Variation Information: ok524

Nameok524 View on WormBase
Species C. elegans
Genetic positionX:24.06 +/- 0.001 cM
Genomic positionX: 16800225..16800632
Protein changeT01C8.1a T01C8.1b T01C8.1c Deletion

Strains carrying this variation

Strain Genotype Species Description
AGD397 aak-1(tm1944) III; aak-2(ok524) X; uthEx202. C. elegans uthEx202 [crtc-1p::crtc-1 cDNA::tdTomato::unc-54 3'UTR + rol-6(su1006)]. Pick Rollers to maintain. Reference: Mair W, et al. Nature. 2011 Feb 17;470(7334):404-8.
MAH28 aak-2(ok524) X; adIs2122. C. elegans adIs2122 [lgg-1::GFP + rol-6(su1006)]. Rollers. Reference: Egan DF, et al. Science. 2011 Jan 28;331(6016):456-61.
MIR13 sir-2.1(ok434) IV; aak-2(ok524) X. C. elegans Slow growing. Maintain under normal conditions. Derived from parental strains RB754 [aak-2(ok524)] and VC199 [sir-2.1(ok434)]. Reference: Schmeisser S, et al. Molecular Metabolism February 15, 2013. DOI: 10.1016/j.molmet.2013.02.002.
PE863 feIs4 V; aak-2(ok524) X. C. elegans feIs4 [sur-5p::luciferase::GFP + rol-6(su1006)] V. Rollers. Strain is bioluminescent when provided with exogenous D-luciferin (potassium salt) due to sur-5 promoter driving expression of firefly (Photinus pyralis) luciferase (lacking the peroxisome tagging signal) fused in-frame to GFP(S65C). Pick animals with high levels of fluorescence to retain expression of luciferase transgene. This strain is for academic use only. This strain cannot be distributed to commercial organizations. This strain cannot be used for any commercial purpose or for work on human subjects. References: Lagido C, et al. BMC Physiol. 2008 Apr 2;8:7. McLaggan D, et al. PLoS One. 2012;7(10):e46503. Lagido C, et al. Toxicol Sci. 2009 May;109(1):88-95.
RB754 aak-2(ok524) X. C. elegans T01C8.1. Homozygous. Outer Left Sequence: TCATTTGCTGCAACTTCCTG. Outer Right Sequence: ATACGTGGCATTTACGGAGG. Inner Left Sequence: ATGTCGTTGGAAAGATTCGC. Inner Right Sequence: AAGGAGTGCTTAACGAGCCA. Inner primer WT PCR product: 2741. 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