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ADAMTS13

Gene

ADAM metallopeptidase with thrombospondin type 1 motif 13

HGNCHGNC:1366EnsemblENSG00000160323NCBI Gene11093
Locus: gene with protein productLocation: 9q34.2

Also known as

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

Also known asC9orf8 · FLJ42993 · VWFCP · TTP · vWF-CP · MGC118899 · MGC118900 · DKFZp434C2322
View full nomenclature history (9)
Previous symbolsC9orf8
Alias symbolsFLJ42993, VWFCP, TTP, vWF-CP, MGC118899, MGC118900, DKFZp434C2322
Previous namesa disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 13

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.

Genetic Diseases, Inborn
Thrombosis
COVID-19
Carcinoma, Hepatocellular
Stroke

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.

ADAM metallopeptidases with thrombospondin type 1 motif

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.