WormBase Tree Display for Gene: WBGene00010437

WBGene00010437 SMap: S_parent: Sequence: JC8
  Identity: Version: 2
    Name: CGC_name: cox-11 Person_evidence: WBPerson261
      Sequence_name: JC8.5
      Molecular_name: JC8.5a
        JC8.5a.1
        CE38202
        JC8.5b
        CE17988
        JC8.5b.1
      Other_name: CELE_JC8.5 Accession_evidence: NDB BX284604
      Public_name: cox-11
    DB_info: Database: AceView gene 4O11
        WormQTL gene WBGene00010437
        WormFlux gene WBGene00010437
        NDB locus_tag CELE_JC8.5
        Panther gene CAEEL|WormBase=WBGene00010437|UniProtKB=Q95QD5
          family PTHR21320
        NCBI gene 186814
        RefSeq protein NM_070146.7
            NM_001306923.3
        TrEMBL UniProtAcc S6F574
            Q95QD5
        UniProt_GCRP UniProtAcc Q95QD5
        OMIM gene 603648
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:51 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
        2 25 Jan 2013 14:30:54 WBPerson2970 Name_change: CGC_name: cox-11
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: cox
    Allele (71)
    Strain: WBStrain00003460
    RNASeq_FPKM (74)
    GO_annotation: 00088349
      00088350
      00117855
    Contained_in_operon: CEOP4536
    Ortholog (38)
    Structured_description: Automated_description: Predicted to enable copper ion binding activity. Predicted to be located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in cytochrome-c oxidase deficiency disease. Is an ortholog of human COX11 (cytochrome c oxidase copper chaperone COX11). 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:0070485 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:2261)
  Molecular_info: Corresponding_CDS: JC8.5a
      JC8.5b
    Corresponding_CDS_history: JC8.5:wp140
    Corresponding_transcript: JC8.5a.1
      JC8.5b.1
    Other_sequence (42)
    Associated_feature: WBsf229399
      WBsf229400
  Experimental_info: RNAi_result: WBRNAi00112816 Inferred_automatically: RNAi_primary
      WBRNAi00008939 Inferred_automatically: RNAi_primary
      WBRNAi00049573 Inferred_automatically: RNAi_primary
      WBRNAi00025826 Inferred_automatically: RNAi_primary
      WBRNAi00033794 Inferred_automatically: RNAi_primary
      WBRNAi00071820 Inferred_automatically: RNAi_primary
      WBRNAi00112936 Inferred_automatically: RNAi_primary
      WBRNAi00112876 Inferred_automatically: RNAi_primary
      WBRNAi00061684 Inferred_automatically: RNAi_primary
      WBRNAi00071488 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr6300
      Expr1011421
      Expr1034553
      Expr1153300
      Expr2010471
      Expr2028711
    Drives_construct: WBCnstr00003921
      WBCnstr00031417
    Construct_product: WBCnstr00031417
    Microarray_results (20)
    Expression_cluster (104)
    Interaction (29)
  Map_info: Map: IV Position: 8.48644
    Positive: Positive_clone: JC8 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: 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