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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
EnamRgsc521
RIKEN Genomic Sciences Center (GSC), 521
MGI:3055587
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
EnamRgsc521/EnamRgsc521 involves: C57BL/6JJcl * DBA/2J MGI:3574667
ht2
EnamRgsc521/Enam+ involves: C57BL/6JJcl * DBA/2J MGI:3574668


Genotype
MGI:3574667
hm1
Allelic
Composition
EnamRgsc521/EnamRgsc521
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 (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• enamel is absent from the incisors and molars

craniofacial
• enamel is absent from the incisors and molars

growth/size/body
• enamel is absent from the incisors and molars

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




Genotype
MGI:3574668
ht2
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 (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
• 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





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last database update
11/29/2016
MGI 6.06
The Jackson Laboratory