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Symbol
Name
ID
Foxf1
forkhead box F1
MGI:1347470
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
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
Availability Mouse Genotype
Foxf1tm1Pca/Foxf1tm1Pca

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/09/2018
MGI 6.12
The Jackson Laboratory