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on page 1 showing 20 out of 2,499 results

Cite this (MGI Cat# 5804554, RRID:MGI:5804554)

Source Database: MGI, catalog # 5804554
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Gprc6a
Genomic Alteration: tm1.1Pwd
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (MGI Cat# 3813702, RRID:MGI:3813702)

Source Database: MGI, catalog # 3813702
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Pum2, Dazl
Genomic Alteration: Gt(XE772)Byg; tm1Hjc
Availability: Availability unknown check source stock center
Reference: PMID:17219433
Notes: reproductive system phenotype, decreased testis weight Allele Detail: Targeted, Gene trapped

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Cite this (MGI Cat# 2677143, RRID:MGI:2677143)

Source Database: MGI, catalog # 2677143
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Gfap
Genomic Alteration: tm1Ldtk
Availability: Availability unknown check source stock center
Reference: PMID:8893019
Notes: abnormal blood-brain barrier function, non-obstructive hydrocephaly, decreased corpus callosum size, abnormal myelination, abnormal astrocyte morphology, abnormal brain white matter morphology, abnormal blood vessel morphology, abnormal oligodendrocyte morphology, abnormal oligodendrocyte physiology Allele Detail: Targeted

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Cite this (MGI Cat# 3719997, RRID:MGI:3719997)

Source Database: MGI, catalog # 3719997
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Hs2st1
Genomic Alteration: Gt(pGT1.8TM)ST125Nimr
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Gene trapped

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Cite this (MGI Cat# 2673511, RRID:MGI:2673511)

Source Database: MGI, catalog # 2673511
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Med1
Genomic Alteration: tm1Jkr
Availability: Availability unknown check source stock center
Reference: PMID:11724781, PMID:10747854
Notes: abnormal placenta vasculature, abnormal placental labyrinth vasculature morphology, abnormal trophoblast giant cell morphology, abnormal lens development, thin myocardium, abnormal cardiovascular system physiology, myocardium hypoplasia, abnormal placenta labyrinth morphology, abnormal definitive hematopoiesis, enlarged liver sinusoidal spaces, absent megakaryocytes, abnormal cardiovascular development, abnormal vascular endothelial cell development, abnormal spongiotrophoblast layer morphology, myocardial trabeculae hypoplasia, thin ventricular wall, abnormal cardiovascular system physiology, trabecula carnea hypoplasia, pericardial effusion, embryonic growth retardation, abnormal lens epithelium morphology, ventricular hypoplasia, decreased embryo size, embryonic lethality during organogenesis, complete penetrance, abnormal placenta vasculature, increased angiogenesis, increased vascular permeability, abnormal retinal pigmentation, abnormal cardiovascular system morphology, abnormal extraembryonic tissue morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5314922, RRID:MGI:5314922)

Source Database: MGI, catalog # 5314922
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Mir138-1
Genomic Alteration: tm1Mtm
Availability: Availability unknown check source stock center
Reference:
Notes: no phenotypic analysis Allele Detail: Targeted

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Cite this (MGI Cat# 3829017, RRID:MGI:3829017)

Source Database: MGI, catalog # 3829017
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ctcf
Genomic Alteration: Tg(Lck-cre)1Cwi; tm1Laat
Availability: Availability unknown check source stock center
Reference: PMID:18923423
Notes: decreased CD8-positive, alpha-beta T cell number, thymus hypoplasia, decreased CD4-positive, alpha beta T cell number Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 3845086, RRID:MGI:3845086)

Source Database: MGI, catalog # 3845086
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Phox2a
Genomic Alteration: tm1Jbr
Availability: Availability unknown check source stock center
Reference: PMID:9115735
Notes: abnormal otic ganglion morphology, small superior cervical ganglion, abnormal parasympathetic ganglion morphology, abnormal pterygopalatine ganglion morphology, abnormal locus ceruleus morphology, small petrosal ganglion, small submandibular ganglion, small nodose ganglion, abnormal cranial ganglia morphology, abnormal autonomic nervous system morphology, small geniculate ganglion Allele Detail: Targeted

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Cite this (MGI Cat# 3575010, RRID:MGI:3575010)

Source Database: MGI, catalog # 3575010
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Gdf7
Genomic Alteration: tm1Tmj
Availability: Availability unknown check source stock center
Reference: PMID:9808626
Notes: hydrocephaly, dilated lateral ventricles, abnormal spinal cord interneuron morphology, dilated fourth ventricle, abnormal cerebral cortex morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3813943, RRID:MGI:3813943)

Source Database: MGI, catalog # 3813943
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Apln
Genomic Alteration: tm1Pngr
Availability: Availability unknown check source stock center
Reference: PMID:17673668
Notes: growth/size/body region phenotype, decreased ventricle muscle contractility, cardiovascular system phenotype, increased response of heart to induced stress, behavior/neurological phenotype Allele Detail: Targeted

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Cite this (MGI Cat# 3822776, RRID:MGI:3822776)

Source Database: MGI, catalog # 3822776
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Nmu
Genomic Alteration: tm1Sjab
Availability: Availability unknown check source stock center
Reference: PMID:19070594
Notes: decreased circulating interleukin-6 level Allele Detail: Targeted

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Cite this (MGI Cat# 3606456, RRID:MGI:3606456)

Source Database: MGI, catalog # 3606456
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Prss12
Genomic Alteration: tm1Dgen
Availability: Availability unknown check source stock center
Reference:
Notes: increased thigmotaxis, hypoactivity Allele Detail: Targeted

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Cite this (MGI Cat# 4831134, RRID:MGI:4831134)

Source Database: MGI, catalog # 4831134
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Faim
Genomic Alteration: tm1Kplm
Availability: Availability unknown check source stock center
Reference: PMID:19300454
Notes: increased hepatocyte apoptosis, liver hemorrhage, increased thymocyte apoptosis, increased circulating alanine transaminase level, increased sensitivity to xenobiotic induced morbidity/mortality, liver failure, liver inflammation, increased B cell apoptosis Allele Detail: Targeted

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Cite this (MGI Cat# 2173367, RRID:MGI:2173367)

Source Database: MGI, catalog # 2173367
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Fgfr2
Genomic Alteration: tm1.1Dsn
Availability: Availability unknown check source stock center
Reference: PMID:10934262, PMID:14697353, PMID:11782400, PMID:10631169, PMID:16720875, PMID:15972105, PMID:15234214
Notes: abnormal salivary gland morphology, abnormal mammary placode morphology, submandibular gland hypoplasia, absent submandibular gland, abnormal rectum morphology, absent lungs, absent forelimb, absent hindlimb, absent rectum, abnormal perineum morphology, hypospadia, curly tail, cecal atresia, abnormal membranous labyrinth morphology, abnormal otic capsule morphology, abnormal semicircular canal morphology, small otic vesicle, absent eyelids, absent lungs, small scapula, premature squamoparietal suture closure, domed cranium, impaired branching involved in trachea morphogenesis, absent Rathke's pouch, abnormal Rathke's pouch apoptosis, absent adenohypophysis, absent hindlimb, translucent skin, small otic capsule, decreased skin pigmentation, abnormal pituitary gland development, abnormal lung development, caudal vertebral fusion, abnormal semicircular canal morphology, abnormal pelvic girdle bone morphology, abnormal stomach morphology, abnormal ilium morphology, abnormal epidermis stratum basale morphology, abnormal clavicle morphology, abnormal endolymphatic duct morphology, absent hypodermis muscle layer, inner ear cysts, abnormal ischium morphology, abnormal limb development, absent pubis, absent acromion, abnormal endolymphatic duct morphology, cleft palate, small stomach, thin dermal layer, thin epidermis, thin skin, abnormal Rathke's pouch development, arrest of tooth development, abnormal cecum development, absent forelimb, decreased body size, perinatal lethality, complete penetrance, curly tail, abnormal cochlea morphology, abnormal vestibulocochlear ganglion morphology, abnormal cochlear sensory epithelium morphology, abnormal epidermis stratum basale morphology, abnormal mammary gland bud morphology, absent mammary gland Allele Detail: Targeted

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Cite this (MGI Cat# 3713995, RRID:MGI:3713995)

Source Database: MGI, catalog # 3713995
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Olfr151
Genomic Alteration: tm21Mom
Availability: Availability unknown check source stock center
Reference: PMID:15186782
Notes: abnormal olfactory bulb development, abnormal axon extension Allele Detail: Targeted

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Cite this (MGI Cat# 3628609, RRID:MGI:3628609)

Source Database: MGI, catalog # 3628609
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Lmbr1l
Genomic Alteration: tm1Dgen
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 4888545, RRID:MGI:4888545)

Source Database: MGI, catalog # 4888545
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Sfn
Genomic Alteration: tm1Mak
Availability: Availability unknown check source stock center
Reference: PMID:21205887
Notes: increased susceptibility to viral infection induced morbidity/mortality, decreased IgG level, decreased IgM level, decreased follicular B cell number, decreased marginal zone B cell number, immune system phenotype, increased B cell apoptosis, increased B cell proliferation, increased susceptibility to viral infection, abnormal spleen morphology, decreased B cell number, decreased B-1a cell number, abnormal B cell differentiation, abnormal spleen B cell follicle morphology, absent spleen marginal zone Allele Detail: Targeted

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Cite this (MGI Cat# 5514152, RRID:MGI:5514152)

Source Database: MGI, catalog # 5514152
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Vwf
Genomic Alteration: tm1Aird
Availability: Availability unknown check source stock center
Reference: PMID:23529929
Notes: no phenotypic analysis Allele Detail: Targeted

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Cite this (MGI Cat# 5293682, RRID:MGI:5293682)

Source Database: MGI, catalog # 5293682
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Noa1
Genomic Alteration: tm1Tze
Availability: Availability unknown check source stock center
Reference: PMID:21118999
Notes: abnormal trophoblast layer morphology, abnormal mitochondrial physiology, abnormal mitochondrial ATP synthesis coupled electron transport, decreased sensitivity to induced cell death, embryonic growth retardation, embryo tissue necrosis, decreased embryonic tissue cell apoptosis, decreased apoptosis, embryonic lethality during organogenesis, complete penetrance, abnormal mitochondrion morphology, abnormal mitochondrial crista morphology, abnormal cell physiology Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 5573199, RRID:MGI:5573199)

Source Database: MGI, catalog # 5573199
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Uchl1
Genomic Alteration: Tg(Thy1-Snca)1S13Putt; tm1Dgen
Availability: Availability unknown check source stock center
Reference: PMID:22355774
Notes: premature death, decreased grip strength, alpha-synuclein inclusion body, impaired coordination, astrocytosis Allele Detail: Transgenic, Targeted

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