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Symbol
Name
ID

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

Phenotype annotations related to vision/eye

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

Human Phenotypes	Lenticonus	Anterior polar cataract	Presenile cataracts	Myopia
Disease(s) Associated with MYH9	Lenticonus	Anterior polar cataract	Presenile cataracts	Myopia
autosomal dominant Alport syndrome
MYH-9 related disease

Mouse Phenotypes		vision/eye phenotype	corneal vascularization	increased incidence of corneal inflammation	abnormal lens fiber morphology	cataract	abnormal eye physiology
Availability	Mouse Genotype	vision/eye phenotype	corneal vascularization	increased incidence of corneal inflammation	abnormal lens fiber morphology	cataract	abnormal eye physiology
	Myh9^tm7.1Rsad/Myh9^tm7.1Rsad
	Myh9^{tm1.1(MYH9*)Mjk}/Myh9⁺
	Myh9^tm1.1Dash/Myh9⁺	*
	Myh9^tm7.1Rsad/Myh9⁺

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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