WormBase Tree Display for Gene: WBGene00007374

WBGene00007374 SMap: S_parent: Sequence: C06C3
  Identity: Version: 1
    Name: Sequence_name: C06C3.3
      Molecular_name: C06C3.3
        C06C3.3.1
        CE35823
      Other_name: CELE_C06C3.3 Accession_evidence: NDB BX284602
      Public_name: C06C3.3
    DB_info: Database: AceView gene 2J658
        WormQTL gene WBGene00007374
        WormFlux gene WBGene00007374
        NDB locus_tag CELE_C06C3.3
        Panther gene CAEEL|WormBase=WBGene00007374|UniProtKB=Q17711
          family PTHR23004
        NCBI gene 182302
        RefSeq protein NM_063594.4
        TrEMBL UniProtAcc Q17711
        UniProt_GCRP UniProtAcc Q17711
        OMIM gene 605755
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:48 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
    Status: Live
  Gene_info: Biotype: SO:0001217
    Allele (56)
    RNASeq_FPKM (74)
    GO_annotation: 00058989
      00058990
      00115515
    Ortholog (28)
    Paralog: WBGene00012332 Caenorhabditis elegans From_analysis: Panther
            WormBase-Compara
      WBGene00012328 Caenorhabditis elegans From_analysis: Panther
            WormBase-Compara
    Structured_description: Automated_description: Predicted to be involved in intracellular signal transduction. Predicted to be located in microtubule and microtubule organizing center. Human ortholog(s) of this gene implicated in several diseases, including attention deficit hyperactivity disorder; autosomal recessive nonsyndromic deafness 66; and dyslexia. Is an ortholog of human DCDC2 (doublecortin domain containing 2). 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:0110517 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:18141)
      DOID:1094 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:18141)
      DOID:14268 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:18141)
      DOID:0111126 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:18141)
      DOID:4428 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:18141)
  Molecular_info: Corresponding_CDS: C06C3.3
    Corresponding_CDS_history: C06C3.3:wp111
    Corresponding_transcript: C06C3.3.1
    Other_sequence: Acan_isotig19176
    Associated_feature: WBsf223640
      WBsf223641
  Experimental_info: RNAi_result: WBRNAi00010286 Inferred_automatically: RNAi_primary
      WBRNAi00115905 Inferred_automatically: RNAi_primary
      WBRNAi00028560 Inferred_automatically: RNAi_primary
      WBRNAi00039864 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1011886
      Expr1143951
      Expr2000516
      Expr2018741
    Drives_construct: WBCnstr00033792
    Construct_product: WBCnstr00033792
    Microarray_results (18)
    Expression_cluster (109)
    Interaction: WBInteraction000458056
      WBInteraction000544334
  Map_info: Positive: Positive_clone: C06C3 Inferred_automatically: From sequence, transcript, pseudogene data
    Interpolated_map_position: II 1.30692
  Method: Gene