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Symbol
Name
ID
Foxf1
forkhead box F1
MGI:1347470
Phenotype annotations related to mortality/aging
Darker colors indicate more annotations
Human Phenotypes
Neonatal death
Disease(s) Associated with FOXF1
persistent fetal circulation syndrome

Mouse Phenotypes
lethality, incomplete penetrance
premature death
lethality throughout fetal growth and development, complete penetrance
neonatal lethality, complete penetrance
neonatal lethality, incomplete penetrance
perinatal lethality, complete penetrance
postnatal lethality, incomplete penetrance
embryonic lethality during organogenesis, complete penetrance
embryonic lethality, complete penetrance
Availability Mouse Genotype
Foxf1em1Vvk/Foxf1em1Vvk
Foxf1tm1Pca/Foxf1tm1Pca
Foxf1tm1Rhc/Foxf1tm1Rhc
Foxf1em1Vvk/Foxf1+
Foxf1tm1Rhc/Foxf1+
Foxf1tm2Rhc/Foxf1tm2Rhc
Tg(Myh11-cre,-EGFP)2Mik/0  (conditional)
Foxf1tm2Rhc/Foxf1+
Tg(Myh11-cre,-EGFP)2Mik/0  (conditional)

Contributing Projects:
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
The Jackson Laboratory