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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cryaatm1Wawr
targeted mutation 1, Eric F Wawrousek
MGI:1858025
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cryaatm1Wawr/Cryaatm1Wawr involves: 129/Sv * 129S4/SvJae MGI:2175799
hm2
Cryaatm1Wawr/Cryaatm1Wawr involves: 129S4/SvJae * C57BL/6 * DBA/2 MGI:2175800
ht3
Cryaatm1Wawr/Cryaa+ involves: 129/Sv * 129S4/SvJae MGI:2681051
ht4
Cryaatm1Wawr/Cryaa+ involves: 129S4/SvJae * C57BL/6 * DBA/2 MGI:2681049


Genotype
MGI:2175799
hm1
Allelic
Composition
Cryaatm1Wawr/Cryaatm1Wawr
Genetic
Background
involves: 129/Sv * 129S4/SvJae
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cryaatm1Wawr mutation (0 available); any Cryaa mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Lens opacity in Cryaatm1Wawr/Cryaatm1Wawr mice

vision/eye
• death of lens epithelial cells was noted in TUNEL and BrdU experiments; cause appeared to be due to defects in mitosis
• mild cataract at 7 weeks of age; progressive severity to dense opacity by 10 weeks of age
• small lens; 25-35% reduced weight and 15% reduced axial and equatorial dimensions
• inclusion bodies composed of crystallin proteins observed in nuclear and inner cortical regions
• small eyes

cellular
• death of lens epithelial cells was noted in TUNEL and BrdU experiments; cause appeared to be due to defects in mitosis

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cataract 9 multiple types DOID:0110266 OMIM:604219
J:38210




Genotype
MGI:2175800
hm2
Allelic
Composition
Cryaatm1Wawr/Cryaatm1Wawr
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cryaatm1Wawr mutation (0 available); any Cryaa mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Lens opacity in Cryaatm1Wawr/Cryaatm1Wawr mice

vision/eye
• death of lens epithelial cells was noted in TUNEL and BrdU experiments; cause appeared to be due to defects in mitosis
• mild cataract at 7 weeks of age; progressive severity to dense opacity by 10 weeks of age
• small lens; 25-35% reduced weight and 15% reduced axial and equatorial dimensions
• inclusion bodies composed of crystallin proteins observed in nuclear and inner cortical regions
• small eyes

cellular
• death of lens epithelial cells was noted in TUNEL and BrdU experiments; cause appeared to be due to defects in mitosis

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cataract 9 multiple types DOID:0110266 OMIM:604219
J:38210




Genotype
MGI:2681051
ht3
Allelic
Composition
Cryaatm1Wawr/Cryaa+
Genetic
Background
involves: 129/Sv * 129S4/SvJae
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cryaatm1Wawr mutation (0 available); any Cryaa mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• small lens; 10-15% reduced weight and 5% reduced axial and equatorial dimensions




Genotype
MGI:2681049
ht4
Allelic
Composition
Cryaatm1Wawr/Cryaa+
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cryaatm1Wawr mutation (0 available); any Cryaa mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• small lens; 10-15% reduced weight and 5% reduced axial and equatorial dimensions





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory