HCN4

hyperpolarization activated cyclic nucleotide gated potassium channel 4
OMIM: 605206, Gene2Phenotype

8 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 8 panels
Amber HCN4 in Aortopathy_Connective Tissue Disorders Level 2: Cardiovascular disorders Version 1.85	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber ClinGen Phenotypes Sick sinus syndrome 2 with cardiac noncompaction and ascending aorta dilation
Green HCN4 in Incidentalome Version 0.301	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green ClinGen Victorian Clinical Genetics Services Phenotypes Sick sinus syndrome 2, MIM# 163800 Aortopathy Tags cardiac
Green HCN4 in Sick sinus syndrome Level 2: Cardiovascular disorders Version 1.4 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Sick sinus syndrome 2, MIM# 163800
Red HCN4 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.33 Component of the following Super Panels: Progressive Neurological Conditions	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert list Phenotypes {Epilepsy, idiopathic generalized, susceptibility to, 18}, MIM# 619521
Green HCN4 in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.192	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green NHS GMS
Red HCN4 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene Phenotypes Brugada syndrome
Red HCN4 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene Expert Review Red Phenotypes Brugada syndrome
Green HCN4 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Sick sinus syndrome 2, MIM# 163800