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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Amelx)42Msnd
transgene insertion 42, Malcolm L Snead
MGI:3584497
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
tg1
Tg(Amelx)42Msnd/Tg(Amelx)42Msnd involves: C57BL/6J * CBA/J * DBA/2J MGI:3584512


Genotype
MGI:3584512
tg1
Allelic
Composition
Tg(Amelx)42Msnd/Tg(Amelx)42Msnd
Genetic
Background
involves: C57BL/6J * CBA/J * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Amelx)42Msnd mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• transmission electron microscopy of the enamel matrix of neonatal incisors reveals non-uniformity in the size of the self-assembled amelogenin nanospheres and disruption of the normally evenly-spaced, parallel arrangement of the hydroxyapatite crystallites
• scanning electron micrographs of incisors of 6 week old mice reveal loss of the normal boundary definiton of the rods comprising the enamel and abnormal porosity of the structure formed by the rods

skeleton
• transmission electron microscopy of the enamel matrix of neonatal incisors reveals non-uniformity in the size of the self-assembled amelogenin nanospheres and disruption of the normally evenly-spaced, parallel arrangement of the hydroxyapatite crystallites
• scanning electron micrographs of incisors of 6 week old mice reveal loss of the normal boundary definiton of the rods comprising the enamel and abnormal porosity of the structure formed by the rods

growth/size/body
• transmission electron microscopy of the enamel matrix of neonatal incisors reveals non-uniformity in the size of the self-assembled amelogenin nanospheres and disruption of the normally evenly-spaced, parallel arrangement of the hydroxyapatite crystallites
• scanning electron micrographs of incisors of 6 week old mice reveal loss of the normal boundary definiton of the rods comprising the enamel and abnormal porosity of the structure formed by the rods

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
NOT amelogenesis imperfecta type 1E DOID:0110058 OMIM:301200
J:100004





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last database update
08/02/2024
MGI 6.24
The Jackson Laboratory