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on page 1 showing 20 out of 1,834 results

Cite this (IMSR Cat# EM:06933, RRID:IMSR_EM:06933)

Source Database: IMSR, catalog # EM:06933
Genetic Background:
Affected Genes: Fyn
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: Fyn proto-oncogene; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# EM:06865, RRID:IMSR_EM:06865)

Source Database: IMSR, catalog # EM:06865
Genetic Background:
Affected Genes: Elmo1
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: engulfment and cell motility 1; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (MGI Cat# 5544023, RRID:MGI:5544023)

Source Database: MGI, catalog # 5544023
Genetic Background: involves: C57BL/6N
Affected Genes: Asxl1
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:23870131
Notes: eye opacity, opacity of vitreous body Allele Detail: Targeted

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Cite this (IMSR Cat# HAR:6775, RRID:IMSR_HAR:6775)

Source Database: IMSR, catalog # HAR:6775
Genetic Background:
Affected Genes: Gtf2e2
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: general transcription factor II E, polypeptide 2 (beta subunit); mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (MGI Cat# 5700880, RRID:MGI:5700880)

Source Database: MGI, catalog # 5700880
Genetic Background: C57BL/6N-Erlin2/Wtsi
Affected Genes: Erlin2
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: decreased circulating insulin level, abnormal bone structure, decreased bone mineral content, abnormal hair growth Allele Detail: Targeted

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Cite this (MGI Cat# 5696540, RRID:MGI:5696540)

Source Database: MGI, catalog # 5696540
Genetic Background: involves: C57BL/6N
Affected Genes: Atg16l1
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:23973919
Notes: prenatal lethality Allele Detail: Targeted

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Cite this (IMSR Cat# HAR:6024, RRID:IMSR_HAR:6024)

Source Database: IMSR, catalog # HAR:6024
Genetic Background:
Affected Genes: Prelid2
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: PRELI domain containing 2; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# EM:08644, RRID:IMSR_EM:08644)

Source Database: IMSR, catalog # EM:08644
Genetic Background:
Affected Genes: Churc1
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: live mouse
Reference:
Notes: gene symbol note: churchill domain containing 1; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (MGI Cat# 5631341, RRID:MGI:5631341)

Source Database: MGI, catalog # 5631341
Genetic Background: C57BL/6N-Ndufb8/Wtsi
Affected Genes: Ndufb8
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 (IMSR Cat# EM:09086, RRID:IMSR_EM:09086)

Source Database: IMSR, catalog # EM:09086
Genetic Background:
Affected Genes: Cyp7a1
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: cytochrome P450, family 7, subfamily a, polypeptide 1; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# EM:05893, RRID:IMSR_EM:05893)

Source Database: IMSR, catalog # EM:05893
Genetic Background:
Affected Genes: Trim66
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: tripartite motif-containing 66; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# HAR:6883, RRID:IMSR_HAR:6883)

Source Database: IMSR, catalog # HAR:6883
Genetic Background:
Affected Genes: Aqp1
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: aquaporin 1; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# EM:07651, RRID:IMSR_EM:07651)

Source Database: IMSR, catalog # EM:07651
Genetic Background:
Affected Genes: Ankrd11
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: ankyrin repeat domain 11; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (IMSR Cat# HAR:7785, RRID:IMSR_HAR:7785)

Source Database: IMSR, catalog # HAR:7785
Genetic Background:
Affected Genes: Lmnb1
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: lamin B1; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (MGI Cat# 5781642, RRID:MGI:5781642)

Source Database: MGI, catalog # 5781642
Genetic Background: B6JTyr;B6N-Ide/Wtsi
Affected Genes: Ide
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: abnormal cranium morphology, decreased circulating cholesterol level, decreased body weight, decreased total body fat amount, decreased circulating aspartate transaminase level, decreased circulating alanine transaminase level, abnormal maxilla morphology, abnormal incisor morphology, increased heart weight, increased circulating amylase level, abnormal hair texture Allele Detail: Targeted

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Cite this (IMSR Cat# EM:10225, RRID:IMSR_EM:10225)

Source Database: IMSR, catalog # EM:10225
Genetic Background:
Affected Genes: Tmem50b
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: live mouse
Reference:
Notes: gene symbol note: transmembrane protein 50B; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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Cite this (MGI Cat# 5806532, RRID:MGI:5806532)

Source Database: MGI, catalog # 5806532
Genetic Background: C57BL/6N-Asns
Affected Genes: Asns
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference: PMID:24139043
Notes: thin cerebral cortex, abnormal short term object recognition memory, enlarged lateral ventricles, abnormal cerebral cortex morphology, behavior/neurological phenotype, abnormal long term object recognition memory, decreased brain size Allele Detail: Targeted

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Cite this (MGI Cat# 5782104, RRID:MGI:5782104)

Source Database: MGI, catalog # 5782104
Genetic Background: Not Specified
Affected Genes: Hgs
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: abnormal coping response Allele Detail: Targeted

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Cite this (MGI Cat# 5782125, RRID:MGI:5782125)

Source Database: MGI, catalog # 5782125
Genetic Background: Not Specified
Affected Genes: March9
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: abnormal tail movements, abnormal bone mineralization, decreased circulating HDL cholesterol level, decreased body weight, decreased B cell number, abnormal bone structure Allele Detail: Targeted

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Cite this (IMSR Cat# EM:07324, RRID:IMSR_EM:07324)

Source Database: IMSR, catalog # EM:07324
Genetic Background:
Affected Genes: Frrs1
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: mouse cells
Reference:
Notes: gene symbol note: ferric-chelate reductase 1; mutant strain: targeted mutation 1a, Wellcome Trust Sanger Institute

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