Symbol Name ID |
Smad2
SMAD family member 2 MGI:108051 |
Darker colors indicate more annotations |
Human Phenotypes | Craniosynostosis |
Micrognathia |
Malar flattening |
Camptodactyly of finger |
Arachnodactyly |
Flexion contracture |
Joint hypermobility |
Pectus carinatum |
Pectus excavatum |
Scoliosis |
Joint dislocation |
Neoplasm of the skeletal system |
Disease(s) Associated with SMAD2 | ||||||||||||
Loeys-Dietz syndrome | ||||||||||||
Lynch syndrome |
Mouse Phenotypes | abnormal Meckel's cartilage morphology |
abnormal mandible morphology |
absent mandible |
mandible hypoplasia |
|
Availability | Mouse Genotype | ||||
Smad2tm1Cxd/Smad2+ | |||||
Smad2tm1Enl/Smad2+ | |||||
Smad2tm2Enl/Smad2+ |
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 07/05/2024 MGI 6.24 |
|
|