Variation Information: n1332
| Name | n1332 View on WormBase |
|---|---|
| Species | C. elegans |
| Genetic position | X:-7.30 +/- 0.022 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 |
|---|---|---|---|
| MT3149 | ham-2(n1332) X. | C. elegans | Egl. HSNs are migration defective and defective in serotonin expression. See also WBPaper00003422. |