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Symbol Name ID |
Acadm
acyl-Coenzyme A dehydrogenase, medium chain MGI:87867 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased circulating carnitine concentration |
Decreased plasma total carnitine |
Hyperammonemia |
Elevated circulating creatine kinase concentration |
Elevated circulating hepatic transaminase concentration |
Abnormal circulating lactate dehydrogenase concentration |
Reduced tissue medium-chain acyl-CoA dehydrogenase activity |
Hypoglycemia |
Metabolic acidosis |
Cerebral edema |
Hepatic steatosis |
Dicarboxylic aciduria |
Medium chain dicarboxylic aciduria |
Elevated urinary 3-hydroxybutyric acid |
Elevated urinary 7-hydroxyoctanoic acid level |
Hyperglycinuria |
Ketosis |
| Disease(s) Associated with ACADM | |||||||||||||||||
| medium chain acyl-CoA dehydrogenase deficiency |
| Mouse Phenotypes | impaired adaptive thermogenesis |
increased circulating carnitine level |
abnormal blood homeostasis |
decreased circulating glucose level |
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| Availability | Mouse Genotype | ||||
| Acadmtm1Uab/Acadmtm1Uab | |||||
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 04/16/2024 MGI 6.23 |
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