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Symbol Name ID |
Mmaa
methylmalonic aciduria (cobalamin deficiency) type A MGI:1923805 |
| Darker colors indicate more annotations |
| Human Phenotypes | Feeding difficulties in infancy |
Lethargy |
| Disease(s) Associated with MMAA | ||
| methylmalonic acidemia cblA type |
| Mouse Phenotypes | decreased exploration in new environment |
decreased thigmotaxis |
increased grip strength |
decreased locomotor activity |
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| Availability | Mouse Genotype | ||||
| Mmaaem1(IMPC)J/Mmaaem1(IMPC)J | |||||
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 04/09/2024 MGI 6.23 |
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