Symbol Name ID |
Amelx
amelogenin, X-linked MGI:88005 |
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 |
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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 |
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 |
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