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on page 1 showing 20 out of 1,378 results

Cite this (MGI Cat# 5474869, RRID:MGI:5474869)

Source Database: MGI, catalog # 5474869
Genetic Background: involves: BALB/c * C57BL/6
Affected Genes: Etv2, Tg(Pgk1-cre)1Lni
Genomic Alteration: tm1Vkou; Tg(Pgk1-cre)1Lni
Availability: Availability unknown check source stock center
Reference: PMID:22570122
Notes: absent erythroid progenitor cell, absent erythrocytes, embryonic lethality during organogenesis, complete penetrance, embryonic growth retardation Allele Detail: Targeted, Transgenic

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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# 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# 2181514, RRID:MGI:2181514)

Source Database: MGI, catalog # 2181514
Genetic Background: either: (involves: 129S/SvEv * 129X1/SvJ) or (involves: 129X1/SvJ * C57BL/6J)
Affected Genes: Jun
Genomic Alteration: tm1Pa
Availability: Availability unknown check source stock center
Reference: PMID:8330736
Notes: decreased fibroblast proliferation, embryonic lethality during organogenesis, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5009024, RRID:MGI:5009024)

Source Database: MGI, catalog # 5009024
Genetic Background: (CKH.Cg-Ebp x NJL)F1
Affected Genes: Ebp
Genomic Alteration: Td-ho
Availability: Availability unknown check source stock center
Reference: PMID:10987663, PMID:9250864
Notes: abnormal embryonic hematopoiesis, embryonic lethality during organogenesis, complete penetrance, abnormal embryonic erythrocyte morphology, abnormal embryonic erythropoiesis Allele Detail: Spontaneous

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Cite this (MGI Cat# 5443840, RRID:MGI:5443840)

Source Database: MGI, catalog # 5443840
Genetic Background: involves: 129S6/SvEvTac * C57BL/6
Affected Genes: Erg
Genomic Alteration: tm2Poet
Availability: Availability unknown check source stock center
Reference: PMID:22932696
Notes: decreased embryo size, internal hemorrhage, abnormal vascular development, embryonic lethality during organogenesis, complete penetrance, abnormal heart development, abnormal placental labyrinth vasculature morphology, abnormal developmental vascular remodeling, intracranial hemorrhage, pericardial effusion Allele Detail: Targeted

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Cite this (MGI Cat# 3711513, RRID:MGI:3711513)

Source Database: MGI, catalog # 3711513
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2
Affected Genes: Cxadr
Genomic Alteration: Tg(Tnnt2-cre)5Blh; tm1.1Mds; tm1Mds
Availability: Availability unknown check source stock center
Reference: PMID:16543498
Notes: abnormal cardinal vein morphology, abnormal heart valve morphology, abnormal heart tube morphology, embryonic lethality during organogenesis, complete penetrance Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 4868429, RRID:MGI:4868429)

Source Database: MGI, catalog # 4868429
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac
Affected Genes: Mmp15, Mmp14
Genomic Alteration: tm1Kohl; tm1Hbh
Availability: Availability unknown check source stock center
Reference: PMID:20858856
Notes: abnormal placenta labyrinth morphology, abnormal placental labyrinth vasculature morphology, dilated vasculature, decreased embryo size, embryonic lethality during organogenesis, complete penetrance, embryonic growth retardation, enlarged pericardium Allele Detail: Targeted

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Cite this (MGI Cat# 4821992, RRID:MGI:4821992)

Source Database: MGI, catalog # 4821992
Genetic Background: B6.129P2-Cdh1
Affected Genes: Cdh1
Genomic Alteration: tm1.1Mpst
Availability: Availability unknown check source stock center
Reference: PMID:20652949
Notes: placental labyrinth hypoplasia, abnormal placental labyrinth vasculature morphology, pallor, pale yolk sac, abnormal placenta physiology, abnormal trophoblast layer morphology, embryonic lethality during organogenesis, complete penetrance, embryonic growth arrest, abnormal placenta morphology, decreased placental labyrinth size 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# 3811915, RRID:MGI:3811915)

Source Database: MGI, catalog # 3811915
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * CBA
Affected Genes: Edil3, Myc
Genomic Alteration: tm2.1Atp; Tg(Sox2-cre)1Amc
Availability: Availability unknown check source stock center
Reference: PMID:18550708
Notes: abnormal proerythroblast morphology, abnormal common myeloid progenitor cell morphology, cardiovascular system phenotype, liver hypoplasia, impaired hematopoiesis, embryonic lethality during organogenesis, complete penetrance, decreased erythroid progenitor cell number, decreased embryo size, pale yolk sac Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 2673583, RRID:MGI:2673583)

Source Database: MGI, catalog # 2673583
Genetic Background: Not Specified
Affected Genes: l11Jus5
Genomic Alteration: l11Jus5
Availability: Availability unknown check source stock center
Reference: PMID:12955145, PMID:16466971
Notes: failure of chorioallantoic fusion, abnormal extraembryonic tissue morphology, embryonic lethality during organogenesis, complete penetrance Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3584534, RRID:MGI:3584534)

Source Database: MGI, catalog # 3584534
Genetic Background: either: (involves: 129S1/Sv) or (involves: 129S1/Sv * C57BL/6)
Affected Genes: Zfpm1
Genomic Alteration: tm2Sho
Availability: Availability unknown check source stock center
Reference: PMID:9553047
Notes: abnormal vitelline vasculature morphology, impaired hematopoiesis, abnormal erythropoiesis, pale liver, anemia, small liver, embryonic lethality during organogenesis, complete penetrance, pallor, abnormal embryonic erythropoiesis, abnormal megakaryocyte differentiation, decreased embryo size, pale yolk sac Allele Detail: Targeted

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Cite this (MGI Cat# 2168563, RRID:MGI:2168563)

Source Database: MGI, catalog # 2168563
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/cIco
Affected Genes: Cdh5
Genomic Alteration: tm1Hub
Availability: Availability unknown check source stock center
Reference: PMID:10207135
Notes: decreased angiogenesis, absent vitelline blood vessels, abnormal visceral yolk sac blood island morphology, irregular heartbeat, abnormal intersomitic vessel morphology, incomplete somite formation, incomplete embryo turning, dilated dorsal aorta, pallor, abnormal cell death, abnormal umbilical cord blood vessel morphology, distended pericardium, abnormal vasculogenesis, embryonic growth retardation, abnormal umbilical artery morphology, embryonic lethality during organogenesis, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 3625275, RRID:MGI:3625275)

Source Database: MGI, catalog # 3625275
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Pttg1, Espl1
Genomic Alteration: tm1.2Kna
Availability: Availability unknown check source stock center
Reference: PMID:16533945
Notes: abnormal mitosis, abnormal cell nucleus morphology, abnormal mitotic spindle morphology, abnormal cell death, embryonic lethality during organogenesis, complete penetrance, decreased embryo size, abnormal somite development, abnormal neural tube morphology Allele Detail: Targeted

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Cite this (MGI Cat# 6195768, RRID:MGI:6195768)

Source Database: MGI, catalog # 6195768
Genetic Background: involves: C57BL/6N * C57BL/6NCrlj * CBA/JNCrlj * SJL
Affected Genes: Bcas3
Genomic Alteration: Tg(Tek-cre)1Ywa; tm1Msin
Availability: Availability unknown check source stock center
Reference: PMID:29618843
Notes: decreased angiogenesis, abnormal intersomitic vessel morphology, abnormal head morphology, small heart, embryonic lethality during organogenesis, complete penetrance, abnormal visceral yolk sac morphology, abnormal endocardium morphology, abnormal dorsal aorta morphology, abnormal placenta morphology, abnormal vascular branching morphogenesis, abnormal vascular development, abnormal capillary morphology, small placenta Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 3042138, RRID:MGI:3042138)

Source Database: MGI, catalog # 3042138
Genetic Background: involves: 129P2/OlaHsd * 129/Sv
Affected Genes: Raf1
Genomic Alteration: tm1Bacc
Availability: Availability unknown check source stock center
Reference: PMID:11296228
Notes: decreased sensitivity to induced cell death, decreased embryo size, abnormal liver sinusoid morphology, increased hepatoblast apoptosis, increased fibroblast apoptosis, abnormal hepatocyte morphology, small placenta, pallor, small liver, embryonic growth retardation, decreased placenta weight, decreased embryo weight, abnormal placenta labyrinth morphology, abnormal placental labyrinth vasculature morphology, decreased spongiotrophoblast size, embryonic lethality during organogenesis, complete penetrance, pale liver, liver hypoplasia, increased sensitivity to induced cell death Allele Detail: Targeted

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Cite this (MGI Cat# 3052977, RRID:MGI:3052977)

Source Database: MGI, catalog # 3052977
Genetic Background: involves: 129S/SvEv * C57BL/6
Affected Genes: Myocd
Genomic Alteration: tm1Eno
Availability: Availability unknown check source stock center
Reference: PMID:12867591
Notes: abnormal blood vessel morphology, absent vitelline blood vessels, embryonic growth retardation, pale yolk sac, cardiovascular system phenotype, abnormal vascular smooth muscle morphology, pericardial effusion, embryonic lethality during organogenesis, complete penetrance, abnormal dorsal aorta morphology Allele Detail: Targeted

  • From Current Category

Cite this (MGI Cat# 5896564, RRID:MGI:5896564)

Source Database: MGI, catalog # 5896564
Genetic Background: involves: C57BL/6J * C57BL/6N
Affected Genes: Brpf1
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:24646517
Notes: embryonic growth arrest, embryonic lethality during organogenesis, complete penetrance, abnormal embryo morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5006951, RRID:MGI:5006951)

Source Database: MGI, catalog # 5006951
Genetic Background: involves: 129S1/Sv * C57BL/6 * FVB/NJ
Affected Genes: arco
Genomic Alteration: arco
Availability: Availability unknown check source stock center
Reference: PMID:21305688
Notes: abnormal nervous system development, abnormal glossopharyngeal ganglion morphology, abnormal cranial ganglia morphology, abnormal pharyngeal arch artery morphology, abnormal blood vessel morphology, small second pharyngeal arch, small pharyngeal arch, embryonic lethality during organogenesis, complete penetrance, decreased embryo size, abnormal trigeminal ganglion morphology Allele Detail: Chemically induced (ENU)

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