F13A1

Gene

coagulation factor XIII A chain

HGNCHGNC:3531 EnsemblENSG00000124491 NCBI Gene2162

Locus: gene with protein productLocation: 6p25.1

Also known as

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

Also known asF13A

View full nomenclature history (2)

Previous symbolsF13A

Previous namescoagulation factor XIII, A1 polypeptide

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 due to thrombin defect

Neurodegenerative Diseases

Placental retention

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.

TransglutaminasesMicroRNA protein coding host genesCoagulation 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.