Progressive cardiac conduction disease
Gene: ANK2
Comment on phenotypes: This gene is also associated with Cardiac arrhythmia, ankyrin-B-related 600919; Long QT syndrome 4 600919Created: 2 Mar 2021, 3:54 p.m. | Last Modified: 2 Mar 2021, 3:54 p.m.
Panel Version: 1.30
Submitted on behalf of the GMS Cardiology specialist group. The group has agreed that this gene should be Red on this panel.Created: 2 Dec 2019, 10:38 a.m. | Last Modified: 2 Dec 2019, 10:38 a.m.
Panel Version: 0.30
Little literature associating this gene with conduction disease in particular.Created: 2 Oct 2019, 10:07 a.m. | Last Modified: 2 Oct 2019, 10:07 a.m.
Panel Version: 0.28
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Cardiac arrhythmia, ankyrin-B-related 600919; Long QT syndrome 4 600919
Publications
Cardiac arrhythmia, ankyrin-B-related (600919), Long QT syndrome 4 (600919)Created: 25 Mar 2019, 4:30 p.m.
Can be associated with Bradycardia. 27785597 - 1 report on HGMDCreated: 25 Mar 2019, 4:27 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Variants in this GENE are reported as part of current diagnostic practice
Phenotypes for gene: ANK2 were changed from to Heart conduction disease, MONDO:0000992
Publications for gene: ANK2 were set to
gene: ANK2 was added gene: ANK2 was added to Progressive cardiac conduction disease. Sources: South West GLH Mode of inheritance for gene: ANK2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted