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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Sppl3tm1Itl
targeted mutation 1, Ingenious Targeting Laboratory
MGI:6467467
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
 		Sppl3tm1Itl/Sppl3tm1Itl
Ncr1tm1.1(icre)Viv/Ncr1+ 		involves: 129S/SvEv * C57BL/6 MGI:6515783
cn2
 		Sppl3tm1Itl/Sppl3tm1Itl
Commd10Tg(Vav1-icre)A2Kio/Commd10+ 		involves: 129S/SvEv * C57BL/6 * C57BL/10 * CBA/Ca MGI:6515779
cn3
 		Sppl3tm1Itl/Sppl3em1Pomz
Ncr1tm1.1(icre)Viv/Ncr1+ 		involves: 129S/SvEv * C57BL/6 * C57BL/6J MGI:6515792
cn4
 		Sppl3tm1Itl/Sppl3tm1Itl
Edil3Tg(Sox2-cre)1Amc/Edil3+ 		involves: 129S/SvEv * C57BL/6 * CBA MGI:6515777


Genotype
MGI:6515783
cn1
Allelic
Composition		 Sppl3tm1Itl/Sppl3tm1Itl
Ncr1tm1.1(icre)Viv/Ncr1+
Genetic
Background		 involves: 129S/SvEv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ncr1tm1.1(icre)Viv mutation (1 available); any Ncr1 mutation (39 available)
Sppl3tm1Itl mutation (0 available); any Sppl3 mutation (75 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
immune system
abnormal NK cell differentiation ( J:280182 )
• mice show subtle changes in the expression of NK cell surface receptors and a defect in NK cell maturation with a 5-fold reduction of CD27+CD11b+ NK cells in spleen and a 2.7-fold loss of CD27+CD11b+ NK cells in the bone marrow
increased immature NK cell number ( J:280182 )
• mice show a 1.3-fold increase in the number of immature CD27+CD11b- NK cells in bone marrow but no significant change in spleen
decreased NK cell number ( J:280182 )
• number of NK cells (Lin-CD122+DX5+) is decreased 4-fold in spleen and 1.5-fold in the bone marrow
decreased mature NK cell number ( J:280182 )
• mice show a 9-fold reduction of mature CD27-CD11b+ NK cells in spleen, and 4-fold loss of CD27-CD11b+ NK cells in the bone marrow
abnormal NK cell physiology ( J:280182 )
• mice show a 2-fold reduction in the % of proliferating Ki67+CD11b- NK cells in the bone marrow, with no change in the % of Ki67+CD11b+ cells
• splenic CD11b- NK cells show no change in Ki67 staining, and even a small increase in the CD11b+ fraction relative to controls (10.8% vs 6.8%)
• annexin V staining showed a modest reduction of cell death CD11b- NK cells in the bone marrow relative to controls (10% vs 14%) but no significant change in splenic CD11b- NK cells
• CD11b+ NK cells show a 2-fold increase in annexin V staining in the bone marrow and a 3-fold increase in spleen
• however, activation of mTOR in response to IL-15 stimulation is normal in immature NK cells
impaired natural killer cell mediated cytotoxicity ( J:280182 )
• mice exhibit reduced clearance of MHC class I-deficient tumors in vivo; 48 h after i.p. injection, recovery of RMA/s tumor cells is 6.5% versus 1.8% in control mice
• in an in vitro YAC-1 target lysis assay, splenic NK cells (DX5+) show 53% of the cytotoxic activity seen in control mice at a 2:1 E:T ratio

hematopoietic system
abnormal NK cell differentiation ( J:280182 )
• mice show subtle changes in the expression of NK cell surface receptors and a defect in NK cell maturation with a 5-fold reduction of CD27+CD11b+ NK cells in spleen and a 2.7-fold loss of CD27+CD11b+ NK cells in the bone marrow
increased immature NK cell number ( J:280182 )
• mice show a 1.3-fold increase in the number of immature CD27+CD11b- NK cells in bone marrow but no significant change in spleen
decreased NK cell number ( J:280182 )
• number of NK cells (Lin-CD122+DX5+) is decreased 4-fold in spleen and 1.5-fold in the bone marrow
decreased mature NK cell number ( J:280182 )
• mice show a 9-fold reduction of mature CD27-CD11b+ NK cells in spleen, and 4-fold loss of CD27-CD11b+ NK cells in the bone marrow
abnormal NK cell physiology ( J:280182 )
• mice show a 2-fold reduction in the % of proliferating Ki67+CD11b- NK cells in the bone marrow, with no change in the % of Ki67+CD11b+ cells
• splenic CD11b- NK cells show no change in Ki67 staining, and even a small increase in the CD11b+ fraction relative to controls (10.8% vs 6.8%)
• annexin V staining showed a modest reduction of cell death CD11b- NK cells in the bone marrow relative to controls (10% vs 14%) but no significant change in splenic CD11b- NK cells
• CD11b+ NK cells show a 2-fold increase in annexin V staining in the bone marrow and a 3-fold increase in spleen
• however, activation of mTOR in response to IL-15 stimulation is normal in immature NK cells
impaired natural killer cell mediated cytotoxicity ( J:280182 )
• mice exhibit reduced clearance of MHC class I-deficient tumors in vivo; 48 h after i.p. injection, recovery of RMA/s tumor cells is 6.5% versus 1.8% in control mice
• in an in vitro YAC-1 target lysis assay, splenic NK cells (DX5+) show 53% of the cytotoxic activity seen in control mice at a 2:1 E:T ratio




Genotype
MGI:6515779
cn2
Allelic
Composition		 Sppl3tm1Itl/Sppl3tm1Itl
Commd10Tg(Vav1-icre)A2Kio/Commd10+
Genetic
Background		 involves: 129S/SvEv * C57BL/6 * C57BL/10 * CBA/Ca
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Commd10Tg(Vav1-icre)A2Kio mutation (3 available); any Commd10 mutation (24 available)
Sppl3tm1Itl mutation (0 available); any Sppl3 mutation (75 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
mortality/aging
mortality/aging ( J:280182 )
N
• mice are born at normal Mendelian ratios and appear healthy

immune system
immune system phenotype ( J:280182 )
N
• mice have normal numbers of T (CD3+CD4+, CD3+CD8+) and B cells (CD19+B220+) in spleen
abnormal NK cell differentiation ( J:280182 )
• mice show reduced expression of several NK cell surface receptors and a severe defect in NK cell maturation, with a 3-fold loss of CD27+CD11b+ in spleen and a 2-fold loss of CD27+CD11b+ in the bone marrow, indicating a partial block in maturation at the CD27+CD11b- stage
increased immature NK cell number ( J:280182 )
• mice show a 2-fold increase in the total number of immature CD27+CD11b- NK cells in the spleen and bone marrow
decreased NK cell number ( J:280182 )
• mice exhibit reduced numbers of peripheral NK cells; the number of NK cells (Lin-CD122+DX5+) is decreased ~2-fold in spleen and 3-fold in liver
• however, NK cell number is normal in the bone marrow
decreased mature NK cell number ( J:280182 )
• mice show a 2.6-fold decrease in the most mature CD27-CD11b+ NK cells in bone marrow, and a 4.9-fold reduction of CD27-CD11b+ cells in spleen
impaired natural killer cell mediated cytotoxicity ( J:280182 )
• mice exhibit reduced clearance of MHC class I-deficient tumors in vivo; 48 h after i.p. injection, recovery of RMA/s tumor cells is 7% versus 1% in control mice
• in an in vitro YAC-1 target lysis assay, splenic NK cells (DX5+) show ~60% of the cytotoxic activity seen in control mice across a range of E:T ratios

hematopoietic system
hematopoietic system phenotype ( J:280182 )
N
• mice have normal numbers of T (CD3+CD4+, CD3+CD8+) and B cells (CD19+B220+) in spleen
abnormal NK cell differentiation ( J:280182 )
• mice show reduced expression of several NK cell surface receptors and a severe defect in NK cell maturation, with a 3-fold loss of CD27+CD11b+ in spleen and a 2-fold loss of CD27+CD11b+ in the bone marrow, indicating a partial block in maturation at the CD27+CD11b- stage
increased immature NK cell number ( J:280182 )
• mice show a 2-fold increase in the total number of immature CD27+CD11b- NK cells in the spleen and bone marrow
decreased NK cell number ( J:280182 )
• however, NK cell number is normal in the bone marrow
• mice exhibit reduced numbers of peripheral NK cells; the number of NK cells (Lin-CD122+DX5+) is decreased ~2-fold in spleen and 3-fold in liver
decreased mature NK cell number ( J:280182 )
• mice show a 2.6-fold decrease in the most mature CD27-CD11b+ NK cells in bone marrow, and a 4.9-fold reduction of CD27-CD11b+ cells in spleen
impaired natural killer cell mediated cytotoxicity ( J:280182 )
• mice exhibit reduced clearance of MHC class I-deficient tumors in vivo; 48 h after i.p. injection, recovery of RMA/s tumor cells is 7% versus 1% in control mice
• in an in vitro YAC-1 target lysis assay, splenic NK cells (DX5+) show ~60% of the cytotoxic activity seen in control mice across a range of E:T ratios




Genotype
MGI:6515792
cn3
Allelic
Composition		 Sppl3tm1Itl/Sppl3em1Pomz
Ncr1tm1.1(icre)Viv/Ncr1+
Genetic
Background		 involves: 129S/SvEv * C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ncr1tm1.1(icre)Viv mutation (1 available); any Ncr1 mutation (39 available)
Sppl3em1Pomz mutation (0 available); any Sppl3 mutation (75 available)
Sppl3tm1Itl mutation (0 available); any Sppl3 mutation (75 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
mortality/aging
mortality/aging ( J:280182 )
N
• mice are born in Mendelian ratios and survive without any overt phenotype

immune system
abnormal NK cell differentiation ( J:280182 )
• mice show a defect in NK cell maturation with a 1.8-fold reduction of CD27+CD11b+ NK cells in the bone marrow and a 3-fold loss of CD27+CD11b+ NK cells in spleen
increased immature NK cell number ( J:280182 )
• mice show a 1.4-fold increase in the number of immature CD27+CD11b- NK cells in bone marrow but no significant change in spleen
decreased NK cell number ( J:280182 )
• mice exhibit reduced numbers of peripheral NK cells with a 2.9-fold reduction of NK cell number in spleen
• however, NK cell number is normal in the bone marrow
decreased mature NK cell number ( J:280182 )
• mice show a 6-fold reduction of mature CD27-CD11b+ NK cells in spleen, and 3-fold loss of CD27-CD11b+ NK cells in the bone marrow

hematopoietic system
abnormal NK cell differentiation ( J:280182 )
• mice show a defect in NK cell maturation with a 1.8-fold reduction of CD27+CD11b+ NK cells in the bone marrow and a 3-fold loss of CD27+CD11b+ NK cells in spleen
increased immature NK cell number ( J:280182 )
• mice show a 1.4-fold increase in the number of immature CD27+CD11b- NK cells in bone marrow but no significant change in spleen
decreased NK cell number ( J:280182 )
• mice exhibit reduced numbers of peripheral NK cells with a 2.9-fold reduction of NK cell number in spleen
• however, NK cell number is normal in the bone marrow
decreased mature NK cell number ( J:280182 )
• mice show a 6-fold reduction of mature CD27-CD11b+ NK cells in spleen, and 3-fold loss of CD27-CD11b+ NK cells in the bone marrow




Genotype
MGI:6515777
cn4
Allelic
Composition		 Sppl3tm1Itl/Sppl3tm1Itl
Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic
Background		 involves: 129S/SvEv * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Edil3Tg(Sox2-cre)1Amc mutation (5 available); any Edil3 mutation (42 available)
Sppl3tm1Itl mutation (0 available); any Sppl3 mutation (75 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
mortality/aging
neonatal lethality, incomplete penetrance ( J:280182 )
• although mice are born in expected Mendelian ratios, a substantial proportion of mice die of undetermined causes shortly after birth
postnatal lethality, incomplete penetrance ( J:280182 )
• only about 10% survive to weaning

growth/size/body
decreased birth body size ( J:280182 )




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Send questions and comments to User Support. 		last database update
05/07/2024
MGI 6.23 		The Jackson Laboratory