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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 (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• enamel is absent from the incisors and molars (J:96349)
• enamel is absent from the incisors and molars (J:96349)

growth/size/body
• enamel is absent from the incisors and molars (J:96349)
• enamel is absent from the incisors and molars (J:96349)

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 (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)
• the incisor occlusion surface shows abnormal wear (J:96349)
• the incisor occlusion surface shows abnormal wear (J:96349)
• the enamel surface appears slightly rougher and abnormal wear at the incisor occlusion surface suggests the enamel is softer, but enamel thickness is normal (J:96349)
• the enamel surface appears slightly rougher and abnormal wear at the incisor occlusion surface suggests the enamel is softer, but enamel thickness is normal (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)
• the incisor occlusion surface shows abnormal wear (J:96349)
• the incisor occlusion surface shows abnormal wear (J:96349)
• the enamel surface appears slightly rougher and abnormal wear at the incisor occlusion surface suggests the enamel is softer, but enamel thickness is normal (J:96349)
• the enamel surface appears slightly rougher and abnormal wear at the incisor occlusion surface suggests the enamel is softer, but enamel thickness is normal (J:96349)

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





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
01/26/2016
MGI 6.02
The Jackson Laboratory