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WormBase Tree Display for Variation: WBVar00089177

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Name Class

WBVar00089177NamePublic_namemn585
Sequence_detailsSeqStatusPending_curation
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratorySP
StatusLive
AffectsGeneWBGene00001194
DescriptionPhenotypeWBPhenotype:0000062Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
Remarkegl-27(mn585) animals exhibited a 68% penetrant embryonic or L1 larval arrest (Table 1)Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
PenetranceIncomplete68% penetrantPaper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
WBPhenotype:0002211Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
RemarkThe egl-27(mn585) mutation results in a 73% penetrant phasmid dye filling defect, indicative of abnormal T cell polarity (Table 1).Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
PenetranceIncomplete73% penetrancePaper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
EQ_annotationsAnatomy_termWBbt:0005425PATO:0000460Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
ReferenceWBPaper00003450
MethodAllele