Symbol Name ID |
Foxf1
forkhead box F1 MGI:1347470 |
Darker colors indicate more annotations |
Human Phenotypes | Pleural effusion |
Pulmonary artery dilatation |
Pulmonary artery stenosis |
Partial anomalous pulmonary venous return |
Misalignment of the pulmonary veins |
Pulmonary lymphangiectasia |
Pulmonary arterial hypertension |
Tracheoesophageal fistula |
Abnormal lung lobation |
Alveolar capillary dysplasia |
Neonatal respiratory distress |
Disease(s) Associated with FOXF1 | |||||||||||
persistent fetal circulation syndrome |
Mouse Phenotypes | abnormal lung vasculature morphology |
lung hemorrhage |
decreased lung endothelial cell proliferation |
lung inflammation |
abnormal lung morphology |
abnormal lung development |
impaired lung alveolus development |
abnormal lung bud morphology |
abnormal lung saccule morphology |
fused right lung lobes |
small lung |
pulmonary hypoplasia |
abnormal pulmonary alveolus morphology |
respiratory distress |
abnormal surfactant secretion |
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Availability | Mouse Genotype | |||||||||||||||
Foxf1em1Vvk/Foxf1+ | ||||||||||||||||
Foxf1tm1Rhc/Foxf1+ |
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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