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on page 1 showing 20 out of 619,294 results from 1 sources

Cite this (IMSR Cat# TIGM:IST14809G7, RRID:IMSR_TIGM:IST14809G7)

Source Database: IMSR, catalog # TIGM:IST14809G7
Genetic Background:
Affected Genes: Camk1d
Genomic Alteration: Gt(IST14809G7)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: calcium/calmodulin-dependent protein kinase ID; unclassified: gene trap IST14809G7, Texas A&M Institute for Genomic Medicine

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Cite this (MMRRC Cat# 024719-UCD, RRID:MMRRC_024719-UCD)

Source Database: MMRRC, catalog # 024719-UCD
Genetic Background: Gene Trap
Affected Genes: Epb41
Genomic Alteration:
Availability:
Reference:
Notes: Mutation type: Gene Trap

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Cite this (IMSR Cat# EM:01263, RRID:IMSR_EM:01263)

Source Database: IMSR, catalog # EM:01263
Genetic Background:
Affected Genes: mhdadcc5
Genomic Alteration: mhdadcc5
Availability: mouse cells
Reference:
Notes: gene symbol note: Martin Hrabe de Angelis dark coat color 5; mutant strain: Martin Hrabe de Angelis dark coat color 5

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Cite this (BDSC Cat# 42814, RRID:BDSC_42814)

Source Database: BDSC, catalog # 42814
Genetic Background:
Affected Genes: CG34202,Scer\UAS,sc,v,y
Genomic Alteration: Chromosome/1;3, breakpoints/68A4, 3L:11070538..11070538 (r6, Ti)
Availability: Available
Reference:
Notes: Expresses dsRNA for RNAi of CG34202 (FBgn0085231) under UAS control.

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Cite this (MMRRC Cat# 024619-UCD, RRID:MMRRC_024619-UCD)

Source Database: MMRRC, catalog # 024619-UCD
Genetic Background: Gene Trap
Affected Genes: R3hdm1
Genomic Alteration:
Availability:
Reference:
Notes: Mutation type: Gene Trap

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Cite this (RGD Cat# 10026, RRID:RGD_10026)

Source Database: RGD, catalog # 10026
Genetic Background: inbred strain
Affected Genes:
Genomic Alteration:
Availability: live
Reference:
Notes: decreased body weight, decreased systemic arterial blood pressure To N 1964 at F18+? from Maas. Developed by Broadhurst, 1954, from a commercial stock, with selection for low defecation response in an open field. A number of parallel sublines are in existence; these differ at least at the agouti and the major histocompatibility loci. NIH Animal Genetic Resource

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Cite this (FlyBase Cat# FBst0204260, RRID:FlyBase_FBst0204260)

Source Database: FlyBase, catalog # FBst0204260
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: Availability unknown check source stock centers
Reference:
Notes:

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Cite this (IMSR Cat# EM:00391, RRID:IMSR_EM:00391)

Source Database: IMSR, catalog # EM:00391
Genetic Background:
Affected Genes: Dmd, Tg(Ckm-Dmd_iDp71)MCA-1Chmb, Utrn
Genomic Alteration: mdx, Tg(Ckm-Dmd_iDp71)MCA-1Chmb, tm1Ked
Availability: mouse cells
Reference:
Notes: gene symbol note: dystrophin, muscular dystrophy, transgene insertion MCA-1, Jeffrey S Chamberlain, utrophin; mutant stock: X linked muscular dystrophy, transgene insertion MCA-1, Jeffrey S Chamberlain, targeted mutation 1, Kay E Davies

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Cite this (IMSR Cat# TIGM:IST13893A9, RRID:IMSR_TIGM:IST13893A9)

Source Database: IMSR, catalog # TIGM:IST13893A9
Genetic Background:
Affected Genes: Gmpr2
Genomic Alteration: Gt(IST13893A9)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: guanosine monophosphate reductase 2; unclassified: gene trap IST13893A9, Texas A&M Institute for Genomic Medicine

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Cite this (BDSC Cat# 56541, RRID:BDSC_56541)

Source Database: BDSC, catalog # 56541
Genetic Background:
Affected Genes: tara,w
Genomic Alteration: Chromosome/1;3, breakpoints/89B8, 3R:16226553..16226553 (r6, Ti)
Availability: Available
Reference:
Notes: Expresses N-terminally truncated, but near full-length tara protein with N-terminal FLAG and mCherry tags under UAS control. Homozygotes &/or P{w[+mC]=GAL4-ninaE.GMR}12 may be present, K.E.

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Cite this (DGGR Cat# 200497, RRID:DGGR_200497)

Source Database: DGGR, catalog # 200497
Genetic Background:
Affected Genes:
Genomic Alteration: Break points/Insertion Site:70D7
Availability: Available
Reference:
Notes: Received from Tokyo Metropolitan University.

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Cite this (MMRRC Cat# 015469-UCD, RRID:MMRRC_015469-UCD)

Source Database: MMRRC, catalog # 015469-UCD
Genetic Background: Gene Trap
Affected Genes: Btbd10
Genomic Alteration:
Availability:
Reference:
Notes: Mutation type: Gene Trap

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Cite this (MGI Cat# 5759404, RRID:MGI:5759404)

Source Database: MGI, catalog # 5759404
Genetic Background: C57BL/6N-Pram1/H
Affected Genes: Pram1
Genomic Alteration: tm1b(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (IMSR Cat# TIGM:IST10880B10, RRID:IMSR_TIGM:IST10880B10)

Source Database: IMSR, catalog # TIGM:IST10880B10
Genetic Background:
Affected Genes: Zfp97
Genomic Alteration: Gt(IST10880B10)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: zinc finger protein 97; unclassified:

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Cite this (BDSC Cat# 63471, RRID:BDSC_63471)

Source Database: BDSC, catalog # 63471
Genetic Background:
Affected Genes: Cerk,Scer\GAL4,w
Genomic Alteration: Chromosome/1;3, breakpoints/83A1, 3R:5367444..5367444 (r6, Ti)
Availability: Available
Reference:
Notes: May be segregating TM6B, Tb[1].

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Cite this (MMRRC Cat# 019078-UCD, RRID:MMRRC_019078-UCD)

Source Database: MMRRC, catalog # 019078-UCD
Genetic Background: Gene Trap
Affected Genes: Wdr82
Genomic Alteration:
Availability:
Reference:
Notes: Mutation type: Gene Trap

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Cite this (MGI Cat# 5317173, RRID:MGI:5317173)

Source Database: MGI, catalog # 5317173
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * SJL
Affected Genes: Gjc1, Tg(Nes-cre)1Kln
Genomic Alteration: tm1.1(Gjd2)Kwi; Tg(Nes-cre)1Kln
Availability: Availability unknown check source stock center
Reference: PMID:20930146
Notes: nervous system phenotype, vision/eye phenotype Allele Detail: Targeted, Transgenic

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Cite this (IMSR Cat# EM:09856, RRID:IMSR_EM:09856)

Source Database: IMSR, catalog # EM:09856
Genetic Background:
Affected Genes: Sbno1
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: strawberry notch 1; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (BDSC Cat# 46768, RRID:BDSC_46768)

Source Database: BDSC, catalog # 46768
Genetic Background:
Affected Genes: bon,Scer\GAL4,Sb,w
Genomic Alteration: Chromosome/1;3, breakpoints/68A4, 3L:11070538..11070538 (r6, Ti)
Availability: Available
Reference:
Notes: Expresses GAL4 under the control of DNA sequences in or near bon (FBgn0023097), G.R.

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Cite this (MGI Cat# 3664570, RRID:MGI:3664570)

Source Database: MGI, catalog # 3664570
Genetic Background: involves: 129/Sv * C57BL/6J * FVB/N
Affected Genes: Lrp5
Genomic Alteration: tm1Lex
Availability: Availability unknown check source stock center
Reference: PMID:15537447
Notes: persistence of hyaloid vascular system, decreased bone mineral density Allele Detail: Targeted

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