Variation Information: n717

Namen717 View on WormBase
Species C. elegans
Genetic positionIV:8.46 +/- 0.000 cM
Genomic positionIV: 13200009..13200009
Protein changeC48D1.2a C48D1.2b Substitution

Strains carrying this variation

Strain Genotype Species Description
DA2356 ced-1(e1735) I; ced-3(n717) IV; lin-15B&lin-15A(n765) X; adEx2342. C. elegans adEx2342 [efl-3::mCherry::FLAG + LIN-15(+)]. Maintain by picking non-Muv. Fluorescence is dim, but array is stable (>95% transmission).
DL308 ced-3(n717) IV; mxIs28 X. C. elegans mxIs28 [ceh-20p::ceh-20::YFP + lin-15(+)] X. Reference: Potts MB, Wang DP, & Cameron S. Dev Biol. 2009 May 15;329(2):374-85.
MT1522 ced-3(n717) IV. C. elegans Abnormal cell death. Cells that normally die survive.
MT2405 ced-3(n717) unc-26(e205) IV. C. elegans Unc. Abnormal cell death. Cells that normally die survive.
MT5729 dpy-20(e1282) unc-30(e191) ced-3(n717) IV. C. elegans Dpy (ts). Unc. Abnormal cell death. Cells that normally die survive.
MT5811 ced-1(e1735) I; ced-3(n717) IV. C. elegans
MT7386 ced-9(n2812) III; ced-3(n717) IV. C. elegans n2812 is a strong loss-of-function allele and a maternal effect lethal.
XR2 ced-3(n717) IV; abl-1(ok171) X. C. elegans
XR5 lagr-1(gk327) I; hyl-1(ok976) IV; ced-3(n717) IV. C. elegans