Back to discover

RAD51C

Gene

RAD51 paralog C

HGNCHGNC:9820EnsemblENSG00000108384NCBI Gene5889
Locus: gene with protein productLocation: 17q22

Also known as

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

Also known asRAD51L2 · FANCO
View full nomenclature history (4)
Alias symbolsRAD51L2, FANCO
Previous namesRAD51 (S. cerevisiae) homolog C, RAD51 homolog C (S. cerevisiae)

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.

Fanconi Anemia
Ovarian Neoplasms
Neoplasms
Inherited cancer-predisposing syndrome
Neoplastic Syndromes, Hereditary
Ovarian carcinoma

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.

FA complementation groupsRAD51 paralogs

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.