Variation Information: tm1761
| Name | tm1761 View on WormBase |
|---|---|
| Species | C. elegans |
| Genetic position | I:5.05 +/- 0.000 cM |
| Genomic position | I: 10483570..10484165 |
| Protein change | F37D6.1 Deletion |
Strains carrying this variation
| Strain | Genotype | Species | Description |
|---|---|---|---|
| AG248 | mus-101(tm1761) I/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). | C. elegans | Homozygous lethal deletion balanced by bli-4- and GFP-marked translocation. Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP+, arrested hT2 aneuploids, and non-GFP tm1761 homozygotes (embryonic lethal). Homozygous hT2[bli-4 let-? qIs48] inviable. Pick WT GFP+ and check for correct segregation of progeny to maintain. Reference: Jaramillo-Lambert A, et al. G3 (2015). |