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on page 1 showing 20 out of 1,384 results

Cite this (MGI Cat# 3580461, RRID:MGI:3580461)

Source Database: MGI, catalog # 3580461
Genetic Background: either: B6.129S2-Hnrnpu or (involves: 129S2/SvPas * C57BL/6J)
Affected Genes: Hnrnpu
Genomic Alteration: Gt(U3Neo)1Rul
Availability: Availability unknown check source stock center
Reference: PMID:16022389
Notes: embryonic growth retardation, abnormal extraembryonic tissue morphology, embryonic lethality during organogenesis, complete penetrance, failure of chorioallantoic fusion, abnormal ectoderm development Allele Detail: Gene trapped

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Cite this (MGI Cat# 4818934, RRID:MGI:4818934)

Source Database: MGI, catalog # 4818934
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Affected Genes: Itga5
Genomic Alteration: tm2.1Hyn
Availability: Availability unknown check source stock center
Reference: PMID:20570943
Notes: embryonic growth retardation, embryonic lethality during organogenesis, complete penetrance, abnormal blood vessel morphology, incomplete somite formation Allele Detail: Targeted

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Cite this (MGI Cat# 6159012, RRID:MGI:6159012)

Source Database: MGI, catalog # 6159012
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac * CBA
Affected Genes: Hspb7, Lmod2
Genomic Alteration: tm1.2Chen; tm1(KOMP)Vlcg
Availability: Availability unknown check source stock center
Reference: PMID:29078393
Notes: abnormal sarcomere morphology, embryonic lethality during organogenesis, complete penetrance, abnormal fetal cardiomyocyte morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3040994, RRID:MGI:3040994)

Source Database: MGI, catalog # 3040994
Genetic Background: involves: 129P2/OlaHsd
Affected Genes: Tfap2c
Genomic Alteration: tm1.1Hsc
Availability: Availability unknown check source stock center
Reference: PMID:11940672
Notes: absent placental labyrinth, decreased embryo size, embryonic lethality during organogenesis, complete penetrance, small ectoplacental cone, abnormal trophoblast giant cell morphology, absent mesoderm, decreased trophoblast giant cell number Allele Detail: Targeted

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Cite this (MGI Cat# 3773267, RRID:MGI:3773267)

Source Database: MGI, catalog # 3773267
Genetic Background: involves: 129 * CD-1
Affected Genes: Ascl2
Genomic Alteration: tm1Alj
Availability: Availability unknown check source stock center
Reference: PMID:7773285
Notes: absent spongiotrophoblast, embryonic lethality during organogenesis, complete penetrance, abnormal chorion morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3511065, RRID:MGI:3511065)

Source Database: MGI, catalog # 3511065
Genetic Background: involves: 129X1/SvJ * C57BL/6J
Affected Genes: Hhex
Genomic Alteration: tm1Cwb
Availability: Availability unknown check source stock center
Reference: PMID:15459110
Notes: abnormal myocardial trabeculae morphology, vascular smooth muscle hypoplasia, increased atrioventricular cushion size, decreased heart right ventricle size, abnormal blood vessel morphology, abnormal vasculogenesis, conotruncal ridge hyperplasia, abnormal cardiac epithelial to mesenchymal transition, abnormal conotruncal ridge morphology, absent liver, decreased forebrain size, pericardial edema, abnormal liver development, edema, heart right ventricle outflow tract stenosis, abnormal atrioventricular valve morphology, double outlet right ventricle, abnormal forebrain development, abnormal thyroid gland development, abnormal atrioventricular cushion morphology, embryonic lethality during organogenesis, complete penetrance, ventricular septal defect, thin myocardium compact layer, thin ventricular wall Allele Detail: Targeted

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Cite this (MGI Cat# 3805987, RRID:MGI:3805987)

Source Database: MGI, catalog # 3805987
Genetic Background: involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * DBA/2
Affected Genes: Smad1
Genomic Alteration: tm1Tako
Availability: Availability unknown check source stock center
Reference: PMID:12351174
Notes: abnormal mesenchyme morphology, decreased primordial germ cell number, absent primordial germ cells, delayed allantois development, embryonic lethality during organogenesis, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 3838394, RRID:MGI:3838394)

Source Database: MGI, catalog # 3838394
Genetic Background: involves: 129/Sv * 129P2/OlaHsd * C57BL/6
Affected Genes: Ccm2, Heg1
Genomic Alteration: tm1Mlkn; Gt(RRG051)Byg
Availability: Availability unknown check source stock center
Reference: PMID:19151727
Notes: pericardial edema, abnormal cardinal vein morphology, dilated aortic sac, abnormal dorsal aorta morphology, embryonic growth retardation, abnormal vasculogenesis, embryonic lethality during organogenesis, complete penetrance, hemopericardium, abnormal vascular endothelial cell development Allele Detail: Gene trapped, Targeted

  • From Current Category

Cite this (MGI Cat# 4839513, RRID:MGI:4839513)

Source Database: MGI, catalog # 4839513
Genetic Background: chimera involves: 129S6/SvEvTac * C57BL/6NCr
Affected Genes: Med12
Genomic Alteration: tm1Hsch
Availability: Availability unknown check source stock center
Reference: PMID:20630950
Notes: embryonic lethality, complete penetrance, abnormal neural tube morphology, embryonic lethality during organogenesis, complete penetrance, abnormal dorsal-ventral polarity of the somites, abnormal head mesenchyme morphology, open neural tube, absent second pharyngeal arch, abnormal first pharyngeal arch morphology, abnormal pharyngeal arch morphology, abnormal neural crest cell migration, failure of heart looping, abnormal heart development, kinked neural tube, caudal body truncation, absent third pharyngeal arch, decreased somite size, abnormal somite shape, abnormal somite development Allele Detail: Targeted

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Cite this (MGI Cat# 2673674, RRID:MGI:2673674)

Source Database: MGI, catalog # 2673674
Genetic Background: Not Specified
Affected Genes: l11Jus41
Genomic Alteration: l11Jus41
Availability: Availability unknown check source stock center
Reference: PMID:16466971
Notes: embryonic lethality during organogenesis, complete penetrance Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3712946, RRID:MGI:3712946)

Source Database: MGI, catalog # 3712946
Genetic Background: involves: BALB/c * C57BL/6 * CBA
Affected Genes: Nrp1, Nrp2
Genomic Alteration: tm1Hfu; tm1Mkl
Availability: Availability unknown check source stock center
Reference: PMID:11891274
Notes: abnormal vascular development, hemorrhage, embryonic lethality during organogenesis, complete penetrance, abnormal dorsal aorta morphology, abnormal vitelline vasculature morphology Allele Detail: Targeted

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Cite this (MGI Cat# 2183176, RRID:MGI:2183176)

Source Database: MGI, catalog # 2183176
Genetic Background: involves: 129S2/SvPas * ICR
Affected Genes: Bmp4
Genomic Alteration: tm1Blh
Availability: Availability unknown check source stock center
Reference: PMID:7657163
Notes: embryonic lethality during organogenesis, complete penetrance, embryonic growth retardation Allele Detail: Targeted

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Cite this (MGI Cat# 3042039, RRID:MGI:3042039)

Source Database: MGI, catalog # 3042039
Genetic Background: Not Specified
Affected Genes: Mapk7
Genomic Alteration: tm1.1Jdl
Availability: Availability unknown check source stock center
Reference: PMID:15085193
Notes: embryonic lethality during organogenesis, complete penetrance, abnormal vitelline vasculature morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3579852, RRID:MGI:3579852)

Source Database: MGI, catalog # 3579852
Genetic Background: involves: 129S6/SvEvTac * C57BL/6
Affected Genes: Tbx20
Genomic Alteration: tm1.1Sev
Availability: Availability unknown check source stock center
Reference: PMID:15843407
Notes: heart hypoplasia, abnormal fetal cardiomyocyte proliferation, embryonic lethality during organogenesis, complete penetrance, embryonic growth arrest, abnormal heart tube morphology, failure of heart looping Allele Detail: Targeted

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Cite this (MGI Cat# 3609628, RRID:MGI:3609628)

Source Database: MGI, catalog # 3609628
Genetic Background: involves: 129S4/SvJae * C57BL/6J
Affected Genes: Ikbkb, Chuk
Genomic Alteration: tm1Ver
Availability: Availability unknown check source stock center
Reference: PMID:10898787
Notes: embryonic lethality during organogenesis, complete penetrance, increased hepatocyte apoptosis, liver degeneration, increased spinal cord apoptosis, abnormal neural fold elevation formation, abnormal hindbrain morphology, abnormal dorsal root ganglion morphology, increased embryonic neuroepithelium apoptosis, open neural tube, small embryonic telencephalon, increased hindbrain apoptosis, abnormal cell physiology Allele Detail: Targeted

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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# 5428758, RRID:MGI:5428758)

Source Database: MGI, catalog # 5428758
Genetic Background: involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * SJL
Affected Genes: Arap3
Genomic Alteration: Tg(Tek-cre)1Ywa; tm1.1Sve; tm1.2Sve
Availability: Availability unknown check source stock center
Reference: PMID:20978237
Notes: abnormal vitelline vascular remodeling, pallor, abnormal placenta labyrinth morphology, abnormal placenta vasculature, decreased placental labyrinth size, embryonic growth arrest, embryonic lethality during organogenesis, complete penetrance, decreased embryo size, excessive folding of visceral yolk sac, pale yolk sac, abnormal vitelline vasculature morphology, abnormal brain vasculature morphology, abnormal developmental vascular remodeling Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 5509043, RRID:MGI:5509043)

Source Database: MGI, catalog # 5509043
Genetic Background: involves: C57BL/6J * C57BL/6N
Affected Genes: Cluap1
Genomic Alteration: tm1a(KOMP)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:23351563
Notes: absent embryonic cilia, embryonic lethality during organogenesis, complete penetrance, abnormal embryo turning, kinked neural tube, decreased body size, enlarged pericardium 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# 4946623, RRID:MGI:4946623)

Source Database: MGI, catalog # 4946623
Genetic Background: involves: 129S4/SvJae * C57BL/6 * SJL
Affected Genes: Hic1
Genomic Alteration: tm1.2Kori
Availability: Availability unknown check source stock center
Reference: PMID:21309068
Notes: embryonic lethality during organogenesis, complete penetrance Allele Detail: Targeted

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