Hereditary bundle branch system defect | Gene-Disease Associations & Pathways | GeDiPNet

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Pathways column key: KEGG Reactome

Disease Term	Disease ID	Gene Symbol	Classification	References	Source	Pathways
HEREDITARY BUNDLE BRANCH SYSTEM DEFECT	C1879286	CASQ2	Unknown	—	Disgenet	Calcium signaling pathway Cardiac muscle contraction Stimuli-sensing channels +1 more
		DSP	Unknown	—	Disgenet	Cytoskeleton in muscle cells Arrhythmogenic right ventricular cardiomyopathy Apoptotic cleavage of cell adhesion proteins +3 more
		HRC	Unknown	—	Disgenet	Calcium signaling pathway Cardiac muscle contraction Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) +1 more
		NKX2-5	Unknown	—	Disgenet	YAP1- and WWTR1 (TAZ)-stimulated gene expression Physiological factors
		SCN1B	Unknown	—	Disgenet	Adrenergic signaling in cardiomyocytes Phase 0 - rapid depolarisation
		SCN5A	Unknown	—	Disgenet	Adrenergic signaling in cardiomyocytes Phase 0 - rapid depolarisation
		TRPM4	Unknown	—	Disgenet	Insulin secretion TRP channels