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WormBase Tree Display for Variation: WBVar00144374

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Name Class

WBVar00144374NamePublic_namee1875
Sequence_detailsSeqStatusPending_curation
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
LaboratoryCB
StatusLive
AffectsGeneWBGene00006605
DescriptionPhenotypeWBPhenotype:0000640Person_evidenceWBPerson261
Curator_confirmedWBPerson712
Remarkslightly Egl hermaphrodite, very weak allelePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
RecessivePerson_evidenceWBPerson261
Curator_confirmedWBPerson712
WBPhenotype:0000930Paper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
Remark31 percent of e1875 XX animals have enlarged, male-like B cells and 49 percent have ventral coelomocytes in the male positionPaper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
PenetranceIncompletePaper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
WBPhenotype:0001220Paper_evidenceWBPaper00001133
WBPaper00001105
Curator_confirmedWBPerson2021
RemarkEither one or both HSNs (which normally undergo apoptosis only in males) die in hermaphroditesPaper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
HSNs undergo embryonic apoptosis in hermaphrodites.Paper_evidenceWBPaper00001105
Curator_confirmedWBPerson2021
PenetranceHighPaper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
Range9494Paper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
EQ_annotationsAnatomy_termWBbt:0006830PATO:0000460Paper_evidenceWBPaper00001133
WBPaper00001105
Curator_confirmedWBPerson2021
WBPhenotype:0001277Paper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
Remarktra-2 XX animals that are heterozygous for e1875 in trans to n196 are transformed into infertile phenotypic malesPaper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
Variation_effectHypomorph_reduction_of_functionPaper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
Phenotype_assayGenotypee1875/n196Paper_evidenceWBPaper00001133
Curator_confirmedWBPerson2021
ReferenceWBPaper00016157
WBPaper00001105
WBPaper00001133
WBPaper00013706
WBPaper00014794
MethodAllele