WormBase Tree Display for Variation: WBVar00143397

WBVar00143397 Name: Public_name: e677
  Sequence_details: SeqStatus: Pending_curation
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00000598
      WBStrain00000599
      WBStrain00000600
      WBStrain00000601
      WBStrain00000607
      WBStrain00000608
      WBStrain00000631
      WBStrain00004196
      WBStrain00027135
      WBStrain00033510
    Laboratory: CB
    Status: Live
  Affects: Gene: WBGene00006794
    Interactor: WBInteraction000519073
  Genetics: Mapping_data: In_2_point: 123
        714
        1724
        2862
        2905
        3032
        3145
        6126
      In_multi_point (17)
      In_pos_neg_data: 1793
        1799
        1805
        2166
        3092
        3257
  Description: Phenotype: WBPhenotype:0000349 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: limp paralysed or very slow; resembles e723 Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
        Ease_of_scoring: ES3_Easy_to_score: Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
      WBPhenotype:0000643 Paper_evidence: WBPaper00001474
        Curator_confirmed: WBPerson712
        Remark: Unc Paper_evidence: WBPaper00001474
            Curator_confirmed: WBPerson712
      WBPhenotype:0000644 Paper_evidence: WBPaper00000031
        Person_evidence: WBPerson261
        Curator_confirmed: WBPerson48
          WBPerson712
        Remark: limp paralysed or very slow; resembles e723 Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
      WBPhenotype:0000646 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: limp paralysed or very slow; resembles e723 Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
      WBPhenotype:0000861 Paper_evidence: WBPaper00000031
        Curator_confirmed: WBPerson48
        Remark: defect in body muscle cells Paper_evidence: WBPaper00000031
            Curator_confirmed: WBPerson48
      WBPhenotype:0000926 Paper_evidence: WBPaper00000031
        Curator_confirmed: WBPerson48
        Remark: defect in body muscle cells Paper_evidence: WBPaper00000031
            Curator_confirmed: WBPerson48
      WBPhenotype:0001292 Paper_evidence: WBPaper00000031
        Curator_confirmed: WBPerson48
        Remark: defect in body muscle cells Paper_evidence: WBPaper00000031
            Curator_confirmed: WBPerson48
    Phenotype_not_observed: WBPhenotype:0001426 Paper_evidence: WBPaper00004883
        Curator_confirmed: WBPerson712
        Variation_effect: Hypomorph_reduction_of_function: Paper_evidence: WBPaper00004883
            Curator_confirmed: WBPerson712
        Phenotype_assay: Genotype: arIs37 Paper_evidence: WBPaper00004883
              Curator_confirmed: WBPerson712
  Reference: WBPaper00001474
    WBPaper00000031
    WBPaper00004883
    WBPaper00016390
    WBPaper00016495
    WBPaper00013649
    WBPaper00014773
    WBPaper00015482
  Method: Allele