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Symbol
Name
ID

Gli3
GLI-Kruppel family member GLI3
MGI:95729

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Keratoconus	Hypertelorism	Microphthalmia
Disease(s) Associated with GLI3	Keratoconus	Hypertelorism	Microphthalmia
Greig cephalopolysyndactyly syndrome
Pallister-Hall syndrome
polydactyly

Mouse Phenotypes		absent optic nerve	abnormal eye morphology	abnormal eye development	microphthalmia	eyelids open at birth	anophthalmia
Availability	Mouse Genotype	absent optic nerve	abnormal eye morphology	abnormal eye development	microphthalmia	eyelids open at birth	anophthalmia
	Gli3^Pdn/Gli3^Pdn
	Gli3^TgBR/Gli3^TgBR
	Gli3^Xt-J/Gli3^Xt-J
	Gli3^tm1.2Zllr/Gli3^Xt-J

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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