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  3. FGB
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Transplant Co-Morbidity Superpanel

Gene: FGB

Green List (high evidence)
FGB (fibrinogen beta chain)
EnsemblGeneIds (GRCh38): ENSG00000171564
EnsemblGeneIds (GRCh37): ENSG00000171564
OMIM: 134830, Gene2Phenotype
FGB is in 7 panels

0 reviews

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Afibrinogenaemia, congenital, MIM# 202400
  • Hypofibrinogenaemia, congenital, MIM# 202400
  • Dysfibrinogenemia, congenital, MIM# 616004
OMIM
134830
Clinvar variants
Variants in FGB
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: FGB was added gene: FGB was added to Transplant Co-Morbidity Superpanel. Sources: Victorian Clinical Genetics Services,Expert Review Green Mode of inheritance for gene: FGB was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FGB were set to 12393540; 16195396 Phenotypes for gene: FGB were set to Afibrinogenaemia, congenital, MIM# 202400; Hypofibrinogenaemia, congenital, MIM# 202400; Dysfibrinogenemia, congenital, MIM# 616004