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Phenotypes Associated with This Genotype
Genotype
MGI:3717735
Allelic
Composition
Foxf2W174R/Foxf2W174R
Genetic
Background
involves: BALB/c * C3H/HeH
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxf2W174R mutation (0 available); any Foxf2 mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Foxf2W174R/Foxf2W174R pups are smaller at 3 days after birth and consume less milk at birth

mortality/aging
• mice die within 14 days of birth

vision/eye
• formation of the ciliary body is absent in the E18.5 eye
• at E18.5, mice fail to exhibit evagination of tissue from the anterior optic cup unlike in wild-type mice

growth/size/body
• mice fail to thrive after birth

craniofacial
N
• mice exhibit normal primary and secondary palate

Mouse Models of Human Disease
OMIM ID Ref(s)
Anterior Segment Mesenchymal Dysgenesis; ASMD 107250 J:178103


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/19/2016
MGI 6.03
The Jackson Laboratory