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Phenotypes Associated with This Genotype
Genotype
MGI:3574666
Allelic
Composition
EnamRgsc514/Enam+
Genetic
Background
involves: C57BL/6JJcl * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
EnamRgsc514 mutation (1 available); any Enam mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• a gap is seen between the enamel and the dentin core (J:96349)
• a gap is seen between the enamel and the dentin core (J:96349)
• enamel surface of the molars appears rough with microscopic cracks and delamination; however, the enamel is of normal thickness (J:96349)
• similar but more prominent enamel defects are seen on the incisors (J:96349)
• enamel surface of the molars appears rough with microscopic cracks and delamination; however, the enamel is of normal thickness (J:96349)
• similar but more prominent enamel defects are seen on the incisors (J:96349)

growth/size/body
• a gap is seen between the enamel and the dentin core (J:96349)
• a gap is seen between the enamel and the dentin core (J:96349)
• enamel surface of the molars appears rough with microscopic cracks and delamination; however, the enamel is of normal thickness (J:96349)
• similar but more prominent enamel defects are seen on the incisors (J:96349)
• enamel surface of the molars appears rough with microscopic cracks and delamination; however, the enamel is of normal thickness (J:96349)
• similar but more prominent enamel defects are seen on the incisors (J:96349)

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
02/02/2016
MGI 6.02
The Jackson Laboratory