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Symbol
Name
ID

Smad2
SMAD family member 2
MGI:108051

Phenotype annotations related to craniofacial

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	Craniosynostosis	Micrognathia	Malar flattening	Adenoma sebaceum	Bifid uvula	High palate	Salivary gland neoplasm	Orofacial cleft
Loeys-Dietz syndrome
Lynch syndrome

Mouse Phenotypes		abnormal craniofacial morphology	abnormal Meckel's cartilage morphology	abnormal mandible morphology	absent mandible	mandible hypoplasia
Availability	Mouse Genotype	abnormal craniofacial morphology	abnormal Meckel's cartilage morphology	abnormal mandible morphology	absent mandible	mandible hypoplasia
	Smad2^tm1Cxd/Smad2⁺
	Smad2^tm1Enl/Smad2⁺
	Smad2^tm2Enl/Smad2⁺

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 04/16/2024 MGI 6.23