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Symbol
Name
ID
Myh9
myosin, heavy polypeptide 9, non-muscle
MGI:107717
Phenotype annotations related to homeostasis/metabolism
*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
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)
Myh9tm1.1Gac/Myh9tm1.1Gac
Tg(NPHS2-cre)295Lbh/0  (conditional)
*
Myh9tm5Rsad/Myh9tm5Rsad
Tg(Nphs2-cre)1Seq/0  (conditional)
Myh9tm1.1Gac/Myh9+
Tg(Pf4-icre)Q3Rsko/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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory