WormBase Tree Display for Gene: WBGene00015050

WBGene00015050 SMap: S_parent: Sequence: B0218
  Identity: Version: 2
    Name: CGC_name: clec-51 Person_evidence: WBPerson655
      Sequence_name: B0218.6
      Molecular_name: B0218.6a
        B0218.6a.1
        CE06689
        B0218.6b
        CE49543
        B0218.6b.1
      Other_name: CELE_B0218.6 Accession_evidence: NDB BX284604
      Public_name: clec-51
    DB_info: Database: AceView gene 4I928
        WormQTL gene WBGene00015050
        WormFlux gene WBGene00015050
        NDB locus_tag CELE_B0218.6
        Panther gene CAEEL|WormBase=WBGene00015050|UniProtKB=Q17450
          family PTHR22803
        NCBI gene 181854
        RefSeq protein NM_068968.7
            NM_001380354.1
        TrEMBL UniProtAcc Q17450
            W6RTE8
        UniProt_GCRP UniProtAcc Q17450
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:30:55 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 29 Apr 2005 13:53:46 WBPerson2970 Name_change: CGC_name: clec-51
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: clec
    Allele (29)
    RNASeq_FPKM (74)
    GO_annotation: 00058203
    Ortholog (43)
    Paralog (12)
    Structured_description: Automated_description: Predicted to enable signaling receptor activity. Human ortholog(s) of this gene implicated in hepatocellular carcinoma and liver cirrhosis. Is an ortholog of several human genes including LY75 (lymphocyte antigen 75); MRC2 (mannose receptor C type 2); and REG3A (regenerating family member 3 alpha). 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:5082 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:8601)
      DOID:684 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:8601)
  Molecular_info: Corresponding_CDS: B0218.6a
      B0218.6b
    Corresponding_transcript: B0218.6a.1
      B0218.6b.1
    Other_sequence (25)
    Associated_feature: WBsf668087
      WBsf230391
  Experimental_info: RNAi_result: WBRNAi00038747 Inferred_automatically: RNAi_primary
      WBRNAi00028001 Inferred_automatically: RNAi_primary
      WBRNAi00009593 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1015614
      Expr1036431
      Expr1142958
      Expr2010184
      Expr2028426
    Drives_construct: WBCnstr00029127
    Construct_product: WBCnstr00029127
    Microarray_results (20)
    Expression_cluster (208)
    Interaction: WBInteraction000119056
      WBInteraction000119057
      WBInteraction000123416
      WBInteraction000123417
      WBInteraction000123418
      WBInteraction000123419
      WBInteraction000319386
      WBInteraction000362017
      WBInteraction000367114
      WBInteraction000417408
  Map_info: Map: IV Position: 3.64706
    Positive: Positive_clone: B0218 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00032258
    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