Variation Information: n5017
| Name | n5017 View on WormBase |
|---|---|
| Species | C. elegans |
| Genetic position | II:0.94 +/- 0.000 cM |
| Genomic position | II: 8939853..8940627 |
| Protein change | T21B10.5a T21B10.5b Deletion |
Strains carrying this variation
| Strain | Genotype | Species | Description |
|---|---|---|---|
| MT17121 | set-17(n5017) II. | C. elegans | Reference: Development 134(16):2991-9 (2007). |
| MT21478 | set-17(n5017) II ; unc-119(ed3) III ; nSi3 IV | C. elegans | nSi3 [set-17p::set-17(+)::GFP::set-17 3’UTR + unc-119(+)] IV. nSi3 expresses a translational fusion of genomic set-17 and GFP. nSi3 rescues the brood size defect of n5017 in this strain. nSi3 is a single copy MOS-mediated transposition into the cxTi10882 site; GFP detectable in the nuclei of the hypoderm, sperm and proximal germline, as well as some other cells. Reference: Engert CG, et al. PLoS Genet. 2018 Apr 27;14(4):e1007295. |