WormBase Tree Display for Gene: WBGene00015692

WBGene00015692 SMap: S_parent: Sequence: C10H11
  Identity (6)
  Gene_info: Biotype: SO:0001217
    Gene_class: ugt
    Allele: WBVar01911578
      WBVar02127223
      WBVar00153326
      WBVar00153327
      WBVar00153328
      WBVar00633899
      WBVar00633900
      WBVar00633901
      WBVar00633902
      WBVar00633903
      WBVar00633904
      WBVar00633905
      WBVar00633906
      WBVar00633907
      WBVar00633908
      WBVar00633909
      WBVar01499919
      WBVar01475446
      WBVar00633910
      WBVar00633911
      WBVar00633912
      WBVar00633913
      WBVar00633914
      WBVar00633915
      WBVar00633916
      WBVar00633917
      WBVar00633918
      WBVar00633919
      WBVar00633920
      WBVar00633921
      WBVar00633922
      WBVar00275820
      WBVar00333062
      WBVar00333063
      WBVar00333064
      WBVar00333065
      WBVar01499786
      WBVar00297975
      WBVar01499985
      WBVar01282522
      WBVar01956986
      WBVar00091031
      WBVar01573975
      WBVar01498959
      WBVar01911577
    RNASeq_FPKM (74)
    GO_annotation: 00049839
      00049840
      00049841
      00049842
      00049843
      00049844
      00049845
      00049846
      00121493
    Ortholog (102)
    Paralog (75)
    Structured_description: Automated_description: Predicted to enable UDP-glycosyltransferase activity. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in osteoporosis. Is an ortholog of several human genes including UGT2B15 (UDP glucuronosyltransferase family 2 member B15); UGT2B4 (UDP glucuronosyltransferase family 2 member B4); and UGT2B7 (UDP glucuronosyltransferase family 2 member B7). 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:11476 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12547)
  Molecular_info: Corresponding_CDS: C10H11.3
    Corresponding_transcript: C10H11.3.1
    Other_sequence: CJC03647_1
      CJC05355_1
      AS10156
      EX559766.1
      ACC12378_1
      ASC04370_1
    Associated_feature: WBsf643234
      WBsf643235
      WBsf656244
      WBsf217573
  Experimental_info: RNAi_result: WBRNAi00040333 Inferred_automatically: RNAi_primary
      WBRNAi00028799 Inferred_automatically: RNAi_primary
      WBRNAi00002939 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1023135
      Expr1036717
      Expr1144402
      Expr2017770
      Expr2035908
    Drives_construct: WBCnstr00028647
    Construct_product: WBCnstr00028647
    Microarray_results (19)
    Expression_cluster (245)
    Interaction: WBInteraction000504188
  Map_info: Map: I Position: -0.77257 Error: 0.008513
    Positive: Positive_clone: C10H11 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00038491
    WBPaper00044018
    WBPaper00055090
    WBPaper00055433
    WBPaper00062388
  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