Back to discover

RSPH9

Gene

radial spoke head component 9

HGNCHGNC:21057EnsemblENSG00000172426NCBI Gene221421
Locus: gene with protein productLocation: 6p21.1

Also known as

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

Also known asMRPS18AL1 · C6orf206 · FLJ30845 · CILD12
View full nomenclature history (7)
Previous symbolsMRPS18AL1, C6orf206
Alias symbolsFLJ30845, CILD12
Previous namesmitochondrial ribosomal protein S18A-like 1, chromosome 6 open reading frame 206, radial spoke head 9 homolog (Chlamydomonas)

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.

Kartagener Syndrome
Bronchiectasis
Alcohol drinking
Urolithiasis
Metabolic Syndrome
Genetic developmental and epileptic encephalopathy

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.

Axonemal radial spoke subunits

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.