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POLR3H

Gene

RNA polymerase III subunit H

HGNCHGNC:30349EnsemblENSG00000100413NCBI Gene171568
Locus: gene with protein productLocation: 22q13.2

Also known as

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

Also known asRPC8 · KIAA1665 · C25
View full nomenclature history (4)
Alias symbolsRPC8, KIAA1665, C25
Previous namespolymerase (RNA) III (DNA directed) polypeptide H (22.9kD)

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.

Optic Atrophy
Genetic Diseases, Inborn
Neurodegenerative Diseases
46,XX gonadal dysgenesis
Iron Metabolism Disorders
Primary Ovarian Insufficiency

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.

RNA polymerase 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.