WormBase Tree Display for Gene: WBGene00000951

WBGene00000951 SMap: S_parent: Sequence: K03B8
  Identity: Version: 1
    Name: CGC_name: deg-3 Person_evidence: WBPerson95
      Sequence_name: K03B8.9
      Molecular_name: K03B8.9
        K03B8.9.1
        CE06083
        K03B8.9.2
      Other_name: CELE_K03B8.9 Accession_evidence: NDB BX284605
      Public_name: deg-3
    DB_info: Database: AceView gene 5L894
        WormQTL gene WBGene00000951
        WormFlux gene WBGene00000951
        NDB locus_tag CELE_K03B8.9
        Panther gene CAEEL|WormBase=WBGene00000951|UniProtKB=P54244
          family PTHR18945
        NCBI gene 3565200
        RefSeq protein NM_001392614.1
        SwissProt UniProtAcc P54244
        UniProt_GCRP UniProtAcc P54244
    Species: Caenorhabditis elegans
    History: Version_change: 1 07 Apr 2004 11:29:22 WBPerson1971 Event: Imported: Initial conversion from geneace
    Status: Live
  Gene_info (11)
  Disease_info: Experimental_model: DOID:1289 Homo sapiens Paper_evidence: WBPaper00002167
            WBPaper00032364
          Curator_confirmed: WBPerson324
            WBPerson38202
          Date_last_updated: 22 May 2018 00:00:00
    Disease_relevance: Defects in human sodium channel proteins cause several disorders including hyperkalemic periodic paralysis and paramyotonia congenita; Chloride channel defects produce cystic fibrosis and acetylcholine receptor defects underlie the congenital myasthenic syndromes. Homo sapiens Curator_confirmed: WBPerson324
          Date_last_updated: 25 Nov 2014 00:00:00
  Models_disease_asserted: WBDOannot00000334
    WBDOannot00000526
  Molecular_info: Corresponding_CDS: K03B8.9
    Corresponding_transcript: K03B8.9.1
      K03B8.9.2
    Other_sequence (22)
    Associated_feature: WBsf234533
  Experimental_info: RNAi_result (5)
    Expr_pattern: Expr224
      Expr9315
      Expr1013101
      Expr1030591
      Expr1153524
      Expr2010844
      Expr2029082
    Drives_construct: WBCnstr00010719
      WBCnstr00013896
      WBCnstr00037183
    Construct_product: WBCnstr00014763
      WBCnstr00037183
    Antibody: WBAntibody00001595
    Microarray_results (20)
    Expression_cluster (150)
    Interaction (43)
  Map_info: Map: V Position: 3.08425 Error: 0.002323
    Well_ordered
    Positive: Positive_clone: K03B8 Inferred_automatically: From sequence, transcript, pseudogene data
        T21D1
    Mapping_data: 2_point: 6220
        7052
      Multi_point: 2781
        2782
        3788
        3971
        4255
        4230
  Reference: WBPaper00002167
    WBPaper00002641
    WBPaper00003024
    WBPaper00003148
    WBPaper00003199
    WBPaper00003300
    WBPaper00003338
    WBPaper00003425
    WBPaper00004218
    WBPaper00004257
    WBPaper00004401
    WBPaper00004462
    WBPaper00004621
    WBPaper00005223
    WBPaper00005391
    WBPaper00005513
    WBPaper00005533
    WBPaper00005594
    WBPaper00005697
    WBPaper00005753
    WBPaper00006018
    WBPaper00006103
    WBPaper00006324
    WBPaper00006402
    WBPaper00010170
    WBPaper00010416
    WBPaper00010638
    WBPaper00011127
    WBPaper00011360
    WBPaper00011362
    WBPaper00011588
    WBPaper00011738
    WBPaper00011839
    WBPaper00015034
    WBPaper00015302
    WBPaper00015304
    WBPaper00016901
    WBPaper00017693
    WBPaper00017986
    WBPaper00018129
    WBPaper00018530
    WBPaper00018532
    WBPaper00018560
    WBPaper00018877
    WBPaper00019381
    WBPaper00019392
    WBPaper00022181
    WBPaper00022305
    WBPaper00022558
    WBPaper00022720
    WBPaper00022915
    WBPaper00023028
    WBPaper00023190
    WBPaper00023812
    WBPaper00024530
    WBPaper00024783
    WBPaper00024811
    WBPaper00025230
    WBPaper00025861
    WBPaper00026649
    WBPaper00027255
    WBPaper00027313
    WBPaper00027349
    WBPaper00027611
    WBPaper00028761
    WBPaper00029012
    WBPaper00029025
    WBPaper00029139
    WBPaper00031030
    WBPaper00031045
    WBPaper00032478
    WBPaper00032839
    WBPaper00035156
    WBPaper00035450
    WBPaper00036308
    WBPaper00037592
    WBPaper00038491
    WBPaper00040041
    WBPaper00040525
    WBPaper00041959
    WBPaper00044839
    WBPaper00054844
    WBPaper00055090
    WBPaper00058383
    WBPaper00061024
    WBPaper00061589
    WBPaper00061945
    WBPaper00062367
    WBPaper00064789
    WBPaper00065135
  Remark: mutation isolated from 'nT1(dm)', a dominant unc and recessive lethal derivative of nT1. u662 is not recessive lethal.
    In an operon with des-2. email 20 from wen chen
  Method: Gene