Variation Information: ok691

Nameok691 View on WormBase
Species C. elegans
Genetic positionIV:2.20 +/- 0.000 cM
Genomic positionIV: 5662027..5664709
Protein changeT19E7.3a T19E7.3b Deletion

Strains carrying this variation

Strain Genotype Species Description
AMH50 juIs76; bec-1(ok691) IV/nT1 [qIs51] (IV;V). C. elegans juIs76 [unc-25p::GFP + lin-15(+)] II.  Heterozygotes are wild-type with pharyngeal GFP signal, and segregate WT GFP, arrested nT1[qIs51] aneuploids, and non-pharyngeal GFP bec-1 homozygotes. Homozygous nT1[qIs51] inviable. Pick WT GFP and check for correct segregation of progeny to maintain.
VC517 bec-1(ok691) IV/nT1 [qIs51] (IV;V). C. elegans T19E7.3. Homozygous lethal deletion balanced by GFP-marked translocation. Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested nT1 aneuploids, and non-GFP ok691 homozygotes (viable and probably fertile, perhaps slow-growing). 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