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Symbol
Name
ID
Hadha
hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha
MGI:2135593
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Hypocalcemia
Hyperammonemia
Hypoketotic hypoglycemia
Lactic acidosis
Hydrops fetalis
Myoglobinuria
Disease(s) Associated with HADHA
mitochondrial trifunctional protein deficiency

Mouse Phenotypes
decreased circulating carnitine level
increased circulating carnitine level
abnormal blood homeostasis
increased blood urea nitrogen level
increased circulating bilirubin level
hypoglycemia
increased circulating insulin level
increased circulating free fatty acid level
increased circulating alanine transaminase level
insulin resistance
abnormal urine homeostasis
Availability Mouse Genotype
Hadhatm1Jib/Hadhatm1Jib
Hadhatm1Jib/Hadha+

Contributing Projects:
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
10/08/2019
MGI 6.14
The Jackson Laboratory