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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
F5tm2Dgi
targeted mutation 2, David Ginsburg
MGI:1931528
Summary 14 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
F5tm2Dgi/F5tm2Dgi 129S1.129(Cg)F5tm2Dgi Tfpitm1Gjb MGI:6119622
hm2
F5tm2Dgi/F5tm2Dgi B6.129S2-F5tm2Dgi MGI:3588767
hm3
F5tm2Dgi/F5tm2Dgi B6.129S2-F5tm2Dgi/J MGI:6275050
hm4
F5tm2Dgi/F5tm2Dgi involves: 129S2/SvPas * C57BL/6 MGI:3789952
hm5
F5tm2Dgi/F5tm2Dgi involves: 129S2/SvPas * C57BL/6J MGI:3588765
ht6
F5tm2Dgi/F5+ B6.129S2-F5tm2Dgi MGI:3588766
cx7
F5tm2Dgi/F5tm2Dgi
Tfpitm1Gjb/Tfpi+
129S1.129(Cg)F5tm2Dgi Tfpitm1Gjb MGI:6119623
cx8
Actr2MF5L12/Actr2+
F5tm2Dgi/F5tm2Dgi
Tfpitm1Gjb/Tfpi+
involves: 129S1/Sv * 129S2/SvPas * C57BL/6 MGI:6119625
cx9
F5tm2Dgi/F5tm2Dgi
MF5L6/MF5L6+
Tfpitm1Gjb/Tfpi+
involves: 129S1/Sv * 129S2/SvPas * C57BL/6 MGI:6119624
cx10
F5tm2Dgi/F5tm2Dgi
Serpina10tm1Gjb/Serpina10tm1Gjb
involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 MGI:3804660
cx11
F5tm2Dgi/F5+
Serpina10tm1Gjb/Serpina10tm1Gjb
involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 MGI:3804661
cx12
F5tm2Dgi/F5tm2Dgi
Proztm1Gjb/Proztm1Gjb
involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 MGI:3789949
cx13
F5tm2Dgi/F5+
Proztm1Gjb/Proztm1Gjb
involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 MGI:3789948
cx14
F5tm2Dgi/F5tm2Dgi
Proztm1Gjb/Proz+
involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 MGI:3789950


Genotype
MGI:6119622
hm1
Allelic
Composition
F5tm2Dgi/F5tm2Dgi
Genetic
Background
129S1.129(Cg)F5tm2Dgi Tfpitm1Gjb
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• Background Sensitivity: mice on a congenic 129S1 background exhibit decreased survival compared with mice on a congenic C57BL/6 background




Genotype
MGI:3588767
hm2
Allelic
Composition
F5tm2Dgi/F5tm2Dgi
Genetic
Background
B6.129S2-F5tm2Dgi
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• Background Sensitivity: do not observe postnatal lethality on the predominately C57BL/6J background like on the mixed 129 and C57BL/6J background, however crossing back to 129/SvJ or 129SvIm/J mice, results in about 50% postnatal loss

homeostasis/metabolism
• chronic, low-grade thrombin generation leading to enhanced fibrin deposition in multiple tissues, however do not observe thrombosis

liver/biliary system
• occasional focal hepatic fibrosis is seen




Genotype
MGI:6275050
hm3
Allelic
Composition
F5tm2Dgi/F5tm2Dgi
Genetic
Background
B6.129S2-F5tm2Dgi/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• Background Sensitivity: mice on a congenic C57BL/6 background exhibit increased survival compared with mice on a congenic 129S1 background




Genotype
MGI:3789952
hm4
Allelic
Composition
F5tm2Dgi/F5tm2Dgi
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• around 20% of homozygotes die in neonatal period

homeostasis/metabolism
• homozygotes that die show microvascular thrombosis in neonatal period




Genotype
MGI:3588765
hm5
Allelic
Composition
F5tm2Dgi/F5tm2Dgi
Genetic
Background
involves: 129S2/SvPas * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• Background Sensitivity: decreased number of expected pups at 3 weeks of age but not at 1-2 days before birth, however do not observe lethality on a predominately C57BL/6J background

homeostasis/metabolism
• more resistant to anticoagulant activated protein C than controls or heterozygotes, however F5 clotting activity is normal
• Background Sensitivity: widespread thrombosis affecting multiple organs, including brain, liver, heart, pancreas, and spleen, in all newborns

behavior/neurological
• subset of mice appear lethargic at birth

integument
• subset of mice appear pale at birth




Genotype
MGI:3588766
ht6
Allelic
Composition
F5tm2Dgi/F5+
Genetic
Background
B6.129S2-F5tm2Dgi
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• more resistant to anticoagulant activated protein C than controls, however F5 clotting activity is normal
• exhibit occasional spontaneous vascular thrombosis (e.g. necrosis of a digit)




Genotype
MGI:6119623
cx7
Allelic
Composition
F5tm2Dgi/F5tm2Dgi
Tfpitm1Gjb/Tfpi+
Genetic
Background
129S1.129(Cg)F5tm2Dgi Tfpitm1Gjb
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
Tfpitm1Gjb mutation (0 available); any Tfpi mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no mice are present at weaning




Genotype
MGI:6119625
cx8
Allelic
Composition
Actr2MF5L12/Actr2+
F5tm2Dgi/F5tm2Dgi
Tfpitm1Gjb/Tfpi+
Genetic
Background
involves: 129S1/Sv * 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Actr2MF5L12 mutation (0 available); any Actr2 mutation (37 available)
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
Tfpitm1Gjb mutation (0 available); any Tfpi mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice exhibit increased survival compared with mice lacking the Actr2mf5l12 mutation




Genotype
MGI:6119624
cx9
Allelic
Composition
F5tm2Dgi/F5tm2Dgi
MF5L6/MF5L6+
Tfpitm1Gjb/Tfpi+
Genetic
Background
involves: 129S1/Sv * 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
MF5L6 mutation (0 available); any MF5L6 mutation (0 available)
Tfpitm1Gjb mutation (0 available); any Tfpi mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• with fewer male than female mice, but less severe mortality than in mice lacking the MF5L6 mutation




Genotype
MGI:3804660
cx10
Allelic
Composition
F5tm2Dgi/F5tm2Dgi
Serpina10tm1Gjb/Serpina10tm1Gjb
Genetic
Background
involves: 129S2/SvPas * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
Serpina10tm1Gjb mutation (0 available); any Serpina10 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no mice survive until 6 weeks of age
• only 4% of embryos out of an expected 25% live until E18.5 with this genotype, which is significantly different from the normal number of E18.5 embryos found with a Proztm1Gjb / Proztm1Gjb F5tm2Dgi / F5tm2Dgi genotype
• normal numbers of double homozygotes are found at E13.5

cardiovascular system
• is often observed in E13.5 embryos
• is often observed in E13.5 embryos

nervous system
• is often observed in E13.5 embryos




Genotype
MGI:3804661
cx11
Allelic
Composition
F5tm2Dgi/F5+
Serpina10tm1Gjb/Serpina10tm1Gjb
Genetic
Background
involves: 129S2/SvPas * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
Serpina10tm1Gjb mutation (0 available); any Serpina10 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only 18% of mice with this genotype are found at 6 weeks of age instead of the expected 25% based on Mendelian inheritance




Genotype
MGI:3789949
cx12
Allelic
Composition
F5tm2Dgi/F5tm2Dgi
Proztm1Gjb/Proztm1Gjb
Genetic
Background
involves: 129S2/SvPas * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
Proztm1Gjb mutation (0 available); any Proz mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mortality of double homozygotes is high; only 1 animal reached adulthood (6 weeks)

cardiovascular system
• at E17.5-18.5, almost all mutants show signs of hemorrhage

homeostasis/metabolism
• at E17.5-18.5, embryos display thrombosis and fibrin depositon in the vasculature




Genotype
MGI:3789948
cx13
Allelic
Composition
F5tm2Dgi/F5+
Proztm1Gjb/Proztm1Gjb
Genetic
Background
involves: 129S2/SvPas * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
Proztm1Gjb mutation (0 available); any Proz mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer (only 10% of expected 50%) animals of this genotype are found at 6 weeks




Genotype
MGI:3789950
cx14
Allelic
Composition
F5tm2Dgi/F5tm2Dgi
Proztm1Gjb/Proz+
Genetic
Background
involves: 129S2/SvPas * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
F5tm2Dgi mutation (1 available); any F5 mutation (159 available)
Proztm1Gjb mutation (0 available); any Proz mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer (37% of expected 50%) animals of this genotype are found at 6 weeks

homeostasis/metabolism
• less severe than in double homozygous embryos





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