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MRPS22

Gene

mitochondrial ribosomal protein S22

HGNCHGNC:14508EnsemblENSG00000175110NCBI Gene56945
Locus: gene with protein productLocation: 3q23

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asMRP-S22 · GK002 · C3orf5 · GIBT · mS22
View full nomenclature history (5)
Alias symbolsMRP-S22, GK002, C3orf5, GIBT, mS22

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

46,XX gonadal dysgenesis
Neurodegenerative Diseases
Genetic Diseases, Inborn
Alopecia
Mitochondrial Diseases

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Mitochondrial ribosomal proteinsSmall subunit mitochondrial ribosomal proteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-07-07.
Open TargetsGene–disease associations from the Open Targets Platform.