WormBase Tree Display for Gene: WBGene00020837

WBGene00020837 SMap: S_parent: Sequence: T27A1
  Identity: Version: 2
    Name: CGC_name: slc-36.2 Person_evidence: WBPerson260
      Sequence_name: T27A1.5
      Molecular_name: T27A1.5a
        T27A1.5a.1
        CE14213
        T27A1.5b
        CE39784
        T27A1.5b.1
      Other_name: CELE_T27A1.5 Accession_evidence: NDB BX284602
      Public_name: slc-36.2
    DB_info: Database: AceView gene 2A815
        WormQTL gene WBGene00020837
        WormFlux gene WBGene00020837
        NDB locus_tag CELE_T27A1.5
        Panther gene CAEEL|WormBase=WBGene00020837|UniProtKB=G4SQY7
          family PTHR22950
        NCBI gene 173442
        RefSeq protein NM_001047347.4
            NM_001047348.4
        TrEMBL UniProtAcc O17275
            G4SQY7
        UniProt_GCRP UniProtAcc G4SQY7
        OMIM gene 608331
    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 29 Apr 2015 12:07:40 WBPerson2970 Name_change: CGC_name: slc-36.2
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: slc
    Allele (53)
    RNASeq_FPKM (74)
    GO_annotation: 00009336
      00009337
      00009338
      00009339
      00009340
    Ortholog (51)
    Paralog (14)
    Structured_description: Automated_description: Predicted to enable L-amino acid transmembrane transporter activity. Predicted to be involved in amino acid transmembrane transport. Predicted to be located in vacuolar membrane. Human ortholog(s) of this gene implicated in iminoglycinuria. Is an ortholog of several human genes including SLC36A1 (solute carrier family 36 member 1); SLC36A2 (solute carrier family 36 member 2); and SLC36A4 (solute carrier family 36 member 4). 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:0112265 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:18762)
  Molecular_info: Corresponding_CDS: T27A1.5a
      T27A1.5b
    Corresponding_CDS_history: T27A1.5:wp154
    Corresponding_transcript: T27A1.5a.1
      T27A1.5b.1
    Other_sequence (42)
    Associated_feature: WBsf717622
      WBsf986428
      WBsf986429
      WBsf1011406
      WBsf220763
  Experimental_info: RNAi_result: WBRNAi00060047 Inferred_automatically: RNAi_primary
      WBRNAi00036012 Inferred_automatically: RNAi_primary
      WBRNAi00060046 Inferred_automatically: RNAi_primary
      WBRNAi00054251 Inferred_automatically: RNAi_primary
      WBRNAi00076713 Inferred_automatically: RNAi_primary
      WBRNAi00060045 Inferred_automatically: RNAi_primary
      WBRNAi00019294 Inferred_automatically: RNAi_primary
      WBRNAi00060048 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr3637
      Expr1020478
      Expr1039082
      Expr1157798
      Expr2015875
      Expr2034108
    Drives_construct: WBCnstr00024849
    Construct_product: WBCnstr00011562
      WBCnstr00024849
    Microarray_results (24)
    Expression_cluster (162)
    Interaction (75)
  Map_info: Map: II Position: -15.5961
    Positive: Positive_clone: T27A1 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00038491
    WBPaper00055090
    WBPaper00059755
  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