Sudden death in young people
Gene: FEVEnsemblGeneIds (GRCh38): ENSG00000163497
EnsemblGeneIds (GRCh37): ENSG00000163497
OMIM: 607150, Gene2Phenotype
FEV is in 1 panel
1 review
Rebecca Foulger (Genomics England curator)
Comment on list classification: Changed rating from red to grey: PMID:17597646 reports 3 polymorphisms in the FEV gene (two in exon 3, and one in the preceeding intron) but they are found in both SIDS cases and matched controls. They also report a heterozygous insertion mutation (IVS-191_190insA) upstream of the 5' exon 3 splice site in the FEV gene, which is unique to African-American SIDS cases. However PMID:19707175 report that this insertion polymorphism seems to be a common, likely nonpathogenic, variant in the African-American population.Created: 6 Dec 2016, 4:33 p.m.
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Removed
- Literature
- Phenotypes
-
- SIDS
- Sudden infant death syndrome
- Tags
- OMIM
- 607150
- Clinvar variants
- Variants in FEV
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
Added Tag
Arina Puzriakova (Genomics England Curator)Tag curated_removed tag was added to gene: FEV.
panel promoted to version 1
Ellen Thomas (Genomics England Curator)This panel contains genes which aren't arrhythmic or metabolic causes of sudden death with normal post mortem.
Gene classified by Genomics England curator
Rebecca Foulger (Genomics England curator)This gene has been removed from the panel.
Created
Rebecca Foulger (Genomics England curator)FEV was created by rfoulger
Added New Source
Rebecca Foulger (Genomics England curator)FEV was added to Sudden death in young peoplepanel. Sources: Literature