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http://www.wormbase.org/db/get?name=WBStrain00037725

Source Database: WormBase (WB)
Affected Genes: WBGene00004237(ptr-23)
Genomic Alteration: WBGene00004237(ptr-23)
Availability: available
Synonyms: ptr-23(ok3663) I.
Alternate IDs: WB-STRAIN:VC3219, CGC_VC3219
Notes: 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.|"ZK270.1. Dpy or Dpyish. External left primer: CAACCAGATGACGCAGCTAA. External right primer: TGATTCCATTTCACGGACAA. Internal left primer: CCGGTCTCCAGGATAACAAA. Internal right primer: GTAGCCATGGAATACACGGG. Internal WT amplicon: 1140 bp. Deletion size: 899 bp. Deletion left flank: GGATAACAAATGTAAAGTCAGTCAAAATGA. Deletion right flank: ATATACACATTTGATGACGACACCGCTGGT."

Proper citation: RRID:WB-STRAIN:WBStrain00037725 Copy   

•   Source: WormBase
  

http://www.wormbase.org/db/get?name=WBStrain00037720

Source Database: WormBase (WB)
Affected Genes: WBGene00013878(atfs-1)
Genomic Alteration: WBGene00013878(atfs-1)
Availability: available
Source References: PMID:33542359, PMID:37902464
Synonyms: atfs-1(gk3094) V.
Alternate IDs: WB-STRAIN:VC3201, CGC_VC3201
Notes: Mutagen:UV/TMP|"Supplementary_genotype atfs-1(gk3094)"|"This strain is homozygous for a deletion (gk3094) in ZC376.7, detectable by PCR using the following primers. External left primer: TTTCAGTCGTTTCAGGACCC. External right primer: TCATCGAGTTGATCTCACGC. Internal left primer: ATAGAAACCGCCTCCTTTCG. Internal right primer: TTCTCGGCTCGTTTCTTCTC. Internal WT amplicon: 2877 bp. Deletion size: 881 bp. Deletion left flank: ACTGGACCTCGACTCATGGCACACTAAGCC. Deletion right flank: ATCAAGTTATCTTCACGGAAAAATGTTCGA. Validation: gk3094 passed by CGH."|"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."

Proper citation: RRID:WB-STRAIN:WBStrain00037720 Copy   

•   Source: WormBase
  

http://www.wormbase.org/db/get?name=WBStrain00037706

Source Database: WormBase (WB)
Affected Genes: WBGene00007630(har-1)
Genomic Alteration: WBGene00007630(har-1)
Availability: available
Synonyms: har-1(gk3124) III.
Alternate IDs: WB-STRAIN:VC3169, CGC_VC3169
Notes: C16C10.11. External left primer: TTGGCTGCTTGTATCGATTG. External right primer: CGAAAGACTGCGAGGAAAAC. Internal left primer: GTTTCCCTGTCGTATTTCGC. Internal right primer: ATCATTGAATCCGTTGCACA. Internal WT amplicon: 855 bp. Deletion size: 260 bp. Deletion left flank: CAGACAAGTGATTTTTGAACTATTTCGTCA. Deletion right flank: TCCTTCGCCGCTCCACCACCAAGACCAGGT. Validation: gk3124 passed by CGH.|"Made_by: Vancouver KO Group"|"Mutagen:UV/TMP"|"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."

Proper citation: RRID:WB-STRAIN:WBStrain00037706 Copy   

•   Source: WormBase
  

http://www.wormbase.org/db/get?name=WBStrain00037717

Source Database: WormBase (WB)
Affected Genes: WBGene00000254(bli-4)|WBGene00008990(smgl-1)
Genomic Alteration: WBGene00000254(bli-4), WBGene00008990(smgl-1)
Availability: available
Synonyms: smgl-1(ok2423) I/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III).
Alternate IDs: WB-STRAIN:VC3196, CGC_VC3196
Notes: F20G4.1. 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 ok2423 homozygotes (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: TCCAACCAATCCAGCTTTTC. External right primer: CCAAAACGAGAAGACGGAGA. Internal left primer: TTCGACTTTTTCGGCGAT. Internal right primer: ATGGAACATCCTGATGCTGA. Internal WT amplicon: 1173 bp. Deletion size: 637 bp. Deletion left flank: TTCTAAAAATAATTAAATTAGAGTGTTAAA. Deletion right flank: CGTATGGTTGCCACGTCGCGAGATCATGAA.|"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."

Proper citation: RRID:WB-STRAIN:WBStrain00037717 Copy   

•   Source: WormBase
  

http://www.wormbase.org/db/get?name=WBStrain00037781

Source Database: WormBase (WB)
Affected Genes: WBGene00001072(dpy-10)|WBGene00011071(R06F6.8)
Genomic Alteration: WBGene00001072(dpy-10), WBGene00011071(R06F6.8)
Availability: available
Synonyms: R06F6.8(ok1318)/mIn1 [mIs14 dpy-10(e128)] II.
Alternate IDs: WB-STRAIN:VC3391, CGC_VC3391
Notes: Mutagen:UV/TMP|"R06F6.8. Homozygous sterile deletion chromosome balanced by GFP- and dpy-10-marked inversion. Heterozygotes are WT with relatively dim pharyngeal GFP signal, and segregate WT dim GFP, Dpy bright GFP (mIn1 homozygotes), and non-GFP ok1318 homozygotes (sterile, lays unfertilized oocytes and very few fertilized eggs that don't hatch). Pick WT dim GFP and check for correct segregation of progeny to maintain. External left primer: CGCGATAAACGTCATTTCCT. External right primer: AACGTTTTTGCGTTCCAAAT. Internal left primer: TTGATTCCTTTTGCACCACA. Internal right primer: CTTCCGAAGCATGAAAAGGA. Internal WT amplicon: 3207 bp. Deletion size: 1673 bp. Deletion left flank: CAACCGACGCATATCGACTGTCAAGTCTCT. Deletion right flank: TTAATTCTCCACGTGTTTCTTTGAAATTGG."|"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."

Proper citation: RRID:WB-STRAIN:WBStrain00037781 Copy   

•   Source: WormBase
  

http://zebrafish.org/fish/lineAll.php?t=ZIRC_Catalog_ID&sverb=exactly+matching&c=ZL12446.07

Source Database: Zebrafish Lines at ZIRC
Affected Genes: (disclaimer)
Genomic Alteration: sa34628
Availability: frozen
Notes: Allele with one point mutation

Proper citation: RRID:ZIRC_ZL12446.07 Copy   

•   Source: Zebrafish International Resource Center
  

http://zebrafish.org/fish/lineAll.php?t=ZIRC_Catalog_ID&sverb=exactly+matching&c=ZL13937.15

Source Database: Zebrafish Lines at ZIRC
Affected Genes: (disclaimer)
Genomic Alteration: sa8817
Availability: frozen
Notes: Allele with one point mutation

Proper citation: RRID:ZIRC_ZL13937.15 Copy   

•   Source: Zebrafish International Resource Center
  

http://zebrafish.org/fish/lineAll.php?t=ZIRC_Catalog_ID&sverb=exactly+matching&c=ZL13979.09

Source Database: Zebrafish Lines at ZIRC
Affected Genes: (disclaimer)
Genomic Alteration: sa9322
Availability: frozen
Notes: Allele with one point mutation

Proper citation: RRID:ZIRC_ZL13979.09 Copy   

•   Source: Zebrafish International Resource Center
  

http://zebrafish.org/fish/lineAll.php?t=ZIRC_Catalog_ID&sverb=exactly+matching&c=ZL13624.10

Source Database: Zebrafish Lines at ZIRC
Affected Genes: (disclaimer)
Genomic Alteration: sa40706
Availability: frozen
Notes: Allele with one point mutation

Proper citation: RRID:ZIRC_ZL13624.10 Copy   

•   Source: Zebrafish International Resource Center
  

http://zebrafish.org/fish/lineAll.php?t=ZIRC_Catalog_ID&sverb=exactly+matching&c=ZL13611.27

Source Database: Zebrafish Lines at ZIRC
Affected Genes: (disclaimer)
Genomic Alteration: sa43180
Availability: frozen
Notes: Allele with one point mutation

Proper citation: RRID:ZIRC_ZL13611.27 Copy   

•   Source: Zebrafish International Resource Center
  

http://zebrafish.org/fish/lineAll.php?t=ZIRC_Catalog_ID&sverb=exactly+matching&c=ZL13723.14

Source Database: Zebrafish Lines at ZIRC
Affected Genes: (disclaimer)
Genomic Alteration: sa43718
Availability: frozen
Notes: Allele with one point mutation

Proper citation: RRID:ZIRC_ZL13723.14 Copy   

•   Source: Zebrafish International Resource Center
  

http://zebrafish.org/fish/lineAll.php?t=ZIRC_Catalog_ID&sverb=exactly+matching&c=ZL891

Source Database: Zebrafish Lines at ZIRC
Genetic Background: AB
Affected Genes: rereatb210/+ (AB)
Genomic Alteration: tb210
Availability: frozen
Notes: Allele with one point mutation

Proper citation: RRID:ZIRC_ZL891 Copy   

•   Source: Zebrafish International Resource Center
  

http://zebrafish.org/fish/lineAll.php?t=ZIRC_Catalog_ID&sverb=exactly+matching&c=ZL906

Source Database: Zebrafish Lines at ZIRC
Genetic Background: AB
Affected Genes: ccdc103tn222a/+ (AB)
Genomic Alteration: tn222a
Availability: frozen
Notes: Allele with one point mutation

Proper citation: RRID:ZIRC_ZL906 Copy   

•   Source: Zebrafish International Resource Center
  

http://zebrafish.org/fish/lineAll.php?t=ZIRC_Catalog_ID&sverb=exactly+matching&c=ZL1390

Source Database: Zebrafish Lines at ZIRC
Genetic Background: AB
Affected Genes: bmp7asb1aub/+ (AB)
Genomic Alteration: sb1aub
Availability: frozen
Notes: Allele with one point mutation

Proper citation: RRID:ZIRC_ZL1390 Copy   

•   Source: Zebrafish International Resource Center
  

http://zebrafish.org/fish/lineAll.php?t=ZIRC_Catalog_ID&sverb=exactly+matching&c=ZL784

Source Database: Zebrafish Lines at ZIRC
Genetic Background: TU
Affected Genes: bgmt21127/+ (TU)
Genomic Alteration: t21127
Availability: frozen
Notes: Unknown

Proper citation: RRID:ZIRC_ZL784 Copy   

•   Source: Zebrafish International Resource Center
  

The record is no longer available at this source.

Source Database: BCBC, Beta Cell Biology Consortium
Genetic Background: TM
Affected Genes: recombination activating gene 1
Genomic Alteration: Rag1tm1Mom
Notes: Backcrossing of the Rag1 null allele onto the NOD/Lt strain background (NOD-Rag1null mice) provided a radio-resistant and longer-lived model for human-cell engraftment. Mutations in X-chromosome-linked Il2rg gene cause X-linked severe combined immunodeficiency (XSCID). Immunodeficient NOD-Rag1null IL2rg nullmice tolerated much higher levels of irradiation conditioning than did NOD-Prkdcscid IL2rg null mice.

Proper citation: RRID:BCBC_212 Copy   

•   Source: Beta Cell Biology Consortium
  

The record is no longer available at this source.

Source Database: BCBC, Beta Cell Biology Consortium
Genetic Background: TM, OTH
Affected Genes: recombination activating gene 1
Genomic Alteration: MGI:97848)
Notes: The NOD-Rag1null Prf1null Ins2Akita mouse is the first immunodeficient, spontaneously hyperglycemic mouse strain described that is based on the Ins2Akita mutation. This strain is suitable as hosts for human islet and human beta stem and progenitor cell transplantation in the absence of the need for pharmacological induction of diabetes. This strain of mice also has low levels of innate immunity and can be engrafted with a human immune system for the study of human islet allograft rejection.

Proper citation: RRID:BCBC_211 Copy   

•   Source: Beta Cell Biology Consortium
  

The record is no longer available at this source.

Source Database: BCBC, Beta Cell Biology Consortium
Genetic Background: TG

Proper citation: RRID:BCBC_185 Copy   

•   Source: Beta Cell Biology Consortium
  

The record is no longer available at this source.

Source Database: BCBC, Beta Cell Biology Consortium
Genetic Background: TM
Affected Genes: Pancreatic and duodenal homeobox 1
Genomic Alteration: Pdx1tmd1Macd
Notes: Mice homozygous for the targeted mutation fail to develop a pancreas. Heterozygous mice have normal pancreatic development, but have partially impaired glucose tolerance in adulthood. The substitution of the targeted Ipf1/Pdx1 gene with tTAoff inactivates the endogenous allele and places tTAoff expression under the control of the endogenous transcriptional regulatory sequences of the Pdx1 locus. Identical to the endogenous allele, mutant locus expression is detectable in the pancreas and adjacent duodenum but not in other visceral organs or salivary glands. This mutant may be useful to direct tetracycline-regulated expression of responder transgenes in studies of pancreatic endocrine/exocrine development and function and diabetes. This mutant can also be bred with other tetO/TRE strains for pancreas-specific applications. This mutant was originally designed to be mated with mice engineered with a heptameric tetracycline operator (tetO)-controlled bicistronic transgene coding for a normal PDX1 protein and with a beta-galactosidase or EGFP reporter (see BCBC mouse M561). The combined modifications allow normal pancreatic development and function until doxycycline-administration renders the mouse conditionally null of the Pdx1 gene. This configuration for conditional expression of Pdx1is most effective when the transgene locus is homozygous. This allows embryonic developmental arrest at desired stages or cessation of function in adult mice by tetracycline administration.

Proper citation: RRID:BCBC_220 Copy   

•   Source: Beta Cell Biology Consortium
  

The record is no longer available at this source.

Source Database: BCBC, Beta Cell Biology Consortium
Notes: These NSG-Abo DR4 mice lack expression of the murine Prkdc gene, the X-linked Il2rg gene, and MHC class II, but express the human leukocyte antigen DR4 gene. These mice may be useful for targeting human CD4+ T cells in transplantation studies in the absence of xeno-GVHD.More details are available at http://jaxmice.jax.org/strain/017637.html.

Proper citation: RRID:BCBC_4612 Copy   

•   Source: Beta Cell Biology Consortium