WormBase Tree Display for Gene: WBGene00020517

WBGene00020517 SMap: S_parent: Sequence: T15B7
  Identity: Version: 2
    Name: CGC_name: hpo-8 Paper_evidence: WBPaper00038231
          Person_evidence: WBPerson26
      Sequence_name: T15B7.2
      Molecular_name: T15B7.2
        T15B7.2.1
        CE33319
      Other_name: CELE_T15B7.2 Accession_evidence: NDB BX284605
      Public_name: hpo-8
    DB_info: Database (13)
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:31:03 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 26 Apr 2011 13:31:47 WBPerson2970 Name_change: CGC_name: hpo-8
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: hpo
    Allele (20)
    Strain: WBStrain00037074
    RNASeq_FPKM (74)
    GO_annotation (13)
    Ortholog (40)
    Paralog: WBGene00011205 Caenorhabditis elegans From_analysis: Panther
            WormBase-Compara
    Structured_description: Automated_description: Predicted to enable 3-hydroxyacyl-CoA dehydratase activity. Predicted to be involved in fatty acid elongation; sphingolipid biosynthetic process; and very long-chain fatty acid biosynthetic process. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in congenital myopathy. Is an ortholog of human HACD2 (3-hydroxyacyl-CoA dehydratase 2). 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:0081337 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:9639)
  Molecular_info: Corresponding_CDS: T15B7.2
    Corresponding_CDS_history: T15B7.2:wp93
    Corresponding_transcript: T15B7.2.1
    Other_sequence (98)
    Associated_feature: WBsf646899
      WBsf646900
      WBsf231916
  Experimental_info: RNAi_result: WBRNAi00088598 Inferred_automatically: RNAi_primary
      WBRNAi00053360 Inferred_automatically: RNAi_primary
      WBRNAi00026299 Inferred_automatically: RNAi_primary
      WBRNAi00009176 Inferred_automatically: RNAi_primary
      WBRNAi00091204 Inferred_automatically: RNAi_primary
      WBRNAi00091205 Inferred_automatically: RNAi_primary
      WBRNAi00091025 Inferred_automatically: RNAi_primary
      WBRNAi00088705 Inferred_automatically: RNAi_primary
      WBRNAi00053364 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1011347
      Expr1038945
      Expr1156945
      Expr2012585
      Expr2030821
    Drives_construct: WBCnstr00025081
    Construct_product: WBCnstr00025081
    Microarray_results (21)
    Expression_cluster (125)
    Interaction (65)
  Map_info: Map: V Position: 0.33102 Error: 0.005764
    Positive: Positive_clone: T15B7 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00038491
    WBPaper00040204
    WBPaper00041683
    WBPaper00042257
    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