RPL36A
Large ribosomal subunit protein eL42
Also known as: L36A, RL36A_HUMAN, RPL44
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P83881
- Gene
- RPL36A
- Ensembl
- ENSG00000241343
- Chromosome
- X
- Canonical length
- 106 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins, Ribosomal proteins
- Subcellular location
- Endoplasmic reticulum,Plasma membrane,Cytosol
OverviewNCBI Gene
Cytoplasmic ribosomes, 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, which shares sequence similarity with yeast ribosomal protein L44, belongs to the L44E (L36AE) family of ribosomal proteins. Although this gene has been referred to as ribosomal protein L44 (RPL44), its official name is ribosomal protein L36a (RPL36A). This gene and the human gene officially named ribosomal protein L36a-like (RPL36AL) encode nearly identical proteins; however, they are distinct genes. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Naturally occurring read-through transcription occurs between this locus and the heterogeneous nuclear ribonucleoprotein H2 (H') gene. [provided by RefSeq, Jan 2011]
Canonical amino-acid sequenceUniProt
106 residues, UniProt reviewed canonical sequence.
>P83881|RPL36A
1 MVNVPKTRRT FCKKCGKHQP HKVTQYKKGK DSLYAQGKRR YDRKQSGYGG QTKPIFRKKA
61 KTTKKIVLRL ECVEPNCRSK RMLAIKRCKH FELGGDKKRK GQVIQFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RPL36A 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)
- 0.47
- Highest tissue expression
- 2,024 nTPM
Expression across tissuesHPA
Tissue
- ovary: 2,024 nTPM
- pancreas: 1,447 nTPM
- skin: 1,376 nTPM
- cervix: 1,090 nTPM
- esophagus: 1,045 nTPM
- vagina: 1,021 nTPM
Single-cell type
- enteric stem cells: 2,483 nCPM
- enteric transient amplifying cells: 2,165 nCPM
- paneth cells: 1,972 nCPM
- epididymal efferent duct absorptive cells: 1,777 nCPM
- goblet cells: 1,513 nCPM
- gastric chief cells: 1,409 nCPM
Immune cell
- total PBMC: 1,802 nTPM
- naive CD4 T-cell: 1,326 nTPM
- memory B-cell: 1,246 nTPM
- memory CD4 T-cell: 1,216 nTPM
- naive CD8 T-cell: 1,183 nTPM
- MAIT T-cell: 1,104 nTPM
Brain region
- white matter: 73 nTPM
- medulla oblongata: 61 nTPM
- spinal cord: 59 nTPM
- hypothalamus: 48 nTPM
- thalamus: 46 nTPM
- pons: 44 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)
- 0.89
- gnomAD pLI
- 0.43
- gnomAD missense Z
- 0.74
- DepMap mean gene effect
- -1.49
- DepMap dependency class
- common
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
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads RPL36A as an antibody target. Whether an autoantibody or antibody against RPL36A could matter depends on whether native RPL36A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RPL36A 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 RPL36A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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