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WormBase Tree Display for Variation: WBVar00142932

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Name Class

WBVar00142932NamePublic_namee47
Sequence_detailsSeqStatusPending_curation
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00004084
WBStrain00004543
WBStrain00007120
WBStrain00007985
WBStrain00008442
WBStrain00022535
WBStrain00022537
WBStrain00022541
WBStrain00022590
WBStrain00023657
WBStrain00023815
WBStrain00023816
WBStrain00023817
WBStrain00023818
WBStrain00023825
WBStrain00023826
WBStrain00023954
WBStrain00023955
WBStrain00023956
WBStrain00023957
WBStrain00023961
WBStrain00023966
WBStrain00023967
WBStrain00054788
LaboratoryCB
StatusLive
AffectsGeneWBGene00006751
InteractorWBInteraction000500226
WBInteraction000501652
WBInteraction000555717
WBInteraction000555718
WBInteraction000555719
WBInteraction000555720
WBInteraction000555721
WBInteraction000555724
WBInteraction000555725
GeneticsMapping_dataIn_2_point4
5
2495
3200
3941
5224
6046
6079
6080
6171
In_multi_point (42)
In_pos_neg_data (21)
DescriptionPhenotypeWBPhenotype:0000017Paper_evidenceWBPaper00032011
Person_evidenceWBPerson261
Curator_confirmedWBPerson712
RemarkAnimals were resistant to 1mM aldicarb, as assayed by the % of animals paralyzed over time.Paper_evidenceWBPaper00032011
Curator_confirmedWBPerson712
RicPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Affected_byMoleculeWBMol:00003650Paper_evidenceWBPaper00032011
Curator_confirmedWBPerson712
WBPhenotype:0000019Paper_evidenceWBPaper00001709
Person_evidenceWBPerson261
Curator_confirmedWBPerson2021
WBPerson712
Remarkslow pharyngeal pumpingPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
EQ_annotationsAnatomy_termWBbt:0003681PATO:0000460Paper_evidenceWBPaper00001709
Curator_confirmedWBPerson2021
WBPhenotype:0000020Paper_evidenceWBPaper00001709
Curator_confirmedWBPerson2021
EQ_annotationsAnatomy_termWBbt:0003681PATO:0000460Paper_evidenceWBPaper00001709
Curator_confirmedWBPerson2021
WBPhenotype:0000153Paper_evidenceWBPaper00032190
Curator_confirmedWBPerson712
RemarkAnimals exhibited increased contractions.Paper_evidenceWBPaper00032190
Curator_confirmedWBPerson712
Phenotype_assayGenotypezxIs6Paper_evidenceWBPaper00032190
Curator_confirmedWBPerson712
WBPhenotype:0000164Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkslightly thinPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000229Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkslightly smallPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000315Paper_evidenceWBPaper00046308
Curator_confirmedWBPerson10425
WBPhenotype:0000352Paper_evidenceWBPaper00001709
Curator_confirmedWBPerson2021
RemarkJerky backward motionPaper_evidenceWBPaper00001709
Curator_confirmedWBPerson2021
WBPhenotype:0000420Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkhypersensitive to levamisolePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000436Paper_evidenceWBPaper00028886
Curator_confirmedWBPerson48
RemarkLocalization of the synaptic protein SNB-1 is abnormal, based on expression analysis of SNB-1::VENUS; expression appears diffuse across the plasma membrane.Paper_evidenceWBPaper00028886
Curator_confirmedWBPerson48
WBPhenotype:0000507Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkelevated acetylcholine levelsPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000544Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkkinker, jerky ratchet-like movement especially in reversePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
Ease_of_scoringES3_Easy_to_scorePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000594Person_evidenceWBPerson261
Curator_confirmedWBPerson712
RemarkSome migration defects.Person_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000616Paper_evidenceWBPaper00025079
Curator_confirmedWBPerson712
RemarkGLR-1::GFP puncta intensity and width were significantly different from those in wild-type animals.Paper_evidenceWBPaper00025079
Curator_confirmedWBPerson712
WBPhenotype:0000643Paper_evidenceWBPaper00000031
Curator_confirmedWBPerson48
WBPhenotype:0000679Paper_evidenceWBPaper00005349
Curator_confirmedWBPerson10038
Remarkquoted from paper: "in a screen for mutants that have increased abundance of GLR-1::GFP in the ventral nerve cord (data not shown). Similar defects in GLR-1::GFP abundance were observed in other unc-11 mutants, including strains carrying the putative null allele, e47 (Figure 2)." Figure 2 title: " Mutants Lacking unc-11 AP180 Had Increased Abundance of GLR-1::GFP in the Ventral Nerve Cord"Paper_evidenceWBPaper00005349
Curator_confirmedWBPerson10038
EQ_annotationsAnatomy_termWBbt:0005829PATO:0000460Paper_evidenceWBPaper00005349
Curator_confirmedWBPerson10038
Phenotype_assayGenotypenuIs24 [GLR-1::GFP]Paper_evidenceWBPaper00005349
Curator_confirmedWBPerson10038
Phenotype_not_observedWBPhenotype:0000306Paper_evidenceWBPaper00032190
Curator_confirmedWBPerson712
RemarkExpression of ChR2-YFP in cholinergic neurons was not affected.Paper_evidenceWBPaper00032190
Curator_confirmedWBPerson712
Phenotype_assayGenotypezxIs6Paper_evidenceWBPaper00032190
Curator_confirmedWBPerson712
WBPhenotype:0000679Paper_evidenceWBPaper00028448
Curator_confirmedWBPerson712
RemarkThe unc-11(e47) mutation does not alter PKD-2 localization to the dendrite or cilium.Paper_evidenceWBPaper00028448
Curator_confirmedWBPerson712
WBPhenotype:0001426Paper_evidenceWBPaper00004883
Curator_confirmedWBPerson712
Variation_effectNullPaper_evidenceWBPaper00004883
Curator_confirmedWBPerson712
Phenotype_assayGenotypearIs37Paper_evidenceWBPaper00004883
Curator_confirmedWBPerson712
Reference (15)
Remark
MethodAllele