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Symbol Name ID |
Foxc2
forkhead box C2 MGI:1347481 |
| Darker colors indicate more annotations |
| Human Phenotypes | Proteinuria |
Glomerulopathy |
Tubulointerstitial nephritis |
Renal duplication |
Recurrent urinary tract infections |
| Disease(s) Associated with FOXC2 | |||||
| lymphedema-distichiasis syndrome |
| Mouse Phenotypes | absent glomerular endothelium fenestra |
decreased glomerular capillary number |
dilated glomerular capillary |
glomerulus hemorrhage |
abnormal mesangial cell morphology |
abnormal podocyte morphology |
absent podocyte foot process |
absent podocyte slit diaphragm |
abnormal renal glomerulus basement membrane morphology |
abnormal renal glomerulus morphology |
abnormal glomerular mesangium morphology |
decreased renal glomerulus number |
small kidney |
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| Availability | Mouse Genotype | |||||||||||||
| Foxc2tm1Blh/Foxc2tm1Blh | ||||||||||||||
| Foxc2tm1Miu/Foxc2tm1Miu | ||||||||||||||
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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