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  2. Bleeding and Platelet Disorders
  3. SERPINF2
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Bleeding and Platelet Disorders

Gene: SERPINF2

Green List (high evidence)
SERPINF2 (serpin family F member 2)
EnsemblGeneIds (GRCh38): ENSG00000167711
EnsemblGeneIds (GRCh37): ENSG00000167711
OMIM: 613168, Gene2Phenotype
SERPINF2 is in 3 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

Mode of inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal

Phenotypes
Alpha-2-plasmin inhibitor deficiency, MIM# 262850

Publications

Created: 4 Jun 2021, 2:38 a.m.
Last Modified: 4 Jun 2021, 2:38 a.m.
Panel version: 0.304

Details

Mode of Inheritance
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Alpha-2-plasmin inhibitor deficiency, MIM# 262850
OMIM
613168
Clinvar variants
Variants in SERPINF2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

4 Jun 2021, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: serpinf2 has been classified as Green List (High Evidence).

4 Jun 2021, Gel status: 3

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: SERPINF2 were changed from to Alpha-2-plasmin inhibitor deficiency, MIM# 262850

4 Jun 2021, Gel status: 3

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: SERPINF2 were set to

4 Jun 2021, Gel status: 3

Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Mode of inheritance for gene: SERPINF2 was changed from Unknown to BOTH monoallelic and 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: SERPINF2 was added gene: SERPINF2 was added to Bleeding Disorders_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: SERPINF2 was set to Unknown