Variation Information: tk69

Nametk69 View on WormBase
Species C. elegans
Genetic positionIII:-0.06 +/- 0.000 cM
Genomic positionIII: 8766367..8766667
Protein changePAR2.4a PAR2.4a PAR2.4a PAR2.4b PAR2.4b PAR2.4b PAR2.4b Deletion

Strains carrying this variation

Strain Genotype Species Description
NF1226 mig-22(tk69) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). C. elegans mig-22(tk69): DTC migration defect and maternal effect embryonic lethal. Heterozygotes are WT with pharyngeal GFP signal. Homozygous hT2[bli-4 let-? qIs48] are inviable.