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Symbol Name ID |
Foxf1
forkhead box F1 MGI:1347470 |
| Darker colors indicate more annotations |
| Human Phenotypes | Thickened nuchal skin fold |
Nonimmune hydrops fetalis |
Single umbilical artery |
Polyhydramnios |
| Disease(s) Associated with FOXF1 | ||||
| persistent fetal circulation syndrome |
| Mouse Phenotypes | absent vitelline blood vessels |
abnormal developmental patterning |
failure of initiation of embryo turning |
abnormal embryonic tissue morphology |
abnormal lateral plate mesoderm morphology |
abnormal posterior primitive streak morphology |
abnormal somite development |
delayed somite formation |
abnormal extraembryonic tissue morphology |
abnormal allantois morphology |
small allantois |
abnormal amnion morphology |
abnormal visceral yolk sac morphology |
abnormal visceral yolk sac mesenchyme morphology |
abnormal extraembryonic mesoderm development |
failure of chorioallantoic fusion |
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| Availability | Mouse Genotype | ||||||||||||||||
| Foxf1tm1Pca/Foxf1tm1Pca | |||||||||||||||||
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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