| BW2063 |
ceh-20(ay38) unc-36(e251) III; svDp1 (III;f). |
May have unc-4(e120) mutation in background. svDp1 balances from pal-1 through unc-36 on III. svDp1 made by fusing array containing [unc-4(+) + sur-5::GFP] to sDp3(III;f). |
| CF1395 |
ceh-20(mu290) III; muIs164. |
muIs164 [tax-4::GFP]. |
| CF1806 |
ceh-20(mu290) III; muEx261. |
muEx261[ceh-20::GFP at C terminus + odr-1::RFP]. |
| HS411 |
ceh-20(os39) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). |
Heterozygotes are WT and GFP+. Segregate GFP- sterile Unc Psa (phasmid socket absent), very rare homozygous hT2 glowing animals, and dead eggs. ceh-20(os39) animals show defects in asymmetric T cell division. |
| MDH17 |
ceh-43(ot406) ceh-20(mu290) III; vtIs1 V; muEx261. |
vtIs1 [dat-1p::GFP + rol-6(su1006)] V. muEx261 [ceh-20::GFP + odr-1::RFP]. Pick RFP+ animals to maintain. Rollers. ot406 has a dopaminergic phenotype. mu290 is Egl and has a PDE dopaminergic phenotype. |
| MDH91 |
ast-1(hd1) rol-6(e187) II; ceh-20(ok541) III; vtIs1 V; ceh-40(gk159) X; muEx261. |
vtIs1 [dat-1p::GFP + rol-6(su1006)] V. muEx261 [ceh-20::GFP + odr-1::RFP]. Pick RFP+ animals to maintain. Rollers. Embryonic lethality of ceh-20(ok541); ceh-40(gk159) double mutants is rescued by muEx261. |
| MDH93 |
ceh-43(ot406) ceh-20(mu290) III; vtIs1 V; ceh-40(gk159) X; muEx261. |
vtIs1 [dat-1p::GFP + rol-6(su1006)] V. muEx261 [ceh-20::GFP at C terminus + odr-1::RFP(su1006)]. Pick RFP+ animals to maintain. Rollers. Embryonic lethality of ceh-20(mu290); ceh-40(gk159) double mutants is rescued by muEx261. ot406 has a dopaminergic phenotype. |
| MDH95 |
ceh-20(mu290) III; vtIs1 V; ceh-40(gk159) X; muEx261. |
vtIs1 [dat-1p::GFP + rol-6(su1006)] V. muEx261 [ceh-20::GFP + odr-1::RFP]. Pick RFP+ animals to maintain. Rollers. Embryonic lethality of ceh-20(mu290); ceh-40(gk159) double mutants is rescued by muEx261. |
| NH2106 |
ceh-20(ay9) III. |
Egl (Vul). 90% penetrant. lesion: M78I. |
| NH2296 |
ceh-20(ay42) unc-36(e251)/sma-3(e491) unc-36(e251) III. |
Heterozygotes are Unc and segregate Unc, SmaUnc and UncVul. ay42 is a strong Vul and is recessive. ay42 has slow growth. |
| NH2552 |
ceh-20(ay38) unc-36(e251)/sma-3(e491) unc-36(e251) III. |
Heterozygotes are Unc and segregate Unc, SmaUnc and larval lethals. Putative null allele. |
| RW12164 |
ceh-20(st12164[ceh-20::GFP + loxP + unc-119(+) + loxP] unc-119(tm4063) III. |
ceh-20(st12164[ceh-20::GFP + loxP + unc-119(+) + loxP]. |
| RW12211 |
ceh-20(st12211[ceh-20::TY1::EGFP::3xFLAG]) III. |
ceh-20(st12211[ceh-20::TY1::EGFP::3xFLAG]) III. |
| VC447 |
ceh-20(ok541) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). |
F31E3.2d. Homozygous lethal deletion chromosome 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 ok541 homozygotes (arrested DpyUnc). Homozygous hT2[bli-4 let-? qIs48] inviable. Note: qIs48 has been observed to recombine off hT2, typically leaving behind a functional homozygous viable hT2 with Bli-4 phenotype. Pick WT GFP and check for correct segregation of progeny to maintain. Attribution: This strain was provided by the C. elegans Reverse Genetics Core Facility at the University of British Columbia, which is part of the international C. elegans Gene Knockout Consortium, which should be acknowledged in any publications resulting from its use. Paper_evidence WBPaper00041807 |