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BAZ1B

Gene

bromodomain adjacent to zinc finger domain 1B

HGNCHGNC:961EnsemblENSG00000009954NCBI Gene9031
Locus: gene with protein productLocation: 7q11.23

Also known as

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

Also known asWBSCR9 · WBSCR10 · WSTF
View full nomenclature history (6)
Previous symbolsWBSCR9, WBSCR10
Alias symbolsWSTF
Alias namesWilliams-Beuren syndrome chromosome region 9, Williams-Beuren syndrome chromosome region 10, transcription factor WSTF

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
Gout
Hyperuricemia
Hyperlipidemias
Non-alcoholic Fatty Liver Disease
Metabolic Diseases
Familial lipoprotein lipase deficiency
Heart Failure
Williams Syndrome

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.

PHD finger proteinsBromodomain containingB-WICH chromatin-remodelling complex subunitsWICH complex

Provenance

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