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Phenotypes Associated with This Genotype
Genotype
MGI:2176478
Allelic
Composition
Fgfr2tm1Cxd/Fgfr2+
Genetic
Background
either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * NIH Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgfr2tm1Cxd mutation (0 available); any Fgfr2 mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• surprisingly, heterozygotes are developmentally normal with no craniofacial or limb defects


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
05/07/2024
MGI 6.23
The Jackson Laboratory