WormBase Tree Display for Gene: WBGene00018181

WBGene00018181 SMap: S_parent: Sequence: F38E1
  Identity: Version: 2
    Name: CGC_name: mpdu-1
      Sequence_name: F38E1.9
      Molecular_name: F38E1.9
        F38E1.9.1
        CE47834
      Other_name: CELE_F38E1.9 Accession_evidence: NDB BX284605
      Public_name: mpdu-1
    DB_info: Database (11)
    Species: Caenorhabditis elegans
    History: Version_change (2)
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: mpdu
    Allele (15)
    RNASeq_FPKM (74)
    GO_annotation: 00067358
      00067359
      00067360
      00105742
    Ortholog (35)
    Structured_description: Automated_description: Acts upstream of or within IRE1-mediated unfolded protein response. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation If. Is an ortholog of human MPDU1 (mannose-P-dolichol utilization defect 1). 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:0080558 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7207)
  Molecular_info: Corresponding_CDS: F38E1.9
    Corresponding_CDS_history: F38E1.9:wp234
    Corresponding_transcript: F38E1.9.1
    Other_sequence (32)
    Associated_feature: WBsf652844
      WBsf234074
      WBsf234075
      WBsf234076
  Experimental_info: RNAi_result (36)
    Expr_pattern: Expr1027460
      Expr1037828
      Expr1150594
      Expr2003480
      Expr2021695
    Drives_construct: WBCnstr00026719
    Construct_product: WBCnstr00026719
    Microarray_results (19)
    Expression_cluster (97)
    Interaction: WBInteraction000124805
      WBInteraction000135942
      WBInteraction000182699
      WBInteraction000196772
      WBInteraction000218971
      WBInteraction000221135
      WBInteraction000224386
      WBInteraction000228273
      WBInteraction000248948
      WBInteraction000263243
      WBInteraction000281596
      WBInteraction000286781
      WBInteraction000292026
      WBInteraction000298053
      WBInteraction000315015
      WBInteraction000318614
      WBInteraction000319096
      WBInteraction000319420
      WBInteraction000324800
      WBInteraction000329192
      WBInteraction000331456
      WBInteraction000336239
      WBInteraction000342836
      WBInteraction000345223
      WBInteraction000362824
      WBInteraction000366186
      WBInteraction000377960
      WBInteraction000381309
      WBInteraction000383000
      WBInteraction000432767
      WBInteraction000454973
      WBInteraction000456790
      WBInteraction000551714
      WBInteraction000582676
      WBInteraction000585756
  Map_info: Map: V Position: 1.32597
    Positive: Positive_clone: F38E1 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00029024
    WBPaper00032078
    WBPaper00038491
    WBPaper00045573
    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