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Symbol
Name
ID

Smad2
SMAD family member 2
MGI:108051

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Blue sclerae	Hypertelorism	Amaurosis fugax	Visual impairment	Visual field defect
Disease(s) Associated with SMAD2	Blue sclerae	Hypertelorism	Amaurosis fugax	Visual impairment	Visual field defect
Loeys-Dietz syndrome
Lynch syndrome

Mouse Phenotypes		abnormal eye morphology	absent optic placodes	abnormal eye development
Availability	Mouse Genotype	abnormal eye morphology	absent optic placodes	abnormal eye development
	Smad2^m1Mag/Smad2^m1Mag
	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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