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on page 1 showing 20 out of 1,232 results

Cite this (MGI Cat# 3698415, RRID:MGI:3698415)

Source Database: MGI, catalog # 3698415
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Htt
Genomic Alteration: tm8Mem
Availability: Availability unknown check source stock center
Reference: PMID:11709539
Notes: preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5484786, RRID:MGI:5484786)

Source Database: MGI, catalog # 5484786
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Grb2
Genomic Alteration: tm1Paw; Tg(Nphs2-cre)1Seq; tm3.1Paw
Availability: Availability unknown check source stock center
Reference: PMID:23226445
Notes: renal/urinary system phenotype Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 3789475, RRID:MGI:3789475)

Source Database: MGI, catalog # 3789475
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Gt(ROSA)26Sor
Genomic Alteration: tm1(CAG-cre)Jphe
Availability: Availability unknown check source stock center
Reference: PMID:18159238
Notes: no phenotypic analysis Allele Detail: Targeted

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Cite this (MGI Cat# 3804962, RRID:MGI:3804962)

Source Database: MGI, catalog # 3804962
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Lin7c
Genomic Alteration: tm1Dsb
Availability: Availability unknown check source stock center
Reference: PMID:17923534
Notes: renal interstitial fibrosis, increased urine sodium level, single kidney, abnormal kidney morphology, decreased kidney weight, increased blood urea nitrogen level, dilated renal tubules, decreased creatinine clearance, increased kidney apoptosis, polycystic kidney, abnormal kidney physiology, polyuria, decreased urine osmolality, decreased body weight, abnormal renal tubule epithelium morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5620355, RRID:MGI:5620355)

Source Database: MGI, catalog # 5620355
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Gt(ROSA)26Sor, Bmi1
Genomic Alteration: tm1(cre/ERT)Mrc; tm2(CAG-Dsred2/EGFP)Luo
Availability: Availability unknown check source stock center
Reference:
Notes: 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: nervous system phenotype, abnormal serotonergic neuron morphology, abnormal neuron differentiation, abnormal GABAergic neuron morphology Allele Detail: Targeted

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Cite this (MGI Cat# 4397539, RRID:MGI:4397539)

Source Database: MGI, catalog # 4397539
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Ilk
Genomic Alteration: tm3Ref
Availability: Availability unknown check source stock center
Reference: PMID:19829382
Notes: abnormal ureteric bud morphology Allele Detail: Targeted

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Cite this (MGI Cat# 2175097, RRID:MGI:2175097)

Source Database: MGI, catalog # 2175097
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Lamb2
Genomic Alteration: tm1Jrs
Availability: Availability unknown check source stock center
Reference: PMID:7670489, PMID:10531444, PMID:7885444
Notes: abnormal glomerular filtration barrier function, abnormal miniature endplate potential, increased urine protein level, postnatal lethality, complete penetrance, postnatal growth retardation, glomerulonephritis, failure of neuromuscular synapse presynaptic differentiation, failure of neuromuscular synapse postsynaptic differentiation, abnormal neuromuscular synapse morphology, fused podocyte foot processes, increased retinal apoptosis, abnormal retina morphology, abnormal retinal rod cell morphology, abnormal retinal outer plexiform layer morphology, abnormal retinal photoreceptor morphology, lethargy, decreased total retina thickness, abnormal eye electrophysiology, short photoreceptor inner segment, short photoreceptor outer segment, postnatal growth retardation, increased renal glomerulus basement membrane thickness, increased urine protein level, abnormal renal glomerulus basement membrane morphology, albuminuria Allele Detail: Targeted

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Cite this (MGI Cat# 4943722, RRID:MGI:4943722)

Source Database: MGI, catalog # 4943722
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Fgf16
Genomic Alteration: tm1(cre)Sms
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (MGI Cat# 3586563, RRID:MGI:3586563)

Source Database: MGI, catalog # 3586563
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Polg
Genomic Alteration: tm1.2Lrsn
Availability: Availability unknown check source stock center
Reference: PMID:15888483
Notes: embryonic lethality between somite formation and embryo turning, complete penetrance, embryonic growth retardation, decreased embryo size Allele Detail: Targeted

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Cite this (MGI Cat# 5315595, RRID:MGI:5315595)

Source Database: MGI, catalog # 5315595
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Col27a1
Genomic Alteration: tm1.1Rpbh
Availability: Availability unknown check source stock center
Reference: PMID:22206015
Notes: sternebra fusion, abnormal long bone epiphyseal plate proliferative zone Allele Detail: Targeted

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Cite this (MGI Cat# 2176445, RRID:MGI:2176445)

Source Database: MGI, catalog # 2176445
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Arnt
Genomic Alteration: tm1Mcs
Availability: Availability unknown check source stock center
Reference: PMID:11124810, PMID:10521392, PMID:9121557
Notes: abnormal chorionic plate morphology, cellular phenotype, disorganized yolk sac vascular plexus, absent vitelline blood vessels, abnormal visceral yolk sac morphology, decreased embryo size, embryonic growth retardation, embryonic lethality, complete penetrance, cardiovascular system phenotype, abnormal spongiotrophoblast layer morphology, absent placental labyrinth, cellular phenotype, abnormal trophoblast layer morphology, abnormal trophoblast giant cell morphology, abnormal angiogenesis, abnormal placenta development, impaired hematopoiesis Allele Detail: Targeted

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Cite this (MGI Cat# 5449367, RRID:MGI:5449367)

Source Database: MGI, catalog # 5449367
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Vsx2, Mitf
Genomic Alteration: Mi; tm1.1Eml
Availability: Availability unknown check source stock center
Reference: PMID:23028343
Notes: abnormal eye morphology, abnormal eye size Allele Detail: Other, Targeted

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Cite this (MGI Cat# 3665430, RRID:MGI:3665430)

Source Database: MGI, catalog # 3665430
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Gt(ROSA)26Sor
Genomic Alteration: tm2(CAG-Dsred2/EGFP)Luo
Availability: Availability unknown check source stock center
Reference:
Notes: reduced female fertility Allele Detail: Targeted

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Cite this (MGI Cat# 2183210, RRID:MGI:2183210)

Source Database: MGI, catalog # 2183210
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Ascl1
Genomic Alteration: tm1And
Availability: Availability unknown check source stock center
Reference: PMID:8221886
Notes: neonatal lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 3703638, RRID:MGI:3703638)

Source Database: MGI, catalog # 3703638
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Neurog2
Genomic Alteration: tm2Fgu
Availability: Availability unknown check source stock center
Reference: PMID:18579678, PMID:16705040
Notes: decreased Cajal-Retzius cell number, abnormal neuron differentiation Allele Detail: Targeted

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Cite this (MGI Cat# 2174714, RRID:MGI:2174714)

Source Database: MGI, catalog # 2174714
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Rapsn
Genomic Alteration: tm1Jrs
Availability: Availability unknown check source stock center
Reference: PMID:7675108
Notes: abnormal neuromuscular synapse morphology, failure of neuromuscular synapse postsynaptic differentiation, respiratory distress, perinatal lethality, complete penetrance, muscle weakness Allele Detail: Targeted

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Cite this (MGI Cat# 5491822, RRID:MGI:5491822)

Source Database: MGI, catalog # 5491822
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Fhl2
Genomic Alteration: tm1Chen
Availability: Availability unknown check source stock center
Reference: PMID:23271052
Notes: cardiac hypertrophy, cardiac fibrosis Allele Detail: Targeted

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Cite this (MGI Cat# 5763182, RRID:MGI:5763182)

Source Database: MGI, catalog # 5763182
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Comp
Genomic Alteration: tm1Aol
Availability: Availability unknown check source stock center
Reference: PMID:25712208
Notes: abnormal vascular wound healing Allele Detail: Targeted

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Cite this (MGI Cat# 2170585, RRID:MGI:2170585)

Source Database: MGI, catalog # 2170585
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Hoxa2, Hoxa1
Genomic Alteration: tm2Mrc; tm1Mrc
Availability: Availability unknown check source stock center
Reference: PMID:10529419
Notes: neonatal lethality, complete penetrance, small middle ear ossicles, abnormal middle ear ossicle morphology, abnormal hindbrain morphology, absent outer ear Allele Detail: Targeted

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