Symbol Name ID |
Myh9
myosin, heavy polypeptide 9, non-muscle MGI:107717 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Increased circulating IgA level |
Increased circulating IgE level |
Hypophosphatemia |
Azotemia |
Elevated circulating hepatic transaminase concentration |
Hematuria |
Microscopic hematuria |
Proteinuria |
Disease(s) Associated with MYH9 | ||||||||
autosomal dominant Alport syndrome | ||||||||
MYH-9 related disease | ||||||||
thrombocytopenia |
Mouse Phenotypes | homeostasis/metabolism phenotype |
abnormal platelet physiology |
abnormal blood coagulation |
increased bleeding time |
albuminuria |
hematuria |
increased susceptibility to injury |
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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+ | ||||||||
Myh9tm1.1Gac/Myh9tm1.1Gac Tg(Pf4-icre)Q3Rsko/0 (conditional) |
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Myh9tm1.1Gac/Myh9tm1.1Gac Tg(NPHS2-cre)295Lbh/0 (conditional) |
* | |||||||
Myh9tm5Rsad/Myh9tm5Rsad Tg(Nphs2-cre)1Seq/0 (conditional) |
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Myh9tm1.1Gac/Myh9+ Tg(Pf4-icre)Q3Rsko/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 04/23/2024 MGI 6.23 |
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