WormBase Tree Display for Gene: WBGene00016628

WBGene00016628 SMap: S_parent: Sequence: C44B7
  Identity: Version: 2
    Name: CGC_name: slc-36.5 Person_evidence: WBPerson260
      Sequence_name: C44B7.6
      Molecular_name: C44B7.6a
        C44B7.6a.1
        CE29720
        C44B7.6b
        CE02544
        C44B7.6b.1
      Other_name: CELE_C44B7.6 Accession_evidence: NDB BX284602
      Public_name: slc-36.5
    DB_info: Database: AceView gene 2H166
        WormQTL gene WBGene00016628
        WormFlux gene WBGene00016628
        NDB locus_tag CELE_C44B7.6
        Panther gene CAEEL|WormBase=WBGene00016628|UniProtKB=Q18595
          family PTHR22950
        NCBI gene 174125
        RefSeq protein NM_001026855.6
            NM_001026856.3
        TrEMBL UniProtAcc Q18595
            H2KY81
        UniProt_GCRP UniProtAcc Q18595
        OMIM gene 608331
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:30:57 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-36.5
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: slc
    Allele (60)
    RNASeq_FPKM (74)
    GO_annotation: 00021404
      00021405
      00021406
      00021407
      00021408
    Ortholog (66)
    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: C44B7.6a
      C44B7.6b
    Corresponding_transcript: C44B7.6a.1
      C44B7.6b.1
    Other_sequence: Oden_isotig13654
      Acan_isotig12679
      Oden_isotig13653
      Oden_isotig26740
    Associated_feature: WBsf665660
      WBsf665661
      WBsf223243
  Experimental_info: RNAi_result: WBRNAi00029786 Inferred_automatically: RNAi_primary
      WBRNAi00042431 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1014116
      Expr1146420
      Expr2015878
      Expr2034111
    Drives_construct: WBCnstr00027925
    Construct_product: WBCnstr00027925
    Microarray_results (24)
    Expression_cluster (226)
    Interaction (20)
  Map_info: Map: II Position: 0.130452
    Positive: Positive_clone: C44B7 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00055090
    WBPaper00065331
  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