WormBase Tree Display for Phenotype: WBPhenotype:0001652

WBPhenotype:0001652 Description: Any variation in the process by which the gonad anchor cell makes contact with vulval cells in order to create a uterine-vulval connection. In C. elegans, this includes the loss of the basement membranes between these cells and the crossing of the basolateral portion of the anchor cell through this gap. Paper_evidence: WBPaper00005989
  Name: Primary_name: anchor cell invasion variant
    Synonym: anchor cell invasion abnormal
  Related_phenotypes: Specialisation_of: WBPhenotype:0000283
  Attribute_of: RNAi: WBRNAi00061041
      WBRNAi00061042
      WBRNAi00061043
      WBRNAi00070210
      WBRNAi00070217
      WBRNAi00070944
      WBRNAi00070945
      WBRNAi00070946
      WBRNAi00078065
      WBRNAi00078066
      WBRNAi00083946
      WBRNAi00083947
      WBRNAi00083948
      WBRNAi00083949
      WBRNAi00083951
      WBRNAi00083955
      WBRNAi00093059
      WBRNAi00112365
      WBRNAi00112366
      WBRNAi00112379
      WBRNAi00114535
      WBRNAi00114537
      WBRNAi00115742
      WBRNAi00115743
    Variation (8)
    Transgene (4)
    Anatomy_function (28)
    Interaction: WBInteraction000050615
      WBInteraction000051961
      WBInteraction000521265
      WBInteraction000521266
      WBInteraction000521267
      WBInteraction000521268
      WBInteraction000524362
      WBInteraction000578854
    Not_in_RNAi: WBRNAi00070204
      WBRNAi00070205
      WBRNAi00070206
      WBRNAi00070207
      WBRNAi00078064
      WBRNAi00078700
      WBRNAi00083950
    Not_in_Variation (107)
    Not_in_Strain: WBStrain00027056
    Not_in_Transgene: WBTransgene00005885
      WBTransgene00005945