RPL22L1
Ribosomal protein eL22-like
Also known as: RL22L_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6P5R6
- Gene
- RPL22L1
- Ensembl
- ENSG00000163584
- Chromosome
- 3
- Canonical length
- 122 aa
- Protein class
- Predicted intracellular proteins, Ribosomal proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Nucleoli rim
OverviewNCBI Gene
Predicted to enable RNA binding activity. Predicted to be a structural constituent of ribosome. Predicted to be involved in cytoplasmic translation. Predicted to be located in ribosome. Predicted to be part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
122 residues, UniProt reviewed canonical sequence.
>Q6P5R6|RPL22L1
1 MAPQKDRKPK RSTWRFNLDL THPVEDGIFD SGNFEQFLRE KVKVNGKTGN LGNVVHIERF
61 KNKITVVSEK QFSKRYLKYL TKKYLKKNNL RDWLRVVASD KETYELRYFQ ISQDEDESES
121 EDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RPL22L1 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)
- 0.39
- Highest tissue expression
- 88 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 88 nTPM
- esophagus: 73 nTPM
- lymph node: 70 nTPM
- spleen: 66 nTPM
- appendix: 61 nTPM
- tonsil: 59 nTPM
Single-cell type
- esophageal basal cells: 807 nCPM
- esophageal suprabasal cells: 694 nCPM
- gastric progenitor cells: 542 nCPM
- erythrocyte progenitors: 479 nCPM
- decidual stromal cells: 458 nCPM
- plasma cells: 453 nCPM
Immune cell
- plasmacytoid DC: 51 nTPM
- memory B-cell: 47 nTPM
- naive B-cell: 35 nTPM
- NK-cell: 29 nTPM
- MAIT T-cell: 27 nTPM
- memory CD4 T-cell: 20 nTPM
Brain region
- white matter: 16 nTPM
- medulla oblongata: 7.7 nTPM
- basal ganglia: 7.5 nTPM
- pons: 7.5 nTPM
- cerebral cortex: 7.2 nTPM
- thalamus: 7.1 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)
- 1.56
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.35
- DepMap mean gene effect
- -0.21
- DepMap dependency class
- selective
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 RPL22L1 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 RPL22L1 as an antibody target. Whether an autoantibody or antibody against RPL22L1 could matter depends on whether native RPL22L1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RPL22L1 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 RPL22L1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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