MRPS24
Small ribosomal subunit protein uS3m
Also known as: HSPC335, MRP-S24, RT24_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96EL2
- Gene
- MRPS24
- Ensembl
- ENSG00000062582
- Chromosome
- 7
- Canonical length
- 167 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 28S subunit protein. A pseudogene corresponding to this gene is found on chromosome 11. Read-through transcription exists between this gene and the upstream upregulator of cell proliferation (URGCP) gene. [provided by RefSeq, Mar 2011]
Canonical amino-acid sequenceUniProt
167 residues, UniProt reviewed canonical sequence.
>Q96EL2|MRPS24
1 MAASVCSGLL GPRVLSWSRE LPCAWRALHT SPVCAKNRAA RVRVSKGDKP VTYEEAHAPH
61 YIAHRKGWLS LHTGNLDGED HAAERTVEDV FLRKFMWGTF PGCLADQLVL KRRGNQLEIC
121 AVVLRQLSPH KYYFLVGYSE TLLSYFYKCP VRLHLQTVPS KVVYKYLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MRPS24 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
- 427 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 427 nTPM
- tongue: 262 nTPM
- heart muscle: 237 nTPM
- liver: 179 nTPM
- kidney: 176 nTPM
- adrenal gland: 166 nTPM
Single-cell type
- other brain neurons: 25 nCPM
- brain excitatory neurons: 20 nCPM
- hepatocytes: 19 nCPM
- brain inhibitory neurons: 18 nCPM
- parietal cells: 18 nCPM
- ependymal cells: 15 nCPM
Immune cell
- myeloid DC: 242 nTPM
- memory B-cell: 224 nTPM
- T-reg: 215 nTPM
- naive B-cell: 197 nTPM
- intermediate monocyte: 182 nTPM
- non-classical monocyte: 182 nTPM
Brain region
- thalamus: 73 nTPM
- hypothalamus: 68 nTPM
- choroid plexus: 67 nTPM
- cerebellum: 67 nTPM
- cerebral cortex: 60 nTPM
- amygdala: 56 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)
- 1.15
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.09
- DepMap mean gene effect
- -0.37
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% 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 uS3m, metazoan
- Mitochondrial ribosome subunit S24
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MRPS24 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 MRPS24 as an antibody target. Whether an autoantibody or antibody against MRPS24 could matter depends on whether native MRPS24 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MRPS24 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 MRPS24 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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