acad9 Phenotypes

Phenotypes

XB-GENEPAGE-5885004

Gene Symbol: acad9 Gene Name: acyl-CoA dehydrogenase family member 9

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: acad9 assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (36 sources): Acute hepatic failure, Cerebellar hemorrhage, Cerebral edema, Congestive heart failure, Decreased activity of mitochondrial complex I, Decreased plasma carnitine, Dicarboxylic aciduria, Dilated cardiomyopathy, EMG: myopathic abnormalities, Elevated circulating acylcarnitine concentration, Elevated circulating hepatic transaminase concentration, Elevated creatine kinase after exercise, Encephalopathy, Exercise intolerance, Failure to thrive, Fatigable weakness, Generalized hypotonia, Generalized muscle weakness, Hepatic failure, Hepatic steatosis, Hyperammonemia, Hypertrophic cardiomyopathy, Hypoglycemia, Hypotonia, Increased circulating lactate concentration, Increased circulating lactate dehydrogenase concentration, Lactic acidosis, Microvesicular hepatic steatosis, Muscle weakness, Myalgia, Myopathy, Nonketotic hypoglycemia, Prolonged prothrombin time, Stroke, Sudden cardiac death, Thrombocytopenia [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Human (36 sources): Acute hepatic failure, Cerebellar hemorrhage, Cerebral edema, Congestive heart failure, Decreased activity of mitochondrial complex I, Decreased plasma carnitine, Dicarboxylic aciduria, Dilated cardiomyopathy, EMG: myopathic abnormalities, Elevated circulating acylcarnitine concentration, [+]