WormBase Tree Display for Gene: WBGene00020516

WBGene00020516 SMap: S_parent: Sequence: T15B7
  Identity: Version: 2
    Name: Sequence_name: T15B7.1
      Molecular_name: T15B7.1
        T15B7.1.1
        CE43669
      Other_name: CELE_T15B7.1 Accession_evidence: NDB BX284605
      Public_name: T15B7.1
    DB_info: Database: AceView gene 5H327
        WormQTL gene WBGene00020516
        WormFlux gene WBGene00020516
        NDB locus_tag CELE_T15B7.1
        Panther gene CAEEL|WormBase=WBGene00020516|UniProtKB=Q5ZR75
          family PTHR19143
        NCBI gene 188512
        RefSeq protein NM_072342.6
        TrEMBL UniProtAcc Q5ZR75
        UniProt_GCRP UniProtAcc Q5ZR75
        OMIM gene 604973
    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 29 Nov 2004 15:51:45 WBPerson2970 Event: Acquires_merge: WBGene00020521
      Acquires_merge: WBGene00020521
    Status: Live
  Gene_info: Biotype: SO:0001217
    Allele (57)
    RNASeq_FPKM (74)
    GO_annotation: 00081529
      00081530
    Ortholog (76)
    Paralog: WBGene00017013 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00002915 Caenorhabditis elegans From_analysis: WormBase-Compara
      WBGene00007687 Caenorhabditis elegans From_analysis: WormBase-Compara
      WBGene00011326 Caenorhabditis elegans From_analysis: WormBase-Compara
    Structured_description: Automated_description: Predicted to be located in collagen-containing extracellular matrix and extracellular space. Is an ortholog of several human genes including FCN1 (ficolin 1); FCN2 (ficolin 2); and MFAP4 (microfibril associated protein 4). 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: EFO:MONDO:0044209 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:3625)
  Molecular_info: Corresponding_CDS: T15B7.1
    Corresponding_CDS_history: T15B7.1:wp131
      T15B7.1:wp202
    Corresponding_transcript: T15B7.1.1
    Other_sequence: Hbac_isotig02250
      Oden_isotig24882
      EX914609.1
      CBC09366_1
      HBC22060_1
    Associated_feature: WBsf1000373
      WBsf231917
      WBsf231918
      WBsf231919
      WBsf231920
  Experimental_info: RNAi_result: WBRNAi00018744 Inferred_automatically: RNAi_primary
      WBRNAi00053362 Inferred_automatically: RNAi_primary
      WBRNAi00053353 Inferred_automatically: RNAi_primary
      WBRNAi00103533 Inferred_automatically: RNAi_primary
      WBRNAi00035584 Inferred_automatically: RNAi_primary
      WBRNAi00053371 Inferred_automatically: RNAi_primary
      WBRNAi00018733 Inferred_automatically: RNAi_primary
      WBRNAi00095073 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1021779
      Expr1156936
      Expr2006192
      Expr2024408
    Drives_construct: WBCnstr00025082
    Construct_product: WBCnstr00025082
    Microarray_results (26)
    Expression_cluster (256)
    Interaction (121)
  Map_info: Positive: Positive_clone: T15B7 Inferred_automatically: From sequence, transcript, pseudogene data
    Interpolated_map_position: V 0.343991
  Reference: WBPaper00038491
    WBPaper00055090
  Method: Gene