Symbol Name ID |
Foxc1
forkhead box C1 MGI:1347466 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal cardiovascular system morphology |
Atrial septal defect |
Patent ductus arteriosus |
Disease(s) Associated with FOXC1 | |||
Axenfeld-Rieger syndrome | |||
Axenfeld-Rieger syndrome type 3 |
Mouse Phenotypes | abnormal pharyngeal arch artery morphology |
abnormal fourth pharyngeal arch artery morphology |
aortic arch coarctation |
interrupted aortic arch |
abnormal kidney arterial blood vessel morphology |
abnormal right renal artery morphology |
abnormal kidney vasculature morphology |
abnormal kidney venous blood vessel morphology |
patent ductus arteriosus |
ventricular septal defect |
abnormal semilunar valve morphology |
abnormal aortic valve morphology |
abnormal aortic valve cusp morphology |
thick aortic valve cusps |
abnormal pulmonary valve morphology |
abnormal pulmonary valve cusp morphology |
thick pulmonary valve cusps |
ovary hemorrhage |
intracranial hemorrhage |
corneal vascularization |
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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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