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VWA3B

Gene

von Willebrand factor A domain containing 3B

HGNCHGNC:28385EnsemblENSG00000168658NCBI Gene200403
Locus: gene with protein productLocation: 2q11.2

Also known as

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

Also known asDKFZp686F2227 · MGC26733
View full nomenclature history (2)
Alias symbolsDKFZp686F2227, MGC26733

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.

Thrombophilia
Graves' Disease
Barrett Esophagus
Cartilage Diseases

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.

Provenance

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