Seroatlas · Human Serome Atlas

MRPL24

Large ribosomal subunit protein uL24m

Also known as: MRP-L18, RM24_HUMAN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q96A35
Gene
MRPL24
Ensembl
ENSG00000143314
Chromosome
1
Canonical length
216 aa
Protein class
Predicted intracellular proteins, Ribosomal proteins

OverviewNCBI Gene

Mammalian mitochondrial ribosomal proteins are encoded by nuclear genes and help in protein synthesis within the mitochondrion. Mitochondrial ribosomes (mitoribosomes) consist of a small 28S subunit and a large 39S subunit. They have an estimated 75% protein to rRNA composition compared to prokaryotic ribosomes, where this ratio is reversed. Another difference between mammalian mitoribosomes and prokaryotic ribosomes is that the latter contain a 5S rRNA. Among different species, the proteins comprising the mitoribosome differ greatly in sequence, and sometimes in biochemical properties, which prevents easy recognition by sequence homology. This gene encodes a 39S subunit protein which is more than twice the size of its E.coli counterpart (EcoL24). Sequence analysis identified two transcript variants that encode the same protein. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

216 residues, UniProt reviewed canonical sequence.

>Q96A35|MRPL24
     1  MRLSALLALA SKVTLPPHYR YGMSPPGSVA DKRKNPPWIR RRPVVVEPIS DEDWYLFCGD
    61  TVEILEGKDA GKQGKVVQVI RQRNWVVVGG LNTHYRYIGK TMDYRGTMIP SEAPLLHRQV
   121  KLVDPMDRKP TEIEWRFTEA GERVRVSTRS GRIIPKPEFP RADGIVPETW IDGPKDTSVE
   181  DALERTYVPC LKTLQEEVME AMGIKETRKY KKVYWY

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against MRPL24 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
141 nTPM

Expression across tissuesHPA

Tissue

  • skeletal muscle: 141 nTPM
  • tongue: 133 nTPM
  • liver: 122 nTPM
  • heart muscle: 102 nTPM
  • pancreas: 95 nTPM
  • epididymis: 89 nTPM

Single-cell type

  • decidual stromal cells: 203 nCPM
  • hepatocytes: 161 nCPM
  • esophageal basal cells: 130 nCPM
  • cytotrophoblasts: 115 nCPM
  • migrating cytotrophoblasts: 114 nCPM
  • esophageal suprabasal cells: 107 nCPM

Immune cell

  • NK-cell: 97 nTPM
  • MAIT T-cell: 96 nTPM
  • total PBMC: 94 nTPM
  • memory B-cell: 88 nTPM
  • naive B-cell: 87 nTPM
  • naive CD8 T-cell: 86 nTPM

Brain region

  • white matter: 55 nTPM
  • cerebellum: 51 nTPM
  • medulla oblongata: 50 nTPM
  • thalamus: 48 nTPM
  • basal ganglia: 48 nTPM
  • hypothalamus: 47 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)
1.35
gnomAD pLI
0
gnomAD missense Z
0.42
DepMap mean gene effect
-0.41
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 11% 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 MRPL24 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 MRPL24 as an antibody target. Whether an autoantibody or antibody against MRPL24 could matter depends on whether native MRPL24 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

MRPL24 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 MRPL24 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/MRPL24. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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