{
    "uniprot_canonical_ac": "P23999-1",
    "uniprot_ac": "P23999",
    "uniprot_id": "MYCS_RAT",
    "mass": {
        "chemical_mass": 47002.0,
        "monoisotopic_mass": 47002.0
    },
    "refseq": {
        "ac": "NP_068609",
        "name": "protein S-Myc",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_068609"
    },
    "gene_names": [
        {
            "name": "Mycs",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/P23999",
            "id": "P23999"
        },
        {
            "name": "Mycs",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_068609",
            "id": "NP_068609"
        }
    ],
    "protein_names": [
        {
            "name": "Protein S-Myc",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "P23999"
        },
        {
            "name": "protein S-Myc",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_068609",
            "id": "NP_068609"
        }
    ],
    "function": [
        {
            "annotation": "Genes are idenetified that are regulated by Myc genes",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_068609",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_068609"
                },
                {
                    "database": "PubMed",
                    "id": "12145275",
                    "url": "https://glygen.org/publication/PubMed/12145275"
                }
            ]
        },
        {
            "annotation": "Has apoptosis-inducing activity.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P23999",
                    "url": "https://www.uniprot.org/uniprot/P23999#function"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0060464",
            "recommended_name": {
                "id": "DOID:0060464",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0060464",
                "name": "Feingold syndrome",
                "description": "A syndrome characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation."
            },
            "synonyms": [
                {
                    "id": "DOID:0060464",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060464",
                    "name": "microcephaly-oculo-digito-esophageal-duodenal syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0060464",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060464",
                    "name": "microcephaly-digital anomalies-normal intelligence syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0060464",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060464",
                    "name": "FGLDS",
                    "description": ""
                },
                {
                    "id": "DOID:0060464",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060464",
                    "name": "MODED syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0060464",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060464",
                    "name": "ODED syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0060464",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060464",
                    "name": "oculo-digito-esophageal-duodenal syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0060464",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060464",
                    "name": "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum",
                    "description": ""
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "Feingold syndrome type 2",
                    "description": "Feingold syndrome type 2 (FS2) is a rare inherited malformation syndrome characterized by skeletal abnormalities and mild intellectual disabilities similar to those seen in Feingold syndrome type 1 (FS1) but that lacks the manifestations of gastrointestinal atresia and short palpebral fissures."
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "Brunner-Winter syndrome type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "FGLDS2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "FS2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "Feingold syndrome type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "MMT type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "brachydactyly-short stature-microcephaly syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "microcephaly-digital anomalies-normal intelligence syndrome type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "Feingold syndrome 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013691",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013691",
                    "name": "brachydactyly with short stature and microcephaly",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "Feingold syndrome type 1",
                    "description": "Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies."
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "Brunner-Winter syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "FGLDS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "FS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "Feingold syndrome caused by mutation in MYCN",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "Feingold syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "MMT type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "MODED syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "MYCN Feingold syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "ODED syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "microcephaly-digital anomalies-normal intelligence syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "oculo-digito-esophageal-duodenal syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "Feingold syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "Feingold syndrome 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "Mmt syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "Oded syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "microcephaly and digital abnormalities with normal intelligence",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "microcephaly, intellectual disability, and tracheoesophageal fistula syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "microcephaly, mental retardation, and tracheoesophageal fistula syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "microcephaly-oculo-digito-esophageal-duodenal syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0008115",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008115",
                    "name": "oculodigitoesophagoduodenal syndrome",
                    "description": ""
                },
                {
                    "id": "MIM:614326",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/614326",
                    "name": "Feingold syndrome 2",
                    "description": "Feingold syndrome 2"
                },
                {
                    "id": "MIM:164280",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/164280",
                    "name": "Feingold syndrome 1",
                    "description": "Feingold syndrome 1"
                }
            ],
            "evidence": [
                {
                    "id": "0060464",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0060464"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P23999",
                    "url": "https://www.uniprot.org/uniprot/P23999"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Mycs",
            "url": "https://www.uniprot.org/uniprot/P23999",
            "locus": {
                "chromosome": "X",
                "start_pos": 17039555,
                "end_pos": 17038263,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSRNOG00000003085",
                        "url": "https://www.ensembl.org/id/ENSRNOG00000003085"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "cd11456",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd11456",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "24581",
            "url": "https://www.ncbi.nlm.nih.gov/gene/24581",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "IPR002418",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR002418",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR011598",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR011598",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR012682",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR012682",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR036638",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR036638",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "rno:24581",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:24581",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "GMICKNS",
            "url": "https://omabrowser.org/oma/group/GMICKNS/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "3039999at2759",
            "url": "http://www.orthodb.org/?query=3039999at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR45851",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR45851",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR45851:SF4",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR45851:SF4",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00010",
            "url": "http://pfam.xfam.org/family/PF00010",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF01056",
            "url": "http://pfam.xfam.org/family/PF01056",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PR_P23999",
            "url": "http://purl.obolibrary.org/obo/PR_P23999",
            "database": "PRO",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "NP_068609",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_068609",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "3133",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=3133",
            "database": "RGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "G3V6D6",
            "url": "https://www.uniprot.org/uniprot/G3V6D6",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "G3V6D6-1",
            "url": "https://www.uniprot.org/uniprot/G3V6D6-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "P23999",
            "url": "https://www.uniprot.org/uniprot/P23999",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "P23999-1",
            "url": "https://www.uniprot.org/uniprot/P23999-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MLSCTTSTMPGMICKNSDLEFDSLKPCFYPEDDDIYFGGRNSTPPGEDIWKKFELLPTPRLSPGRALAEDSLEPANWATEMLLPEADLWSNPAEEEDIFGLKGLSGSSSNPVVLQDCMWSGFSSREKPETVVSEKLPGGCGSLAVGAGTLVPGAAAATSAGHARSGTAGVGRRKAAWLTELSHLDSECVDSAVIFPANKRESMPVATIPASAGAAISLGDHQGLSSSLEDFLSNSGYVEEGGEEIYVVMLGETQFSKTVTKLPTAAHSENAALTPECAQSGELILKRSDLIQEQHNYAAPPLPYAEDARPLKKPRSQDPLGPLKCVLRPKAPRLRSRSNSDLEDIERRRNHNRMERQRRDIMRSSFLNLRDLVPELVHNEKAAKVVILKKATEYIHTLQTDESKLLVEREKLYERKQQLLEKIKQSAVC",
        "length": 429,
        "header": "sp|P23999-1|MYCS_RAT Isoform 1 of Protein S-Myc  OS=Rattus norvegicus OX=10116 GN=Mycs PE=3 SV=1 CANONICAL=P23999-1"
    },
    "isoforms": [
        {
            "isoform_ac": "G3V6D6-1",
            "url": "",
            "sequence": {
                "sequence": "MLSCTTSTMPGMICKNSDLEFDSLKPCFYPEDDDIYFGGRNSTPPGEDIWKKFELLPTPRLSPGRALAEDSLEPANWATEMLLPEADLWSNPAEEEDIFGLKGLSGSSSNPVVLQDCMWSGFSSREKPETVVSEKLPGGCGSLAVGAGTLVPGAAAAASSAGHARSGTAGVGRRKAAWLTELSHLDSECVDSAVIFPANKRESMPVATIPASAGAAISLGDHQGLSSSLEDFLSNSGYVEEGGEEIYVVMLGETQFSKTVTKLPTAAHSENAALTPECAQSGELILKRSDLIQEQHNYAAPPLPYAEDARPLKKPRSQDPLGPLKCVLRPKAPRLRSRSNSDLEDIERRRNHNRMERQRRDIMRSSFLNLRDLVPELVHNEKAAKVVILKKATEYIHTLQTDESKLLVEREKLYERKQQLLEKIKQSAVC",
                "length": 430,
                "header": "tr|G3V6D6-1|MYCS_RAT Computationally mapped isoform of Protein S-Myc  OS=Rattus norvegicus OX=10116 GN=Mycs PE=3 SV=1 CANONICAL=P23999-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 17039552,
                "end_pos": 17038263,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000004118.3",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000004118.3"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000004118.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000004118.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "P23999-1",
            "url": "",
            "sequence": {
                "sequence": "MLSCTTSTMPGMICKNSDLEFDSLKPCFYPEDDDIYFGGRNSTPPGEDIWKKFELLPTPRLSPGRALAEDSLEPANWATEMLLPEADLWSNPAEEEDIFGLKGLSGSSSNPVVLQDCMWSGFSSREKPETVVSEKLPGGCGSLAVGAGTLVPGAAAATSAGHARSGTAGVGRRKAAWLTELSHLDSECVDSAVIFPANKRESMPVATIPASAGAAISLGDHQGLSSSLEDFLSNSGYVEEGGEEIYVVMLGETQFSKTVTKLPTAAHSENAALTPECAQSGELILKRSDLIQEQHNYAAPPLPYAEDARPLKKPRSQDPLGPLKCVLRPKAPRLRSRSNSDLEDIERRRNHNRMERQRRDIMRSSFLNLRDLVPELVHNEKAAKVVILKKATEYIHTLQTDESKLLVEREKLYERKQQLLEKIKQSAVC",
                "length": 429,
                "header": "sp|P23999-1|MYCS_RAT Isoform 1 of Protein S-Myc  OS=Rattus norvegicus OX=10116 GN=Mycs PE=3 SV=1 CANONICAL=P23999-1"
            },
            "locus": {}
        }
    ],
    "glycosylation": [],
    "phosphorylation": [
        {
            "start_pos": 36,
            "end_pos": 36,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Tyr",
            "comment": "Phosphotyrosine; by Tyr-kinases",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P23999",
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    "publication": [
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            "title": "Identifying genes regulated in a Myc-dependent manner.",
            "journal": "The Journal of biological chemistry",
            "date": "2002",
            "authors": "Watson JD, Oster SK, Shago M, Khosravi F, Penn LZ",
            "evidence": [
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                    "database": "RefSeq",
                    "id": "NP_068609",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_068609"
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                    "type": "PubMed",
                    "id": "12145275",
                    "url": "https://glygen.org/publication/PubMed/12145275"
                }
            ]
        },
        {
            "title": "Isolation and characterization of s-myc, a member of the rat myc gene family.",
            "journal": "Proc. Natl. Acad. Sci. U.S.A.",
            "date": "1989",
            "authors": "Sugiyama A., Nishimura S., Lee S.Y., Kuchino Y., Kume A., Nemoto K., Asami Y., Nemoto F.",
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            ]
        }
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        {
            "id": "rno:24581",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:24581",
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            "tax_id": 9606,
            "organism": "Homo sapiens",
            "sequence": {
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