Mouse Genome Informatics
hm1
    CryaaAey7/CryaaAey7
C3HeB/FeJ
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
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; more severe than heterozygotes
• 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; more severe than heterozygotes
• small eyes

Mouse Models of Human Disease
OMIM IDRef(s)
Cataract 9, Multiple Types; CTRCT9 604219 J:72928


Mouse Genome Informatics
ht2
    CryaaAey7/Cryaa+
C3HeB/FeJ
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
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
OMIM IDRef(s)
Cataract 9, Multiple Types; CTRCT9 604219 J:72928