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Symbol
Name
ID
Amtn
amelotin
MGI:1918671
Phenotype annotations related to craniofacial
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
Availability Mouse Genotype
Amtntm1Tigm/Amtntm1Tigm

Contributing Projects:
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
The Jackson Laboratory