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on page 3 showing 20 out of 623,700 results

Cite this (MGI Cat# 3525260, RRID:MGI:3525260)

Source Database: MGI, catalog # 3525260
Genetic Background: involves: 129X1/SvJ * C57BL/6
Affected Genes: Sgk3
Genomic Alteration: tm1Dpea
Availability: Availability unknown check source stock center
Reference: PMID:15240817
Notes: curly vibrissae, abnormal hair follicle inner root sheath morphology, homeostasis/metabolism phenotype, abnormal hair follicle development, abnormal hair follicle orientation, abnormal hair growth, abnormal hair shaft morphology, sparse hair, waved hair, disorganized outer root sheath cells, abnormal postnatal growth Allele Detail: Targeted

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Cite this (WB Cat# LS2342, RRID:WB-STRAIN:LS2342)

Source Database: WB, catalog # LS2342
Genetic Background:
Affected Genes:
Genomic Alteration: WBVar00066489(cxTi4314)
Availability: live
Reference: WBPaper00024297
Notes: other notes: For further information and strain requests please visit http://ums3421.univ-lyon1.fr/

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Cite this (MGI Cat# 3689219, RRID:MGI:3689219)

Source Database: MGI, catalog # 3689219
Genetic Background: Mixed stock
Affected Genes: Nell1
Genomic Alteration: l7R6-1R; l7R6-4R
Availability: Availability unknown check source stock center
Reference:
Notes: perinatal lethality, complete penetrance, prenatal lethality, incomplete penetrance Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 5518458, RRID:MGI:5518458)

Source Database: MGI, catalog # 5518458
Genetic Background: involves: C57BL/6 * C57BL/6NTac
Affected Genes: Epas1
Genomic Alteration: tm1.1Fsl
Availability: Availability unknown check source stock center
Reference: PMID:23640890
Notes: increased spleen weight, abnormal heart right ventricle pressure, thick ventricular wall, lethality, incomplete penetrance, increased circulating erythropoietin level, pulmonary artery hypoplasia, increased erythrocyte cell number, increased heart weight, increased hematocrit, increased hemoglobin content, increased leukocyte cell number, increased monocyte cell number, increased pulmonary respiratory rate Allele Detail: Targeted

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Cite this (WB Cat# IE35100, RRID:WB-STRAIN:IE35100)

Source Database: WB, catalog # IE35100
Genetic Background:
Affected Genes:
Genomic Alteration: WBVar00261970(ttTi35100)
Availability: live
Reference: WBPaper00040752, WBPaper00028894
Notes: other notes: For further information and strain requests please visit http://ums3421.univ-lyon1.fr/"|"Hermaphrodites carrying both the Mos1 transposon substrate and transposase extrachromosomal arrays were subjected to a heat-shock to induce transposase expression. Five days later, progeny of the F1 at the L4 stage carrying the Mos1 substrate array were singled. After a further 5 days of culture, worms of the F3 generation were transferred to fresh plates and 3 days later a single F4 worm that did not carry the Mos1 substrate array was transferred to a fresh plate. These worms were allowed to reproduce to give the F6 generation that was then subject to molecular characterization

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Cite this (MGI Cat# 3624330, RRID:MGI:3624330)

Source Database: MGI, catalog # 3624330
Genetic Background: involves: 129S4/SvJae
Affected Genes: Trp53
Genomic Alteration: tm1Wahl
Availability: Availability unknown check source stock center
Reference: PMID:16006521, PMID:10973245
Notes: abnormal cell cycle, abnormal cell cycle, increased fibroblast proliferation, decreased cellular sensitivity to gamma-irradiation Allele Detail: Targeted

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Cite this (MGI Cat# 4456249, RRID:MGI:4456249)

Source Database: MGI, catalog # 4456249
Genetic Background: involves: 129S/SvEv * C57BL/6J * DBA * MF1
Affected Genes: Ghr, Igf1
Genomic Alteration: tm1Arge
Availability: Availability unknown check source stock center
Reference: PMID:11133160
Notes: decreased width of hypertrophic chondrocyte zone, abnormal trabecular bone morphology, abnormal long bone epiphyseal plate proliferative zone, abnormal chondrocyte morphology, proportional dwarf, postnatal growth retardation, delayed endochondral bone ossification, abnormal long bone hypertrophic chondrocyte zone Allele Detail: Targeted

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Cite this (MGI Cat# 4366459, RRID:MGI:4366459)

Source Database: MGI, catalog # 4366459
Genetic Background: involves: 129X1/SvJ * FVB/N
Affected Genes: Ctnnb1
Genomic Alteration: tm1Mmt; Tg(Cryaa-cre)10Mlr
Availability: Availability unknown check source stock center
Reference: PMID:19570848
Notes: microphthalmia, increased lens epithelium apoptosis, abnormal lens epithelium morphology Allele Detail: Targeted, Transgenic

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Cite this (WB Cat# JN1715, RRID:WB-STRAIN:JN1715)

Source Database: WB, catalog # JN1715
Genetic Background:
Affected Genes: NULL
Genomic Alteration: NULL
Availability: No longer indexed by source database
Reference:
Notes:

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Cite this (WB Cat# JN1715, RRID:WB-STRAIN:JN1715)

Source Database: WB, catalog # JN1715
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: live
Reference:
Notes: mutagen: UV for integration of Ex into the genome; outcrossed: x4; other notes: peIs1715 [str-1p::mCasp-1 + unc-122p::mCherry]. AWB neurons are eliminated. Abnormal odor chemotaxis. Reference: Yoshida K, et al. Nat Commun. 2012 Mar 13;3:739.

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Cite this (MGI Cat# 3775385, RRID:MGI:3775385)

Source Database: MGI, catalog # 3775385
Genetic Background: involves: 129S4/SvJae * C57BL/6 * DBA/2
Affected Genes: Speer6-ps1, Insr
Genomic Alteration: tm1Khn; Tg(Alb-cre)21Mgn
Availability: Availability unknown check source stock center
Reference: PMID:17416680
Notes: increased pancreatic beta cell mass, decreased circulating glucose level, increased circulating insulin level, insulin resistance, hyperglycemia, impaired glucose tolerance Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 3789308, RRID:MGI:3789308)

Source Database: MGI, catalog # 3789308
Genetic Background: involves: 129S2/SvPas * Swiss Webster
Affected Genes: En2
Genomic Alteration: tm2Alj
Availability: Availability unknown check source stock center
Reference: PMID:17537797
Notes: abnormal cerebellum morphology, small cerebellum, abnormal cerebellum vermis morphology, abnormal cerebellum posterior vermis morphology, decreased inferior colliculus size Allele Detail: Targeted

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Cite this (MGI Cat# 6209484, RRID:MGI:6209484)

Source Database: MGI, catalog # 6209484
Genetic Background: involves: 129S2/SvPas * C57BL/6
Affected Genes: E2f4
Genomic Alteration: tm1Lees
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (WB Cat# IE37709, RRID:WB-STRAIN:IE37709)

Source Database: WB, catalog # IE37709
Genetic Background:
Affected Genes:
Genomic Alteration: WBVar00263036(ttTi37709)
Availability: live
Reference: WBPaper00028894, WBPaper00040752
Notes: other notes: For further information and strain requests please visit http://ums3421.univ-lyon1.fr/"|"Hermaphrodites carrying both the Mos1 transposon substrate and transposase extrachromosomal arrays were subjected to a heat-shock to induce transposase expression. Five days later, progeny of the F1 at the L4 stage carrying the Mos1 substrate array were singled. After a further 5 days of culture, worms of the F3 generation were transferred to fresh plates and 3 days later a single F4 worm that did not carry the Mos1 substrate array was transferred to a fresh plate. These worms were allowed to reproduce to give the F6 generation that was then subject to molecular characterization

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Cite this (MGI Cat# 6161263, RRID:MGI:6161263)

Source Database: MGI, catalog # 6161263
Genetic Background: C57BL/6N-Brd2/WtsiIeg
Affected Genes: Brd2
Genomic Alteration: em1(IMPC)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: abnormal physiological umbilical hernia morphology, persistent trigeminal artery, thoracoschisis, enlarged brain ventricles, abnormal pectinate muscle morphology, increased rib number, abnormal ductus venosus morphology, abnormal vertebral body morphology, abnormal external carotid artery origin, dual inferior vena cava, small thymus, basisphenoid bone foramen, abnormal optic cup morphology, scoliosis, abnormal optic stalk morphology, abnormal pineal gland morphology, persistent truncus arteriosis, reduced sympathetic cervical ganglion size, abnormal umbilical vein topology, transposition of great arteries, perimembraneous ventricular septal defect, atrioventricular septal defect, fusion of vertebral arches, rib bifurcation, enlarged liver sinusoidal spaces, abnormal interatrial septum morphology, double outlet right ventricle, absent vertebral arch, interrupted aortic arch, type b, exencephaly, enlarged heart, abnormal forebrain morphology, absent eye muscles, abnormal olfactory nerve morphology, heterochrony, abnormal Mullerian duct topology, retroesophageal right subclavian artery, abnormal adenohypophysis morphology, abnormal choroid plexus morphology, artery stenosis, abnormal ductus venosus topology, duplication of ductus venosus, abnormal vertebral artery topology, rib fusion, myelocele, abnormal optic chiasm morphology, abnormal common carotid artery morphology, aphakia, abnormal middle ear ossicle morphology, abnormal pulmonary valve morphology, hemorrhage, decreased rib number, abnormal aortic valve morphology, abnormal semilunar valve morphology, abnormal hepatic portal vein connection, abnormal brain artery topology, thin myocardium compact layer, aorta coarctation, abnormal hypoglossal nerve topology, muscular ventricular septal defect, small kidney, abnormal gallbladder morphology, abnormal vertebral arch morphology, persistent right dorsal aorta, absent pectinate muscle, abnormal thymus topology, common truncal valve, small thyroid gland, absent costovertebral joint, abnormal vagus ganglion morphology, absent vagus nerve, fetal growth retardation, abnormal nasal septum morphology, retropleural edema, subcutaneous edema, absent superior cervical ganglion, abnormal lung position or orientation, blood in lymph vessels, absent connection between subcutaneous lymph vessels and lymph sac Allele Detail: Endonuclease-mediated

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Cite this (MGI Cat# 2662461, RRID:MGI:2662461)

Source Database: MGI, catalog # 2662461
Genetic Background: involves: C57BL/6
Affected Genes: Sh2b1
Genomic Alteration: tm1Ayos
Availability: Availability unknown check source stock center
Reference: PMID:11940664
Notes: proportional dwarf, oligozoospermia, ovary hypoplasia, reduced male fertility, reduced female fertility, endocrine/exocrine gland phenotype, abnormal ovulation, testis hypoplasia, decreased testis weight, postnatal growth retardation, asthenozoospermia, abnormal ovarian folliculogenesis, neonatal lethality, incomplete penetrance, abnormal oocyte morphology, abnormal epididymis morphology, immune system phenotype, decreased ovary weight, abnormal uterus development, decreased body weight, Leydig cell hypoplasia Allele Detail: Targeted

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Cite this (MGI Cat# 3040919, RRID:MGI:3040919)

Source Database: MGI, catalog # 3040919
Genetic Background: either: (involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6) or (involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6 * NIH Black Swiss) or (involves: 129S/SvEv * 129S6/SvEvTac * NIH Black Swiss)
Affected Genes: Inpp5b, Ocrl
Genomic Alteration: tm1Nbm
Availability: Availability unknown check source stock center
Reference: PMID:9593760
Notes: 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

  • From Current Category

Cite this (MGI Cat# 3793282, RRID:MGI:3793282)

Source Database: MGI, catalog # 3793282
Genetic Background: B6.129S1-Ror2
Affected Genes: Ror2
Genomic Alteration: tm1Anec
Availability: Availability unknown check source stock center
Reference: PMID:18353862
Notes: abnormal vertebrae morphology, broad nasal bone, short snout, short nasal bone, abnormal axial skeleton morphology, increased lean body mass, abnormal digit morphology, brachydactyly, decreased body length, kinked tail, short mandible, abnormal caudal vertebrae morphology, abnormal limb morphology, abnormal phalanx morphology, homeostasis/metabolism phenotype, brachyphalangia, caudal vertebral fusion, short metacarpal bones, vertebral body hypoplasia, excessive tearing, entropion, decreased body size, decreased total body fat amount, large orbits, abnormal bone mineralization, abnormal seminiferous tubule morphology, decreased testis weight, oligozoospermia, reduced male fertility, small seminiferous tubules, abnormal cartilage development, abnormal digit development, abnormal intervertebral disk morphology, abnormal limb development, abnormal skeleton development, abnormal thoracic vertebrae morphology, delayed endochondral bone ossification, rib fusion, abnormal nasal bone morphology, decreased bone trabecula number, decreased trabecular bone volume Allele Detail: Targeted

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Cite this (MGI Cat# 6193928, RRID:MGI:6193928)

Source Database: MGI, catalog # 6193928
Genetic Background: Not Specified
Affected Genes: Lepr
Genomic Alteration: db
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Spontaneous

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