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on page 1 showing 16 out of 16 results

Cite this (MGI Cat# 2167065, RRID:MGI:2167065)

Source Database: MGI, catalog # 2167065
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Map2k4
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (MGI Cat# 4887241, RRID:MGI:4887241)

Source Database: MGI, catalog # 4887241
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Cacna2d3
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:21074052
Notes: behavior/neurological phenotype, abnormal nervous system physiology, abnormal nociception after inflammation, increased thermal nociceptive threshold Allele Detail: Targeted

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Cite this (MGI Cat# 3759065, RRID:MGI:3759065)

Source Database: MGI, catalog # 3759065
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Hace1
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:17694067
Notes: increased lung tumor incidence Allele Detail: Targeted

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Cite this (MGI Cat# 2680203, RRID:MGI:2680203)

Source Database: MGI, catalog # 2680203
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Cblc
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:14560016
Notes: no abnormal phenotype detected Allele Detail: Targeted

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Cite this (MGI Cat# 3759064, RRID:MGI:3759064)

Source Database: MGI, catalog # 3759064
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Hace1
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:17694067
Notes: increased lung tumor incidence, increased T cell derived lymphoma incidence, increased tumor incidence Allele Detail: Targeted

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Cite this (MGI Cat# 2661729, RRID:MGI:2661729)

Source Database: MGI, catalog # 2661729
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ace2
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:12075344
Notes: decreased cardiac muscle contractility Allele Detail: Targeted

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Cite this (MGI Cat# 3716872, RRID:MGI:3716872)

Source Database: MGI, catalog # 3716872
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Card11
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:17486093
Notes: immune system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3619226, RRID:MGI:3619226)

Source Database: MGI, catalog # 3619226
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Pik3cg
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:17723215, PMID:10669416
Notes: decreased interferon-gamma secretion, abnormal NK cell differentiation, decreased thymocyte number, decreased T cell proliferation, increased monocyte cell number, increased neutrophil cell number, impaired neutrophil recruitment, decreased interleukin-2 secretion, abnormal definitive hematopoiesis, abnormal T cell differentiation, decreased cytotoxic T cell cytolysis, abnormal T cell activation, impaired neutrophil chemotaxis, decreased CD4-positive, alpha beta T cell number, abnormal T cell physiology, abnormal neutrophil physiology, abnormal T-helper 2 physiology, thymus hypoplasia, increased eosinophil cell number, abnormal immune cell physiology, decreased interferon-gamma secretion Allele Detail: Targeted

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Cite this (MGI Cat# 3801009, RRID:MGI:3801009)

Source Database: MGI, catalog # 3801009
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Tnfsf11
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:11051546, PMID:9950424
Notes: absent mesenteric lymph nodes, abnormal immune system morphology, abnormal pro-B cell differentiation, immune system phenotype, abnormal immune system physiology, increased bone mineral density, thin neurocranium, abnormal neurocranium morphology, increased diameter of long bones, increased spleen weight, decreased interleukin-2 secretion, postnatal growth retardation, abnormal long bone epiphyseal plate morphology, absent peripheral lymph nodes, macrocytic anemia, decreased thymus weight, round face, decreased interferon-gamma secretion, lactation failure, abnormal mammary gland growth during pregnancy, failure of tooth eruption, extramedullary hematopoiesis, osteopetrosis, decreased osteoclast cell number, decreased mature B cell number, decreased length of long bones, decreased interleukin-6 secretion, decreased immature B cell number, decreased interleukin-5 secretion, hematopoietic system phenotype, decreased interleukin-4 secretion, osteopetrosis, arrested T cell differentiation, thymus hypoplasia, failure of tooth eruption, homeostasis/metabolism phenotype, small Peyer's patches Allele Detail: Targeted

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Cite this (MGI Cat# 3813941, RRID:MGI:3813941)

Source Database: MGI, catalog # 3813941
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Apln
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:17673668
Notes: cardiovascular system phenotype, decreased ventricle muscle contractility, behavior/neurological phenotype, growth/size/body region phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3813943, RRID:MGI:3813943)

Source Database: MGI, catalog # 3813943
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Apln
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:17673668
Notes: growth/size/body region phenotype, decreased ventricle muscle contractility, cardiovascular system phenotype, increased response of heart to induced stress, behavior/neurological phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 5912245, RRID:MGI:5912245)

Source Database: MGI, catalog # 5912245
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ace2, Pik3cg
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:17499227
Notes: increased cardiac muscle contractility Allele Detail: Targeted

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Cite this (MGI Cat# 3851170, RRID:MGI:3851170)

Source Database: MGI, catalog # 3851170
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Kcnip3
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:11792319
Notes: abnormal motor capabilities/coordination/movement, increased thermal nociceptive threshold, behavior/neurological phenotype, hypoalgesia, increased chemical nociceptive threshold, abnormal nociception after inflammation, hyporesponsive to tactile stimuli Allele Detail: Targeted

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Cite this (MGI Cat# 2661730, RRID:MGI:2661730)

Source Database: MGI, catalog # 2661730
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ace2
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:17499227, PMID:12075344
Notes: congestive heart failure, abnormal heart echocardiography feature, hypotension, thin ventricular wall, decreased cardiac muscle contractility, increased NAD(P)H oxidase activity, heart inflammation, dilated heart ventricle, dilated heart left ventricle, abnormal cardiovascular system physiology, dilated cardiomyopathy, decreased cardiac muscle contractility, cardiac hypertrophy, oxidative stress, increased left ventricle diastolic pressure, abnormal cytokine level Allele Detail: Targeted

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Cite this (MGI Cat# 2664000, RRID:MGI:2664000)

Source Database: MGI, catalog # 2664000
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Fkbp6
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:12764197
Notes: male infertility, small testis, azoospermia, abnormal spermatocyte morphology, arrest of male meiosis Allele Detail: Targeted

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Cite this (MGI Cat# 2167066, RRID:MGI:2167066)

Source Database: MGI, catalog # 2167066
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Map2k4
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:9876179
Notes: embryonic lethality during organogenesis, complete penetrance, anemia, abnormal liver development Allele Detail: Targeted

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