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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Stag2tm1.1Alos
targeted mutation 1.1, Ana Losada
MGI:6490260
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Stag2tm1.1Alos/Stag2tm1.1Alos
involves: 129S6/SvEvTac * C57BL/6NCrl MGI:6490362
cn2
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Stag2tm1.1Alos/Y
involves: 129S6/SvEvTac * C57BL/6NCrl MGI:6490363
cn3
Stag2tm1.1Alos/Y
Tg(CAG-cre)1Nagy/0
involves: 129S6/SvEvTac * C57BL/6NCrl MGI:6490364


Genotype
MGI:6490362
cn1
Allelic
Composition
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Stag2tm1.1Alos/Stag2tm1.1Alos
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6NCrl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ndor1Tg(UBC-cre/ERT2)1Ejb mutation (6 available); any Ndor1 mutation (32 available)
Stag2tm1.1Alos mutation (0 available); any Stag2 mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 4 weeks after initiation of tamoxifen treatment

cellular
• tamoxifen-treated mouse embryonic fibroblasts exhibit increased chromosome adhesion and mis-segregation compared with control cells
• increased caspase-3-positive cells in tamoxifen-treated mouse embryonic fibroblasts
• 8 week old tamoxifen-treated mice exhibit increased intestinal erosion and necrosis compared with wild-type mice
• reduced in intestinal crypts of tamoxifen-treated mice indicating reduced cellular renewal
• increased doubling time in tamoxifen-treated mouse embryonic fibroblasts

digestive/alimentary system
• reduced in intestinal crypts of tamoxifen-treated mice indicating reduced cellular renewal
• 8 week old tamoxifen-treated mice exhibit increased intestinal erosion and necrosis compared with wild-type mice

growth/size/body
• in tamoxifen-treated mice

hematopoietic system
• tamoxifen-treated mice exhibit normal adult hematopoiesis
• enhanced self-renewal in cells from tamoxifen-treated mice

neoplasm
• tamoxifen-treated mice do not exhibit increased spontaneous tumors




Genotype
MGI:6490363
cn2
Allelic
Composition
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Stag2tm1.1Alos/Y
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6NCrl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ndor1Tg(UBC-cre/ERT2)1Ejb mutation (6 available); any Ndor1 mutation (32 available)
Stag2tm1.1Alos mutation (0 available); any Stag2 mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 4 weeks after initiation of tamoxifen treatment

cellular
• tamoxifen-treated mouse embryonic fibroblasts exhibit increased chromosome adhesion and mis-segregation compared with control cells
• increased caspase-3-positive cells in tamoxifen-treated mouse embryonic fibroblasts
• 8 week old tamoxifen-treated mice exhibit increased intestinal erosion and necrosis compared with wild-type mice
• reduced in intestinal crypts of tamoxifen-treated mice indicating reduced cellular renewal
• increased doubling time in tamoxifen-treated mouse embryonic fibroblasts

digestive/alimentary system
• reduced in intestinal crypts of tamoxifen-treated mice indicating reduced cellular renewal
• 8 week old tamoxifen-treated mice exhibit increased intestinal erosion and necrosis compared with wild-type mice

growth/size/body
• in tamoxifen-treated mice

hematopoietic system
N
• tamoxifen-treated mice exhibit normal adult hematopoiesis
• enhanced self-renewal in cells from tamoxifen-treated mice

neoplasm
N
• tamoxifen-treated mice do not exhibit increased spontaneous tumors




Genotype
MGI:6490364
cn3
Allelic
Composition
Stag2tm1.1Alos/Y
Tg(CAG-cre)1Nagy/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6NCrl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Stag2tm1.1Alos mutation (0 available); any Stag2 mutation (15 available)
Tg(CAG-cre)1Nagy mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• shortened length and rightward turning at the junction with the ventricular myocardium in mildly affect mice at E9.5
• distended atria and ventricles at E9.5
• distended OFT and IFT
• severe cardiac anomalies at E10.5 in all mice with extensive necrosis and apoptosis
• in mildly affect mice at E9.5

cellular
• in E9.5 embryos

embryo
• indicated by reduced somite number at E9.5 measuring a day behind
• mild and severe at E9.5

growth/size/body
• indicated by reduced somite number at E9.5 measuring a day behind
• mild and severe at E9.5





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory