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on page 1 showing 20 out of 2,451 results

Cite this (MGI Cat# 3721134, RRID:MGI:3721134)

Source Database: MGI, catalog # 3721134
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Atf7, Atf2
Genomic Alteration: tm1Nicj; tm2Nicj
Availability: Availability unknown check source stock center
Reference: PMID:17699753
Notes: anemia, heart hypoplasia, hemopericardium, increased apoptosis, increased hepatocyte apoptosis, liver hypoplasia, decreased cell proliferation, abnormal liver morphology, abnormal common myeloid progenitor cell morphology, embryonic growth arrest, embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 3720353, RRID:MGI:3720353)

Source Database: MGI, catalog # 3720353
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Rag1
Genomic Alteration: tm1Mnz
Availability: Availability unknown check source stock center
Reference: PMID:15021880
Notes: abnormal T cell morphology, decreased T cell number, abnormal double-positive T cell morphology, abnormal double-negative T cell morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3056551, RRID:MGI:3056551)

Source Database: MGI, catalog # 3056551
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ptgfr
Genomic Alteration: tm1Aic
Availability: Availability unknown check source stock center
Reference: PMID:12606450, PMID:9235889
Notes: parturition failure, abnormal ovarian secretion, parturition failure, reproductive system phenotype, abnormal reproductive system physiology Allele Detail: Targeted

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Cite this (MGI Cat# 4821751, RRID:MGI:4821751)

Source Database: MGI, catalog # 4821751
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Gata3
Genomic Alteration: Tg(Dbh-icre)1Gsc; tm3Gsv
Availability: Availability unknown check source stock center
Reference: PMID:20702712
Notes: abnormal sympathetic ganglion morphology, abnormal embryo development, abnormal nervous system development Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 3815330, RRID:MGI:3815330)

Source Database: MGI, catalog # 3815330
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Bag4
Genomic Alteration: tm1Yeh
Availability: Availability unknown check source stock center
Reference: PMID:12748303
Notes: increased interleukin-6 secretion, increased inflammatory response, spleen hypoplasia, increased circulating interleukin-6 level, thymus hypoplasia, abnormal macrophage physiology Allele Detail: Targeted

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Cite this (MGI Cat# 2674285, RRID:MGI:2674285)

Source Database: MGI, catalog # 2674285
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Meox1, Meox2
Genomic Alteration: tm1Vpa; tm1Bmk
Availability: Availability unknown check source stock center
Reference: PMID:12925591
Notes: absent ribs, abnormal myotome development, decreased brown adipose tissue amount, fused dorsal root ganglion, abnormal dorsal root ganglion morphology, loose skin, abnormal vertebral column morphology, abnormal vertebrae morphology, abnormal sternum morphology, abnormal spinal nerve morphology, abnormal somite size, abnormal sclerotome morphology, abnormal somite shape, abnormal axial skeleton morphology, abnormal dermomyotome development, abnormal epaxial muscle morphology, occipital bone hypoplasia, abnormal somite development, cyanosis, vestigial tail, neonatal lethality, complete penetrance, abnormal skeletal muscle morphology, abnormal hypaxial muscle morphology, decreased body length, absent caudal vertebrae, abnormal dorsal-ventral polarity of the somites Allele Detail: Targeted

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Cite this (MGI Cat# 5563689, RRID:MGI:5563689)

Source Database: MGI, catalog # 5563689
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Il18
Genomic Alteration: tm1Aki; Tg(KRT14-CASP1)1Miz
Availability: Availability unknown check source stock center
Reference: PMID:12151598
Notes: integument phenotype, immune system phenotype, decreased IgE level, decreased IgG1 level Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 4881786, RRID:MGI:4881786)

Source Database: MGI, catalog # 4881786
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Nox4
Genomic Alteration: tm1.1Hwsc
Availability: Availability unknown check source stock center
Reference: PMID:20877715
Notes: abnormal blood-brain barrier function, decreased neuron apoptosis, oxidative stress, decreased susceptibility to ischemic brain injury, cardiovascular system phenotype, decreased cerebral infarction size Allele Detail: Targeted

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Cite this (MGI Cat# 2653477, RRID:MGI:2653477)

Source Database: MGI, catalog # 2653477
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ski
Genomic Alteration: tm1Cco
Availability: Availability unknown check source stock center
Reference: PMID:11781823
Notes: increased fibroblast proliferation, increased lymphoma incidence, increased incidence of tumors by chemical induction Allele Detail: Targeted

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Cite this (MGI Cat# 4431243, RRID:MGI:4431243)

Source Database: MGI, catalog # 4431243
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Plppr4
Genomic Alteration: tm2.1Roni
Availability: Availability unknown check source stock center
Reference: PMID:19766573
Notes: abnormal miniature excitatory postsynaptic currents, nervous system phenotype, abnormal excitatory postsynaptic currents, behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3770157, RRID:MGI:3770157)

Source Database: MGI, catalog # 3770157
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Adipor2
Genomic Alteration: tm2Dgen
Availability: Availability unknown check source stock center
Reference: PMID:17068142
Notes: increased adiponectin level, increased circulating glucose level, abnormal glucose homeostasis, decreased circulating HDL cholesterol level, decreased circulating LDL cholesterol level, decreased circulating VLDL cholesterol level, decreased circulating cholesterol level, decreased circulating insulin level, decreased circulating triglyceride level, decreased pancreatic beta cell number, decreased susceptibility to diet-induced obesity Allele Detail: Targeted

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Cite this (MGI Cat# 3038368, RRID:MGI:3038368)

Source Database: MGI, catalog # 3038368
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Rorb
Genomic Alteration: tm1Mba
Availability: Availability unknown check source stock center
Reference: PMID:9670004
Notes: behavior/neurological phenotype, limb grasping, impaired coordination, abnormal motor capabilities/coordination/movement, decreased body size, abnormal learning/memory/conditioning, abnormal eye physiology, abnormal retina morphology, decreased aggression, abnormal gait, abnormal social/conspecific interaction, retinal degeneration, disorganized retinal layers, decreased exploration in new environment, abnormal sexual interaction, nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 5509364, RRID:MGI:5509364)

Source Database: MGI, catalog # 5509364
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Krt1, Il18
Genomic Alteration: tm1Tmm; tm1Khe
Availability: Availability unknown check source stock center
Reference: PMID:23132931
Notes: mortality/aging, integument phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3521740, RRID:MGI:3521740)

Source Database: MGI, catalog # 3521740
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Satb1
Genomic Alteration: tm1Kos
Availability: Availability unknown check source stock center
Reference: PMID:10716941
Notes: small lymph nodes, postnatal lethality, complete penetrance, decreased body size, limb grasping, decreased thymocyte number, abnormal T cell differentiation, abnormal T cell proliferation, small thymus, postnatal growth retardation, arrested T cell differentiation, delayed eyelid opening, small spleen Allele Detail: Targeted

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Cite this (MGI Cat# 3054439, RRID:MGI:3054439)

Source Database: MGI, catalog # 3054439
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Furin
Genomic Alteration: tm1Ajmr
Availability: Availability unknown check source stock center
Reference: PMID:9811571
Notes: abnormal allantois morphology, abnormal neural plate morphology, decreased embryo size, failure of heart looping, abnormal dorsal-ventral axis patterning, excessive folding of visceral yolk sac, absent vitelline blood vessels, short rostral-caudal axis, cardia bifida, abnormal visceral yolk sac blood island morphology, abnormal developmental patterning, embryonic lethality during organogenesis, complete penetrance, abnormal somite shape, failure of chorioallantoic fusion, abnormal extraembryonic tissue morphology, failure of initiation of embryo turning, kinked neural tube, absent midgut, abnormal ventral body wall morphology, decreased somite size, abnormal heart development, abnormal heart tube morphology, abnormal cardinal vein morphology, exencephaly Allele Detail: Targeted

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Cite this (MGI Cat# 3796072, RRID:MGI:3796072)

Source Database: MGI, catalog # 3796072
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Glis2
Genomic Alteration: tm1Amj
Availability: Availability unknown check source stock center
Reference: PMID:18227149
Notes: polydipsia, kidney failure, renal cast, renal glomerulus atrophy, renal tubule atrophy, kidney degeneration, increased glomerular capsule space, increased circulating creatinine level, glomerulosclerosis, dilated renal tubules, decreased kidney weight, glomerulonephritis, albuminuria, abnormal renal glomerular capsule morphology, increased blood urea nitrogen level, pale kidney, polyuria, premature death, renal interstitial fibrosis, increased renal tubule apoptosis, increased urine protein level, kidney atrophy Allele Detail: Targeted

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Cite this (MGI Cat# 2662584, RRID:MGI:2662584)

Source Database: MGI, catalog # 2662584
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Chl1
Genomic Alteration: tm1Mtg
Availability: Availability unknown check source stock center
Reference: PMID:12391163
Notes: abnormal olfactory sensory neuron morphology, abnormal olfactory neuron innervation pattern, abnormal hippocampal mossy fiber morphology, nervous system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3654100, RRID:MGI:3654100)

Source Database: MGI, catalog # 3654100
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Nfatc2
Genomic Alteration: tm1Srf
Availability: Availability unknown check source stock center
Reference: PMID:9710223
Notes: abnormal B cell number, abnormal lymphocyte physiology, abnormal spleen germinal center morphology, enlarged spleen, abnormal lymph node B cell domain morphology, enlarged thymus, thymus hyperplasia, abnormal thymus involution, abnormal T cell physiology, increased activated T cell number, abnormal B cell physiology Allele Detail: Targeted

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Cite this (MGI Cat# 3530651, RRID:MGI:3530651)

Source Database: MGI, catalog # 3530651
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: F2rl1
Genomic Alteration: tm1Bpd
Availability: Availability unknown check source stock center
Reference: PMID:17623652, PMID:15458925
Notes: decreased inflammatory response, increased inflammatory response, increased susceptibility to induced pancreatitis, abnormal pain threshold Allele Detail: Targeted

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Cite this (MGI Cat# 2662384, RRID:MGI:2662384)

Source Database: MGI, catalog # 2662384
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Sp3
Genomic Alteration: tm1Sus
Availability: Availability unknown check source stock center
Reference: PMID:17584888, PMID:10675334, PMID:11472836, PMID:12676787
Notes: abnormal osteoblast differentiation, abnormal ameloblast morphology, abnormal tooth development, abnormal enamel development, decreased birth body size, abnormal pulmonary alveolus morphology, abnormal dentin development, neonatal lethality, complete penetrance, respiratory failure, abnormal bone mineralization, abnormal phalanx morphology, abnormal cranium morphology, abnormal metatarsal bone morphology, abnormal metacarpal bone morphology, abnormal cervical atlas morphology, abnormal xiphoid process morphology, abnormal trophoblast glycogen cell morphology, abnormal spongiotrophoblast cell morphology, abnormal vertebral body morphology, abnormal supraoccipital bone morphology, abnormal presphenoid bone morphology, abnormal parietal bone morphology, abnormal nasal bone morphology, abnormal interparietal bone morphology, delayed bone ossification, abnormal frontal bone morphology, abnormal basicranium morphology, abnormal basisphenoid bone morphology, abnormal sternum ossification, delayed intramembranous bone ossification, delayed endochondral bone ossification, abnormal sagittal suture morphology, small thymus, decreased CD4-positive, alpha beta T cell number, abnormal B cell differentiation, abnormal erythropoiesis, abnormal placenta labyrinth morphology, decreased spongiotrophoblast size, liver hypoplasia Allele Detail: Targeted

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