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on page 1 showing 20 out of 1,751 results

Cite this (MGI Cat# 3589021, RRID:MGI:3589021)

Source Database: MGI, catalog # 3589021
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6
Affected Genes: Spp1
Genomic Alteration: tm1Rit
Availability: Availability unknown check source stock center
Reference: PMID:17211411, PMID:10411681, PMID:10657301, PMID:16939396, PMID:9661074, PMID:15165989, PMID:11181551, PMID:17301681, PMID:10825241, PMID:10393964, PMID:11278791
Notes: nervous system phenotype, increased osteoclast cell number, skeleton phenotype, decreased osteoclast cell number, delayed wound healing, abnormal inflammatory response, decreased interleukin-12 secretion, abnormal osteoclast physiology, decreased susceptibility to viral infection, increased interleukin-10 secretion, abnormal physiological neovascularization, decreased cardiac muscle contractility, increased osteoclast cell number, abnormal osteoclast physiology, decreased heart weight, abnormal cardiovascular system physiology, decreased sensitivity to induced cell death, mortality/aging, decreased interferon-gamma secretion, increased blood urea nitrogen level, hyporesponsive to tactile stimuli, increased interleukin-4 secretion, abnormal response to infection, increased bone mineral density, increased circulating creatinine level, abnormal osteoblast physiology, dilated renal tubules, increased susceptibility to injury, renal tubular necrosis, decreased fibroblast chemotaxis, increased trabecular bone thickness, decreased susceptibility to type IV hypersensitivity reaction, decreased bone resorption Allele Detail: Targeted

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Cite this (MGI Cat# 3807188, RRID:MGI:3807188)

Source Database: MGI, catalog # 3807188
Genetic Background: Not Specified
Affected Genes: Cplx3, Cplx2
Genomic Alteration: tm1Rmnd
Availability: Availability unknown check source stock center
Reference: PMID:18505837
Notes: nervous system phenotype, mortality/aging, reproductive system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 6120521, RRID:MGI:6120521)

Source Database: MGI, catalog # 6120521
Genetic Background: involves: C57BL/6 * SJL
Affected Genes: Myo9a
Genomic Alteration: tm1.2Bah
Availability: Availability unknown check source stock center
Reference: PMID:19828736
Notes: dilated lateral ventricles, abnormal gait, postnatal growth retardation, obstructive hydrocephaly, nervous system phenotype, enlarged third ventricle, brain ventricle stenosis, abnormal third ventricle morphology, abnormal neural tube ventricular layer morphology, abnormal cerebral aqueduct morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3764493, RRID:MGI:3764493)

Source Database: MGI, catalog # 3764493
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Camk2a
Genomic Alteration: tm4Sva
Availability: Availability unknown check source stock center
Reference: PMID:17660813
Notes: enhanced long term potentiation, nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3765152, RRID:MGI:3765152)

Source Database: MGI, catalog # 3765152
Genetic Background: involves: C57BL/6N
Affected Genes: Grid2
Genomic Alteration: tm1Mmsh
Availability: Availability unknown check source stock center
Reference: PMID:17978051
Notes: nervous system phenotype, abnormal Purkinje cell morphology, abnormal CNS synaptic transmission, behavior/neurological phenotype, abnormal excitatory postsynaptic currents, reduced long term depression Allele Detail: Targeted

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Cite this (MGI Cat# 3046975, RRID:MGI:3046975)

Source Database: MGI, catalog # 3046975
Genetic Background: involves: C57BL/6 * CBA
Affected Genes: Otx2
Genomic Alteration: tm5Sia
Availability: Availability unknown check source stock center
Reference: PMID:15201224
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 2447466, RRID:MGI:2447466)

Source Database: MGI, catalog # 2447466
Genetic Background: involves: 129S/SvEv * C57BL/6
Affected Genes: Cx3cl1
Genomic Alteration: tm1Lira
Availability: Availability unknown check source stock center
Reference: PMID:11287620
Notes: hematopoietic system phenotype, nervous system phenotype, immune system phenotype, behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 2656252, RRID:MGI:2656252)

Source Database: MGI, catalog # 2656252
Genetic Background: Not Specified
Affected Genes: St8sia1
Genomic Alteration: tm1Kfk
Availability: Availability unknown check source stock center
Reference: PMID:11682464
Notes: nervous system phenotype, increased T cell proliferation, abnormal nervous system regeneration, behavior/neurological phenotype, decreased CD8-positive, alpha-beta T cell number, immune system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5307044, RRID:MGI:5307044)

Source Database: MGI, catalog # 5307044
Genetic Background: involves: 129S6/SvEvTac * C3H * C57BL/6
Affected Genes: Mir124a-1hg
Genomic Alteration: Tg(Syn1-DsRed,-Mir124a-2)#Tfur; tm1Tfur
Availability: Availability unknown check source stock center
Reference: PMID:21857657
Notes: nervous system phenotype Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 3613783, RRID:MGI:3613783)

Source Database: MGI, catalog # 3613783
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Sim1
Genomic Alteration: tm1Jlmd
Availability: Availability unknown check source stock center
Reference: PMID:16291793, PMID:17356169
Notes: neonatal lethality, decreased apoptosis, abnormal hypothalamus morphology, nervous system phenotype, abnormal neuronal migration, abnormal hypothalamus morphology, abnormal nervous system tract morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5751210, RRID:MGI:5751210)

Source Database: MGI, catalog # 5751210
Genetic Background: C57BL/6-C9orf72
Affected Genes: C9orf72
Genomic Alteration: em5Lutzy
Availability: Availability unknown check source stock center
Reference:
Notes: enlarged lymph nodes, abnormal spinal cord white matter morphology, nervous system phenotype, lysosomal protein accumulation, behavior/neurological phenotype, enlarged spleen, abnormal spinal cord grey matter morphology, abnormal microglial cell physiology, abnormal macrophage physiology Allele Detail: Endonuclease-mediated

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Cite this (MGI Cat# 3851194, RRID:MGI:3851194)

Source Database: MGI, catalog # 3851194
Genetic Background: involves: 129/Sv * C57BL/6
Affected Genes: Rasgrf1
Genomic Alteration: tm1Kln
Availability: Availability unknown check source stock center
Reference: PMID:9384379
Notes: impaired synaptic plasticity, nervous system phenotype, reduced long term potentiation, abnormal long term spatial reference memory, abnormal excitatory postsynaptic potential, abnormal active avoidance behavior, behavior/neurological phenotype, impaired contextual conditioning behavior Allele Detail: Targeted

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Cite this (MGI Cat# 3700130, RRID:MGI:3700130)

Source Database: MGI, catalog # 3700130
Genetic Background: involves: 129 * C57BL/6
Affected Genes: Gria1
Genomic Alteration: tm2Rlh
Availability: Availability unknown check source stock center
Reference: PMID:16007085
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5698610, RRID:MGI:5698610)

Source Database: MGI, catalog # 5698610
Genetic Background: involves: 129S4/SvJae
Affected Genes: Olig1
Genomic Alteration: tm1(cre)Rth
Availability: Availability unknown check source stock center
Reference: PMID:24507192
Notes: abnormal brain interneuron morphology, decreased oligodendrocyte number, abnormal olfactory bulb interneuron morphology, abnormal cerebellum morphology, abnormal cerebral cortex pyramidal cell morphology, nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 4436742, RRID:MGI:4436742)

Source Database: MGI, catalog # 4436742
Genetic Background: B6.Cg-Npc1/Npc1 Tg(Pcp2-cre)2Mpin
Affected Genes: Npc1
Genomic Alteration: Tg(Pcp2-cre)2Mpin; tm1.1Apl; tm1.2Apl
Availability: Availability unknown check source stock center
Reference: PMID:20007718
Notes: Purkinje cell degeneration, growth/size/body region phenotype, impaired coordination, microgliosis, increased cholesterol level, mortality/aging, tremors, nervous system phenotype, ataxia Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 5800563, RRID:MGI:5800563)

Source Database: MGI, catalog # 5800563
Genetic Background: B6.129(Cg)-Dnm1
Affected Genes: Dnm1
Genomic Alteration: tm1.2Frk
Availability: Availability unknown check source stock center
Reference: PMID:27363778
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5882502, RRID:MGI:5882502)

Source Database: MGI, catalog # 5882502
Genetic Background: involves: 129S/Sv * C57BL/6 * C57BL/6J * SJL/J
Affected Genes: Cpeb2
Genomic Alteration: tm1.2Yshu
Availability: Availability unknown check source stock center
Reference: PMID:27810937
Notes: abnormal parasympathetic neuron morphology, bronchoconstriction, abnormal whole-body plethysmography, growth/size/body region phenotype, abnormal breathing pattern, decreased heart rate, decreased pulmonary respiratory rate, respiratory failure, increased brain choline acetyltransferase activity, apnea, increased acetylcholine level, nervous system phenotype, abnormal parasympathetic nervous system physiology, postnatal lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5285584, RRID:MGI:5285584)

Source Database: MGI, catalog # 5285584
Genetic Background: involves: 129P2/OlaHsd
Affected Genes: Camk2b
Genomic Alteration: tm1Yelg
Availability: Availability unknown check source stock center
Reference: PMID:21752990
Notes: nervous system phenotype, impaired contextual conditioning behavior, reduced long term potentiation Allele Detail: Targeted

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Cite this (MGI Cat# 3795859, RRID:MGI:3795859)

Source Database: MGI, catalog # 3795859
Genetic Background: involves: 129/Sv * Black Swiss * Swiss Webster
Affected Genes: Gli2, Gli1
Genomic Alteration: tm2Alj; tm3.1(Gli1)Alj
Availability: Availability unknown check source stock center
Reference: PMID:12361967
Notes: nervous system phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 5475097, RRID:MGI:5475097)

Source Database: MGI, catalog # 5475097
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Affected Genes: Ei24, Tg(Nes-cre)1Kln
Genomic Alteration: Tg(Nes-cre)1Kln; tm1Hzha
Availability: Availability unknown check source stock center
Reference: PMID:23074225, PMID:23479740
Notes: astrocytosis, abnormal cerebral cortex morphology, axonal dystrophy, abnormal brain white matter morphology, abnormal behavior, abnormal motor capabilities/coordination/movement, brain vacuoles, decreased Purkinje cell number, decreased myelin sheath thickness, decreased neuron number, neuronal cytoplasmic inclusions, reduced cerebellar foliation, thin cerebellar molecular layer, impaired autophagy, decreased cerebral cortex pyramidal cell number, premature death, postnatal growth retardation, limb grasping, increased neuron apoptosis, impaired coordination, enlarged lateral ventricles, decreased hippocampus pyramidal cell number, decreased body weight, axon degeneration, ataxia, nervous system phenotype, axonal spheroids, abnormal involuntary movement, abnormal hippocampus pyramidal cell layer, tremors, abnormal Purkinje cell morphology, abnormal axon morphology, abnormal cerebellum fissure morphology, abnormal nervous system morphology, thin cerebral cortex, abnormal oligodendrocyte morphology Allele Detail: Transgenic, Targeted

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