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F5

Gene

coagulation factor V

HGNCHGNC:3542EnsemblENSG00000198734NCBI Gene2153
Locus: gene with protein productLocation: 1q24.2

Also known as

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

Also known asfV
View full nomenclature history (2)
Alias symbolsfV
Previous namescoagulation factor V (proaccelerin, labile factor)

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.

Ischemic Stroke
Venous Thromboembolism
Pulmonary Embolism
Venous Thrombosis

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.

Multicopper oxidase familyCoagulation factors

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-03-18.
Open TargetsGene–disease associations from the Open Targets Platform.