About   Help   FAQ
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 (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• a gap is seen between the enamel and the dentin core
• enamel surface of the molars appears rough with microscopic cracks and delamination; however, the enamel is of normal thickness
• similar but more prominent enamel defects are seen on the incisors

craniofacial
• a gap is seen between the enamel and the dentin core
• enamel surface of the molars appears rough with microscopic cracks and delamination; however, the enamel is of normal thickness
• similar but more prominent enamel defects are seen on the incisors

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

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
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
09/20/2016
MGI 6.05
The Jackson Laboratory