Cardiac arrhythmias - previous panel
Gene: ANK2EnsemblGeneIds (GRCh38): ENSG00000145362
EnsemblGeneIds (GRCh37): ENSG00000145362
OMIM: 106410, Gene2Phenotype
ANK2 is in 12 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
- Sources
-
- Expert Review Green
- Phenotypes
-
- Brugada/Brugada like syndrome
- Long QT syndrome-4
- Long QT syndrome 4 600919
- Cardiac arrhythmia, ankyrin-B-related 600919
- catecholaminergic polymorphic ventricular tachycardia
- OMIM
- 106410
- Clinvar variants
- Variants in ANK2
- Penetrance
- None
- Panels with this gene
-
- Cardiac arrhythmias - additional genes
- Intellectual disability
- Dilated and arrhythmogenic cardiomyopathy
- DDG2P
- Long QT syndrome
- Paediatric or syndromic cardiomyopathy
- Arrhythmogenic right ventricular cardiomyopathy
- Short QT syndrome
- Early onset or syndromic epilepsy
- Brugada syndrome and cardiac sodium channel disease
- Catecholaminergic polymorphic VT
- Progressive cardiac conduction disease
History Filter Activity
Panel promoted to version 1.0
Ellen McDonagh (Genomics England Curator)Checked against the component panels, and ready to be promoted to version 1.
Set Phenotypes
Rebecca Foulger (Genomics England curator)Added phenotypes Cardiac arrhythmia, ankyrin-B-related 600919; Long QT syndrome 4 600919 for gene: ANK2
Set Phenotypes
Rebecca Foulger (Genomics England curator)Added phenotypes catecholaminergic polymorphic ventricular tachycardia for gene: ANK2
Set Phenotypes
Rebecca Foulger (Genomics England curator)Added phenotypes Brugada/Brugada like syndrome for gene: ANK2
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Rebecca Foulger (Genomics England curator)gene: ANK2 was added gene: ANK2 was added to Cardiac arrythmias. Sources: Expert Review Green Mode of inheritance for gene: ANK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: ANK2 were set to Long QT syndrome-4