WormBase Tree Display for Gene: WBGene00002270

WBGene00002270 SMap: S_parent: Sequence: R07B1
  Identity: Version: 1
    Name: CGC_name: lec-7
      Sequence_name: R07B1.2
      Molecular_name: R07B1.2
        R07B1.2.1
        CE26722
      Other_name: CELE_R07B1.2 Accession_evidence: NDB BX284606
      Public_name: lec-7
    DB_info: Database: AceView gene XK471
        WormQTL gene WBGene00002270
        WormFlux gene WBGene00002270
        NDB locus_tag CELE_R07B1.2
        Panther gene CAEEL|WormBase=WBGene00002270|UniProtKB=Q09605
          family PTHR11346
        NCBI gene 181199
        RefSeq protein NM_001392828.1
        SwissProt UniProtAcc Q09605
        UniProt_GCRP UniProtAcc Q09605
    Species: Caenorhabditis elegans
    History: Version_change: 1 07 Apr 2004 11:29:27 WBPerson1971 Event: Imported: Initial conversion from geneace
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: lec
    Allele (19)
    Legacy_information: [Arata Y] No mutants known. Encodes predicted galectin. Predicted gene R07B1.2
    Strain: WBStrain00032637
    RNASeq_FPKM (74)
    GO_annotation: 00055067
      00055068
      00110342
    Ortholog (38)
    Paralog (26)
    Structured_description: Automated_description: Predicted to enable galactoside binding activity. Human ortholog(s) of this gene implicated in several diseases, including COVID-19; aortic valve stenosis; and liver cirrhosis. Is an ortholog of human LGALS3 (galectin 3). Paper_evidence: WBPaper00065943
          Curator_confirmed: WBPerson324
            WBPerson37462
          Inferred_automatically: This description was generated automatically by a script based on data from the WS291 version of WormBase
          Date_last_updated: 29 Nov 2023 00:00:00
  Disease_info: Potential_model: DOID:0080600 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:6563)
      DOID:2841 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:6563)
      DOID:5082 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:6563)
      DOID:1712 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:6563)
  Molecular_info: Corresponding_CDS: R07B1.2
    Corresponding_CDS_history: R07B1.2:wp40
      R07B1.2a:wp75
      R07B1.2b:wp75
      R07B1.2c:wp75
    Corresponding_transcript: R07B1.2.1
    Associated_feature: WBsf648429
      WBsf236203
  Experimental_info: RNAi_result: WBRNAi00034676 Inferred_automatically: RNAi_primary
      WBRNAi00017501 Inferred_automatically: RNAi_primary
      WBRNAi00051411 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1019289
      Expr1155101
      Expr2013040
      Expr2031272
    Drives_construct: WBCnstr00036343
    Construct_product: WBCnstr00036343
    Microarray_results (37)
    Expression_cluster (155)
    Interaction: WBInteraction000134060
      WBInteraction000134062
      WBInteraction000168785
      WBInteraction000359552
      WBInteraction000368837
      WBInteraction000373141
      WBInteraction000381796
      WBInteraction000404470
      WBInteraction000414119
  Map_info: Map: X Position: 1.72893 Error: 0.000496
    Positive: Positive_clone: R07B1 Person_evidence: WBPerson763
          Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00011877
    WBPaper00032075
    WBPaper00034766
    WBPaper00038491
    WBPaper00055090
  Remark: Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC. CGC_data_submission
  Method: Gene