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on page 1 showing 14 out of 14 results

Cite this (MGI Cat# 5792693, RRID:MGI:5792693)

Source Database: MGI, catalog # 5792693
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Ptchd1
Genomic Alteration: tm2.2Gfng
Availability: Availability unknown check source stock center
Reference: PMID:27007844
Notes: abnormal sleep pattern, hypotonia, abnormal gait, impaired cued conditioning behavior, abnormal single cell response, hyperactivity, behavior/neurological phenotype, increased aggression, impaired contextual conditioning behavior, impaired avoidance learning behavior, nervous system phenotype, abnormal cognition Allele Detail: Targeted

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Cite this (MGI Cat# 4415255, RRID:MGI:4415255)

Source Database: MGI, catalog # 4415255
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Nefm
Genomic Alteration: tm1Dwc
Availability: Availability unknown check source stock center
Reference: PMID:19193875
Notes: abnormal axon morphology, homeostasis/metabolism phenotype, nervous system phenotype, behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5000281, RRID:MGI:5000281)

Source Database: MGI, catalog # 5000281
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes:
Genomic Alteration: Tg(AR*100Q)#Als
Availability: Availability unknown check source stock center
Reference: PMID:21317158
Notes: nervous system phenotype, motor neuron degeneration Allele Detail: Transgenic

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Cite this (MGI Cat# 5634918, RRID:MGI:5634918)

Source Database: MGI, catalog # 5634918
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Tg(Camk2a-tTA)1Mmay, Bace1
Genomic Alteration: Tg(Camk2a-tTA)1Mmay; tm1Pcw; Tg(tetO-CDK5R1/GFP)337Lht
Availability: Availability unknown check source stock center
Reference: PMID:22049418
Notes: nervous system phenotype, hippocampal neuron degeneration, decreased brain weight, behavior/neurological phenotype, astrocytosis Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 2686964, RRID:MGI:2686964)

Source Database: MGI, catalog # 2686964
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Nefm
Genomic Alteration: tm1Mvr
Availability: Availability unknown check source stock center
Reference: PMID:14662746
Notes: abnormal neuron differentiation, abnormal axon morphology, nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3717260, RRID:MGI:3717260)

Source Database: MGI, catalog # 3717260
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Arc
Genomic Alteration: tm1.1Kuhl
Availability: Availability unknown check source stock center
Reference: PMID:17088210
Notes: decreased fear-related response, abnormal contextual conditioning behavior, abnormal long term object recognition memory, enhanced long term potentiation, reduced long term potentiation, nervous system phenotype, abnormal cued conditioning behavior, abnormal conditioned taste aversion behavior, abnormal spatial learning Allele Detail: Targeted

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Cite this (MGI Cat# 5141223, RRID:MGI:5141223)

Source Database: MGI, catalog # 5141223
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Neto2
Genomic Alteration: tm1Mci
Availability: Availability unknown check source stock center
Reference: PMID:21734292
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 2675280, RRID:MGI:2675280)

Source Database: MGI, catalog # 2675280
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Hoxb1
Genomic Alteration: tm1Mrc
Availability: Availability unknown check source stock center
Reference: PMID:8898234
Notes: abnormal digastric posterior belly morphology, abnormal temporalis muscle morphology, abnormal masseter muscle morphology, postnatal lethality, incomplete penetrance, facial paralysis, abnormal tooth morphology, absent facial nuclei, narrow face, decreased body size, nervous system phenotype, abnormal facial nerve morphology, facial muscle degeneration, abnormal buccinator muscle morphology, abnormal lower lip morphology, small facial motor nucleus, abnormal zygomaticus muscle morphology, absent facial muscle, absent levator nasolabialis muscle, abnormal neuron differentiation, abnormal depressor anguli oris muscle morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5705386, RRID:MGI:5705386)

Source Database: MGI, catalog # 5705386
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Bbs7
Genomic Alteration: tm1Vcs
Availability: Availability unknown check source stock center
Reference: PMID:23572516
Notes: abnormal brain ependyma motile cilium morphology, small hippocampus, thin cerebral cortex, abnormal sperm axoneme morphology, enlarged lateral ventricles, obese, abnormal cilium morphology, increased body weight, renal/urinary system phenotype, increased food intake, retinal degeneration, photoreceptor outer segment degeneration, enlarged third ventricle, retinal outer nuclear layer degeneration, nervous system phenotype, decreased body weight, abnormal sperm principal piece morphology, decreased birth body size, male infertility, abnormal sperm flagellum morphology, taste/olfaction phenotype, photoreceptor inner segment degeneration, preweaning lethality, incomplete penetrance, decreased brain ependyma motile cilium number, limbs/digits/tail phenotype, decreased striatum area, cellular phenotype, absent sperm flagellum, decreased brain ependyma motile cilium length Allele Detail: Targeted

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Cite this (MGI Cat# 2656901, RRID:MGI:2656901)

Source Database: MGI, catalog # 2656901
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Kif5a
Genomic Alteration: tm1Gsn
Availability: Availability unknown check source stock center
Reference: PMID:12682084
Notes: neonatal lethality, complete penetrance, nervous system phenotype, atelectasis, abnormal breathing pattern, cyanosis, abnormal motor neuron morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5508328, RRID:MGI:5508328)

Source Database: MGI, catalog # 5508328
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Adra2c
Genomic Alteration: tm1Gsb
Availability: Availability unknown check source stock center
Reference: PMID:19225179
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 2675282, RRID:MGI:2675282)

Source Database: MGI, catalog # 2675282
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Hoxb1
Genomic Alteration: tm2Mrc
Availability: Availability unknown check source stock center
Reference: PMID:8898234
Notes: abnormal neuron differentiation, nervous system phenotype, decreased body size, narrow face, absent facial muscle, small facial motor nucleus, absent facial nuclei, abnormal zygomaticus muscle morphology, postnatal lethality, incomplete penetrance, facial muscle degeneration, abnormal masseter muscle morphology, abnormal temporalis muscle morphology, abnormal digastric posterior belly morphology, abnormal depressor anguli oris muscle morphology, absent levator nasolabialis muscle, abnormal buccinator muscle morphology, neonatal lethality, incomplete penetrance, abnormal lower lip morphology, facial paralysis, abnormal facial nerve morphology, abnormal tooth morphology Allele Detail: Targeted

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Cite this (MGI Cat# 2173304, RRID:MGI:2173304)

Source Database: MGI, catalog # 2173304
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Hmx2
Genomic Alteration: tm1Tlu
Availability: Availability unknown check source stock center
Reference: PMID:11748138
Notes: abnormal inner ear canal fusion, circling, absent semicircular canals, abnormal inner ear morphology, head tilt, nervous system phenotype, abnormal crista ampullaris morphology, hyperactivity, abnormal ear development, abnormal inner ear vestibule morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3842785, RRID:MGI:3842785)

Source Database: MGI, catalog # 3842785
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Affected Genes: Nefh
Genomic Alteration: tm2Dwc
Availability: Availability unknown check source stock center
Reference: PMID:12186852
Notes: abnormal axon morphology, nervous system phenotype Allele Detail: Targeted

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