Genes in panel
Regions in panel
Prev Next

Mendeliome

Gene: F7

Green List (high evidence)

F7 (coagulation factor VII)
EnsemblGeneIds (GRCh38): ENSG00000057593
EnsemblGeneIds (GRCh37): ENSG00000057593
OMIM: 613878, Gene2Phenotype
F7 is in 7 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

Variable severity of bleeding, well established gene-disease association.
Created: 2 Jun 2021, 8:31 p.m. | Last Modified: 2 Jun 2021, 8:31 p.m.
Panel Version: 0.7758

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

2 Jun 2021, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: f7 has been classified as Green List (High Evidence).

2 Jun 2021, Gel status: 3

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

2 Jun 2021, Gel status: 3

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: F7 were set to

2 Jun 2021, Gel status: 3

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

17 Nov 2019, Gel status: 3

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 Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: F7 was set to Unknown