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Symbol
Name
ID
Smad2
SMAD family member 2
MGI:108051
Phenotype annotations related to mortality/aging
Darker colors indicate more annotations
Human Phenotypes
Death in early adulthood
Death in infancy
Disease(s) Associated with SMAD2
Lynch syndrome

Mouse Phenotypes
premature death
embryonic lethality during organogenesis
embryonic lethality during organogenesis, complete penetrance
embryonic lethality between implantation and somite formation, complete penetrance
embryonic lethality, complete penetrance
Availability Mouse Genotype
Smad2m1Mag/Smad2m1Mag
Smad2tm1Cxd/Smad2tm1Cxd
Smad2tm1Enl/Smad2tm1Enl
Smad2tm1Rak/Smad2tm1Rak
Smad2tm1Rob/Smad2tm1Rob
Smad2tm2.1Rob/Smad2tm2.1Rob
Smad2tm2Enl/Smad2tm2Enl
Smad2m1Mag/Smad2tm1Rob
Smad2tm1Cxd/Smad2tm1Mwst
Smad2tm1Mwst/Smad2tm1.2Mwst
Smad2tm1Rob/Smad2tm2.1Rob
Smad2tm1.1Nomu/Smad2tm1.1Nomu
Tg(Nes-cre)1Kln/0  (conditional)

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)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory