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Phenotypes Associated with This Genotype
Genotype
MGI:3047564
Allelic
Composition
Col18a1tm1Hms/Col18a1tm1Hms
Hspg2tm1Soin/Hspg2tm1Soin
Genetic
Background
involves: C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Col18a1tm1Hms mutation (2 available); any Col18a1 mutation (138 available)
Hspg2tm1Soin mutation (1 available); any Hspg2 mutation (308 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• double mutant newborns display accelerated lens degeneration relative to Hspg2tm1Soin mice, as well as more severe lens defects relative to single mutant mice
• the first signs of abnormal development are already apparent in neonates in that leakages of cells are detected in the anterior region of the lens; in Hspg2tm1Soin mice, leakages are observed in a more posterior region and are less severe
• in double mutant lenses, epithelial cells migrate focally outwards, proliferate and remain external for several weeks


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
04/09/2024
MGI 6.23
The Jackson Laboratory