WormBase Tree Display for Gene: WBGene00008921

WBGene00008921 SMap: S_parent: Sequence: F17C11
  Identity: Version: 2
    Name: CGC_name: ctf-4 Person_evidence: WBPerson30546
      Sequence_name: F17C11.10
      Molecular_name: F17C11.10
        F17C11.10.1
        CE05657
      Other_name: CELE_F17C11.10 Accession_evidence: NDB BX284605
      Public_name: ctf-4
    DB_info: Database: AceView gene 5L442
        WormQTL gene WBGene00008921
        WormFlux gene WBGene00008921
        NDB locus_tag CELE_F17C11.10
        Panther gene CAEEL|WormBase=WBGene00008921|UniProtKB=Q19520
          family PTHR19932
        NCBI gene 179521
        RefSeq protein NM_073398.5
        TREEFAM TREEFAM_ID TF105988
        TrEMBL UniProtAcc Q19520
        UniProt_GCRP UniProtAcc Q19520
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:49 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
        2 05 Apr 2017 11:17:23 WBPerson2970 Name_change: CGC_name: ctf-4
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: ctf
    Allele (49)
    RNASeq_FPKM (74)
    GO_annotation: 00064969
      00064970
      00064971
      00064972
      00064973
      00064974
      00064975
      00064976
    Contained_in_operon: CEOP5268
    Ortholog (35)
    Structured_description: Automated_description: Predicted to enable chromatin binding activity. Predicted to be involved in DNA repair; DNA-templated DNA replication; and mitotic cell cycle. Predicted to be located in nuclear replication fork. Predicted to be part of replication fork protection complex. Human ortholog(s) of this gene implicated in cholangiocarcinoma. Is an ortholog of human WDHD1 (WD repeat and HMG-box DNA binding protein 1). 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:4947 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:23170)
  Molecular_info: Corresponding_CDS: F17C11.10
    Corresponding_transcript: F17C11.10.1
    Other_sequence: CR00891
      CR04214
      CJC12789_1
      CJC13735_1
      CRC02477_1
      CRC12170_1
      CR00103
      CBC13226_1
    Associated_feature: WBsf653052
      WBsf234475
      WBsf234476
  Experimental_info: RNAi_result: WBRNAi00013456 Inferred_automatically: RNAi_primary
      WBRNAi00108113 Inferred_automatically: RNAi_primary
      WBRNAi00007584 Inferred_automatically: RNAi_primary
      WBRNAi00094296 Inferred_automatically: RNAi_primary
      WBRNAi00108114 Inferred_automatically: RNAi_primary
      WBRNAi00044871 Inferred_automatically: RNAi_primary
      WBRNAi00108126 Inferred_automatically: RNAi_primary
      WBRNAi00094214 Inferred_automatically: RNAi_primary
      WBRNAi00108115 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1027543
      Expr1033883
      Expr1148835
      Expr2010570
      Expr2028810
    Drives_construct: WBCnstr00032593
    Construct_product: WBCnstr00032593
    Antibody: WBAntibody00002991
    Microarray_results (20)
    Expression_cluster (187)
    Interaction (129)
  Map_info: Positive: Positive_clone: F17C11 Inferred_automatically: From sequence, transcript, pseudogene data
    Interpolated_map_position: V 2.85487
  Reference: WBPaper00038491
    WBPaper00055090
    WBPaper00066002
  Method: Gene