About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Amelx+
wild type
MGI:2439023
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Amelxem1(IMPC)Ccpcz/Amelx+ C57BL/6N-Amelxem1(IMPC)Ccpcz/Ccpcz MGI:7471859
ht2
Amelxtm1Msnd/Amelx+ involves: 129X1/SvJ MGI:3695922
ht3
Amelxtm2Msnd/Amelx+ involves: 129X1/SvJ MGI:3695924
ht4
AmelxRgsc888/Amelx+ involves: C57BL/6JJcl * DBA/2J MGI:4438260
ht5
AmelxRgsc888/Amelx+ involves: C57BL/6JJcl * DBA/2JJcl MGI:3807979


Genotype
MGI:7471859
ht1
Allelic
Composition
Amelxem1(IMPC)Ccpcz/Amelx+
Genetic
Background
C57BL/6N-Amelxem1(IMPC)Ccpcz/Ccpcz
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Amelxem1(IMPC)Ccpcz mutation (1 available); any Amelx mutation (26 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial

growth/size/body

hematopoietic system

immune system
IMPC - CCP-IMG

skeleton




Genotype
MGI:3695922
ht2
Allelic
Composition
Amelxtm1Msnd/Amelx+
Genetic
Background
involves: 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Amelxtm1Msnd mutation (1 available); any Amelx mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• sections of abnormal rod pattern next to sections of normal rod pattern resulting from X inactivation of either the mutant or wild-type allele
• enamel fractures

growth/size/body
• sections of abnormal rod pattern next to sections of normal rod pattern resulting from X inactivation of either the mutant or wild-type allele
• enamel fractures

skeleton
• sections of abnormal rod pattern next to sections of normal rod pattern resulting from X inactivation of either the mutant or wild-type allele
• enamel fractures




Genotype
MGI:3695924
ht3
Allelic
Composition
Amelxtm2Msnd/Amelx+
Genetic
Background
involves: 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Amelxtm2Msnd mutation (1 available); any Amelx mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• sections of abnormal rod pattern next to sections of normal rod pattern resulting from X inactivation of either the mutant or wild-type allele
• enamel fractures

growth/size/body
• sections of abnormal rod pattern next to sections of normal rod pattern resulting from X inactivation of either the mutant or wild-type allele
• enamel fractures

skeleton
• sections of abnormal rod pattern next to sections of normal rod pattern resulting from X inactivation of either the mutant or wild-type allele
• enamel fractures




Genotype
MGI:4438260
ht4
Allelic
Composition
AmelxRgsc888/Amelx+
Genetic
Background
involves: C57BL/6JJcl * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
AmelxRgsc888 mutation (0 available); any Amelx mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• incisors display patchy regions of roughened, chalky white enamel
• patchy regions of chalky white enamel
• the upper and lower incisors are shortened
• incisors display patchy regions of roughened, chalky white enamel
• occasional small blister like structures of variable size are apparent from the late secretory stage onwards
• within the blister like structures aberrant matrix is present with areas appearing less eosinophilic than the original enamel matrix
• decrease in enamel mineral content
• no defect in dentine mineral levels
• by SEM the prismatic structure is less highly ordered with greater inter-prismatic spacing
• shortened with irregular incisal edge

skeleton
• incisors display patchy regions of roughened, chalky white enamel
• patchy regions of chalky white enamel
• the upper and lower incisors are shortened
• incisors display patchy regions of roughened, chalky white enamel
• occasional small blister like structures of variable size are apparent from the late secretory stage onwards
• within the blister like structures aberrant matrix is present with areas appearing less eosinophilic than the original enamel matrix
• decrease in enamel mineral content
• no defect in dentine mineral levels
• by SEM the prismatic structure is less highly ordered with greater inter-prismatic spacing
• shortened with irregular incisal edge

growth/size/body
• incisors display patchy regions of roughened, chalky white enamel
• patchy regions of chalky white enamel
• the upper and lower incisors are shortened
• incisors display patchy regions of roughened, chalky white enamel
• occasional small blister like structures of variable size are apparent from the late secretory stage onwards
• within the blister like structures aberrant matrix is present with areas appearing less eosinophilic than the original enamel matrix
• decrease in enamel mineral content
• no defect in dentine mineral levels
• by SEM the prismatic structure is less highly ordered with greater inter-prismatic spacing
• shortened with irregular incisal edge

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
amelogenesis imperfecta type 1E DOID:0110058 OMIM:301200
J:157947




Genotype
MGI:3807979
ht5
Allelic
Composition
AmelxRgsc888/Amelx+
Genetic
Background
involves: C57BL/6JJcl * DBA/2JJcl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
AmelxRgsc888 mutation (0 available); any Amelx mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• rough tooth surface

growth/size/body
• rough tooth surface

skeleton
• rough tooth surface





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
01/06/2026
MGI 6.24
The Jackson Laboratory