Variation Information: tk69
| Name | tk69 View on WormBase |
|---|---|
| Species | C. elegans |
| Genetic position | III:-0.06 +/- 0.000 cM |
| Genomic position | III: 8766367..8766667 |
| Protein change | PAR2.4a PAR2.4a PAR2.4a PAR2.4b PAR2.4b PAR2.4b PAR2.4b Deletion |
Strains carrying this variation
| Strain | Genotype | Species | Description |
|---|---|---|---|
| NF1226 | mig-22(tk69) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). | C. elegans | mig-22(tk69): DTC migration defect and maternal effect embryonic lethal. Heterozygotes are WT with pharyngeal GFP signal. Homozygous hT2[bli-4 let-? qIs48] are inviable. |