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on page 1 showing 20 out of 1,085 results from 1 sources

Cite this (MGI Cat# 4410441, RRID:MGI:4410441)

Source Database: MGI, catalog # 4410441
Genetic Background: involves: C57BL/6
Affected Genes:
Genomic Alteration: Tg(Prm1-cre)1Mrc
Availability: Availability unknown check source stock center
Reference: PMID:11087830
Notes: reproductive system phenotype, male infertility, impaired fertilization Allele Detail: Transgenic

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Cite this (MGI Cat# 3799539, RRID:MGI:3799539)

Source Database: MGI, catalog # 3799539
Genetic Background: involves: 129S1/Sv * NOR2/LtDn
Affected Genes: Vsx2
Genomic Alteration: or-J; or-2J
Availability: Availability unknown check source stock center
Reference:
Notes: reproductive system phenotype Allele Detail: Spontaneous

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Cite this (MGI Cat# 4839333, RRID:MGI:4839333)

Source Database: MGI, catalog # 4839333
Genetic Background: C57BL/6JEi-Chr Y/EiJ
Affected Genes: Sry
Genomic Alteration: AKR/J; RIII
Availability: Availability unknown check source stock center
Reference: PMID:12750339
Notes: reproductive system phenotype Allele Detail: Spontaneous

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Cite this (MGI Cat# 5301419, RRID:MGI:5301419)

Source Database: MGI, catalog # 5301419
Genetic Background: involves: 129S/SvEv * BALB/cJ * C57BL/6
Affected Genes: Col4a3bp
Genomic Alteration: tm1.1Jsau
Availability: Availability unknown check source stock center
Reference: PMID:21832087
Notes: abnormal muscle development, reproductive system phenotype, homeostasis/metabolism phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 4360936, RRID:MGI:4360936)

Source Database: MGI, catalog # 4360936
Genetic Background: involves: 129/Sv * C57BL/6 * SJL
Affected Genes: Plekha5, Dicer1
Genomic Alteration: Tg(AMH-cre)1Flor; tm1Bdh
Availability: Availability unknown check source stock center
Reference: PMID:19071104
Notes: reproductive system phenotype, decreased testis weight, abnormal Sertoli cell morphology, male infertility, abnormal spermatogenesis, ectopic Sertoli cells, seminiferous tubule degeneration, testis degeneration, abnormal seminiferous tubule epithelium morphology, Leydig cell hyperplasia, azoospermia, abnormal spermatid morphology, abnormal male germ cell apoptosis, abnormal male germ cell morphology, small testis, small seminiferous tubules, decreased male germ cell number Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 5013562, RRID:MGI:5013562)

Source Database: MGI, catalog # 5013562
Genetic Background: involves: 129/Sv * BALB/c * C57BL/6 * SJL
Affected Genes: Hormad1
Genomic Alteration: tm1.2Atot
Availability: Availability unknown check source stock center
Reference: PMID:21478856
Notes: abnormal male germ cell apoptosis, female infertility, azoospermia, abnormal chiasmata formation, abnormal double-strand DNA break repair, abnormal female meiosis, abnormal male meiosis, abnormal synaptonemal complex, arrest of spermatogenesis, reproductive system phenotype, male infertility Allele Detail: Targeted

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Cite this (MGI Cat# 4837219, RRID:MGI:4837219)

Source Database: MGI, catalog # 4837219
Genetic Background: B6.129-Paip2b
Affected Genes: Paip2b
Genomic Alteration: tm1.2Nso
Availability: Availability unknown check source stock center
Reference: PMID:20739757
Notes: reproductive system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 2167486, RRID:MGI:2167486)

Source Database: MGI, catalog # 2167486
Genetic Background: C57BL/6J-Kit/J
Affected Genes: Kit
Genomic Alteration: W-42J
Availability: Availability unknown check source stock center
Reference: PMID:7274658, PMID:8951075
Notes: macrocytic anemia, small testis, abnormal ovarian follicle number, absent coat pigmentation, reproductive system phenotype, irregular coat pigmentation Allele Detail: Spontaneous

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Cite this (MGI Cat# 3622318, RRID:MGI:3622318)

Source Database: MGI, catalog # 3622318
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Fzd4
Genomic Alteration: tm1Nat
Availability: Availability unknown check source stock center
Reference: PMID:11425903, PMID:16093361, PMID:15035989
Notes: reproductive system phenotype, cochlear inner hair cell degeneration, cochlear outer hair cell degeneration, hemorrhage, retinal hemorrhage, abnormal retinal vasculature morphology, short stride length, failure of embryo implantation, decreased circulating progesterone level, absent corpus luteum, abnormal digestion, decreased skeletal muscle fiber diameter, absent startle reflex, abnormal esophagus morphology, abnormal astrocyte physiology, decreased startle reflex, enlarged esophagus, abnormal cerebellum morphology, cochlear hair cell degeneration, persistence of hyaloid vascular system, stria vascularis degeneration, weight loss, abnormal posture, diluted coat color, cerebellum hypoplasia, impaired hearing, premature death, abnormal gait, male infertility, abnormal vascular development, impaired luteinization, abnormal corpus luteum morphology, abnormal organ of Corti morphology, hunched posture, abnormal cerebellar granule layer morphology, increased or absent threshold for auditory brainstem response, abnormal stria vascularis vasculature morphology, abnormal stria vascularis morphology, abnormal esophageal squamous epithelium morphology, impaired luteal cell differentiation, decreased Purkinje cell number, ataxia, female infertility Allele Detail: Targeted

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Cite this (MGI Cat# 5569412, RRID:MGI:5569412)

Source Database: MGI, catalog # 5569412
Genetic Background: Not Specified
Affected Genes: Oca2
Genomic Alteration: p-d
Availability: Availability unknown check source stock center
Reference: PMID:1495987
Notes: decreased eye pigmentation, abnormal coat/hair pigmentation, diluted coat color, reproductive system phenotype Allele Detail: Radiation induced

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Cite this (MGI Cat# 5499210, RRID:MGI:5499210)

Source Database: MGI, catalog # 5499210
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Hdac6
Genomic Alteration: tm1.1Pmt
Availability: Availability unknown check source stock center
Reference: PMID:18180281
Notes: decreased IgM level, increased bone mineral density, increased bone mineral content, reproductive system phenotype, nervous system phenotype, immune system phenotype, increased body weight, decreased IgG level Allele Detail: Targeted

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Cite this (MGI Cat# 6115792, RRID:MGI:6115792)

Source Database: MGI, catalog # 6115792
Genetic Background: involves: C57BL/6
Affected Genes: B3gat2
Genomic Alteration: tm1Shok
Availability: Availability unknown check source stock center
Reference: PMID:26659409
Notes: nervous system phenotype, reproductive system phenotype, mortality/aging Allele Detail: Targeted

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Cite this (MGI Cat# 5296633, RRID:MGI:5296633)

Source Database: MGI, catalog # 5296633
Genetic Background: B6.Cg-Cttn
Affected Genes: Cttn
Genomic Alteration: tm1.2Dvst
Availability: Availability unknown check source stock center
Reference: PMID:21788407
Notes: preweaning lethality, incomplete penetrance, reproductive system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5568948, RRID:MGI:5568948)

Source Database: MGI, catalog # 5568948
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Setd1a
Genomic Alteration: Tg(Gdf9-icre)5092Coo; tm1.1Afst
Availability: Availability unknown check source stock center
Reference: PMID:24121738
Notes: reproductive system phenotype Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 3694476, RRID:MGI:3694476)

Source Database: MGI, catalog # 3694476
Genetic Background: involves: 129S4/SvJae
Affected Genes: Catsper1
Genomic Alteration: tm1Clph
Availability: Availability unknown check source stock center
Reference: PMID:26429887, PMID:17227845
Notes: abnormal sperm motility, asthenozoospermia, abnormal sperm physiology, reproductive system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3621305, RRID:MGI:3621305)

Source Database: MGI, catalog # 3621305
Genetic Background: involves: 129S2/SvPas
Affected Genes: Vim
Genomic Alteration: tm1Cba
Availability: Availability unknown check source stock center
Reference: PMID:9888296, PMID:7954832, PMID:20963821, PMID:12177195, PMID:9625752, PMID:9294120
Notes: impaired balance, abnormal cerebellar Purkinje cell layer, abnormal motor learning, Purkinje cell degeneration, decreased Purkinje cell number, abnormal Purkinje cell dendrite morphology, reproductive system phenotype, nervous system phenotype, increased anxiety-related response, hyperactivity, impaired coordination, embryo phenotype, abnormal cerebellum morphology, abnormal locomotor behavior, abnormal astrocyte morphology, abnormal Purkinje cell morphology, abnormal cell physiology, abnormal cell morphology, abnormal cell migration, abnormal vasodilation, cardiovascular system phenotype, decreased mean systemic arterial blood pressure, increased circulating creatinine level, respiratory system phenotype, increased sensitivity to induced morbidity/mortality, abnormal vasoconstriction Allele Detail: Targeted

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Cite this (MGI Cat# 3603175, RRID:MGI:3603175)

Source Database: MGI, catalog # 3603175
Genetic Background: involves: 129X1/SvJ
Affected Genes: Nab1, Nab2
Genomic Alteration: tm1Jmi
Availability: Availability unknown check source stock center
Reference: PMID:16136673
Notes: increased Schwann cell proliferation, abnormal Schwann cell morphology, abnormal long bone hypertrophic chondrocyte zone, increased keratinocyte proliferation, abnormal myelination, epidermal hyperplasia, hyperkeratosis, reproductive system phenotype, thick skin, postnatal lethality, complete penetrance, decreased body size, tremors, weakness, impaired coordination, abnormal breathing pattern, decreased bone mineral density Allele Detail: Targeted

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Cite this (MGI Cat# 4949887, RRID:MGI:4949887)

Source Database: MGI, catalog # 4949887
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl
Affected Genes: Mecp2
Genomic Alteration: tm1Vnar
Availability: Availability unknown check source stock center
Reference: PMID:20163734
Notes: behavior/neurological phenotype, mortality/aging, reproductive system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5903628, RRID:MGI:5903628)

Source Database: MGI, catalog # 5903628
Genetic Background: FVB/NCrl-Poln
Affected Genes: Poln
Genomic Alteration: em1Rwd
Availability: Availability unknown check source stock center
Reference: PMID:28570559
Notes: mortality/aging, reproductive system phenotype Allele Detail: Endonuclease-mediated

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Cite this (MGI Cat# 5522969, RRID:MGI:5522969)

Source Database: MGI, catalog # 5522969
Genetic Background: involves: 129 * CD-1
Affected Genes: Hoxd
Genomic Alteration: tm1.1Ssp
Availability: Availability unknown check source stock center
Reference: PMID:23760953
Notes: reduced female fertility, abnormal vas deferens morphology, reproductive system phenotype, decreased litter size, male infertility, abnormal copulation Allele Detail: Targeted

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