WormBase Tree Display for Gene: WBGene00018361

WBGene00018361 SMap: S_parent: Sequence: F42G8
  Identity: Version: 2
    Name: CGC_name: ndub-11 Person_evidence: WBPerson555
      Sequence_name: F42G8.10
      Molecular_name: F42G8.10
        F42G8.10.1
        CE17069
      Other_name: CELE_F42G8.10 Accession_evidence: NDB BX284604
      Public_name: ndub-11
    DB_info: Database: AceView gene 4I894
        WormQTL gene WBGene00018361
        WormFlux gene WBGene00018361
        NDB locus_tag CELE_F42G8.10
        Panther gene CAEEL|WormBase=WBGene00018361|UniProtKB=O44509
          family PTHR13327
        NCBI gene 177606
        RefSeq protein NM_001028030.6
        TrEMBL UniProtAcc O44509
        UniProt_GCRP UniProtAcc O44509
        OMIM gene 300403
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:31:00 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 16 Jan 2023 18:37:21 WBPerson51134 Name_change: CGC_name: ndub-11
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: ndub
    Allele (28)
    Strain: WBStrain00031923
    RNASeq_FPKM (74)
    GO_annotation: 00032605
      00032606
      00032607
      00032608
      00032609
      00032610
    Ortholog (40)
    Structured_description: Automated_description: Predicted to be located in membrane and mitochondrion. Predicted to be part of mitochondrial respiratory chain complex I. Human ortholog(s) of this gene implicated in linear skin defects with multiple congenital anomalies 3 and nuclear type mitochondrial complex I deficiency 30. Is an ortholog of human NDUFB11 (NADH:ubiquinone oxidoreductase subunit B11). 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:0112098 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:20372)
      DOID:0111876 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:20372)
  Molecular_info: Corresponding_CDS: F42G8.10
    Corresponding_CDS_history: F42G8.10b:wp241
    Corresponding_transcript: F42G8.10.1
    Other_sequence (71)
    Associated_feature: WBsf651982
      WBsf230384
      WBsf230385
  Experimental_info: RNAi_result: WBRNAi00106847 Inferred_automatically: RNAi_primary
      WBRNAi00109841 Inferred_automatically: RNAi_primary
      WBRNAi00047122 Inferred_automatically: RNAi_primary
      WBRNAi00032151 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1013992
      Expr1037908
      Expr1150990
      Expr2003650
      Expr2021869
    Drives_construct: WBCnstr00026581
    Construct_product: WBCnstr00026581
    Microarray_results (30)
    Expression_cluster (101)
    Interaction (61)
  Map_info: Map: IV Position: 3.60866
    Positive: Positive_clone: F42G8 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