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 08/02/2024 MGI 6.24 |
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