Symbol Name ID |
Mmut
methylmalonyl-Coenzyme A mutase MGI:97239 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hepatomegaly |
Disease(s) Associated with MMUT | |
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 |
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Availability | Mouse Genotype | |||||
Mmuttm1Cpv/Mmuttm1Cpv | ||||||
Mmuttm1Cpv/Mmuttm1Cpv Tg(Alb-Mut)#Cpv/0 |
* | |||||
Mmuttm1Pai/Mmuttm1Pai |
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 06/12/2024 MGI 6.13 |
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