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on page 1 showing 20 out of 2,473 results

Cite this (MGI Cat# 3723117, RRID:MGI:3723117)

Source Database: MGI, catalog # 3723117
Genetic Background: involves: BALB/cJ * C57BL/6
Affected Genes: Ackr3
Genomic Alteration: tm1.1Fma
Availability: Availability unknown check source stock center
Reference: PMID:17804806
Notes: neonatal lethality, incomplete penetrance, abnormal pulmonary valve morphology, ventricular septal defect, calcified aortic valve, decreased marginal zone B cell number, digestive/alimentary phenotype, dilated heart right ventricle, abnormal aortic valve morphology, premature death, abnormal cardiac outflow tract development, atrial septal defect, nervous system phenotype, overriding aortic valve, abnormal heart morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5141026, RRID:MGI:5141026)

Source Database: MGI, catalog # 5141026
Genetic Background: C57BL/6J-bc<8J>/GrsrJ
Affected Genes: Kcnn2
Genomic Alteration: bc-8J
Availability: Availability unknown check source stock center
Reference:
Notes: tremors, ataxia, decreased body size Allele Detail: Spontaneous

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Cite this (MGI Cat# 3849330, RRID:MGI:3849330)

Source Database: MGI, catalog # 3849330
Genetic Background: either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S6/SvEvTac * C57BL/6NCr)
Affected Genes: Celsr3
Genomic Alteration: tm1Mrc
Availability: Availability unknown check source stock center
Reference: PMID:19332558
Notes: abnormal neuronal migration, neonatal lethality, complete penetrance, nervous system phenotype, abnormal globus pallidus morphology, abnormal innervation, abnormal embryonic/fetal subventricular zone morphology Allele Detail: Targeted

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Cite this (MGI Cat# 4938269, RRID:MGI:4938269)

Source Database: MGI, catalog # 4938269
Genetic Background: C57BL/6N-Slx4
Affected Genes: Slx4
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:22922648, PMID:21240276
Notes: abnormal eyelid aperture, impaired glucose tolerance, nervous system phenotype, increased circulating glucose level, increased erythrocyte cell number, lethality throughout fetal growth and development, incomplete penetrance, abnormal male germ cell apoptosis, microphthalmia, abnormal eye morphology, abnormal cranium morphology, increased caudal vertebrae number, obstructive hydrocephaly, oligozoospermia, abnormal cornea morphology, abnormal cerebral cortex morphology, perinatal lethality, incomplete penetrance, postnatal growth retardation, azoospermia, abnormal tooth morphology, abnormal third ventricle morphology, reduced female fertility, reduced male fertility, vertebral fusion, abnormal pupil morphology, early cellular replicative senescence, hydrocephaly, abnormal primordial germ cell morphology, abnormal lymphopoiesis, abnormal iris morphology, increased physiological sensitivity to xenobiotic, increased sensitivity to induced cell death, thin cerebral cortex, absent corpus luteum, absent mature ovarian follicles, absent oocytes, absent optic nerve, anophthalmia, abnormal spermatogenesis, abnormal spine curvature, abnormal retinal vasculature morphology, chromosomal instability, corneal opacity, decreased body size, decreased body weight, decreased common myeloid progenitor cell number, decreased leukocyte cell number, decreased litter size, thrombocytopenia, dilated lateral ventricles, domed cranium, enlarged cranium 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# 2654530, RRID:MGI:2654530)

Source Database: MGI, catalog # 2654530
Genetic Background: involves: 129S6/SvEvTac
Affected Genes: Dvl1
Genomic Alteration: tm1Awb
Availability: Availability unknown check source stock center
Reference: PMID:16116426, PMID:9298901
Notes: hearing/vestibular/ear phenotype, abnormal social/conspecific interaction, behavior/neurological phenotype, nervous system phenotype, abnormal nest building behavior, decreased startle reflex, abnormal huddling behavior, reduced sensorimotor gating, decreased prepulse inhibition, abnormal whisker trimming behavior 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: postnatal lethality, incomplete penetrance, decreased serotonin level, nervous system phenotype, abnormal catecholamine level, decreased anxiety-related response, abnormal emotion/affect behavior, hypoactivity Allele Detail: Targeted

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Cite this (MGI Cat# 2175856, RRID:MGI:2175856)

Source Database: MGI, catalog # 2175856
Genetic Background: involves: 129S6/SvEvTac
Affected Genes: En2
Genomic Alteration: tm3Alj
Availability: Availability unknown check source stock center
Reference: PMID:10640701
Notes: 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 hippocampus CA1 region morphology, abnormal corpus callosum morphology, abnormal cell physiology, abnormal neuronal precursor cell migration, decreased neuronal precursor cell number, abnormal dentate gyrus morphology, nervous system phenotype, postnatal lethality, incomplete penetrance, prenatal growth retardation, thin cortical plate, abnormal hippocampal mossy fiber morphology, limb grasping, decreased neuronal precursor proliferation, decreased neocortex size, decreased food intake, decreased corpus callosum size, decreased body size, abnormal nest building behavior, abnormal behavior, prenatal lethality, incomplete penetrance, abnormal neocortex morphology, increased subiculum size, decreased radial glial cell number, abnormal radial glial cell morphology, abnormal hippocampus neuron morphology, abnormal cell cycle checkpoint function, abnormal hippocampus region morphology, abnormal hippocampus development, decreased neuronal precursor proliferation, abnormal neuronal stem cell morphology, decreased dentate gyrus size, abnormal neocortex morphology, abnormal hippocampus morphology, postnatal lethality, incomplete penetrance, abnormal hippocampus pyramidal cell layer Allele Detail: Targeted

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Cite this (MGI Cat# 5297855, RRID:MGI:5297855)

Source Database: MGI, catalog # 5297855
Genetic Background: involves: C3H/HeJ * C57BL/6J
Affected Genes:
Genomic Alteration: Tg(Prnp-SNCA)22Dpr
Availability: Availability unknown check source stock center
Reference: PMID:12084935
Notes: nervous system phenotype Allele Detail: Transgenic

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Cite this (MGI Cat# 4418655, RRID:MGI:4418655)

Source Database: MGI, catalog # 4418655
Genetic Background: B6.129P2-Ccr5
Affected Genes: Ccr5
Genomic Alteration: tm1Kuz
Availability: Availability unknown check source stock center
Reference: PMID:12807425, PMID:12556387, PMID:16105698
Notes: mortality/aging, behavior/neurological phenotype, corneal vascularization, increased alcohol consumption, abnormal conditioned taste aversion behavior, nervous system phenotype, increased fluid intake Allele Detail: Targeted

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Cite this (MGI Cat# 2678257, RRID:MGI:2678257)

Source Database: MGI, catalog # 2678257
Genetic Background: C57BL/6J-nmf111/J
Affected Genes: nmf111
Genomic Alteration: nmf111
Availability: Availability unknown check source stock center
Reference:
Notes: decreased body size, tremors Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3513684, RRID:MGI:3513684)

Source Database: MGI, catalog # 3513684
Genetic Background: involves: 129S4/SvJae * C57BL/6J
Affected Genes: Jph3
Genomic Alteration: tm1Hta
Availability: Availability unknown check source stock center
Reference: PMID:11906164
Notes: nervous system phenotype, impaired coordination, behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5052381, RRID:MGI:5052381)

Source Database: MGI, catalog # 5052381
Genetic Background: involves: C57BL/6 * DBA/2
Affected Genes:
Genomic Alteration: Tg(HTT*/EGFP)150Nn
Availability: Availability unknown check source stock center
Reference: PMID:15836623
Notes: premature death, abnormal involuntary movement, abnormal striatum morphology, abnormal hippocampus morphology, abnormal cerebral cortex morphology, ataxia, abnormal nervous system morphology, tremors, limb grasping, neuronal intranuclear inclusions Allele Detail: Transgenic

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Cite this (MGI Cat# 2181781, RRID:MGI:2181781)

Source Database: MGI, catalog # 2181781
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Ank3
Genomic Alteration: tm1Bnt
Availability: Availability unknown check source stock center
Reference: PMID:9832557
Notes: Purkinje cell degeneration, impaired ability to fire action potentials, hypoactivity, tremors, decreased Purkinje cell number, convulsive seizures, ataxia, abnormal gait, thin cerebellar molecular layer, small cerebellum, premature death Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 3723444, RRID:MGI:3723444)

Source Database: MGI, catalog # 3723444
Genetic Background: involves: 129S4/SvJae * C57BL/6
Affected Genes: Bdnf, Omp
Genomic Alteration: tm1(tTA)Gogo; Tg(tetO-tetX,lacZ)2Gogo; tm1Jae
Availability: Availability unknown check source stock center
Reference: PMID:17493809
Notes: nervous system phenotype Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 6276568, RRID:MGI:6276568)

Source Database: MGI, catalog # 6276568
Genetic Background: involves: FVB/N
Affected Genes:
Genomic Alteration: Tg(Mpz*S63C)32Mes
Availability: Availability unknown check source stock center
Reference: PMID:16495463
Notes: muscular atrophy, dysmyelination, abnormal nervous system physiology, weakness, tremors, ataxia, demyelination Allele Detail: Transgenic

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Cite this (MGI Cat# 3513190, RRID:MGI:3513190)

Source Database: MGI, catalog # 3513190
Genetic Background: involves: 129X1/SvJ * C57BL/6
Affected Genes: Neurl1a
Genomic Alteration: tm1Ynj
Availability: Availability unknown check source stock center
Reference: PMID:11481456
Notes: abnormal locomotor coordination, homeostasis/metabolism phenotype, reproductive system phenotype, behavior/neurological phenotype, nervous system phenotype, abnormal olfactory discrimination memory Allele Detail: Targeted

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Cite this (MGI Cat# 4818570, RRID:MGI:4818570)

Source Database: MGI, catalog # 4818570
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: En1, Gata2
Genomic Alteration: tm1Msal; tm2(cre)Wrst
Availability: Availability unknown check source stock center
Reference: PMID:19088086
Notes: abnormal serotonergic neuron morphology, abnormal neuron differentiation, abnormal GABAergic neuron morphology, nervous system phenotype Allele Detail: Targeted

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