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Symbol
Name
ID
Amelx
amelogenin, X-linked
MGI:88005
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Abnormal jaw morphology
Amelogenesis imperfecta
Enamel hypomineralization
Hypocalcification of dental enamel
Hypomature dental enamel
Enamel hypoplasia
Disease(s) Associated with AMELX
amelogenesis imperfecta
amelogenesis imperfecta type 1E

Mouse Phenotypes
abnormal tooth morphology
abnormal incisor morphology
abnormal incisor color
short lower incisors
short upper incisors
short incisors
abnormal molar morphology
abnormal molar cusp morphology
abnormal tooth color
abnormal tooth development
abnormal ameloblast morphology
abnormal enamel mineralization
abnormal enamel morphology
abnormal enamel rod pattern
enamel pits
reduced enamel thickness
abnormal tooth wear
absent teeth
brittle teeth
abnormal mandible morphology
large mandible
abnormal zygomatic bone morphology
abnormal vertebral arch morphology
vertebral transformation
Availability Mouse Genotype
Amelxem1(IMPC)Ccpcz/Amelxem1(IMPC)Ccpcz
AmelxRgsc888/AmelxRgsc888
Amelxtm1Kul/Amelxtm1Kul
Tg(Amelx)42Msnd/Tg(Amelx)42Msnd
Amelxem1(IMPC)Ccpcz/Amelx+
AmelxRgsc888/Amelx+
Amelxem1(IMPC)Ccpcz/Y
AmelxRgsc888/Y

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
04/30/2024
MGI 6.23
The Jackson Laboratory