SERPINE1

serpin family E member 1
OMIM: 173360, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green SERPINE1 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.43

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Plasminogen activator inhibitor-1 deficiency, MIM# 613329

Green SERPINE1 in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Plasminogen activator inhibitor-1 deficiency, MIM# 613329

Green SERPINE1 in Transplant Co-Morbidity Superpanel


Level 2: Screening
Version 0.18

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Plasminogen activator inhibitor-1 deficiency, MIM# 613329