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on page 1 showing 20 out of 1,145 results

Cite this (MGI Cat# 3605490, RRID:MGI:3605490)

Source Database: MGI, catalog # 3605490
Genetic Background: involves: 129S7/SvEvBrd
Affected Genes: Asl
Genomic Alteration: tm1Wjc
Availability: Availability unknown check source stock center
Reference: PMID:12559843
Notes: abnormal food intake, decreased circulating arginine level, increased circulating ammonia level, homeostasis/metabolism phenotype, abnormal enzyme/coenzyme activity, lethargy, increased circulating glutamine level, abnormal circulating amino acid level, postnatal lethality, complete penetrance, increased circulating citrulline level Allele Detail: Targeted

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Cite this (MGI Cat# 5806513, RRID:MGI:5806513)

Source Database: MGI, catalog # 5806513
Genetic Background: C57BL/6J-Kbtbd2
Affected Genes: Kbtbd2
Genomic Alteration: m1Btlr
Availability: Availability unknown check source stock center
Reference: PMID:27708159
Notes: increased circulating alanine transaminase level, homeostasis/metabolism phenotype, increased circulating aspartate transaminase level, increased circulating insulin level, increased fasted circulating glucose level, increased lean body mass, increased liver triglyceride level, increased liver weight, insulin resistance, male infertility, pale liver, postnatal growth retardation, abnormal white adipose tissue physiology, decreased adiponectin level, decreased body size, enlarged liver, decreased inguinal fat pad weight, decreased epididymal fat pad weight, decreased circulating leptin level, decreased body weight, female infertility, hepatic steatosis Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3831161, RRID:MGI:3831161)

Source Database: MGI, catalog # 3831161
Genetic Background: involves: 129 * C57BL/6 * CBA * SJL
Affected Genes: Foxa2, Foxa1
Genomic Alteration: tm1Khk; Tg(Pdx1-cre)6Cvw
Availability: Availability unknown check source stock center
Reference: PMID:19141476
Notes: homeostasis/metabolism phenotype, endocrine/exocrine gland phenotype Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 2684306, RRID:MGI:2684306)

Source Database: MGI, catalog # 2684306
Genetic Background: involves: 129P2/OlaHsd * CBA/Ca
Affected Genes: F13a1
Genomic Alteration: tm1Gdi
Availability: Availability unknown check source stock center
Reference: PMID:12529747
Notes: hemothorax, pregnancy-related premature death, homeostasis/metabolism phenotype, abnormal pregnancy, increased bleeding time, hemoperitoneum, hematopoietic system phenotype, abnormal blood coagulation, hemorrhage, premature death Allele Detail: Targeted

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Cite this (MGI Cat# 5554950, RRID:MGI:5554950)

Source Database: MGI, catalog # 5554950
Genetic Background: involves: 129 * C57BL/6
Affected Genes: Gpr83
Genomic Alteration: tm1.2Lex
Availability: Availability unknown check source stock center
Reference: PMID:23088626
Notes: impaired spatial learning, hyperactivity, homeostasis/metabolism phenotype, behavior/neurological phenotype, decreased anxiety-related response, sweet preference Allele Detail: Targeted

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Cite this (MGI Cat# 5661928, RRID:MGI:5661928)

Source Database: MGI, catalog # 5661928
Genetic Background: C3N.C-Pdgfrb
Affected Genes: Pdgfrb
Genomic Alteration: redeye
Availability: Availability unknown check source stock center
Reference: PMID:23633653
Notes: increased vascular permeability, abnormal pericyte morphology, renal/urinary system phenotype, decreased retinal ganglion cell number, increased retinal apoptosis, retinal ganglion cell degeneration, homeostasis/metabolism phenotype, abnormal retinal blood vessel morphology, abnormal retinal blood vessel pattern, vision/eye phenotype, abnormal basement membrane morphology, abnormal retinal vasculature morphology, eye hemorrhage, abnormal blood-retinal barrier function Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3769129, RRID:MGI:3769129)

Source Database: MGI, catalog # 3769129
Genetic Background: involves: 129S6/SvEvTac * C57BL/6
Affected Genes: Mapk11
Genomic Alteration: tm2Okee
Availability: Availability unknown check source stock center
Reference: PMID:17855341
Notes: homeostasis/metabolism phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3850438, RRID:MGI:3850438)

Source Database: MGI, catalog # 3850438
Genetic Background: involves: C57BL/6 * SJL
Affected Genes:
Genomic Alteration: Tg(tetO-Egfr*)2-9Jek; Tg(Prl-tTA)6-5Jek
Availability: Availability unknown check source stock center
Reference: PMID:11266511
Notes: homeostasis/metabolism phenotype, reproductive system phenotype, growth/size/body region phenotype, endocrine/exocrine gland phenotype Allele Detail: Transgenic

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Cite this (MGI Cat# 5707195, RRID:MGI:5707195)

Source Database: MGI, catalog # 5707195
Genetic Background: involves: C57BL/6
Affected Genes: Del(4Cyp2j13-Cyp2j5)1Brs
Genomic Alteration: Del(4Cyp2j13-Cyp2j5)1Brs; Tg(CYP2J2)#Brs
Availability: Availability unknown check source stock center
Reference: PMID:24278032
Notes: cardiovascular system phenotype, homeostasis/metabolism phenotype Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 5689331, RRID:MGI:5689331)

Source Database: MGI, catalog # 5689331
Genetic Background: B6J.D2-Dtnbp1
Affected Genes: Dtnbp1
Genomic Alteration: sdy
Availability: Availability unknown check source stock center
Reference: PMID:25677649, PMID:23261874
Notes: abnormal operant conditioning behavior, abnormal circadian behavior, hyperactivity, homeostasis/metabolism phenotype, decreased anxiety-related response, decreased prepulse inhibition Allele Detail: Spontaneous

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Cite this (MGI Cat# 3618379, RRID:MGI:3618379)

Source Database: MGI, catalog # 3618379
Genetic Background: either: (involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6)
Affected Genes: Mapk8ip1
Genomic Alteration: tm1Wae
Availability: Availability unknown check source stock center
Reference: PMID:11390367
Notes: homeostasis/metabolism phenotype, reproductive system phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 2174766, RRID:MGI:2174766)

Source Database: MGI, catalog # 2174766
Genetic Background: involves: 129/Sv * C57BL/6J * SJL
Affected Genes: Terc
Genomic Alteration: tm1Rdp
Availability: Availability unknown check source stock center
Reference: PMID:17360455, PMID:12505991, PMID:15084742, PMID:10064584, PMID:15731767, PMID:10654945, PMID:9335332, PMID:11809709
Notes: reduced female fertility, decreased fetal size, prenatal lethality, incomplete penetrance, abnormal telomere length, open neural tube, infertility, prenatal lethality, incomplete penetrance, decreased litter size, abnormal meiosis, hypoactivity, increased cardiomyocyte apoptosis, abnormal telomere length, abnormal developmental patterning, increased embryonic tissue cell apoptosis, increased left ventricle diastolic pressure, abnormal cardiovascular system physiology, abnormal fetal cardiomyocyte proliferation, abnormal myocardial fiber morphology, abnormal telomere length, abnormal cardiac muscle relaxation, weight loss, decreased left ventricle developed pressure, cardiac hypertrophy, congestive heart failure, premature death, abnormal cardiac muscle contractility, heart left ventricle hypertrophy, dilated cardiomyopathy, decreased myocardial fiber number, decreased heart left ventricle weight, decreased heart weight, abnormal telomere length, decreased incidence of tumors by chemical induction, homeostasis/metabolism phenotype, abnormal spleen B cell follicle morphology, abnormal telomere length, decreased spleen germinal center number, decreased T cell proliferation, increased B cell apoptosis, decreased B cell proliferation, abnormal angiogenesis, decreased incidence of induced tumors, abnormal telomere length, decreased body size, decreased body weight, abnormal male germ cell apoptosis, kyphosis, testicular atrophy, increased apoptosis, abnormal telomere length, abnormal male germ cell apoptosis, abnormal oocyte morphology, abnormal spermatocyte morphology, premature aging, abnormal male meiosis, abnormal female meiosis, abnormal chromosome morphology, abnormal intestine morphology, abnormal telomere length, alopecia Allele Detail: Targeted

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Cite this (MGI Cat# 3807520, RRID:MGI:3807520)

Source Database: MGI, catalog # 3807520
Genetic Background: involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL
Affected Genes: Gpsm1
Genomic Alteration: tm1.1Lajb
Availability: Availability unknown check source stock center
Reference: PMID:18450958
Notes: nervous system phenotype, increased energy expenditure, increased vasodilation, cardiovascular system phenotype, decreased body weight, decreased white adipose tissue amount, homeostasis/metabolism phenotype, decreased mean systemic arterial blood pressure, abnormal eating behavior, abnormal baroreceptor physiology Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 4818925, RRID:MGI:4818925)

Source Database: MGI, catalog # 4818925
Genetic Background: B6.Cg-Tg(SMN2)11Tro Tg(SMN2)46Tro Smn1/J
Affected Genes: Smn1
Genomic Alteration: Tg(SMN2)46Tro; tm1Msd; Tg(SMN2)11Tro
Availability: Availability unknown check source stock center
Reference: PMID:20085811
Notes: apnea, abnormal respiration, abnormal phrenic nerve morphology, abnormal gait, postnatal lethality, incomplete penetrance, decreased survivor rate, progressive muscle weakness, decreased pulmonary ventilation, abnormal autopod morphology, abnormal tail morphology, abnormal synaptic bouton morphology, positive geotaxis, abnormal muscle electrophysiology, abnormal skeletal muscle fiber morphology, abnormal sciatic nerve morphology, muscular atrophy, abnormal neuromuscular synapse morphology, increased thermal nociceptive threshold, homeostasis/metabolism phenotype, abnormal outer ear morphology, axon degeneration, behavior/neurological phenotype, decreased motor neuron number, slow postnatal weight gain, abnormal respiratory mechanics Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 5487467, RRID:MGI:5487467)

Source Database: MGI, catalog # 5487467
Genetic Background: involves: C57BL/6 * DBA
Affected Genes: Speer6-ps1, Sqstm1
Genomic Alteration: tm2.1Jmos; Tg(Alb-cre)21Mgn
Availability: Availability unknown check source stock center
Reference: PMID:23257354
Notes: homeostasis/metabolism phenotype, growth/size/body region phenotype, behavior/neurological phenotype, liver/biliary system phenotype Allele Detail: Transgenic, Targeted

  • From Current Category

Cite this (MGI Cat# 4939499, RRID:MGI:4939499)

Source Database: MGI, catalog # 4939499
Genetic Background: involves: 129S6/SvEvTac * C57BL/6
Affected Genes: Pnpla3
Genomic Alteration: tm1Eek
Availability: Availability unknown check source stock center
Reference: PMID:21068004
Notes: homeostasis/metabolism phenotype Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 5319230, RRID:MGI:5319230)

Source Database: MGI, catalog # 5319230
Genetic Background: involves: 129 * C57BL/6J * FVB
Affected Genes: Tg(Col1a1-cre)1Kry, Ptpn1
Genomic Alteration: Tg(Col1a1-cre)1Kry; tm1.1Kry
Availability: Availability unknown check source stock center
Reference: PMID:22252315
Notes: homeostasis/metabolism phenotype Allele Detail: Transgenic, Targeted

  • From Current Category

Cite this (MGI Cat# 3835380, RRID:MGI:3835380)

Source Database: MGI, catalog # 3835380
Genetic Background: involves: C57BL/6J * CBA/J
Affected Genes:
Genomic Alteration: Tg(CETP)5203Tall
Availability: Availability unknown check source stock center
Reference: PMID:15761619, PMID:9598833
Notes: homeostasis/metabolism phenotype, decreased circulating HDL cholesterol level Allele Detail: Transgenic

  • From Current Category

Cite this (MGI Cat# 4888960, RRID:MGI:4888960)

Source Database: MGI, catalog # 4888960
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J
Affected Genes: Gria1
Genomic Alteration: tm1Rsp
Availability: Availability unknown check source stock center
Reference: PMID:20699120
Notes: abnormal emotion/affect behavior, homeostasis/metabolism phenotype, induced hyperactivity, increased exploration in new environment, hyperactivity Allele Detail: Targeted

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Cite this (MGI Cat# 3841490, RRID:MGI:3841490)

Source Database: MGI, catalog # 3841490
Genetic Background: B6.Cg-Htr2c Tg(Pomc1-cre)16Lowl
Affected Genes: Htr2c
Genomic Alteration: tm1Jke; Tg(Pomc1-cre)16Lowl
Availability: Availability unknown check source stock center
Reference: PMID:19038216
Notes: premature death, behavior/neurological phenotype, homeostasis/metabolism phenotype, tonic-clonic seizures, growth/size/body region phenotype, adipose tissue phenotype Allele Detail: Transgenic, Targeted

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