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MRPS9

Gene

mitochondrial ribosomal protein S9

HGNCHGNC:14501EnsemblENSG00000135972NCBI Gene64965
Locus: gene with protein productLocation: 2q12.1

Also known as

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

Also known asRPMS9 · MRP-S9 · S9mt · uS9m
View full nomenclature history (5)
Alias symbolsRPMS9, MRP-S9, S9mt, uS9m
Alias names28S ribosomal protein S9, mitochondrial

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.

Neurodegenerative Diseases
Kidney Diseases
Major depressive disorder
Eye Diseases
Duodenal Diseases
Liver 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 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.