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Phenotypes Associated with This Genotype
Genotype
MGI:2653234
Allelic
Composition
CryaaAey7/Cryaa+
Genetic
Background
C3HeB/FeJ-CryaaAey7/Ieg
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
CryaaAey7 mutation (1 available); any Cryaa mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• clefts apparent in the subcortical zone and nucleus at 7 weeks of age; this region corresponded to regions of developing opacity
• described as progressive, starting as a visible opacity in the embryonic nucleus and resulting in a zonal and nuclear opacity by 2 months of age
• small eyes

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cataract 9 multiple types DOID:0110266 OMIM:604219
J:72928


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
03/19/2024
MGI 6.23
The Jackson Laboratory