ADAMTS13 Chromosome 9

ADAM metallopeptidase with thrombospondin type 1 motif 13
166 variants 166 Health Risk

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What This Gene Does
This gene encodes a member of a family of proteins containing several distinct regions, including a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. The enzyme encoded by this gene specifically cleaves von Willebrand Factor (vWF). Defects in this gene are associated with thrombotic thrombocytopenic purpura. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Gene Info
Gene Group
ADAM metallopeptidases with thrombospondin type 1 motif
Locus Type
gene with protein product
Location
9q34.2
Ensembl
ENSG00000160323
Associated Conditions (11)
Upshaw-Schulman syndrome
Inborn genetic diseases
ADAMTS13-related disorder
Thrombus
See cases
Ovarian serous cystadenocarcinoma
Cervical cancer
Atypical hemolytic-uremic syndrome
Thrombotic thrombocytopenic purpura
Thrombocytopenia
Abnormal bleeding
Key Variants
RS11575933
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
Health Risk
RS1183963868
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS138014548
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
Health Risk
RS138489501
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
Health Risk
RS138699340
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Inborn genetic diseases, Upshaw-Schulman syndrome
Health Risk
RS139214644
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Inborn genetic diseases, ADAMTS13-related disorder
Health Risk
RS1393965473
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
Health Risk
RS139951127
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
Health Risk
RS140628579
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
Health Risk
RS140639242
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Thrombus, ADAMTS13-related disorder
Health Risk
RS141811556
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
Health Risk
RS142214608
Conflicting classifications of pathogenicity
Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
Health Risk
All Variants (166)
RSID Category Clinical Significance Conditions
RS372953477 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS373530345 Health Risk Conflicting classifications of pathogenicity ADAMTS13-related disorder, Upshaw-Schulman syndrome, ADAMTS13-related disorder
RS373569027 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS374444423 Health Risk Conflicting classifications of pathogenicity ADAMTS13-related disorder, Upshaw-Schulman syndrome, ADAMTS13-related disorder
RS374606481 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Inborn genetic diseases, Upshaw-Schulman syndrome
RS375335095 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS377220995 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Upshaw-Schulman syndrome, Inborn genetic diseases
RS377454829 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS587602874 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS587701622 Health Risk Conflicting classifications of pathogenicity
RS587750566 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS587768675 Health Risk Conflicting classifications of pathogenicity
RS754541465 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS756898709 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS762112077 Health Risk Conflicting classifications of pathogenicity See cases, Inborn genetic diseases, See cases
RS77985067 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS781862563 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS781938740 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS781945326 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS782090689 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS782109481 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Upshaw-Schulman syndrome, Inborn genetic diseases
RS782235228 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS782239711 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS782311486 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Inborn genetic diseases, Upshaw-Schulman syndrome
RS782472825 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Inborn genetic diseases, Upshaw-Schulman syndrome
RS782604159 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Inborn genetic diseases, Upshaw-Schulman syndrome
RS782661001 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS782724202 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS782748173 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS886063636 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS898957135 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS944652890 Health Risk Conflicting classifications of pathogenicity Upshaw-Schulman syndrome, Inborn genetic diseases, Upshaw-Schulman syndrome
RS1060499780 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS121908471 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS1474290508 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS1554785114 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS1554789680 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS1554793379 Health Risk Likely pathogenic
RS1554795391 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS1554796161 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS1554797078 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS1841759683 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS201457594 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS2130769073 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS2130845614 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
RS2491096625 Health Risk Likely pathogenic
RS2491124231 Health Risk Likely pathogenic ADAMTS13-related disorder, ADAMTS13-related disorder
RS2491164601 Health Risk Likely pathogenic ADAMTS13-related disorder, ADAMTS13-related disorder
RS2491212714 Health Risk Likely pathogenic
RS2491219604 Health Risk Likely pathogenic Upshaw-Schulman syndrome, Upshaw-Schulman syndrome
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