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Symbol
Name
ID

Gli3
GLI-Kruppel family member GLI3
MGI:95729

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Inguinal hernia	Omphalocele	Umbilical hernia	Short stature	Growth delay	Intrauterine growth retardation
Disease(s) Associated with GLI3	Inguinal hernia	Omphalocele	Umbilical hernia	Short stature	Growth delay	Intrauterine growth retardation
Greig cephalopolysyndactyly syndrome
Pallister-Hall syndrome
polydactyly

Mouse Phenotypes		abnormal tooth development	abnormal palatine bone horizontal plate morphology	abnormal facial morphology	bilateral cleft upper lip	unilateral cleft upper lip	cleft palate	abnormal ear position	embryonic growth retardation	increased embryo size	herniated abdominal wall
Availability	Mouse Genotype	abnormal tooth development	abnormal palatine bone horizontal plate morphology	abnormal facial morphology	bilateral cleft upper lip	unilateral cleft upper lip	cleft palate	abnormal ear position	embryonic growth retardation	increased embryo size	herniated abdominal wall
	Gli3^Pdn/Gli3^Pdn
	Gli3^TgBR/Gli3^TgBR
	Gli3^tm1Urt/Gli3^tm1Urt
	Gli3^Xt-3H/Gli3^Xt-3H
	Gli3^Xt-J/Gli3^Xt-J
	Gli3^Xt-3H/Gli3⁺

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 04/30/2024 MGI 6.23