WormBase Tree Display for Gene: WBGene00011878

WBGene00011878 SMap: S_parent: Sequence: T21B4
  Identity: Version: 2
    Name: CGC_name: ador-1 Person_evidence: WBPerson2467
      Sequence_name: T21B4.4
      Molecular_name: T21B4.4a
        T21B4.4a.1
        CE40126
        T21B4.4b
        CE40127
        T21B4.4b.1
      Other_name: CELE_T21B4.4 Accession_evidence: NDB BX284602
      Public_name: ador-1
    DB_info: Database: AceView gene 2M788
        WormQTL gene WBGene00011878
        WormFlux gene WBGene00011878
        NDB locus_tag CELE_T21B4.4
        Panther gene CAEEL|WormBase=WBGene00011878|UniProtKB=Q1ZXT2
          family PTHR24246
        NCBI gene 174890
        RefSeq protein NM_001047344.4
            NM_001047345.5
        TREEFAM TREEFAM_ID TF325296
        TrEMBL UniProtAcc Q1ZXT1
            Q1ZXT2
        UniProt_GCRP UniProtAcc Q1ZXT2
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:53 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
        2 10 Feb 2012 15:49:10 WBPerson2970 Name_change: CGC_name: ador-1
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: ador
    Allele (146)
    RNASeq_FPKM (74)
    GO_annotation (12)
    Ortholog (46)
    Paralog (17)
    Structured_description: Automated_description: Predicted to enable G protein-coupled receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in asthma; hypertension; and obesity. Is an ortholog of several human genes including ADORA1 (adenosine A1 receptor); ADORA2A (adenosine A2a receptor); and ADORA2B (adenosine A2b receptor). 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:9970 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:262)
      DOID:2841 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:262,HGNC:263)
      DOID:10763 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:262,HGNC:263)
  Molecular_info: Corresponding_CDS: T21B4.4a
      T21B4.4b
    Corresponding_CDS_history: T21B4.4:wp156
    Corresponding_transcript: T21B4.4a.1
      T21B4.4b.1
    Other_sequence (11)
    Associated_feature (16)
  Experimental_info: RNAi_result: WBRNAi00072226 Inferred_automatically: RNAi_primary
      WBRNAi00053696 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1018537
      Expr1157249
      Expr2009237
      Expr2027474
    Drives_construct: WBCnstr00030316
    Construct_product: WBCnstr00030316
    Microarray_results (23)
    Expression_cluster (95)
    Interaction: WBInteraction000134302
      WBInteraction000211772
      WBInteraction000231973
      WBInteraction000254303
      WBInteraction000270411
      WBInteraction000285004
      WBInteraction000295099
      WBInteraction000393717
      WBInteraction000398458
  Map_info: Map: II Position: 10.1552
    Positive: Positive_clone: T21B4 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00038491
    WBPaper00043208
    WBPaper00054831
    WBPaper00055090
    WBPaper00055319
    WBPaper00060134
    WBPaper00063830
    WBPaper00064944
    WBPaper00065953
  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