Variation Information: n4337
| Name | n4337 View on WormBase |
|---|---|
| Species | C. elegans |
| Genetic position | I:-1.53 +/- 0.000 cM |
| Genomic position | I: 4256308..4258167 |
| Protein change | C43E11.3a C43E11.3b C43E11.3b C43E11.3b Deletion |
Strains carrying this variation
| Strain | Genotype | Species | Description |
|---|---|---|---|
| MT14171 | met-1(n4337) I/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III); met-2(n4256) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). | C. elegans | n4256 is a deletion of R05D3.11 (met-2). n4337 is a deletion of C43E11.3 from the splice donor for the 4th exon through exon 7. Heterozygotes are WT with pharyngeal GFP signal. Homozygous hT2[bli-4 let-? qIs48] are inviable. |
| MT16973 | met-1(n4337) I. | C. elegans | Deletion of C43E11.3 splice donor for the 4th exon through exon 7. |