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on page 1 showing 20 out of 1,132 results from 1 sources

Cite this (MGI Cat# 5502225, RRID:MGI:5502225)

Source Database: MGI, catalog # 5502225
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Ilk
Genomic Alteration: tm1Star; Tg(Acp5-cre)1Star; tm2Star
Availability: Availability unknown check source stock center
Reference: PMID:20564195
Notes: abnormal osteoclast physiology, craniofacial phenotype, growth/size/body region phenotype, increased bone volume, increased osteoclast cell number, increased trabecular bone thickness Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 5749543, RRID:MGI:5749543)

Source Database: MGI, catalog # 5749543
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Fzd6
Genomic Alteration: tm1Nat
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (MGI Cat# 3845244, RRID:MGI:3845244)

Source Database: MGI, catalog # 3845244
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Pax1
Genomic Alteration: tm1Neu
Availability: Availability unknown check source stock center
Reference: PMID:9671740
Notes: abnormal cervical atlas morphology, abnormal lumbar vertebrae morphology, abnormal sternum morphology, abnormal vertebrae morphology, abnormal ventral tubercle of atlas morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5310750, RRID:MGI:5310750)

Source Database: MGI, catalog # 5310750
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Arl6
Genomic Alteration: tm2Vcs
Availability: Availability unknown check source stock center
Reference: PMID:22139371
Notes: vision/eye phenotype, abnormal retinal neuronal layer morphology, abnormal retinal outer nuclear layer morphology, abnormal retinal photoreceptor morphology, absent photoreceptor inner segment, absent photoreceptor outer segment, male infertility, absent sperm flagellum, wide cranial sutures, domed cranium, decreased striatum area, abnormal telencephalon morphology, small hippocampus, thin cerebral cortex, abnormal brain ventricular system morphology, hydroencephaly, abnormal brain ependyma motile cilium morphology, abnormal sympathetic nervous system physiology, abnormal brain ependyma motile cilium physiology, cellular phenotype, increased percent body fat/body weight, increased systemic arterial blood pressure, behavior/neurological phenotype, increased heart rate Allele Detail: Targeted

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Cite this (MGI Cat# 3531210, RRID:MGI:3531210)

Source Database: MGI, catalog # 3531210
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes:
Genomic Alteration: Tg(Pcp2-cre)2Mpin
Availability: Availability unknown check source stock center
Reference: PMID:11105049
Notes: no abnormal phenotype detected Allele Detail: Transgenic

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Cite this (MGI Cat# 2668196, RRID:MGI:2668196)

Source Database: MGI, catalog # 2668196
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Cnmd
Genomic Alteration: tm1Ref
Availability: Availability unknown check source stock center
Reference: PMID:12192060
Notes: no abnormal phenotype detected Allele Detail: Targeted

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Cite this (MGI Cat# 4397673, RRID:MGI:4397673)

Source Database: MGI, catalog # 4397673
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Kcnq3
Genomic Alteration: tm1.1Naas
Availability: Availability unknown check source stock center
Reference: PMID:18483067
Notes: abnormal neuron physiology, prenatal lethality, incomplete penetrance, seizures Allele Detail: Targeted

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Cite this (MGI Cat# 2674122, RRID:MGI:2674122)

Source Database: MGI, catalog # 2674122
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Cacna1c
Genomic Alteration: tm2Hfm
Availability: Availability unknown check source stock center
Reference: PMID:10973973
Notes: lethality throughout fetal growth and development, complete penetrance, abnormal embryonic tissue morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3583813, RRID:MGI:3583813)

Source Database: MGI, catalog # 3583813
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Itga7
Genomic Alteration: tm1Umr
Availability: Availability unknown check source stock center
Reference: PMID:12588796, PMID:9354797, PMID:24227711
Notes: increased variability of skeletal muscle fiber size, skeletal muscle fiber atrophy, centrally nucleated skeletal muscle fibers, embryonic lethality during organogenesis, incomplete penetrance, muscle degeneration, dystrophic muscle, abnormal skeletal muscle morphology, abnormal skeletal muscle morphology, abnormal soleus morphology, abnormal diaphragm morphology, increased skeletal muscle fiber size, increased circulating creatine kinase level, abnormal Schwann cell physiology Allele Detail: Targeted

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Cite this (MGI Cat# 5523684, RRID:MGI:5523684)

Source Database: MGI, catalog # 5523684
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Notch1, Notch2
Genomic Alteration: tm3.1Grid; tm1Con; tm3.1Rko
Availability: Availability unknown check source stock center
Reference: PMID:23806616
Notes: renal/urinary system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3695306, RRID:MGI:3695306)

Source Database: MGI, catalog # 3695306
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Polq
Genomic Alteration: tm2Jow
Availability: Availability unknown check source stock center
Reference: PMID:16890500
Notes: abnormal somatic hypermutation frequency Allele Detail: Targeted

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Cite this (MGI Cat# 5504446, RRID:MGI:5504446)

Source Database: MGI, catalog # 5504446
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Smarcc2, Neurod6
Genomic Alteration: tm1.1Stoy; tm1(cre)Kan
Availability: Availability unknown check source stock center
Reference: PMID:23643363
Notes: nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3834193, RRID:MGI:3834193)

Source Database: MGI, catalog # 3834193
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Lyz2
Genomic Alteration: tm1(DTR)Mtka
Availability: Availability unknown check source stock center
Reference: PMID:17404282
Notes: abnormal alveolar macrophage morphology, abnormal liver morphology, abnormal lung interstitium morphology, abnormal surfactant secretion, abnormal pulmonary alveolus morphology, absent type II pneumocytes, hunched posture, hypoactivity, increased lactate dehydrogenase level, lung hemorrhage, premature death, respiratory failure, ruffled hair Allele Detail: Targeted

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Cite this (MGI Cat# 3510832, RRID:MGI:3510832)

Source Database: MGI, catalog # 3510832
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Pax7
Genomic Alteration: tm1(cre)Mrc
Availability: Availability unknown check source stock center
Reference: PMID:15520281
Notes: no abnormal phenotype detected Allele Detail: Targeted

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Cite this (MGI Cat# 3027115, RRID:MGI:3027115)

Source Database: MGI, catalog # 3027115
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Ifi47
Genomic Alteration: tm1Gat
Availability: Availability unknown check source stock center
Reference: PMID:11457893
Notes: increased susceptibility to parasitic infection, immune system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3850629, RRID:MGI:3850629)

Source Database: MGI, catalog # 3850629
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Man2a1, Man2a2
Genomic Alteration: tm1Mfu; tm1Jxm
Availability: Availability unknown check source stock center
Reference: PMID:16754854
Notes: postnatal lethality, incomplete penetrance, abnormal pulmonary alveolus morphology, abnormal pulmonary alveolus epithelial cell morphology, abnormal breathing pattern, abnormal liver morphology, abnormal proximal convoluted tubule morphology, lethality throughout fetal growth and development, incomplete penetrance, neonatal lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 2175762, RRID:MGI:2175762)

Source Database: MGI, catalog # 2175762
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Cdkn1c
Genomic Alteration: tm1Bbd
Availability: Availability unknown check source stock center
Reference: PMID:9136926, PMID:14671317
Notes: lethality throughout fetal growth and development, incomplete penetrance, neonatal lethality, incomplete penetrance, abnormal suckling behavior, abnormal long bone epiphysis morphology, abnormal bone ossification, cleft palate, delayed endochondral bone ossification, abnormal hard palate morphology, abnormal soft palate morphology, abnormal intestine morphology, absent jejunum, abnormal ileum morphology, abnormal duodenum morphology, abnormal digestive system development, abnormal midbrain morphology, absent gastric milk in neonates, meteorism, palatal shelves fail to meet at midline, short limbs, increased midbrain apoptosis Allele Detail: Targeted

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Cite this (MGI Cat# 3799086, RRID:MGI:3799086)

Source Database: MGI, catalog # 3799086
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Syt6, Syt5, Syt10, Syt3
Genomic Alteration: tm1Sud
Availability: Availability unknown check source stock center
Reference:
Notes: no abnormal phenotype detected Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 3526729, RRID:MGI:3526729)

Source Database: MGI, catalog # 3526729
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Hmox1
Genomic Alteration: tm1Ysh
Availability: Availability unknown check source stock center
Reference: PMID:11273999
Notes: prenatal lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 3843982, RRID:MGI:3843982)

Source Database: MGI, catalog # 3843982
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Adar
Genomic Alteration: Tg(Tal1-cre/ERT)42-056Jrg; tm2Phs; tm1.1Phs
Availability: Availability unknown check source stock center
Reference: PMID:19060901
Notes: abnormal hematopoietic stem cell morphology, decreased bone marrow cell number Allele Detail: Targeted, Transgenic

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