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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Epor+
wild type
MGI:1857576
Summary 13 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Eportm1Jae/Epor+ either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6) MGI:3835199
ht2
Eportm1.3(EPOR*)Jtp/Epor+ involves: 129P2/OlaHsd * C57BL/6 MGI:2386209
ht3
Eportm1.4(EPOR*)Jtp/Epor+ involves: 129P2/OlaHsd * C57BL/6 MGI:2386211
cn4
Bcl11atm1Pwt/Bcl11atm1Pwt
Kdm1atm1.1Sho/Kdm1a+
Eportm1.1(EGFP/icre)Uk/Epor+
involves: 129 * BALB/cJ MGI:5515311
cn5
Kdm1atm1.1Sho/Kdm1atm1.1Sho
Eportm1.1(EGFP/icre)Uk/Epor+
involves: 129 * BALB/cJ MGI:5515313
cn6
Bcl11atm1Mbu/Bcl11atm1Mbu
Eportm1.1(EGFP/icre)Uk/Epor+
Tg(HBB)8.1Gvs/0
involves: 129 * BALB/cJ * FVB/N MGI:5496871
cn7
Bcl11atm1Mbu/Bcl11atm1Mbu
Klf1tm1Nimr/Klf1+
Eportm1.1(EGFP/icre)Uk/Epor+
Tg(HBB)8.1Gvs/0
involves: 129P2/OlaHsd * BALB/cJ * FVB/N MGI:5496872
cn8
Eedtm1Sho/Eedtm1Sho
Eportm1.1(EGFP/icre)Uk/Epor+
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sortm1(EYFP)Cos
involves: 129S1/Sv * 129X1/SvJ * BALB/cJ MGI:4410547
cn9
Eportm1.1(EGFP/icre)Uk/Epor+
Rasa3tm1.1Llp/Rasa3tm1.3Llp
involves: 129S1/SvImJ * BALB/cJ * C57BL/6J MGI:6510263
cn10
Eportm1.1(EGFP/icre)Uk/Epor+
Rasa3tm1.1Llp/Rasa3tm1.1Llp
involves: 129S1/SvImJ * BALB/cJ * C57BL/6J MGI:6509624
cn11
Slc29a1tm2Msg/Slc29a1tm2Msg
Eportm1.1(EGFP/icre)Uk/Epor+
involves: 129X1/SvJ * BALB/cJ MGI:6151074
cn12
Bcl11atm1Pwt/Bcl11atm1Pwt
Eportm1.1(EGFP/icre)Uk/Epor+
involves: BALB/cJ MGI:5515310
cn13
Il22ra1tm1.1Koll/Il22ra1tm1.1Koll
Eportm1.1(EGFP/icre)Uk/Epor+
involves: BALB/cJ * C57BL/6 MGI:6712738


Genotype
MGI:3835199
ht1
Allelic
Composition
Eportm1Jae/Epor+
Genetic
Background
either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eportm1Jae mutation (0 available); any Epor mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
liver/biliary system




Genotype
MGI:2386209
ht2
Allelic
Composition
Eportm1.3(EPOR*)Jtp/Epor+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eportm1.3(EPOR*)Jtp mutation (0 available); any Epor mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype




Genotype
MGI:2386211
ht3
Allelic
Composition
Eportm1.4(EPOR*)Jtp/Epor+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eportm1.4(EPOR*)Jtp mutation (0 available); any Epor mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• develop polycythemia within 3-6 weeks after birth, however do not exhibit any red blood cell morphological abnormalities

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
familial erythrocytosis 1 DOID:0060652 OMIM:133100
J:67205




Genotype
MGI:5515311
cn4
Allelic
Composition
Bcl11atm1Pwt/Bcl11atm1Pwt
Kdm1atm1.1Sho/Kdm1a+
Eportm1.1(EGFP/icre)Uk/Epor+
Genetic
Background
involves: 129 * BALB/cJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bcl11atm1Pwt mutation (0 available); any Bcl11a mutation (42 available)
Eportm1.1(EGFP/icre)Uk mutation (4 available); any Epor mutation (30 available)
Kdm1atm1.1Sho mutation (1 available); any Kdm1a mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• mild




Genotype
MGI:5515313
cn5
Allelic
Composition
Kdm1atm1.1Sho/Kdm1atm1.1Sho
Eportm1.1(EGFP/icre)Uk/Epor+
Genetic
Background
involves: 129 * BALB/cJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eportm1.1(EGFP/icre)Uk mutation (4 available); any Epor mutation (30 available)
Kdm1atm1.1Sho mutation (1 available); any Kdm1a mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• embryos are smaller than control at E13.5

growth/size/body
• embryos are smaller than control at E13.5

hematopoietic system
• 300% increase in CD71hi Ter119low proerythroblasts found in fetal liver cells
• 20-fold decrease in number of erythrocytes found in fetal (E13.5) liver cells
• 20-fold decrease in number of reticulocytes found in fetal (E13.5) liver cells

liver/biliary system
• E13.5 livers exhibit a disturbed architecture with multiple pyknotic cells displaying karyorrhexis
• fetal liver (E13.5) is pale




Genotype
MGI:5496871
cn6
Allelic
Composition
Bcl11atm1Mbu/Bcl11atm1Mbu
Eportm1.1(EGFP/icre)Uk/Epor+
Tg(HBB)8.1Gvs/0
Genetic
Background
involves: 129 * BALB/cJ * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bcl11atm1Mbu mutation (0 available); any Bcl11a mutation (42 available)
Eportm1.1(EGFP/icre)Uk mutation (4 available); any Epor mutation (30 available)
Tg(HBB)8.1Gvs mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• mice are produced in expected Mendelian ratios

hematopoietic system
• increased Ter119+/CD71+ cells in the blood
• increased Ter119+/DRAQ5+ cells in the blood
• mild

homeostasis/metabolism
• indicating anemic stress




Genotype
MGI:5496872
cn7
Allelic
Composition
Bcl11atm1Mbu/Bcl11atm1Mbu
Klf1tm1Nimr/Klf1+
Eportm1.1(EGFP/icre)Uk/Epor+
Tg(HBB)8.1Gvs/0
Genetic
Background
involves: 129P2/OlaHsd * BALB/cJ * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bcl11atm1Mbu mutation (0 available); any Bcl11a mutation (42 available)
Eportm1.1(EGFP/icre)Uk mutation (4 available); any Epor mutation (30 available)
Klf1tm1Nimr mutation (0 available); any Klf1 mutation (23 available)
Tg(HBB)8.1Gvs mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• increased Ter119+/CD71+ cells in the blood




Genotype
MGI:4410547
cn8
Allelic
Composition
Eedtm1Sho/Eedtm1Sho
Eportm1.1(EGFP/icre)Uk/Epor+
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sortm1(EYFP)Cos
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * BALB/cJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eedtm1Sho mutation (1 available); any Eed mutation (116 available)
Eportm1.1(EGFP/icre)Uk mutation (4 available); any Epor mutation (30 available)
Gt(ROSA)26Sortm1(EYFP)Cos mutation (23 available); any Gt(ROSA)26Sor mutation (1095 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• increase in the percentage of cells in the R2 stage (lin-,CD71+,Ter119-) and reduction in the percentage of cells in the R3 stage (lin-,CD71+,Ter119+)




Genotype
MGI:6510263
cn9
Allelic
Composition
Eportm1.1(EGFP/icre)Uk/Epor+
Rasa3tm1.1Llp/Rasa3tm1.3Llp
Genetic
Background
involves: 129S1/SvImJ * BALB/cJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eportm1.1(EGFP/icre)Uk mutation (4 available); any Epor mutation (30 available)
Rasa3tm1.1Llp mutation (0 available); any Rasa3 mutation (62 available)
Rasa3tm1.3Llp mutation (0 available); any Rasa3 mutation (62 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
N
• although there is efficient deletion of exon 3 in red cell precursors, mice are normal at birth and at 6-8 weeks of age with normal spleen weights, normal blood morphology, and normal blood counts except for a clinically insignificant decrease in platelet number and slight increase in circulating reticulocytes




Genotype
MGI:6509624
cn10
Allelic
Composition
Eportm1.1(EGFP/icre)Uk/Epor+
Rasa3tm1.1Llp/Rasa3tm1.1Llp
Genetic
Background
involves: 129S1/SvImJ * BALB/cJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eportm1.1(EGFP/icre)Uk mutation (4 available); any Epor mutation (30 available)
Rasa3tm1.1Llp mutation (0 available); any Rasa3 mutation (62 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
N
• although there is efficient deletion of exon 3 in red cell precursors, mice are normal at birth and at 6-8 weeks of age with normal spleen weights, normal blood morphology, and normal blood counts except for a clinically insignificant decrease in platelet number and slight increase in circulating reticulocytes




Genotype
MGI:6151074
cn11
Allelic
Composition
Slc29a1tm2Msg/Slc29a1tm2Msg
Eportm1.1(EGFP/icre)Uk/Epor+
Genetic
Background
involves: 129X1/SvJ * BALB/cJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eportm1.1(EGFP/icre)Uk mutation (4 available); any Epor mutation (30 available)
Slc29a1tm2Msg mutation (0 available); any Slc29a1 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• under acute hypoxic conditions, mice exhibit a faster increase in serum adenosine levels than in wild-type mice
• under acute hypoxic conditions, mice exhibit reduced tissue hypoxia in the heart, kidney and lung with reduced total cell numbers, albumin and IL6 concentration bronchoalveolar lavage fluid, pulmonary myeloperoxidase activity, and perivascular edema compared with wild-type mice

immune system
• in the lungs of mice exposed to hypoxic conditions




Genotype
MGI:5515310
cn12
Allelic
Composition
Bcl11atm1Pwt/Bcl11atm1Pwt
Eportm1.1(EGFP/icre)Uk/Epor+
Genetic
Background
involves: BALB/cJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bcl11atm1Pwt mutation (0 available); any Bcl11a mutation (42 available)
Eportm1.1(EGFP/icre)Uk mutation (4 available); any Epor mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
N
• mice exhibit normal red blood cell numbers, white blood cell numbers and hemoglobin content




Genotype
MGI:6712738
cn13
Allelic
Composition
Il22ra1tm1.1Koll/Il22ra1tm1.1Koll
Eportm1.1(EGFP/icre)Uk/Epor+
Genetic
Background
involves: BALB/cJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eportm1.1(EGFP/icre)Uk mutation (4 available); any Epor mutation (30 available)
Il22ra1tm1.1Koll mutation (1 available); any Il22ra1 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• mice treated with phenylhydrazine to induce stress erythropoiesis show an increase in RIII and RIV erythroid precursors in the bone marrow compared to controls
• mice treated with phenylhydrazine to induce stress erythropoiesis show an increase in peripheral blood red blood cell numbers compared to controls
• mice treated with phenylhydrazine to induce stress erythropoiesis show an increase in hematocrit compared to controls

homeostasis/metabolism
• mice show alleviation of stress-induced anemia, showing increased peripheral blood cell counts, increased hematocrit, and increase in erythroid precursors in the bone marrow following phenylhydrazine-induced stress erythropoiesis





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last database update
03/18/2025
MGI 6.24
The Jackson Laboratory