WormBase Tree Display for Gene: WBGene00019725

WBGene00019725 SMap: S_parent: Sequence: M02B7
  Identity: Version: 3
    Name: CGC_name: algn-14 Person_evidence: WBPerson261
      Sequence_name: M02B7.4
      Molecular_name: M02B7.4a
        M02B7.4a.1
        CE48746
        M02B7.4b
        CE48609
        M02B7.4b.1
      Other_name: hpo-16 Paper_evidence: WBPaper00038231
          Person_evidence: WBPerson26
        CELE_M02B7.4 Accession_evidence: NDB BX284604
      Public_name: algn-14
    DB_info: Database: AceView gene 4E566
        WormQTL gene WBGene00019725
        WormFlux gene WBGene00019725
        NDB locus_tag CELE_M02B7.4
        Panther gene CAEEL|WormBase=WBGene00019725|UniProtKB=U4PE03
          family PTHR12154
        NCBI gene 187398
        RefSeq protein NM_001307358.3
            NM_001307357.2
        TrEMBL UniProtAcc U4PQW2
            U4PE03
        UniProt_GCRP UniProtAcc U4PE03
        OMIM gene 612866
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:31:02 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 26 Apr 2011 13:31:47 WBPerson2970 Name_change: CGC_name: hpo-16
        3 29 Apr 2015 12:07:40 WBPerson2970 Name_change: CGC_name: algn-14
                Other_name: hpo-16
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: algn
    Allele (42)
    Strain: WBStrain00002519
    RNASeq_FPKM (74)
    GO_annotation: 00105047
      00105048
      00105049
      00105050
      00105051
      00105052
      00105053
      00105054
      00124505
    Ortholog (40)
    Structured_description: Automated_description: Predicted to enable transferase activity. Predicted to contribute to N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase activity. Predicted to be involved in dolichol-linked oligosaccharide biosynthetic process. Predicted to be located in endoplasmic reticulum membrane and nuclear membrane. Predicted to be part of UDP-N-acetylglucosamine transferase complex. Human ortholog(s) of this gene implicated in congenital myasthenic syndrome 15. Is an ortholog of human ALG14 (ALG14 UDP-N-acetylglucosaminyltransferase subunit). 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:0110658 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:28287)
  Molecular_info: Corresponding_CDS: M02B7.4a
      M02B7.4b
    Corresponding_CDS_history: M02B7.4:wp202
      M02B7.4:wp239
    Corresponding_transcript: M02B7.4a.1
      M02B7.4b.1
    Other_sequence (37)
    Associated_feature: WBsf651714
  Experimental_info: RNAi_result: WBRNAi00017120 Inferred_automatically: RNAi_primary
      WBRNAi00115262 Inferred_automatically: RNAi_primary
      WBRNAi00115271 Inferred_automatically: RNAi_primary
      WBRNAi00088741 Inferred_automatically: RNAi_primary
      WBRNAi00103458 Inferred_automatically: RNAi_primary
      WBRNAi00088634 Inferred_automatically: RNAi_primary
      WBRNAi00050811 Inferred_automatically: RNAi_primary
      WBRNAi00115300 Inferred_automatically: RNAi_primary
    Expr_pattern: Chronogram1057
      Expr1028984
      Expr1038527
      Expr1154502
      Expr2009295
      Expr2027532
    Drives_construct: WBCnstr00004507
    Microarray_results (16)
    Expression_cluster (58)
    Interaction (17)
  Map_info: Map: IV Position: -2.18965 Error: 0.007262
    Positive: Positive_clone: M02B7 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00035925
    WBPaper00038491
    WBPaper00045573
    WBPaper00055090
  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