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WormBase Tree Display for Variation: WBVar00248951

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Name Class

WBVar00248951EvidencePaper_evidenceWBPaper00014894
NamePublic_namesy254
Sequence_detailsMapping_targetC37F5
SeqStatusPending_curation
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00027299
WBStrain00027326
LaboratoryPS
StatusLive
AffectsGeneWBGene00002990
InteractorWBInteraction000502206
DescriptionPhenotypeWBPhenotype:0000700Paper_evidenceWBPaper00002125
Curator_confirmedWBPerson625
RemarkmultivulvaPaper_evidenceWBPaper00002125
Curator_confirmedWBPerson625
EQ_annotationsAnatomy_termWBbt:0006748PATO:0000460Paper_evidenceWBPaper00002125
Curator_confirmedWBPerson625
WBPhenotype:0000961Paper_evidenceWBPaper00004481
Curator_confirmedWBPerson2987
Remark"Similar to lin-15 mutants, lin-1 loss-of-function mutants have all VPCs adopting vulval fates, and the AC is closest to P6.p, which always becomes 1°. We found that the zmp-1::GFP expression pattern in P6.pxxx was abnormal in 18 of 23 animals examined (Table 5), suggesting that lin-1 is involved in 1° lineage patterning."Paper_evidenceWBPaper00004481
Curator_confirmedWBPerson2987
"Simply activating RAS signaling by let-23(gf) can partially rescue the 1° patterning defect caused by the absence of the AC (Table 5), suggesting that the inner and outer 1° VPC descendants can differentiate from one another independent of the AC. Furthermore, when the AC was ablated, RAS signaling disrupted by heat shock induced RAS(dn) after the induction of VPC fates, or lin-1 mutated, the 1° VPC descendants expressed zmp-1::GFP in a variable fashion (Tables 1D, 4, 5). However, a careful examination of the pattern of zmp-1::GFP expression shows that among the pairs of 1° inner and outer P6.pxxx cells that adopted different fates, 64/70, 33/38 and 48/52 had the proper orientation with vulF facing the normal position of the AC, respectively (Table 7)."Paper_evidenceWBPaper00004481
Curator_confirmedWBPerson2987
EQ_annotationsAnatomy_termWBbt:0007809PATO:0000460Paper_evidenceWBPaper00004481
Curator_confirmedWBPerson2987
Phenotype_assayGenotypesyIs49 [zmp-1::GFP]Paper_evidenceWBPaper00004481
Curator_confirmedWBPerson2987
ReferenceWBPaper00002125
WBPaper00004481
WBPaper00014894
RemarkExons 3 and 6 are deleted and exons 4 and 5 are reaaranged.Paper_evidenceWBPaper00024367
MethodAllele