WormBase Tree Display for Variation: WBVar00090993

WBVar00090993 Evidence: Paper_evidence: WBPaper00026736
  Name: Public_name: ne1373
    Other_name: F38E1.7.1:c.566A>C
      CE17806:p.His189Pro
    HGVSg: CHROMOSOME_V:g.8357272A>C
  Sequence_details: SMap: S_parent: Sequence: F38E1
    Flanking_sequences: ggaaattcgtggaccagtacgatcgccagc cgcaaccgagccacgttctcagatgaattt
    Mapping_target: F38E1
    Type_of_mutation: Substitution: a c Paper_evidence: WBPaper00026736
    SeqStatus: Sequenced
  Variation_type: Allele
  Origin: Species: Caenorhabditis elegans
    Laboratory: WM
    Status: Live
  Affects: Gene: WBGene00003395
    Transcript: F38E1.7.1 (12)
  Genetics: Interpolated_map_position: V 1.32396
  Description: Phenotype: WBPhenotype:0000050 Paper_evidence: WBPaper00026736
        Curator_confirmed: WBPerson2021
        Remark: Mutants have defects in P2/EMS signaling Paper_evidence: WBPaper00026736
            Curator_confirmed: WBPerson2021
        EQ_annotations: Life_stage: WBls:0000003 PATO:0000460 Paper_evidence: WBPaper00026736
                Curator_confirmed: WBPerson2021
        Temperature_sensitive: Heat_sensitive: 25C Paper_evidence: WBPaper00026736
              Curator_confirmed: WBPerson2021
        Phenotype_assay: Temperature: 25C Paper_evidence: WBPaper00026736
              Curator_confirmed: WBPerson2021
  Reference: WBPaper00026736
  Method: Substitution_allele