Mouse Genome Informatics
hm1
     CryaaAey7/CryaaAey7
C3HeB/FeJ
Key:
♀ phenotype observed in females WTSI Wellcome Trust Sanger Institute
♂ phenotype observed in males Euro Europhenome
N normal phenotype
vision/eye
abnormal lens morphology ( J:72928 )
• 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
cataracts ( J:72928 )
• 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
microphthalmia ( J:72928 )
• small eyes

Mouse Models of Human Disease
 OMIM IDRef(s)
Crystallin, Alpha-A; CRYAA 123580 J:72928


Mouse Genome Informatics
ht2
     CryaaAey7/Cryaa+
C3HeB/FeJ
Key:
♀ phenotype observed in females WTSI Wellcome Trust Sanger Institute
♂ phenotype observed in males Euro Europhenome
N normal phenotype
vision/eye
abnormal lens morphology ( J:72928 )
• clefts apparent in the subcortical zone and nucleus at 7 weeks of age; this region corresponded to regions of developing opacity
cataracts ( J:72928 )
• 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
microphthalmia ( J:72928 )
• small eyes

Mouse Models of Human Disease
 OMIM IDRef(s)
Crystallin, Alpha-A; CRYAA 123580 J:72928