WormBase Tree Display for Gene: WBGene00006638

WBGene00006638 SMap: S_parent: Sequence: T14G10
  Identity: Version: 1
    Name: CGC_name: tsp-12 Person_evidence: WBPerson522
      Sequence_name: T14G10.6
      Molecular_name: T14G10.6
        T14G10.6.1
        CE06452
      Other_name: CELE_T14G10.6 Accession_evidence: NDB BX284604
      Public_name: tsp-12
    DB_info: Database: AceView gene 4K914
        WormQTL gene WBGene00006638
        WormFlux gene WBGene00006638
        NDB locus_tag CELE_T14G10.6
        Panther gene CAEEL|WormBase=WBGene00006638|UniProtKB=Q22495
          family PTHR19282
        NCBI gene 177890
        RefSeq protein NM_069452.5
        SwissProt UniProtAcc Q22495
        UniProt_GCRP UniProtAcc Q22495
    Species: Caenorhabditis elegans
    History: Version_change: 1 07 Apr 2004 11:29:41 WBPerson1971 Event: Imported: Initial conversion from geneace
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: tsp
    Allele (27)
    Strain: WBStrain00035713
    RNASeq_FPKM (74)
    GO_annotation (27)
    Contained_in_operon: CEOP4356
    Ortholog (46)
    Paralog (20)
    Structured_description: Automated_description: Enables protease binding activity. Involved in several processes, including nematode male tail tip morphogenesis; positive regulation of egg-laying behavior; and regulation of developmental process. Located in cytoplasmic vesicle membrane and plasma membrane. Expressed in several structures, including M lineage cell; germ line; intestine; pharynx; and vulval precursor cell. Used to study cancer. Is an ortholog of human TSPAN14 (tetraspanin 14); TSPAN17 (tetraspanin 17); and TSPAN5 (tetraspanin 5). 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: Experimental_model: DOID:162 Homo sapiens Paper_evidence: WBPaper00046810
          Curator_confirmed: WBPerson324
          Date_last_updated: 15 Jul 2015 00:00:00
  Models_disease_in_annotation: WBDOannot00000356
  Molecular_info: Corresponding_CDS: T14G10.6
    Corresponding_transcript: T14G10.6.1
    Other_sequence (27)
    Associated_feature: WBsf652110
      WBsf652111
      WBsf976938
      WBsf976939
      WBsf230686
  Experimental_info: RNAi_result: WBRNAi00018719 Inferred_automatically: RNAi_primary
      WBRNAi00053335 Inferred_automatically: RNAi_primary
      WBRNAi00084275 Inferred_automatically: RNAi_primary
      WBRNAi00008262 Inferred_automatically: RNAi_primary
      WBRNAi00035574 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr13208
      Expr13209
      Expr15990
      Expr1025636
      Expr1032756
      Expr1156921
      Expr2017541
      Expr2035679
    Drives_construct: WBCnstr00006015
      WBCnstr00006016
      WBCnstr00006017
      WBCnstr00006018
      WBCnstr00034248
    Construct_product: WBCnstr00006015
      WBCnstr00006016
      WBCnstr00034248
    Microarray_results (19)
    Expression_cluster (115)
    Interaction (24)
  Map_info: Map: IV Position: 4.54671 Error: 0.000826
    Positive: Positive_clone: T14G10 Inferred_automatically: From sequence, transcript, pseudogene data
    Mapping_data: Multi_point: 4498
        4743
        5002
        5525
    Pseudo_map_position
  Reference (14)
  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