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WormBase Tree Display for Variation: WBVar00145405

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Name Class

WBVar00145405EvidencePaper_evidenceWBPaper00027609
NamePublic_namega62
Other_nameCE34955:p.His329Tyr
R06B9.6.1:c.985C>T
HGVSgCHROMOSOME_II:g.13746999C>T
Sequence_detailsSMapS_parentSequenceR06B9
Flanking_sequencesttctcgttttggctcatttttgccggcgagatctgatcgatgataataccagaaataatt
Mapping_targetR06B9
Type_of_mutationSubstitutionctPaper_evidenceWBPaper00027609
SeqStatusSequenced
Variation_typeAllele
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00007433
LaboratorySD
StatusLive
AffectsGeneWBGene00305552
WBGene00003246
TranscriptR06B9.7
R06B9.6.1 (12)
InteractorWBInteraction000001247
WBInteraction000504807
WBInteraction000521345
WBInteraction000524019
WBInteraction000524372
WBInteraction000524373
WBInteraction000535541
GeneticsInterpolated_map_positionII20.2552
DescriptionPhenotype (15)
Phenotype_not_observedWBPhenotype:0000062Paper_evidenceWBPaper00031356
Curator_confirmedWBPerson712
WBPhenotype:0000306Paper_evidenceWBPaper00027035
Curator_confirmedWBPerson2987
Remark"We first analyzed the expression pattern of lin-39::GFP in bar-1(ga80) and mig-14(ga62) mutants where Wnt signaling is compromised (Eisenmann et al., 1998; Eisenmann and Kim, 2000). In these mutants, we found that GFP levels were upregulated in P6.p, as in wild type animals (data not shown). This is consistent with the phenotypes of bar-1(ga80) and mig-14(ga62), which show a highly penetrant Fused fate phenotype for P3.p and P4.p, but a weaker phenotype for the remaining VPCs where lin-39::GFP expression is robust."Paper_evidenceWBPaper00027035
Curator_confirmedWBPerson2987
EQ_annotationsAnatomy_termWBbt:0006894PATO:0000460Paper_evidenceWBPaper00027035
Curator_confirmedWBPerson2987
Phenotype_assayGenotypelin-39::GFPPaper_evidenceWBPaper00027035
Curator_confirmedWBPerson2987
WBPhenotype:0000822Paper_evidenceWBPaper00036019
Curator_confirmedWBPerson712
RemarkMale gonads do not exhibit any apparent gonadal feminization.Paper_evidenceWBPaper00036019
Curator_confirmedWBPerson712
WBPhenotype:0001652Paper_evidenceWBPaper00032446
Curator_confirmedWBPerson2021
Reference (11)
MethodSubstitution_allele