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Symbol Name ID |
Acadvl
acyl-Coenzyme A dehydrogenase, very long chain MGI:895149 |
| Darker colors indicate more annotations |
| Human Phenotypes | Atrial septal defect |
Patent foramen ovale |
Ventricular septal defect |
Dilated cardiomyopathy |
Hypertrophic cardiomyopathy |
Pericardial effusion |
Cardiomegaly |
Reduced left ventricular ejection fraction |
Prolonged QT interval |
Arrhythmia |
Sudden cardiac death |
Tachycardia |
Ventricular tachycardia |
Ventricular fibrillation |
Atrioventricular block |
| Disease(s) Associated with ACADVL | |||||||||||||||
| very long chain acyl-CoA dehydrogenase deficiency |
| Mouse Phenotypes | abnormal myocardial fiber morphology |
myocardial fiber degeneration |
abnormal heart morphology |
increased heart weight |
abnormal heart left ventricle morphology |
dilated heart left ventricle |
dilated cardiomyopathy |
abnormal cardiovascular system physiology |
decreased ventricle muscle contractility |
decreased heart rate |
irregular heartbeat |
cardiomyopathy |
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| Availability | Mouse Genotype | ||||||||||||
| Acadvltm1Uab/Acadvltm1Uab | |||||||||||||
| Acadvltm1Vje/Acadvltm1Vje | |||||||||||||
| Acadvltm1Zkhu/Acadvltm1Zkhu Tg(Myh6-cre)1Jmk/0 (conditional) |
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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 04/23/2024 MGI 6.23 |
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