Mouse Genome Informatics
hm1
    EnamRgsc521/EnamRgsc521
involves: C57BL/6JJcl * DBA/2J
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
craniofacial
• enamel is absent from the incisors and molars

Mouse Models of Human Disease
OMIM IDRef(s)
Amelogenesis Imperfecta, Type IB; AI1B 104500 J:96349


Mouse Genome Informatics
ht2
    EnamRgsc521/Enam+
involves: C57BL/6JJcl * DBA/2J
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
N normal phenotype
craniofacial
• a gap is seen between the enamel and the dentin core
• the incisor occlusion surface shows abnormal wear
• the enamel surface appears slightly rougher and abnormal wear at the incisor occlusion surface suggests the enamel is softer, but enamel thickness is normal

Mouse Models of Human Disease
OMIM IDRef(s)
Amelogenesis Imperfecta, Type IB; AI1B 104500 J:96349