Strain Information

Name IB16   View On Wormbase
Species C. elegans
Genotypeceh-17(np1) I.
DescriptionWT 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.
MutagenUV/TMP
Outcrossedx3
Made byNathalie Pujol
Laboratory IB
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