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Symbol
Name
ID

Myo1e
myosin IE
MGI:106621

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Hypoalbuminemia	Edema	Hematuria	Proteinuria
Disease(s) Associated with MYO1E
focal segmental glomerulosclerosis 6

Mouse Phenotypes		increased blood urea nitrogen level	abnormal urine homeostasis	increased urine protein level	albuminuria	hemoglobinuria	hematuria	leukocyturia
Availability	Mouse Genotype	increased blood urea nitrogen level	abnormal urine homeostasis	increased urine protein level	albuminuria	hemoglobinuria	hematuria	leukocyturia
	Myo1e^tm1.1Flv/Myo1e^tm1.1Flv
	Myo1e^tm1Flv/Myo1e^tm1Flv Tg(NPHS2-cre)295Lbh/0 (conditional)
	Myo1e^tm1Flv/Myo1e^tm1.1Flv 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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