Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Krt14tm1(cre)Wbm mutation
(0 available);
any
Krt14 mutation
(36 available)
Pard3tm1Shoh mutation
(0 available);
any
Pard3 mutation
(96 available)
Tg(HIST1H2BB/EGFP)1Pa mutation
(1 available)
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pigmentation
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• in P58 tail whole mounts, melanocytes (MCs) show a more stubby dendritic morphology with dendritic shortening and a more spread cell body area relative to MCs in control mice
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bub1btm1.1Hsl mutation
(0 available);
any
Bub1b mutation
(58 available)
Tg(HIST1H2BB/EGFP)1Pa mutation
(1 available)
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cellular
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• micronuclei due to lagging chromosomes in mouse embryonic fibroblasts, regenerating hepatocytes and hepatocellular carcinoma
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• in mouse embryonic fibroblasts
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• premature sister chromatid separation in mouse embryonic fibroblasts
• shortened mitotic timing
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• weakened with chromosome mis-segregation, congression failure and severe defects in kinetochore-microtubule attachment in mouse embryonic fibroblasts
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(HIST1H2BB/EGFP)1Pa mutation
(1 available)
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normal phenotype
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• homozygotes are viable and fertile; the reporter is developmentally neutral
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