Bleeding and Platelet Disorders
Gene: F7EnsemblGeneIds (GRCh38): ENSG00000057593
EnsemblGeneIds (GRCh37): ENSG00000057593
OMIM: 613878, Gene2Phenotype
F7 is in 7 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Variable severity of bleeding, well established gene-disease association.Created: 2 Jun 2021, 8:28 p.m. | Last Modified: 2 Jun 2021, 8:28 p.m.
Panel Version: 0.245
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Factor VII deficiency, MIM# 227500; MONDO:0009211
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Victorian Clinical Genetics Services
- Phenotypes
-
- Factor VII deficiency, MIM# 227500
- MONDO:0009211
- OMIM
- 613878
- Clinvar variants
- Variants in F7
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: f7 has been classified as Green List (High Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: F7 were changed from to Factor VII deficiency, MIM# 227500; MONDO:0009211
Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Publications for gene: F7 were set to
Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Mode of inheritance for gene: F7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Created, Added New Source, Set mode of inheritance
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: F7 was added gene: F7 was added to Bleeding Disorders_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: F7 was set to Unknown