RPL10L
Ribosomal protein uL16-like
Also known as: RL10L_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96L21
- Gene
- RPL10L
- Ensembl
- ENSG00000165496
- Chromosome
- 14
- Canonical length
- 214 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins, Ribosomal proteins
- Subcellular location
- Endoplasmic reticulum,Cytosol
OverviewNCBI Gene
This gene encodes a protein sharing sequence similarity with ribosomal protein L10. It is not currently known whether the encoded protein is a functional ribosomal protein or whether it has evolved a function that is independent of the ribosome. This gene is intronless. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
214 residues, UniProt reviewed canonical sequence.
>Q96L21|RPL10L
1 MGRRPARCYR YCKNKPYPKS RFCRGVPDAK IRIFDLGRKK AKVDEFPLGG HMVSDEYEQL
61 SSEALEAARI CANKYMVKSC GRDGFHMRVR LHPFHVIRIN KMLSCAGADR LQTGMRGAFG
121 KPQGTVARVH IGQVIMSIRT KLQNEEHVIE ALRRAKFKFP GRQKIHISKK WGFTKFNADE
181 FEDMVAKKCL IPDGCGVKYV PSHGPLDKWR VLHSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RPL10L 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
- 92 nTPM
Expression across tissuesHPA
Tissue
- testis: 92 nTPM
- rectum: 2.5 nTPM
- colon: 2.3 nTPM
- duodenum: 0.6 nTPM
- appendix: 0.2 nTPM
- small intestine: 0.2 nTPM
Single-cell type
- late primary spermatocytes: 892 nCPM
- early spermatids: 527 nCPM
- late spermatids: 280 nCPM
- early primary spermatocytes: 35 nCPM
- undifferentiated spermatogonia: 12 nCPM
- differentiating spermatogonia: 10 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 0.1 nTPM
- hypothalamus: 0.1 nTPM
- medulla oblongata: 0.1 nTPM
- midbrain: 0.1 nTPM
- pons: 0.1 nTPM
- thalamus: 0.1 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about RPL10L.
Disease | AllUniProt
Conditions RPL10L is implicated in, by any mechanism.
- Spermatogenic failure 63 (SPGF63) MIM:619689
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 51 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Spermatogenesis maturation arrest
- Spermatogenic failure 63
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)
- 1.49
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.25
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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 RPL10L 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 RPL10L as an antibody target. Whether an autoantibody or antibody against RPL10L could matter depends on whether native RPL10L is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RPL10L 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 RPL10L as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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