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on page 1 showing 20 out of 2,729 results

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

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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# 5790646, RRID:MGI:5790646)

Source Database: MGI, catalog # 5790646
Genetic Background: involves: BALB/cAnNHsd * C3H/HeNHsd
Affected Genes: Gnptab
Genomic Alteration: nym
Availability: Availability unknown check source stock center
Reference: PMID:25107912
Notes: kyphosis, thick eyelids, demyelination, abnormal skin turgor, brain atrophy, penis prolapse, limb grasping, impaired coordination, abnormal cerebellum white matter morphology, Purkinje cell axonal dystrophy, abnormal cerebellar molecular layer, premature death, thick skin, abnormal fertility/fecundity, small nasal bridge, abnormal gait, decreased brain size, axonal spheroids, abnormal cerebellar cortex morphology, postnatal growth retardation, abnormal skeleton morphology, abnormal facial morphology, astrocytosis, ataxia, abnormal cognition, decreased body size, decreased survivor rate, flattened snout, prenatal lethality, incomplete penetrance, abnormal hippocampus CA1 region morphology, abnormal enzyme/coenzyme activity, abnormal spine curvature, Purkinje cell degeneration, abnormal chondrocyte morphology, abnormal hippocampus CA3 region morphology, abnormal pancreas morphology, abnormal pancreatic acinar cell morphology, brain inflammation, lysosomal protein accumulation, cerebellum atrophy, progressive muscle weakness Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3811792, RRID:MGI:3811792)

Source Database: MGI, catalog # 3811792
Genetic Background: involves: 129S4/SvJae * BALB/cJ * C57BL/6J * C57BL/6NTac * CBA
Affected Genes: Tsc1
Genomic Alteration: tm1Djk; Tg(Camk2a-cre)#Szi
Availability: Availability unknown check source stock center
Reference: PMID:18568033
Notes: postnatal lethality, complete penetrance, neuron hypertrophy, astrocytosis, limb grasping, increased brain weight, hypoactivity 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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Cite this (MGI Cat# 3613509, RRID:MGI:3613509)

Source Database: MGI, catalog # 3613509
Genetic Background: involves: 129S1/SvImJ * C57BL/6J
Affected Genes: Mobp
Genomic Alteration: tm1Irg
Availability: Availability unknown check source stock center
Reference: PMID:12203392
Notes: nervous system phenotype, behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 4439363, RRID:MGI:4439363)

Source Database: MGI, catalog # 4439363
Genetic Background: involves: 129/Sv * BALB/cJ * C57BL/6
Affected Genes: Lrrc3b
Genomic Alteration: tm1.1Reed
Availability: Availability unknown check source stock center
Reference: PMID:20080187
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3798665, RRID:MGI:3798665)

Source Database: MGI, catalog # 3798665
Genetic Background: involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m musculus
Affected Genes: Dmd, Utrn
Genomic Alteration: tm1Ked; mdx-3Cv
Availability: Availability unknown check source stock center
Reference: PMID:10204788
Notes: nervous system phenotype, renal/urinary system phenotype, abnormal skeletal muscle morphology, liver/biliary system phenotype, reproductive system phenotype, respiratory system phenotype Allele Detail: Chemically induced (ENU), Targeted

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Cite this (MGI Cat# 3720209, RRID:MGI:3720209)

Source Database: MGI, catalog # 3720209
Genetic Background: involves: FVB
Affected Genes:
Genomic Alteration: Tg(Thy1-MAPT)1Vln
Availability: Availability unknown check source stock center
Reference: PMID:11007782, PMID:10595944
Notes: tau protein deposits, muscular atrophy, impaired coordination, limb grasping, muscle weakness, muscular atrophy, nervous system phenotype, decreased body weight, abnormal axon morphology, abnormal locomotor activation, abnormal neuron morphology, abnormal postural reflex, skeletal muscle fiber atrophy, astrocytosis, axon degeneration, decreased skeletal muscle mass, impaired coordination, abnormal cell cytoskeleton morphology, abnormal axon morphology, impaired righting response Allele Detail: Transgenic

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Cite this (MGI Cat# 5513846, RRID:MGI:5513846)

Source Database: MGI, catalog # 5513846
Genetic Background: involves: 129S6/SvEvTac * C57BL/6NTac
Affected Genes: Cnih2
Genomic Alteration: tm1.1Ran
Availability: Availability unknown check source stock center
Reference: PMID:23522044
Notes: reduced AMPA-mediated synaptic currents, nervous system phenotype, abnormal AMPA-mediated synaptic currents, abnormal miniature excitatory postsynaptic currents Allele Detail: Targeted

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Cite this (MGI Cat# 5629974, RRID:MGI:5629974)

Source Database: MGI, catalog # 5629974
Genetic Background: involves: C57BL/6J * DBA/2J
Affected Genes: Pitpna, Nxf1
Genomic Alteration: vb; em1Haml
Availability: Availability unknown check source stock center
Reference: PMID:25835743
Notes: tremors, abnormal survival Allele Detail: Spontaneous, Endonuclease-mediated

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Cite this (MGI Cat# 3759418, RRID:MGI:3759418)

Source Database: MGI, catalog # 3759418
Genetic Background: B6.129-Cln3
Affected Genes: Cln3
Genomic Alteration: tm1Blda
Availability: Availability unknown check source stock center
Reference: PMID:17855597, PMID:20219947
Notes: abnormal locomotor activation, renal/urinary system phenotype, increased circulating potassium level, increased blood osmolality, decreased urine potassium level, decreased urine osmolality, abnormal kidney morphology, polydipsia, polyuria, abnormal brain morphology, tremors, increased susceptibility to pharmacologically induced seizures, limb grasping, impaired coordination, abnormal lysosome morphology Allele Detail: Targeted

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Cite this (MGI Cat# 4459065, RRID:MGI:4459065)

Source Database: MGI, catalog # 4459065
Genetic Background: involves: 129X1/SvJ * C57BL/6
Affected Genes: Ret
Genomic Alteration: tm2(RET)Jmi; tm1Heno
Availability: Availability unknown check source stock center
Reference: PMID:20392943
Notes: absent enteric neurons, postnatal lethality, incomplete penetrance, premature death, abnormal feces composition, abnormal enteric neural crest cell migration, renal/urinary system phenotype, nervous system phenotype, decreased body weight, abnormal defecation, postnatal growth retardation Allele Detail: Targeted

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Cite this (MGI Cat# 5824114, RRID:MGI:5824114)

Source Database: MGI, catalog # 5824114
Genetic Background: involves: 129S/SvEv * C3H * C57BL/6 * C57BL/6N
Affected Genes: Ndor1, Fus
Genomic Alteration: Tg(UBC-cre/ERT2)1Ejb; tm1c(EUCOMM)Wtsi; tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:26842965
Notes: nervous system phenotype Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 5520084, RRID:MGI:5520084)

Source Database: MGI, catalog # 5520084
Genetic Background: CByJ(Cg)-Zfp24/GrsrJ
Affected Genes: Zfp24
Genomic Alteration: hmcns-2J
Availability: Availability unknown check source stock center
Reference:
Notes: increased or absent threshold for auditory brainstem response, vision/eye phenotype, tonic seizures, tremors, abnormal myelination, premature death, decreased myelin sheath thickness Allele Detail: Spontaneous

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