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CMSS1

Gene

cms1 ribosomal small subunit homolog

HGNCHGNC:28666EnsemblENSG00000184220NCBI Gene84319
Locus: gene with protein productLocation: 3q12.1

Also known as

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

Also known asC3orf26 · MGC4308
View full nomenclature history (4)
Previous symbolsC3orf26
Alias symbolsMGC4308
Previous nameschromosome 3 open reading frame 26, cms1 ribosomal small subunit homolog (yeast)

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.

Anemia
Atrioventricular Block
Atrial Fibrillation
Basal cell carcinoma
Osteoarthritis, Knee

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.

Provenance

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