Sudden death in young people
Gene: SLC25A4EnsemblGeneIds (GRCh38): ENSG00000151729
EnsemblGeneIds (GRCh37): ENSG00000151729
OMIM: 103220, Gene2Phenotype
SLC25A4 is in 15 panels
1 review
Rebecca Foulger (Genomics England curator)
Comment on list classification: Changed rating from red to grey: SLC25A4 is red on the V1.8 Hypertrophic Cardiomyopathy panel.Created: 6 Dec 2016, 4:35 p.m.
Details
- Sources
-
- Expert Review Removed
- UKGTN
- Phenotypes
-
- Molecular autopsy
- Familial Hypertrophic Cardiomyopathy
- HCM
- Tags
- OMIM
- 103220
- Clinvar variants
- Variants in SLC25A4
- Penetrance
- Complete
- Panels with this gene
-
- Fetal anomalies
- Sudden death in young people
- White matter disorders and cerebral calcification - narrow panel
- Undiagnosed metabolic disorders
- Mitochondrial DNA maintenance disorder
- Likely inborn error of metabolism
- Inherited white matter disorders
- Paediatric or syndromic cardiomyopathy
- Mitochondrial disorders
- Arthrogryposis
- Congenital myopathy
- Hypertrophic cardiomyopathy
- Childhood onset dystonia, chorea or related movement disorder
- DDG2P
- Possible mitochondrial disorder - nuclear genes
History Filter Activity
Added Tag
Arina Puzriakova (Genomics England Curator)Tag curated_removed tag was added to gene: SLC25A4.
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.
Added New Source
Rebecca Foulger (Genomics England curator)SLC25A4 was added to Sudden death in young peoplepanel. Sources: UKGTN
Created
Rebecca Foulger (Genomics England curator)SLC25A4 was created by rfoulger