Transplant Co-Morbidity Superpanel
Gene: SERPINE1
SERPINE1 (serpin family E member 1)
EnsemblGeneIds (GRCh38): ENSG00000106366
EnsemblGeneIds (GRCh37): ENSG00000106366
OMIM: 173360, Gene2Phenotype
SERPINE1 is in 3 panels
EnsemblGeneIds (GRCh38): ENSG00000106366
EnsemblGeneIds (GRCh37): ENSG00000106366
OMIM: 173360, Gene2Phenotype
SERPINE1 is in 3 panels
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Details
- Mode of Inheritance
- 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
- OMIM
- 173360
- Clinvar variants
- Variants in SERPINE1
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
1 Aug 2023, Gel status: 3
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)gene: SERPINE1 was added gene: SERPINE1 was added to Transplant Co-Morbidity Superpanel. Sources: Victorian Clinical Genetics Services,Expert Review Green Mode of inheritance for gene: SERPINE1 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal Publications for gene: SERPINE1 were set to 15650551; 9207454 Phenotypes for gene: SERPINE1 were set to Plasminogen activator inhibitor-1 deficiency, MIM# 613329