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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rasa3tm1.1Llp
targeted mutation 1.1, Luanne Peters
MGI:6509614
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Eportm1.1(EGFP/icre)Uk/Epor+
Rasa3tm1.1Llp/Rasa3tm1.1Llp
involves: 129S1/SvImJ * BALB/cJ * C57BL/6J MGI:6509624
cn2
Eportm1.1(EGFP/icre)Uk/Epor+
Rasa3tm1.1Llp/Rasa3tm1.3Llp
involves: 129S1/SvImJ * BALB/cJ * C57BL/6J MGI:6510263
cn3
Rasa3tm1.1Llp/Rasa3tm1.3Llp
Tg(CMV-cre)1Cgn/?
involves: 129S1/SvImJ * BALB/cJ * C57BL/6J MGI:6510839
cn4
Rasa3tm1.1Llp/Rasa3tm1.1Llp
Tg(Vav1-cre)1Cgp/?
involves: 129S1/SvImJ * C57BL/6J MGI:6510265
cn5
Rasa3tm1.1Llp/Rasa3tm1.1Llp
Tg(Mx1-cre)1Cgn/?
involves: 129S1/SvImJ * C57BL/6J * CBA/J MGI:6510806
cn6
Rasa3tm1.1Llp/Rasa3tm1.1Llp
Tg(Tek-cre)1Ywa/?
involves: 129S1/SvImJ * C57BL/6J * SJL/J MGI:6510800


Genotype
MGI:6509624
cn1
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 (2 available); any Epor mutation (26 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:6510263
cn2
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 (2 available); any Epor mutation (26 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:6510839
cn3
Allelic
Composition
Rasa3tm1.1Llp/Rasa3tm1.3Llp
Tg(CMV-cre)1Cgn/?
Genetic
Background
involves: 129S1/SvImJ * BALB/cJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rasa3tm1.1Llp mutation (0 available); any Rasa3 mutation (62 available)
Rasa3tm1.3Llp mutation (0 available); any Rasa3 mutation (62 available)
Tg(CMV-cre)1Cgn mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• intercrosses of heterozygotes in the presence of a cre deleter yield no homozygous null animals at birth, showing the homozygous lethality of the null allele




Genotype
MGI:6510265
cn4
Allelic
Composition
Rasa3tm1.1Llp/Rasa3tm1.1Llp
Tg(Vav1-cre)1Cgp/?
Genetic
Background
involves: 129S1/SvImJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rasa3tm1.1Llp mutation (0 available); any Rasa3 mutation (62 available)
Tg(Vav1-cre)1Cgp mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system

embryo

hematopoietic system

mortality/aging
• all die in utero at E12.5 and E13.5 with severe hemorrhage and diminished fetal liver erythropoiesis




Genotype
MGI:6510806
cn5
Allelic
Composition
Rasa3tm1.1Llp/Rasa3tm1.1Llp
Tg(Mx1-cre)1Cgn/?
Genetic
Background
involves: 129S1/SvImJ * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rasa3tm1.1Llp mutation (0 available); any Rasa3 mutation (62 available)
Tg(Mx1-cre)1Cgn mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• resulting from stress erythropoiesis after Poly(I:C) treatment
• adults at 8-12 weeks of age were assessed after being injected with 300 ug Poly(I:C) every other day for 5 days and were found to have suppressed basal erythropoiesis with severe anemia, thrombocytopenia, and leukopenia, with very low CD45- erythroid and CD45+ non-erythroid cell counts in bone marrow, but progression between precursor stages is not affected, and stress erythropoiesis is found with markedly increased spleen size, increased red pulp, increased BFU-E and CFU-E, increased erythroblasts, and reticulocytosis
• profound anemia after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment
• in spleen after Poly(I:C) treatment
• indicated by increased LDH and bilirubin after Poly(I:C) treatment
• after Poly(I:C) treatment

homeostasis/metabolism
• after Poly(I:C) treatment

immune system
• resulting from stress erythropoiesis after Poly(I:C) treatment
• after Poly(I:C) treatment
• after Poly(I:C) treatment

growth/size/body
• resulting from stress erythropoiesis after Poly(I:C) treatment




Genotype
MGI:6510800
cn6
Allelic
Composition
Rasa3tm1.1Llp/Rasa3tm1.1Llp
Tg(Tek-cre)1Ywa/?
Genetic
Background
involves: 129S1/SvImJ * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rasa3tm1.1Llp mutation (0 available); any Rasa3 mutation (62 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system

mortality/aging
• all die in utero at E12.5 and E13.5 with severe hemorrhage and diminished fetal liver erythropoiesis

embryo

hematopoietic system





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory