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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Setd5tm1c(EUCOMM)Wtsi
targeted mutation 1c, Wellcome Trust Sanger Institute
MGI:7438258
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Setd5tm1c(EUCOMM)Wtsi/Setd5+
Tbx1tm1Bld/Tbx1+
Tmem163Tg(ACTB-cre)2Mrt/Tmem163+
involves: 129S7/SvEvBrd * C57BL/6 * FVB/N MGI:7543763
cn2
Setd5tm1c(EUCOMM)Wtsi/Setd5tm1c(EUCOMM)Wtsi
Tbx1tm6(cre)Bld/Tbx1+
involves: C57BL/6N MGI:7543765
cn3
Setd5tm1c(EUCOMM)Wtsi/Setd5tm1c(EUCOMM)Wtsi
Mesp1tm2(cre)Ysa/Mesp1+
involves: C57BL/6N * C57BL/6NCrlj * CBA/JNCrlj MGI:7543766
cn4
Setd5tm1c(EUCOMM)Wtsi/Setd5+
Mesp1tm2(cre)Ysa/Mesp1+
involves: C57BL/6N * C57BL/6NCrlj * CBA/JNCrlj MGI:7543767
cn5
Setd5tm1c(EUCOMM)Wtsi/Setd5+
Tmem163Tg(ACTB-cre)2Mrt/Tmem163+
involves: C57BL/6N * FVB/N MGI:7543762


Genotype
MGI:7543763
cn1
Allelic
Composition
Setd5tm1c(EUCOMM)Wtsi/Setd5+
Tbx1tm1Bld/Tbx1+
Tmem163Tg(ACTB-cre)2Mrt/Tmem163+
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Setd5tm1c(EUCOMM)Wtsi mutation (0 available); any Setd5 mutation (120 available)
Tbx1tm1Bld mutation (1 available); any Tbx1 mutation (34 available)
Tmem163Tg(ACTB-cre)2Mrt mutation (3 available); any Tmem163 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• double heterozygotes are recovered at normal Mendelian ratios at E14.5

cardiovascular system
• at E14.5, 21% of double heterozygotes exhibit an aberrant right subclavian artery
• at E14.5, 57% of double heterozygotes show OFT rotational defects, including DORV and overriding aorta
• however, no common arterial trunk is identified at E14.5
• at E14.5, 86% of double heterozygotes exhibit a perimembranous VSD




Genotype
MGI:7543765
cn2
Allelic
Composition
Setd5tm1c(EUCOMM)Wtsi/Setd5tm1c(EUCOMM)Wtsi
Tbx1tm6(cre)Bld/Tbx1+
Genetic
Background
involves: C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Setd5tm1c(EUCOMM)Wtsi mutation (0 available); any Setd5 mutation (120 available)
Tbx1tm6(cre)Bld mutation (1 available); any Tbx1 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
N
• at E15.5, hearts show no great vessel defects; outflow tract septation is largely normal and the atrial septum and atrioventricular valves are intact




Genotype
MGI:7543766
cn3
Allelic
Composition
Setd5tm1c(EUCOMM)Wtsi/Setd5tm1c(EUCOMM)Wtsi
Mesp1tm2(cre)Ysa/Mesp1+
Genetic
Background
involves: C57BL/6N * C57BL/6NCrlj * CBA/JNCrlj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mesp1tm2(cre)Ysa mutation (1 available); any Mesp1 mutation (17 available)
Setd5tm1c(EUCOMM)Wtsi mutation (0 available); any Setd5 mutation (120 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos are recovered at expected Mendelian ratios at E10.5 but die before E12.5

growth/size/body
• at E10.5, embryos are significantly smaller than control embryos, as determined by crown-to-rump length

embryo
• at E10.5, embryos are significantly smaller than control embryos, as determined by crown-to-rump length

cardiovascular system
• at E10.5, all (100%) of hearts exhibit a shorter OFT than control hearts
• at E10.5, embryos show varying degrees of abnormal cardiac morphogenesis
• at E10.5, some embryos show poorly developed atria and a thickened atrial wall
• at E10.5, 25% of embryos have dumbbell-shaped hearts with a single atrium and a single ventricle
• at E10.5, some embryos exhibit right ventricular hypoplasia
• at E10.5, some embryos show no evidence of the interventricular groove
• at E10.5, 74% of embryos exhibit pericardial effusion
• at E10.5, 95% of embryos show abnormal cardiac chamber ballooning by external analysis
• at E10.5, all (100%) hearts show abnormal atrial ballooning by H&E analysis
• at E10.5, all (100%) hearts show abnormal ventricular ballooning by H&E analysis
• at E10.5, 16% of embryos exhibit hemorrhage

homeostasis/metabolism
• at E10.5, 74% of embryos exhibit pericardial effusion




Genotype
MGI:7543767
cn4
Allelic
Composition
Setd5tm1c(EUCOMM)Wtsi/Setd5+
Mesp1tm2(cre)Ysa/Mesp1+
Genetic
Background
involves: C57BL/6N * C57BL/6NCrlj * CBA/JNCrlj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mesp1tm2(cre)Ysa mutation (1 available); any Mesp1 mutation (17 available)
Setd5tm1c(EUCOMM)Wtsi mutation (0 available); any Setd5 mutation (120 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• at E10.5, one of 6 (17%) hearts show abnormal ventricular ballooning
• however, no OFT phenotype or abnormal atrial ballooning is observed




Genotype
MGI:7543762
cn5
Allelic
Composition
Setd5tm1c(EUCOMM)Wtsi/Setd5+
Tmem163Tg(ACTB-cre)2Mrt/Tmem163+
Genetic
Background
involves: C57BL/6N * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Setd5tm1c(EUCOMM)Wtsi mutation (0 available); any Setd5 mutation (120 available)
Tmem163Tg(ACTB-cre)2Mrt mutation (3 available); any Tmem163 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• at E14.5, 50% of heterozygotes show outflow tract (OFT) rotational defects (OFT fails to align with the two future ventricles at the looping stage), including DORV and overriding aorta
• however, OFT septation is normal; no aberrant right subclavian artery or common arterial trunk are identified at E14.5
• at E14.5, 75% of heterozygotes exhibit a perimembranous VSD





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory