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on page 2 showing 20 out of 620,331 results

Cite this (DGGR Cat# 204956, RRID:DGGR_204956)

Source Database: DGGR, catalog # 204956
Genetic Background:
Affected Genes:
Genomic Alteration: Break points/Insertion Site:076C05
Availability: Available
Reference:
Notes: Received from Tokyo Metropolitan University.

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Cite this (ZIRC Cat# ZL12423.16, RRID:ZIRC_ZL12423.16)

Source Database: ZIRC, catalog # ZL12423.16
Genetic Background: disclaimer
Affected Genes: tigara
Genomic Alteration: sa38040
Availability: frozen
Reference:
Notes: - Point Mutation

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Cite this (BDSC Cat# 24645, RRID:BDSC_24645)

Source Database: BDSC, catalog # 24645
Genetic Background:
Affected Genes: Dcr-2,Scer\UAS,Sb,sens,w
Genomic Alteration: Chromosome/1;3, breakpoints/70A2-70A3;70A5-70A6 (Df)
Availability: Available
Reference:
Notes: Expresses Dicer-2 under UAS control; X and second chromosomes isogenic with stock 5905, B.D. TM3 may also carry Ser[1].

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Cite this (ZIRC Cat# ZL13602.22, RRID:ZIRC_ZL13602.22)

Source Database: ZIRC, catalog # ZL13602.22
Genetic Background: disclaimer
Affected Genes: c7b
Genomic Alteration: sa43625
Availability: frozen
Reference:
Notes: - Point Mutation

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Cite this (IMSR Cat# TIGM:IST13549H8, RRID:IMSR_TIGM:IST13549H8)

Source Database: IMSR, catalog # TIGM:IST13549H8
Genetic Background:
Affected Genes: Macf1
Genomic Alteration: Gt(IST13549H8)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: microtubule-actin crosslinking factor 1; unclassified: gene trap IST13549H8, Texas A&M Institute for Genomic Medicine

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Cite this (IMSR Cat# TIGM:IST14653C4, RRID:IMSR_TIGM:IST14653C4)

Source Database: IMSR, catalog # TIGM:IST14653C4
Genetic Background:
Affected Genes: Wwp2
Genomic Alteration: Gt(IST14653C4)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: WW domain containing E3 ubiquitin protein ligase 2; unclassified: gene trap IST14653C4, Texas A&M Institute for Genomic Medicine

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Cite this (WB Cat# RB2336, RRID:WB-STRAIN:RB2336)

Source Database: WB, catalog # RB2336
Genetic Background:
Affected Genes: WBGene00017442(F13H8.9)
Genomic Alteration: WBVar00094245(ok3172)
Availability: live
Reference:
Notes: mutagen: EMS; outcrossed: x0; other notes: F13H8.9. Homozygous. Outer Left Sequence: TCTCAATCGGTGATGATGGA. Outer Right Sequence: AAGGCTGCTGATGCAATTCT. Inner Left Sequence: TCTTCTTAAGACGGGGAGCA. Inner Right Sequence: GAAGCAAGAAGTCATCTCGGA. Inner Primer PCR Length: 1198 bp. Deletion Size: 754 bp. Deletion left flank: CCACACTTGATGTATTTGGAAGTCTCTGGG. Deletion right flank: GAAGTTTTGAAACTTTCTTAGCATTTCTTA. Insertion Sequence: TGCTCGATATTTGTAGTGATAATATGTA."|"Made_by: OMRF Knockout Group"|"This strain was provided by the C. elegans Gene Knockout Project at the Oklahoma Medical Research Foundation, which was part of the International C. elegans Gene Knockout Consortium, which should be acknowledged in any publications resulting from its use.

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Cite this (MGI Cat# 5653009, RRID:MGI:5653009)

Source Database: MGI, catalog # 5653009
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: Availability unknown check source stock center
Reference:
Notes: Strain Type: Not Specified

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Cite this (IMSR Cat# TIGM:IST12604A4, RRID:IMSR_TIGM:IST12604A4)

Source Database: IMSR, catalog # TIGM:IST12604A4
Genetic Background:
Affected Genes: Ccdc58
Genomic Alteration: Gt(IST12604A4)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: coiled-coil domain containing 58; unclassified: gene trap IST12604A4, Texas A&M Institute for Genomic Medicine

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Cite this (MGI Cat# 3655091, RRID:MGI:3655091)

Source Database: MGI, catalog # 3655091
Genetic Background: involves: 129S2/SvPas * 129S4/SvJae
Affected Genes: Foxk1, Cdkn1a
Genomic Alteration: tm1Djg; tm1Tyj
Availability: Availability unknown check source stock center
Reference: PMID:12446708
Notes: growth/size/body region phenotype, muscle phenotype, cellular phenotype Allele Detail: Targeted

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Cite this (WB Cat# VC1833, RRID:WB-STRAIN:VC1833)

Source Database: WB, catalog # VC1833
Genetic Background:
Affected Genes: WBGene00000254(bli-4), WBGene00004771(sem-2)
Genomic Alteration: WBVar00093571(ok2422)|WBVar00143617(e937)|WBVar00241187(q782)
Availability: live
Reference:
Notes: mutagen: EMS; outcrossed: x1; other notes: C32E12.5. Homozygous lethal deletion chromosome balanced by bli-4- and GFP-marked translocation. Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested hT2 aneuploids, and non-GFP ok2422 homozygotes (embryonic or early larval arrest). Homozygous hT2[bli-4 let-? qIs48] inviable. Pick WT GFP and check for correct segregation of progeny to maintain. External left primer: AACGAATGAAAACTGGCTCG. External right primer: ATATGATGCCGCCGATTAAC. Internal left primer: CAATCGCTTGGATTTGTTGA. Internal right primer: CAATTGCAGTAGCCTCATCG. Internal WT amplicon: 3044 bp. Deletion size: 2389 bp. Deletion left flank: AAGTTGGTGCTGGTGATGGTGCGAAGTGGT. Deletion right flank: CCAGAAGTCGATGAGGCTACTGCAATTGCG."|"This strain was provided by the C. elegans Reverse Genetics Core Facility at the University of British Columbia, which is part of the international C. elegans Gene Knockout Consortium, which should be acknowledged in any publications resulting from its use.

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Cite this (BDSC Cat# 70616, RRID:BDSC_70616)

Source Database: BDSC, catalog # 70616
Genetic Background:
Affected Genes: Dh31-R,Hsap\RELA,Tb,w
Genomic Alteration: Chromosome/1;2;3, breakpoints/25C6, 2L:5108448..5108448 (r6, Ti)
Availability: Available
Reference:
Notes: Expresses the p65 activation domain under control of sequences in/near Dh31-R (FBgn0052843). Chromosome 2 homozygotes may be present.

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Cite this (IMSR Cat# TIGM:IST12413B4m35, RRID:IMSR_TIGM:IST12413B4m35)

Source Database: IMSR, catalog # TIGM:IST12413B4m35
Genetic Background:
Affected Genes: Pcdhga8
Genomic Alteration: Gt(IST12413B4m35)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: protocadherin gamma subfamily A, 8; unclassified:

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Cite this (IMSR Cat# TIGM:IST14370D6, RRID:IMSR_TIGM:IST14370D6)

Source Database: IMSR, catalog # TIGM:IST14370D6
Genetic Background:
Affected Genes: Akap12
Genomic Alteration: Gt(IST14370D6)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: A kinase (PRKA) anchor protein (gravin) 12; unclassified: gene trap IST14370D6, Texas A&M Institute for Genomic Medicine

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Cite this (IMSR Cat# EM:07678, RRID:IMSR_EM:07678)

Source Database: IMSR, catalog # EM:07678
Genetic Background:
Affected Genes: Baiap2l2
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: mouse cells
Reference:
Notes: gene symbol note: BAI1-associated protein 2-like 2; mutant strain: targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH

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Cite this (MGI Cat# 2161365, RRID:MGI:2161365)

Source Database: MGI, catalog # 2161365
Genetic Background:
Affected Genes: Phex
Genomic Alteration:
Availability: Availability unknown check source stock center
Reference:
Notes: Strain Type: congenic

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Cite this (MMRRC Cat# 039457-MU, RRID:MMRRC_039457-MU)

Source Database: MMRRC, catalog # 039457-MU
Genetic Background: Chemically Induced
Affected Genes: 2900026A02Rik, 4932431P20Rik, A330070K13Rik, Abcc2, Adgrv1, Ankrd27, Arhgap11a, Arhgap12, Arhgef12, Asb3, C2cd5, Ccdc85a, Cep128, Cep192, Col20a1, Cylc2, Eef1a1, Esyt3, Extl3, Fat3, Fcgbp, Fdxacb1, Fryl, Gm597, Gm8374, Gria1, Gse1, Gtf3c3, Hectd4, Herc1, Ift172, Ift81, Klrb1b, Lactb, Map1a, Map1lc3b, Mlh1, Myo1f, Ncoa4, Neto1, Nf1, Nkain2, Obsl1, Olfr12, Olfr1347, Olfr564, Olfr615, Phlpp1, Prrxl1, Psen1, Ralgapa2, Rdh12, Rgma, Sag, Scaf1, Slc4a10, Sned1, Spata46, Tgm2, Tub, Ugt3a1, Vmn2r15, Wdr44, Zfp322a, Zfp663
Genomic Alteration:
Availability:
Reference:
Notes: Mutation type: Chemically Induced

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Cite this (IMSR Cat# TIGM:IST11387C2, RRID:IMSR_TIGM:IST11387C2)

Source Database: IMSR, catalog # TIGM:IST11387C2
Genetic Background:
Affected Genes: Rbm6
Genomic Alteration: Gt(IST11387C2)Tigm
Availability: mouse cells
Reference:
Notes: gene symbol note: RNA binding motif protein 6; unclassified: gene trap IST11387C2, Texas A&M Institute for Genomic Medicine

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Cite this (ZIRC Cat# ZL5498.05, RRID:ZIRC_ZL5498.05)

Source Database: ZIRC, catalog # ZL5498.05
Genetic Background: disclaimer
Affected Genes:
Genomic Alteration: la013154Tg
Availability: frozen
Reference:
Notes: - Transgenic Insertion

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Cite this (MGI Cat# 5706067, RRID:MGI:5706067)

Source Database: MGI, catalog # 5706067
Genetic Background: C57BL/6N-Pop4/Wtsi
Affected Genes: Pop4
Genomic Alteration: tm1a(EUCOMM)Wtsi
Availability: Availability unknown check source stock center
Reference:
Notes: decreased circulating insulin level Allele Detail: Targeted

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