Variation Information: ok1002

Nameok1002 View on WormBase
Species C. elegans
Genetic positionIV:4.34 +/- 0.001 cM
Genomic positionIV: 9617005..9618204
Protein changeW09C2.1a W09C2.1b W09C2.1c W09C2.1d W09C2.1f Deletion

Strains carrying this variation

Strain Genotype Species Description
OH14408 elt-1(ok1002) IV; otEx6750. C. elegans otEx6750 [unc-47p::mChopti + elt-1(+)(fosmid)]. Array rescues lethal elt-1 mutation; contains fosmid WRM0619bE05. Line 1-2. Reference: Gendrel M, et al. Elife. 2016 Oct 14;5.
OH14619 elt-1(ok1002) IV; him-5(e1490) V; otIs549 X; otEx6751. C. elegans otIs549 [unc-25p::unc-25(partial)::mChopti::unc-54 3'UTR + pha-1(+)]. otEx6751 [unc-47p::GFP + elt-1(+)(fosmid)]. Him. otEx6751 rescues lethal elt-1 mutation; contains fosmid WRM0619bE05. otIs549 contains 1.8 kb upstream of the unc-25 start codon through exon 4; derived from injection of pMG154; line 2-1. Reference: Gendrel M, et al. Elife. 2016 Oct 14;5.
VC744 elt-1(ok1002) IV/nT1 [qIs51] (IV;V). C. elegans W09C2.1. Homozygous lethal deletion chromosome balanced by GFP-marked translocation. Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested nT1 aneuploids, and non-GFP ok1002 homozygotes (probable embryonic arrest). Homozygous nT1[qIs51] inviable. Pick WT GFP and check for correct segregation of progeny to maintain. 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