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WormBase Tree Display for Variation: WBVar00144802

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Name Class

WBVar00144802EvidencePaper_evidenceWBPaper00012673
NamePublic_namee2394
Sequence_detailsSeqStatusPending_curation
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryCB
StatusLive
AffectsGeneWBGene00001194
DescriptionPhenotypeWBPhenotype:0000062Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
Remarkegl-27(e2394) animals exhibited an 11% penetrant embryonic or L1 larval arrest (Table 1)Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
PenetranceIncomplete11% penetrantPaper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
WBPhenotype:0000816Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
RemarkApproximately 40% of egl-27(e2394) animals exhibited missing QL and/or QR neuroblasts at hatching (Table 1)Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
PenetranceIncomplete40% penetrantPaper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
EQ_annotationsAnatomy_termWBbt:0004056PATO:0000460Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
WBbt:0004054PATO:0000460Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
Life_stageWBls:0000024PATO:0000460Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
WBPhenotype:0000828Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
Remarkegl-27(e2394) mutants exhibited an abnormal pattern of T cell lineages, with all descendants of T adopting a hypodermal or hypodermal-like fate, unlike wild type (Figure 1).Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
EQ_annotationsAnatomy_termWBbt:0006994PATO:0000460Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
WBbt:0006996PATO:0000460Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
WBbt:0006995PATO:0000460Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
WBbt:0006997PATO:0000460Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
WBPhenotype:0002211Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
RemarkThe egl-27(e2394) mutation results in a completely penetrant phasmid dye filling defect, indicative of abnormal T cell polarity (Table 1).Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
PenetranceCompletePaper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
EQ_annotationsAnatomy_termWBbt:0005425PATO:0000460Paper_evidenceWBPaper00003450
Curator_confirmedWBPerson2987
ReferenceWBPaper00012673
WBPaper00003450
MethodAllele