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Strain Species Genotype
FK430 C. elegans lin-15B&lin-15A(n309) X; ksEx30. Show Description
ksEx30 [dyf-3::GFP + lin-15(+)].
MT309 C. elegans lin-15B&lin-15A(n309) X. Show Description
Multivulva. See also WBPaper00001990. n309 extends into both lin-15B and lin-15A.
HS1673 C. elegans lin-17(n3091) mom-5(ne12) I/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III); vpIs1 X. Show Description
vpIs1 [elt-3::GFP + lin-15(+)] X. Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested hT2 aneuploids, and non-GFP n3091 homozygotes (Sys Unc Psa). Homozygous hT2[bli-4 let-? qIs48] inviable. Pick WT GFP and check for correct segregation of progeny to maintain. Reference: Yamamoto Y, et al. PLoS Genet. 2011 Oct;7(10):e1002308.
MT8904 C. elegans lin-17(n3091) I. Show Description
Mail tale abnormal. Bivulva.
MT8987 C. elegans pag-3(n3098) X. Show Description
Kinker Unc, neuronal lineage defects including lineage reiterations and abnormal corpse pattern in ventral cord. Allele causes W113 opal.