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on page 1 showing 20 out of 1,556 results

Cite this (MGI Cat# 6261904, RRID:MGI:6261904)

Source Database: MGI, catalog # 6261904
Genetic Background: B6Brd;B6Dnk;B6N-Tyr Arid2/Wtsi
Affected Genes: Arid2
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 3609649, RRID:MGI:3609649)

Source Database: MGI, catalog # 3609649
Genetic Background: involves: 129S5/SvEvBrd
Affected Genes: Spns1
Genomic Alteration: Gt(OST214133)Lex
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Gene trapped

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Cite this (MGI Cat# 6262982, RRID:MGI:6262982)

Source Database: MGI, catalog # 6262982
Genetic Background: C57BL/6N-Ndel1/J
Affected Genes: Ndel1
Genomic Alteration: tm1b(KOMP)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: abnormal embryo size, respiratory system phenotype, preweaning lethality, complete penetrance, embryonic growth retardation, abnormal tail morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5757912, RRID:MGI:5757912)

Source Database: MGI, catalog # 5757912
Genetic Background: C57BL/6N-Zfp536/Ucd
Affected Genes: Zfp536
Genomic Alteration: tm1.1(KOMP)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: cyanosis, respiratory system phenotype, preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5757552, RRID:MGI:5757552)

Source Database: MGI, catalog # 5757552
Genetic Background: C57BL/6N-Ppp4r2/Rbrc
Affected Genes: Ppp4r2
Genomic Alteration: tm2b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5757345, RRID:MGI:5757345)

Source Database: MGI, catalog # 5757345
Genetic Background: C57BL/6N-Mat2a/Rbrc
Affected Genes: Mat2a
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 6262632, RRID:MGI:6262632)

Source Database: MGI, catalog # 6262632
Genetic Background: C57BL/6NJ-Hmg20a/Mmjax
Affected Genes: Hmg20a
Genomic Alteration: em1(IMPC)J
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Endonuclease-mediated

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Cite this (MGI Cat# 5003067, RRID:MGI:5003067)

Source Database: MGI, catalog # 5003067
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Anp32b, Anp32a, Anp32e
Genomic Alteration: tm1Mak
Availability: Availability unknown check source stock center
Reference: PMID:21636789
Notes: preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 6263134, RRID:MGI:6263134)

Source Database: MGI, catalog # 6263134
Genetic Background: C57BL/6N-Pdx1/Bay
Affected Genes: Pdx1
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5767742, RRID:MGI:5767742)

Source Database: MGI, catalog # 5767742
Genetic Background: C57BL/6N-Notch1/H
Affected Genes: Notch1
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5757874, RRID:MGI:5757874)

Source Database: MGI, catalog # 5757874
Genetic Background: C57BL/6N-Vezt/J
Affected Genes: Vezt
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 6288471, RRID:MGI:6288471)

Source Database: MGI, catalog # 6288471
Genetic Background: C57BL/6N-Foxred1/Bay
Affected Genes: Foxred1
Genomic Alteration: em1(IMPC)Bay
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Endonuclease-mediated

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Cite this (MGI Cat# 3609770, RRID:MGI:3609770)

Source Database: MGI, catalog # 3609770
Genetic Background: involves: 129S5/SvEvBrd
Affected Genes: Rptor
Genomic Alteration: tm1Lex
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5756728, RRID:MGI:5756728)

Source Database: MGI, catalog # 5756728
Genetic Background: B6N(Cg)-Arid3a/J
Affected Genes: Arid3a
Genomic Alteration: tm1b(KOMP)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: hemorrhage, abnormal limb bud morphology, abnormal placenta morphology, abnormal embryo size, preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 6261902, RRID:MGI:6261902)

Source Database: MGI, catalog # 6261902
Genetic Background: C57BL/6N-Arid1b/Tcp
Affected Genes: Arid1b
Genomic Alteration: em1(IMPC)Tcp
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance, edema Allele Detail: Endonuclease-mediated

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Cite this (MGI Cat# 3697462, RRID:MGI:3697462)

Source Database: MGI, catalog # 3697462
Genetic Background: either: B6.129P2-Crb1 or (involves: 129P2/OlaHsd * C57BL/6)
Affected Genes: Crb1
Genomic Alteration: tm2Wij
Availability: Availability unknown check source stock center
Reference: PMID:17234588
Notes: preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5700966, RRID:MGI:5700966)

Source Database: MGI, catalog # 5700966
Genetic Background: C57BL/6N-Psph/Wtsi
Affected Genes: Psph
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: short Meckel's cartilage, abnormal vertebral body morphology, preweaning lethality, complete penetrance, umbilical vein stenosis, muscular ventricular septal defect, spleen hypoplasia, abnormal thyroid gland morphology, absent portal vein segment, abnormal pulmonary artery origin, absent maxilla, subcutaneous edema, absent pineal gland, absent optic chiasm, abnormal nasal septum morphology, abnormal nasal cavity morphology, abnormal optic stalk morphology, abnormal optic cup morphology, abnormal parasellar internal carotid artery branch morphology, oligodactyly, abnormal vertebral artery origin, absent stapedial artery, abnormal facial nerve topology, abnormal infrahyoid muscle connection, perimembraneous ventricular septal defect, abnormal eye muscle morphology, thin cerebral cortex, abnormal external auditory canal morphology, abnormal forebrain morphology, abnormal hindbrain morphology, absent posterior commissure, absent celiac artery, abnormal vitelline vein connection, abnormal inferior vena cava morphology, abnormal duodenum topology, heterochrony, absent neurohypophysis, absent eye muscles, abnormal olfactory nerve morphology, abnormal adenohypophysis morphology, abnormal neurohypophysis morphology, absent tongue, herniated liver, holoprosencephaly, abnormal thymus topology, basal brain tissue herniation, abnormal bile duct morphology, abnormal salivary gland morphology, abnormal olfactory bulb morphology, absent salivary gland, absent vomeronasal organ, absent segment of posterior cerebral artery, absent abducens nerve, small superior cervical ganglion, tongue hypoplasia, abnormal outer ear morphology, abnormal semicircular canal morphology, fusion of vertebral arches, fusion of vertebral bodies, abnormal pineal gland morphology, abnormal dorsal root ganglion topology, intestinal/bowel diverticulum, abnormal interatrial septum morphology, double outlet right ventricle, abnormal Wolffian duct morphology, persistent trigeminal artery, abnormal ductus venosus valve topology, trigeminal neuroma, anastomosis between middle cerebral arteries, abnormal oral cavity morphology, abnormal femur morphology, fragmented Meckel's cartilage, absent trochlear nerve, epithelioid cysts, abnormal spinal cord central canal morphology, aphakia, absent external auditory canal, aorta coarctation, absent hypoglossal nerve, abnormal hypoglossal nerve topology, absent olfactory nerve, small salivary gland, athymia, embryo cyst, abnormal thymus morphology, intraembryonal intestine elongation, abnormal larynx morphology, abnormal vomeronasal organ morphology, absent brain internal capsule, abnormal brain internal capsule morphology, abnormal middle ear ossicle morphology, rib fusion, abnormal pelvic girdle bone morphology, increased rib number, persistent truncus arteriosis, absent olfactory bulb, abnormal midbrain morphology, blood in lymph vessels, absent connection between subcutaneous lymph vessels and lymph sac, thoracoschisis, abnormal choroid plexus morphology, abnormal lens morphology, fetal growth retardation, small kidney, abnormal sphenoid bone morphology, abnormal brain commissure morphology, abnormal posterior semicircular canal morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3609658, RRID:MGI:3609658)

Source Database: MGI, catalog # 3609658
Genetic Background: involves: 129S5/SvEvBrd * C57BL/6J
Affected Genes: Cdc25a
Genomic Alteration: Gt(OST186277)Lex
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance Allele Detail: Gene trapped

  • From Current Category

Cite this (MGI Cat# 5630969, RRID:MGI:5630969)

Source Database: MGI, catalog # 5630969
Genetic Background: C57BL/6N-Chtop/Wtsi
Affected Genes: Chtop
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: fused dorsal root ganglion, abnormal optic cup morphology, subcutaneous edema, spleen hypoplasia, absent extracranial vertebral artery segment, abnormal vertebral artery topology, ductus venosus stenosis, heterochrony, common atrium, abnormal pineal gland morphology, ostium primum atrial septal defect, absent hypoglossal nerve, fusion of vertebral arches, absent vertebral arch, abnormal cervical atlas morphology, anomalous pulmonary venous connection, absent dorsal root ganglion, abnormal eye morphology, perimembraneous ventricular septal defect, thyroid hypoplasia, abnormal hyoid bone body morphology, abnormal neurohypophysis morphology, absent celiac artery, abnormal olfactory bulb position, abnormal vertebral body morphology, abnormal rectum morphology, abnormal small intestine placement, decreased rib number, thin hypoglossal nerve, retro-esophageal left subclavian artery, internal hemorrhage, muscular ventricular septal defect, abnormal optic stalk morphology, rib fusion, reduced sympathetic cervical ganglion size, abnormal pancreas topology, anastomosis between common carotid and vertebral artery, abnormal adenohypophysis morphology, abnormal dorsal pancreas topology, double outlet right ventricle, abnormal subclavian artery origin, absent costovertebral joint, abnormal choroid plexus morphology, small superior cervical ganglion, abnormal abdominal muscle morphology, abnormal hepatic portal vein formation, abnormal viscerocranium morphology, persistent truncus arteriosis, myelocele, embryo cyst, abnormal atrioventricular valve morphology, diaphragmatic hernia, abnormal interventricular foramen morphology, abnormal brachial plexus formation, intestinal stenosis, fetal growth retardation, abnormal ureter topology, abnormal eye muscle morphology, absent parasellar internal carotid artery, retroesophageal right subclavian artery, fused right lung lobes, abnormal maxilla morphology, abnormal salivary gland morphology, decreased cervical vertebrae number, absent vertebrae, urinary bladder hypoplasia, holoprosencephaly, fusion of atlas and occipital bones, right aortic arch, abnormal forebrain morphology, abnormal hepatic portal vein morphology, abnormal Wolffian duct morphology, blind ureter, absent olfactory bulb, arteriovenous malformation, abnormal vitelline vein topology, absent intrahepatic inferior vena cava segment, absent spleen, scoliosis, abnormal vitelline vein connection, bicuspid aortic valve, decreased thoracic vertebrae number, abnormal fetal atrioventricular canal morphology, abnormal thyroid gland morphology, abnormal ductus venosus valve topology, pelvic kidney, absent hypoglossal canal, anal atresia, absent ductus venosus valve, small nodose ganglion, rib bifurcation, abnormal carotid artery origin, abnormal azygos vein topology, preweaning lethality, complete penetrance, abnormal ductus venosus morphology Allele Detail: Targeted

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Cite this (MGI Cat# 6288348, RRID:MGI:6288348)

Source Database: MGI, catalog # 6288348
Genetic Background: C57BL/6N-Atp6v1h/Bay
Affected Genes: Atp6v1h
Genomic Alteration: em1(IMPC)Bay
Availability: Availability unknown check source stock center
Reference:
Notes: embryonic lethality prior to organogenesis, preweaning lethality, complete penetrance Allele Detail: Endonuclease-mediated

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