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WormBase Tree Display for Variation: WBVar00266521

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Name Class

WBVar00266521EvidencePaper_evidenceWBPaper00003414
NamePublic_nameu63
Other_nameCE24843:p.Glu415Lys
C44B11.3.1:c.1243G>A
HGVSgCHROMOSOME_III:g.3131843C>T
Sequence_detailsSMapS_parentSequenceC44B11
Flanking_sequencesgtccactggtatgttggtgaaggaatggagaaggagaatttagtgaggctcgtgaagatt
Mapping_targetC44B11
Type_of_mutationSubstitutiongaPaper_evidenceWBPaper00003414
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryTU
StatusLive
AffectsGeneWBGene00003175
TranscriptC44B11.3.1 (11)
InteractorWBInteraction000502025
WBInteraction000504762
WBInteraction000504764
GeneticsInterpolated_map_positionIII-7.53489
DescriptionPhenotypeWBPhenotype:0000315Paper_evidenceWBPaper00001125
Curator_confirmedWBPerson712
WBPhenotype:0000962Paper_evidenceWBPaper00038206
Curator_confirmedWBPerson712
RemarkAnimals exhibited reduced fluorescence in GFP-expressing touch receptor neurons (TRNs).Paper_evidenceWBPaper00038206
Curator_confirmedWBPerson712
Phenotype_assayGenotypeuIs22(Pmec-3::GFP)Paper_evidenceWBPaper00038206
Curator_confirmedWBPerson712
WBPhenotype:0002364Paper_evidenceWBPaper00044649
Curator_confirmedWBPerson9270
RemarkSpontaneous axon degeneration affecting PLM, PVM, ALM, and AVM. (Figure 5C, S3G)Paper_evidenceWBPaper00044649
Curator_confirmedWBPerson9270
EQ_annotationsAnatomy_termWBbt:0005490PATO:0000460Paper_evidenceWBPaper00044649
Curator_confirmedWBPerson9270
WBbt:0004086PATO:0000460Paper_evidenceWBPaper00044649
Curator_confirmedWBPerson9270
WBbt:0005406PATO:0000460Paper_evidenceWBPaper00044649
Curator_confirmedWBPerson9270
WBbt:0003832PATO:0000460Paper_evidenceWBPaper00044649
Curator_confirmedWBPerson9270
Phenotype_not_observedWBPhenotype:0001676Paper_evidenceWBPaper00001125
Curator_confirmedWBPerson712
RemarkTouch cell processes have normal numbers of large diameter microtubules compared to processes in control animals.Paper_evidenceWBPaper00001125
Curator_confirmedWBPerson712
ReferenceWBPaper00038206
WBPaper00001125
WBPaper00003414
WBPaper00044649
MethodSubstitution_allele