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Symbol Name ID |
Acad9
acyl-Coenzyme A dehydrogenase family, member 9 MGI:1914272 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cerebellar hemorrhage |
Dilated cardiomyopathy |
Hypertrophic cardiomyopathy |
Stroke |
Sudden cardiac death |
Congestive heart failure |
| Disease(s) Associated with ACAD9 | ||||||
| nuclear type mitochondrial complex I deficiency 20 |
| Mouse Phenotypes | myocardial fiber disarray |
abnormal heart morphology |
thick ventricular wall |
decreased cardiac muscle contractility |
cardiomyopathy |
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| Availability | Mouse Genotype | |||||
| Acad9tm1c(KOMP)Wtsi/Acad9tm1c(KOMP)Wtsi Tg(Myh6-cre)2182Mds/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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