WormBase Tree Display for Gene: WBGene00010755

WBGene00010755 SMap: S_parent: Sequence: CHROMOSOME_III
  Identity: Version: 2
    Name: CGC_name: vglu-2 Person_evidence: WBPerson260
      Sequence_name: K10G9.1
      Molecular_name: K10G9.1
        K10G9.1.1
        CE01603
      Other_name: CELE_K10G9.1 Accession_evidence: NDB BX284603
      Public_name: vglu-2
    DB_info: Database: AceView gene 3L387
        WormQTL gene WBGene00010755
        WormFlux gene WBGene00010755
        NDB locus_tag CELE_K10G9.1
        Panther gene CAEEL|WormBase=WBGene00010755|UniProtKB=G5EEK1
          family PTHR11662
        NCBI gene 176441
        RefSeq protein NM_066875.6
        TrEMBL UniProtAcc G5EEK1
        UniProt_GCRP UniProtAcc G5EEK1
        OMIM gene 607557
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:51 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
        2 01 Apr 2010 13:55:15 WBPerson2970 Name_change: CGC_name: vglu-2
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: vglu
    Allele (52)
    Strain: WBStrain00032512
      WBStrain00047428
    RNASeq_FPKM (74)
    GO_annotation (13)
    Ortholog (50)
    Paralog (58)
    Structured_description: Automated_description: Predicted to enable L-glutamate transmembrane transporter activity and neurotransmitter transmembrane transporter activity. Predicted to be involved in several processes, including glutamatergic synaptic transmission; monoatomic anion transport; and neurotransmitter loading into synaptic vesicle. Predicted to be located in excitatory synapse. Expressed in AIAL; AIAR; hyp7 syncytium; uterine epithelial cell; and in male. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 25. Is an ortholog of human SLC17A6 (solute carrier family 17 member 6); SLC17A7 (solute carrier family 17 member 7); and SLC17A8 (solute carrier family 17 member 8). 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:0110555 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:20151)
  Molecular_info: Corresponding_CDS: K10G9.1
    Corresponding_transcript: K10G9.1.1
    Other_sequence: Acan_isotig16296
    Associated_feature (15)
  Experimental_info: RNAi_result: WBRNAi00050563 Inferred_automatically: RNAi_primary
      WBRNAi00022400 Inferred_automatically: RNAi_primary
      WBRNAi00001951 Inferred_automatically: RNAi_primary
      WBRNAi00034270 Inferred_automatically: RNAi_primary
      WBRNAi00006027 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr14915
      Expr14916
      Expr14917
      Expr1027561
      Expr1034705
      Expr1154268
      Expr2017974
      Expr2036110
    Drives_construct: WBCnstr00031170
    Construct_product: WBCnstr00031170
    Microarray_results (22)
    Expression_cluster (173)
    Interaction (11)
  Map_info: Map: III Position: 2.2476 Error: 0.00858
    Positive: Positive_clone: K10G9 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00038491
    WBPaper00039208
    WBPaper00039414
    WBPaper00055090
    WBPaper00058928
  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