Familial Genetic Generalised Epilepsies
Gene: TRAK1EnsemblGeneIds (GRCh38): ENSG00000182606
EnsemblGeneIds (GRCh37): ENSG00000182606
OMIM: 608112, Gene2Phenotype
TRAK1 is in 3 panels
1 review
Sarah Leigh (Genomics England Curator)
c.287-2A>C homozygous variant reported in four cases in three apparently unrelated Israeli families (no haplotype information provided), segregation with condition reported with disease in these families. Functional studies included. From PMID 28364549Created: 4 May 2017, 12:04 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Fatal encephalopathy
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- Fatal encephalopathy
- OMIM
- 608112
- Clinvar variants
- Variants in TRAK1
- Penetrance
- Complete
- Publications
- Panels with this gene
History Filter Activity
Gene classified by Genomics England curator
Sarah Leigh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Added New Source
Sarah Leigh (Genomics England Curator)TRAK1 was added to Familial Genetic Generalised Epilepsiespanel. Sources: Literature
Created
Sarah Leigh (Genomics England Curator)TRAK1 was created by sleigh