|
Symbol Name ID |
Acad9
acyl-Coenzyme A dehydrogenase family, member 9 MGI:1914272 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased activity of mitochondrial complex I |
Decreased circulating carnitine concentration |
Elevated circulating acylcarnitine concentration |
Hyperammonemia |
Elevated creatine kinase after exercise |
Elevated circulating hepatic transaminase concentration |
Increased circulating lactate dehydrogenase concentration |
Hypoglycemia |
Nonketotic hypoglycemia |
Increased circulating lactate concentration |
Lactic acidosis |
Cerebral edema |
Hepatic steatosis |
Microvesicular hepatic steatosis |
Dicarboxylic aciduria |
Exercise intolerance |
| Disease(s) Associated with ACAD9 | ||||||||||||||||
| nuclear type mitochondrial complex I deficiency 20 |
| Mouse Phenotypes | impaired exercise endurance |
lactic acidosis |
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| Availability | Mouse Genotype | ||
| Acad9tm1c(KOMP)Wtsi/Acad9tm1c(KOMP)Wtsi Tg(ACTA1-cre)79Jme/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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