WormBase Tree Display for Gene: WBGene00010510

WBGene00010510 SMap: S_parent: Sequence: K02E11
  Identity: Version: 3
    Name: CGC_name: ent-3 Person_evidence: WBPerson1318
      Sequence_name: K02E11.1
      Molecular_name: K02E11.1
        K02E11.1.1
        CE37978
      Other_name: CELE_K02E11.1 Accession_evidence: NDB BX284605
      Public_name: ent-3
    DB_info: Database (11)
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:51 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
        2 04 Nov 2004 16:11:20 WBPerson2970 Name_change: CGC_name: ent-3
        3 10 Jan 2005 12:17:44 WBPerson2970 Event: Acquires_merge: WBGene00001321
      Acquires_merge: WBGene00001321
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: ent
    Allele (62)
    Strain: WBStrain00035587
      WBStrain00035945
    RNASeq_FPKM (74)
    GO_annotation: 00070402
      00070403
      00070404
      00070405
      00070406
      00117888
      00117889
      00117890
    Ortholog (58)
    Paralog: WBGene00001320 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00008123 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00009499 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00009686 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00017532 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00010701 Caenorhabditis elegans From_analysis: Panther
            WormBase-Compara
    Structured_description: Automated_description: Predicted to enable nucleoside transmembrane transporter activity. Predicted to be involved in nucleoside transmembrane transport. Predicted to be located in plasma membrane. Human ortholog(s) of this gene implicated in histiocytosis-lymphadenopathy plus syndrome. Is an ortholog of human SLC29A2 (solute carrier family 29 member 2) and SLC29A3 (solute carrier family 29 member 3). 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:0111278 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:23096)
  Molecular_info: Corresponding_CDS: K02E11.1
    Corresponding_CDS_history: K02E11.1:wp138
    Corresponding_transcript: K02E11.1.1
    Other_sequence: CRC00025_1
      CR06836
      CJC16007_1
      CR02783
      CR00015
      CRC01103_1
      CRC02587_1
    Associated_feature: WBsf1001968
      WBsf1001969
      WBsf1001970
      WBsf1001971
      WBsf1001972
      WBsf1001973
      WBsf1020813
      WBsf1020814
      WBsf1020815
      WBsf234918
  Experimental_info: RNAi_result: WBRNAi00016459 Inferred_automatically: RNAi_primary
      WBRNAi00001923 Inferred_automatically: RNAi_primary
      WBRNAi00049711 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1024929
      Expr1153429
      Expr2011325
      Expr2029561
    Drives_construct: WBCnstr00031366
    Construct_product: WBCnstr00031366
    Microarray_results (18)
    Expression_cluster (161)
    Interaction: WBInteraction000164342
      WBInteraction000170214
      WBInteraction000171104
      WBInteraction000192882
      WBInteraction000223184
      WBInteraction000244262
      WBInteraction000264156
      WBInteraction000285679
      WBInteraction000301213
      WBInteraction000326268
      WBInteraction000329413
      WBInteraction000375264
      WBInteraction000379753
      WBInteraction000390566
      WBInteraction000391394
      WBInteraction000406970
      WBInteraction000420691
      WBInteraction000441609
      WBInteraction000460520
      WBInteraction000460521
      WBInteraction000460522
      WBInteraction000462217
      WBInteraction000464146
      WBInteraction000464984
      WBInteraction000472423
      WBInteraction000472799
      WBInteraction000472800
      WBInteraction000472801
      WBInteraction000472802
  Map_info: Map: V Position: 6.2055 Error: 0.001795
    Positive: Positive_clone: K02E11 Inferred_automatically: From sequence, transcript, pseudogene data
    Mapping_data: Multi_point: 5653
    Pseudo_map_position
  Reference: WBPaper00011438
    WBPaper00018608
    WBPaper00024337
    WBPaper00038491
    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