RPL26L1
Ribosomal protein uL24-like
Also known as: RL26L_HUMAN, RPL26P1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UNX3
- Gene
- RPL26L1
- Ensembl
- ENSG00000037241
- Chromosome
- 5
- Canonical length
- 145 aa
- Protein class
- Predicted intracellular proteins, Ribosomal proteins
- Subcellular location
- Nucleoli,Endoplasmic reticulum,Cytosol
OverviewNCBI Gene
This gene encodes a protein that shares high sequence similarity with ribosomal protein L26. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Dec 2015]
Canonical amino-acid sequenceUniProt
145 residues, UniProt reviewed canonical sequence.
>Q9UNX3|RPL26L1
1 MKFNPFVTSD RSKNRKRHFN APSHVRRKIM SSPLSKELRQ KYNVRSMPIR KDDEVQVVRG
61 HYKGQQIGKV VQVYRKKYVI YIERVQREKA NGTTVHVGIH PSKVVITRLK LDKDRKKILE
121 RKAKSRQVGK EKGKYKEELI EKMQELocalizationUniProt · AlphaFold · HPA
Whether an antibody against RPL26L1 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)
- 0.38
- Highest tissue expression
- 87 nTPM
Expression across tissuesHPA
Tissue
- testis: 87 nTPM
- kidney: 46 nTPM
- liver: 45 nTPM
- adrenal gland: 43 nTPM
- bone marrow: 37 nTPM
- skeletal muscle: 36 nTPM
Single-cell type
- late primary spermatocytes: 611 nCPM
- early spermatids: 334 nCPM
- early primary spermatocytes: 188 nCPM
- oocytes: 161 nCPM
- differentiating spermatogonia: 146 nCPM
- esophageal basal cells: 135 nCPM
Immune cell
- myeloid DC: 100 nTPM
- classical monocyte: 87 nTPM
- intermediate monocyte: 81 nTPM
- non-classical monocyte: 73 nTPM
- plasmacytoid DC: 68 nTPM
- T-reg: 56 nTPM
Brain region
- cerebral cortex: 26 nTPM
- hippocampal formation: 26 nTPM
- pons: 26 nTPM
- hypothalamus: 24 nTPM
- cerebellum: 24 nTPM
- thalamus: 24 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)
- 1.58
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.23
- DepMap mean gene effect
- -0.42
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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
- Large ribosomal subunit protein uL24, eukaryota_archaea
- KOW
- Large ribosomal subunit protein uL24, conserved site
- Translation protein SH3-like domain superfamily
- Large ribosomal subunit protein uL2, domain 2
- Large ribosomal subunit protein uL24, KOW domain
- KOW motif
- Ribosomal proteins L26 eukaryotic, L24P archaeal
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RPL26L1 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 RPL26L1 as an antibody target. Whether an autoantibody or antibody against RPL26L1 could matter depends on whether native RPL26L1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RPL26L1 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 RPL26L1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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