Symbol Name ID |
Foxf1
forkhead box F1 MGI:1347470 |
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 |
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Availability | Mouse Genotype | |||||||||
Foxf1em1Vvk/Foxf1em1Vvk | ||||||||||
Foxf1tm1Pca/Foxf1tm1Pca | ||||||||||
Foxf1tm1Rhc/Foxf1tm1Rhc | ||||||||||
Foxf1em1Vvk/Foxf1+ | ||||||||||
Foxf1tm1Rhc/Foxf1+ | ||||||||||
Foxf1tm2Rhc/Foxf1tm2Rhc Tg(Myh11-cre,-EGFP)2Mik/0 (conditional) |
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Foxf1tm2Rhc/Foxf1+ Tg(Myh11-cre,-EGFP)2Mik/0 (conditional) |
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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