WormBase Tree Display for Gene: WBGene00011573

WBGene00011573 SMap: S_parent: Sequence: T07C12
  Identity: Version: 2
    Name: CGC_name: anmt-3 Person_evidence: WBPerson260
      Sequence_name: T07C12.9
      Molecular_name: T07C12.9
        T07C12.9.1
        CE21160
      Other_name: CELE_T07C12.9 Accession_evidence: NDB BX284605
      Public_name: anmt-3
    DB_info: Database: AceView gene 5K438
        WormQTL gene WBGene00011573
        WormFlux gene WBGene00011573
        NDB locus_tag CELE_T07C12.9
        Panther gene CAEEL|WormBase=WBGene00011573|UniProtKB=Q22279
          family PTHR10867
        NCBI gene 179385
        RefSeq protein NM_073162.9
        TREEFAM TREEFAM_ID TF313114
        TrEMBL UniProtAcc Q22279
        UniProt_GCRP UniProtAcc Q22279
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:52 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
        2 04 Sep 2012 12:07:47 WBPerson2970 Name_change: CGC_name: anmt-3
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: anmt
    Allele (25)
    Strain: WBStrain00055508
    RNASeq_FPKM (74)
    GO_annotation: 00074761
      00074762
      00074763
      00118808
    Ortholog (37)
    Paralog: WBGene00015124 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00018340 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
    Structured_description: Automated_description: Predicted to enable N-methyltransferase activity. Predicted to be located in cytosol. Expressed in body wall musculature and pharyngeal muscle cell. Human ortholog(s) of this gene implicated in renal cell carcinoma. Is an ortholog of human NNMT (nicotinamide N-methyltransferase). 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:7693 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7861)
      DOID:4450 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7861)
      DOID:3393 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7861)
  Molecular_info: Corresponding_CDS: T07C12.9
    Corresponding_transcript: T07C12.9.1
    Other_sequence (26)
    Associated_feature: WBsf655587
      WBsf669272
      WBsf669273
      WBsf669274
      WBsf669275
      WBsf1001019
      WBsf1001020
      WBsf1020242
      WBsf1020243
      WBsf234300
  Experimental_info: RNAi_result: WBRNAi00018343 Inferred_automatically: RNAi_primary
      WBRNAi00052720 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr4923
      Expr1021180
      Expr1035102
      Expr1156330
      Expr2009340
      Expr2027576
    Drives_construct: WBCnstr00012336
      WBCnstr00030549
    Construct_product: WBCnstr00030549
    Microarray_results (20)
    Expression_cluster (178)
    Interaction (11)
  Map_info: Map: V Position: 2.21937
    Positive: Positive_clone: T07C12 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00031003
    WBPaper00038491
    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