Symbol Name ID |
Cacna1c
calcium channel, voltage-dependent, L type, alpha 1C subunit MGI:103013 |
Darker colors indicate more annotations |
Human Phenotypes | Single umbilical artery |
Patent foramen ovale |
Ventricular septal defect |
Tetralogy of Fallot |
Cardiomegaly |
Patent ductus arteriosus |
Pulmonary arterial hypertension |
Prolonged QT interval |
Prolonged QTc interval |
Shortened QT interval |
J wave |
Sinus bradycardia |
Bradycardia |
Aborted sudden cardiac death |
Sudden cardiac death |
Atrial fibrillation |
Ventricular tachycardia |
Ventricular arrhythmia |
Ventricular fibrillation |
Atrioventricular block |
Syncope |
Disease(s) Associated with CACNA1C | |||||||||||||||||||||
Brugada syndrome 3 | |||||||||||||||||||||
long QT syndrome 8 | |||||||||||||||||||||
neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures | |||||||||||||||||||||
Timothy syndrome |
Mouse Phenotypes | patent ductus arteriosus |
increased myocardial fiber size |
heart right ventricle hypertrophy |
increased heart weight |
cardiac hypertrophy |
dilated heart ventricle |
internal hemorrhage |
abnormal cardiac muscle contractility |
decreased cardiac muscle contractility |
abnormal fetal cardiomyocyte physiology |
decreased heart rate |
irregular heartbeat |
abnormal myocardial fiber physiology |
decreased calcium uptake by cardiac muscle |
congestive heart failure |
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Availability | Mouse Genotype | |||||||||||||||
Cacna1ctm1.1Wac/Cacna1ctm1.1Wac | ||||||||||||||||
Cacna1ctm1Itl/Cacna1ctm1Itl | ||||||||||||||||
Cacna1ctm1Jst/Cacna1ctm1Jst | ||||||||||||||||
Cacna1ctm2.1Wac/Cacna1ctm2.1Wac | ||||||||||||||||
Cacna1ctm5.1Hfm/Cacna1ctm5.1Hfm | ||||||||||||||||
Cacna1ctm1Ggm/Cacna1ctm1Ggm A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 05/14/2024 MGI 6.23 |
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