WormBase Tree Display for Variation: WBVar00143856

WBVar00143856 Evidence: Paper_evidence: WBPaper00013703
  Name: Public_name: e1245
  Sequence_details: SeqStatus: Pending_curation
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00004480
    Laboratory: CB
    Status: Live
  Affects: Gene: WBGene00003106
  Genetics: Mapping_data: In_2_point: 652
        653
        6131
      In_multi_point: 564
        565
        1672
        1674
      In_pos_neg_data: 2613
        2614
        2615
  Description: Phenotype: WBPhenotype:0000054 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: Many males die or rupture during L4 molt. e1245/Df similar. Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
        EQ_annotations: Life_stage: WBls:0000073 PATO:0000460 Person_evidence: WBPerson261
                Curator_confirmed: WBPerson712
        Ease_of_scoring: ES3_Easy_to_score: Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
      WBPhenotype:0000070 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: Male tail morphology and development grossly abnormal. e1245/Df similar. Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
      WBPhenotype:0000347 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: Hermaphrodite grossly WT, sometimes constipated as a result of rectal abnormalities, rectal cells. Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
      WBPhenotype:0000651 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: Hermaphrodite grossly WT, sometimes constipated as a result of rectal abnormalities, rectal cells. Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
      WBPhenotype:0000758 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: Many males die or rupture during L4 molt. e1245/Df similar. Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
        EQ_annotations: Life_stage: WBls:0000073 PATO:0000460 Person_evidence: WBPerson261
                Curator_confirmed: WBPerson712
      WBPhenotype:0000830 Paper_evidence: WBPaper00001189
        Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
          WBPerson105
        Remark: B lineage defective, resembles Y lineage. e1245/Df similar. Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
        EQ_annotations: Anatomy_term: WBbt:0008608 PATO:0000460 Paper_evidence: WBPaper00001189
                Curator_confirmed: WBPerson105
      WBPhenotype:0000835 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: Probable F to U lineage transformation. e1245/Df similar. Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
      WBPhenotype:0001297 Person_evidence: WBPerson261
        Curator_confirmed: WBPerson712
        Remark: Male tail morphology and development grossly abnormal. e1245/Df similar. Person_evidence: WBPerson261
            Curator_confirmed: WBPerson712
    Phenotype_not_observed: WBPhenotype:0001524 Paper_evidence: WBPaper00036308
        Curator_confirmed: WBPerson2987
        Remark: "MAB-9 is a T-box transcription factor that has been observed to be expressed in ALA (Appleford et_al, 2008), but the null mutation mab-9(e1245) has no discernable effect on ALA function (Table 3)." Paper_evidence: WBPaper00036308
            Curator_confirmed: WBPerson2987
        EQ_annotations: Anatomy_term: WBbt:0003955 PATO:0000460 Paper_evidence: WBPaper00036308
                Curator_confirmed: WBPerson2987
        Phenotype_assay: Genotype: hs:LIN-3 Paper_evidence: WBPaper00036308
              Curator_confirmed: WBPerson2987
  Reference: WBPaper00036308
    WBPaper00013703
    WBPaper00001189
  Method: Allele