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Phenotypes Associated with This Genotype
Genotype
MGI:2176812
Allelic
Composition
Fgf8tm1.2Mrt/Fgf8tm1.2Mrt
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf8tm1.2Mrt mutation (0 available); any Fgf8 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all homozygotes are resorbed by E10.5
• by E9.5 embryos begin to die likely because the heart does not form

embryo
• ectoderm on the anterior side of the embryo appears undifferentiated and fails to form a neural tube
• all embryonic mesoderm-derived structures appear to be absent including the heart (J:45909)
• at E8.5 embryos lack all mesodermally-derived tissues including the heart and somites; little mesoderm is detected anterior to the primitive streak (J:56519)
• embryos are significantly smaller than wild-type or heterozygous littermates at E8.5 and E9.5
• after cells undergo epithelial-mesenchymal transition, at E7.5, majority of nascent mesodermal cells fail to migrate away from the primitive streak, resulting in deformation of the epiblast and inward collapse of the posterior side of the embryo
• node does not form in mutants
• somites do not develop
• at E7.5 in mutant embryos the streak never extends to the distal tip of the embryo
• allantois is displaced anteriorly
• a chorion can be identified but is often tortuous

growth/size/body
• embryos are significantly smaller than wild-type or heterozygous littermates at E8.5 and E9.5

cardiovascular system
• the heart does not form (J:45909)


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
01/28/2026
MGI 6.24
The Jackson Laboratory