Variation Information: n2812

Namen2812 View on WormBase
Species C. elegans
Genetic positionIII:2.35 +/- 0.000 cM
Genomic positionIII: 10335307..10335307
Protein changeT07C4.8 Substitution

Strains carrying this variation

Strain Genotype Species Description
MT7386 ced-9(n2812) III; ced-3(n717) IV. C. elegans n2812 is a strong loss-of-function allele and a maternal effect lethal.
MT7686 ced-9(n2812)/qC1 [dpy-19(e1259) glp-1(q339)] III. C. elegans Heterozygotes are WT. Segregates Dpy Steriles.
MT7735 ced-9(n2812) III; ced-3(n2427) IV. C. elegans
PD9927 ced-9(n2812) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III); nIs106 X. C. elegans nIs106 [lin-11::GFP + lin-15(+)] X. Homozygous maternal effect lethal ced-9 mutation balanced by bli-4- and GFP-marked translocation. Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested hT2 aneuploids, and non-GFP ced-9 homozygotes (maternal effect lethal). Homozygous hT2[bli-4 let-? qIs48] inviable. Pick WT GFP and check for correct segregation of progeny to maintain.