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FBXO8

Gene

F-box protein 8

HGNCHGNC:13587EnsemblENSG00000164117NCBI Gene26269
Locus: gene with protein productLocation: 4q34.1

Also known as

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

Also known asFBX8 · FBS
View full nomenclature history (3)
Alias symbolsFBX8, FBS
Previous namesF-box only protein 8

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.

Neurodegenerative Diseases
Cataract
Alcohol drinking
Gastrointestinal Neoplasms
Multiple Sclerosis
Actinic keratosis
Muscular Atrophy
Pericarditis
Stroke

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.

F-boxes otherSec7 family

Provenance

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