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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
CrygdLop12
lens opacity 12
MGI:1858026
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
CrygdLop12/CrygdLop12 involves: BALB/cJ * SJL/J MGI:3796549
ht2
CrygdLop12/Crygd+ involves: BALB/cJ * SJL/J MGI:2175808


Genotype
MGI:3796549
hm1
Allelic
Composition
CrygdLop12/CrygdLop12
Genetic
Background
involves: BALB/cJ * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
CrygdLop12 mutation (1 available); any Crygd mutation (8 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• characterized by irregular nuclear opacity that develops by one month of age
• develops mild cortical opacification with age
• early in life, the lens cortex and nuclear material extrude into the vitreous and posterior chambers




Genotype
MGI:2175808
ht2
Allelic
Composition
CrygdLop12/Crygd+
Genetic
Background
involves: BALB/cJ * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
CrygdLop12 mutation (1 available); any Crygd mutation (8 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• first detectable by 1 month of age; progressive opacity with age

Mouse Models of Human Disease
OMIM ID Ref(s)
Cataract 2, Multiple Types; CTRCT2 604307 J:60856





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/19/2016
MGI 6.03
The Jackson Laboratory