Symbol Name ID |
Smad2
SMAD family member 2 MGI:108051 |
Darker colors indicate more annotations |
Human Phenotypes | Craniosynostosis |
Micrognathia |
Malar flattening |
Adenoma sebaceum |
Bifid uvula |
High palate |
Salivary gland neoplasm |
Orofacial cleft |
Disease(s) Associated with SMAD2 | ||||||||
Loeys-Dietz syndrome | ||||||||
Lynch syndrome |
Mouse Phenotypes | abnormal craniofacial morphology |
abnormal Meckel's cartilage morphology |
abnormal mandible morphology |
absent mandible |
mandible hypoplasia |
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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) |
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last database update 07/05/2024 MGI 6.24 |
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