About   Help   FAQ
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 (46 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





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
11/19/2024
MGI 6.24
The Jackson Laboratory