Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lect2tm1Ymg mutation
(0 available);
any
Lect2 mutation
(12 available)
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hematopoietic system
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• the percent of hepatic CD3int and CD4+ NK1.1+ T cells is significantly higher compared to wild-type mice
• the proportion of CD4+ among the CD3int NK1.1+ T cells is also increased
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• hepatic but not splenic mononuclear cells are significantly more cytotoxic to syngeneic thymocytes and YAC-1 cells
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• 3 hours after Con A injection CD3int NK1.1+ T cells show increased apoptosis
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immune system
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• the percent of hepatic CD3int and CD4+ NK1.1+ T cells is significantly higher compared to wild-type mice
• the proportion of CD4+ among the CD3int NK1.1+ T cells is also increased
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• hepatic but not splenic mononuclear cells are significantly more cytotoxic to syngeneic thymocytes and YAC-1 cells
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• 3 hours after Con A injection CD3int NK1.1+ T cells show increased apoptosis
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• in response to alpha-GalCer mutant mice produce significantly more IL-4 and slightly more IFN-gamma
• in response to Con A injection mutant mice produce significantly more IL-4
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• 5 hours after Con A injection mutant livers show focal degenerative change and clusters of apoptotic cells
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liver/biliary system
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• 5 hours after Con A injection mutant livers show focal degenerative change and clusters of apoptotic cells
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cellular
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• 3 hours after Con A injection CD3int NK1.1+ T cells show increased apoptosis
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm2.1Cip mutation
(2 available);
any
Apc mutation
(154 available)
Lect2tm1Ymg mutation
(0 available);
any
Lect2 mutation
(12 available)
Tg(Ttr-cre/Esr1*)1Vco mutation
(1 available)
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mortality/aging
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• tamoxifen treated mutants exhibit a decrease in survival rate
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liver/biliary system
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• increase in liver apoptosis in tamoxifen treated mutants
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• liver inflammation is increased in tamoxifen treated mutants compared to single Apc mutants
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• livers of tamoxifen treated mutants exhibit a flaccid and loose texture compared to livers from single Apc homozygotes
• mutants injected with tamoxifen exhibit significantly higher total numbers of nonparenchymal cells (NPCs) in the liver
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• in tamoxifen treated mutants
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immune system
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• number of iNKT cells in the liver is increased in tamoxifen-treated double mutants compared to single Apc mutants
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• liver infiltrating immune cells of tamoxifen treated mutants have an increase in neutrophils compared to infiltrating immune cells in single Apc mutants
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• invariant NKTs (iNKTs) are more activated in tamoxifen treated double mutant livers than in single Apc mutant livers
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• chemokines in the liver of tamoxifen treated mutants, such as Cxcl1, Cxcl12, and Cxcl12 are induced to higher levels in double mutants than in single Apc mutants
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• CD4- iNKTs from tamoxifen treated mutants produce less IFN-gamma than CD4- iNKTs of single Apc mutants
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• CD4- iNKTs from tamoxifen treated mutants produce more IL-4 than CD4- iNKTs of single Apc mutants
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• liver inflammation is increased in tamoxifen treated mutants compared to single Apc mutants
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homeostasis/metabolism
hematopoietic system
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• number of iNKT cells in the liver is increased in tamoxifen-treated double mutants compared to single Apc mutants
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• liver infiltrating immune cells of tamoxifen treated mutants have an increase in neutrophils compared to infiltrating immune cells in single Apc mutants
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• invariant NKTs (iNKTs) are more activated in tamoxifen treated double mutant livers than in single Apc mutant livers
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cellular
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• increase in liver apoptosis in tamoxifen treated mutants
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• in tamoxifen treated mutants
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lect2tm1Ymg mutation
(0 available);
any
Lect2 mutation
(12 available)
Tg(Pklr-Myc)73Ak mutation
(0 available)
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neoplasm
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• tumors have higher grades of malignancy and are less differentiated than those of single Tg(Pklr-Myc)73Ak mice
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• mutants develop hepatocellular carcinoma
• the number and size of tumor nodules in double mutants is greater than in single Tg(Pklr-Myc)73Ak mice
• some tumors in double mutants exhibit a very poorly differentiated phenotype (fetal-like phenotype) that is never seen in tumors of single Tg(Pklr-Myc)73Ak mice
• tumors have higher mitotic indices compared with tumors from single Tg(Pklr-Myc)73Ak mice
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liver/biliary system
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• mutants develop hepatocellular carcinoma
• the number and size of tumor nodules in double mutants is greater than in single Tg(Pklr-Myc)73Ak mice
• some tumors in double mutants exhibit a very poorly differentiated phenotype (fetal-like phenotype) that is never seen in tumors of single Tg(Pklr-Myc)73Ak mice
• tumors have higher mitotic indices compared with tumors from single Tg(Pklr-Myc)73Ak mice
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