Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hip1rtm1Tsr mutation
(1 available);
any
Hip1r mutation
(45 available)
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normal phenotype
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• no gross or histological phenotype observable by 12 months of age
• mice were viable, of normal size, and were fertile, producing normal sized litters
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hip1rtm1Tsr mutation
(1 available);
any
Hip1r mutation
(45 available)
Hip1tm3Tsr mutation
(0 available);
any
Hip1 mutation
(67 available)
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skeleton
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• mice exhibit more severe kypholordosis than age-matched than Hip1tm5.1(HIP1)Tsr homozygotes
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hip1rtm1Tsr mutation
(1 available);
any
Hip1r mutation
(45 available)
Hip1tm3Tsr mutation
(0 available);
any
Hip1 mutation
(67 available)
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growth/size/body
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• although not apparent at birth, dwarfism is noticeable by early adulthood
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mortality/aging
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• spontaneous death in two mice at 3 months of age
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skeleton
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• skeletal disorganization in both thoracic and lumbar spinal regions at 13 weeks of age
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• abnormalities in spinal curvature noticeable as early as 2 weeks of age
• all mice exhibit the deformity by weaning
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• dramatically accelerated kypholordosis relative to Hip1tm3Tsr homozygotes
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• vertebral bodies show asymmetry with encroachment of cartilage into areas normally occupied by bone marrow
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behavior/neurological
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hip1rtm1Tsr mutation
(1 available);
any
Hip1r mutation
(45 available)
Hip1tm3Tsr mutation
(0 available);
any
Hip1 mutation
(67 available)
Hip1tm5.2(HIP1)Tsr mutation
(0 available);
any
Hip1 mutation
(67 available)
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skeleton
N |
• mice exhibit no kypholordotic spine, indicating rescue of the spinal phenotype by a single copy of human HIP1
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