MRPL18
Large ribosomal subunit protein uL18m
Also known as: HSPC071, RM18_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H0U6
- Gene
- MRPL18
- Ensembl
- ENSG00000112110
- Chromosome
- 6
- Canonical length
- 180 aa
- Protein class
- Predicted intracellular proteins, Ribosomal proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
This nuclear gene encodes a protein component of the larger 39S subunit of mitochondrial ribosome. This protein may also aid in the import of nuclear-encoded 5S rRNA into mitochondria. Alternative splicing results in multiple transcript variants, most of which are not predicted to encode a protein. A pseudogene of this gene is found on chromosome 16. [provided by RefSeq, Jan 2016]
Canonical amino-acid sequenceUniProt
180 residues, UniProt reviewed canonical sequence.
>Q9H0U6|MRPL18
1 MALRSRFWGL FSVCRNPGCR FAALSTSSEP AAKPEVDPVE NEAVAPEFTN RNPRNLELLS
61 VARKERGWRT VFPSREFWHR LRVIRTQHHV EALVEHQNGK VVVSASTREW AIKKHLYSTR
121 NVVACESIGR VLAQRCLEAG INFMVYQPTP WEAASDSMKR LQSAMTEGGV VLREPQRIYELocalizationUniProt · AlphaFold · HPA
Whether an antibody against MRPL18 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)
- 0.43
- Highest tissue expression
- 73 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 73 nTPM
- tongue: 69 nTPM
- cerebral cortex: 62 nTPM
- liver: 62 nTPM
- heart muscle: 61 nTPM
- amygdala: 60 nTPM
Single-cell type
- pancreatic duct cells: 489 nCPM
- oocytes: 295 nCPM
- early primary spermatocytes: 263 nCPM
- epididymal principal cells: 251 nCPM
- epididymal efferent duct absorptive cells: 239 nCPM
- megakaryocytes: 235 nCPM
Immune cell
- total PBMC: 193 nTPM
- non-classical monocyte: 177 nTPM
- plasmacytoid DC: 168 nTPM
- memory B-cell: 155 nTPM
- intermediate monocyte: 153 nTPM
- T-reg: 138 nTPM
Brain region
- cerebral cortex: 60 nTPM
- white matter: 46 nTPM
- cerebellum: 40 nTPM
- hypothalamus: 38 nTPM
- basal ganglia: 37 nTPM
- spinal cord: 37 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)
- 1.31
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.35
- DepMap mean gene effect
- -0.39
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 1% 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
- Small ribosomal subunit protein uS11 superfamily
- Large ribosomal subunit protein uL18
- Large ribosomal subunit protein uL18, bacterial/plantae/animalia
- Ribosomal L18 of archaea, bacteria, mitoch. and chloroplast
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MRPL18 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 MRPL18 as an antibody target. Whether an autoantibody or antibody against MRPL18 could matter depends on whether native MRPL18 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MRPL18 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 MRPL18 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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