Results for "ventricular compact myocardium morphogenesis": 7 genes

Name

LVNC2 Gene

noncompaction of left ventricular myocardium, familial isolated, autosomal dominant 2

CPVT3 Gene

Ventricular tachycardia, catecholaminergic polymorphic, 3

ARVD4 Gene

arrhythmogenic right ventricular dysplasia 4

ARVD6 Gene

arrhythmogenic right ventricular dysplasia 6

ARVD3 Gene

arrhythmogenic right ventricular dysplasia 3

MYL3 Gene

myosin, light chain 3, alkali; ventricular, skeletal, slow

MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]

VEPH1 Gene

ventricular zone expressed PH domain-containing 1

Predicted to enable phosphatidylinositol-5-phosphate binding activity. Involved in negative regulation of SMAD protein signal transduction and negative regulation of transforming growth factor beta receptor signaling pathway. Predicted to be located in endomembrane system. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]