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| Gene: Trpm4 (transient receptor potential cation channel, subfamily M, member 4) Rattus norvegicus |  Analyze |
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Analyze GeneStrainQTL List
 Functional Annotation unavailable |
 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) | Bradycardia | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Bradycardia | ClinVar | PMID:25741868 PMID:28492532 | Brugada syndrome | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:21887725 PMID:28492532 | Brugada syndrome | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:21887725 more ... | Brugada syndrome | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:25741868 PMID:28492532 | Brugada syndrome | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:25741868 | Brugada syndrome | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Sudden unexplained nocturnal death syndrome | ClinVar | PMID:20562447 more ... | cardiac arrest | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Cardiac arrest | ClinVar | | Cardiac Conduction Defect, Nonspecific | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Cardiac conduction defect, nonspecific | ClinVar | | catecholaminergic polymorphic ventricular tachycardia | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Catecholaminergic polymorphic ventricular tachycardia | ClinVar | | catecholaminergic polymorphic ventricular tachycardia 1 | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Ventricular tachycardia, catecholaminergic polymorphic, 1 | ClinVar | | epilepsy | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Epilepsy | ClinVar | PMID:25741868 PMID:28492532 | Failure to Thrive | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Failure to thrive | ClinVar | PMID:25741868 PMID:28492532 | genetic disease | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:19726882 more ... | hypertrophic cardiomyopathy | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Hypertrophic cardiomyopathy | ClinVar | | Hypoxia | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Hypoxemia | ClinVar | PMID:25741868 PMID:28492532 | long QT syndrome | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:28492532 | patent foramen ovale | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Patent foramen ovale | ClinVar | PMID:25741868 PMID:28492532 | progressive familial heart block | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: LENEGRE-LEV DISEASE | ClinVar | PMID:26820365 PMID:28492532 | progressive familial heart block | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: LENEGRE-LEV DISEASE | ClinVar | PMID:25741868 PMID:28492532 | progressive familial heart block | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Progressive familial heart block | ClinVar | PMID:25741868 | progressive familial heart block | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: LENEGRE-LEV DISEASE | ClinVar | | progressive familial heart block | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: LENEGRE-LEV DISEASE | ClinVar | PMID:28492532 | progressive familial heart block type IA | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: LENEGRE-LEV DISEASE | ClinVar | PMID:26820365 PMID:28492532 | progressive familial heart block type IA | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: LENEGRE-LEV DISEASE | ClinVar | PMID:25741868 PMID:28492532 | progressive familial heart block type IA | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: LENEGRE-LEV DISEASE | ClinVar | | progressive familial heart block type IA | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: LENEGRE-LEV DISEASE | ClinVar | PMID:28492532 | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:26820365 PMID:28492532 | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:21887725 more ... | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:21887725 more ... | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:21887725 more ... | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:21887725 more ... | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:20562447 more ... | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:20562447 more ... | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by OMIM:604559 | ClinVar | | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:25741868 | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:25741868 PMID:28492532 | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:23382873 more ... | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:21887725 PMID:28492532 | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by OMIM:604559 | ClinVar | PMID:19726882 PMID:897853 | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by OMIM:604559 | ClinVar | PMID:20562447 | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by OMIM:604559 | ClinVar | PMID:21887725 | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:19726882 PMID:25741868 | progressive familial heart block type IB | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | ClinVar | PMID:28492532 | short QT syndrome | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: short QT syndrome | ClinVar | | Sudden Death, Cardiac | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Sudden cardiac death | ClinVar | | Sudden Death, Cardiac | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Sudden cardiac death | ClinVar | PMID:28492532 | Tachycardia | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Tachycardia | ClinVar | PMID:25741868 PMID:28492532 | Ventricular Fibrillation | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Ventricular fibrillation | ClinVar | PMID:21887725 more ... | visual epilepsy | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Seizures | ClinVar | PMID:25741868 PMID:28492532 | West syndrome | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Hypsarrhythmia | ClinVar | PMID:25741868 PMID:28492532 | Wolff-Parkinson-White syndrome | | ISO | RGD:1348019 | 8554872 | ClinVar Annotator: match by term: Wolff-Parkinson-White pattern | ClinVar | | |
Imported Annotations - CTD
Imported Annotations - OMIM
Gene-Chemical Interaction AnnotationsGene Ontology Annotations
