|
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 | Hematuria |
Microscopic hematuria |
Proteinuria |
Abnormality of the kidney |
Glomerular basement membrane lamellation |
Thickened glomerular basement membrane |
Glomerulonephritis |
Nephrocalcinosis |
Nephritis |
Nephropathy |
Nephrotic syndrome |
Renal insufficiency |
Stage 5 chronic kidney disease |
| Disease(s) Associated with MYH9 | |||||||||||||
| autosomal dominant Alport syndrome | |||||||||||||
| MYH-9 related disease |
| Mouse Phenotypes | renal/urinary system phenotype |
albuminuria |
hematuria |
abnormal podocyte morphology |
fused podocyte foot processes |
podocyte foot process effacement |
podocyte microvillus transformation |
increased renal glomerulus basement membrane thickness |
glomerulosclerosis |
renal cast |
|
| Availability | Mouse Genotype | ||||||||||
| Myh9tm1.1(MYH9*)Mjk/Myh9tm1.1(MYH9*)Mjk | |||||||||||
| Myh9tm7.1Rsad/Myh9tm7.1Rsad | |||||||||||
| Myh9Gt(Betageo-btk)1Dash/Myh9+ | * | ||||||||||
| Myh9tm1.1(MYH9*)Mjk/Myh9+ | |||||||||||
| Myh9tm1.1Dash/Myh9+ | |||||||||||
| Myh9tm7.1Rsad/Myh9+ | |||||||||||
| Myh9tm8.1Rsad/Myh9+ | |||||||||||
| Myh9tm1.1Gac/Myh9tm1.1Gac Tg(NPHS2-cre)295Lbh/0 (conditional) |
* | ||||||||||
| Myh9tm5Rsad/Myh9tm5Rsad Tg(Nphs2-cre)1Seq/0 (conditional) |
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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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