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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cdh11tm1Mta
targeted mutation 1, Masatoshi Takeichi
MGI:1861184
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cdh11tm1Mta/Cdh11tm1Mta involves: 129S1/Sv * C57BL/6 MGI:2175752
cx2
Cdh11tm1Mta/Cdh11tm1Mta
Cdh2tm1Hyn/Cdh2tm1Hyn
involves: 129S1/Sv * 129S2/SvPas * C57BL/6 MGI:2662271
cx3
Bhlhe22tm1Meg/Bhlhe22tm1Meg
Cdh11tm1Mta/Cdh11tm1Mta
involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J MGI:5315766


Genotype
MGI:2175752
hm1
Allelic
Composition
Cdh11tm1Mta/Cdh11tm1Mta
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdh11tm1Mta mutation (1 available); any Cdh11 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
N
• at E9.0, homozygous mutant embryos display normal epitheial somite patterning relative to wild-type embryos
• moreover, homozygous mutant mice survive to adulthood




Genotype
MGI:2662271
cx2
Allelic
Composition
Cdh11tm1Mta/Cdh11tm1Mta
Cdh2tm1Hyn/Cdh2tm1Hyn
Genetic
Background
involves: 129S1/Sv * 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdh11tm1Mta mutation (1 available); any Cdh11 mutation (42 available)
Cdh2tm1Hyn mutation (1 available); any Cdh2 mutation (50 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• at E9.0, double mutant embryos display a more severe disorganization and fragmentation of the epithelial somites than single Cdh2tm1Hyn embryos
• each epithelial somite is cleaved into rostral and caudal halves just after somite formation, as in single Cdh2tm1Hyn embryos; however, in double mutant embryos, each half is further fragmented into smaller clusters, and the caudal and rostral compartments tend to separate from each other




Genotype
MGI:5315766
cx3
Allelic
Composition
Bhlhe22tm1Meg/Bhlhe22tm1Meg
Cdh11tm1Mta/Cdh11tm1Mta
Genetic
Background
involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bhlhe22tm1Meg mutation (0 available); any Bhlhe22 mutation (12 available)
Cdh11tm1Mta mutation (1 available); any Cdh11 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
integument
• at 13 weeks, delayed compared to in Bhlhe22tm1Meg homozygotes

nervous system
• mice exhibit a reduction of the corticospinal tract compared with wild-type mice although not as severe as in Bhlhe22tm1Meg homozygotes





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last database update
06/12/2024
MGI 6.13
The Jackson Laboratory