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  3. FOXF2
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Familial cerebral small vessel disease

Gene: FOXF2

Red List (low evidence)
FOXF2 (forkhead box F2)
EnsemblGeneIds (GRCh38): ENSG00000137273
EnsemblGeneIds (GRCh37): ENSG00000137273
OMIM: 603250, Gene2Phenotype
FOXF2 is in 2 panels

1 review

Louise Daugherty (Genomics England Curator)

Red List (low evidence)

Sources: Literature
Created: 20 Jan 2019, 3:15 p.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Phenotypes
Small vessel stroke

Publications

Created: 20 Jan 2019, 3:15 p.m.

Panel version: 1.6

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
Phenotypes
  • Small vessel stroke
OMIM
603250
Clinvar variants
Variants in FOXF2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

20 Jan 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Louise Daugherty (Genomics England Curator)

gene: FOXF2 was added gene: FOXF2 was added to Familial cerebral small vessel disease. Sources: Literature Mode of inheritance for gene: FOXF2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: FOXF2 were set to 27068588 Phenotypes for gene: FOXF2 were set to Small vessel stroke Review for gene: FOXF2 was set to RED