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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Foxf1tm1Pca
targeted mutation 1, Peter Carlsson
MGI:1929432
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Foxf1tm1Pca/Foxf1tm1Pca either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129X1/SvJ * C57BL/6) MGI:2171425
hm2
Foxf1tm1Pca/Foxf1tm1Pca involves: 129P2/OlaHsd * C57BL/6 MGI:3818881


Genotype
MGI:2171425
hm1
Allelic
Composition
Foxf1tm1Pca/Foxf1tm1Pca
Genetic
Background
either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1) or (involves: 129X1/SvJ * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxf1tm1Pca mutation (0 available); any Foxf1 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos die at midgestation, between E9.5 and E10

embryo
• the posterior part of the embryo is developmentally retarded compared with the anterior part
• embryos are severely disfigured at E9.5
• impaired lateral plate differentiation and coelom formation
• incomplete separation of splanchnic and somatic mesoderm
• mutants exhibit a lower proliferation rate of mesodermal cells in the posterior primitive streak, resulting in an underdeveloped posterior end
• somites become asymmetrically arranged on either side of the neural tube
• somite formation is retarded such that fewer somites are seen at E8.5
• vascular plexus does not form
• although the allantois grows, it retains a primitive, bud-like shape, does not elongate and fails to contact the chorion
• defective mesodermal expansion and lack of vascularization of the allantois
• allantois does not elongate
• amnion is small, but thicker, consisting of multiple layers of rounded cells instead of the normal flattened bilayer, and does not expand with the growth of the embryo
• impaired differentiation of amniotic mesoderm; expression analysis indicates that the amniotic mesoderm resembles yolk sac mesoderm
• ectopic hematopoiesis in the amnion
• yolk sacs at E9.5 are wrinkled, shrunken, anemic and lack vasculature
• endodermal and mesodermal layers of the yolk sac are separated from each other, first seen at E8.5
• defects in extraembryonic mesoderm differentiation
• mesodermal layers of the amnion and yolk sack frequently adhere to each other, indicating enhanced intramesodermal cohesion, and as the yolk sac mesoderm separates from the endoderm, it occasionally fuses with the amnion
• yolk sac and amniotic mesoderm are unable to expand
• no placentation due to the lack of chorioallantoic fusion

digestive/alimentary system
• formation of the involuted hindgut diverticulum is delayed and the posterior visceral endoderm is flat and enclosed in a wide yolk-sac pocket
• midgut does not form because embryos fail to turn

cardiovascular system
• vascular plexus does not form




Genotype
MGI:3818881
hm2
Allelic
Composition
Foxf1tm1Pca/Foxf1tm1Pca
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxf1tm1Pca mutation (0 available); any Foxf1 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• yolk sacs are completely avascular
• at E9.5, yolk sac surface has wrinkles which are folds in the visceral endoderm which are prevented from expanding by constricted mesodermal layer
• yolk sac mesoderm has abnormal adhesion properties
• much of yolk sac mesoderm is detached and forms thick layer between yolk sac and amnion
• amnion appears normal but yolk sac mesoderm is hypoplastic and is reduced to thin lining of the endoderm

cardiovascular system
• yolk sacs are completely avascular





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory