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on page 1 showing 20 out of 1,105 results from 1 sources

Cite this (MGI Cat# 5797925, RRID:MGI:5797925)

Source Database: MGI, catalog # 5797925
Genetic Background: Not Specified
Affected Genes: Zfp148
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: No longer indexed by source database
Reference:
Notes: NULL Allele Detail: Targeted

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Cite this (IMSR Cat# RBRC06442, RRID:IMSR_RBRC06442)

Source Database: IMSR, catalog # RBRC06442
Genetic Background:
Affected Genes: Atp13a2
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: ATPase type 13A2; mutant strain: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH

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Cite this (MGI Cat# 5757386, RRID:MGI:5757386)

Source Database: MGI, catalog # 5757386
Genetic Background: C57BL/6N-Mybbp1a/Ieg
Affected Genes: Mybbp1a
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# 5887314, RRID:MGI:5887314)

Source Database: MGI, catalog # 5887314
Genetic Background: C57BL/6N-Bhmt/Bay
Affected Genes: Bhmt
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (IMSR Cat# EM:08418, RRID:IMSR_EM:08418)

Source Database: IMSR, catalog # EM:08418
Genetic Background:
Affected Genes: Sgip1
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: SH3-domain GRB2-like (endophilin) interacting protein 1; mutant strain: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH

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Cite this (MGI Cat# 5887489, RRID:MGI:5887489)

Source Database: MGI, catalog # 5887489
Genetic Background: C57BL/6N-Psmf1/Rbrc
Affected Genes: Psmf1
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (MGI Cat# 5631265, RRID:MGI:5631265)

Source Database: MGI, catalog # 5631265
Genetic Background: C57BL/6N-Lifr/H
Affected Genes: Lifr
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: No longer indexed by source database
Reference:
Notes: NULL Allele Detail: Targeted

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Cite this (IMSR Cat# EM:10112, RRID:IMSR_EM:10112)

Source Database: IMSR, catalog # EM:10112
Genetic Background:
Affected Genes: Slc44a4
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: solute carrier family 44, member 4; mutant strain: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH

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Cite this (MGI Cat# 5756795, RRID:MGI:5756795)

Source Database: MGI, catalog # 5756795
Genetic Background: C57BL/6N-BC055324/H
Affected Genes: BC055324
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage, preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (IMSR Cat# EM:09352, RRID:IMSR_EM:09352)

Source Database: IMSR, catalog # EM:09352
Genetic Background:
Affected Genes: Slc13a5
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: solute carrier family 13 (sodium-dependent citrate transporter), member 5; mutant strain: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH

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Cite this (MGI Cat# 5797909, RRID:MGI:5797909)

Source Database: MGI, catalog # 5797909
Genetic Background: C57BL/6N-Vsig4/J
Affected Genes: Vsig4
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: hyperactivity, decreased leukocyte cell number, abnormal behavior, decreased grip strength, increased vertical activity, increased circulating potassium level, abnormal sleep behavior, abnormal behavioral response to light, shortened PQ interval, decreased circulating glucose level, increased circulating alanine transaminase level, improved glucose tolerance Allele Detail: Targeted

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Cite this (MGI Cat# 5757291, RRID:MGI:5757291)

Source Database: MGI, catalog # 5757291
Genetic Background: C57BL/6N-Klhl29/Ics
Affected Genes: Klhl29
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: increased or absent threshold for auditory brainstem response Allele Detail: Targeted

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Cite this (MGI Cat# 5757380, RRID:MGI:5757380)

Source Database: MGI, catalog # 5757380
Genetic Background: C57BL/6N-Mtch2/Cnrm
Affected Genes: Mtch2
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: embryonic lethality prior to tooth bud stage, preweaning lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5757525, RRID:MGI:5757525)

Source Database: MGI, catalog # 5757525
Genetic Background: C57BL/6N-Pla2g10/Ieg
Affected Genes: Pla2g10
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: abnormal lens morphology, oligodactyly Allele Detail: Targeted

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Cite this (MGI Cat# 5756974, RRID:MGI:5756974)

Source Database: MGI, catalog # 5756974
Genetic Background: C57BL/6N-Dcps/J
Affected Genes: Dcps
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (IMSR Cat# EM:09252, RRID:IMSR_EM:09252)

Source Database: IMSR, catalog # EM:09252
Genetic Background:
Affected Genes: Zfp445
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: zinc finger protein 445; mutant strain: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH

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Cite this (MGI Cat# 5757778, RRID:MGI:5757778)

Source Database: MGI, catalog # 5757778
Genetic Background: C57BL/6N-Supt4a/Tcp
Affected Genes: Supt4a
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: preweaning lethality, complete penetrance, embryonic lethality prior to tooth bud stage, embryonic lethality prior to organogenesis Allele Detail: Targeted

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Cite this (MGI Cat# 5756940, RRID:MGI:5756940)

Source Database: MGI, catalog # 5756940
Genetic Background: C57BL/6N-Cyp27b1/Tcp
Affected Genes: Cyp27b1
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: decreased heart weight, decreased bone mineral density, decreased circulating glucose level, abnormal behavior, decreased total body fat amount, abnormal scapula morphology, abnormal joint morphology, abnormal ulna morphology, abnormal clavicle morphology, abnormal humerus morphology, decreased circulating HDL cholesterol level, abnormal cranium morphology, increased erythrocyte cell number, hypoactivity, absent mammary gland, decreased skeletal muscle mass, thin skin, short tibia, decreased lean body mass, abnormal radius morphology, abnormal tibia morphology, abnormal femur morphology, abnormal pelvic girdle bone morphology, small uterus, increased circulating bilirubin level, abnormal vertebrae morphology, small heart, abnormal fibula morphology, increased circulating alkaline phosphatase level, abnormal rib morphology, decreased grip strength, abnormal bone structure, decreased circulating calcium level, decreased leukocyte cell number, small ovary, decreased circulating cholesterol level, decreased body length, decreased bone mineral content, decreased vertical activity, small kidney, small spleen, increased respiratory quotient Allele Detail: Targeted

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Cite this (MGI Cat# 5757624, RRID:MGI:5757624)

Source Database: MGI, catalog # 5757624
Genetic Background: C57BL/6N-Ric8b/Cnrm
Affected Genes: Ric8b
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: decreased bone mineral content, decreased kidney weight, increased leukocyte cell number, decreased heart weight, decreased lean body mass, decreased bone mineral density Allele Detail: Targeted

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Cite this (MGI Cat# 5887442, RRID:MGI:5887442)

Source Database: MGI, catalog # 5887442
Genetic Background: C57BL/6N-Mfsd8/H
Affected Genes: Mfsd8
Genomic Alteration: tm1b(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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