WormBase Tree Display for Gene: WBGene00018067

WBGene00018067 SMap: S_parent: Sequence: F35G8
  Identity: Version: 2
    Name: CGC_name: npr-7 Paper_evidence: WBPaper00033064
          Person_evidence: WBPerson2441
      Sequence_name: F35G8.1
      Molecular_name: F35G8.1
        F35G8.1.1
        CE39498
      Other_name: CELE_F35G8.1 Accession_evidence: NDB BX284606
      Public_name: npr-7
    DB_info: Database: AceView gene XJ932
            XJ930
        WormQTL gene WBGene00018067
        WormFlux gene WBGene00018067
        NDB locus_tag CELE_F35G8.1
        Panther gene CAEEL|WormBase=WBGene00018067|UniProtKB=Q20067
          family PTHR24235
        NCBI gene 185321
        RefSeq protein NM_077169.5
        TrEMBL UniProtAcc Q20067
        UniProt_GCRP UniProtAcc Q20067
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:30:59 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 20 Dec 2011 16:46:04 WBPerson2970 Name_change: CGC_name: npr-7
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: npr
    Allele (54)
    Strain: WBStrain00031475
    RNASeq_FPKM (74)
    GO_annotation (16)
    Ortholog (34)
    Paralog (19)
    Structured_description: Automated_description: Predicted to enable neuropeptide binding activity and neuropeptide receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to be located in neuron projection and plasma membrane. Human ortholog(s) of this gene implicated in artery disease (multiple); lipid metabolism disorder; and obesity. Is an ortholog of human NPY5R (neuropeptide Y receptor Y5) and PRLHR (prolactin releasing hormone 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:7958)
      DOID:3146 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7958)
      DOID:0050830 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7958)
      DOID:10763 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:4464)
  Molecular_info: Corresponding_CDS: F35G8.1
    Corresponding_CDS_history: F35G8.1:wp129
      F35G8.1:wp152
    Corresponding_transcript: F35G8.1.1
    Associated_feature: WBsf1006393
      WBsf1006394
      WBsf1023541
      WBsf1023542
      WBsf237760
  Experimental_info: RNAi_result: WBRNAi00046415 Inferred_automatically: RNAi_primary
      WBRNAi00075426 Inferred_automatically: RNAi_primary
      WBRNAi00014373 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1013623
      Expr1150280
      Expr2014427
      Expr2032668
    Microarray_results (18)
    Expression_cluster (96)
    Interaction (16)
  Map_info: Map: X Position: 1.01482
    Positive: Positive_clone: F35G8 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00006132
    WBPaper00027520
    WBPaper00032196
    WBPaper00038491
    WBPaper00043908
    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