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Phenotypes Associated with This Genotype
Genotype
MGI:4437476
Allelic
Composition
Cryaatm1Ady/Cryaa+
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cryaatm1Ady mutation (0 available); any Cryaa mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Lens opacity in Cryaatm1Ady/Cryaa+, Cryaatm1Ady/Cryaatm1Ady, and Cryaatm1.1Ady/Cryaatm1.1Ady mice

vision/eye
• at 9 months, mice exhibit severe posterior rupture of the lens, curling up of the posterior capsule, and migration of cells to the posterior lens unlike wild-type mice
• at 9 months, mice exhibit severe posterior rupture of the lens unlike wild-type mice
• at 3 weeks, lenses contain small and large swollen cells or vacuoles in the lens cortical fiber unlike in wild-type mice
• beginning at 2 to 3 months of age and worsening with age in the posterior and nuclear regions of the lens

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cataract 9 multiple types DOID:0110266 OMIM:604219
J:157274


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
04/23/2024
MGI 6.23
The Jackson Laboratory