WormBase Tree Display for Gene: WBGene00020319

WBGene00020319 SMap: S_parent: Sequence: T07F8
  Identity: Version: 2
    Name: CGC_name: npr-31 Person_evidence: WBPerson260
            WBPerson42
      Sequence_name: T07F8.2
      Molecular_name: T07F8.2
        T07F8.2.1
        CE39767
      Other_name: CELE_T07F8.2 Accession_evidence: NDB BX284602
      Public_name: npr-31
    DB_info: Database: AceView gene 2H437
        WormQTL gene WBGene00020319
        WormFlux gene WBGene00020319
        NDB locus_tag CELE_T07F8.2
        Panther gene CAEEL|WormBase=WBGene00020319|UniProtKB=P91439
          family PTHR24228
        NCBI gene 188235
        RefSeq protein NM_063080.3
        TrEMBL UniProtAcc P91439
        UniProt_GCRP UniProtAcc P91439
        OMIM gene 600804
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:31:03 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 12 Apr 2012 16:15:57 WBPerson2970 Name_change: CGC_name: npr-31
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: npr
    Allele (28)
    Strain: WBStrain00051544
    RNASeq_FPKM (74)
    GO_annotation: 00051043
      00051044
      00051045
      00051046
      00051047
      00051048
      00051049
      00124969
      00124970
      00124971
    Ortholog (35)
    Paralog (24)
    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 Huntington's disease and type 2 diabetes mellitus. Is an ortholog of several human genes including APLNR (apelin receptor); MTNR1A (melatonin receptor 1A); and MTNR1B (melatonin receptor 1B). 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:12858 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7463)
      DOID:9352 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7464)
  Molecular_info: Corresponding_CDS: T07F8.2
    Corresponding_CDS_history: T07F8.2:wp151
      T07F8.2:wp154
    Corresponding_transcript: T07F8.2.1
    Other_sequence: BXC05297_1
      JI172983.1
    Associated_feature: WBsf717001
      WBsf988364
      WBsf988365
  Experimental_info: RNAi_result: WBRNAi00018386 Inferred_automatically: RNAi_primary
      WBRNAi00052779 Inferred_automatically: RNAi_primary
      WBRNAi00103513 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr16036
      Expr1020890
      Expr1156386
      Expr2014418
      Expr2032659
    Drives_construct: WBCnstr00025224
      WBCnstr00042705
    Construct_product: WBCnstr00025224
    Microarray_results (18)
    Expression_cluster (67)
    Interaction: WBInteraction000326821
      WBInteraction000398165
  Map_info: Map: II Position: 0.495807
    Positive: Positive_clone: T07F8 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  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