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Phenotypes Associated with This Genotype
Genotype
MGI:3574668
Allelic
Composition
EnamRgsc521/Enam+
Genetic
Background
involves: C57BL/6JJcl * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
EnamRgsc521 mutation (1 available); any Enam mutation (32 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• 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

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

growth/size/body
• 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 ID Ref(s)
Amelogenesis Imperfecta, Type IB; AI1B 104500 J:96349


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
05/24/2016
MGI 6.04
The Jackson Laboratory