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: 00071001
      00071002
      00071003
      00071004
      00113572
    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 abdominal aortic aneurysm; coronary artery disease; and 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 WS292 version of WormBase
          Date_last_updated: 24 Apr 2024 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 (179)
    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