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on page 1 showing 20 out of 1,158 results

Cite this (MGI Cat# 2665094, RRID:MGI:2665094)

Source Database: MGI, catalog # 2665094
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Fshr
Genomic Alteration: tm1Mha
Availability: Availability unknown check source stock center
Reference: PMID:10803590
Notes: decreased testis weight, increased circulating luteinizing hormone level, increased circulating follicle stimulating hormone level, increased follicle stimulating hormone level, impaired ovarian folliculogenesis, decreased uterus weight, abnormal ovarian secretion, vagina atresia, female infertility, absent corpus luteum, absent mature ovarian follicles, uterus atrophy, decreased ovary weight, small seminiferous tubules, absent estrous cycle, abnormal ovary morphology, abnormal testes secretion, small ovary Allele Detail: Targeted

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Cite this (MGI Cat# 3694560, RRID:MGI:3694560)

Source Database: MGI, catalog # 3694560
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Nefh
Genomic Alteration: tm1Jpj
Availability: Availability unknown check source stock center
Reference: PMID:10461886
Notes: abnormal axon morphology, abnormal ventral spinal root morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5572012, RRID:MGI:5572012)

Source Database: MGI, catalog # 5572012
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Gt(ROSA)26Sor
Genomic Alteration: tm4(ACTB-tdTomato,-EGFP)Luo; Tg(Cck-cre)CKres
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 4946508, RRID:MGI:4946508)

Source Database: MGI, catalog # 4946508
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Phc2, Mtf2
Genomic Alteration: tm1Hko; tm1.1Hko
Availability: Availability unknown check source stock center
Reference: PMID:21059868
Notes: prenatal lethality, complete penetrance, abnormal skeleton morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3707681, RRID:MGI:3707681)

Source Database: MGI, catalog # 3707681
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Cyp26c1, Cyp26a1
Genomic Alteration: tm1.1Hmd; tm1.1Keya
Availability: Availability unknown check source stock center
Reference: PMID:17067568
Notes: abnormal geniculate ganglion morphology, embryonic lethality during organogenesis, complete penetrance, abnormal ectomesenchyme morphology, abnormal nervous system development, open neural tube, abnormal hindbrain development, abnormal rhombomere morphology, abnormal head morphology, midbrain hypoplasia, first pharyngeal arch hypoplasia, forebrain hypoplasia, abnormal facial morphology, nervous system phenotype, second pharyngeal arch hypoplasia, absent trigeminal ganglion, truncated tail bud, abnormal neural crest cell migration, abnormal cranial ganglia morphology, cochlear ganglion hypoplasia, increased hindbrain size, microcephaly Allele Detail: Targeted

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Cite this (MGI Cat# 3812195, RRID:MGI:3812195)

Source Database: MGI, catalog # 3812195
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Slc46a2
Genomic Alteration: tm1Moki
Availability: Availability unknown check source stock center
Reference: PMID:18684012
Notes: thymus hypoplasia Allele Detail: Targeted

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Cite this (MGI Cat# 3718029, RRID:MGI:3718029)

Source Database: MGI, catalog # 3718029
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Aldh1a3, Aldh1a1
Genomic Alteration: tm1Gdu
Availability: Availability unknown check source stock center
Reference: PMID:16611695
Notes: abnormal vitreous body morphology, increased corneal stroma thickness, decreased periocular mesenchyme apoptosis, abnormal periocular mesenchyme morphology, persistent hyperplastic primary vitreous, thick eyelids, abnormal posterior eye segment morphology, increased total retina thickness Allele Detail: Targeted

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Cite this (MGI Cat# 3789903, RRID:MGI:3789903)

Source Database: MGI, catalog # 3789903
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Cckar
Genomic Alteration: tm1Kpn
Availability: Availability unknown check source stock center
Reference: PMID:15152034
Notes: abnormal neuronal migration, abnormal forebrain morphology Allele Detail: Targeted

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Cite this (MGI Cat# 4353028, RRID:MGI:4353028)

Source Database: MGI, catalog # 4353028
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Chat
Genomic Alteration: tm1(cre/ERT)Nat; Tg(CAG-Bgeo/ALPP)1Lbe
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 6157359, RRID:MGI:6157359)

Source Database: MGI, catalog # 6157359
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Eprs, Rps6kb1
Genomic Alteration: tm2.1Xen; tm1Nte
Availability: Availability unknown check source stock center
Reference: PMID:28178239
Notes: decreased epididymal fat pad weight, decreased body size, decreased inguinal fat pad weight, decreased interscapular fat pad weight, decreased mesenteric fat pad weight, decreased retroperitoneal fat pad weight Allele Detail: Targeted

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Cite this (MGI Cat# 3623123, RRID:MGI:3623123)

Source Database: MGI, catalog # 3623123
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Drd2
Genomic Alteration: tm1Schm
Availability: Availability unknown check source stock center
Reference: PMID:10391470
Notes: decreased body size, abnormal dopamine level, abnormal locomotor behavior, bradykinesia, decreased body weight, hunched posture, premature death Allele Detail: Targeted

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Cite this (MGI Cat# 4867023, RRID:MGI:4867023)

Source Database: MGI, catalog # 4867023
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Tg(CAG-Bgeo/GFP)21Lbe, Tg(Itgam-cre)AJva
Genomic Alteration: Tg(CAG-Bgeo/GFP)21Lbe; Tg(Itgam-cre)AJva
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Transgenic

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Cite this (MGI Cat# 4887394, RRID:MGI:4887394)

Source Database: MGI, catalog # 4887394
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Ryr1
Genomic Alteration: tm2.1Alle
Availability: Availability unknown check source stock center
Reference: PMID:17122579
Notes: abnormal calcium ion homeostasis, lethality throughout fetal growth and development, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 3762653, RRID:MGI:3762653)

Source Database: MGI, catalog # 3762653
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Gatad2a
Genomic Alteration: tm1Rnu
Availability: Availability unknown check source stock center
Reference: PMID:17565372
Notes: abnormal embryo turning, decreased embryo size, abnormal vitelline vasculature morphology, embryonic growth arrest, embryonic lethality during organogenesis, complete penetrance, abnormal neural fold morphology, incomplete rostral neuropore closure Allele Detail: Targeted

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Cite this (MGI Cat# 2677318, RRID:MGI:2677318)

Source Database: MGI, catalog # 2677318
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Recql4
Genomic Alteration: tm1Abe
Availability: Availability unknown check source stock center
Reference: PMID:12915449
Notes: growth retardation of incisors, abnormal small intestine morphology, postnatal lethality, incomplete penetrance, neonatal lethality, incomplete penetrance, decreased body weight, vision/eye phenotype, small thymus, abnormal long bone metaphysis morphology, skin lesions, postnatal growth retardation, alopecia, abnormal thymus corticomedullary boundary morphology, absent coat pigmentation, growth retardation of molars, decreased body size, decreased spleen white pulp amount Allele Detail: Targeted

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Cite this (MGI Cat# 5297331, RRID:MGI:5297331)

Source Database: MGI, catalog # 5297331
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Six1
Genomic Alteration: tm1Mair
Availability: Availability unknown check source stock center
Reference: PMID:21364285
Notes: abnormal common carotid artery morphology, abnormal midface morphology, abnormal face development, abnormal cardiac outflow tract development, abnormal skeletal muscle morphology, micrognathia Allele Detail: Targeted

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Cite this (MGI Cat# 5546335, RRID:MGI:5546335)

Source Database: MGI, catalog # 5546335
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Wfikkn1, Gdf11
Genomic Alteration: tm1.1Sjl; tm1Sjl
Availability: Availability unknown check source stock center
Reference: PMID:24019467
Notes: increased rib number, abnormal axial skeleton morphology, cleft palate, increased lumbar vertebrae number, increased thoracic vertebrae number Allele Detail: Targeted

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Cite this (MGI Cat# 2678488, RRID:MGI:2678488)

Source Database: MGI, catalog # 2678488
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Zfp143
Genomic Alteration: Gt(U3Betageo)1Ruiz
Availability: Availability unknown check source stock center
Reference: PMID:12904583
Notes: infertility Allele Detail: Gene trapped

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Cite this (MGI Cat# 3721064, RRID:MGI:3721064)

Source Database: MGI, catalog # 3721064
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Clcn3
Genomic Alteration: tm1Tjj
Availability: Availability unknown check source stock center
Reference: PMID:11182090, PMID:20351103
Notes: decreased body weight, abnormal eye morphology, stereotypic behavior, decreased retinal photoreceptor cell number, abnormal response to new environment, photoreceptor inner segment degeneration, premature death, decreased brain size, small hippocampus, retinal degeneration, photoreceptor outer segment degeneration, hippocampal neuron degeneration, abnormal eye physiology, tremors, abnormal posture, abnormal motor capabilities/coordination/movement, abnormal hippocampus pyramidal cell morphology, abnormal nervous system physiology, abnormal hippocampus morphology, hyperactivity, abnormal eye electrophysiology, blindness, abnormal synaptic vesicle morphology, abnormal nervous system morphology, disorganized photoreceptor outer segment, impaired synaptic plasticity, impaired coordination, abnormal microglial cell physiology, renal/urinary system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5443814, RRID:MGI:5443814)

Source Database: MGI, catalog # 5443814
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Mgat5, Mgat5b
Genomic Alteration: tm1Jwd; tm1.1Itl
Availability: Availability unknown check source stock center
Reference: PMID:22715095
Notes: nervous system phenotype, abnormal homeostasis Allele Detail: Targeted

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