Variation Information: gk49

Namegk49 View on WormBase
Species C. elegans
Genetic positionI:29.27 +/- 0.000 cM
Genomic positionI: 15009009..15010764
Protein changeF33H2.5 Deletion

Strains carrying this variation

Strain Genotype Species Description
VC129 F33H2.5(gk49)/mIs13 I. C. elegans F33H2.5. mIs13 [myo-2p::GFP + pes-10p::GFP + gut-promoter::GFP] I. GFP expression in 4-cell embryos, pharyngeal muscle and gut. Heterozygotes are WT with dim GFP signal in pharynx, and segregate WT with dim GFP, WT with brighter GFP (WT homozygotes), and GFP- sterile Uncs with a vulval blip. Pick dim GFP+ WT 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