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on page 1 showing 20 out of 883 results

Cite this (MGI Cat# 5757219, RRID:MGI:5757219)

Source Database: MGI, catalog # 5757219
Genetic Background: C57BL/6N-Hells/Ieg
Affected Genes: Hells
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# 5813004, RRID:MGI:5813004)

Source Database: MGI, catalog # 5813004
Genetic Background: C57BL/6N-Eml2/Bay
Affected Genes: Eml2
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: increased exploration in new environment, abnormal eye morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5757398, RRID:MGI:5757398)

Source Database: MGI, catalog # 5757398
Genetic Background: C57BL/6N-Nae1/Ics
Affected Genes: Nae1
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# 5756925, RRID:MGI:5756925)

Source Database: MGI, catalog # 5756925
Genetic Background: C57BL/6N-Ctnnbip1/H
Affected Genes: Ctnnbip1
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (IMSR Cat# EM:08060, RRID:IMSR_EM:08060)

Source Database: IMSR, catalog # EM:08060
Genetic Background:
Affected Genes: Epc2
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: enhancer of polycomb homolog 2; mutant strain: targeted mutation 1b, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# EM:07760, RRID:IMSR_EM:07760)

Source Database: IMSR, catalog # EM:07760
Genetic Background:
Affected Genes: Kif3b
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: live mouse
Reference:
Notes: gene symbol note: kinesin family member 3B; mutant strain: targeted mutation 1b, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# EM:09125, RRID:IMSR_EM:09125)

Source Database: IMSR, catalog # EM:09125
Genetic Background:
Affected Genes: Exosc9
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: exosome component 9; mutant strain: targeted mutation 1b, Wellcome Trust Sanger Institute

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Cite this (MGI Cat# 5757908, RRID:MGI:5757908)

Source Database: MGI, catalog # 5757908
Genetic Background: C57BL/6N-Zfp287/Wtsi
Affected Genes: Zfp287
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: increased grip strength, abnormal gait, decreased grip strength, increased rib number, abnormal thoracic vertebrae morphology, abnormal cervical vertebrae morphology Allele Detail: Targeted

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Cite this (IMSR Cat# EM:08098, RRID:IMSR_EM:08098)

Source Database: IMSR, catalog # EM:08098
Genetic Background:
Affected Genes: Ggps1
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: geranylgeranyl diphosphate synthase 1; mutant strain: targeted mutation 1b, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# HAR:5424, RRID:IMSR_HAR:5424)

Source Database: IMSR, catalog # HAR:5424
Genetic Background:
Affected Genes: Emc10
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: ER membrane protein complex subunit 10; mutant strain: targeted mutation 1b, Wellcome Trust Sanger Institute

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Cite this (MGI Cat# 5767633, RRID:MGI:5767633)

Source Database: MGI, catalog # 5767633
Genetic Background: C57BL/6N-Dhx35/Wtsi
Affected Genes: Dhx35
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: common truncal valve, scoliosis, persistent truncus arteriosis, absent connection between subcutaneous lymph vessels and lymph sac, symmetric azygos veins, abnormal vertebral artery origin, retro-esophageal left subclavian artery, abnormal adenohypophysis morphology, holoprosencephaly, abnormal vertebrae morphology, perimembraneous ventricular septal defect, absent mammary gland, abnormal brain internal capsule morphology, right aortic arch, short snout, double lumen aortic arch, thoracoschisis, muscular ventricular septal defect, preweaning lethality, complete penetrance, double outlet right ventricle, basisphenoid bone foramen, absent olfactory bulb, abnormal hypoglossal nerve topology, abnormal basilar artery morphology, abnormal optic cup morphology Allele Detail: Targeted

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Cite this (MGI Cat# 5757741, RRID:MGI:5757741)

Source Database: MGI, catalog # 5757741
Genetic Background: C57BL/6N-Smdt1/Bay
Affected Genes: Smdt1
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: prenatal lethality, preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5797921, RRID:MGI:5797921)

Source Database: MGI, catalog # 5797921
Genetic Background: C57BL/6N-Xkrx/Wtsi
Affected Genes: Xkrx
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: decreased gamma-delta T cell number, decreased KLRG1-positive NK cell number Allele Detail: Targeted

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Cite this (MGI Cat# 5757168, RRID:MGI:5757168)

Source Database: MGI, catalog # 5757168
Genetic Background: C57BL/6N-Gfpt2/Ieg
Affected Genes: Gfpt2
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: decreased threshold for auditory brainstem response, abnormal tooth morphology, decreased total body fat amount, abnormal lens morphology Allele Detail: Targeted

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Cite this (IMSR Cat# EM:08100, RRID:IMSR_EM:08100)

Source Database: IMSR, catalog # EM:08100
Genetic Background:
Affected Genes: Nxn
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: nucleoredoxin; mutant strain: targeted mutation 1b, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# EM:11852, RRID:IMSR_EM:11852)

Source Database: IMSR, catalog # EM:11852
Genetic Background:
Affected Genes: Kdm6b
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: live mouse
Reference:
Notes: gene symbol note: KDM1 lysine (K)-specific demethylase 6B; mutant strain: EUCOMM targeted mutation 1b, Wellcome Trust Sanger Institute

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Cite this (MGI Cat# 5797869, RRID:MGI:5797869)

Source Database: MGI, catalog # 5797869
Genetic Background: C57BL/6N-Tmem181a/J
Affected Genes: Tmem181a
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: increased bone mineral density Allele Detail: Targeted

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Cite this (IMSR Cat# EM:10354, RRID:IMSR_EM:10354)

Source Database: IMSR, catalog # EM:10354
Genetic Background:
Affected Genes: Zkscan17
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: zinc finger with KRAB and SCAN domains 17; mutant strain: targeted mutation 1b, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# EM:10110, RRID:IMSR_EM:10110)

Source Database: IMSR, catalog # EM:10110
Genetic Background:
Affected Genes: Gpbp1
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: GC-rich promoter binding protein 1; mutant strain: targeted mutation 1b, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# EM:10636, RRID:IMSR_EM:10636)

Source Database: IMSR, catalog # EM:10636
Genetic Background:
Affected Genes: Ifitm1
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: interferon induced transmembrane protein 1; mutant strain: targeted mutation 1b, Wellcome Trust Sanger Institute

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