WormBase Tree Display for Gene: WBGene00010421

WBGene00010421 SMap: S_parent: Sequence: H32K16
  Identity: Version: 2
    Name: CGC_name: slc-36.4 Person_evidence: WBPerson260
      Sequence_name: H32K16.1
      Molecular_name: H32K16.1
        H32K16.1.1
        CE16186
      Other_name: CELE_H32K16.1 Accession_evidence: NDB BX284601
      Public_name: slc-36.4
    DB_info: Database: AceView gene 1J729
        WormQTL gene WBGene00010421
        WormFlux gene WBGene00010421
        NDB locus_tag CELE_H32K16.1
        Panther gene CAEEL|WormBase=WBGene00010421|UniProtKB=O62286
          family PTHR22950
        NCBI gene 186798
        RefSeq protein NM_060052.3
        TrEMBL UniProtAcc O62286
        UniProt_GCRP UniProtAcc O62286
        OMIM gene 608331
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:51 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
        2 29 Apr 2015 12:07:40 WBPerson2970 Name_change: CGC_name: slc-36.4
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: slc
    Allele (41)
    RNASeq_FPKM (74)
    GO_annotation: 00039353
      00039354
      00039355
      00039356
      00039357
      00039358
      00039359
      00039360
    Ortholog (56)
    Paralog (14)
    Structured_description: Automated_description: Predicted to enable L-amino acid transmembrane transporter activity. Predicted to be involved in L-amino acid transport and 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
            WBPaper00067038
          Curator_confirmed: WBPerson324
            WBPerson37462
          Inferred_automatically: This description was generated automatically by a script based on data from the WS296 version of WormBase
          Date_last_updated: 20 Mar 2025 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: H32K16.1
    Corresponding_transcript: H32K16.1.1
    Other_sequence: BXC07383_1
    Associated_feature: WBsf643572
      WBsf656681
      WBsf656682
      WBsf984600
      WBsf984601
      WBsf1010321
      WBsf218254
  Experimental_info: RNAi_result: WBRNAi00049529 Inferred_automatically: RNAi_primary
      WBRNAi00003888 Inferred_automatically: RNAi_primary
      WBRNAi00033772 Inferred_automatically: RNAi_primary
      WBRNAi00073167 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1014248
      Expr1153249
      Expr2015877
      Expr2034110
    Drives_construct: WBCnstr00031427
    Construct_product: WBCnstr00031427
    Microarray_results (22)
    Expression_cluster (128)
  Map_info: Map: I Position: 3.62539
    Positive: Positive_clone: H32K16 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: 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