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WDSUB1

Gene

WD repeat, sterile alpha motif and U-box domain containing 1

HGNCHGNC:26697EnsemblENSG00000196151NCBI Gene151525
Locus: gene with protein productLocation: 2q24.2

Also known as

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

Also known asWDSAM1 · UBOX6 · FLJ36175
View full nomenclature history (5)
Previous symbolsWDSAM1
Alias symbolsUBOX6, FLJ36175
Previous namesWD repeat, SAM and U-box domain containing 1, WD repeat and SAM domain containing 1

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
Joint Diseases
Liver Diseases
Cardiomyopathies
Restless Legs Syndrome
Autoimmune disorder of central nervous system
Death, Sudden, Cardiac

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 containingU-box domain containingSterile alpha motif 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.