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: WBVar00092476 Inferred_automatically: From strain object: RB1224
      WBVar01283041
      WBVar00264261
      WBVar00335235
      WBVar00335236
      WBVar00335237
      WBVar00335238
      WBVar00335239
      WBVar00335240
      WBVar02151301
      WBVar01909612
      WBVar01499786
      WBVar01499054
      WBVar00261045
      WBVar00261048
      WBVar00640799
      WBVar00640800
      WBVar00640801
      WBVar00640802
      WBVar00640803
      WBVar00640804
      WBVar00640805
      WBVar00640806
      WBVar00640807
      WBVar00640808
      WBVar00640809
      WBVar00640810
      WBVar00640811
      WBVar00640812
      WBVar00640813
      WBVar00640814
      WBVar00640815
      WBVar00640816
      WBVar00640817
      WBVar00640818
      WBVar00640819
      WBVar00640820
      WBVar00640821
      WBVar00640822
      WBVar01694795
      WBVar00153858
      WBVar00153859
      WBVar01498959
      WBVar01500249
    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 (47)
    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: Map: I Position: 0.475289 Error: 0.001229
    Positive: Positive_clone: C34G6 Inferred_automatically: From sequence, transcript, pseudogene data
    Mapping_data: Multi_point: 5068
        4575
        4601
    Pseudo_map_position
  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