| NL132 |
C. elegans |
pgp-1(pk17) IV. Show Description
pgp-1 deletion allele. No visible phenotype. Might be sensitive to drugs. |
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| NL130 |
C. elegans |
pgp-1(pk17) IV; pgp-3(pk18) X. Show Description
Drug sensitive. No visible phenotype. pgp-1 and pgp-3 deletion alleles. |
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| NL152 |
C. elegans |
pgp-1(pk17) IV; pgp-3(pk18) X; mrp-1(pk89) Show Description
pgp-1, pgp-3 and mrp-1 triple deletion mutant. Hypersensitive to cadmium and arsenite. |
|
| RB1041 |
C. elegans |
pgp-15(ok987) X. Show Description
F22E10.4. Homozygous. Outer Left Sequence: GATCTCGAACCAACGCTCTC. Outer Right Sequence: TGGAGTCGCAATGCTTGTAG. Inner Left Sequence: CCTTCTCTCCGACGTCAGTC. Inner Right Sequence: CGTTGCACCCACTTGTATTG. Inner Primer WT PCR product: 3156. Deletion size: 2256 bp. Attribution: 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. Paper_evidence WBPaper00041807 |
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| RB1045 |
C. elegans |
pgp-10(ok991) X. Show Description
C54D1.1. Homozygous. Outer Left Sequence: AGCTCTTCACTTCCGCGATA. Outer Right Sequence: GTGGCGTTGTACATTCGTTG. Inner Left Sequence: TGGTAGTGGAAAAAGCACCC. Inner Right Sequence: ACCCGGAAGGTCCTACAAGT. Inner Primer WT PCR product: 3218. Deletion size: 2060 bp. Attribution: 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. Paper_evidence WBPaper00041807 |
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| RB2008 |
C. elegans |
pgp-14(ok2660) X. Show Description
F22E10.3. Homozygous. Outer Left Sequence: TCCAGAAGCAGAATTTTGGG. Outer Right Sequence: TGGGTTTTCGAAGGTTTCAC. Inner Left Sequence: GGACCAAAGCTCTGGCAAT. Inner Right Sequence: TTGTTTGCTGTTGTTTCGGA. Inner Primer PCR Length: 1234 bp. Deletion Size: 688 bp. Deletion left flank: GACCAAAGCTCTGGCAATTGCAATTCTCTG. Deletion right flank: AAAGATTGAGTTAGACTGTAATTGATGGCT. Attribution: 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. Paper_evidence WBPaper00041807 |
|
| RB894 |
C. elegans |
pgp-13(ok747) X. Show Description
F22E10.2. Homozygous. Outer Left Sequence: GACAAAATGCAGGGTGGTTT. Outer Right Sequence: CGGGTAAGTTGCCAAGAAAA. Inner Left Sequence: CTGATTCCCGTCTCCACAAT. Inner Right Sequence: CTCAAGTGGCACGTCTTTCA. Inner primer WT PCR product: 3297. Attribution: 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. Paper_evidence WBPaper00041807 |
|
| RP3412 |
C. elegans |
pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3414 |
C. elegans |
tat-3(tm1275) III; pgp-14(ok2660) X. Show Description
Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3452 |
C. elegans |
nhr-70(tr685) V; pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. nhr-70(tr685) is an A23T missense allele. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3453 |
C. elegans |
pgp-13(tr686) pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. pgp-13(tr686) is a splice site mutation in exon 5. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3458 |
C. elegans |
tat-3(tr691) III; pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. tat-3(tr691) is a W1155X nonsense allele. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3459 |
C. elegans |
nhr-70(tr692) V; pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. nhr-70(tr692) is a G220D missense allele in the LBD. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3463 |
C. elegans |
pgp-13(tr696) pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. pgp-13(tr696) is a K416X nonsense allele. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3464 |
C. elegans |
pgp-13(tr697) pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. pgp-13(tr697) is a G813E missense allele in TM helix 8. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3467 |
C. elegans |
nhr-107(tr700) V; pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. nhr-107(tr700) is a splice site mutation in exon 4. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3469 |
C. elegans |
pgp-13(tr702) pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. pgp-13(tr702) is a G813E missense allele in TM helix 8. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3471 |
C. elegans |
nhr-107(tr704) V; pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. nhr-107(tr704) is a G210R missense allele in the LBD. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3473 |
C. elegans |
pgp-13(tr706) pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. pgp-13(tr706) is a splice site mutation in exon 3. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3475 |
C. elegans |
pgp-13(tr708) pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. pgp-13(tr708) is a Q654X nonsense allele. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3476 |
C. elegans |
tat-3(tr709) III; pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. tat-3(tr709) is a single-nucleotide deletion within exon 8 of tat-3 (III: 10,727,273). Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3480 |
C. elegans |
pgp-13(tr713) pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. pgp-13(tr713) is a splice site mutation in exon 9. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3483 |
C. elegans |
nhr-107(tr716) V; pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. nhr-107(tr716) is an R54K missense allele in the DBD. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3484 |
C. elegans |
pgp-13(tr717) pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. pgp-13(tr717) is a S1124N missense allele in NBD II. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3487 |
C. elegans |
nhr-107(tr720) V; pgp-14(ok2660) X; trIs104. Show Description
trIs104 [pgp-14p::sms-5B(genomic)::FLAG::mCherry + pgp-14p::YFP]. nhr-107(tr720) is a splice site mutation. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3510 |
C elegans |
trEx1010. Show Description
trEx1010 [pgp-14p::sms-5B(genomic)::Flag::mCherry + pgp-14p::YFP::pgp-14]. Pick animals with mCherry+ pharynx to maintain. Fluorescence is more apparent in older animals (late stage larvae to young adults). Generated in N2 background. Reference: Kamal M, et al. bioRxiv 2022.03.11.483951; doi: https://doi.org/10.1101/2022.03.11.483951. |
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| RP3518 |
C. elegans |
nhr-70(tm1697) V; trIs114. Show Description
trIs114 [pgp-13p::YFP + myo-2p::mCherry]. Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| RP3522 |
C. elegans |
nhr-70(tm1697) V; pgp-14(ok2660) X. Show Description
Reference: Tokmakjian L, et al. bioRxiv 2026.01.03.697488; doi: https://doi.org/10.64898/2026.01.03.697488 |
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| VC26 |
C. elegans |
pgp-12(gk19) X. Show Description
F22E10.1. Superficially wild type. Attribution: 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. Paper_evidence WBPaper00041807 |
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| VC2921 |
C. elegans |
F55G1.5(gk1250) IV; pgp-10(gk3148) X. Show Description
C54D1.1, F55G1.5. The gk1250 allele was identified by PCR and validated by CGH, and can be detected with PCR using the following primers. External left primer: GCACGTTGCGAAGTAGATGA. External right primer: GCGGTACAACGATTGAAGGT. Internal left primer: TCGTTGCCTGTTGTATGGAA. Internal right primer: CCGATGAAATGGCAAAATCT. Internal WT amplicon: 1387 bp. Deletion size: 621 bp. Deletion left flank: AGTCGTAATCACCACACCAATGGAGCTATT. Deletion right flank: TGCGTCGGTTTCGCCTAGAGCATTTATTTT. The gk3148 allele was identified by CGH. Attribution: 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. Paper_evidence WBPaper00041807 |
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