WormBase Tree Display for Gene: WBGene00016860

WBGene00016860 SMap: S_parent: Sequence: C50H11
  Identity: Version: 2
    Name: CGC_name: cyp-33C9
      Sequence_name: C50H11.15
      Molecular_name: C50H11.15
        C50H11.15.1
        CE08931
      Other_name: CELE_C50H11.15 Accession_evidence: NDB BX284605
      Public_name: cyp-33C9
    DB_info: Database: AceView gene 5D570
        WormQTL gene WBGene00016860
        WormFlux gene WBGene00016860
        NDB locus_tag CELE_C50H11.15
        Panther gene CAEEL|WormBase=WBGene00016860|UniProtKB=O16482
          family PTHR24300
        NCBI gene 178752
        RefSeq protein NM_071445.5
        TrEMBL UniProtAcc O16482
        UniProt_GCRP UniProtAcc O16482
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:30:58 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 21 Sep 2004 09:38:16 WBPerson1971 Name_change: CGC_name: cyp-33C9
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: cyp
    Allele (61)
    RNASeq_FPKM (74)
    GO_annotation (14)
    Ortholog (110)
    Paralog (44)
    Structured_description: Automated_description: Predicted to enable heme binding activity; oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen; and steroid hydroxylase activity. Predicted to be involved in organic acid metabolic process and xenobiotic metabolic process. Predicted to be located in cytoplasm and intracellular membrane-bounded organelle. Human ortholog(s) of this gene implicated in end stage renal disease and renal hypertension. Is an ortholog of human CYP2C8 (cytochrome P450 family 2 subfamily C member 8). 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:783 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:2622)
      DOID:1073 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:2622)
  Molecular_info: Corresponding_CDS: C50H11.15
    Corresponding_transcript: C50H11.15.1
    Other_sequence (25)
    Associated_feature: WBsf999573
      WBsf233457
  Experimental_info: RNAi_result: WBRNAi00012252 Inferred_automatically: RNAi_primary
      WBRNAi00030060 Inferred_automatically: RNAi_primary
      WBRNAi00092663 Inferred_automatically: RNAi_primary
      WBRNAi00042966 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1010215
      Expr1037232
      Expr1146933
      Expr2010720
      Expr2028958
    Drives_construct: WBCnstr00027746
    Construct_product: WBCnstr00027746
    Microarray_results (18)
    Expression_cluster (155)
    Interaction (35)
  Map_info: Map: V Position: -12.7512 Error: 0.002406
    Positive: Positive_clone: C50H11 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00031529
    WBPaper00036738
    WBPaper00038491
    WBPaper00044578
    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