Cardiac arrhythmias - previous panel
Gene: AKAP9EnsemblGeneIds (GRCh38): ENSG00000127914
EnsemblGeneIds (GRCh37): ENSG00000127914
OMIM: 604001, Gene2Phenotype
AKAP9 is in 3 panels
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Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Red
- Phenotypes
-
- ?Long QT syndrome-11 611820
- Long QT syndrome-11
- OMIM
- 604001
- Clinvar variants
- Variants in AKAP9
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Panel promoted to version 1.0
Ellen McDonagh (Genomics England Curator)Eleanor Williams: Sources: Literature
Set Phenotypes
Rebecca Foulger (Genomics England curator)Added phenotypes Long QT syndrome-11 for gene: AKAP9
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Rebecca Foulger (Genomics England curator)gene: AKAP9 was added gene: AKAP9 was added to Cardiac arrythmias. Sources: Expert Review Red Mode of inheritance for gene: AKAP9 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: AKAP9 were set to 18093912 Phenotypes for gene: AKAP9 were set to ?Long QT syndrome-11 611820