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| Gene: Cacna1c (calcium voltage-gated channel subunit alpha1 C) Rattus norvegicus |  Analyze |
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Analyze GeneStrainQTL List
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 Annotation Distribution unavailable |
 Genomic Variants unavailble for Mouse Genomic Variants unavailable |
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| Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | breast ductal carcinoma | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Ductal breast carcinoma | ClinVar | | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:25741868 PMID:28492532 | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS) | ClinVar | PMID:23861362 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS) | ClinVar | PMID:20817017 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS) | ClinVar | PMID:20817017 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | PMID:20817017 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS) | ClinVar | PMID:20817017 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:23861362 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:20031608 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | PMID:20817017 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | PMID:12166659 PMID:28492532 | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:25741868 | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | PMID:20817017 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:23861362 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | PMID:25637381 | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | PMID:20817017 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | PMID:17224476 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | PMID:20031608 PMID:25741868 | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | PMID:17224476 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:23861362 PMID:28492532 | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:23757202 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | PMID:23861362 more ... | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome | ClinVar | | Brugada syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:28492532 | Brugada syndrome 3 | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome 3 | ClinVar | PMID:20817017 more ... | Brugada syndrome 3 | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome 3 | ClinVar | PMID:23861362 more ... | Brugada syndrome 3 | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome 3 | ClinVar | PMID:17224476 more ... | Brugada syndrome 3 | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Brugada syndrome 3 | ClinVar | PMID:17224476 more ... | Cardiac Arrhythmias | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by synonym: EXTRASYSTOLES | ClinVar | | Cardiac Arrhythmias | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Cardiac arrhythmia | ClinVar | PMID:24690944 more ... | Cardiac Arrhythmias | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Cardiac arrhythmia | ClinVar | PMID:25741868 PMID:28492532 | Cardiac Arrhythmias | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Cardiac arrhythmia | ClinVar | PMID:20031608 PMID:25741868 | Cardiac Complexes, Premature | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: EXTRASYSTOLES | ClinVar | PMID:25741868 PMID:28492532 | Cardiac Complexes, Premature | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: EXTRASYSTOLES | ClinVar | PMID:24690944 more ... | Cardiac Complexes, Premature | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: EXTRASYSTOLES | ClinVar | | congenital myasthenic syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Myasthenia, limb-girdle, familial | ClinVar | PMID:25741868 PMID:28492532 | congenital myasthenic syndrome 10 | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: MYASTHENIC SYNDROME, CONGENITAL, 10 | ClinVar | PMID:25741868 PMID:28492532 | dilated cardiomyopathy | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Primary dilated cardiomyopathy | ClinVar | | epilepsy | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Seizure Disorders | ClinVar | | genetic disease | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:12417552 more ... | hypertrophic cardiomyopathy 1 | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Familial hypertrophic cardiomyopathy 1 | ClinVar | PMID:26253506 PMID:28492532 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:28492532 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:23861362 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:20817017 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:20817017 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:20817017 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:23677916 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:20817017 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:20817017 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:15454078 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:23861362 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:26253506 PMID:28492532 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:25633834 PMID:28492532 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:24690944 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:23861362 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:25341504 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:24981977 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:20031608 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:20817017 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:12166659 PMID:28492532 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:23861362 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:20817017 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:23861362 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:25741868 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:20817017 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:17224476 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:26743238 PMID:28492532 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:24033266 PMID:28492532 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Congenital long QT syndrome | ClinVar | PMID:15863612 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:22840528 PMID:28492532 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by null | ClinVar | | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:23861362 PMID:28492532 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:23757202 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:23677916 | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:23861362 more ... | long QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:25741868 PMID:28492532 | melanoma | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Malignant melanoma | ClinVar | PMID:28492532 | Multiple Abnormalities | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Multiple congenital anomalies | ClinVar | | Paroxysmal Ventricular Fibrillation | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Paroxysmal ventricular fibrillation | ClinVar | | restrictive cardiomyopathy | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Cardiomyopathy, restrictive | ClinVar | PMID:20817017 more ... | schizophrenia | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Schizophrenia | ClinVar | PMID:21681106 PMID:27240532 | short QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Short QT Syndrome 4 | ClinVar | PMID:25741868 PMID:28492532 | short QT syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: short QT syndrome | ClinVar | PMID:20031608 more ... | Sudden Death, Cardiac | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Sudden cardiac death | ClinVar | | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:25741868 PMID:28492532 | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:23861362 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:20817017 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:22106044 | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:20817017 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:15454078 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:23861362 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:24690944 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:23861362 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:20031608 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:20817017 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:12166659 PMID:28492532 | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:20817017 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:23861362 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:17224476 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by OMIM:601005 | ClinVar | PMID:20031608 PMID:25741868 | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by OMIM:601005 | ClinVar | PMID:25741868 | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:15863612 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by OMIM:601005 | ClinVar | | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:23861362 PMID:28492532 | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:23757202 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:15454078 | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:23861362 more ... | Timothy syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Timothy syndrome | ClinVar | PMID:28492532 | Ventricular Fibrillation, Paroxysmal Familial, 1 | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Paroxysmal familial ventricular fibrillation 1 | ClinVar | | Ventricular Tachycardia | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Ventricular tachycardia | ClinVar | | Wolff-Parkinson-White syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Wolff-Parkinson-White pattern | ClinVar | PMID:28492532 | Wolff-Parkinson-White syndrome | | ISO | RGD:10268 | 8554872 | ClinVar Annotator: match by term: Wolff-Parkinson-White pattern | ClinVar | | 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Imported Annotations - CTD
Imported Annotations - OMIM
Gene-Chemical Interaction AnnotationsGene Ontology AnnotationsMolecular Pathway Annotations
