Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Variation: WBVar00239430

expand all nodes | collapse all nodes | view schema

Name Class

WBVar00239430NamePublic_namepk2083
Sequence_detailsSeqStatusPending_curation
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00028979
LaboratoryNL
StatusLive
AffectsGeneWBGene00011908
InteractorWBInteraction000502008
GeneticsMapping_dataIn_multi_point5599
DescriptionPhenotypeWBPhenotype:0000038Paper_evidenceWBPaper00024573
Curator_confirmedWBPerson712
RemarkDefects in structures are easily detected in pash-1 RNAi knock-down animals and to a lesser degree in a pash-1(pk2083) nonsense mutant. Typical defects include protrusion or bursting of the vulva.Paper_evidenceWBPaper00024573
Curator_confirmedWBPerson712
WBPhenotype:0000280Paper_evidenceWBPaper00024573
Curator_confirmedWBPerson712
RemarkDefects in structures are easily detected in pash-1 RNAi knock-down animals and to a lesser degree in a pash-1(pk2083) nonsense mutant. Typical defects include gaps or absence of the alae.Paper_evidenceWBPaper00024573
Curator_confirmedWBPerson712
WBPhenotype:0000745Paper_evidenceWBPaper00024573
Curator_confirmedWBPerson712
RemarkThis mutation lead to re-expression of the pkIs2084 reporter in the adult stage; in wild type worms, this expression is silenced.Paper_evidenceWBPaper00024573
Curator_confirmedWBPerson712
WBPhenotype:0001096Paper_evidenceWBPaper00024573
Curator_confirmedWBPerson712
RemarkDefects in structures are easily detected in pash-1 RNAi knock-down animals and to a lesser degree in a pash-1(pk2083) nonsense mutant. Typical defects include protrusion or bursting of the vulva.Paper_evidenceWBPaper00024573
Curator_confirmedWBPerson712
WBPhenotype:0001228Paper_evidenceWBPaper00024573
Curator_confirmedWBPerson712
RemarkDefects in structures are easily detected in pash-1 RNAi knock-down animals and to a lesser degree in a pash-1(pk2083) nonsense mutant. Typical defects include gaps or absence of the alae.Paper_evidenceWBPaper00024573
Curator_confirmedWBPerson712
ReferenceWBPaper00029257
WBPaper00024573
RemarkThis variation is reported to effect T22A3.5 with a premature stop giving rise to a sterile phenotype (Sup. Table 2)Paper_evidenceWBPaper00029257
MethodAllele