WormBase Tree Display for Gene: WBGene00016419

WBGene00016419 SMap: S_parent: Sequence: C34G6
  Identity: Version: 2
    Name: CGC_name: tyr-4 Person_evidence: WBPerson69
      Sequence_name: C34G6.2
      Molecular_name: C34G6.2
        C34G6.2.1
        CE08574
      Other_name: CELE_C34G6.2 Accession_evidence: NDB BX284601
      Public_name: tyr-4
    DB_info: Database (11)
    Species: Caenorhabditis elegans
    History: Version_change (2)
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: tyr
    Allele (44)
    Strain: WBStrain00031924
    RNASeq_FPKM (74)
    GO_annotation: 00024775
      00122059
    Ortholog (46)
    Paralog: WBGene00009001 Caenorhabditis elegans From_analysis: TreeFam
            Inparanoid_8
            Panther
            WormBase-Compara
      WBGene00010060 Caenorhabditis elegans From_analysis: Panther
            WormBase-Compara
      WBGene00010661 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00015332 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00021553 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00022231 Caenorhabditis elegans From_analysis: TreeFam
            Panther
            WormBase-Compara
      WBGene00017483 Caenorhabditis elegans From_analysis: Panther
    Structured_description: Automated_description: Predicted to enable oxidoreductase activity. Human ortholog(s) of this gene implicated in several diseases, including ocular albinism 1; oculocutaneous albinism (multiple); and vitiligo. Is an ortholog of human DCT (dopachrome tautomerase); TYR (tyrosinase); and TYRP1 (tyrosinase related protein 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:0050633 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12442)
      DOID:8465 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12442)
      DOID:0070097 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12450)
      DOID:8923 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12442)
      DOID:0050632 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12442,HGNC:12450,HGNC:2709)
      DOID:12306 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12442)
      DOID:0070095 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12442)
      DOID:0070094 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12442)
      DOID:1909 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12442)
      DOID:10123 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:12442,HGNC:12450)
  Molecular_info: Corresponding_CDS: C34G6.2
    Corresponding_transcript: C34G6.2.1
    Other_sequence: GPC00773_1
      JI175612.1
      HG08456
      Oden_isotig28382
      ES741208.1
      GP01349
      ACC12891_1
      JI167525.1
      Oden_isotig24062
      GP00144
      OOC02687_1
      Oden_isotig21980
      ACC13333_1
      BXC00809_1
      Oden_isotig25876
      EX565319.1
      GPC00633_1
      PP02555
      MHC08297_1
      Oden_isotig23990
      EY471748.1
      MAC00577_1
      OFC00690_1
      Dviv_isotig19515
      HBC09297_1
      MH10231
      EX543524.1
      JI482770.1
      JI180031.1
      EW743995.1
      Hbac_isotig07717
      ACC10306_1
      CJC06472_1
      Dviv_isotig19514
      HGC08490_1
      HSC00770_1
      GT738128.1
      OF01282
      MA01266
      FG589538.1
      JI475897.1
      Oden_isotig23753
      BXC03867_1
      HS01042
      Dviv_isotig27906
      JI464508.1
      PPC02458_1
    Associated_feature: WBsf656345
      WBsf217724
      WBsf217725
      WBsf217726
  Experimental_info: RNAi_result: WBRNAi00098215 Inferred_automatically: RNAi_primary
      WBRNAi00029552 Inferred_automatically: RNAi_primary
      WBRNAi00003081 Inferred_automatically: RNAi_primary
      WBRNAi00098219 Inferred_automatically: RNAi_primary
      WBRNAi00001841 Inferred_automatically: RNAi_primary
      WBRNAi00041928 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1010270
      Expr1037037
      Expr1145935
      Expr2017688
      Expr2035826
    Drives_construct: WBCnstr00028083
    Construct_product: WBCnstr00028083
    Microarray_results (19)
    Expression_cluster (185)
    Interaction (25)
  Map_info (4)
  Reference: WBPaper00044177
    WBPaper00055090
    WBPaper00061547
    WBPaper00065140
  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