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on page 1 showing 20 out of 926 results

Cite this (MGI Cat# 5450473, RRID:MGI:5450473)

Source Database: MGI, catalog # 5450473
Genetic Background: Not Specified
Affected Genes: Abcd4
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: abnormal response to new environment, abnormal response to tactile stimuli Allele Detail: Targeted

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Cite this (MGI Cat# 6192632, RRID:MGI:6192632)

Source Database: MGI, catalog # 6192632
Genetic Background: C57BL/6-Rem2
Affected Genes: Rem2
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference: PMID:29809135
Notes: decreased litter size, decreased survivor rate Allele Detail: Targeted

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Cite this (MGI Cat# 5782154, RRID:MGI:5782154)

Source Database: MGI, catalog # 5782154
Genetic Background: C57BL/6N-Pacs2/Ics
Affected Genes: Pacs2
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: short tibia, decreased grip strength, abnormal behavior Allele Detail: Targeted

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Cite this (MGI Cat# 5608494, RRID:MGI:5608494)

Source Database: MGI, catalog # 5608494
Genetic Background: C57BL/6N-Xxylt1/Wtsi
Affected Genes: Xxylt1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: increased total body fat amount, decreased blood urea nitrogen level, increased KLRG1-positive NK cell number, abnormal retina morphology, absent vibrissae, decreased lean body mass, abnormal retinal pigmentation Allele Detail: Targeted

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Cite this (MGI Cat# 5705958, RRID:MGI:5705958)

Source Database: MGI, catalog # 5705958
Genetic Background: C57BL/6N-Bap1/Wtsi
Affected Genes: Bap1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: increased effector memory CD4-positive, alpha-beta T cell number, decreased KLRG1-positive NK cell number, increased circulating alkaline phosphatase level, increased monocyte cell number Allele Detail: Targeted

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Cite this (MGI Cat# 5782233, RRID:MGI:5782233)

Source Database: MGI, catalog # 5782233
Genetic Background: C57BL/6N-Zfp760/Ieg
Affected Genes: Zfp760
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: decreased IgE level, increased hematocrit, thrombocytopenia, decreased body weight, increased circulating serum albumin level, increased erythrocyte cell number Allele Detail: Targeted

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Cite this (MGI Cat# 5782171, RRID:MGI:5782171)

Source Database: MGI, catalog # 5782171
Genetic Background: C57BL/6N-Ric1/H
Affected Genes: Ric1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: decreased erythrocyte cell number, decreased B cell number, decreased hematocrit, increased mean corpuscular volume, abnormal bone mineralization, decreased mature B cell number, increased circulating alkaline phosphatase level, increased heart weight, decreased leukocyte cell number, decreased body weight, increased grip strength, decreased hemoglobin content, abnormal bone structure 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: abnormal outer ear morphology, blood in lymph vessels, fusion of vertebral arches, fusion of vertebral bodies, small superior cervical ganglion, abnormal lens morphology, abnormal brain internal capsule morphology, absent abducens nerve, abnormal posterior semicircular canal morphology, absent brain internal capsule, abnormal nasal septum morphology, abnormal nasal cavity morphology, absent optic chiasm, absent pineal gland, rib fusion, persistent trigeminal artery, abnormal Wolffian duct morphology, absent segment of posterior cerebral artery, abnormal thyroid gland morphology, abnormal dorsal root ganglion topology, absent vomeronasal organ, absent olfactory bulb, oligodactyly, abnormal parasellar internal carotid artery branch morphology, absent maxilla, preweaning lethality, complete penetrance, abnormal pulmonary artery origin, thoracoschisis, persistent truncus arteriosis, muscular ventricular septal defect, abnormal pineal gland morphology, spleen hypoplasia, absent salivary gland, subcutaneous edema, abnormal pelvic girdle bone morphology, absent portal vein segment, abnormal olfactory bulb morphology, abnormal salivary gland morphology, abnormal facial nerve topology, small salivary gland, athymia, embryo cyst, abnormal thymus morphology, tongue hypoplasia, perimembraneous ventricular septal defect, abnormal bile duct morphology, abnormal midbrain morphology, basal brain tissue herniation, abnormal thymus topology, short Meckel's cartilage, intraembryonal intestine elongation, abnormal choroid plexus morphology, aorta coarctation, abnormal infrahyoid muscle connection, holoprosencephaly, abnormal femur morphology, absent external auditory canal, abnormal middle ear ossicle morphology, absent tongue, abnormal neurohypophysis morphology, abnormal adenohypophysis morphology, abnormal olfactory nerve morphology, absent eye muscles, absent neurohypophysis, aphakia, herniated liver, umbilical vein stenosis, abnormal vertebral body morphology, intestinal/bowel diverticulum, abnormal interatrial septum morphology, absent stapedial artery, abnormal eye muscle morphology, abnormal semicircular canal morphology, double outlet right ventricle, heterochrony, abnormal duodenum topology, thin cerebral cortex, abnormal external auditory canal morphology, abnormal ductus venosus valve topology, trigeminal neuroma, absent trochlear nerve, absent hypoglossal nerve, abnormal hypoglossal nerve topology, absent olfactory nerve, abnormal hindbrain morphology, abnormal larynx morphology, absent posterior commissure, absent celiac artery, abnormal vitelline vein connection, abnormal inferior vena cava morphology, abnormal optic stalk morphology, abnormal optic cup morphology, anastomosis between middle cerebral arteries, abnormal spinal cord central canal morphology, abnormal vomeronasal organ morphology, epithelioid cysts, abnormal sphenoid bone morphology, abnormal oral cavity morphology, abnormal brain commissure morphology, abnormal vertebral artery origin, abnormal forebrain morphology, fetal growth retardation, small kidney, increased rib number, absent connection between subcutaneous lymph vessels and lymph sac, fragmented Meckel's cartilage Allele Detail: Targeted

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Cite this (MGI Cat# 5782071, RRID:MGI:5782071)

Source Database: MGI, catalog # 5782071
Genetic Background: C57BL/6N-Elmod1/H
Affected Genes: Elmod1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: decreased body weight, abnormal behavior, increased circulating alkaline phosphatase level, decreased circulating cholesterol level, decreased grip strength, decreased leukocyte cell number, increased hemoglobin content, thrombocytopenia, increased blood urea nitrogen level, decreased circulating HDL cholesterol level, decreased B cell number, decreased prepulse inhibition, decreased hemoglobin content, abnormal locomotor activation, tremors, decreased circulating glucose level, abnormal coping response, increased circulating chloride level, abnormal response to tactile stimuli, abnormal startle reflex, abnormal gait Allele Detail: Targeted

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Cite this (MGI Cat# 5780454, RRID:MGI:5780454)

Source Database: MGI, catalog # 5780454
Genetic Background: C57BL/6-Katnb1
Affected Genes: Katnb1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference: PMID:25521379
Notes: increased brain apoptosis, thin cerebral cortex, abnormal embryo morphology, abnormal erythropoiesis, abnormal forebrain morphology, decreased brain size, small limb buds, loss of cortex neurons, microphthalmia, pale liver, lethality throughout fetal growth and development, complete penetrance, abnormal cortical ventricular zone morphology, abnormal cell morphology, abnormal neuronal precursor proliferation, anophthalmia, decreased embryo size, abnormal mitotic spindle morphology, abnormal mitosis, holoprosencephaly, aneuploidy, binucleate, decreased fibroblast proliferation, abnormal primary cilium morphology, decreased neuronal precursor cell number Allele Detail: Targeted

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Cite this (MGI Cat# 5631451, RRID:MGI:5631451)

Source Database: MGI, catalog # 5631451
Genetic Background: C57BL/6N-Pth1r/Wtsi
Affected Genes: Pth1r
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: increased hemangioma incidence, anastomosis between internal carotid artery and basilar artery, hemorrhage, dilated bile duct, blood in lymph vessels, jugular vein stenosis, decreased total retina thickness, abnormal thymus morphology, enlarged paraumbilical vein, preweaning lethality, complete penetrance, herniated liver, enlarged lymphatic vessel, abnormal lens morphology, abnormal inferior vena cava valve morphology, retropharyngeal edema, absent ductus venosus valve, abnormal brain morphology, abnormal ductus venosus valve morphology, absent segment of posterior cerebral artery, abnormal vertebral artery topology Allele Detail: Targeted

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Cite this (IMSR Cat# EM:07605, RRID:IMSR_EM:07605)

Source Database: IMSR, catalog # EM:07605
Genetic Background:
Affected Genes: Krt8
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: keratin 8; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:07824, RRID:IMSR_EM:07824)

Source Database: IMSR, catalog # EM:07824
Genetic Background:
Affected Genes: Plscr1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: phospholipid scramblase 1; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:04697, RRID:IMSR_EM:04697)

Source Database: IMSR, catalog # EM:04697
Genetic Background:
Affected Genes: Tbc1d2b
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: TBC1 domain family, member 2B; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# HAR:5871, RRID:IMSR_HAR:5871)

Source Database: IMSR, catalog # HAR:5871
Genetic Background:
Affected Genes: F7
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: coagulation factor VII; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:04455, RRID:IMSR_EM:04455)

Source Database: IMSR, catalog # EM:04455
Genetic Background:
Affected Genes: Mtch2
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: mitochondrial carrier 2; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# HAR:3396, RRID:IMSR_HAR:3396)

Source Database: IMSR, catalog # HAR:3396
Genetic Background:
Affected Genes: Dpm2
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: dolichol-phosphate (beta-D) mannosyltransferase 2; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:09370, RRID:IMSR_EM:09370)

Source Database: IMSR, catalog # EM:09370
Genetic Background:
Affected Genes: Rbl1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: RB transcriptional corepressor like 1; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:09698, RRID:IMSR_EM:09698)

Source Database: IMSR, catalog # EM:09698
Genetic Background:
Affected Genes: Stx5a
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: syntaxin 5A; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# HAR:4981, RRID:IMSR_HAR:4981)

Source Database: IMSR, catalog # HAR:4981
Genetic Background:
Affected Genes: Tpcn2
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: two pore segment channel 2; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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