Phenotypes Associated with This Genotype

Genotype
MGI:2175798

• Allelic Composition: Cryaa^lop18/Cryaa^lop18
• Genetic Background: involves: CBA/CaGnLeJ

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

vision/eye

abnormal lens morphology ( J:34933 )

• degeneration of lens cortex

• posterior migration of lens epithelial nuclei

lens vacuoles ( J:34933 )

• vacuoles in lens noted at E14; prominent by E16

abnormal lens fiber morphology ( J:34933 )

• abnormal fibers form at posterior pole of lens

cataract ( J:34933 )

• apparent at weaning age; progressive severity with age

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
cataract 9 multiple types		DOID:0110266	OMIM:604219	J:34933