ANK2

ankyrin 2
OMIM: 106410, ClinGen, DECIPHER

13 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 13 panels
Green ANK2 in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.233	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Complex neurodevelopmental disorder, MONDO:0100038
Red ANK2 in Brugada syndrome Level 2: Cardiovascular disorders Version 0.44 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red ClinGen Phenotypes Brugada syndrome, MONDO:0015263 Tags disputed
Red ANK2 in Catecholaminergic Polymorphic Ventricular Tachycardia Level 2: Cardiovascular disorders Version 0.37 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red ClinGen Phenotypes Catecholaminergic polymorphic ventricular tachycardia, MONDO:0017990 Tags disputed
Red ANK2 in Incidentalome Version 0.370	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Long QT syndrome 4, MIM# 600919 Tags disputed cardiac
Red ANK2 in Long QT Syndrome Level 2: Cardiovascular disorders Version 0.62 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Victorian Clinical Genetics Services Phenotypes Long QT syndrome 4, MIM# 600919 Tags disputed
Green ANK2 in Mendeliome Version 1.3802	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red ClinGen Expert Review Green Expert Review Phenotypes Long QT syndrome 4, MIM# 600919 Complex neurodevelopmental disorder, MONDO:0100038
Green ANK2 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.309 Component of the following Super Panels: Progressive Neurological Conditions	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Complex neurodevelopmental disorder, MONDO:0100038, ANK2-related
Green ANK2 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.578	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green ANK2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.508	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Other Phenotypes Complex neurodevelopmental disorder, MONDO:0100038
Red ANK2 in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.208	1 review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red NHS GMS Phenotypes Cardiac arrhythmia, ankyrin-B-related MIM#600919 Long QT syndrome 4 MIM#600919
Green ANK2 in Additional findings_Paediatric Level 2: Screening Version 0.278	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green BabySeq Category B gene Phenotypes Complex neurodevelopmental disorder, MONDO:0100038
Red ANK2 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.141	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category B gene Phenotypes Complex neurodevelopmental disorder, MONDO:0100038
Red ANK2 in Speech apraxia Level 2: Neurology and neurodevelopmental disorders Version 1.27	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert Review Phenotypes Neurodevelopmental disorder (MONDO:0700092), gene-related