F7

Gene

coagulation factor VII

HGNCHGNC:3544 EnsemblENSG00000057593 NCBI Gene2155

Locus: gene with protein productLocation: 13q34

Also known as

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

View full nomenclature history (4)

Previous namescoagulation factor VII (serum prothrombin conversion accelerator)

Alias nameseptacog alfa, FVII coagulation protein, factor VII

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.

Hemophilia B

Hemophilia A

Blood Coagulation Disorders

Cerebral Hemorrhage

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.

Serine proteasesGla domain containingCoagulation factors

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.