Symbol Name ID |
Smad2
SMAD family member 2 MGI:108051 |
Darker colors indicate more annotations |
Human Phenotypes | Tall stature |
Weight loss |
Disease(s) Associated with SMAD2 | ||
Loeys-Dietz syndrome | ||
Lynch syndrome |
Mouse Phenotypes | embryonic growth retardation |
decreased embryo size |
slow postnatal weight gain |
decreased body size |
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Availability | Mouse Genotype | ||||
Smad2tm1.2Mwst/Smad2tm1.2Mwst | |||||
Smad2tm1Cxd/Smad2tm1Cxd | |||||
Smad2tm1Enl/Smad2tm1Enl | |||||
Smad2tm2Enl/Smad2tm2Enl | |||||
Smad2tm1Enl/Smad2+ | |||||
Smad2tm2Enl/Smad2+ | |||||
Smad2tm1.1Nomu/Smad2tm1.1Nomu Tg(Nes-cre)1Kln/0 (conditional) |
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 04/09/2024 MGI 6.23 |
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