WormBase Tree Display for Gene: WBGene00018260

WBGene00018260 SMap: S_parent: Sequence: F41B5
  Identity: Version: 2
    Name: CGC_name: cyp-33C7
      Sequence_name: F41B5.2
      Molecular_name: F41B5.2
        F41B5.2.1
        CE42114
      Other_name: CELE_F41B5.2 Accession_evidence: NDB BX284605
      Public_name: cyp-33C7
    DB_info: Database: AceView gene 5C729
        WormQTL gene WBGene00018260
        WormFlux gene WBGene00018260
        NDB locus_tag CELE_F41B5.2
        Panther gene CAEEL|WormBase=WBGene00018260|UniProtKB=O16673
          family PTHR24300
        NCBI gene 185589
        RefSeq protein NM_071217.3
        TrEMBL UniProtAcc O16673
        UniProt_GCRP UniProtAcc O16673
    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 21 Sep 2004 09:38:16 WBPerson1971 Name_change: CGC_name: cyp-33C7
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: cyp
    Allele (51)
    RNASeq_FPKM (74)
    GO_annotation (14)
    Ortholog (134)
    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: F41B5.2
    Corresponding_CDS_history: F41B5.2:wp187
    Corresponding_transcript: F41B5.2.1
    Other_sequence (18)
    Associated_feature: WBsf646701
      WBsf231496
  Experimental_info: RNAi_result: WBRNAi00070141 Inferred_automatically: RNAi_primary
      WBRNAi00046944 Inferred_automatically: RNAi_primary
      WBRNAi00092661 Inferred_automatically: RNAi_primary
      WBRNAi00014717 Inferred_automatically: RNAi_primary
      WBRNAi00032071 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1026428
      Expr1150811
      Expr2010718
      Expr2028956
    Microarray_results (20)
    Expression_cluster (192)
    Interaction (97)
  Map_info: Map: V Position: -15.1587 Error: 0.002076
    Positive: Positive_clone: F41B5 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