Symbol Name ID |
Mmut
methylmalonyl-Coenzyme A mutase MGI:97239 |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties |
Lethargy |
Disease(s) Associated with MMUT | ||
methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency |
Mouse Phenotypes | absent gastric milk in neonates |
abnormal suckling behavior |
decreased locomotor activity |
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Availability | Mouse Genotype | |||
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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