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WormBase Tree Display for Variation: WBVar01429502

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Name Class

WBVar01429502EvidencePaper_evidenceWBPaper00040041
NamePublic_nameu701
Other_nameCE06083:p.Trp232AlafsTer9
K03B8.9.1:c.694_1301del
K03B8.9.2:c.694_1301del
HGVSgCHROMOSOME_V:g.11413627_11414337del
Sequence_detailsSMapS_parentSequenceK03B8
Flanking_sequencesagcatgcaatcattcattccaaatgaagaagccacagtcggctggaagtgtttctgaaaa
Mapping_targetK03B8
Type_of_mutationDeletion
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryTU
StatusLive
AffectsGeneWBGene00000951
TranscriptK03B8.9.2 (11)
K03B8.9.1 (11)
InteractorWBInteraction000518320
GeneticsInterpolated_map_positionV3.08423
DescriptionPhenotypeWBPhenotype:0000643Paper_evidenceWBPaper00041959
Curator_confirmedWBPerson557
RemarkExhibited significantly reduced general locomotor activity compared to control worms. Authors refer to this allele as tu1851, which is the strain name. The allele of deg-3 in this strain is u701.Paper_evidenceWBPaper00041959
Curator_confirmedWBPerson557
WBPhenotype:0001790Paper_evidenceWBPaper00044839
Curator_confirmedWBPerson661
Remarkimaging study shows reduced responses to coldPaper_evidenceWBPaper00044839
Curator_confirmedWBPerson661
WBPhenotype:0002028Paper_evidenceWBPaper00044839
Curator_confirmedWBPerson661
Remarkimaging study shows reduced responses to high threshold mechanical stimuliPaper_evidenceWBPaper00044839
Curator_confirmedWBPerson661
Phenotype_not_observedWBPhenotype:0000384Paper_evidenceWBPaper00040041
Curator_confirmedWBPerson712
RemarkAnimals do not exhibit axon guidance defects.Paper_evidenceWBPaper00040041
Curator_confirmedWBPerson712
EQ_annotationsAnatomy_termWBbt:0003832PATO:0000460Paper_evidenceWBPaper00040041
Curator_confirmedWBPerson712
WBPhenotype:0000643Paper_evidenceWBPaper00002167
Curator_confirmedWBPerson712
Remarkrevertant of the dominant Unc phenotype associated with the u662 mutationPaper_evidenceWBPaper00002167
Curator_confirmedWBPerson712
Variation_effectNullPaper_evidenceWBPaper00002167
Curator_confirmedWBPerson712
WBPhenotype:0000886Paper_evidenceWBPaper00002167
Curator_confirmedWBPerson712
Remarkrevertant of u662; these revertants are phenotypically wild typePaper_evidenceWBPaper00002167
Curator_confirmedWBPerson712
Variation_effectNullPaper_evidenceWBPaper00002167
Curator_confirmedWBPerson712
ReferenceWBPaper00040041
WBPaper00041959
WBPaper00002167
WBPaper00044839
MethodDeletion_allele