Variation Information: gk5048
| Name | gk5048 View on WormBase |
|---|---|
| Species | C. elegans |
| Genetic position | II:-1.12 +/- 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 |
|---|---|---|---|
| VC3964 | aps-3(gk5047) I; C17C3.3(gk5048) II. | C. elegans | Homozygous viable. Nonsense allele and splicing defect identified by amplicon sequencing. |
| VC3965 | clec-118(gk5049) C17C3.3(gk5048) II. | C. elegans | Homozygous viable. Nonsense allele and splicing defect identified by amplicon sequencing. |