WormBase Tree Display for Gene: HGNC:12450

HGNC:12450 Identity: Name: CGC_name: Tyrp1 Inferred_automatically: AGR_import
      Other_name (17)
      Public_name: Tyrp1
    DB_info: Database: HGNC id 12450
        AGR cURI HGNC:12450
        EnsEMBL ENSEMBL_geneID ENSG00000107165
        UniProt UniProt_AC P17643
        OMIM gene 115501
        DO id DOID:0070097
            DOID:10123
            DOID:0050632
    Species: Homo sapiens
    Status: Live
  Gene_info: Biotype: SO:0001217
    Ortholog: WBGene00016419 Caenorhabditis elegans From_analysis: EnsEMBL-Compara
            OrthoFinder
            OrthoInspector
            Panther
            SonicParanoid
      WBGene00009001 Caenorhabditis elegans From_analysis: Inparanoid
            OrthoFinder
            OrthoInspector
            Panther
            SonicParanoid
      WBGene00015332 Caenorhabditis elegans From_analysis: Inparanoid
            OrthoFinder
            OrthoInspector
            Panther
            SonicParanoid
      WBGene00010661 Caenorhabditis elegans From_analysis: Inparanoid
            OrthoFinder
            OrthoInspector
            Panther
            SonicParanoid
      WBGene00022231 Caenorhabditis elegans From_analysis: EnsEMBL-Compara
            OrthoFinder
            OrthoInspector
            Panther
            SonicParanoid
      WBGene00021553 Caenorhabditis elegans From_analysis: Inparanoid
            OrthoFinder
            OrthoInspector
            Panther
            SonicParanoid
    Structured_description: Automated_description: This gene encodes a melanosomal enzyme that belongs to the tyrosinase family and plays an important role in the melanin biosynthetic pathway. Defects in this gene are the cause of rufous oculocutaneous albinism and oculocutaneous albinism type III. [provided by RefSeq, Mar 2009] Inferred_automatically: AGR_import