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on page 1 showing 20 out of 965 results

Cite this (MGI Cat# 6305410, RRID:MGI:6305410)

Source Database: MGI, catalog # 6305410
Genetic Background: involves: C57BL/6 * C57BL/6N
Affected Genes: Ttbk2
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference: PMID:30532139
Notes: hydrocephaly, polycystic kidney, abnormal cell morphology Allele Detail: Targeted

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Cite this (IMSR Cat# EM:05474, RRID:IMSR_EM:05474)

Source Database: IMSR, catalog # EM:05474
Genetic Background:
Affected Genes: Map3k10
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: mitogen-activated protein kinase kinase kinase 10; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:08646, RRID:IMSR_EM:08646)

Source Database: IMSR, catalog # EM:08646
Genetic Background:
Affected Genes: Me2
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: malic enzyme 2, NAD(+)-dependent, mitochondrial; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:06911, RRID:IMSR_EM:06911)

Source Database: IMSR, catalog # EM:06911
Genetic Background:
Affected Genes: Casz1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: castor zinc finger 1; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:09849, RRID:IMSR_EM:09849)

Source Database: IMSR, catalog # EM:09849
Genetic Background:
Affected Genes: Usp5
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: ubiquitin specific peptidase 5 (isopeptidase T); mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:09827, RRID:IMSR_EM:09827)

Source Database: IMSR, catalog # EM:09827
Genetic Background:
Affected Genes: Ube2t
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: ubiquitin-conjugating enzyme E2T; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# CMMR:AATS, RRID:IMSR_CMMR:AATS)

Source Database: IMSR, catalog # CMMR:AATS
Genetic Background:
Affected Genes: Grtp1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: GH regulated TBC protein 1; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:10551, RRID:IMSR_EM:10551)

Source Database: IMSR, catalog # EM:10551
Genetic Background:
Affected Genes: Rap1gap2
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: RAP1 GTPase activating protein 2; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (MGI Cat# 5782034, RRID:MGI:5782034)

Source Database: MGI, catalog # 5782034
Genetic Background: C57BL/6N-BC055324/H
Affected Genes: BC055324
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: increased mean corpuscular volume, abnormal bone mineralization, increased circulating cholesterol level, decreased bone mineral density, increased circulating HDL cholesterol level, increased circulating alkaline phosphatase level Allele Detail: Targeted

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Cite this (IMSR Cat# EM:04978, RRID:IMSR_EM:04978)

Source Database: IMSR, catalog # EM:04978
Genetic Background:
Affected Genes: Wtap
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: Wilms tumour 1-associating protein; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:08576, RRID:IMSR_EM:08576)

Source Database: IMSR, catalog # EM:08576
Genetic Background:
Affected Genes: Akr7a5
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: aldo-keto reductase family 7, member A5 (aflatoxin aldehyde reductase); mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:05200, RRID:IMSR_EM:05200)

Source Database: IMSR, catalog # EM:05200
Genetic Background:
Affected Genes: Abcb11
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: ATP-binding cassette, sub-family B (MDR/TAP), member 11; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (MGI Cat# 5782159, RRID:MGI:5782159)

Source Database: MGI, catalog # 5782159
Genetic Background: C57BL/6N-Per2/H
Affected Genes: Per2
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: increased circulating alkaline phosphatase level, abnormal bone mineralization, abnormal coat/hair pigmentation Allele Detail: Targeted

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Cite this (MGI Cat# 5782182, RRID:MGI:5782182)

Source Database: MGI, catalog # 5782182
Genetic Background: C57BL/6N-Serf1/H
Affected Genes: Serf1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: increased circulating cholesterol level, increased circulating HDL cholesterol level, decreased T cell number, decreased CD8-positive, alpha-beta T cell number, increased heart weight Allele Detail: Targeted

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Cite this (IMSR Cat# HAR:4174, RRID:IMSR_HAR:4174)

Source Database: IMSR, catalog # HAR:4174
Genetic Background:
Affected Genes: Bmp7
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: bone morphogenetic protein 7; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# HAR:4243, RRID:IMSR_HAR:4243)

Source Database: IMSR, catalog # HAR:4243
Genetic Background:
Affected Genes: Dnase2b
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: deoxyribonuclease II beta; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# EM:11374, RRID:IMSR_EM:11374)

Source Database: IMSR, catalog # EM:11374
Genetic Background:
Affected Genes: Pdgfc
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: platelet-derived growth factor, C polypeptide; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (IMSR Cat# CMMR:AAYM, RRID:IMSR_CMMR:AAYM)

Source Database: IMSR, catalog # CMMR:AAYM
Genetic Background:
Affected Genes: Atp6v0d1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: ATPase, H+ transporting, lysosomal V0 subunit D1; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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

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Cite this (MGI Cat# 5782039, RRID:MGI:5782039)

Source Database: MGI, catalog # 5782039
Genetic Background: C57BL/6N-Btk/Ics
Affected Genes: Btk
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: increased CD4-positive, alpha beta T cell number, decreased body weight Allele Detail: Targeted

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