WormBase Tree Display for Gene: WBGene00017013

WBGene00017013 SMap: S_parent: Sequence: D1009
  Identity: Version: 2
    Name: CGC_name: ensh-1 Person_evidence: WBPerson95
      Sequence_name: D1009.3
      Molecular_name: D1009.3a
        D1009.3a.1
        CE27893
        D1009.3b
        CE04287
        D1009.3b.1
        D1009.3b.2
      Other_name: CELE_D1009.3 Accession_evidence: NDB BX284606
      Public_name: ensh-1
    DB_info: Database: AceView gene XJ529
        WormQTL gene WBGene00017013
        WormFlux gene WBGene00017013
        NDB locus_tag CELE_D1009.3
        Panther gene CAEEL|WormBase=WBGene00017013|UniProtKB=Q18914
          family PTHR19143
        NCBI gene 181135
        RefSeq protein NM_001029338.7
            NM_001029337.4
        TrEMBL UniProtAcc Q18914
            H2KYR5
        UniProt_GCRP UniProtAcc Q18914
        OMIM gene 604774
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:30:58 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 16 Jun 2015 13:39:51 WBPerson2970 Name_change: CGC_name: ensh-1
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: ensh
    Allele (109)
    Strain: WBStrain00031967
    RNASeq_FPKM (74)
    GO_annotation: 00021839
      00021840
      00021841
    Ortholog (31)
    Paralog: WBGene00020516 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00002915 Caenorhabditis elegans From_analysis: WormBase-Compara
      WBGene00007687 Caenorhabditis elegans From_analysis: WormBase-Compara
      WBGene00011326 Caenorhabditis elegans From_analysis: WormBase-Compara
    Structured_description: Automated_description: Predicted to be located in collagen-containing extracellular matrix and extracellular space. Human ortholog(s) of this gene implicated in familial hypobetalipoproteinemia 2. Is an ortholog of human ANGPTL3 (angiopoietin like 3). 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:0111061 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:491)
  Molecular_info: Corresponding_CDS: D1009.3a
      D1009.3b
    Corresponding_transcript: D1009.3a.1
      D1009.3b.1
      D1009.3b.2
    Other_sequence: CBC00868_1
    Associated_feature: WBsf663062
      WBsf718659
      WBsf718660
      WBsf718661
      WBsf1006273
      WBsf1006274
      WBsf236094
      WBsf236095
  Experimental_info: RNAi_result: WBRNAi00030316 Inferred_automatically: RNAi_primary
      WBRNAi00043337 Inferred_automatically: RNAi_primary
      WBRNAi00012492 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1020441
      Expr1037311
      Expr1147317
      Expr1200326
      Expr2011322
      Expr2029558
    Drives_construct: WBCnstr00027638
    Construct_product: WBCnstr00027638
    Microarray_results (23)
    Expression_cluster (116)
    Interaction: WBInteraction000162650
      WBInteraction000167813
  Map_info: Map: X Position: 0.442968
    Positive: Positive_clone: D1009 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00038491
    WBPaper00043346
    WBPaper00047943
    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