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  3. F7
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Factor VII deficiency

Gene: F7

Green List (high evidence)
F7 (coagulation factor VII)
EnsemblGeneIds (GRCh38): ENSG00000057593
EnsemblGeneIds (GRCh37): ENSG00000057593
OMIM: 613878, Gene2Phenotype
F7 is in 4 panels

1 review

Achchuthan Shanmugasundram (Genomics England Curator)

Green List (high evidence)

Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #227500) and the OMIM record was last accessed on 18 December 2025.
Created: 18 Dec 2025, 10:36 a.m. | Last Modified: 18 Dec 2025, 10:36 a.m.
Panel Version: 1.2
F7 has been added to the panel for R116 Factor VII deficiency with a green rating as agreed with the NHS Genomic Medicine Service.
Created: 30 Jun 2023, 1:02 p.m. | Last Modified: 30 Jun 2023, 1:02 p.m.
Panel Version: 0.1

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Created: 30 Jun 2023, 1:02 p.m.
Last Modified: 30 Jun 2023, 1:02 p.m.
Panel version: 0.1

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Factor VII deficiency, OMIM:227500
  • congenital factor VII deficiency, MONDO:0009211
OMIM
613878
Clinvar variants
Variants in F7
Penetrance
None
Panels with this gene

History Filter Activity

18 Dec 2025, Gel status: 3

Set Phenotypes

Achchuthan Shanmugasundram (Genomics England Curator)

Phenotypes for gene: F7 were changed from to Factor VII deficiency, OMIM:227500; congenital factor VII deficiency, MONDO:0009211

29 Jun 2023, Gel status: 3

Created, Added New Source, Set mode of inheritance

Achchuthan Shanmugasundram (Genomics England Curator)

gene: F7 was added gene: F7 was added to Factor VII deficiency. Sources: NHS GMS,Expert Review Green Mode of inheritance for gene: F7 was set to BIALLELIC, autosomal or pseudoautosomal