Symbol Name ID |
Myo1e
myosin IE MGI:106621 |
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 |
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Availability | Mouse Genotype | |||||||
Myo1etm1.1Flv/Myo1etm1.1Flv | ||||||||
Myo1etm1Flv/Myo1etm1Flv Tg(NPHS2-cre)295Lbh/0 (conditional) |
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Myo1etm1Flv/Myo1etm1.1Flv Tg(NPHS2-cre)295Lbh/0 (conditional) |
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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last database update 09/03/2024 MGI 6.24 |
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