Gene Information: mig-22

Namemig-22 View on WormBase
Species C. elegans
Genetic positionIII:-0.06 +/- 0.001 cM
Genomic positionIII: 8763291..8767342

Strains carrying this gene

Strain Genotype Description
BC10306 dpy-5(e907) I; sEx10306. sEx10306 [rCes PAR2.4::GFP + pCeh361]. Maintain by picking WT. WT animals are GFP+. Strain construction supported by Genome British Columbia and Genome Canada. Please acknowledge McKay et al, Cold Spring Harbor Symposia on Quantitative Biology 68: 159-169 2004 (WBPaper00006525).
NF1226 mig-22(tk69) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). 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.
NF591 mig-22(tk24) III. DTC migration defect.
NF68 mig-22(k141) III. DTC migration defect.