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WormBase Tree Display for Variation: WBVar00090239

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Name Class

WBVar00090239EvidencePaper_evidenceWBPaper00001105
NamePublic_namen1706
Sequence_detailsSeqStatusPending_curation
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryMT
StatusLive
AffectsGeneWBGene00003244
DescriptionPhenotypeWBPhenotype:0000006Paper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
PenetranceIncompletePaper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
Range2929Paper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
EQ_annotationsLife_stageWBls:0000057PATO:0000460Paper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
WBPhenotype:0000024Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkinsensitive to serotoninPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000470Paper_evidenceWBPaper00001105
Person_evidenceWBPerson261
Curator_confirmedWBPerson2021
WBPerson712
RemarkHSNs fail to arrive at their final destination (between P5/6 and V4)Paper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
defective HSN migrationPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
EQ_annotationsAnatomy_termWBbt:0006830PATO:0000460Paper_evidenceWBPaper00001105
Person_evidenceWBPerson261
Curator_confirmedWBPerson2021
WBPerson712
Life_stageWBls:0000057PATO:0000460Paper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
WBPhenotype:0000594Paper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
RemarkMigration defects (which include those of ALM and CAN neurons)Paper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
WBPhenotype:0000640Person_evidenceWBPerson261
Curator_confirmedWBPerson712
RemarkEglPerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000643Paper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
WBPhenotype:0000695Paper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
ReferenceWBPaper00001105
MethodAllele