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Symbol
Name
ID

Eogt
EGF domain specific O-linked N-acetylglucosamine transferase
MGI:2141669

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Cataract	Developmental cataract	Optic atrophy	Hypertelorism	Microphthalmia	Strabismus	Esotropia	Visual impairment
Disease(s) Associated with EOGT
Adams-Oliver syndrome

Mouse Phenotypes		abnormal retina vasculature morphology
Availability	Mouse Genotype	abnormal retina vasculature morphology
	Eogt^tm1.2Okaj/Eogt^tm1.2Okaj
	Eogt^tm1.1Okaj/Eogt^tm1.1Okaj Tg(Tek-cre)1Ywa/0 (conditional)

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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