Symbol Name ID |
Myh9
myosin, heavy polypeptide 9, non-muscle MGI:107717 |
Darker colors indicate more annotations |
Human Phenotypes | Increased circulating IgA level |
Increased circulating IgE level |
Leukocytosis |
Neutrophil inclusion bodies |
Leukocyte inclusion bodies |
Glomerulonephritis |
Nephritis |
Eczematoid dermatitis |
Disease(s) Associated with MYH9 | ||||||||
autosomal dominant Alport syndrome | ||||||||
MYH-9 related disease | ||||||||
thrombocytopenia |
Mouse Phenotypes | abnormal leukocyte migration |
abnormal leukocyte adhesion |
abnormal thrombopoiesis |
abnormal neutrophil morphology |
decreased CD8-positive, alpha-beta T cell number |
abnormal T cell physiology |
abnormal CD8-positive, alpha-beta T cell physiology |
abnormal lymph node cell ratio |
increased incidence of corneal inflammation |
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Availability | Mouse Genotype | |||||||||
Myh9tm1.1(MYH9*)Mjk/Myh9tm1.1(MYH9*)Mjk | ||||||||||
Myh9tm7.1Rsad/Myh9tm7.1Rsad | ||||||||||
Myh9tm1.1(MYH9*)Mjk/Myh9+ | ||||||||||
Myh9tm1.1Dash/Myh9+ | ||||||||||
Myh9tm6.1(EGFP/MYH9*)Rsad/Myh9+ | ||||||||||
Myh9tm7.1Rsad/Myh9+ | ||||||||||
Myh9tm5Rsad/Myh9tm5Rsad (conditional) | ||||||||||
Myh9tm5Rsad/Myh9tm5Rsad Tg(Lck-cre)#Nik/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 04/16/2024 MGI 6.23 |
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