RFWD3

Gene

ring finger and WD repeat domain 3

HGNCHGNC:25539 EnsemblENSG00000168411 NCBI Gene55159

Locus: gene with protein productLocation: 16q23.1

Also known as

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

Also known asFLJ10520 · RNF201 · FANCW

View full nomenclature history (3)

Alias symbolsFLJ10520, RNF201, FANCW

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

Multiple Myeloma

Lymphoid neoplasm

Neurodegenerative Diseases

Testicular Neoplasms

Restless Legs Syndrome

Carcinoma, Hepatocellular

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.

Ring finger proteinsWD repeat domain containingFA complementation groups

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.