WormBase Tree Display for Gene: WBGene00019760

WBGene00019760 SMap: S_parent: Sequence: M03F4
  Identity: Version: 2
    Name: CGC_name: calu-1 Person_evidence: WBPerson3007
            WBPerson746
      Sequence_name: M03F4.7
      Molecular_name (6)
      Other_name: CELE_M03F4.7 Accession_evidence: NDB BX284606
      Public_name: calu-1
    DB_info: Database: AceView gene XF588
        WormQTL gene WBGene00019760
        WormFlux gene WBGene00019760
        NDB locus_tag CELE_M03F4.7
        Panther gene CAEEL|WormBase=WBGene00019760|UniProtKB=G5EBH7
          family PTHR10827
        NCBI gene 180769
        RefSeq protein NM_001383568.2
            NM_001383569.1
        TrEMBL UniProtAcc H2L0I1
            G5EBH7
        UniProt_GCRP UniProtAcc G5EBH7
    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 14 Nov 2006 10:33:09 WBPerson2970 Name_change: CGC_name: calu-1
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: calu
    Allele (20)
    Strain: WBStrain00001695
    RNASeq_FPKM (74)
    GO_annotation: 00009591
      00009592
      00009593
      00009594
      00009595
      00105695
      00105727
      00124534
    Contained_in_operon: CEOPX149
    Ortholog (45)
    Paralog: WBGene00016965 Caenorhabditis elegans From_analysis: Panther
            WormBase-Compara
      WBGene00017240 Caenorhabditis elegans From_analysis: Panther
            WormBase-Compara
      WBGene00023408 Caenorhabditis elegans From_analysis: Panther
      WBGene00023407 Caenorhabditis elegans From_analysis: Panther
            WormBase-Compara
    Structured_description: Automated_description: Enables calcium ion binding activity. Involved in cuticle development. Located in endoplasmic reticulum. Expressed in tail. Human ortholog(s) of this gene implicated in colorectal carcinoma. Is an ortholog of human CALU (calumenin). 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:13207 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:1458)
      DOID:0080199 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:1458)
  Molecular_info: Corresponding_CDS: M03F4.7a
      M03F4.7b
    Corresponding_transcript: M03F4.7a.1
      M03F4.7b.1
    Other_sequence: SR00564
      MI03885
      MC00445
      MHC01334_1
      NBC05853_1
      AS14115
      RS09584
      Tcol_isotig09884
      AYC02339_1
      AI095964.1
      Tcir_isotig06672
      ES742825.1
      AS11576
      AS13140
      AS12559
      ES411659.1
      DN190875.1
      MH00475
      EX013810.1
      ACC03616_1
      FG352309.1
      SS01050
      EX551697.1
      ES412613.1
      BM00289
      EX916652.1
      DN191219.1
      GR10937
      JI466738.1
      JI172394.1
      CRC00279_1
      GO239520.1
      Tcir_isotig28529
      MH05290
      JI460863.1
      AS14039
      FE916772.1
      AS14604
      AS12434
      TSC02322_1
      ACC19019_1
      CJC00299_1
      HCC00296_1
      FC815723.1
      ASC02223_1
      AS12428
      FG975533.1
      BM00704
      GR979211.1
      EX567076.1
      AS11577
      MIC00966_1
      Oden_isotig10962
      BMC02427_1
      HBC01583_1
      AS11443
      FC821077.1
      AS12493
      JI171757.1
      MC00164
      BM00990
      AS12649
      JI459615.1
      MCC00322_1
      HBC17902_1
      GW412721.1
      Dviv_isotig23396
      AS12054
      DN190472.1
      FK800719.1
      EX540656.1
      ES411252.1
      ASC12388_1
      AS02576
      SSC02904_1
      CJC12529_1
      Acan_isotig09409
      AS14444
      BXC06670_1
      HC00736
      SRC01148_1
      HC02752
      CK850205.1
      EX911558.1
      EX010061.1
      TLC00053_1
      GW408625.1
      GW406625.1
      ES739469.1
      EL890209.1
      AAC00216_1
      EX913681.1
      FK807101.1
      PSC00208
      EV850561.1
      AS13209
      ES409190.1
      DVC02320_1
      GRC05006_1
      RSC01865_1
      MHC01808_1
      EX012165.1
      AS14125
      EX910994.1
      CK725703.1
      FG586855.1
      EX561104.1
      ES743476.1
      NB09776
      EX911642.1
      OVC00558_1
      PPC00263_1
      Oden_isotig10960
      MI01420
      AS13265
      Hbac_isotig02134
      EX912037.1
      CJC13084_1
      GW408666.1
      EX915052.1
      CR00764
      AE03563
      SC01268
      ES741596.1
      EX559089.1
      GW408873.1
      Oden_isotig10961
      ES412207.1
      AS13080
      PSC02833_1
      JO474585.1
      ES880592.1
      EV850573.1
      AS00119
      EG025690.1
      WBC01698
      Tcol_isotig09885
      FC810332.1
      CBC00217_1
      FC543025.1
      MHC11328_1
      OOC00502_1
      TX00314
      PVC03034_1
      EX540130.1
      TCC01204_1
      DN190453.1
      Name_isotig01455
      GPC00399_1
      FC821696.1
      ES562940.1
      EX554269.1
      GP00870
      FG352312.1
      EX501723.1
      EX012873.1
      PP00415
      ASC04502_1
      ES568994.1
    Associated_feature (12)
  Experimental_info: RNAi_result (16)
    Expr_pattern (13)
    Drives_construct: WBCnstr00002519
      WBCnstr00004368
      WBCnstr00013525
      WBCnstr00025615
      WBCnstr00043034
      WBCnstr00043035
    Construct_product: WBCnstr00014114
      WBCnstr00025615
      WBCnstr00043035
    Antibody: WBAntibody00001974
    Microarray_results (30)
    Expression_cluster (235)
    Interaction (74)
  Map_info: Map: X Position: -6.19941 Error: 0.000507
    Positive: Positive_clone: M03F4 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference (12)
  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