|
Symbol Name ID |
Amt
aminomethyltransferase MGI:3646700 |
| Darker colors indicate more annotations |
| Human Phenotypes | Agenesis of corpus callosum |
Myoclonus |
Irritability |
Lethargy |
Aggressive behavior |
Hyperactivity |
Impulsivity |
Restlessness |
Intellectual disability |
Hyperreflexia |
Hyporeflexia |
Encephalopathy |
Seizure |
| Disease(s) Associated with AMT | |||||||||||||
| glycine encephalopathy |
| Mouse Phenotypes | abnormal neural tube morphology |
incomplete rostral neuropore closure |
spina bifida |
craniorachischisis |
exencephaly |
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| Availability | Mouse Genotype | |||||
| Amtem1(IMPC)Tcp/Amtem1(IMPC)Tcp | ||||||
| AmtGt(OST181110)Lex/AmtGt(OST181110)Lex | ||||||
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 05/28/2024 MGI 6.13 |
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