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Symbol
Name
ID

Myo9a
myosin IXa
MGI:107735

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Polyhydramnios	Decreased fetal movement
Disease(s) Associated with MYO9A	Polyhydramnios	Decreased fetal movement
congenital myasthenic syndrome

Mouse Phenotypes		abnormal Mullerian duct morphology	abnormal Wolffian duct morphology	abnormal neural tube ventricular layer morphology
Availability	Mouse Genotype	abnormal Mullerian duct morphology	abnormal Wolffian duct morphology	abnormal neural tube ventricular layer morphology
	Myo9a^tm1.2Bah/Myo9a^tm1.2Bah
	Myo9a^{tm1b(EUCOMM)Wtsi}/Myo9a^{tm1b(EUCOMM)Wtsi}

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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