Symbol Name ID |
Mmut
methylmalonyl-Coenzyme A mutase MGI:97239 |
Darker colors indicate more annotations |
Human Phenotypes | Cerebellar hemorrhage |
Delayed CNS myelination |
Abnormal globus pallidus morphology |
Ataxia |
Choreoathetosis |
Paraparesis |
Tetraparesis |
Abnormality of speech or vocalization |
Lethargy |
Intellectual disability |
Coma |
Global developmental delay |
Seizure |
Disease(s) Associated with MMUT | |||||||||||||
methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency |
Mouse Phenotypes | abnormal brain morphology |
increased brain weight |
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Availability | Mouse Genotype | ||
Mmuttm1Cpv/Mmuttm1Cpv | |||
Mmuttm1Cpv/Mmuttm1Cpv Tg(Alb-Mut)#Cpv/0 |
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Mmuttm1Pai/Mmuttm1.1Mrb |
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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