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on page 1 showing 20 out of 1,702 results from 1 sources

Cite this (MGI Cat# 3808124, RRID:MGI:3808124)

Source Database: MGI, catalog # 3808124
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * CBA
Affected Genes: Emx1, Hes1
Genomic Alteration: tm1(cre)Ito; tm1Kag
Availability: Availability unknown check source stock center
Reference: PMID:18579678
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5660929, RRID:MGI:5660929)

Source Database: MGI, catalog # 5660929
Genetic Background: 129S2/SvPasCrl-Disc1 Disc1
Affected Genes: Disc1
Genomic Alteration: tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho; del
Availability: Availability unknown check source stock center
Reference: PMID:24908665
Notes: increased prepulse inhibition, low sweet preference, decreased hemoglobin content, increased startle reflex, increased red blood cell distribution width, decreased body size, anemia, abnormal behavioral response to xenobiotic, decreased body weight, behavioral despair, nervous system phenotype Allele Detail: Spontaneous, Targeted

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Cite this (MGI Cat# 5521492, RRID:MGI:5521492)

Source Database: MGI, catalog # 5521492
Genetic Background: involves: 129S2/SvPas * C57BL/6J * CBA
Affected Genes: Rapgef3
Genomic Alteration: tm1.1Geno; Tg(Camk2a-cre)2Szi
Availability: Availability unknown check source stock center
Reference: PMID:22365550
Notes: nervous system phenotype Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 4868621, RRID:MGI:4868621)

Source Database: MGI, catalog # 4868621
Genetic Background: C57BL/6J-Cars2
Affected Genes: Cars2
Genomic Alteration: m1Btlr
Availability: Availability unknown check source stock center
Reference:
Notes: head bobbing, hearing/vestibular/ear phenotype, tremors, nervous system phenotype, induced hyperactivity Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3715612, RRID:MGI:3715612)

Source Database: MGI, catalog # 3715612
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Clcn2
Genomic Alteration: tm1Tjj
Availability: Availability unknown check source stock center
Reference: PMID:17567819, PMID:24647135, PMID:11250895
Notes: retinal degeneration, endocrine/exocrine gland phenotype, abnormal retinal outer nuclear layer morphology, abnormal male germ cell morphology, seminiferous tubule degeneration, abnormal testis development, abnormal spermatocyte morphology, abnormal seminiferous tubule morphology, abnormal brain morphology, abnormal brainstem morphology, abnormal cerebellum morphology, abnormal blood-brain barrier function, nervous system phenotype, abnormal brain internal capsule morphology, abnormal corpus callosum morphology, abnormal microglial cell physiology, abnormal myelin sheath morphology, abnormal nerve conduction, homeostasis/metabolism phenotype, abnormal spinal cord morphology, abnormal myelin sheath morphology, behavior/neurological phenotype, male infertility, behavior/neurological phenotype, brain vacuoles, abnormal oligodendrocyte physiology, abnormal glial cell physiology, abnormal photoreceptor outer segment morphology, disorganized photoreceptor inner segment, abnormal eye physiology, disorganized photoreceptor outer segment, Leydig cell hyperplasia, azoospermia, small testis, abnormal Sertoli cell development, brain vacuoles, abnormal Sertoli cell morphology Allele Detail: Targeted

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Cite this (MGI Cat# 4836484, RRID:MGI:4836484)

Source Database: MGI, catalog # 4836484
Genetic Background: involves: C57BL/6N
Affected Genes: Nedd4
Genomic Alteration: tm2Bros
Availability: Availability unknown check source stock center
Reference: PMID:20159449
Notes: abnormal miniature excitatory postsynaptic currents, abnormal neuron morphology, abnormal synaptic vesicle number, abnormal synapse morphology, perinatal lethality, complete penetrance, nervous system phenotype, abnormal dendrite morphology, lethality throughout fetal growth and development, incomplete penetrance, hemorrhage, abnormal excitatory postsynaptic currents, fetal growth retardation Allele Detail: Targeted

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Cite this (MGI Cat# 5487389, RRID:MGI:5487389)

Source Database: MGI, catalog # 5487389
Genetic Background: involves: C57BL/6
Affected Genes: Tph2
Genomic Alteration: tm1Dmkh
Availability: Availability unknown check source stock center
Reference: PMID:20722968
Notes: decreased serotonin level, nervous system phenotype, increased core body temperature Allele Detail: Targeted

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Cite this (MGI Cat# 2684657, RRID:MGI:2684657)

Source Database: MGI, catalog # 2684657
Genetic Background: involves: FVB/N
Affected Genes: Psen1
Genomic Alteration: Tg(Thy1-cre)1Vln; tm1Vln
Availability: Availability unknown check source stock center
Reference: PMID:11978821
Notes: behavior/neurological phenotype, abnormal long term potentiation, nervous system phenotype, amyloid beta deposits Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 5702670, RRID:MGI:5702670)

Source Database: MGI, catalog # 5702670
Genetic Background: D2.Cg-Tg(APPswe,PSEN1dE9)85Dbo
Affected Genes: Tg(APPswe,PSEN1dE9)85Dbo, Hc
Genomic Alteration: Tg(APPswe,PSEN1dE9)85Dbo; 1
Availability: Availability unknown check source stock center
Reference: PMID:25933409
Notes: premature death, convulsive seizures, amyloid beta deposits, nervous system phenotype Allele Detail: Transgenic, Not Applicable

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Cite this (MGI Cat# 3831872, RRID:MGI:3831872)

Source Database: MGI, catalog # 3831872
Genetic Background: B6.129P2-Cnr1
Affected Genes: Cnr1
Genomic Alteration: tm1.1Ltz
Availability: Availability unknown check source stock center
Reference: PMID:21050275, PMID:12152079
Notes: nervous system phenotype, abnormal axon fasciculation, abnormal nervous system development, behavior/neurological phenotype, abnormal learning/memory/conditioning, decreased exploration in new environment, enhanced long term potentiation, abnormal paired-pulse facilitation, absent long term depression, abnormal nervous system morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5800419, RRID:MGI:5800419)

Source Database: MGI, catalog # 5800419
Genetic Background: B6.129S7(C)-Shank3
Affected Genes: Shank3
Genomic Alteration: tm1.2Yhj
Availability: Availability unknown check source stock center
Reference: PMID:27161151
Notes: abnormal response to new environment, abnormal synapse morphology, decreased amygdala size, decreased vocalization, enhanced contextual conditioning behavior, abnormal social/conspecific interaction, hypoactivity, impaired coordination, impaired learning, impaired spatial learning, abnormal social investigation, abnormal single cell response, abnormal olfactory lobe morphology, increased anxiety-related response, increased grooming behavior, abnormal odor adaptation, increased startle reflex, nervous system phenotype, reduced long term depression, abnormal nervous system electrophysiology, skin lesions, small hippocampus, thalamus hyperplasia, abnormal excitatory postsynaptic currents, abnormal ear development, abnormal dendritic spine morphology, abnormal cingulum morphology, abnormal cerebellar peduncle morphology, abnormal brain white matter morphology, abnormal brain internal capsule morphology, abnormal brain commissure morphology, abnormal behavior, abnormal basal ganglion morphology, abnormal autopod morphology, abnormal spinal cord commissure morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3806249, RRID:MGI:3806249)

Source Database: MGI, catalog # 3806249
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
Affected Genes: Ndst3
Genomic Alteration: tm1.1Grob
Availability: Availability unknown check source stock center
Reference: PMID:18385133
Notes: decreased lymphocyte cell number, nervous system phenotype, decreased CD8-positive, alpha-beta T cell number, decreased anxiety-related response, decreased circulating cholesterol level, decreased circulating HDL cholesterol level Allele Detail: Targeted

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Cite this (MGI Cat# 5661729, RRID:MGI:5661729)

Source Database: MGI, catalog # 5661729
Genetic Background: C3H.Cg-Scrib
Affected Genes: Scrib
Genomic Alteration: Crc
Availability: Availability unknown check source stock center
Reference: PMID:25128525
Notes: nervous system phenotype Allele Detail: Spontaneous

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Cite this (MGI Cat# 5316843, RRID:MGI:5316843)

Source Database: MGI, catalog # 5316843
Genetic Background: involves: C57BL/6 * CBA
Affected Genes: Pax6
Genomic Alteration: Sey; Tg(PAX6)77Ndha
Availability: Availability unknown check source stock center
Reference: PMID:8689689
Notes: nervous system phenotype, taste/olfaction phenotype, vision/eye phenotype Allele Detail: Transgenic, Spontaneous

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Cite this (MGI Cat# 4450933, RRID:MGI:4450933)

Source Database: MGI, catalog # 4450933
Genetic Background: B6.Cg-Fem1c
Affected Genes: Fem1c
Genomic Alteration: Gt(ROSABetageo)3Sor
Availability: Availability unknown check source stock center
Reference: PMID:15082774
Notes: reproductive system phenotype, nervous system phenotype Allele Detail: Gene trapped

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Cite this (MGI Cat# 3613527, RRID:MGI:3613527)

Source Database: MGI, catalog # 3613527
Genetic Background: involves: 129X1/SvJ * C57BL/6
Affected Genes: Cntn6
Genomic Alteration: tm1Kwat
Availability: Availability unknown check source stock center
Reference: PMID:12884264
Notes: nervous system phenotype, impaired coordination Allele Detail: Targeted

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Cite this (MGI Cat# 3835528, RRID:MGI:3835528)

Source Database: MGI, catalog # 3835528
Genetic Background: involves: 129 * C57BL/6
Affected Genes: Ptpn5
Genomic Alteration: tm1Pjlo
Availability: Availability unknown check source stock center
Reference: PMID:18932218
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3715457, RRID:MGI:3715457)

Source Database: MGI, catalog # 3715457
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Syt5
Genomic Alteration: tm2Sud
Availability: Availability unknown check source stock center
Reference: PMID:17521570
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5497000, RRID:MGI:5497000)

Source Database: MGI, catalog # 5497000
Genetic Background: involves: 129S1/Sv * C57BL/6J
Affected Genes: Slc18a2, Slc6a4
Genomic Alteration: tm1.1Bgir; tm1(cre)Xz
Availability: Availability unknown check source stock center
Reference: PMID:21814181
Notes: abnormal emotion/affect behavior, decreased anxiety-related response, decreased serotonin level, abnormal catecholamine level, hypoactivity, postnatal lethality, incomplete penetrance, nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5896655, RRID:MGI:5896655)

Source Database: MGI, catalog # 5896655
Genetic Background: involves: 129S2/SvPas * C57BL/6J * C57BL/6N
Affected Genes: Brpf1, Emx1
Genomic Alteration: tm1c(EUCOMM)Wtsi; tm1(cre)Krj
Availability: Availability unknown check source stock center
Reference: PMID:25568313, PMID:25757017, PMID:27939640
Notes: abnormal neocortex morphology, abnormal cell physiology, decreased food intake, abnormal behavior, abnormal nest building behavior, decreased body size, abnormal hippocampal mossy fiber morphology, abnormal dentate gyrus morphology, decreased corpus callosum size, decreased dentate gyrus size, abnormal corpus callosum morphology, abnormal neocortex morphology, increased subiculum size, prenatal lethality, incomplete penetrance, decreased neocortex size, limb grasping, nervous system phenotype, prenatal growth retardation, abnormal hippocampus region morphology, abnormal hippocampus pyramidal cell layer, abnormal hippocampus development, decreased neuronal precursor proliferation, abnormal hippocampus CA1 region morphology, postnatal lethality, incomplete penetrance, decreased radial glial cell number, abnormal radial glial cell morphology, abnormal hippocampus neuron morphology, thin cortical plate, abnormal cell cycle checkpoint function, decreased neuronal precursor cell number, abnormal neuronal stem cell morphology, abnormal neuronal migration, postnatal lethality, incomplete penetrance, abnormal hippocampus morphology, decreased neuronal precursor proliferation Allele Detail: Targeted

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