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Phenotypes Associated with This Genotype
Genotype
MGI:5297593
Allelic
Composition
Foxf2W174R/Foxf2+
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 (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Iris abnormalities in Foxf2W174R/Foxf2+ mice

vision/eye
• mice exhibit extraneous amorphous tissue between the retina and the lens unlike in wild-type mice
• 2 of 18 mice exhibit swelling of the optic nerve, which disrupts the outer nuclear layer of the retina
• one mouse exhibits hypoplastic ciliary muscle compared with wild-type mice
• 6 of 10 mice exhibit reduced angle between cornea and iris compared with wild-type mice
• smaller in 7 of 10 mice
• absent in 2 of 10 mice
• hypoplastic ciliary body or ciliary body process
• hypoplastic ciliary body or ciliary body process
• the iris stroma sows irregular thinning of the tissue and loss of structural organization at P45
• iridocorneal adhesion is present
• in two mice at 6 months of age
• disrupted in 2 of 18 mice due to swelling of the optic nerve

nervous system
• 2 of 18 mice exhibit swelling of the optic nerve, which disrupts the outer nuclear layer of the retina

homeostasis/metabolism
• 2 of 18 mice exhibit swelling of the optic nerve, which disrupts the outer nuclear layer of the retina

muscle
• one mouse exhibits hypoplastic ciliary muscle compared with wild-type mice


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
05/21/2024
MGI 6.23
The Jackson Laboratory