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  3. F13A1
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Factor XIII deficiency

Gene: F13A1

Green List (high evidence)
F13A1 (coagulation factor XIII A chain)
EnsemblGeneIds (GRCh38): ENSG00000124491
EnsemblGeneIds (GRCh37): ENSG00000124491
OMIM: 134570, Gene2Phenotype
F13A1 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 #613225) and the OMIM record was last accessed on 18 December 2025.
Created: 18 Dec 2025, 10:44 a.m. | Last Modified: 18 Dec 2025, 10:44 a.m.
Panel Version: 1.2
F13A1 has been added to the panel for R122 Factor XIII deficiency with a green rating as agreed with the NHS Genomic Medicine Service.
Created: 30 Jun 2023, 1:07 p.m. | Last Modified: 30 Jun 2023, 1:07 p.m.
Panel Version: 0.1

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Created: 30 Jun 2023, 1:07 p.m.
Last Modified: 30 Jun 2023, 1:07 p.m.
Panel version: 0.1

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Factor XIIIA deficiency, OMIM:613225
  • factor XIII, A subunit, deficiency of, MONDO:0013187
OMIM
134570
Clinvar variants
Variants in F13A1
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: F13A1 were changed from to Factor XIIIA deficiency, OMIM:613225; factor XIII, A subunit, deficiency of, MONDO:0013187

29 Jun 2023, Gel status: 3

Created, Added New Source, Set mode of inheritance

Achchuthan Shanmugasundram (Genomics England Curator)

gene: F13A1 was added gene: F13A1 was added to Factor XIII deficiency. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: F13A1 was set to BIALLELIC, autosomal or pseudoautosomal