WormBase Tree Display for Gene: WBGene00000983

WBGene00000983 SMap: S_parent: Sequence: F35B12
  Identity: Version: 1
    Name: CGC_name: dhs-20 Person_evidence: WBPerson651
      Sequence_name: F35B12.2
      Molecular_name: F35B12.2
        F35B12.2.1
        CE39496
      Other_name: CELE_F35B12.2 Accession_evidence: NDB BX284605
      Public_name: dhs-20
    DB_info: Database: AceView gene 5M84
        WormQTL gene WBGene00000983
        WormFlux gene WBGene00000983
        NDB locus_tag CELE_F35B12.2
        Panther gene CAEEL|WormBase=WBGene00000983|UniProtKB=Q20012
          family PTHR43313
        NCBI gene 179590
        RefSeq protein NM_073540.6
        TrEMBL UniProtAcc Q20012
        UniProt_GCRP UniProtAcc Q20012
        OMIM gene 601617
            609769
    Species: Caenorhabditis elegans
    History: Version_change: 1 07 Apr 2004 11:29:22 WBPerson1971 Event: Imported: Initial conversion from geneace
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: dhs
    Allele (29)
    RNASeq_FPKM (74)
    GO_annotation: 00066820
      00066821
      00066822
      00066823
    Ortholog (61)
    Paralog (38)
    Structured_description: Concise_description: dhs-20 encodes a short-chain dehydrogenase predicted to be mitochondrial. Paper_evidence: WBPaper00004424
          Curator_confirmed: WBPerson567
          Date_last_updated: 17 Jun 2004 00:00:00
      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: F35B12.2
    Corresponding_CDS_history: F35B12.2:wp87
      F35B12.2:wp152
    Corresponding_transcript: F35B12.2.1
    Other_sequence (75)
    Associated_feature: WBsf653131
      WBsf669390
      WBsf234552
  Experimental_info: RNAi_result: WBRNAi00014283 Inferred_automatically: RNAi_primary
      WBRNAi00046270 Inferred_automatically: RNAi_primary
      WBRNAi00046271 Inferred_automatically: RNAi_primary
      WBRNAi00031741 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1025422
      Expr1150162
      Expr2010904
      Expr2029143
    Drives_construct: WBCnstr00037159
    Construct_product: WBCnstr00037159
    Microarray_results (19)
    Expression_cluster (225)
    Interaction (35)
  Map_info: Map: V Position: 3.21084 Error: 0.00022
    Positive: Positive_clone: F35B12 Inferred_automatically: From CDS info
            From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00038491
    WBPaper00042257
    WBPaper00045631
    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