Seroatlas · Human Serome Atlas

RPL23

Large ribosomal subunit protein uL14

Also known as: L23, RL23_HUMAN, rpL17

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
P62829
Gene
RPL23
Ensembl
ENSG00000125691
Chromosome
17
Canonical length
140 aa
Protein class
Plasma proteins, Predicted intracellular proteins, Ribosomal proteins
Subcellular location
Cytosol

OverviewNCBI Gene

Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L14P family of ribosomal proteins. It is located in the cytoplasm. This gene has been referred to as rpL17 because the encoded protein shares amino acid identity with ribosomal protein L17 from Saccharomyces cerevisiae; however, its official symbol is RPL23. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

140 residues, UniProt reviewed canonical sequence.

>P62829|RPL23
     1  MSKRGRGGSS GAKFRISLGL PVGAVINCAD NTGAKNLYII SVKGIKGRLN RLPAAGVGDM
    61  VMATVKKGKP ELRKKVHPAV VIRQRKSYRR KDGVFLYFED NAGVIVNNKG EMKGSAITGP
   121  VAKECADLWP RIASNAGSIA

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against RPL23 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
4,082 nTPM

Expression across tissuesHPA

Tissue

  • ovary: 4,082 nTPM
  • breast: 2,364 nTPM
  • bone marrow: 2,304 nTPM
  • skin: 2,177 nTPM
  • tonsil: 2,117 nTPM
  • pancreas: 2,016 nTPM

Single-cell type

  • esophageal suprabasal cells: 4,036 nCPM
  • esophageal basal cells: 3,714 nCPM
  • decidual stromal cells: 3,214 nCPM
  • extravillous trophoblasts: 3,205 nCPM
  • ovarian stromal cells: 3,131 nCPM
  • erythrocyte progenitors: 3,098 nCPM

Immune cell

  • total PBMC: 3,247 nTPM
  • plasmacytoid DC: 2,586 nTPM
  • naive CD4 T-cell: 2,481 nTPM
  • memory B-cell: 2,384 nTPM
  • naive B-cell: 2,169 nTPM
  • naive CD8 T-cell: 2,149 nTPM

Brain region

  • spinal cord: 418 nTPM
  • white matter: 410 nTPM
  • medulla oblongata: 394 nTPM
  • hypothalamus: 381 nTPM
  • choroid plexus: 372 nTPM
  • thalamus: 344 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)
0.74
gnomAD pLI
0.33
gnomAD missense Z
1.95
DepMap mean gene effect
-2.65
DepMap dependency class
pan

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of RPL23 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 RPL23 as an antibody target. Whether an autoantibody or antibody against RPL23 could matter depends on whether native RPL23 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

RPL23 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 RPL23 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/RPL23. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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