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Symbol Name ID |
Foxc1
forkhead box C1 MGI:1347466 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypospadias |
| Disease(s) Associated with FOXC1 | |
| Axenfeld-Rieger syndrome |
| Mouse Phenotypes | abnormal kidney arterial blood vessel morphology |
abnormal right renal artery morphology |
abnormal kidney vasculature morphology |
abnormal kidney venous blood vessel morphology |
enlarged kidney |
abnormal renal/urinary system morphology |
abnormal kidney morphology |
abnormal kidney development |
abnormal metanephros morphology |
hydronephrosis |
duplex kidney |
abnormal ureter development |
bifid ureter |
blind ureter |
ectopic ureter |
hydroureter |
ectopic ureteric bud |
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| Availability | Mouse Genotype | |||||||||||||||||
| Foxc1ch/Foxc1ch | ||||||||||||||||||
| Foxc1tm1Blh/Foxc1tm1Blh | ||||||||||||||||||
| Foxc1ch/Foxc1+ | ||||||||||||||||||
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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