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Phenotypes Associated with This Genotype
Genotype
MGI:5305581
Allelic
Composition
Hsf4ldis1/Hsf4ldis1
Genetic
Background
involves: C57BL/6 * CAST/EiJ * RIIIS/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hsf4ldis1 mutation (0 available); any Hsf4 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• persistence of nuclei in lens fiber cells as early as P0.5
• by P10-12, lenses develop severely vauolated cataracts often accompanied by rupture of the lens capsule and release of the lenticular material in the vitreous cavity, such that cataracts are visible upon eyelid opening between P12-14
• vacuoles are seen in the cortex and nucleus of the lens

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cataract 5 multiple types DOID:0110255 OMIM:116800
J:179658


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
04/30/2024
MGI 6.23
The Jackson Laboratory