RPP40
Ribonuclease P protein subunit p40
Also known as: bA428J1.3, RNASEP1, RPP40_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75818
- Gene
- RPP40
- Ensembl
- ENSG00000124787
- Chromosome
- 6
- Canonical length
- 363 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables ribonuclease P RNA binding activity. Contributes to ribonuclease P activity. Involved in tRNA 5'-leader removal. Part of multimeric ribonuclease P complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
363 residues, UniProt reviewed canonical sequence.
>O75818|RPP40
1 MATLRRLREA PRHLLVCEKS NFGNHKSRHR HLVQTHYYNY RVSFLIPECG ILSEELKNLV
61 MNTGPYYFVK NLPLHELITP EFISTFIKKG SCYALTYNTH IDEDNTVALL PNGKLILSLD
121 KDTYEETGLQ GHPSQFSGRK IMKFIVSIDL MELSLNLDSK KYERISWSFK EKKPLKFDFL
181 LAWHKTGSEE STMMSYFSKY QIQEHQPKVA LSTLRDLQCP VLQSSELEGT PEVSCRALEL
241 FDWLGAVFSN VDLNNEPNNF ISTYCCPEPS TVVAKAYLCT ITGFILPEKI CLLLEHLCHY
301 FDEPKLAPWV TLSVQGFADS PVSWEKNEHG FRKGGEHLYN FVIFNNQDYW LQMAVGANDH
361 CPPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RPP40 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)
- 0.25
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- adrenal gland: 11 nTPM
- esophagus: 8.4 nTPM
- urinary bladder: 7.5 nTPM
- liver: 7 nTPM
- breast: 6.2 nTPM
- skin: 5.8 nTPM
Single-cell type
- oocytes: 120 nCPM
- esophageal basal cells: 42 nCPM
- esophageal suprabasal cells: 35 nCPM
- gastric progenitor cells: 33 nCPM
- differentiating spermatogonia: 32 nCPM
- decidual stromal cells: 30 nCPM
Immune cell
- myeloid DC: 13 nTPM
- intermediate monocyte: 12 nTPM
- T-reg: 9.2 nTPM
- NK-cell: 8.7 nTPM
- memory B-cell: 8.1 nTPM
- naive CD4 T-cell: 7.6 nTPM
Brain region
- hypothalamus: 5.6 nTPM
- white matter: 4.3 nTPM
- pons: 4.2 nTPM
- cerebral cortex: 4.1 nTPM
- spinal cord: 4 nTPM
- midbrain: 3.9 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)
- 0.9
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.24
- DepMap mean gene effect
- -0.88
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- endonucleolytic cleavage in ITS1 to separate SSU-rRNA from 5.8S rRNA and LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)
- tRNA 5'-leader removal
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ribonuclease P protein subunit Rpp40
- Ribonuclease P 40kDa (Rpp40) subunit
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RPP40 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 RPP40 as an antibody target. Whether an autoantibody or antibody against RPP40 could matter depends on whether native RPP40 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RPP40 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 RPP40 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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