Strain Information
| Name | IB16 View On Wormbase |
|---|---|
| Species | C. elegans |
| Genotype | ceh-17(np1) I. |
| Description | WT behavioral phenotype. Axon guidance defect in ceh-17 expressing neurons ALA and 4SIA. ceh-17 = D1007.1, a C. elegans paired homeodomain transcription factor, Phox2 orthologue. np1 is a molecular null. np1 is a 1353 bp deletion inculding 549 bp upstream of the initiator ATG and extending to the 5th codon of the homeodomain. [NOTE: Miyazaki, et al. (2022) report that this strain carries the fln-2(ot611) mutation in the background, and outcrossing the strain resulted in significantly reduced quiescence during lethargus.] |
| Mutagen | UV/TMP |
| Outcrossed | x3 |
| Made by | Nathalie Pujol |
| Laboratory | IB |
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