Variation Information: tm1086

Nametm1086 View on WormBase
Species C. elegans
Genetic positionIII:-0.91 +/- 0.001 cM
Genomic positionIII: 6901776..6902447
Protein changeT07E3.5 Deletion

Strains carrying this variation

Strain Genotype Species Description
DW104 brc-2(tm1086) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). C. elegans tm1086 is homozygous lethal. Maternally rescued. Fails to produce viable progeny due to a defect in repairing meiotic DNA double-strand breaks. Chromosomes are visibly aggregated at diakinesis. Maintain by picking GFP progeny and checking that the non-GFP progeny that are produced fail to give viable progeny. qIs48 is an insertion of ccEx9747 with markers: myo-2::GFP expressed brightly in the pharynx throughout development, pes-10::GFP expressed in embryos, and a gut promoter driving GFP in the intestine, and is homozygous lethal.