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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(CD68-icre)1Bwlx
transgene insertion 1, Ben Wielockx
MGI:5474196
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Egln1tm1.1Brei/Egln1tm1.1Brei
Hif1atm3Rsjo/Hif1atm3Rsjo
Tg(CD68-icre)1Bwlx/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5568401
cn2
Hif1atm3Rsjo/Hif1atm3Rsjo
Tg(CD68-icre)1Bwlx/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5568404
cn3
Egln1tm1.1Brei/Egln1tm1.1Brei
Egln3tm2Fong/Egln3tm2Fong
Tg(CD68-icre)1Bwlx/0
involves: 129S6/SvEvTac * C57BL/6 MGI:5568402
cn4
Egln1tm1.1Brei/Egln1tm1.1Brei
Epas1tm1Mcs/Epas1tm1Mcs
Tg(CD68-icre)1Bwlx/0
involves: 129X1/SvJ * C57BL/6 MGI:5568400
cn5
Epas1tm1Mcs/Epas1tm1Mcs
Tg(CD68-icre)1Bwlx/0
involves: 129X1/SvJ * C57BL/6 MGI:5568403
cn6
Egln1tm1.1Brei/Egln1tm1.1Brei
Tg(CD68-icre)1Bwlx/0
involves: C57BL/6 MGI:5568399


Genotype
MGI:5568401
cn1
Allelic
Composition
Egln1tm1.1Brei/Egln1tm1.1Brei
Hif1atm3Rsjo/Hif1atm3Rsjo
Tg(CD68-icre)1Bwlx/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egln1tm1.1Brei mutation (0 available); any Egln1 mutation (21 available)
Hif1atm3Rsjo mutation (3 available); any Hif1a mutation (48 available)
Tg(CD68-icre)1Bwlx mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice start dying suddenly at 5 weeks with 95% mortality by 16 weeks (mean survival time = 11 weeks)

hematopoietic system
N
• no cardiovascular complications or thromboses are observed
• not different from CD68cre/Phd2fl mice

craniofacial
• 3/16 mice show this

nervous system
• mice with domed skulls show dramatic hydrocephalus

skeleton
• 3/16 mice show this




Genotype
MGI:5568404
cn2
Allelic
Composition
Hif1atm3Rsjo/Hif1atm3Rsjo
Tg(CD68-icre)1Bwlx/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hif1atm3Rsjo mutation (3 available); any Hif1a mutation (48 available)
Tg(CD68-icre)1Bwlx mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• no premature death observed




Genotype
MGI:5568402
cn3
Allelic
Composition
Egln1tm1.1Brei/Egln1tm1.1Brei
Egln3tm2Fong/Egln3tm2Fong
Tg(CD68-icre)1Bwlx/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egln1tm1.1Brei mutation (0 available); any Egln1 mutation (21 available)
Egln3tm2Fong mutation (1 available); any Egln3 mutation (24 available)
Tg(CD68-icre)1Bwlx mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• mice display severe erythrocytosis

mortality/aging
• animals start dying shortly after birth




Genotype
MGI:5568400
cn4
Allelic
Composition
Egln1tm1.1Brei/Egln1tm1.1Brei
Epas1tm1Mcs/Epas1tm1Mcs
Tg(CD68-icre)1Bwlx/0
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egln1tm1.1Brei mutation (0 available); any Egln1 mutation (21 available)
Epas1tm1Mcs mutation (1 available); any Epas1 mutation (64 available)
Tg(CD68-icre)1Bwlx mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• no premature death is observed

hematopoietic system
N
• erythropoiesis phenotype seen in Phd2 single mutants is absent from double mutants
• HCT is lower than wild type
• lower than in wild-type




Genotype
MGI:5568403
cn5
Allelic
Composition
Epas1tm1Mcs/Epas1tm1Mcs
Tg(CD68-icre)1Bwlx/0
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epas1tm1Mcs mutation (1 available); any Epas1 mutation (64 available)
Tg(CD68-icre)1Bwlx mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• no premature death observed




Genotype
MGI:5568399
cn6
Allelic
Composition
Egln1tm1.1Brei/Egln1tm1.1Brei
Tg(CD68-icre)1Bwlx/0
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Egln1tm1.1Brei mutation (0 available); any Egln1 mutation (21 available)
Tg(CD68-icre)1Bwlx mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• no premature death is observed; some erythrocytotic mutants live for more than 20 months with no observed decrease in hematocrit

growth/size/body
• severe growth retardation occurs in conjunction with skin redness until adulthood

hematopoietic system
N
• F4/80+ macrophages and neutrophils are not significantly different from wild type, but red pulp macrophages are highly induced in the spleen
• megakaryocyte-erythroid progenitors (MEPs) are significantly induced (>2.5 fold) in the spleen, but not in bone marrow
• splenic CD71+ve/Ter119+ve erythroblasts are increase >10-fold with mild increase in bone marrow
• results in splenomegaly
• increases with age to >85% in some animals
• splenomegaly occurs with increase in nucleated cells
• significantly decreased
• fraction of B and T cells in spleen is significantly decreased but in lymph nodes these numbers are increased
• splenomegaly occurs with loss of splenic architecture

cardiovascular system
• viscosity is increased but no differences in heart rate, blood pressure or cardiac hypertrophy is observed
• blood volume increased by 65%

immune system
• fraction of B and T cells in spleen is significantly decreased but in lymph nodes these numbers are increased
• splenomegaly occurs with loss of splenic architecture

integument
• redness of paws and snouts is observed by 4 weeks of age





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