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Human Disease and Mouse Model Detail
Human Disease Amelogenesis Imperfecta, Type IE; AI1E
OMIM ID: 301200
Human Phenotype Ontology associations
Synonyms Amelogenesis Imperfecta; Amelogenesis Imperfecta, Hypomaturation Type, with Snow-Capped Teeth; Amelogenesis Imperfecta, Hypoplastic/Hypomaturation, X-Linked 1; Amelogenesis Imperfecta, X-Linked 1; AIH1; Enamel Hypoplasia, X-Linked
View all models View ALL (6) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     AMELX*, AMELY Amelx* View 6 models HGNC
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(AMELX*P70T)2Gibs View 2 models
References Disease References using Mouse Models (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory