About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:2175799
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 (15 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


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory