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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
CryaaAey7
dominant cataract 7
MGI:2653028
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
CryaaAey7/CryaaAey7 C3HeB/FeJ MGI:2653233
ht2
CryaaAey7/Cryaa+ C3HeB/FeJ MGI:2653234


Genotype
MGI:2653233
hm1
Allelic
Composition
CryaaAey7/CryaaAey7
Genetic
Background
C3HeB/FeJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
CryaaAey7 mutation (0 available); any Cryaa mutation (5 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; more severe than heterozygotes (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 (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 (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 (J:72928)
• small eyes (J:72928)
• small eyes (J:72928)

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




Genotype
MGI:2653234
ht2
Allelic
Composition
CryaaAey7/Cryaa+
Genetic
Background
C3HeB/FeJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
CryaaAey7 mutation (0 available); any Cryaa mutation (5 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 (J:72928)
• clefts apparent in the subcortical zone and nucleus at 7 weeks of age; this region corresponded to regions of developing opacity (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 (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 (J:72928)
• small eyes (J:72928)
• small eyes (J:72928)

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





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last database update
02/02/2016
MGI 6.02
The Jackson Laboratory