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XB-GENEPAGE-955811
acad8 acyl-CoA dehydrogenase family member 8
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (12 sources): Anemia, Decreased plasma carnitine, Dehydration, Delayed speech and language development, Dicarboxylic aciduria, Dilated cardiomyopathy, Elevated circulating acylcarnitine concentration, Hypotonia, Ketotic hypoglycemia, Mild global developmental delay, [+] |
Mouse (9 sources): abnormal hepatocyte morphology, abnormal mitochondrial crista morphology, abnormal mitochondrial matrix morphology, decreased brown fat cell lipid droplet size, homeostasis/metabolism phenotype, impaired adaptive thermogenesis, increased oxygen consumption, macrovesicular hepatic steatosis, microvesicular hepatic steatosis |
View all ortholog results at Monarch |