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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Runx1tm1Yg
targeted mutation 1, Yoram Groner
MGI:3760788
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Runx1tm1Yg/Runx1tm1Yg either: (involves: 129/Sv * 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1) MGI:3760800
hm2
Runx1tm1Yg/Runx1tm1Yg involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:4458936
ht3
Runx1tm1Yg/Runx1tm2Spe either: (involves: 129/Sv) or (involves: 129/Sv * ICR) or (involves: 129/Sv * MF1) MGI:3760802
ht4
Runx1tm1Spe/Runx1tm1Yg involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 MGI:4459011
cn5
Runx1tm1Yg/Runx1tm1Yg
Tg(Lck-cre)1Jtak/?
either: (involves: 129/Sv * 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1) MGI:3760803
cx6
Runx1tm1Yg/Runx1tm1Yg
Tg(Runx1-GFP)#Itan/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA MGI:4459013
cx7
Runx1tm1Yg/Runx1+
Tg(Runx1-GFP)#Itan/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA MGI:4459014


Genotype
MGI:3760800
hm1
Allelic
Composition
Runx1tm1Yg/Runx1tm1Yg
Genetic
Background
either: (involves: 129/Sv * 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Runx1tm1Yg mutation (2 available); any Runx1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die 2 to 3 days after birth

immune system
• at E16.5, the thymus has a scalloped capsular surface of predominantly epithelial cells with no evidence of an organized medulla or cortex
• at E17.5, the thymus lacks corticomedullary organization
• at P1.5, the thymus is one third of the size of a normal thymus
• in embryos and neonates
• at E14.5, thymocyte numbers are reduced 3-fold compared to in wild-type mice due to increased thymocyte apoptosis
• however, thymocyte proliferation and cell cycle progression is normal
• at E14.5 and E15.5, thymi contain scattered cysts from accelerated epithelial turnover
• at E17.5, the thymus occasionally contains cysts
• mice exhibit a 4-fold reduction in T cell precursors compared to wild-type mice
• when E15.5 fetal liver cells are cultured under limiting dilution conditions in fetal thymic organ culture successful repopulation was lower than for wild-type cells
• mice display an increased proportion of DN3 cells and a corresponding reduction in DN4 cells relative to levels in wild-type mice (DN3 to DN4 ratio 1.51+/-0.31 compared to 0.65+/-0.15 in wild-type mice)
• however, by P3.5 T cell differentiation is recovered to wild-type proportions
• at E16.5, mice exhibit a 2.5-fold increase in double positive cells compared to wild-type mice
• at E17.5, the decrease in double positive cells is more pronounced and accompanied by an increase in CD4+CD8low cells
• after 16 days in a fetal thymic organ culture, an increased proportion of double positive CD4+CD8low cells and a 2-fold reduction in single positive cells was observed
• after 16 days in a fetal thymic organ culture, an increased proportion of double positive CD4+CD8low cells and a 2-fold reduction in single positive cells was observed

growth/size/body
• at E14.5 and E15.5, thymi contain scattered cysts from accelerated epithelial turnover
• at E17.5, the thymus occasionally contains cysts

hematopoietic system
• at E16.5, the thymus has a scalloped capsular surface of predominantly epithelial cells with no evidence of an organized medulla or cortex
• at E17.5, the thymus lacks corticomedullary organization
• at P1.5, the thymus is one third of the size of a normal thymus
• in embryos and neonates
• at E14.5, thymocyte numbers are reduced 3-fold compared to in wild-type mice due to increased thymocyte apoptosis
• however, thymocyte proliferation and cell cycle progression is normal
• at E14.5 and E15.5, thymi contain scattered cysts from accelerated epithelial turnover
• at E17.5, the thymus occasionally contains cysts
in vitro colony formation ability by fetal liver cells is reduced compared to that for wild-type cells
• fetal liver cells contain few hematopoietic progenitor cells compared to wild-type fetal liver cells
• at E17.5 and E18.5, mice display fewer Gr-1/CD18+ and CD11a+/CD11b+ cells compared to wild-type mice
• at E17.5 and E18.5, mice exhibit a 2-fold reduction in the proportion of CD44+ to c-Kit+ hematopoietic progenitor cells and an even greater reduction in CD34+ cells compared to wild-type mice
• mice exhibit a 4-fold reduction in T cell precursors compared to wild-type mice
• when E15.5 fetal liver cells are cultured under limiting dilution conditions in fetal thymic organ culture successful repopulation was lower than for wild-type cells
• mice display an increased proportion of DN3 cells and a corresponding reduction in DN4 cells relative to levels in wild-type mice (DN3 to DN4 ratio 1.51+/-0.31 compared to 0.65+/-0.15 in wild-type mice)
• however, by P3.5 T cell differentiation is recovered to wild-type proportions
• at E16.5, mice exhibit a 2.5-fold increase in double positive cells compared to wild-type mice
• at E17.5, the decrease in double positive cells is more pronounced and accompanied by an increase in CD4+CD8low cells
• after 16 days in a fetal thymic organ culture, an increased proportion of double positive CD4+CD8low cells and a 2-fold reduction in single positive cells was observed
• after 16 days in a fetal thymic organ culture, an increased proportion of double positive CD4+CD8low cells and a 2-fold reduction in single positive cells was observed

cellular

endocrine/exocrine glands
• at E16.5, the thymus has a scalloped capsular surface of predominantly epithelial cells with no evidence of an organized medulla or cortex
• at E17.5, the thymus lacks corticomedullary organization
• at P1.5, the thymus is one third of the size of a normal thymus
• in embryos and neonates
• at E14.5, thymocyte numbers are reduced 3-fold compared to in wild-type mice due to increased thymocyte apoptosis
• however, thymocyte proliferation and cell cycle progression is normal
• at E14.5 and E15.5, thymi contain scattered cysts from accelerated epithelial turnover
• at E17.5, the thymus occasionally contains cysts




Genotype
MGI:4458936
hm2
Allelic
Composition
Runx1tm1Yg/Runx1tm1Yg
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Runx1tm1Yg mutation (2 available); any Runx1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• the number of colony forming units in culture (CFU-Cs) produced from E8.5 hematopoietic tissues is decreased 8.8-fold compared to CFU-Cs produced from wild-type tissue
• at E8.5, CFU-C tend to be smaller than wild-type colonies
• the number of CFU-Cs generated from E11.5 yolk sac is decreased 10.1-fold compared to CFU-Cs produced from wild-type tissues
• the number of CFU-Cs generated from E11.5 vitelline and umbilical arteries is decreased 12.8-fold compared to CFU-Cs produced from wild-type tissues
• at E11.5, the number of fetal liver (FL) CFU-Cs is reduced 5.9-fold and the size of colonies is decreased compared to in wild-type mice




Genotype
MGI:3760802
ht3
Allelic
Composition
Runx1tm1Yg/Runx1tm2Spe
Genetic
Background
either: (involves: 129/Sv) or (involves: 129/Sv * ICR) or (involves: 129/Sv * MF1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Runx1tm1Yg mutation (2 available); any Runx1 mutation (35 available)
Runx1tm2Spe mutation (0 available); any Runx1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die between E11.5 and E12.5 of hemorrhages in the central nervous system

cardiovascular system
• mice die of hemorrhages in the central nervous system extensively in the fourth ventricle, ventral metencephalon and spinal cord

nervous system




Genotype
MGI:4459011
ht4
Allelic
Composition
Runx1tm1Spe/Runx1tm1Yg
Genetic
Background
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Runx1tm1Spe mutation (1 available); any Runx1 mutation (35 available)
Runx1tm1Yg mutation (2 available); any Runx1 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

hematopoietic system
• severe in the fetal liver at E12.5

cardiovascular system
• in the central nervous system at E12.5




Genotype
MGI:3760803
cn5
Allelic
Composition
Runx1tm1Yg/Runx1tm1Yg
Tg(Lck-cre)1Jtak/?
Genetic
Background
either: (involves: 129/Sv * 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Runx1tm1Yg mutation (2 available); any Runx1 mutation (35 available)
Tg(Lck-cre)1Jtak mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• despite normal thymus development and a complete rescue of embryonic lethality, mice display a reduction in the number of Runx1+ T cells

hematopoietic system
• despite normal thymus development and a complete rescue of embryonic lethality, mice display a reduction in the number of Runx1+ T cells




Genotype
MGI:4459013
cx6
Allelic
Composition
Runx1tm1Yg/Runx1tm1Yg
Tg(Runx1-GFP)#Itan/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Runx1tm1Yg mutation (2 available); any Runx1 mutation (35 available)
Tg(Runx1-GFP)#Itan mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• mice lack GFP+ hematopoietic cells or clusters in the dorsal aorta compared with Tg(Runx1-GFP)#Itan mice
• mesenchyme beneath the dorsal aorta is compact unlike in wild-type mice

hematopoietic system
• mice lack GFP+ hematopoietic cells or clusters in the dorsal aorta compared with Tg(Runx1-GFP)#Itan mice




Genotype
MGI:4459014
cx7
Allelic
Composition
Runx1tm1Yg/Runx1+
Tg(Runx1-GFP)#Itan/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Runx1tm1Yg mutation (2 available); any Runx1 mutation (35 available)
Tg(Runx1-GFP)#Itan mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• mice exhibit fewer large GFP+ hematopoietic cells or clusters in the dorsal aorta compared with Tg(Runx1-GFP)#Itan mice

hematopoietic system
• mice exhibit fewer large GFP+ hematopoietic cells or clusters in the dorsal aorta compared with Tg(Runx1-GFP)#Itan mice





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory