WormBase Tree Display for Gene: WBGene00009773

WBGene00009773 SMap: S_parent: Sequence: F46B6
  Identity (6)
  Gene_info: Biotype: SO:0001217
    Gene_class: lipl
    Allele (29)
    RNASeq_FPKM (74)
    GO_annotation: 00068196
      00068197
      00117373
      00117374
    Ortholog (64)
    Paralog: WBGene00008510 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00022642 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00010062 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00020016 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00019376 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00021963 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00013050 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
    Structured_description: Automated_description: Predicted to enable hydrolase activity, acting on ester bonds. Predicted to be involved in lipid catabolic process. Human ortholog(s) of this gene implicated in Wolman disease; autosomal recessive congenital ichthyosis 8; and cholesterol ester storage disease. Is an ortholog of several human genes including LIPA (lipase A, lysosomal acid type); LIPF (lipase F, gastric type); and LIPJ (lipase family member J). 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:0080217 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:6617)
      DOID:14502 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:6617)
      DOID:14497 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:6617)
      DOID:0060717 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:23452)
  Molecular_info: Corresponding_CDS: F46B6.8
    Corresponding_transcript: F46B6.8.1
    Other_sequence (16)
    Associated_feature: WBsf647111
      WBsf232297
  Experimental_info: RNAi_result: WBRNAi00032350 Inferred_automatically: RNAi_primary
      WBRNAi00102885 Inferred_automatically: RNAi_primary
      WBRNAi00015069 Inferred_automatically: RNAi_primary
      WBRNAi00047500 Inferred_automatically: RNAi_primary
      WBRNAi00114802 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1023504
      Expr1034274
      Expr1151337
      Expr2013205
      Expr2031437
    Drives_construct: WBCnstr00017677
      WBCnstr00031933
    Construct_product: WBCnstr00031933
    Microarray_results (16)
    Expression_cluster (354)
    Interaction (71)
  Map_info: Map: V Position: 2.19757 Error: 0.000312
    Positive: Positive_clone: F46B6 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference (12)
  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