Variation Information: gk3766
| Name | gk3766 View on WormBase |
|---|---|
| Species | C. elegans |
| Genetic position | V:2.28 +/- 0.000 cM |
| Genomic position | genomic coordinates unknown or not listed |
| Protein change | protein change unknown or not listed |
Strains carrying this variation
| Strain | Genotype | Species | Description |
|---|---|---|---|
| VC3880 | C51E3.9(gk3766) C27A7.9(gk3765) V. | C. elegans | Homozygous viable. Nonsense allele and splicing defect identified by amplicon sequencing. |