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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
MipCat-Fr
dominant cataract Fraser
MGI:1857104
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
MipCat-Fr/MipCat-Fr involves: A/J MGI:2175110


Genotype
MGI:2175110
hm1
Allelic
Composition
MipCat-Fr/MipCat-Fr
Genetic
Background
involves: A/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
MipCat-Fr mutation (1 available); any Mip mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• at 14 days of gestation, the centrally located nuclei of the lens fibers are seen to be abnormally small and dark with indistinct nucleoli (J:5104)
• nuclear degeneration is followed by swelling and vacuolization of the lens fibers (J:5104)
• the main lens fiber mass degenerates (J:5114)
• the epithelial cells form multiple layers of atypical cells (J:5114)
• by electron microscopy, changes can be seen in the nuclear envelope of the primary lens fibers in 12-day embryos (J:30791)
• lens opacities are visible when the eyes first open at 14 days

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cataract 15 multiple types DOID:0110251 OMIM:615274
J:31574





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)
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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory