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on page 1 showing 20 out of 99,581 results

Cite this (MGI Cat# 5694213, RRID:MGI:5694213)

Source Database: MGI, catalog # 5694213
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Affected Genes: Ctnnb1
Genomic Alteration: Tg(Msx2-cre)5Rem; tm2Kem
Availability: Availability unknown check source stock center
Reference: PMID:23358455
Notes: decreased diameter of humerus, short ulna, absent radius, absent hindlimb, absent deltoid tuberosity, abnormal autopod morphology Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 6202728, RRID:MGI:6202728)

Source Database: MGI, catalog # 6202728
Genetic Background: involves: 129P2/OlaHsd * FVB/N
Affected Genes: Ezh2, Ezh1
Genomic Alteration: Tg(MMTV-cre)1Mam; tm1Tara; tm1Jnw
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 3046320, RRID:MGI:3046320)

Source Database: MGI, catalog # 3046320
Genetic Background: Not Specified
Affected Genes: Myo15
Genomic Alteration: sh2
Availability: Availability unknown check source stock center
Reference: PMID:6889851
Notes: abnormal cochlear hair cell morphology, abnormal tectorial membrane morphology, abnormal utricular macula morphology, abnormal stria vascularis morphology, circling, abnormal cochlear hair cell morphology, organ of Corti degeneration, abnormal organ of Corti morphology, abnormal cochlear ganglion morphology, cochlear ganglion degeneration, deafness, head shaking Allele Detail: Radiation induced

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Cite this (MGI Cat# 5696659, RRID:MGI:5696659)

Source Database: MGI, catalog # 5696659
Genetic Background: involves: C57BL/6 * DBA/2 * SJL
Affected Genes: Nmt2, Nmt1
Genomic Alteration: Tg(Lck-cre)1Cwi; tm1.1Poru
Availability: Availability unknown check source stock center
Reference: PMID:26423150
Notes: decreased single-positive T cell number, decreased interleukin-2 secretion, decreased splenocyte proliferation, decreased interferon-gamma secretion, decreased double-positive T cell number, abnormal CD8-positive, alpha beta T cell morphology, decreased DN4 thymocyte number, abnormal CD4-positive, alpha beta T cell morphology, decreased circulating tumor necrosis factor level, small thymus medulla, increased gamma-delta T cell number, increased double-negative T cell number, increased T cell apoptosis, immune system phenotype, decreased susceptibility to endotoxin shock, decreased T cell number, decreased T cell proliferation, decreased circulating interferon-gamma level, decreased circulating interleukin-2 level Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 5317843, RRID:MGI:5317843)

Source Database: MGI, catalog # 5317843
Genetic Background: involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6
Affected Genes: Ccr5, Cxcr4
Genomic Alteration: tm1Kuz; tm1Qma
Availability: Availability unknown check source stock center
Reference: PMID:16841089
Notes: decreased susceptibility to viral infection, abnormal nervous system physiology Allele Detail: Targeted

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Cite this (MGI Cat# 4450916, RRID:MGI:4450916)

Source Database: MGI, catalog # 4450916
Genetic Background: C57BL/6-Phex
Affected Genes: Phex
Genomic Alteration: Ska1
Availability: Availability unknown check source stock center
Reference: PMID:12414538
Notes: decreased bone mineral density, decreased circulating phosphate level, exostosis, decreased compact bone thickness, abnormal rib morphology, abnormal hindlimb morphology, abnormal obturator foramen morphology, abnormal skeleton morphology, abnormal pelvic girdle bone morphology, abnormal caudal vertebrae morphology, abnormal limb long bone morphology, short ulna, short humerus, short tibia, short fibula, short femur, abnormal acetabulum morphology, small clavicle, short radius, increased circulating alkaline phosphatase level, abnormal gait Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 5474869, RRID:MGI:5474869)

Source Database: MGI, catalog # 5474869
Genetic Background: involves: BALB/c * C57BL/6
Affected Genes: Etv2, Tg(Pgk1-cre)1Lni
Genomic Alteration: tm1Vkou; Tg(Pgk1-cre)1Lni
Availability: Availability unknown check source stock center
Reference: PMID:22570122
Notes: absent erythroid progenitor cell, absent erythrocytes, embryonic lethality during organogenesis, complete penetrance, embryonic growth retardation Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 4440638, RRID:MGI:4440638)

Source Database: MGI, catalog # 4440638
Genetic Background: involves: A * C3H/He * C57BL/6
Affected Genes: Sec24b, Vangl2
Genomic Alteration: Y613X; Lp
Availability: Availability unknown check source stock center
Reference: PMID:19966784
Notes: spina bifida, postnatal lethality, incomplete penetrance, lethality throughout fetal growth and development, incomplete penetrance Allele Detail: Spontaneous, Chemically induced (ENU)

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Cite this (MGI Cat# 3576739, RRID:MGI:3576739)

Source Database: MGI, catalog # 3576739
Genetic Background: involves: 129S4/SvJae * C57BL/6
Affected Genes: Sh2d1a
Genomic Alteration: tm1Cpt
Availability: Availability unknown check source stock center
Reference: PMID:11323694, PMID:22613797
Notes: abnormal immunoglobulin level, decreased NK T cell number, abnormal NK T cell physiology, abnormal germinal center B cell physiology, increased susceptibility to viral infection, increased T cell proliferation, abnormal cytokine secretion, abnormal humoral immune response Allele Detail: Targeted

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Cite this (MGI Cat# 3803705, RRID:MGI:3803705)

Source Database: MGI, catalog # 3803705
Genetic Background: involves: 129S1/Sv * C57BL/6
Affected Genes: Cdk2, Cdk4
Genomic Alteration: tm1Kiyo; tm1Kald
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (MGI Cat# 5291648, RRID:MGI:5291648)

Source Database: MGI, catalog # 5291648
Genetic Background: C57BL/6J-Krt71/GrsrJ
Affected Genes: Krt71
Genomic Alteration: Ca-17J
Availability: Availability unknown check source stock center
Reference:
Notes: curly vibrissae, waved hair Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 6188325, RRID:MGI:6188325)

Source Database: MGI, catalog # 6188325
Genetic Background: NOD.Cg-Lag3 Tg(Foxp3-EGFP/cre)1cJbs
Affected Genes: Lag3
Genomic Alteration: tm1Daav; Tg(Foxp3-EGFP/cre)1cJbs
Availability: Availability unknown check source stock center
Reference: PMID:28783703
Notes: decreased susceptibility to autoimmune diabetes, abnormal CD8-positive, alpha-beta T cell physiology, abnormal effector T cell number, abnormal interleukin level, abnormal tumor necrosis factor level Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 5767558, RRID:MGI:5767558)

Source Database: MGI, catalog # 5767558
Genetic Background: C57BL/6N-Aif1l/Bay
Affected Genes: Aif1l
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: enlarged spleen, abnormal spleen morphology, abnormal skin morphology, small thymus, abnormal liver morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5897775, RRID:MGI:5897775)

Source Database: MGI, catalog # 5897775
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * FVB/NCr
Affected Genes: Pten, Prkar1a
Genomic Alteration: Tg(TPO-cre)1Shk; tm1.2Lsk; tm1.1Mwst
Availability: Availability unknown check source stock center
Reference: PMID:24512487
Notes: neoplasm, decreased survivor rate Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 2669213, RRID:MGI:2669213)

Source Database: MGI, catalog # 2669213
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Aldh1a1
Genomic Alteration: tm1Gdu
Availability: Availability unknown check source stock center
Reference: PMID:12808103
Notes: abnormal hepatobiliary system physiology, vision/eye phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 4397677, RRID:MGI:4397677)

Source Database: MGI, catalog # 4397677
Genetic Background: FVB.129-Kcnq3
Affected Genes: Kcnq3
Genomic Alteration: tm1.1Naas
Availability: Availability unknown check source stock center
Reference: PMID:18483067
Notes: decreased body size, nervous system phenotype, abnormal hippocampus morphology, astrocytosis, premature death, neonatal lethality, incomplete penetrance, seizures Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 5307019, RRID:MGI:5307019)

Source Database: MGI, catalog # 5307019
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J
Affected Genes: Col3a1
Genomic Alteration: m1Lsmi
Availability: Availability unknown check source stock center
Reference: PMID:21071432
Notes: aortic dissection, premature death, abnormal aorta smooth muscle morphology, abnormal aorta elastic tissue morphology, aortic dissection, premature death, increased systemic arterial systolic blood pressure, increased vasoconstriction, abnormal response/metabolism to endogenous compounds Allele Detail: Spontaneous

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Cite this (MGI Cat# 6256504, RRID:MGI:6256504)

Source Database: MGI, catalog # 6256504
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: Availability unknown check source stock center
Reference:
Notes: Strain Type: Not Specified

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Cite this (MGI Cat# 4431220, RRID:MGI:4431220)

Source Database: MGI, catalog # 4431220
Genetic Background: involves: C57BL/6J
Affected Genes: Phex
Genomic Alteration: Hyp; Tg(Bglap2-Phex)1Ldq
Availability: Availability unknown check source stock center
Reference: PMID:11713245
Notes: osteomalacia, abnormal bone mineralization, rickets, decreased bone mass, decreased circulating phosphate level Allele Detail: Spontaneous, Transgenic

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Cite this (MGI Cat# 2661449, RRID:MGI:2661449)

Source Database: MGI, catalog # 2661449
Genetic Background: involves: 129P2/OlaHsd * C57BL
Affected Genes: Pzp
Genomic Alteration: tm1Vln
Availability: Availability unknown check source stock center
Reference: PMID:7544347
Notes: greasy coat, abnormal bile color, hypoactivity, homeostasis/metabolism phenotype, hepatic steatosis, decreased sensitivity to induced morbidity/mortality, enlarged liver, disheveled coat, decreased susceptibility to weight gain, pancreas inflammation, neoplasm, increased susceptibility to induced pancreatitis, respiratory system phenotype, liver/biliary system phenotype, gallstones Allele Detail: Targeted

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