WormBase Tree Display for Gene: WBGene00017858

WBGene00017858 SMap: S_parent: Sequence: F27C1
  Identity: Version: 2
    Name: Sequence_name: F27C1.11
      Molecular_name: F27C1.11a
        F27C1.11a.1
        CE53755
        F27C1.11b
        CE53725
        F27C1.11b.1
      Other_name: CELE_F27C1.11 Accession_evidence: NDB BX284601
      Public_name: F27C1.11
    DB_info: Database: AceView gene 1G2
        WormQTL gene WBGene00017858
        WormFlux gene WBGene00017858
        NDB locus_tag CELE_F27C1.11
        Panther gene CAEEL|WormBase=WBGene00017858|UniProtKB=E5QCF1
          family PTHR45901
        NCBI gene 3565116
        RefSeq protein NM_001374894.3
            NM_001374895.3
        TrEMBL UniProtAcc A0A5K1IAB7
            A0A5K1IBA0
        UniProt_GCRP UniProtAcc A0A5K1IAB7
        OMIM gene 613072
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:30:59 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 23 Nov 2010 10:08:28 WBPerson1867 Event: Acquires_merge: WBGene00017857
      Acquires_merge: WBGene00017857
    Status: Live
  Gene_info: Biotype: SO:0001217
    Allele (116)
    RNASeq_FPKM (74)
    GO_annotation: 00123165
    Ortholog (29)
    Paralog: WBGene00017860 Caenorhabditis elegans From_analysis: WormBase-Compara
    Structured_description: Automated_description: Predicted to be involved in intracellular signal transduction. Human ortholog(s) of this gene implicated in Fuchs' endothelial dystrophy; autosomal recessive nonsyndromic deafness 77; and orofacial cleft. Is an ortholog of human LOXHD1 (lipoxygenase homology PLAT domains 1). 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:0110525 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:26521)
      DOID:11555 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:26521)
      DOID:0050567 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:26521)
  Molecular_info: Corresponding_CDS: F27C1.11a
      F27C1.11b
    Corresponding_CDS_history: F27C1.11:wp157
      F27C1.11:wp221
      F27C1.11:wp273
    Corresponding_transcript: F27C1.11a.1
      F27C1.11b.1
    Other_sequence: MH08937
      MHC06478_1
    Associated_feature: WBsf664240
      WBsf664241
      WBsf983698
      WBsf1009827
      WBsf219431
  Experimental_info: RNAi_result: WBRNAi00003495 Inferred_automatically: RNAi_primary
      WBRNAi00045721 Inferred_automatically: RNAi_primary
      WBRNAi00003502 Inferred_automatically: RNAi_primary
      WBRNAi00003496 Inferred_automatically: RNAi_primary
      WBRNAi00045719 Inferred_automatically: RNAi_primary
      WBRNAi00045720 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1023888
      Expr1149631
      Expr2003054
      Expr2021269
    Microarray_results (40)
    Expression_cluster (138)
    Interaction: WBInteraction000367527
  Map_info: Positive: Positive_clone: F27C1 Inferred_automatically: From sequence, transcript, pseudogene data
    Interpolated_map_position: I 0.00219081
  Method: Gene