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Symbol Name ID |
Foxo1
forkhead box O1 MGI:1890077 |
| Darker colors indicate more annotations |
| Mouse Phenotypes | pharyngeal arch artery hypoplasia |
abnormal vitelline vasculature morphology |
absent vitelline blood vessels |
small first pharyngeal arch |
absent second pharyngeal arch |
small second pharyngeal arch |
pharyngeal arch hypoplasia |
abnormal embryo development |
embryonic growth retardation |
abnormal somite development |
abnormal somite shape |
decreased somite size |
abnormal visceral yolk sac morphology |
abnormal vitelline vascular remodeling |
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| Availability | Mouse Genotype | ||||||||||||||
| Foxo1tm1.1Dac/Foxo1tm1.1Dac | |||||||||||||||
| Foxo1tm1Tf/Foxo1tm1Tf | |||||||||||||||
| Foxo1tm1Whb/Foxo1tm1Whb | |||||||||||||||
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 04/16/2024 MGI 6.23 |
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