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FBXW12

Gene

F-box and WD repeat domain containing 12

HGNCHGNC:20729EnsemblENSG00000164049NCBI Gene285231
Locus: gene with protein productLocation: 3p21.31

Also known as

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

Also known asFBXO35 · Fbw12
View full nomenclature history (4)
Previous symbolsFBXO35
Alias symbolsFbw12
Previous namesF-box only protein 35, F-box and WD-40 domain protein 12

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.

Myelofibrosis
Primary myelofibrosis

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.