Gene Information: unc-54

Nameunc-54 View on WormBase
Species C. elegans
SequenceF11C3.3
Genetic positionI:27.96 +/- 0.002 cM
Genomic positionI: 14855901..14863482

Strains carrying this gene

Strain Genotype Description
AM140 rmIs132 I. rmIs132 [unc-54p::Q35::YFP]. AM140 animals show a Q35::YFP progressive transition from soluble to aggregated as they age.
AM141 rmIs133. rmIs133 [unc-54p::Q40::YFP]. AM141 animals show a soluble Q40::YFP distribution in body wall muscle cells immediately after hatching. As these worms age the rapid formation of foci is observed. When they reach adulthood, AM141 animals show an entirely Q40::YFP aggregated phenotype.
ATD6 par-6(zu222) unc-101(m1)/hIn1[unc-54(h1040)] I; unc-119(ed3) III; zuIs45 V. zuIs45 [nmy-2p::nmy-2::GFP + unc-119(+)] V. Balanced worms are wild-type and segregate wild-type (heterozygotes), Coil Par (par-6 unc-101 homozygotes; maternal effect lethal), and paralyzed Unc (hIn1 homozygotes). Par phenotype is slightly leaky, but survivors are agametic. NMY-2::GFP is expressed in the germline and somatic gonad. Cross of JJ1473 and KK818. Unknown if unc-119(ed3) is still present or homozygous in background. Reference: Small LE & Dawes AT. Mol Biol Cell. 2017 Aug 1;28(16):2220-2231.
BC347 unc-54(s74) I. Paralyzed Rigid Unc. Muscle birefrigence normal. Muscle normal in EM.
CB1008 unc-54(e1008) I. Unc. Suppressed by sup-5 and sup-7.
CB1009 unc-54(e1009) I. Paralyzed Unc. Null allele.
CB1092 unc-54(e1092) I. Paralyzed Unc. Null allele.
CB1108 unc-54(e1108) I. Slow moving Unc.
CB1157 unc-54(e1157) I. Temperature sensitive. Unc. Recessive. Dominant Slow.
CB1168 unc-54(e1168) I. Paralyzed Unc. Null allele.
CB1201 unc-54(e1201) I. Paralyzed Unc. Null allele.
CB1258 unc-54(e1258) I. Paralyzed Unc. Null allele.
CB1300 unc-54(e1300) I. Unc. Suppressed by sup-5 and sup-7. Null allele? Milder than most null.
CB1301 unc-54(e1301) I. Temperature sensitive Unc.
CB1315 unc-54(e1315) I. Paralyzed Unc. Severe phenotype. Recessive. Null allele.
CB1419 unc-54(e1419) I. Unc. Suppressed by sup-5 and sup-7.
CB190 unc-54(e190) I. Semi-paralyzed Unc. Null allele. Recessive. M-MATING-NO SUCCESS.
CB2203 unc-54(e190) I; dpy-11(e224) eDp22 V. Dpy. Movement Slow. Unc partially suppressed.
CB2204 unc-54(e190) I; eDp22 V. Movement slow. Unc partially suppressed.
CB2221 unc-54(e1315) I; dpy-11(e224) eDp23 V. Dpy. Movement Slow. Unc partially suppressed.
CB2779 let-201(e1716) unc-54(e1092)/eDf24 I. Heterozygotes are WT. eDf24 homozygotes arrest as early larvae. eDf24 = let(e2000).
CB2780 let-203(e1717) unc-54(e1092)/eDf24 I. Heterozygotes are WT. eDf24 homozygotes arrest as early larvae. eDf24 = let(e2000).
CB2781 unc-54(e1092) let-208(e1718)/eDf24 I. Heterozygotes are WT. eDf24 homozygotes arrest as early larvae. eDf24 = let(e2000).
CB2782 let-204(e1719) unc-54(e1092)/eDf24 I. Heterozygotes are WT. eDf24 homozygotes arrest as early larvae. eDf24 = let(e2000).
CB2784 let-202(e1720) unc-54(e1092)/eDf24 I. Heterozygotes are WT. eDf24 homozygotes arrest as early larvae. eDf24 = let(e2000).
CB2785 let-206(e1721) unc-54(e1092)/eDf24 I. Heterozygotes are WT. eDf24 homozygotes arrest as early larvae. eDf24 = let(e2000).
CB2786 let-205(e1722) unc-54(e1092)/eDf24 I. Heterozygotes are WT. eDf24 homozygotes arrest as early larvae. eDf24 = let(e2000).
CB2787 let-207(e1723) unc-54(e1092)/eDf24 I. Heterozygotes are WT. eDf24 homozygotes arrest as early larvae. eDf24 = let(e2000).
CB3019 unc-54(e1258) I; eDf1 eDp21/+ V. Movement slow. Suppressed Unc. Revertant. Heterozygotes move slowly and segregate larval lethals (eDf1 eDp21 homozygotes), and paralyzed Uncs.
CB3035 unc-54(e1258) I; wdDp1 V. Suppressed Unc.
CB569 unc-54(e569) I. Paralyzed Unc.
CB576 unc-54(e576) I. Slow movement.
CB651 unc-54(e651) I.
CB675 unc-54(e675) I. Slow moving Unc. Semi-dominant.
CB843 unc-54(e843) I. Stiff. Body muscle abnormal.
CGC58 C54E10.3(umn2[LoxP + myo-2p::GFP::unc-54 3' UTR + rps-27p::neoR::unc-54 3' UTR + LoxP]) V. Homozygous viable. Deletion of 745 bp with Calarco/Colaiacovo selection cassette conferring myo-2::GFP and G418 resistance inserted at break in parental strain N2. Left flanking Sequence: tgtacccccgatgggattcgaacctgtggc ; Right flanking sequence: gggtatgcaaaatgaccgcgttttctgtga. Please reference Au et al., G3 9(1): 135-144 2019 in any work resulting from use of this mutation.
CGC59 gnrr-7(umn3[LoxP + myo-2p::GFP::unc-54 3' UTR + rps-27p::neoR::unc-54 3' UTR + LoxP]) X. Homozygous viable. Deletion of 1004 bp with Calarco/Colaiacovo selection cassette conferring myo-2 GFP and G418 resistance inserted at break in parental strain N2. Left flanking Sequence: ttgttctggtttaaagccgcaaagtcttgg ; Right flanking sequence: agggtaccatcaagcaatggcattctggtt. Please reference Au et al., G3 9(1): 135-144 2019 in any work resulting from use of this mutation.
CGC61 F36D4.4(umn4[LoxP + myo-2p::GFP::unc-54 3' UTR + rps-27p::neoR::unc-54 3' UTR + LoxP]) V. Homozygous viable. Deletion of 917 bp with Calarco/Colaiacovo selection cassette conferring myo-2 GFP and G418 resistance inserted at break in parental strain N2. Left flanking Sequence: CATGTACTCCCCTATATCTTCCAAACATTC ; Right flanking sequence: TGGACATCTTGGAGCACTTTCTGTGATTCT. Please reference Au et al., G3 9(1): 135-144 2019 in any work resulting from use of this mutation.
CGC72 npr-23(umn5[LoxP + myo-2p::GFP::unc-54 3' UTR + rps-27p::neoR::unc-54 3' UTR + LoxP]) I. Homozygous viable. Deletion of 280 bp with Calarco/Colaiacovo selection cassette conferring myo-2 GFP and G418 resistance inserted at break in parental strain N2. Left flanking Sequence: AAGGCGTCATCTGGAGAGAAGAACGAAgtg ; Right flanking sequence: CGGACACTTGTGCTTCACCAACTTGATCGC. Please reference Au et al., G3 9(1): 135-144 2019 in any work resulting from use of this mutation.
CGC73 npr-28(umn6[LoxP + myo-2p::GFP::unc-54 3' UTR + rps-27p::neoR::unc-54 3' UTR + LoxP]) X. Homozygous viable. Deletion of 842 bp with Calarco/Colaiacovo selection cassette conferring myo-2 GFP and G418 resistance inserted at break in parental strain N2. Left flanking Sequence: TATTTGGTATCATTTTTCTAGCCGACTTTC ; Right flanking sequence: TGGACTTGTTTTCACTCATCCCTGTACCGA. Please reference Au et al., G3 9(1): 135-144 2019 in any work resulting from use of this mutation.
CGC78 C04C3.6(umn8[LoxP + myo-2p::GFP::unc-54 3' UTR + rps-27p::neoR::unc-54 3' UTR + LoxP]) IV. Homozygous viable. Deletion of 1123 bp with Calarco/Colaiacovo selection cassette conferring myo-2 GFP and G418 resistance inserted at break in parental strain N2. Left flanking Sequence: aaaaatcaactatttttaatgaaaatttca ; Right flanking sequence: TGGTCACTTTACCTGCGTTGATATTCATGT. Please reference Au et al., G3 9(1): 135-144 2019 in any work resulting from use of this mutation.
CGC81 C09F12.3(umn9[LoxP + myo-2p::GFP::unc-54 3' UTR + rps-27p::neoR::unc-54 3' UTR + LoxP]) X. Homozgous viable. Deletion of 1171 bp with Calarco/Colaiacovo selection cassette conferring myo-2 GFP and G418 resistance inserted at break in parental strain N2. Left flanking Sequence: acaatttacattaacttttcattatttcag ; Right flanking sequence: tggatgtgcattttttcgctgctcactctt. Please reference Au et al., G3 9(1): 135-144 2019 in any work resulting from use of this mutation.
CL2006 dvIs2. dvIs2 [pCL12(unc-54/human Abeta peptide 1-42 minigene) + rol-6(su1006)]. Temperature-sensitive. Maintain at 15C. Adult onset paralysis and egg-laying deficiency when raised at 20C. A few animals will be paralyzed even at permissive temperatures. Received new stock from CL 8/2005.
CL2122 dvIs15. dvIs15 [(pPD30.38) unc-54(vector) + (pCL26) mtl-2::GFP]. Control strain for CL2120. Phenotype apparently WT.
CZ3086 kin-1(ok338)/unc-54(r293) I. Heterozygotes are WT and segregate WT, Unc, and early larval lethal.
DR115 unc-15(e73) unc-54(e675) I. Slow movement.
DR119 unc-54(e1258) I; dpy-11(e224) wdDp1 V. DPY.
DR120 unc-54(e1258) I; eDp23 V.
DR176 unc-54(e190) I; eDp23 V. Suppressed-movement slow. Unlinked double.
DR177 unc-54(e1258) I; eDp22 V. Suppressed-movement slow.