Back to discover

FBXW10

Gene

F-box and WD repeat domain containing 10

HGNCHGNC:1211EnsemblENSG00000171931NCBI Gene10517
Locus: gene with protein productLocation: 17p11.2

Also known as

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

Also known asC17orf1 · C17orf1A · SM2SH2 · HREP · Fbw10
View full nomenclature history (7)
Previous symbolsC17orf1, C17orf1A
Alias symbolsSM2SH2, HREP, Fbw10
Previous nameschromosome 17 open reading frame 1A, F-box and WD-40 domain protein 10

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.

Spinal Fractures
Carcinoma, Hepatocellular
Neoplasms

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.

WD repeat domain containingF-box and WD repeat domain containing

Provenance

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