Variation Information: n4066

Namen4066 View on WormBase
Species C. elegans
Genetic positionIII:-0.99 +/- 0.000 cM
Genomic positionIII: 6707642..6708947
Protein changeF37A4.8 Deletion

Strains carrying this variation

Strain Genotype Species Description
MT13516 isw-1(n4066) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). C. elegans Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested hT2 aneuploids, and non-GFP n4066 homozygotes (sterile). n4066 is a deletion of F37A4.8.