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  3. F10
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Factor X deficiency

Gene: F10

Green List (high evidence)
F10 (coagulation factor X)
EnsemblGeneIds (GRCh38): ENSG00000126218
EnsemblGeneIds (GRCh37): ENSG00000126218
OMIM: 613872, Gene2Phenotype
F10 is in 3 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 #227600) and the OMIM record was last accessed on 18 December 2025.
Created: 18 Dec 2025, 10:40 a.m. | Last Modified: 18 Dec 2025, 10:40 a.m.
Panel Version: 1.2
F10 has been added to the panel for R119 Factor X deficiency with a green rating as agreed with the NHS Genomic Medicine Service.
Created: 30 Jun 2023, 1:04 p.m. | Last Modified: 30 Jun 2023, 1:04 p.m.
Panel Version: 0.1

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Created: 30 Jun 2023, 1:04 p.m.
Last Modified: 30 Jun 2023, 1:04 p.m.
Panel version: 0.1

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Factor X deficiency, OMIM:227600
  • congenital factor X deficiency, MONDO:0009212
OMIM
613872
Clinvar variants
Variants in F10
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: F10 were changed from to Factor X deficiency, OMIM:227600; congenital factor X deficiency, MONDO:0009212

29 Jun 2023, Gel status: 3

Created, Added New Source, Set mode of inheritance

Achchuthan Shanmugasundram (Genomics England Curator)

gene: F10 was added gene: F10 was added to Factor X deficiency. Sources: NHS GMS,Expert Review Green Mode of inheritance for gene: F10 was set to BIALLELIC, autosomal or pseudoautosomal