WormBase Tree Display for Gene: WBGene00018885

WBGene00018885 SMap: S_parent: Sequence: F55E10
  Identity: Version: 2
    Name: CGC_name: drd-5 Person_evidence: WBPerson10050
      Sequence_name: F55E10.6
      Molecular_name: F55E10.6
        F55E10.6.1
        CE41820
      Other_name: CELE_F55E10.6 Accession_evidence: NDB BX284606
      Public_name: drd-5
    DB_info: Database: AceView gene XI964
        WormQTL gene WBGene00018885
        WormFlux gene WBGene00018885
        NDB locus_tag CELE_F55E10.6
        Panther gene CAEEL|WormBase=WBGene00018885|UniProtKB=Q20840
          family PTHR43313
        NCBI gene 186315
        RefSeq protein NM_077014.5
        TrEMBL UniProtAcc Q20840
        UniProt_GCRP UniProtAcc Q20840
        OMIM gene 601617
            609769
    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 29 Apr 2015 12:07:40 WBPerson2970 Name_change: CGC_name: drd-5
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: drd
    Allele (30)
    RNASeq_FPKM (74)
    GO_annotation: 00069289
      00069290
      00069291
      00069292
      00069293
    Ortholog (40)
    Paralog (38)
    Structured_description: Automated_description: Predicted to enable oxidoreductase activity. Predicted to be involved in steroid metabolic process. Predicted to be located in intracellular membrane-bounded organelle. Human ortholog(s) of this gene implicated in autosomal recessive congenital ichthyosis 13; fundus albipunctatus; and night blindness. Is an ortholog of several human genes including DHRS9 (dehydrogenase/reductase 9); HSD17B6 (hydroxysteroid 17-beta dehydrogenase 6); and RDH5 (retinol dehydrogenase 5). 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:0080257 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:29958)
      DOID:11105 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:9940)
      DOID:8499 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:9940)
  Molecular_info: Corresponding_CDS: F55E10.6
    Corresponding_CDS_history: F55E10.6:wp184
    Corresponding_transcript: F55E10.6.1
    Other_sequence: CBC05688_1
    Associated_feature: WBsf654209
      WBsf670830
      WBsf237672
      WBsf237673
  Experimental_info: RNAi_result: WBRNAi00015735 Inferred_automatically: RNAi_primary
      WBRNAi00048510 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1019201
      Expr1152298
      Expr2011086
      Expr2029322
    Drives_construct: WBCnstr00026212
    Construct_product: WBCnstr00026212
    Microarray_results (18)
    Expression_cluster (204)
    Interaction (31)
  Map_info: Positive: Positive_clone: F55E10 Inferred_automatically: From sequence, transcript, pseudogene data
    Interpolated_map_position: X -0.157767
  Reference: WBPaper00038491
    WBPaper00042257
    WBPaper00044557
    WBPaper00045631
    WBPaper00051037
    WBPaper00055090
    WBPaper00058665
    WBPaper00065331
  Method: Gene