Symbol Name ID |
Amtn
amelotin MGI:1918671 |
Darker colors indicate more annotations |
Human Phenotypes | Amelogenesis imperfecta |
Enamel hypomineralization |
Disease(s) Associated with AMTN | ||
amelogenesis imperfecta type 3B |
Mouse Phenotypes | abnormal incisor color |
abnormal ameloblast morphology |
abnormal enamel mineralization |
abnormal enamel morphology |
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Availability | Mouse Genotype | ||||
Amtntm1Tigm/Amtntm1Tigm |
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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