Phenotypes Associated with This Genotype

Genotype
MGI:3574668

• Allelic Composition: Enam^Rgsc521/Enam⁺
• Genetic Background: involves: C57BL/6JJcl * DBA/2J

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

craniofacial

abnormal tooth morphology ( J:96349 )

• a gap is seen between the enamel and the dentin core

abnormal incisor morphology ( J:96349 )

• the incisor occlusion surface shows abnormal wear

abnormal enamel morphology ( 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

growth/size/body

abnormal tooth morphology ( J:96349 )

• a gap is seen between the enamel and the dentin core

abnormal incisor morphology ( J:96349 )

• the incisor occlusion surface shows abnormal wear

abnormal enamel morphology ( 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

skeleton

abnormal tooth morphology ( J:96349 )

• a gap is seen between the enamel and the dentin core

abnormal incisor morphology ( J:96349 )

• the incisor occlusion surface shows abnormal wear

abnormal enamel morphology ( 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

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
amelogenesis imperfecta type 1B		DOID:0110052	OMIM:104500	J:96349