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Symbol
Name
ID

Mmut
methylmalonyl-Coenzyme A mutase
MGI:97239

Phenotype annotations related to liver/biliary system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Hepatomegaly
Disease(s) Associated with MMUT	Hepatomegaly
methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency

Mouse Phenotypes		liver/biliary system phenotype	abnormal hepatocyte mitochondrial morphology	abnormal liver morphology	abnormal liver parenchyma morphology	hepatic steatosis
Availability	Mouse Genotype	liver/biliary system phenotype	abnormal hepatocyte mitochondrial morphology	abnormal liver morphology	abnormal liver parenchyma morphology	hepatic steatosis
	Mmut^tm1Cpv/Mmut^tm1Cpv
	Mmut^tm1Cpv/Mmut^tm1Cpv Tg(Alb-Mut)#Cpv/0	*
	Mmut^tm1Pai/Mmut^tm1Pai

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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