|
Symbol Name ID |
Foxc2
forkhead box C2 MGI:1347481 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Conjunctivitis |
Abnormal cardiovascular system morphology |
Ventricular septal defect |
Tetralogy of Fallot |
Patent ductus arteriosus |
Varicose veins |
Arrhythmia |
Abnormality of the pulmonary vasculature |
| Disease(s) Associated with FOXC2 | ||||||||
| lymphedema-distichiasis syndrome |
| Mouse Phenotypes | cardiovascular system phenotype |
abnormal blood vessel morphology |
abnormal fourth pharyngeal arch artery morphology |
abnormal third pharyngeal arch artery morphology |
abnormal aortic arch morphology |
aortic arch coarctation |
interrupted aortic arch, type b |
absent glomerular endothelium fenestra |
decreased glomerular capillary number |
dilated glomerular capillary |
thin myocardium |
perimembraneous ventricular septal defect |
ventricular septal defect |
pericardial effusion |
abnormal lymph circulation |
intracranial hemorrhage |
glomerulus hemorrhage |
spinal hemorrhage |
|
| Availability | Mouse Genotype | ||||||||||||||||||
| Foxc2tm1.2Tsku/Foxc2tm1.2Tsku | |||||||||||||||||||
| Foxc2tm1Blh/Foxc2tm1Blh | |||||||||||||||||||
| Foxc2tm1Miu/Foxc2tm1Miu | |||||||||||||||||||
| Foxc2tm1Miu/Foxc2+ | |||||||||||||||||||
| Foxc2tm1.1Miu/Foxc2tm1.1Miu Nkx2-5tm1(cre)Rjs/Nkx2-5+ (conditional) |
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| Foxc2tm1.1Miu/Foxc2tm1.1Miu Tg(Tek-cre)1Ywa/0 (conditional) |
* | ||||||||||||||||||
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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