nTPM
- total PBMC: 46 nTPM
- non-classical monocyte: 43 nTPM
Brain region
- white matter: 13 nTPM
- medulla oblongata: 12 nTPM
- cerebellum: 12 nTPM
- pons: 12 nTPM
- spinal cord: 12 nTPM
- hypothalamus: 11 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)
- 1.21
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.13
- DepMap mean gene effect
- -0.96
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 12% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
- multimeric ribonuclease P complex
- nucleolus
- nucleoplasm
- ribonuclease MRP complex
- ribonuclease P complex
Protein domainsUniProt · Pfam · InterPro
- Ribonuclease P protein subunit Rpp29/RNP1
- Ribonuclease P/MRP subunit Rpp29
- Rof/RNase P-like
- Ribonuclease P/MRP subunit Rpp29 superfamily
- Ribonuclease P/MRP, subunit p29
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of POP4 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 POP4 as an antibody target. Whether an autoantibody or antibody against POP4 could matter depends on whether native POP4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
POP4 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 POP4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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