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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Col1a1tm11(tetO-Nup88)Jvd
targeted mutation 11, Jan MA van Deursen
MGI:6343326
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Col1a1tm11(tetO-Nup88)Jvd/Col1a1+ involves: 129S4/SvJae * C57BL/6 MGI:6377632
cx2
ApcMin/Apc+
Col1a1tm11(tetO-Nup88)Jvd/Col1a1+
involves: 129S4/SvJae * C57BL/6 * C57BL/6J MGI:6377634


Genotype
MGI:6377632
ht1
Allelic
Composition
Col1a1tm11(tetO-Nup88)Jvd/Col1a1+
Genetic
Background
involves: 129S4/SvJae * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Col1a1tm11(tetO-Nup88)Jvd mutation (0 available); any Col1a1 mutation (163 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• dox-treated MEFs exhibit higher aneuploidy rates
• splenocytes from 5 month old dox-treated mice show about 4-fold higher rates of aneuploidy than control splenocytes
• lung tissues from 5 month old dox-treated mice are more aneuploid than control lung tissues
• dox-treated MEFs exhibit mitotic checkpoint defects
• dox-treated MEFs have higher rates of chromatin bridges and lagging chromosomes, indicating chromosomal segregation defects
• dox-treated MEFs exhibit increased incomplete centrosome separation
• MEFs treated with the PLK inhibitor BI2536 show restoration of normal centrosome separation
• dox-treated MEFs exhibit more frequent spindle geometry defects showing mitotic spindle asymmetry

neoplasm
• mice administered doxycycline (dox) beginning at weaning are prone to spontaneous tumors, particularly lung tumors, by 14 months of age, with 56% of mice having at least one neoplastic lesion compared to 21% of controls
• in dox-treated mice

respiratory system
• in dox-treated mice




Genotype
MGI:6377634
cx2
Allelic
Composition
ApcMin/Apc+
Col1a1tm11(tetO-Nup88)Jvd/Col1a1+
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
ApcMin mutation (12 available); any Apc mutation (158 available)
Col1a1tm11(tetO-Nup88)Jvd mutation (0 available); any Col1a1 mutation (163 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
• doxycycline (dox)-treated mice show increased incidence of colon tumors compared to single ApcMin heterozygotes, but tumor multiplicity or size is unaffected and there is no difference in the multiplicity of small intestinal polyps
• mice in which dox is discontinued 30 days before analysis, show the same incidence of colon tumors as in mice with continuous administration of dox

neoplasm
• doxycycline (dox)-treated mice show increased incidence of colon tumors compared to single ApcMin heterozygotes, but tumor multiplicity or size is unaffected and there is no difference in the multiplicity of small intestinal polyps
• mice in which dox is discontinued 30 days before analysis, show the same incidence of colon tumors as in mice with continuous administration of dox





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory