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Symbol
Name
ID

Smad2
SMAD family member 2
MGI:108051

Phenotype annotations related to skeleton

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	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)
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