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on page 1 showing 20 out of 1,141 results

Cite this (MGI Cat# 5629717, RRID:MGI:5629717)

Source Database: MGI, catalog # 5629717
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Gt(ROSA)26Sor, Pou4f2
Genomic Alteration: tm2.1Nat; tm1(cre/ERT)Nat
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (MGI Cat# 3521754, RRID:MGI:3521754)

Source Database: MGI, catalog # 3521754
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Ccr9
Genomic Alteration: tm1Ccb
Availability: Availability unknown check source stock center
Reference: PMID:15484191
Notes: abnormal T cell differentiation, decreased thymocyte number Allele Detail: Targeted

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Cite this (MGI Cat# 3045954, RRID:MGI:3045954)

Source Database: MGI, catalog # 3045954
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Kit
Genomic Alteration: tm1Ber
Availability: Availability unknown check source stock center
Reference: PMID:15067126
Notes: immune system phenotype, decreased mast cell number, absent coat pigmentation, white spotting, variable depigmentation, abnormal coat/hair pigmentation, reproductive system phenotype, digestive/alimentary phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 4887827, RRID:MGI:4887827)

Source Database: MGI, catalog # 4887827
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Slc17a6
Genomic Alteration: tm1Kldr; Tg(PLAT-cre)116Sdu
Availability: Availability unknown check source stock center
Reference: PMID:21040852
Notes: excessive scratching, increased thermal nociceptive threshold, increased pruritus Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 3664568, RRID:MGI:3664568)

Source Database: MGI, catalog # 3664568
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Itgb1bp1
Genomic Alteration: Gt(SA-IRES-betaGeo)10Pgr
Availability: Availability unknown check source stock center
Reference: PMID:9626504
Notes: no abnormal phenotype detected Allele Detail: Gene trapped

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Cite this (MGI Cat# 3764493, RRID:MGI:3764493)

Source Database: MGI, catalog # 3764493
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Camk2a
Genomic Alteration: tm4Sva
Availability: Availability unknown check source stock center
Reference: PMID:17660813
Notes: enhanced long term potentiation, nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3045949, RRID:MGI:3045949)

Source Database: MGI, catalog # 3045949
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Kit
Genomic Alteration: tm3Ber
Availability: Availability unknown check source stock center
Reference: PMID:15067126
Notes: spleen hyperplasia, increased megakaryocyte cell number, abnormal coat/hair pigmentation, variable depigmentation, lethality at weaning, incomplete penetrance, white spotting, enlarged spleen, absent coat pigmentation, digestive/alimentary phenotype, reproductive system phenotype, decreased mast cell number, meteorism, arrested B cell differentiation, premature death, increased B cell number Allele Detail: Targeted

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Cite this (MGI Cat# 4461059, RRID:MGI:4461059)

Source Database: MGI, catalog # 4461059
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Igh-J
Genomic Alteration: tm1Aigl; Tg(Tcra2D2,Tcrb2D2)1Kuch
Availability: Availability unknown check source stock center
Reference: PMID:19483694
Notes: muscle hypertonia, CNS inflammation, abnormal nervous system morphology, abnormal optic nerve morphology, abnormal spinal cord morphology, demyelination, increased susceptibility to experimental autoimmune encephalomyelitis, paralysis Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 5461346, RRID:MGI:5461346)

Source Database: MGI, catalog # 5461346
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Pitx2
Genomic Alteration: tm1Rsd
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (MGI Cat# 3613783, RRID:MGI:3613783)

Source Database: MGI, catalog # 3613783
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Sim1
Genomic Alteration: tm1Jlmd
Availability: Availability unknown check source stock center
Reference: PMID:16291793, PMID:17356169
Notes: decreased apoptosis, abnormal neuronal migration, nervous system phenotype, abnormal hypothalamus morphology, neonatal lethality, abnormal nervous system tract morphology, abnormal hypothalamus morphology Allele Detail: Targeted

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Cite this (MGI Cat# 2180490, RRID:MGI:2180490)

Source Database: MGI, catalog # 2180490
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Lamc1
Genomic Alteration: tm1Edg
Availability: Availability unknown check source stock center
Reference: PMID:9885251
Notes: abnormal primitive endoderm morphology, embryonic lethality between implantation and somite formation, complete penetrance, absent visceral yolk sac Allele Detail: Targeted

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Cite this (MGI Cat# 3784009, RRID:MGI:3784009)

Source Database: MGI, catalog # 3784009
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: App
Genomic Alteration: tm1Sud
Availability: Availability unknown check source stock center
Reference:
Notes: no abnormal phenotype detected Allele Detail: Targeted

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Cite this (MGI Cat# 3583444, RRID:MGI:3583444)

Source Database: MGI, catalog # 3583444
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Vezf1
Genomic Alteration: tm1Stmn
Availability: Availability unknown check source stock center
Reference: PMID:15882861
Notes: perinatal lethality, incomplete penetrance, embryo phenotype, abnormal blood vessel morphology, hemorrhage Allele Detail: Targeted

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Cite this (MGI Cat# 3045535, RRID:MGI:3045535)

Source Database: MGI, catalog # 3045535
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Mfge8
Genomic Alteration: tm1Osa
Availability: Availability unknown check source stock center
Reference: PMID:15155946, PMID:23443560, PMID:16275924
Notes: spleen hyperplasia, enlarged spleen, increased spleen white pulp amount, increased spleen weight, impaired macrophage phagocytosis, increased anti-double stranded DNA antibody level, abnormal spleen B cell follicle morphology, abnormal lactation, abnormal spleen morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3707682, RRID:MGI:3707682)

Source Database: MGI, catalog # 3707682
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Cyp26a1, Cyp26c1, Aldh1a2
Genomic Alteration: tm1.1Keya; tm1Ipc; tm1.1Hmd
Availability: Availability unknown check source stock center
Reference: PMID:17067568
Notes: abnormal head mesenchyme morphology, nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3693809, RRID:MGI:3693809)

Source Database: MGI, catalog # 3693809
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Irf6
Genomic Alteration: tm1Mjd
Availability: Availability unknown check source stock center
Reference: PMID:17041603
Notes: neonatal lethality, incomplete penetrance, abnormal mouth morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3589555, RRID:MGI:3589555)

Source Database: MGI, catalog # 3589555
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Psen1
Genomic Alteration: tm1Tak
Availability: Availability unknown check source stock center
Reference: PMID:15908021
Notes: increased grip strength, increased startle reflex, abnormal spatial learning Allele Detail: Targeted

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Cite this (MGI Cat# 3718030, RRID:MGI:3718030)

Source Database: MGI, catalog # 3718030
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Aldh1a3, Aldh1a2, Aldh1a1
Genomic Alteration: tm1Gdu
Availability: Availability unknown check source stock center
Reference: PMID:16611695
Notes: abnormal optic cup morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3758961, RRID:MGI:3758961)

Source Database: MGI, catalog # 3758961
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Nlgn3
Genomic Alteration: tm1Sud
Availability: Availability unknown check source stock center
Reference: PMID:17823315
Notes: abnormal social investigation, abnormal spatial learning, abnormal inhibitory postsynaptic currents Allele Detail: Targeted

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Cite this (MGI Cat# 2656013, RRID:MGI:2656013)

Source Database: MGI, catalog # 2656013
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Bak1
Genomic Alteration: tm1Thsn
Availability: Availability unknown check source stock center
Reference: PMID:11163212
Notes: no abnormal phenotype detected Allele Detail: Targeted

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