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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Smad1tm1Rjle
targeted mutation 1, Robert J Lechleider
MGI:2157982
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Smad1tm1Rjle/Smad1tm1Rjle either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) MGI:2448124
ht2
Smad1tm1Rjle/Smad1+ involves: 129S6/SvEvTac * C57BL/6 MGI:5827844
ht3
Smad1tm1Rjle/Smad1+ involves: 129S6/SvEvTac * NIH Black Swiss MGI:3582566
cx4
Bmpr2tm1Mmue/Bmpr2+
Smad1tm1Rjle/Smad1+
involves: 129S1/SvImJ * 129S6/SvEvTac * C57BL/6 MGI:5827848


Genotype
MGI:2448124
hm1
Allelic
Composition
Smad1tm1Rjle/Smad1tm1Rjle
Genetic
Background
either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Smad1tm1Rjle mutation (0 available); any Smad1 mutation (32 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
• defective allantois formation
• allantois failed to fuse to chorion




Genotype
MGI:5827844
ht2
Allelic
Composition
Smad1tm1Rjle/Smad1+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Smad1tm1Rjle mutation (0 available); any Smad1 mutation (32 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
N
• mice do not exhibit increased right ventricular systolic pressure or right ventricular hypertrophy at 3 or 6 months of age




Genotype
MGI:3582566
ht3
Allelic
Composition
Smad1tm1Rjle/Smad1+
Genetic
Background
involves: 129S6/SvEvTac * NIH Black Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Smad1tm1Rjle mutation (0 available); any Smad1 mutation (32 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• significant reduction in the number of heterozygous mutant mice at weaning

nervous system
• increased cellular proliferation in the dorsal region of the neural tube but not in the ventral region, resulting in neuroectodermal hypercellularity
• about 22% of E11.5 embryos exhibit reductions in the midbrain and hindbrain
• about 22% of E11.5 embryos exhibit reductions in the midbrain and hindbrain
• have a curved cranial nerve likely to be a secondary effect caused by the abnormal architecture of the hindbrain
• exhibit a truncated spinal accessory nerve at E11.5

embryo
• increased cellular proliferation in the dorsal region of the neural tube but not in the ventral region, resulting in neuroectodermal hypercellularity




Genotype
MGI:5827848
cx4
Allelic
Composition
Bmpr2tm1Mmue/Bmpr2+
Smad1tm1Rjle/Smad1+
Genetic
Background
involves: 129S1/SvImJ * 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bmpr2tm1Mmue mutation (0 available); any Bmpr2 mutation (45 available)
Smad1tm1Rjle mutation (0 available); any Smad1 mutation (32 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• right ventricular hypertrophy by 6 months of age
• by 6 months of age, mice develop more severe elevations in right ventricular systolic pressure than single Bmpr2 heterozygotes

growth/size/body
• right ventricular hypertrophy by 6 months of age

muscle
• right ventricular hypertrophy by 6 months of age





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