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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tbx2tm1.1(cre)Vmc
targeted mutation 1.1, Vincent M Christoffels
MGI:4415614
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Tbx2tm1.1(cre)Vmc/Tbx2tm1.1(cre)Vmc involves: 129P2/OlaHsd * FVB MGI:4418058
hm2
Tbx2tm1.1(cre)Vmc/Tbx2tm1.1(cre)Vmc involves: 129P2/OlaHsd * NMRI MGI:4418054
ht3
Tbx2tm1.1(cre)Vmc/Tbx2+ involves: 129P2/OlaHsd * NMRI MGI:4418056
cx4
Tbx2tm1.1(cre)Vmc/Tbx2tm1.1(cre)Vmc
Tbx3tm1.1(cre)Vmc/Tbx3tm1.1(cre)Vmc
involves: 129P2/OlaHsd MGI:5314603
cx5
Tbx2tm1.1(cre)Vmc/Tbx2tm1.1(cre)Vmc
Tbx3tm1.1(cre)Vmc/Tbx3tm1.1(cre)Vmc
involves: 129P2/OlaHsd * FVB/N MGI:4418050
cx6
Tbx2tm1.1(cre)Vmc/Tbx2tm1.1(cre)Vmc
Tbx3tm1.1(cre)Vmc/Tbx3+
involves: 129P2/OlaHsd * FVB/N * NMRI MGI:4418052
cx7
Tbx2tm1.1(cre)Vmc/Tbx2+
Tbx3tm1.1(cre)Vmc/Tbx3tm1.1(cre)Vmc
involves: 129P2/OlaHsd * FVB/N * NMRI MGI:4418051
cx8
Tbx2tm1.1(cre)Vmc/Tbx2+
Tbx3tm1.1(cre)Vmc/Tbx3+
involves: 129P2/OlaHsd * FVB/N * NMRI MGI:4418053


Genotype
MGI:4418058
hm1
Allelic
Composition
Tbx2tm1.1(cre)Vmc/Tbx2tm1.1(cre)Vmc
Genetic
Background
involves: 129P2/OlaHsd * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx2tm1.1(cre)Vmc mutation (0 available); any Tbx2 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• bilateral hindlimb-specific duplication of digit IV is observed




Genotype
MGI:4418054
hm2
Allelic
Composition
Tbx2tm1.1(cre)Vmc/Tbx2tm1.1(cre)Vmc
Genetic
Background
involves: 129P2/OlaHsd * NMRI
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx2tm1.1(cre)Vmc mutation (0 available); any Tbx2 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• mesenchymal cell proliferation is significantly increased at E12.5 in the anterior region, but not in the posterior region at this age, or in either region at E14.0
• at E13.5, palatal shelves appear smaller and have moved less down the tongue compared to wild type
• at E14.0, a significant reduction in size of the anterior region of the palatal shelves is detected with no significant changes in cell densities in the anterior or posterior aspects
• at E18.5 and 15.5, 18 of 21 embryos analyzed show a complete cleft of the secondary palate
• morphogenesis of the palatal shelves is severely retarded and comes to a premature hold with elevated palatal shelves only apparent at E14.5 in contrast to wild-type where elevated shelves are seen at E14.25 and fusion occurs between E14.5 and 15.5

limbs/digits/tail
• bilateral hindlimb-specific duplication of digit IV is observed

digestive/alimentary system
• mesenchymal cell proliferation is significantly increased at E12.5 in the anterior region, but not in the posterior region at this age, or in either region at E14.0
• at E13.5, palatal shelves appear smaller and have moved less down the tongue compared to wild type
• at E14.0, a significant reduction in size of the anterior region of the palatal shelves is detected with no significant changes in cell densities in the anterior or posterior aspects
• at E18.5 and 15.5, 18 of 21 embryos analyzed show a complete cleft of the secondary palate
• morphogenesis of the palatal shelves is severely retarded and comes to a premature hold with elevated palatal shelves only apparent at E14.5 in contrast to wild-type where elevated shelves are seen at E14.25 and fusion occurs between E14.5 and 15.5

growth/size/body
• mesenchymal cell proliferation is significantly increased at E12.5 in the anterior region, but not in the posterior region at this age, or in either region at E14.0
• at E13.5, palatal shelves appear smaller and have moved less down the tongue compared to wild type
• at E14.0, a significant reduction in size of the anterior region of the palatal shelves is detected with no significant changes in cell densities in the anterior or posterior aspects
• at E18.5 and 15.5, 18 of 21 embryos analyzed show a complete cleft of the secondary palate
• morphogenesis of the palatal shelves is severely retarded and comes to a premature hold with elevated palatal shelves only apparent at E14.5 in contrast to wild-type where elevated shelves are seen at E14.25 and fusion occurs between E14.5 and 15.5




Genotype
MGI:4418056
ht3
Allelic
Composition
Tbx2tm1.1(cre)Vmc/Tbx2+
Genetic
Background
involves: 129P2/OlaHsd * NMRI
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx2tm1.1(cre)Vmc mutation (0 available); any Tbx2 mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice are phenotypically normal on this outbred background




Genotype
MGI:5314603
cx4
Allelic
Composition
Tbx2tm1.1(cre)Vmc/Tbx2tm1.1(cre)Vmc
Tbx3tm1.1(cre)Vmc/Tbx3tm1.1(cre)Vmc
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx2tm1.1(cre)Vmc mutation (0 available); any Tbx2 mutation (27 available)
Tbx3tm1.1(cre)Vmc mutation (0 available); any Tbx3 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• mice exhibit abrogation of myocardial patterning of the atrioventricular canal and largely lack the constriction between the left ventricle and atrium

embryo
• slightly retarded at E9.5

growth/size/body
• slightly retarded at E9.5




Genotype
MGI:4418050
cx5
Allelic
Composition
Tbx2tm1.1(cre)Vmc/Tbx2tm1.1(cre)Vmc
Tbx3tm1.1(cre)Vmc/Tbx3tm1.1(cre)Vmc
Genetic
Background
involves: 129P2/OlaHsd * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx2tm1.1(cre)Vmc mutation (0 available); any Tbx2 mutation (27 available)
Tbx3tm1.1(cre)Vmc mutation (0 available); any Tbx3 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• 11 of 13 embryos show complete cleft palate

digestive/alimentary system
• 11 of 13 embryos show complete cleft palate

growth/size/body
• 11 of 13 embryos show complete cleft palate




Genotype
MGI:4418052
cx6
Allelic
Composition
Tbx2tm1.1(cre)Vmc/Tbx2tm1.1(cre)Vmc
Tbx3tm1.1(cre)Vmc/Tbx3+
Genetic
Background
involves: 129P2/OlaHsd * FVB/N * NMRI
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx2tm1.1(cre)Vmc mutation (0 available); any Tbx2 mutation (27 available)
Tbx3tm1.1(cre)Vmc mutation (0 available); any Tbx3 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• the limited number of embryos obtained from intercrosses die at E10.5 due to hemodynamic failure




Genotype
MGI:4418051
cx7
Allelic
Composition
Tbx2tm1.1(cre)Vmc/Tbx2+
Tbx3tm1.1(cre)Vmc/Tbx3tm1.1(cre)Vmc
Genetic
Background
involves: 129P2/OlaHsd * FVB/N * NMRI
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx2tm1.1(cre)Vmc mutation (0 available); any Tbx2 mutation (27 available)
Tbx3tm1.1(cre)Vmc mutation (0 available); any Tbx3 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• the limited number of embryos obtained from intercrosses die at E10.5 due to hemodynamic failure




Genotype
MGI:4418053
cx8
Allelic
Composition
Tbx2tm1.1(cre)Vmc/Tbx2+
Tbx3tm1.1(cre)Vmc/Tbx3+
Genetic
Background
involves: 129P2/OlaHsd * FVB/N * NMRI
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx2tm1.1(cre)Vmc mutation (0 available); any Tbx2 mutation (27 available)
Tbx3tm1.1(cre)Vmc mutation (0 available); any Tbx3 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• 5 of 13 embryos show complete cleft palate at E18.5

digestive/alimentary system
• 5 of 13 embryos show complete cleft palate at E18.5

growth/size/body
• 5 of 13 embryos show complete cleft palate at E18.5





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory