WormBase Tree Display for Gene: WBGene00012370

WBGene00012370 SMap: S_parent: Sequence: CHROMOSOME_I
  Identity: Version: 1
    Name: Sequence_name: W09G3.7
      Molecular_name: W09G3.7a
        W09G3.7a.1
        CE41036
        W09G3.7b
        CE34217
        W09G3.7b.1
      Other_name: CELE_W09G3.7 Accession_evidence: NDB BX284601
      Public_name: W09G3.7
    DB_info: Database: AceView gene 1O390
        WormQTL gene WBGene00012370
        WormFlux gene WBGene00012370
        NDB locus_tag CELE_W09G3.7
        Panther gene CAEEL|WormBase=WBGene00012370|UniProtKB=G5EEZ1
          family PTHR46337
        NCBI gene 173245
        RefSeq protein NM_001026501.6
            NM_001026500.5
        TREEFAM TREEFAM_ID TF317425
        TrEMBL UniProtAcc Q7YTU8
            G5EEZ1
        UniProt_GCRP UniProtAcc G5EEZ1
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:53 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
    Status: Live
  Gene_info: Biotype: SO:0001217
    Allele (66)
    RNASeq_FPKM (74)
    GO_annotation: 00017118
      00017119
      00017120
      00017121
    Contained_in_operon: CEOP1998
    Ortholog (38)
    Paralog: WBGene00175036 Caenorhabditis elegans From_analysis: modENCODE_Pseudogenes
      WBGene00013510 Caenorhabditis elegans From_analysis: modENCODE_Pseudogenes
      WBGene00004304 Caenorhabditis elegans From_analysis: WormBase-Compara
      WBGene00010768 Caenorhabditis elegans From_analysis: WormBase-Compara
      WBGene00017195 Caenorhabditis elegans From_analysis: WormBase-Compara
    Structured_description: Automated_description: Predicted to enable guanyl-nucleotide exchange factor activity and rRNA binding activity. Predicted to be involved in positive regulation of mitochondrial translation. Predicted to be located in mitochondrial inner membrane. Expressed in amphid neurons; hypodermis; and intestine. Human ortholog(s) of this gene implicated in Williams-Beuren syndrome. Is an ortholog of human RCC1L (RCC1 like). 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:1928 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:14948)
  Molecular_info: Corresponding_CDS: W09G3.7a
      W09G3.7b
    Corresponding_CDS_history: W09G3.7a:wp132
      W09G3.7a:wp175
    Corresponding_transcript: W09G3.7a.1
      W09G3.7b.1
    Other_sequence (18)
    Associated_feature: WBsf649719
      WBsf220543
      WBsf220544
  Experimental_info: RNAi_result: WBRNAi00055065 Inferred_automatically: RNAi_primary
      WBRNAi00009275 Inferred_automatically: RNAi_primary
      WBRNAi00004458 Inferred_automatically: RNAi_primary
      WBRNAi00116616 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr11308
      Expr1014396
      Expr1158604
      Expr2006898
      Expr2025125
    Drives_construct: WBCnstr00018758
    Microarray_results (26)
    Expression_cluster (53)
  Map_info: Positive: Positive_clone: W09G3 Inferred_automatically: From sequence, transcript, pseudogene data
    Interpolated_map_position: I 21.7594
  Reference: WBPaper00038491
    WBPaper00055090
    WBPaper00064339
  Method: Gene