WormBase Tree Display for Gene: WBGene00016624

WBGene00016624 SMap: S_parent: Sequence: C44B7
  Identity: Version: 2
    Name: CGC_name: hrpl-1 Person_evidence: WBPerson260
      Sequence_name: C44B7.2
      Molecular_name: C44B7.2a
        C44B7.2a.1
        CE34752
        C44B7.2b
        CE25812
        C44B7.2a.2
        C44B7.2b.1
      Other_name: CELE_C44B7.2 Accession_evidence: NDB BX284602
      Public_name: hrpl-1
    DB_info: Database: AceView gene 2H191C
            2H191
        WormQTL gene WBGene00016624
        WormFlux gene WBGene00016624
        NDB locus_tag CELE_C44B7.2
        Panther gene CAEEL|WormBase=WBGene00016624|UniProtKB=Q95QR5
          family PTHR15592
        NCBI gene 3565706
        RefSeq protein NM_063011.6
            NM_001393108.1
        TREEFAM TREEFAM_ID TF354318
        TrEMBL UniProtAcc Q95QR5
            Q95QR6
        UniProt_GCRP UniProtAcc Q95QR5
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:30:57 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 07 Dec 2017 13:24:47 WBPerson1983 Name_change: CGC_name: hrpl-1
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: hrpl
    Allele (38)
    RNASeq_FPKM (74)
    GO_annotation: 00091828
      00091829
      00091830
      00091831
      00091832
      00126133
      00126134
      00126135
      00126136
    Contained_in_operon: CEOP2264
    Ortholog (47)
    Paralog: WBGene00004207 Caenorhabditis elegans From_analysis: WormBase-Compara
    Structured_description: Automated_description: Predicted to enable mRNA binding activity. Predicted to be involved in regulation of RNA splicing. Predicted to be located in nucleus. Human ortholog(s) of this gene implicated in several diseases, including Sertoli cell-only syndrome; hepatocellular carcinoma; and systemic scleroderma. Is an ortholog of human HNRNPLL (heterogeneous nuclear ribonucleoprotein L like). Paper_evidence: WBPaper00065943
            WBPaper00067038
          Curator_confirmed: WBPerson324
            WBPerson37462
          Inferred_automatically: This description was generated automatically by a script based on data from the WS296 version of WormBase
          Date_last_updated: 20 Mar 2025 00:00:00
  Disease_info: Potential_model: DOID:0050457 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:5045)
      DOID:1324 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:5045)
      DOID:1319 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:5045)
      DOID:684 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:5045)
      DOID:418 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:5045)
  Molecular_info: Corresponding_CDS: C44B7.2a
      C44B7.2b
    Corresponding_CDS_history: C44B7.2:wp21
      C44B7.2a:wp104
    Corresponding_transcript: C44B7.2a.1
      C44B7.2a.2
      C44B7.2b.1
    Other_sequence (28)
    Associated_feature: WBsf644335
      WBsf221520
  Experimental_info: RNAi_result: WBRNAi00102169 Inferred_automatically: RNAi_primary
      WBRNAi00042427 Inferred_automatically: RNAi_primary
      WBRNAi00011909 Inferred_automatically: RNAi_primary
      WBRNAi00042426 Inferred_automatically: RNAi_primary
      WBRNAi00076213 Inferred_automatically: RNAi_primary
      WBRNAi00061751 Inferred_automatically: RNAi_primary
      WBRNAi00033365 Inferred_automatically: RNAi_primary
      WBRNAi00062160 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1020702
      Expr1037145
      Expr1146416
      Expr2001616
      Expr2019840
    Drives_construct: WBCnstr00027929
    Construct_product: WBCnstr00027929
    Microarray_results (36)
    Expression_cluster (91)
    Interaction (12)
  Map_info: Map: II Position: 0.137677
    Positive: Positive_clone: C44B7 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00038491
    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
    [210510 skd] Modified Map position as it was a reverse physical that could not be fixed by automated methods. (0.13752)
  Method: Gene