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Symbol
Name
ID

Myh9
myosin, heavy polypeptide 9, non-muscle
MGI:107717

Phenotype annotations related to cardiovascular system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Joint hemorrhage	Bruising susceptibility	Petechiae	Hypertension	Myocardial infarction
Disease(s) Associated with MYH9	Joint hemorrhage	Bruising susceptibility	Petechiae	Hypertension	Myocardial infarction
autosomal dominant Alport syndrome
MYH-9 related disease
thrombocytopenia

Mouse Phenotypes		cardiovascular system phenotype	abnormal brain vasculature morphology	abnormal placental labyrinth vasculature morphology	abnormal vascular branching morphogenesis	abnormal vitelline vasculature morphology	corneal vascularization
Availability	Mouse Genotype	cardiovascular system phenotype	abnormal brain vasculature morphology	abnormal placental labyrinth vasculature morphology	abnormal vascular branching morphogenesis	abnormal vitelline vasculature morphology	corneal vascularization
	Myh9^{tm2(GFP/MYH10)Rsad}/Myh9^{tm2(GFP/MYH10)Rsad}
	Myh9^{tm3(GFP/MYH9/MYH10)Rsad}/Myh9^{tm3(GFP/MYH9/MYH10)Rsad}
	Myh9^{tm4(GFP/MYH10/MYH9)Rsad}/Myh9^{tm4(GFP/MYH10/MYH9)Rsad}
	Myh9^{tm1.1(MYH9*)Mjk}/Myh9⁺
	Myh9^tm1.1Gac/Myh9^tm1.1Gac Tg(NPHS2-cre)295Lbh/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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