|
Symbol Name ID |
Dnmt1
DNA methyltransferase 1 MGI:94912 |
| Darker colors indicate more annotations |
| Human Phenotypes | Depression |
Apathy |
Polyphagia |
Hyperactivity |
Impulsivity |
| Disease(s) Associated with DNMT1 | |||||
| autosomal dominant cerebellar ataxia, deafness and narcolepsy | |||||
| Graves' disease | |||||
| hereditary sensory neuropathy type 1E |
| Mouse Phenotypes | impaired spatial learning |
abnormal spatial reference memory |
abnormal spatial working memory |
abnormal response to novel object |
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| Availability | Mouse Genotype | ||||
| Dnmt1em2Jiemw/Dnmt1+ | |||||
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 04/16/2024 MGI 6.23 |
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