[
    {
        "title": "PDK1-stabilized LncRNA SPRY4-IT1 promotes breast cancer progression via activating NF-\u03baB signaling pathway.",
        "journal": "Molecular carcinogenesis",
        "date": "2023-04-12",
        "authors": "Zhang Yulu, Chen Hongling, Yuan Renjie, Wang Yange, Zhang Dian, Zeng Qian, Jiang Weiqian, Zhang Ruiming, Chen Tingmei, Chai Chengsen, Guo Bianqin",
        "reference": {
            "type": "PubMed",
            "id": "37042573",
            "url": "https://pubmed.ncbi.nlm.nih.gov/37042573"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q68CZ6-1",
                "protein_name": "HAUS augmin-like complex subunit 3",
                "gene_name": "HAUS3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9C004-1",
                "protein_name": "Protein sprouty homolog 4",
                "gene_name": "SPRY4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q68CZ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q68CZ6"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.37042573",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "RUNX1-IT1 acts as a scaffold of STAT1 and NuRD complex to promote ROS-mediated NF-\u03baB activation and ovarian cancer progression.",
        "journal": "Oncogene",
        "date": "2024-02",
        "authors": "Yu Xiao, Zhao Pengfei, Luo Qingyu, Wu Xiaowei, Wang Yating, Nan Yabing, Liu Shi, Gao Wenyan, Li Bin, Liu Zhihua, Cui Zhumei",
        "reference": {
            "type": "PubMed",
            "id": "38092960",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38092960"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q68CZ6-1",
                "protein_name": "HAUS augmin-like complex subunit 3",
                "gene_name": "HAUS3",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q68CZ6",
                        "url": "https://www.uniprot.org/uniprotkb/Q68CZ6"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38092960",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis.",
        "journal": "Gut",
        "date": "2018",
        "authors": "Rosendahl J, Kirsten H, Hegyi E, Kovacs P, Weiss FU, Laumen H, Lichtner P, Ruffert C, Chen JM, Masson E, Beer S, Zimmer C, Seltsam K, Algul H, Buhler F, Bruno MJ, Bugert P, Burkhardt R, Cavestro GM, Cichoz-Lach H, Farre A, Frank J, Gambaro G, Gimpfl S, Grallert H, Griesmann H, Grutzmann R, Hellerbrand C, Hegyi P, Hollenbach M, Iordache S, Jurkowska G, Keim V, Kiefer F, Krug S, Landt O, Leo MD, Lerch MM, Levy P, Loffler M, Lohr M, Ludwig M, Macek M, Malats N, Malecka-Panas E, Malerba G, Mann K, Mayerle J, Mohr S, Te Morsche RHM, Motyka M, Mueller S, Muller T, Nothen MM, Pedrazzoli S, Pereira SP, Peters A, Pfutzer R, Real FX, Rebours V, Ridinger M, Rietschel M, Rosmann E, Saftoiu A, Schneider A, Schulz HU, Soranzo N, Soyka M, Simon P, Skipworth J, Stickel F, Strauch K, Stumvoll M, Testoni PA, Tonjes A, Werner L, Werner J, Wodarz N, Ziegler M, Masamune A, Mossner J, Ferec C, Michl P, P H Drenth J, Witt H, Scholz M, Sahin-Toth M",
        "reference": {
            "type": "PubMed",
            "id": "28754779",
            "url": "https://pubmed.ncbi.nlm.nih.gov/28754779"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q6GPI1-1",
                "protein_name": "Chymotrypsinogen B2",
                "gene_name": "CTRB2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P17538-1",
                "protein_name": "Chymotrypsinogen B",
                "gene_name": "CTRB1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q6GPI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q6GPI1"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.28754779",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Sequencing of the complex CTRB1-CTRB2 locus in chronic pancreatitis.",
        "journal": "Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]",
        "date": "2020",
        "authors": "Seltsam K, Pentner C, Weigl F, Sutedjo S, Zimmer C, Beer S, Bugert P, Ewers M, Ruffert C, Michl P, Laumen H, Witt H, Rosendahl J",
        "reference": {
            "type": "PubMed",
            "id": "33036922",
            "url": "https://pubmed.ncbi.nlm.nih.gov/33036922"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q6GPI1-1",
                "protein_name": "Chymotrypsinogen B2",
                "gene_name": "CTRB2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P17538-1",
                "protein_name": "Chymotrypsinogen B",
                "gene_name": "CTRB1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q6GPI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q6GPI1"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.33036922",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "A 584 bp deletion in CTRB2 inhibits chymotrypsin B2 activity and secretion and confers risk of pancreatic cancer.",
        "journal": "American journal of human genetics",
        "date": "2021",
        "authors": "Jermusyk A, Zhong J, Connelly KE, Gordon N, Perera S, Abdolalizadeh E, Zhang T, O'Brien A, Hoskins JW, Collins I, Eiser D, Yuan C, Risch HA, Jacobs EJ, Li D, Du M, Stolzenberg-Solomon RZ, Klein AP, Smith JP, Wolpin BM, Chanock SJ, Shi J, Petersen GM, Westlake CJ, Amundadottir LT",
        "reference": {
            "type": "PubMed",
            "id": "34559995",
            "url": "https://pubmed.ncbi.nlm.nih.gov/34559995"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q6GPI1-1",
                "protein_name": "Chymotrypsinogen B2",
                "gene_name": "CTRB2",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q6GPI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q6GPI1"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.34559995",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Arg236 in human chymotrypsin B2 (CTRB2) is a key determinant of high enzyme activity, trypsinogen degradation capacity, and protection against pancreatitis.",
        "journal": "Biochimica et biophysica acta. Proteins and proteomics",
        "date": "2022",
        "authors": "Nemeth BZ, Demcsak A, Micsonai A, Kiss B, Schlosser G, Geisz A, Hegyi E, Sahin-Toth M, Pal G",
        "reference": {
            "type": "PubMed",
            "id": "35934298",
            "url": "https://pubmed.ncbi.nlm.nih.gov/35934298"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q6GPI1-1",
                "protein_name": "Chymotrypsinogen B2",
                "gene_name": "CTRB2",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q6GPI1",
                        "url": "https://www.uniprot.org/uniprotkb/Q6GPI1"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.35934298",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger protein.",
        "journal": "Nat. Genet.",
        "date": "2006",
        "authors": "Birnbaum Ramon Y, Zvulunov Alex, Hallel-Halevy Dafna, Cagnano Emanuella, Finer Gal, Ofir Rivka, Geiger Dan, Silberstein Eldad, Feferman Yael, Birk Ohad S",
        "reference": {
            "type": "PubMed",
            "id": "16751772",
            "url": "https://pubmed.ncbi.nlm.nih.gov/16751772"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q32MQ0-1",
                "protein_name": "Zinc finger protein 750",
                "gene_name": "ZNF750",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.16751772",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "A promoter sequence variant of ZNF750 is linked with familial psoriasis.",
        "journal": "The Journal of investigative dermatology",
        "date": "2008",
        "authors": "Yang CF, Hwu WL, Yang LC, Chung WH, Chien YH, Hung CF, Chen HC, Tsai PJ, Fann CS, Liao F, Chen YT",
        "reference": {
            "type": "PubMed",
            "id": "18256691",
            "url": "https://pubmed.ncbi.nlm.nih.gov/18256691"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q32MQ0-1",
                "protein_name": "Zinc finger protein 750",
                "gene_name": "ZNF750",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.18256691",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Association analysis identifies ZNF750 regulatory variants in psoriasis.",
        "journal": "BMC medical genetics",
        "date": "2011",
        "authors": "Birnbaum RY, Hayashi G, Cohen I, Poon A, Chen H, Lam ET, Kwok PY, Birk OS, Liao W",
        "reference": {
            "type": "PubMed",
            "id": "22185198",
            "url": "https://pubmed.ncbi.nlm.nih.gov/22185198"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q32MQ0-1",
                "protein_name": "Zinc finger protein 750",
                "gene_name": "ZNF750",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.22185198",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "ZNF750 is a p63 target gene that induces KLF4 to drive terminal epidermal differentiation.",
        "journal": "Developmental cell",
        "date": "2012",
        "authors": "Sen GL, Boxer LD, Webster DE, Bussat RT, Qu K, Zarnegar BJ, Johnston D, Siprashvili Z, Khavari PA",
        "reference": {
            "type": "PubMed",
            "id": "22364861",
            "url": "https://pubmed.ncbi.nlm.nih.gov/22364861"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q32MQ0-1",
                "protein_name": "Zinc finger protein 750",
                "gene_name": "ZNF750",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "mutagenesis": [
            {
                "start_pos": 27,
                "end_pos": 27,
                "sequence_org": "C",
                "sequence_mut": "A",
                "comment": "Abolishes the ability to induce epidermal terminal differentiation; when associated with A-30.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    },
                    {
                        "database": "PubMed",
                        "id": "22364861",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/22364861"
                    }
                ],
                "uniprot_canonical_ac": "Q32MQ0-1"
            },
            {
                "start_pos": 30,
                "end_pos": 30,
                "sequence_org": "C",
                "sequence_mut": "A",
                "comment": "Abolishes the ability to induce epidermal terminal differentiation; when associated with A-27.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    },
                    {
                        "database": "PubMed",
                        "id": "22364861",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/22364861"
                    }
                ],
                "uniprot_canonical_ac": "Q32MQ0-1"
            },
            {
                "start_pos": 39,
                "end_pos": 39,
                "sequence_org": "H",
                "sequence_mut": "A",
                "comment": "Abolishes the ability to induce epidermal terminal differentiation; when associated with A-43. Retains the ability to bind zinc; when associated with A-34.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    },
                    {
                        "database": "PubMed",
                        "id": "22364861",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/22364861"
                    },
                    {
                        "database": "PubMed",
                        "id": "37655311",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/37655311"
                    }
                ],
                "uniprot_canonical_ac": "Q32MQ0-1"
            },
            {
                "start_pos": 43,
                "end_pos": 43,
                "sequence_org": "H",
                "sequence_mut": "A",
                "comment": "Abolishes the ability to induce epidermal terminal differentiation; when associated with A-39.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    },
                    {
                        "database": "PubMed",
                        "id": "22364861",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/22364861"
                    }
                ],
                "uniprot_canonical_ac": "Q32MQ0-1"
            }
        ],
        "record_id": "pubmed.22364861",
        "abstract": "",
        "glycosylation": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "ZNF750 is expressed in differentiated keratinocytes and regulates epidermal late differentiation genes.",
        "journal": "PloS one",
        "date": "2012",
        "authors": "Cohen I, Birnbaum RY, Leibson K, Taube R, Sivan S, Birk OS",
        "reference": {
            "type": "PubMed",
            "id": "22936986",
            "url": "https://pubmed.ncbi.nlm.nih.gov/22936986"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q32MQ0-1",
                "protein_name": "Zinc finger protein 750",
                "gene_name": "ZNF750",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.22936986",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "ZNF750: A Novel Prognostic Biomarker in Metastatic Prostate Cancer.",
        "journal": "International journal of molecular sciences",
        "date": "2023-03-30",
        "authors": "Montanaro Manuela, Agostini Massimiliano, Anemona Lucia, Bonanno Elena, Servadei Francesca, Finazzi Agr\u00f2 Enrico, Asimakopoulos Anastasios D, Ganini Carlo, Cipriani Chiara, Signoretti Marta, Bove Pierluigi, Rugolo Francesco, Imperiali Benedetta, Melino Gerry, Mauriello Alessandro, Scimeca Manuel",
        "reference": {
            "type": "PubMed",
            "id": "37047491",
            "url": "https://pubmed.ncbi.nlm.nih.gov/37047491"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q32MQ0-1",
                "protein_name": "Zinc finger protein 750",
                "gene_name": "ZNF750",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.37047491",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "NMR structure verifies the eponymous zinc finger domain of transcription factor ZNF750.",
        "journal": "Journal of structural biology: X",
        "date": "2023-12",
        "authors": "Rua Antonio J, Whitehead Richard D, Alexandrescu Andrei T",
        "reference": {
            "type": "PubMed",
            "id": "37655311",
            "url": "https://pubmed.ncbi.nlm.nih.gov/37655311"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q32MQ0-1",
                "protein_name": "Zinc finger protein 750",
                "gene_name": "ZNF750",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "mutagenesis": [
            {
                "start_pos": 34,
                "end_pos": 34,
                "sequence_org": "C",
                "sequence_mut": "A",
                "comment": "Retains the ability to bind zinc; when associated with A-39.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    },
                    {
                        "database": "PubMed",
                        "id": "37655311",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/37655311"
                    }
                ],
                "uniprot_canonical_ac": "Q32MQ0-1"
            },
            {
                "start_pos": 39,
                "end_pos": 39,
                "sequence_org": "H",
                "sequence_mut": "A",
                "comment": "Abolishes the ability to induce epidermal terminal differentiation; when associated with A-43. Retains the ability to bind zinc; when associated with A-34.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    },
                    {
                        "database": "PubMed",
                        "id": "22364861",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/22364861"
                    },
                    {
                        "database": "PubMed",
                        "id": "37655311",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/37655311"
                    }
                ],
                "uniprot_canonical_ac": "Q32MQ0-1"
            }
        ],
        "record_id": "pubmed.37655311",
        "abstract": "",
        "glycosylation": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "The transcription regulators ZNF750 and LSD1/KDM1A dampen inflammation on the skin's surface by silencing pattern recognition receptors.",
        "journal": "Immunity",
        "date": "2024-10-08",
        "authors": "Liu Ye, Chen Yifang, Batzorig Uyanga, Li Jingting, Fern\u00e1ndez-M\u00e9ndez Celia, Mahapatra Samiksha, Li Fengwu, Sam Shebin, Dokoshi Tatsuya, Hong Seung-Phil, Nakatsuji Teruaki, Gallo Richard L, Sen George L",
        "reference": {
            "type": "PubMed",
            "id": "39353440",
            "url": "https://pubmed.ncbi.nlm.nih.gov/39353440"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q32MQ0-1",
                "protein_name": "Zinc finger protein 750",
                "gene_name": "ZNF750",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O60341-1",
                "protein_name": "Lysine-specific histone demethylase 1A",
                "gene_name": "KDM1A",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q32MQ0",
                        "url": "https://www.uniprot.org/uniprotkb/Q32MQ0"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.39353440",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Human GLUT4/muscle-fat glucose-transporter gene. Characterization and genetic variation.",
        "journal": "Diabetes",
        "date": "1992",
        "authors": "Buse JB, Yasuda K, Lay TP, Seo TS, Olson AL, Pessin JE, Karam JH, Seino S, Bell GI",
        "reference": {
            "type": "PubMed",
            "id": "1397719",
            "url": "https://pubmed.ncbi.nlm.nih.gov/1397719"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "P14672",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P14672"
                    },
                    {
                        "id": "rs121434581",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs121434581"
                    },
                    {
                        "id": "rs121434581",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs121434581"
                    },
                    {
                        "id": "rs121434581",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs121434581"
                    },
                    {
                        "id": "rs121434581",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs121434581#frequency_tab"
                    },
                    {
                        "id": "rs121434581",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs121434581"
                    },
                    {
                        "id": "1397719",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/1397719"
                    },
                    {
                        "id": "1918382",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/1918382"
                    },
                    {
                        "id": "7814014",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/7814014"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 383,
                "end_pos": 383,
                "subjects_tested": "4177",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "V",
                "sequence_mut": "I",
                "comment": "Somatic mutation passed 1 filters: protein-of-interest(glycogene, carbohydrate synthesis and metabolism/transporter).",
                "chr_id": "17",
                "chr_pos": "7285729",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "V383",
                "disease": [
                    {
                        "disease_id": "DOID:10283",
                        "recommended_name": {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:10283",
                            "name": "prostate cancer",
                            "description": "A male reproductive organ cancer that is located_in the prostate."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "NGP - new growth of prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "hereditary prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "malignant tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate cancer, familial",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "HPCX1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "HPCX2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene."
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "RNASEL familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "familial prostate cancer caused by mutation in RNASEL",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "HPC1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, type 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "HPC8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, susceptibility to, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "HPC3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, susceptibility to, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "HPC4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, type 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "HPC5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, type 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "HPC6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "HPC7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "HPC9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "HPC10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene."
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "EHBP1 familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "familial prostate cancer caused by mutation in EHBP1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "HPC12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene."
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "MSMB familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "familial prostate cancer caused by mutation in MSMB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, type 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "HPC13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "HPC11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "HPC14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "HPC15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0700275",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0700275",
                                "name": "prostate cancer, hereditary",
                                "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents."
                            },
                            {
                                "id": "MIM:601518",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601518",
                                "name": "Prostate cancer, hereditary, 1",
                                "description": "Prostate cancer, hereditary, 1"
                            },
                            {
                                "id": "MIM:610997",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610997",
                                "name": "Prostate cancer, hereditary, 9",
                                "description": "Prostate cancer, hereditary, 9"
                            },
                            {
                                "id": "MIM:611868",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611868",
                                "name": "Prostate cancer, hereditary, 12",
                                "description": "Prostate cancer, hereditary, 12"
                            },
                            {
                                "id": "MIM:611928",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611928",
                                "name": "Prostate cancer, hereditary, 13",
                                "description": "Prostate cancer, hereditary, 13"
                            },
                            {
                                "id": "MIM:611955",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611955",
                                "name": "Prostate cancer, hereditary, 11",
                                "description": "Prostate cancer, hereditary, 11"
                            },
                            {
                                "id": "MIM:176807",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/176807",
                                "name": "Prostate cancer",
                                "description": "Prostate cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10283",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10283"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:9352",
                        "recommended_name": {
                            "id": "DOID:9352",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9352",
                            "name": "type 2 diabetes mellitus",
                            "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "NIDDM",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "non-insulin-dependent diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "type 2 diabetes",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "type II diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "insulin resistance",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type 2 diabetes mellitus",
                                "description": "A type of diabetes mellitus that is characterized by insulin resistance or desensitization and increased blood glucose levels. This is a chronic disease that can develop gradually over the life of a patient and can be linked to both environmental factors and heredity."
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "NIDDM",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "T2D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "T2DM",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "T2DM - type 2 diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "adult onset diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "adult-onset diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitis type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitis type II",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, noninsulin-dependent",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, noninsulin-dependent, association with",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, noninsulin-dependent, late onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, type II",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes, type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "insulin resistance, severe, digenic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "non-insulin dependent diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "non-insulin dependent diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "noninsulin dependent diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "noninsulin-dependent diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type 2 diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type 2 diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type 2 diabetes mellitus non-insulin dependent",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type II diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type II diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, noninsulin-dependent, 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011027",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                                "name": "diabetes mellitus, noninsulin-dependent, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011027",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                                "name": "diabetes mellitus, noninsulin-dependent 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011027",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                                "name": "diabetes mellitus, noninsulin-dependent, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011027",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                                "name": "diabetes mellitus, noninsulin-dependent, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011027",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                                "name": "NIDDM1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011072",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011072",
                                "name": "diabetes mellitus, noninsulin-dependent, 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011072",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011072",
                                "name": "NIDDM2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011072",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011072",
                                "name": "diabetes mellitus, noninsulin-dependent, 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011363",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                                "name": "diabetes mellitus, noninsulin-dependent, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011363",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                                "name": "diabetes mellitus, noninsulin-dependent, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011363",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                                "name": "diabetes mellitus, noninsulin-dependent, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011363",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                                "name": "type 2 diabetes mellitus 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011363",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                                "name": "NIDDM3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                                "name": "diabetes mellitus, noninsulin-dependent, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                                "name": "diabetes mellitus, noninsulin-dependent, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                                "name": "diabetes mellitus, noninsulin-dependent, type 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:125853",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/125853",
                                "name": "Type 2 diabetes mellitus",
                                "description": "Type 2 diabetes mellitus"
                            },
                            {
                                "id": "MIM:601283",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601283",
                                "name": "Type 2 diabetes mellitus 1",
                                "description": "Type 2 diabetes mellitus 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9352",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9352"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ],
                "filter_code": "000000000000000000010.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P14672-1"
            }
        ],
        "record_id": "pubmed.1397719",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Insulin receptor and insulin-responsive glucose transporter (GLUT 4) mutations and polymorphisms in a Welsh type 2 (non-insulin-dependent) diabetic population.",
        "journal": "Diabetologia",
        "date": "1992",
        "authors": "O'Rahilly S, Krook A, Morgan R, Rees A, Flier JS, Moller DE",
        "reference": {
            "type": "PubMed",
            "id": "1521731",
            "url": "https://pubmed.ncbi.nlm.nih.gov/1521731"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.1521731",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "DHHC7 Palmitoylates Glucose Transporter 4 (Glut4) and Regulates Glut4 Membrane Translocation.",
        "journal": "The Journal of biological chemistry",
        "date": "2017",
        "authors": "Du K, Murakami S, Sun Y, Kilpatrick CL, Luscher B",
        "reference": {
            "type": "PubMed",
            "id": "28057756",
            "url": "https://pubmed.ncbi.nlm.nih.gov/28057756"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q91WU6-1",
                "protein_name": "Palmitoyltransferase ZDHHC7",
                "gene_name": "Zdhhc7",
                "tax_name": "Mouse"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "mutagenesis": [
            {
                "start_pos": 223,
                "end_pos": 223,
                "sequence_org": "C",
                "sequence_mut": "S",
                "comment": "Loss of palmitoylation.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    },
                    {
                        "database": "PubMed",
                        "id": "28057756",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/28057756"
                    }
                ],
                "uniprot_canonical_ac": "P14672-1"
            }
        ],
        "record_id": "pubmed.28057756",
        "abstract": "",
        "glycosylation": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Regulated dynamic subcellular GLUT4 localization revealed by proximal proteome mapping in human muscle cells.",
        "journal": "Journal of cell science",
        "date": "2023-12-01",
        "authors": "Ray Anuttoma, Wen Jennifer, Yammine Lucie, Culver Jeff, Parida Isabella Supardi, Garren Jeonifer, Xue Liang, Hales Katherine, Xiang Qing, Birnbaum Morris J, Zhang Bei B, Monetti Mara, McGraw Timothy E",
        "reference": {
            "type": "PubMed",
            "id": "38126809",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38126809"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38126809",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Phosphorylation of Syntaxin 4 by the Insulin Receptor Drives Exocytic SNARE Complex Formation to Deliver GLUT4 to the Cell Surface.",
        "journal": "Biomolecules",
        "date": "2023-12-02",
        "authors": "Kioumourtzoglou Dimitrios, Black Hannah L, Al Tobi Mohammed, Livingstone Rachel, Petrie John R, Boyle James G, Gould Gwyn W, Bryant Nia J",
        "reference": {
            "type": "PubMed",
            "id": "38136609",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38136609"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P70452-1",
                "protein_name": "Syntaxin-4",
                "gene_name": "Stx4a; Stx4",
                "tax_name": "Mouse"
            },
            {
                "uniprot_canonical_ac": "Q12846-1",
                "protein_name": "Syntaxin-4",
                "gene_name": "STX4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38136609",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 3
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "GLUT4 localisation with the plasma membrane is unaffected by an increase in plasma free fatty acid availability.",
        "journal": "Lipids in health and disease",
        "date": "2024-04-02",
        "authors": "Barrett J S, Strauss J A, Chow L S, Shepherd S O, Wagenmakers A J M, Wang Y",
        "reference": {
            "type": "PubMed",
            "id": "38566151",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38566151"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38566151",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Insulin-Activated Signaling Pathway and GLUT4 Membrane Translocation in hiPSC-Derived Cardiomyocytes.",
        "journal": "International journal of molecular sciences",
        "date": "2024-07-27",
        "authors": "Querio Giulia, Antoniotti Susanna, Levi Renzo, Fleischmann Bernd K, Gallo Maria Pia, Malan Daniela",
        "reference": {
            "type": "PubMed",
            "id": "39125765",
            "url": "https://pubmed.ncbi.nlm.nih.gov/39125765"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.39125765",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Failure to detect Glut4-Ile383 and IR-Gln1152 variants in NIDDM (non-insulin dependent diabetes mellitus) and control subjects in an Italian population.",
        "journal": "Human genetics",
        "date": "1995-01",
        "authors": "Esposito L, Carrera P, Pontiroli A E, Ferrari M",
        "reference": {
            "type": "PubMed",
            "id": "7814014",
            "url": "https://pubmed.ncbi.nlm.nih.gov/7814014"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "P14672",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P14672"
                    },
                    {
                        "id": "rs121434581",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs121434581"
                    },
                    {
                        "id": "rs121434581",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs121434581"
                    },
                    {
                        "id": "rs121434581",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs121434581"
                    },
                    {
                        "id": "rs121434581",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs121434581#frequency_tab"
                    },
                    {
                        "id": "rs121434581",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs121434581"
                    },
                    {
                        "id": "1397719",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/1397719"
                    },
                    {
                        "id": "1918382",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/1918382"
                    },
                    {
                        "id": "7814014",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/7814014"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 383,
                "end_pos": 383,
                "subjects_tested": "4177",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "V",
                "sequence_mut": "I",
                "comment": "Somatic mutation passed 1 filters: protein-of-interest(glycogene, carbohydrate synthesis and metabolism/transporter).",
                "chr_id": "17",
                "chr_pos": "7285729",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "V383",
                "disease": [
                    {
                        "disease_id": "DOID:10283",
                        "recommended_name": {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:10283",
                            "name": "prostate cancer",
                            "description": "A male reproductive organ cancer that is located_in the prostate."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "NGP - new growth of prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "hereditary prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "malignant tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate cancer, familial",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "HPCX1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "HPCX2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene."
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "RNASEL familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "familial prostate cancer caused by mutation in RNASEL",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "HPC1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, type 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "HPC8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, susceptibility to, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "HPC3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, susceptibility to, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "HPC4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, type 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "HPC5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, type 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "HPC6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "HPC7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "HPC9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "HPC10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene."
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "EHBP1 familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "familial prostate cancer caused by mutation in EHBP1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "HPC12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene."
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "MSMB familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "familial prostate cancer caused by mutation in MSMB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, type 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "HPC13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "HPC11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "HPC14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "HPC15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0700275",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0700275",
                                "name": "prostate cancer, hereditary",
                                "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents."
                            },
                            {
                                "id": "MIM:601518",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601518",
                                "name": "Prostate cancer, hereditary, 1",
                                "description": "Prostate cancer, hereditary, 1"
                            },
                            {
                                "id": "MIM:610997",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610997",
                                "name": "Prostate cancer, hereditary, 9",
                                "description": "Prostate cancer, hereditary, 9"
                            },
                            {
                                "id": "MIM:611868",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611868",
                                "name": "Prostate cancer, hereditary, 12",
                                "description": "Prostate cancer, hereditary, 12"
                            },
                            {
                                "id": "MIM:611928",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611928",
                                "name": "Prostate cancer, hereditary, 13",
                                "description": "Prostate cancer, hereditary, 13"
                            },
                            {
                                "id": "MIM:611955",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611955",
                                "name": "Prostate cancer, hereditary, 11",
                                "description": "Prostate cancer, hereditary, 11"
                            },
                            {
                                "id": "MIM:176807",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/176807",
                                "name": "Prostate cancer",
                                "description": "Prostate cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10283",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10283"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:9352",
                        "recommended_name": {
                            "id": "DOID:9352",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9352",
                            "name": "type 2 diabetes mellitus",
                            "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "NIDDM",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "non-insulin-dependent diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "type 2 diabetes",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "type II diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "insulin resistance",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type 2 diabetes mellitus",
                                "description": "A type of diabetes mellitus that is characterized by insulin resistance or desensitization and increased blood glucose levels. This is a chronic disease that can develop gradually over the life of a patient and can be linked to both environmental factors and heredity."
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "NIDDM",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "T2D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "T2DM",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "T2DM - type 2 diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "adult onset diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "adult-onset diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitis type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitis type II",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, noninsulin-dependent",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, noninsulin-dependent, association with",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, noninsulin-dependent, late onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, type II",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes, type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "insulin resistance, severe, digenic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "non-insulin dependent diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "non-insulin dependent diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "noninsulin dependent diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "noninsulin-dependent diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type 2 diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type 2 diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type 2 diabetes mellitus non-insulin dependent",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type II diabetes",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type II diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "diabetes mellitus, noninsulin-dependent, 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011027",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                                "name": "diabetes mellitus, noninsulin-dependent, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011027",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                                "name": "diabetes mellitus, noninsulin-dependent 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011027",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                                "name": "diabetes mellitus, noninsulin-dependent, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011027",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                                "name": "diabetes mellitus, noninsulin-dependent, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011027",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011027",
                                "name": "NIDDM1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011072",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011072",
                                "name": "diabetes mellitus, noninsulin-dependent, 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011072",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011072",
                                "name": "NIDDM2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011072",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011072",
                                "name": "diabetes mellitus, noninsulin-dependent, 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011363",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                                "name": "diabetes mellitus, noninsulin-dependent, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011363",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                                "name": "diabetes mellitus, noninsulin-dependent, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011363",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                                "name": "diabetes mellitus, noninsulin-dependent, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011363",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                                "name": "type 2 diabetes mellitus 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011363",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011363",
                                "name": "NIDDM3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                                "name": "diabetes mellitus, noninsulin-dependent, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                                "name": "diabetes mellitus, noninsulin-dependent, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011955",
                                "name": "diabetes mellitus, noninsulin-dependent, type 4",
                                "description": ""
                            },
                            {
                                "id": "MIM:125853",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/125853",
                                "name": "Type 2 diabetes mellitus",
                                "description": "Type 2 diabetes mellitus"
                            },
                            {
                                "id": "MIM:601283",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601283",
                                "name": "Type 2 diabetes mellitus 1",
                                "description": "Type 2 diabetes mellitus 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9352",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9352"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ],
                "filter_code": "000000000000000000010.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P14672-1"
            }
        ],
        "record_id": "pubmed.7814014",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Identification of the 5' end of the gene encoding a human insulin-responsive glucose transporter.",
        "journal": "Gene",
        "date": "1993",
        "authors": "Chiaramonte R, Martini R, Taramelli R, Comi P",
        "reference": {
            "type": "PubMed",
            "id": "7916714",
            "url": "https://pubmed.ncbi.nlm.nih.gov/7916714"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.7916714",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "A Leu-Leu sequence is essential for COOH-terminal targeting signal of GLUT4 glucose transporter in fibroblasts.",
        "journal": "The Journal of biological chemistry",
        "date": "1994",
        "authors": "Verhey KJ, Birnbaum MJ",
        "reference": {
            "type": "PubMed",
            "id": "8300557",
            "url": "https://pubmed.ncbi.nlm.nih.gov/8300557"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "mutagenesis": [
            {
                "start_pos": 489,
                "end_pos": 490,
                "sequence_org": "LL",
                "sequence_mut": "AA",
                "comment": "Changes subcellular location mainly to the plasma membrane.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    },
                    {
                        "database": "PubMed",
                        "id": "8300557",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/8300557"
                    }
                ],
                "uniprot_canonical_ac": "P14672-1"
            }
        ],
        "record_id": "pubmed.8300557",
        "abstract": "",
        "glycosylation": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Mutational analysis of the carboxy-terminal phosphorylation site of GLUT-4 in 3T3-L1 adipocytes.",
        "journal": "The American journal of physiology",
        "date": "1998",
        "authors": "Marsh BJ, Martin S, Melvin DR, Martin LB, Alm RA, Gould GW, James DE",
        "reference": {
            "type": "PubMed",
            "id": "9725807",
            "url": "https://pubmed.ncbi.nlm.nih.gov/9725807"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "phosphorylation": [
            {
                "start_pos": 488,
                "end_pos": 488,
                "kinase_uniprot_canonical_ac": "",
                "kinase_gene_name": "",
                "residue": "Ser",
                "comment": "Phosphoserine",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P14672",
                        "url": "https://www.uniprot.org/uniprotkb/P14672"
                    },
                    {
                        "database": "iPTMnet",
                        "id": "P14672",
                        "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P14672"
                    },
                    {
                        "database": "PubMed",
                        "id": "9725807",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/9725807"
                    }
                ],
                "site_lbl": "Ser488",
                "uniprot_canonical_ac": "P14672-1"
            }
        ],
        "record_id": "pubmed.9725807",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    },
                    {
                        "field": "total_sites",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "start_pos",
                    "end_pos",
                    "kinase_uniprot_canonical_ac",
                    "kinase_gene_name",
                    "residue",
                    "comment",
                    "site_lbl",
                    "uniprot_canonical_ac"
                ]
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Sex-determining region Y-related protein SOX13 is a diabetes autoantigen expressed in pancreatic islets.",
        "journal": "Diabetes",
        "date": "2000-04",
        "authors": "Kasimiotis H, Myers M A, Argentaro A, Mertin S, Fida S, Ferraro T, Olsson J, Rowley M J, Harley V R",
        "reference": {
            "type": "PubMed",
            "id": "10871192",
            "url": "https://pubmed.ncbi.nlm.nih.gov/10871192"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q9UN79-1",
                "protein_name": "Transcription factor SOX-13",
                "gene_name": "SOX13",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q04891-1",
                "protein_name": "Transcription factor SOX-13",
                "gene_name": "Sox13",
                "tax_name": "Mouse"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9UN79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9UN79"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.10871192",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Sex-determining Region Y-box transcription factor 13 promotes breast cancer cell proliferation and glycolysis by activating the tripartite motif containing 11-mediated Wnt/beta-catenin signaling pathway.",
        "journal": "Bioengineered",
        "date": "2022",
        "authors": "Jin X, Shao X, Pang W, Wang Z, Huang J",
        "reference": {
            "type": "PubMed",
            "id": "35611828",
            "url": "https://pubmed.ncbi.nlm.nih.gov/35611828"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q9UN79-1",
                "protein_name": "Transcription factor SOX-13",
                "gene_name": "SOX13",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9UN79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9UN79"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.35611828",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Sox13 and M2-like leukemia-associated macrophages contribute to endogenous IL-34 caused accelerated progression of acute myeloid leukemia.",
        "journal": "Cell death & disease",
        "date": "2023-05-06",
        "authors": "Zhang Dongyue, Cui Xiaoxi, Li Yifei, Wang Rong, Wang Hao, Dai Yibo, Ren Qian, Wang Lina, Zheng Guoguang",
        "reference": {
            "type": "PubMed",
            "id": "37149693",
            "url": "https://pubmed.ncbi.nlm.nih.gov/37149693"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q9UN79-1",
                "protein_name": "Transcription factor SOX-13",
                "gene_name": "SOX13",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9UN79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9UN79"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.37149693",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Hsa_circ_0071589 aggravates stemness and oxaliplatin resistance in colorectal cancer through sponging miR-133b to upregulate SOX13 expression.",
        "journal": "Molecular and cellular biochemistry",
        "date": "2024-08",
        "authors": "Lv Lv, Yi Lu, Huang Bojie, Zhou Cong, Zhang Lei",
        "reference": {
            "type": "PubMed",
            "id": "37522976",
            "url": "https://pubmed.ncbi.nlm.nih.gov/37522976"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q9UN79-1",
                "protein_name": "Transcription factor SOX-13",
                "gene_name": "SOX13",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9UN79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9UN79"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.37522976",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "THAP9-AS1 promotes nasopharyngeal carcinoma progression through targeted regulation of the miR-185-5p/SOX13 axis.",
        "journal": "Physiology international",
        "date": "2024-01-25",
        "authors": "Mo Jinhua, Gong Zengyi, Liu Hong, Zhou Lian, Zhao Yanguang",
        "reference": {
            "type": "PubMed",
            "id": "38270621",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38270621"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q9UN79-1",
                "protein_name": "Transcription factor SOX-13",
                "gene_name": "SOX13",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9UN79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9UN79"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38270621",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "High expression of the HMG box factor sox-13 in arterial walls during embryonic development.",
        "journal": "Nucleic Acids Res.",
        "date": "1998",
        "authors": "Roose J, Korver W, Oving E, Wilson A, Wagenaar G, Markman M, Lamers W, Clevers H",
        "reference": {
            "type": "PubMed",
            "id": "9421502",
            "url": "https://pubmed.ncbi.nlm.nih.gov/9421502"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q9UN79-1",
                "protein_name": "Transcription factor SOX-13",
                "gene_name": "SOX13",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q04891-1",
                "protein_name": "Transcription factor SOX-13",
                "gene_name": "Sox13",
                "tax_name": "Mouse"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q9UN79",
                        "url": "https://www.uniprot.org/uniprotkb/Q9UN79"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.9421502",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "The subunit 1 of the COP9 signalosome suppresses gene expression through its N-terminal domain and incorporates into the complex through the PCI domain.",
        "journal": "J. Mol. Biol.",
        "date": "2001",
        "authors": "Tsuge T, Matsui M, Wei N",
        "reference": {
            "type": "PubMed",
            "id": "11114242",
            "url": "https://pubmed.ncbi.nlm.nih.gov/11114242"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q13098-4",
                "protein_name": "COP9 signalosome complex subunit 1",
                "gene_name": "GPS1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q13098",
                        "url": "https://www.uniprot.org/uniprotkb/Q13098"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.11114242",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Inositol 1,3,4-trisphosphate 5/6-kinase associates with the COP9 signalosome by binding to CSN1.",
        "journal": "J. Biol. Chem.",
        "date": "2002",
        "authors": "Sun Young, Wilson Monita P, Majerus Philip W",
        "reference": {
            "type": "PubMed",
            "id": "12324474",
            "url": "https://pubmed.ncbi.nlm.nih.gov/12324474"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q13098-4",
                "protein_name": "COP9 signalosome complex subunit 1",
                "gene_name": "GPS1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q13572-1",
                "protein_name": "Inositol-tetrakisphosphate 1-kinase",
                "gene_name": "ITPK1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q13098",
                        "url": "https://www.uniprot.org/uniprotkb/Q13098"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.12324474",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "CSN1 facilitates proliferation and migration of hepatocellular carcinoma cells by upregulating cyclin A2 expression.",
        "journal": "Molecular medicine reports",
        "date": "2021",
        "authors": "Fu H, Zhang Y, Chen Y, Chen J, Chen P",
        "reference": {
            "type": "PubMed",
            "id": "33200803",
            "url": "https://pubmed.ncbi.nlm.nih.gov/33200803"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q13098-4",
                "protein_name": "COP9 signalosome complex subunit 1",
                "gene_name": "GPS1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q13098",
                        "url": "https://www.uniprot.org/uniprotkb/Q13098"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.33200803",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "USP48 and A20 synergistically promote cell survival in Helicobacter pylori infection.",
        "journal": "Cell. Mol. Life Sci.",
        "date": "2022",
        "authors": "Jantaree P, Chaithongyot S, Sokolova O, Naumann M",
        "reference": {
            "type": "PubMed",
            "id": "35913642",
            "url": "https://pubmed.ncbi.nlm.nih.gov/35913642"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q13098-4",
                "protein_name": "COP9 signalosome complex subunit 1",
                "gene_name": "GPS1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q86UV5-1",
                "protein_name": "Ubiquitin carboxyl-terminal hydrolase 48",
                "gene_name": "USP48",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q13098",
                        "url": "https://www.uniprot.org/uniprotkb/Q13098"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.35913642",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Bioinformatics analysis of GPS1 expression and biological function in breast cancer.",
        "journal": "Journal of cancer research and clinical oncology",
        "date": "2024-01-30",
        "authors": "Wei Hong, Niu Zhaocan, Ji Ruixue, Jiang Wenwen, Tang Jiawei, Meng Zhexuan, Cao Xiaoyang, Zhang Xinyi, Liu Xue",
        "reference": {
            "type": "PubMed",
            "id": "38289496",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38289496"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q13098-4",
                "protein_name": "COP9 signalosome complex subunit 1",
                "gene_name": "GPS1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q13098",
                        "url": "https://www.uniprot.org/uniprotkb/Q13098"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38289496",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Functional interaction of general transcription initiation factor TFIIE with general chromatin factor SPT16/CDC68.",
        "journal": "Genes Cells",
        "date": "2000",
        "authors": "Kang SW, Kuzuhara T, Horikoshi M",
        "reference": {
            "type": "PubMed",
            "id": "10792464",
            "url": "https://pubmed.ncbi.nlm.nih.gov/10792464"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P29084-1",
                "protein_name": "Transcription initiation factor IIE subunit beta",
                "gene_name": "GTF2E2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y5B9-1",
                "protein_name": "FACT complex subunit SPT16",
                "gene_name": "SUPT16H",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P29084",
                        "url": "https://www.uniprot.org/uniprotkb/P29084"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.10792464",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Conserved sequence motifs in the small subunit of human general transcription factor TFIIE.",
        "journal": "Nature",
        "date": "1991",
        "authors": "Sumimoto H, Ohkuma Y, Sinn E, Kato H, Shimasaki S, Horikoshi M, Roeder RG",
        "reference": {
            "type": "PubMed",
            "id": "1956404",
            "url": "https://pubmed.ncbi.nlm.nih.gov/1956404"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P29084-1",
                "protein_name": "Transcription initiation factor IIE subunit beta",
                "gene_name": "GTF2E2",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P29084",
                        "url": "https://www.uniprot.org/uniprotkb/P29084"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.1956404",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy.",
        "journal": "American journal of human genetics",
        "date": "2016",
        "authors": "Kuschal C, Botta E, Orioli D, Digiovanna JJ, Seneca S, Keymolen K, Tamura D, Heller E, Khan SG, Caligiuri G, Lanzafame M, Nardo T, Ricotti R, Peverali FA, Stephens R, Zhao Y, Lehmann AR, Baranello L, Levens D, Kraemer KH, Stefanini M",
        "reference": {
            "type": "PubMed",
            "id": "26996949",
            "url": "https://pubmed.ncbi.nlm.nih.gov/26996949"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P29084-1",
                "protein_name": "Transcription initiation factor IIE subunit beta",
                "gene_name": "GTF2E2",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P29084",
                        "url": "https://www.uniprot.org/uniprotkb/P29084"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.26996949",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "GTF2E2 is a novel biomarker for recurrence after surgery and promotes progression of esophageal squamous cell carcinoma via miR-139-5p/GTF2E2/FUS axis.",
        "journal": "Oncogene",
        "date": "2022-02",
        "authors": "Zhang Yujie, Zhang Yuxin, Ai Bo, Gong Juejun, Li Yichen, Yu Shiying, Cai Xiuyu, Zhang Li",
        "reference": {
            "type": "PubMed",
            "id": "34853466",
            "url": "https://pubmed.ncbi.nlm.nih.gov/34853466"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P29084-1",
                "protein_name": "Transcription initiation factor IIE subunit beta",
                "gene_name": "GTF2E2",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P29084",
                        "url": "https://www.uniprot.org/uniprotkb/P29084"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.34853466",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Mayaro Virus Non-Structural Protein 2 Circumvents the Induction of Interferon in Part by Depleting Host Transcription Initiation Factor IIE Subunit 2.",
        "journal": "Cells",
        "date": "2021",
        "authors": "Ishida R, Cole J, Lopez-Orozco J, Fayad N, Felix-Lopez A, Elaish M, Luo SY, Julien O, Kumar A, Hobman TC",
        "reference": {
            "type": "PubMed",
            "id": "34944018",
            "url": "https://pubmed.ncbi.nlm.nih.gov/34944018"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P29084-1",
                "protein_name": "Transcription initiation factor IIE subunit beta",
                "gene_name": "GTF2E2",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P29084",
                        "url": "https://www.uniprot.org/uniprotkb/P29084"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.34944018",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "GTF2E2 downregulated by miR-340-5p inhibits the malignant progression of glioblastoma.",
        "journal": "Cancer gene therapy",
        "date": "2023-12",
        "authors": "Qiao Xiaolong, Chen Yinan, Wang Zixuan, Peng Nan, Niu Wanxiang, Hou Shiqiang, Wu Jiaying, Ji Ying, Niu Chaoshi, Cheng Chuandong",
        "reference": {
            "type": "PubMed",
            "id": "37845349",
            "url": "https://pubmed.ncbi.nlm.nih.gov/37845349"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P29084-1",
                "protein_name": "Transcription initiation factor IIE subunit beta",
                "gene_name": "GTF2E2",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P29084",
                        "url": "https://www.uniprot.org/uniprotkb/P29084"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.37845349",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "DELE1 haploinsufficiency causes resistance to mitochondrial stress-induced apoptosis in monosomy 5/del(5q) AML.",
        "journal": "Leukemia",
        "date": "2024-03",
        "authors": "Spinella Jean-Fran\u00e7ois, Chagraoui Jalila, Moison C\u00e9line, Lavall\u00e9e Vincent P, Boivin Isabel, Gracias Deanne, Lavall\u00e9e Sylvie, Carpentier Guillaume Richard, Beliveau Fran\u00e7ois, H\u00e9bert Jos\u00e9e, Sauvageau Guy",
        "reference": {
            "type": "PubMed",
            "id": "38102204",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38102204"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q14154-1",
                "protein_name": "DAP3-binding cell death enhancer 1",
                "gene_name": "DELE1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q14154",
                        "url": "https://www.uniprot.org/uniprotkb/Q14154"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38102204",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "The HRI branch of the integrated stress response selectively triggers mitophagy.",
        "journal": "Molecular cell",
        "date": "2024-02-06",
        "authors": "Chakrabarty Yogaditya, Yang Zheng, Chen Hsiuchen, Chan David C",
        "reference": {
            "type": "PubMed",
            "id": "38340717",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38340717"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q14154-1",
                "protein_name": "DAP3-binding cell death enhancer 1",
                "gene_name": "DELE1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P05198-1",
                "protein_name": "Eukaryotic translation initiation factor 2 subunit 1",
                "gene_name": "EIF2S1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BQI3-1",
                "protein_name": "Eukaryotic translation initiation factor 2-alpha kinase 1",
                "gene_name": "EIF2AK1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q14154",
                        "url": "https://www.uniprot.org/uniprotkb/Q14154"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "mutagenesis": [
            {
                "start_pos": 52,
                "end_pos": 52,
                "sequence_org": "S",
                "sequence_mut": "A",
                "comment": "Abolished phosphorylation by EIF2AK1/HRI in response to stress. Abolished relocalization to the mitochondrial surface in response to mitochondrial damage.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P05198",
                        "url": "https://www.uniprot.org/uniprotkb/P05198"
                    },
                    {
                        "database": "PubMed",
                        "id": "38340717",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/38340717"
                    }
                ],
                "uniprot_canonical_ac": "P05198-1"
            },
            {
                "start_pos": 52,
                "end_pos": 52,
                "sequence_org": "S",
                "sequence_mut": "D",
                "comment": "Mimics phosphorylation; promotes relocalization to the mitochondrial surface in response to mitochondrial damage.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P05198",
                        "url": "https://www.uniprot.org/uniprotkb/P05198"
                    },
                    {
                        "database": "PubMed",
                        "id": "38340717",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/38340717"
                    }
                ],
                "uniprot_canonical_ac": "P05198-1"
            }
        ],
        "phosphorylation": [
            {
                "start_pos": 52,
                "end_pos": 52,
                "kinase_uniprot_canonical_ac": "",
                "kinase_gene_name": "",
                "residue": "Ser",
                "comment": "Phosphoserine",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P05198",
                        "url": "https://www.uniprot.org/uniprotkb/P05198"
                    },
                    {
                        "database": "PubMed",
                        "id": "19690332",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19690332"
                    },
                    {
                        "database": "PubMed",
                        "id": "38340717",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/38340717"
                    },
                    {
                        "database": "PubMed",
                        "id": "24275569",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/24275569"
                    },
                    {
                        "database": "iPTMnet",
                        "id": "P05198",
                        "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P05198"
                    },
                    {
                        "database": "PubMed",
                        "id": "10542257",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/10542257"
                    },
                    {
                        "database": "PubMed",
                        "id": "1677563",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/1677563"
                    },
                    {
                        "database": "PubMed",
                        "id": "9819435",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/9819435"
                    },
                    {
                        "database": "PRO",
                        "id": "P05198",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=P05198"
                    }
                ],
                "site_lbl": "Ser52",
                "uniprot_canonical_ac": "P05198-1"
            }
        ],
        "record_id": "pubmed.38340717",
        "abstract": "",
        "glycosylation": [],
        "snv": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 3
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    },
                    {
                        "field": "total_sites",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "start_pos",
                    "end_pos",
                    "kinase_uniprot_canonical_ac",
                    "kinase_gene_name",
                    "residue",
                    "comment",
                    "site_lbl",
                    "uniprot_canonical_ac"
                ]
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Prox1 is differentially localized during lens development.",
        "journal": "Mechanisms of development",
        "date": "2002",
        "authors": "Duncan MK, Cui W, Oh DJ, Tomarev SI",
        "reference": {
            "type": "PubMed",
            "id": "11850194",
            "url": "https://pubmed.ncbi.nlm.nih.gov/11850194"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q92786-1",
                "protein_name": "Prospero homeobox protein 1",
                "gene_name": "PROX1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q92786",
                        "url": "https://www.uniprot.org/uniprotkb/Q92786"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.11850194",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Determination of solution structures of proteins up to 40 kDa using CS-Rosetta with sparse NMR data from deuterated samples.",
        "journal": "Proc. Natl. Acad. Sci. U.S.A.",
        "date": "2012",
        "authors": "Lange Oliver F, Rossi Paolo, Sgourakis Nikolaos G, Song Yifan, Lee Hsiau-Wei, Aramini James M, Ertekin Asli, Xiao Rong, Acton Thomas B, Montelione Gaetano T, Baker David",
        "reference": {
            "type": "PubMed",
            "id": "22733734",
            "url": "https://pubmed.ncbi.nlm.nih.gov/22733734"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q92786-1",
                "protein_name": "Prospero homeobox protein 1",
                "gene_name": "PROX1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q92786",
                        "url": "https://www.uniprot.org/uniprotkb/Q92786"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.22733734",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "PROX1 interaction with \u03b1-SMA-rich cancer-associated fibroblasts facilitates colorectal cancer progression and correlates with poor clinical outcomes and therapeutic resistance.",
        "journal": "Aging",
        "date": "2024-01-18",
        "authors": "Lai Shiue-Wei, Cheng Yi-Chiao, Kiu Kee-Thai, Yen Min-Hsuan, Chen Ying-Wei, Yadav Vijesh Kumar, Yeh Chi-Tai, Kuo Kuang-Tai, Chang Tung-Cheng",
        "reference": {
            "type": "PubMed",
            "id": "38244581",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38244581"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q92786-1",
                "protein_name": "Prospero homeobox protein 1",
                "gene_name": "PROX1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q92786",
                        "url": "https://www.uniprot.org/uniprotkb/Q92786"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38244581",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Prox1 Suppresses Proliferation and Drug Resistance of Retinoblastoma Cells via Targeting Notch1.",
        "journal": "Current medical science",
        "date": "2024-02",
        "authors": "Zhang Hong-Li, Li Na, Dong Lin, Ma Hong-Xia, Yang Mo-Chi",
        "reference": {
            "type": "PubMed",
            "id": "38277016",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38277016"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q92786-1",
                "protein_name": "Prospero homeobox protein 1",
                "gene_name": "PROX1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q92786",
                        "url": "https://www.uniprot.org/uniprotkb/Q92786"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38277016",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "PROX1 drives neuroendocrine plasticity and liver metastases in prostate cancer.",
        "journal": "Cancer letters",
        "date": "2024-08-10",
        "authors": "Liu Chunyu, Chen Jiawei, Cong Yukun, Chen Kang, Li Haoran, He Qingliu, Chen Liang, Song Yarong, Xing Yifei",
        "reference": {
            "type": "PubMed",
            "id": "38901665",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38901665"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q92786-1",
                "protein_name": "Prospero homeobox protein 1",
                "gene_name": "PROX1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q92786",
                        "url": "https://www.uniprot.org/uniprotkb/Q92786"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38901665",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "PROX1 is a regulator of neuroendocrine-related gene expression in lung carcinoid.",
        "journal": "Human cell",
        "date": "2024-09",
        "authors": "Sakurai Kouhei, Ando Tatsuya, Sakai Yasuhiro, Mori Yuichiro, Nakamura Satoru, Kato Taku, Ito Hiroyasu",
        "reference": {
            "type": "PubMed",
            "id": "39066858",
            "url": "https://pubmed.ncbi.nlm.nih.gov/39066858"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q92786-1",
                "protein_name": "Prospero homeobox protein 1",
                "gene_name": "PROX1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q92786",
                        "url": "https://www.uniprot.org/uniprotkb/Q92786"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.39066858",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Structure and chromosomal localization of the human homeobox gene Prox 1.",
        "journal": "Genomics",
        "date": "1996",
        "authors": "Zinovieva RD, Duncan MK, Johnson TR, Torres R, Polymeropoulos MH, Tomarev SI",
        "reference": {
            "type": "PubMed",
            "id": "8812486",
            "url": "https://pubmed.ncbi.nlm.nih.gov/8812486"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q92786-1",
                "protein_name": "Prospero homeobox protein 1",
                "gene_name": "PROX1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q92786",
                        "url": "https://www.uniprot.org/uniprotkb/Q92786"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.8812486",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Defective glucose transport across brain tissue barriers: a newly recognized neurological syndrome.",
        "journal": "Neurochemical research",
        "date": "1999",
        "authors": "Klepper J, Wang D, Fischbarg J, Vera JC, Jarjour IT, O'Driscoll KR, De Vivo DC",
        "reference": {
            "type": "PubMed",
            "id": "10227690",
            "url": "https://pubmed.ncbi.nlm.nih.gov/10227690"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.10227690",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Golgi targeting of the GLUT1 glucose transporter in lactating mouse mammary gland.",
        "journal": "Pediatric research",
        "date": "2000",
        "authors": "Nemeth BA, Tsang SW, Geske RS, Haney PM",
        "reference": {
            "type": "PubMed",
            "id": "10759149",
            "url": "https://pubmed.ncbi.nlm.nih.gov/10759149"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P00709-1",
                "protein_name": "Alpha-lactalbumin",
                "gene_name": "LALBA",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15291-1",
                "protein_name": "Beta-1,4-galactosyltransferase 1",
                "gene_name": "B4GALT1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.10759149",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 3
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Hexose permeation pathways in Plasmodium falciparum-infected erythrocytes.",
        "journal": "Proceedings of the National Academy of Sciences of the United States of America",
        "date": "2000-08-29",
        "authors": "Woodrow C J, Burchmore R J, Krishna S",
        "reference": {
            "type": "PubMed",
            "id": "10954735",
            "url": "https://pubmed.ncbi.nlm.nih.gov/10954735"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.10954735",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome.",
        "journal": "Human mutation",
        "date": "2000",
        "authors": "Wang D, Kranz-Eble P, De Vivo DC",
        "reference": {
            "type": "PubMed",
            "id": "10980529",
            "url": "https://pubmed.ncbi.nlm.nih.gov/10980529"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs80359816",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359816"
                    },
                    {
                        "id": "rs80359816",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs80359816"
                    },
                    {
                        "id": "10980529",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/10980529"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 126,
                "end_pos": 126,
                "sequence_org": "R",
                "sequence_mut": "L",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42930765",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R126",
                "disease": [
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            },
            {
                "evidence": [
                    {
                        "id": "rs80359822",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359822"
                    },
                    {
                        "id": "rs80359822",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs80359822"
                    },
                    {
                        "id": "10980529",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/10980529"
                    },
                    {
                        "id": "20687207",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/20687207"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 256,
                "end_pos": 256,
                "sequence_org": "K",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42929693_42929694delin",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "K256",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090044",
                        "recommended_name": {
                            "id": "DOID:0090044",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090044",
                            "name": "dystonia 9",
                            "description": "A dystonia that is characterized by paroxysmal choreoathetosis and progressive spastic paraplegia, with episodes often precipitated by alcohol, fatigue, or emotional stress, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090044",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090044",
                                "name": "paroxysmal choreoathetosis with spasticity",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": "A dystonia characterized by autosomal dominant inheritance of paroxysmal choreoathetosis and progressive spastic paraplegia, episodes are often precipitated by alcohol, fatigue, or emotional stress that has material basis in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "DYT9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "episodic choreoathetosis/spasticity",
                                "description": ""
                            },
                            {
                                "id": "MIM:601042",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601042",
                                "name": "Dystonia 9",
                                "description": "Dystonia 9"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            },
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111313",
                        "recommended_name": {
                            "id": "DOID:0111313",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111313",
                            "name": "obsolete idiopathic generalized epilepsy 12",
                            "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC2A1 on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111313",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111313",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "susceptibility to idiopathic generalised epilepsy 12",
                                "description": ""
                            },
                            {
                                "id": "MIM:614847",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614847",
                                "name": "Epilepsy, idiopathic generalized 12",
                                "description": "Epilepsy, idiopathic generalized 12"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "614847",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/614847"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000000001000000000.00000000000000.000000000001000000.00001.10.000.100",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.10980529",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Autosomal dominant transmission of GLUT1 deficiency.",
        "journal": "Human molecular genetics",
        "date": "2001",
        "authors": "Klepper J, Willemsen M, Verrips A, Guertsen E, Herrmann R, Kutzick C, Florcken A, Voit T",
        "reference": {
            "type": "PubMed",
            "id": "11136715",
            "url": "https://pubmed.ncbi.nlm.nih.gov/11136715"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs80359814",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359814"
                    },
                    {
                        "id": "rs80359814",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs80359814"
                    },
                    {
                        "id": "11136715",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11136715"
                    },
                    {
                        "id": "11389907",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11389907"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 91,
                "end_pos": 91,
                "sequence_org": "G",
                "sequence_mut": "D",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42931049",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G91",
                "disease": [
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000010000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.11136715",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene.",
        "journal": "FEBS letters",
        "date": "2001-06-01",
        "authors": "Klepper J, Monden I, Guertsen E, Voit T, Willemsen M, Keller K",
        "reference": {
            "type": "PubMed",
            "id": "11389907",
            "url": "https://pubmed.ncbi.nlm.nih.gov/11389907"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs80359814",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359814"
                    },
                    {
                        "id": "rs80359814",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs80359814"
                    },
                    {
                        "id": "11136715",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11136715"
                    },
                    {
                        "id": "11389907",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11389907"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 91,
                "end_pos": 91,
                "sequence_org": "G",
                "sequence_mut": "D",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42931049",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G91",
                "disease": [
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000010000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.11389907",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Autosomal dominant glut-1 deficiency syndrome and familial epilepsy.",
        "journal": "Annals of neurology",
        "date": "2001",
        "authors": "Brockmann K, Wang D, Korenke CG, von Moers A, Ho YY, Pascual JM, Kuang K, Yang H, Ma L, Kranz-Eble P, Fischbarg J, Hanefeld F, De Vivo DC",
        "reference": {
            "type": "PubMed",
            "id": "11603379",
            "url": "https://pubmed.ncbi.nlm.nih.gov/11603379"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs80359816",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359816"
                    },
                    {
                        "id": "rs80359816",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs80359816"
                    },
                    {
                        "id": "11603379",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11603379"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 126,
                "end_pos": 126,
                "sequence_org": "R",
                "sequence_mut": "H",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42930765",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R126",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.11603379",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Purification of lactose synthetase a protein from human milk and demonstration of its interaction with alpha-lactalbumin.",
        "journal": "FEBS letters",
        "date": "1970",
        "authors": "Andrews P",
        "reference": {
            "type": "PubMed",
            "id": "11947697",
            "url": "https://pubmed.ncbi.nlm.nih.gov/11947697"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P00709-1",
                "protein_name": "Alpha-lactalbumin",
                "gene_name": "LALBA",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15291-1",
                "protein_name": "Beta-1,4-galactosyltransferase 1",
                "gene_name": "B4GALT1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.11947697",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 3
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Imaging the metabolic footprint of Glut1 deficiency on the brain.",
        "journal": "Annals of neurology",
        "date": "2002",
        "authors": "Pascual JM, Van Heertum RL, Wang D, Engelstad K, De Vivo DC",
        "reference": {
            "type": "PubMed",
            "id": "12325075",
            "url": "https://pubmed.ncbi.nlm.nih.gov/12325075"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.12325075",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "GLUT-1 deficiency without epilepsy--an exceptional case.",
        "journal": "Journal of inherited metabolic disease",
        "date": "2003",
        "authors": "Overweg-Plandsoen WC, Groener JE, Wang D, Onkenhout W, Brouwer OF, Bakker HD, De Vivo DC",
        "reference": {
            "type": "PubMed",
            "id": "14605501",
            "url": "https://pubmed.ncbi.nlm.nih.gov/14605501"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs80359812",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359812"
                    },
                    {
                        "id": "rs80359812",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs80359812"
                    },
                    {
                        "id": "14605501",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/14605501"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 34,
                "end_pos": 34,
                "sequence_org": "N",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42943239",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N34",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "001000000000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.14605501",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "The ubiquitous glucose transporter GLUT-1 is a receptor for HTLV.",
        "journal": "Cell",
        "date": "2003",
        "authors": "Manel N, Kim FJ, Kinet S, Taylor N, Sitbon M, Battini JL",
        "reference": {
            "type": "PubMed",
            "id": "14622599",
            "url": "https://pubmed.ncbi.nlm.nih.gov/14622599"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.14622599",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.",
        "journal": "Annals of neurology",
        "date": "2005",
        "authors": "Wang D, Pascual JM, Yang H, Engelstad K, Jhung S, Sun RP, De Vivo DC",
        "reference": {
            "type": "PubMed",
            "id": "15622525",
            "url": "https://pubmed.ncbi.nlm.nih.gov/15622525"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.15622525",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Transmembrane segment 6 of the Glut1 glucose transporter is an outer helix and contains amino acid side chains essential for transport activity.",
        "journal": "The Journal of biological chemistry",
        "date": "2008",
        "authors": "Mueckler M, Makepeace C",
        "reference": {
            "type": "PubMed",
            "id": "18245775",
            "url": "https://pubmed.ncbi.nlm.nih.gov/18245775"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "mutagenesis": [
            {
                "start_pos": 192,
                "end_pos": 192,
                "sequence_org": "I",
                "sequence_mut": "C",
                "comment": "Strongly decreases glucose transport.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    },
                    {
                        "database": "PubMed",
                        "id": "18245775",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18245775"
                    }
                ],
                "uniprot_canonical_ac": "P11166-1"
            },
            {
                "start_pos": 204,
                "end_pos": 204,
                "sequence_org": "L",
                "sequence_mut": "C",
                "comment": "Abolishes glucose transport.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    },
                    {
                        "database": "PubMed",
                        "id": "18245775",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18245775"
                    }
                ],
                "uniprot_canonical_ac": "P11166-1"
            },
            {
                "start_pos": 205,
                "end_pos": 205,
                "sequence_org": "P",
                "sequence_mut": "C",
                "comment": "Abolishes glucose transport.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    },
                    {
                        "database": "PubMed",
                        "id": "18245775",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18245775"
                    }
                ],
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.18245775",
        "abstract": "",
        "glycosylation": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "GLUT1 deficiency without epilepsy: yet another case.",
        "journal": "Journal of child neurology",
        "date": "2008-07",
        "authors": "Joshi Charuta, Greenberg Cheryl R, De Vivo Darryl, Dong Wang , Chan-Lui Winifred, Booth Frances A",
        "reference": {
            "type": "PubMed",
            "id": "18403583",
            "url": "https://pubmed.ncbi.nlm.nih.gov/18403583"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs267607061",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs267607061"
                    },
                    {
                        "id": "rs267607061",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs267607061"
                    },
                    {
                        "id": "18403583",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18403583"
                    },
                    {
                        "id": "19996082",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19996082"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 93,
                "end_pos": 93,
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42930865",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R93",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.18403583",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak.",
        "journal": "The Journal of clinical investigation",
        "date": "2008",
        "authors": "Weber YG, Storch A, Wuttke TV, Brockmann K, Kempfle J, Maljevic S, Margari L, Kamm C, Schneider SA, Huber SM, Pekrun A, Roebling R, Seebohm G, Koka S, Lang C, Kraft E, Blazevic D, Salvo-Vargas A, Fauler M, Mottaghy FM, Munchau A, Edwards MJ, Presicci A, Margari F, Gasser T, Lang F, Bhatia KP, Lehmann-Horn F, Lerche H",
        "reference": {
            "type": "PubMed",
            "id": "18451999",
            "url": "https://pubmed.ncbi.nlm.nih.gov/18451999"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs121909740",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs121909740"
                    },
                    {
                        "id": "rs121909740",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs121909740#frequency_tab"
                    },
                    {
                        "id": "rs121909740",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs121909740"
                    },
                    {
                        "id": "18451999",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18451999"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 275,
                "end_pos": 275,
                "sequence_org": "A",
                "sequence_mut": "T",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42929637",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "A275",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "100000000000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            },
            {
                "evidence": [
                    {
                        "id": "rs121909739",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs121909739"
                    },
                    {
                        "id": "rs121909739",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs121909739"
                    },
                    {
                        "id": "18451999",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18451999"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 314,
                "end_pos": 314,
                "sequence_org": "G",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42929242",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G314",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090044",
                        "recommended_name": {
                            "id": "DOID:0090044",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090044",
                            "name": "dystonia 9",
                            "description": "A dystonia that is characterized by paroxysmal choreoathetosis and progressive spastic paraplegia, with episodes often precipitated by alcohol, fatigue, or emotional stress, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090044",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090044",
                                "name": "paroxysmal choreoathetosis with spasticity",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": "A dystonia characterized by autosomal dominant inheritance of paroxysmal choreoathetosis and progressive spastic paraplegia, episodes are often precipitated by alcohol, fatigue, or emotional stress that has material basis in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "DYT9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "episodic choreoathetosis/spasticity",
                                "description": ""
                            },
                            {
                                "id": "MIM:601042",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601042",
                                "name": "Dystonia 9",
                                "description": "Dystonia 9"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            },
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000010000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.18451999",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.",
        "journal": "Brain : a journal of neurology",
        "date": "2008-07",
        "authors": "Suls Arvid, Dedeken Peter, Goffin Karolien, Van Esch Hilde, Dupont Patrick, Cassiman David, Kempfle Judith, Wuttke Thomas V, Weber Yvonne, Lerche Holger, Afawi Zaid, Vandenberghe Wim, Korczyn Amos D, Berkovic Samuel F, Ekstein Dana, Kivity Sara, Ryvlin Philippe, Claes Lieve R F, Deprez Liesbet, Maljevic Snezana, Vargas Alberto, Van Dyck Tine, Goossens Dirk, Del-Favero Jurgen, Van Laere Koen, De Jonghe Peter, Van Paesschen Wim",
        "reference": {
            "type": "PubMed",
            "id": "18577546",
            "url": "https://pubmed.ncbi.nlm.nih.gov/18577546"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs267607060",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs267607060"
                    },
                    {
                        "id": "rs267607060",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs267607060"
                    },
                    {
                        "id": "18577546",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18577546"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 95,
                "end_pos": 95,
                "sequence_org": "S",
                "sequence_mut": "I",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42930858_42930859delin",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "S95",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000000000000100000.00000000000000.000000000001000000.00001.10.000.001",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.18577546",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Paroxysmal movement disorders in GLUT1 deficiency syndrome.",
        "journal": "Neurology",
        "date": "2008-07-08",
        "authors": "Zorzi G, Castellotti B, Zibordi F, Gellera C, Nardocci N",
        "reference": {
            "type": "PubMed",
            "id": "18606970",
            "url": "https://pubmed.ncbi.nlm.nih.gov/18606970"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs80359818",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359818"
                    },
                    {
                        "id": "rs80359818",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs80359818"
                    },
                    {
                        "id": "18606970",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18606970"
                    },
                    {
                        "id": "19798636",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19798636"
                    },
                    {
                        "id": "21832227",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/21832227"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 126,
                "end_pos": 126,
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42930766",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R126",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090044",
                        "recommended_name": {
                            "id": "DOID:0090044",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090044",
                            "name": "dystonia 9",
                            "description": "A dystonia that is characterized by paroxysmal choreoathetosis and progressive spastic paraplegia, with episodes often precipitated by alcohol, fatigue, or emotional stress, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090044",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090044",
                                "name": "paroxysmal choreoathetosis with spasticity",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": "A dystonia characterized by autosomal dominant inheritance of paroxysmal choreoathetosis and progressive spastic paraplegia, episodes are often precipitated by alcohol, fatigue, or emotional stress that has material basis in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "DYT9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "episodic choreoathetosis/spasticity",
                                "description": ""
                            },
                            {
                                "id": "MIM:601042",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601042",
                                "name": "Dystonia 9",
                                "description": "Dystonia 9"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            },
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.18606970",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Model of the exofacial substrate-binding site and helical folding of the human Glut1 glucose transporter based on scanning mutagenesis.",
        "journal": "Biochemistry",
        "date": "2009",
        "authors": "Mueckler M, Makepeace C",
        "reference": {
            "type": "PubMed",
            "id": "19449892",
            "url": "https://pubmed.ncbi.nlm.nih.gov/19449892"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "mutagenesis": [
            {
                "start_pos": 340,
                "end_pos": 340,
                "sequence_org": "G",
                "sequence_mut": "C",
                "comment": "Strongly decreases glucose transport.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    },
                    {
                        "database": "PubMed",
                        "id": "19449892",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19449892"
                    }
                ],
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.19449892",
        "abstract": "",
        "glycosylation": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias.",
        "journal": "Movement disorders : official journal of the Movement Disorder Society",
        "date": "2009",
        "authors": "Schneider SA, Paisan-Ruiz C, Garcia-Gorostiaga I, Quinn NP, Weber YG, Lerche H, Hardy J, Bhatia KP",
        "reference": {
            "type": "PubMed",
            "id": "19630075",
            "url": "https://pubmed.ncbi.nlm.nih.gov/19630075"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs202060209",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs202060209"
                    },
                    {
                        "id": "rs202060209",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs202060209"
                    },
                    {
                        "id": "rs202060209",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs202060209"
                    },
                    {
                        "id": "rs202060209",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs202060209#frequency_tab"
                    },
                    {
                        "id": "rs202060209",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs202060209"
                    },
                    {
                        "id": "19630075",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19630075"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 92,
                "end_pos": 92,
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42931047",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R92",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.19630075",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1.",
        "journal": "Annals of neurology",
        "date": "2009",
        "authors": "Suls A, Mullen SA, Weber YG, Verhaert K, Ceulemans B, Guerrini R, Wuttke TV, Salvo-Vargas A, Deprez L, Claes LR, Jordanova A, Berkovic SF, Lerche H, De Jonghe P, Scheffer IE",
        "reference": {
            "type": "PubMed",
            "id": "19798636",
            "url": "https://pubmed.ncbi.nlm.nih.gov/19798636"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs80359818",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359818"
                    },
                    {
                        "id": "rs80359818",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs80359818"
                    },
                    {
                        "id": "18606970",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18606970"
                    },
                    {
                        "id": "19798636",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19798636"
                    },
                    {
                        "id": "21832227",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/21832227"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 126,
                "end_pos": 126,
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42930766",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R126",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090044",
                        "recommended_name": {
                            "id": "DOID:0090044",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090044",
                            "name": "dystonia 9",
                            "description": "A dystonia that is characterized by paroxysmal choreoathetosis and progressive spastic paraplegia, with episodes often precipitated by alcohol, fatigue, or emotional stress, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090044",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090044",
                                "name": "paroxysmal choreoathetosis with spasticity",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": "A dystonia characterized by autosomal dominant inheritance of paroxysmal choreoathetosis and progressive spastic paraplegia, episodes are often precipitated by alcohol, fatigue, or emotional stress that has material basis in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "DYT9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "episodic choreoathetosis/spasticity",
                                "description": ""
                            },
                            {
                                "id": "MIM:601042",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601042",
                                "name": "Dystonia 9",
                                "description": "Dystonia 9"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            },
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            },
            {
                "evidence": [
                    {
                        "id": "rs397514564",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs397514564"
                    },
                    {
                        "id": "rs397514564",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs397514564"
                    },
                    {
                        "id": "rs397514564",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs397514564#frequency_tab"
                    },
                    {
                        "id": "rs397514564",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs397514564"
                    },
                    {
                        "id": "19798636",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19798636"
                    },
                    {
                        "id": "25982116",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/25982116"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 223,
                "end_pos": 223,
                "sequence_org": "R",
                "sequence_mut": "P",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42929884",
                "ref_nt": "G",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R223",
                "disease": [
                    {
                        "disease_id": "DOID:0111313",
                        "recommended_name": {
                            "id": "DOID:0111313",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111313",
                            "name": "obsolete idiopathic generalized epilepsy 12",
                            "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC2A1 on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111313",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111313",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "susceptibility to idiopathic generalised epilepsy 12",
                                "description": ""
                            },
                            {
                                "id": "MIM:614847",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614847",
                                "name": "Epilepsy, idiopathic generalized 12",
                                "description": "Epilepsy, idiopathic generalized 12"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "614847",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/614847"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.19798636",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Childhood chorea with cerebral hypotrophy: a treatable GLUT1 energy failure syndrome.",
        "journal": "Archives of neurology",
        "date": "2009",
        "authors": "Perez-Duenas B, Prior C, Ma Q, Fernandez-Alvarez E, Setoain X, Artuch R, Pascual JM",
        "reference": {
            "type": "PubMed",
            "id": "19901175",
            "url": "https://pubmed.ncbi.nlm.nih.gov/19901175"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.19901175",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Glut1 deficiency and alternating hemiplegia of childhood.",
        "journal": "Neurology",
        "date": "2009-12-08",
        "authors": "Rotstein M, Doran J, Yang H, Ullner P M, Engelstad K, De Vivo D C",
        "reference": {
            "type": "PubMed",
            "id": "19996082",
            "url": "https://pubmed.ncbi.nlm.nih.gov/19996082"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs267607061",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs267607061"
                    },
                    {
                        "id": "rs267607061",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs267607061"
                    },
                    {
                        "id": "18403583",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18403583"
                    },
                    {
                        "id": "19996082",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19996082"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 93,
                "end_pos": 93,
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42930865",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R93",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.19996082",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.",
        "journal": "Brain : a journal of neurology",
        "date": "2010",
        "authors": "Leen WG, Klepper J, Verbeek MM, Leferink M, Hofste T, van Engelen BG, Wevers RA, Arthur T, Bahi-Buisson N, Ballhausen D, Bekhof J, van Bogaert P, Carrilho I, Chabrol B, Champion MP, Coldwell J, Clayton P, Donner E, Evangeliou A, Ebinger F, Farrell K, Forsyth RJ, de Goede CG, Gross S, Grunewald S, Holthausen H, Jayawant S, Lachlan K, Laugel V, Leppig K, Lim MJ, Mancini G, Marina AD, Martorell L, McMenamin J, Meuwissen ME, Mundy H, Nilsson NO, Panzer A, Poll-The BT, Rauscher C, Rouselle CM, Sandvig I, Scheffner T, Sheridan E, Simpson N, Sykora P, Tomlinson R, Trounce J, Webb D, Weschke B, Scheffer H, Willemsen MA",
        "reference": {
            "type": "PubMed",
            "id": "20129935",
            "url": "https://pubmed.ncbi.nlm.nih.gov/20129935"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.20129935",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Autosomal recessive inheritance of GLUT1 deficiency syndrome.",
        "journal": "Neuropediatrics",
        "date": "2009",
        "authors": "Klepper J, Scheffer H, Elsaid MF, Kamsteeg EJ, Leferink M, Ben-Omran T",
        "reference": {
            "type": "PubMed",
            "id": "20221955",
            "url": "https://pubmed.ncbi.nlm.nih.gov/20221955"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs267607059",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs267607059"
                    },
                    {
                        "id": "rs267607059",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs267607059"
                    },
                    {
                        "id": "20221955",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/20221955"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 468,
                "end_pos": 468,
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42927118",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R468",
                "disease": [
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.20221955",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency.",
        "journal": "Neurology",
        "date": "2010",
        "authors": "Mullen SA, Suls A, De Jonghe P, Berkovic SF, Scheffer IE",
        "reference": {
            "type": "PubMed",
            "id": "20574033",
            "url": "https://pubmed.ncbi.nlm.nih.gov/20574033"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.20574033",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Paroxysmal exercise-induced dyskinesia, writer's cramp, migraine with aura and absence epilepsy in twin brothers with a novel SLC2A1 missense mutation.",
        "journal": "Journal of the neurological sciences",
        "date": "2010",
        "authors": "Urbizu A, Cuenca-Leon E, Raspall-Chaure M, Gratacos M, Conill J, Redecillas S, Roig-Quilis M, Macaya A",
        "reference": {
            "type": "PubMed",
            "id": "20621801",
            "url": "https://pubmed.ncbi.nlm.nih.gov/20621801"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.20621801",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Glut1 deficiency: inheritance pattern determined by haploinsufficiency.",
        "journal": "Annals of neurology",
        "date": "2010",
        "authors": "Rotstein M, Engelstad K, Yang H, Wang D, Levy B, Chung WK, De Vivo DC",
        "reference": {
            "type": "PubMed",
            "id": "20687207",
            "url": "https://pubmed.ncbi.nlm.nih.gov/20687207"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs80359822",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359822"
                    },
                    {
                        "id": "rs80359822",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs80359822"
                    },
                    {
                        "id": "10980529",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/10980529"
                    },
                    {
                        "id": "20687207",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/20687207"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 256,
                "end_pos": 256,
                "sequence_org": "K",
                "sequence_mut": "V",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42929693_42929694delin",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "K256",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090044",
                        "recommended_name": {
                            "id": "DOID:0090044",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090044",
                            "name": "dystonia 9",
                            "description": "A dystonia that is characterized by paroxysmal choreoathetosis and progressive spastic paraplegia, with episodes often precipitated by alcohol, fatigue, or emotional stress, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090044",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090044",
                                "name": "paroxysmal choreoathetosis with spasticity",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": "A dystonia characterized by autosomal dominant inheritance of paroxysmal choreoathetosis and progressive spastic paraplegia, episodes are often precipitated by alcohol, fatigue, or emotional stress that has material basis in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "DYT9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "episodic choreoathetosis/spasticity",
                                "description": ""
                            },
                            {
                                "id": "MIM:601042",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601042",
                                "name": "Dystonia 9",
                                "description": "Dystonia 9"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            },
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111313",
                        "recommended_name": {
                            "id": "DOID:0111313",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111313",
                            "name": "obsolete idiopathic generalized epilepsy 12",
                            "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC2A1 on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111313",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111313",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "susceptibility to idiopathic generalised epilepsy 12",
                                "description": ""
                            },
                            {
                                "id": "MIM:614847",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614847",
                                "name": "Epilepsy, idiopathic generalized 12",
                                "description": "Epilepsy, idiopathic generalized 12"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "614847",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/614847"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000000001000000000.00000000000000.000000000001000000.00001.10.000.100",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.20687207",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Excellent response to acetazolamide in a case of paroxysmal dyskinesias due to GLUT1-deficiency.",
        "journal": "Journal of neurology",
        "date": "2011",
        "authors": "Anheim M, Maillart E, Vuillaumier-Barrot S, Flamand-Rouviere C, Pineau F, Ewenczyk C, Riant F, Apartis E, Roze E",
        "reference": {
            "type": "PubMed",
            "id": "20830593",
            "url": "https://pubmed.ncbi.nlm.nih.gov/20830593"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.20830593",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Mild adolescent/adult onset epilepsy and paroxysmal exercise-induced dyskinesia due to GLUT1 deficiency.",
        "journal": "Epilepsia",
        "date": "2010",
        "authors": "Afawi Z, Suls A, Ekstein D, Kivity S, Neufeld MY, Oliver K, De Jonghe P, Korczyn AD, Berkovic SF",
        "reference": {
            "type": "PubMed",
            "id": "21204808",
            "url": "https://pubmed.ncbi.nlm.nih.gov/21204808"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.21204808",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome.",
        "journal": "Blood",
        "date": "2011",
        "authors": "Flatt JF, Guizouarn H, Burton NM, Borgese F, Tomlinson RJ, Forsyth RJ, Baldwin SA, Levinson BE, Quittet P, Aguilar-Martinez P, Delaunay J, Stewart GW, Bruce LJ",
        "reference": {
            "type": "PubMed",
            "id": "21791420",
            "url": "https://pubmed.ncbi.nlm.nih.gov/21791420"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs864309514",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs864309514"
                    },
                    {
                        "id": "rs864309514",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs864309514"
                    },
                    {
                        "id": "21791420",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/21791420"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 286,
                "end_pos": 286,
                "sequence_org": "G",
                "sequence_mut": "D",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42929603",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "G286",
                "keywords": [
                    "ebi",
                    "germline"
                ],
                "filter_code": "000000010000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            },
            {
                "evidence": [
                    {
                        "id": "rs864309522",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs864309522"
                    },
                    {
                        "id": "21791420",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/21791420"
                    },
                    {
                        "id": "22492876",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/22492876"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 436,
                "end_pos": 436,
                "sequence_org": "I",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42927214TGA",
                "ref_nt": "]",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I436",
                "disease": [
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000000100000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.21791420",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect.",
        "journal": "Neurology",
        "date": "2011",
        "authors": "Weber YG, Kamm C, Suls A, Kempfle J, Kotschet K, Schule R, Wuttke TV, Maljevic S, Liebrich J, Gasser T, Ludolph AC, Van Paesschen W, Schols L, De Jonghe P, Auburger G, Lerche H",
        "reference": {
            "type": "PubMed",
            "id": "21832227",
            "url": "https://pubmed.ncbi.nlm.nih.gov/21832227"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs80359818",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359818"
                    },
                    {
                        "id": "rs80359818",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs80359818"
                    },
                    {
                        "id": "18606970",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18606970"
                    },
                    {
                        "id": "19798636",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19798636"
                    },
                    {
                        "id": "21832227",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/21832227"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 126,
                "end_pos": 126,
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42930766",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R126",
                "disease": [
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090044",
                        "recommended_name": {
                            "id": "DOID:0090044",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090044",
                            "name": "dystonia 9",
                            "description": "A dystonia that is characterized by paroxysmal choreoathetosis and progressive spastic paraplegia, with episodes often precipitated by alcohol, fatigue, or emotional stress, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090044",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090044",
                                "name": "paroxysmal choreoathetosis with spasticity",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": "A dystonia characterized by autosomal dominant inheritance of paroxysmal choreoathetosis and progressive spastic paraplegia, episodes are often precipitated by alcohol, fatigue, or emotional stress that has material basis in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "DYT9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "episodic choreoathetosis/spasticity",
                                "description": ""
                            },
                            {
                                "id": "MIM:601042",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601042",
                                "name": "Dystonia 9",
                                "description": "Dystonia 9"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            },
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            },
            {
                "evidence": [
                    {
                        "id": "rs387907312",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs387907312"
                    },
                    {
                        "id": "rs387907312",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs387907312"
                    },
                    {
                        "id": "21832227",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/21832227"
                    },
                    {
                        "id": "8808284",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/8808284"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 212,
                "end_pos": 212,
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42929918",
                "ref_nt": "A",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "R212",
                "disease": [
                    {
                        "disease_id": "DOID:0090044",
                        "recommended_name": {
                            "id": "DOID:0090044",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090044",
                            "name": "dystonia 9",
                            "description": "A dystonia that is characterized by paroxysmal choreoathetosis and progressive spastic paraplegia, with episodes often precipitated by alcohol, fatigue, or emotional stress, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090044",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090044",
                                "name": "paroxysmal choreoathetosis with spasticity",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": "A dystonia characterized by autosomal dominant inheritance of paroxysmal choreoathetosis and progressive spastic paraplegia, episodes are often precipitated by alcohol, fatigue, or emotional stress that has material basis in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "DYT9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "episodic choreoathetosis/spasticity",
                                "description": ""
                            },
                            {
                                "id": "MIM:601042",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601042",
                                "name": "Dystonia 9",
                                "description": "Dystonia 9"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            },
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.21832227",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy.",
        "journal": "Neurology",
        "date": "2012",
        "authors": "Striano P, Weber YG, Toliat MR, Schubert J, Leu C, Chaimana R, Baulac S, Guerrero R, LeGuern E, Lehesjoki AE, Polvi A, Robbiano A, Serratosa JM, Guerrini R, Nurnberg P, Sander T, Zara F, Lerche H, Marini C",
        "reference": {
            "type": "PubMed",
            "id": "22282645",
            "url": "https://pubmed.ncbi.nlm.nih.gov/22282645"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "P11166",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P11166"
                    },
                    {
                        "id": "rs387907313",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs387907313"
                    },
                    {
                        "id": "rs387907313",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs387907313"
                    },
                    {
                        "id": "rs387907313",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs387907313"
                    },
                    {
                        "id": "22282645",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/22282645"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 232,
                "end_pos": 232,
                "subjects_tested": "1704",
                "subjects_positive": "1",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "C",
                "comment": "Somatic mutation passed 1 filters: protein-of-interest(glycogene, carbohydrate synthesis and metabolism/transporter).",
                "chr_id": "1",
                "chr_pos": "42929766",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R232",
                "disease": [
                    {
                        "disease_id": "DOID:363",
                        "recommended_name": {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:363",
                            "name": "uterine cancer",
                            "description": "A female reproductive organ cancer that is located_in the uterus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "CA - cancer of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "Tumour of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "malignant uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "neoplasm of uterus",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterine tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
                                "name": "uterus neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:9460",
                            "DOID:5166",
                            "DOID:2021",
                            "DOID:4114"
                        ],
                        "evidence": [
                            {
                                "id": "363",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:363"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:9256",
                        "recommended_name": {
                            "id": "DOID:9256",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9256",
                            "name": "colorectal cancer",
                            "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": "A primary or metastatic malignant neoplasm that affects the colon or rectum. Representative examples include carcinoma, lymphoma, and sarcoma."
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "cancer of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, advanced, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colon cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer with chromosomal instability, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectal cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "colorectum cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectal tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant colorectum neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large bowel tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant large intestine tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of colorectum",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant neoplasm of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumor of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large bowel",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "malignant tumour of the large intestine",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005575",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005575",
                                "name": "CRC",
                                "description": ""
                            },
                            {
                                "id": "MIM:114500",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114500",
                                "name": "Colorectal cancer",
                                "description": "Colorectal cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "9256",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:9256"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111313",
                        "recommended_name": {
                            "id": "DOID:0111313",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111313",
                            "name": "obsolete idiopathic generalized epilepsy 12",
                            "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC2A1 on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111313",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111313",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "susceptibility to idiopathic generalised epilepsy 12",
                                "description": ""
                            },
                            {
                                "id": "MIM:614847",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614847",
                                "name": "Epilepsy, idiopathic generalized 12",
                                "description": "Epilepsy, idiopathic generalized 12"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "614847",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/614847"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.22282645",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "An infant with pseudohyperkalemia, hemolysis, and seizures: cation-leaky GLUT1-deficiency syndrome due to a SLC2A1 mutation.",
        "journal": "The Journal of clinical endocrinology and metabolism",
        "date": "2012",
        "authors": "Bawazir WM, Gevers EF, Flatt JF, Ang AL, Jacobs B, Oren C, Grunewald S, Dattani M, Bruce LJ, Stewart GW",
        "reference": {
            "type": "PubMed",
            "id": "22492876",
            "url": "https://pubmed.ncbi.nlm.nih.gov/22492876"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs864309522",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs864309522"
                    },
                    {
                        "id": "21791420",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/21791420"
                    },
                    {
                        "id": "22492876",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/22492876"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 436,
                "end_pos": 436,
                "sequence_org": "I",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42927214TGA",
                "ref_nt": "]",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "I436",
                "disease": [
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000000100000000000.00000000000000.000000000001000000.00001.10.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.22492876",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Structures of the asparagine-linked sugar chain of glucose transporter from human erythrocytes.",
        "journal": "Biochemistry",
        "date": "1990",
        "authors": "Endo T, Kasahara M, Kobata A",
        "reference": {
            "type": "PubMed",
            "id": "2271582",
            "url": "https://pubmed.ncbi.nlm.nih.gov/2271582"
        },
        "referenced_glycans": [
            {
                "glytoucan_ac": "G06580KR"
            },
            {
                "glytoucan_ac": "G82959GZ"
            },
            {
                "glytoucan_ac": "G97547WF"
            },
            {
                "glytoucan_ac": "G60230HH"
            },
            {
                "glytoucan_ac": "G54569PE"
            },
            {
                "glytoucan_ac": "G70101JE"
            },
            {
                "glytoucan_ac": "G71333AK"
            },
            {
                "glytoucan_ac": "G03509EL"
            },
            {
                "glytoucan_ac": "G69440RD"
            },
            {
                "glytoucan_ac": "G62187QU"
            }
        ],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "glycosylation": [
            {
                "glytoucan_ac": "G60230HH",
                "type": "N-linked",
                "subtype": "other",
                "prediction_tool_list": [],
                "site_category": "reported_with_glycan",
                "site_category_dict": {
                    "reported_with_glycan": true
                },
                "site_seq": "",
                "relation": "attached",
                "comment": "",
                "icn3d_view": {},
                "evidence": [
                    {
                        "id": "2271582",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/2271582"
                    },
                    {
                        "id": "573",
                        "database": "GlyConnect",
                        "url": "https://glyconnect.expasy.org/browser/proteins/573"
                    }
                ],
                "filter_code": "000000000000000000000.0000000.00010000000000.0100000.1100000000.110100100001101010.10000.01000",
                "uniprot_canonical_ac": "P11166-1"
            },
            {
                "glytoucan_ac": "G70101JE",
                "type": "N-linked",
                "subtype": "other",
                "prediction_tool_list": [],
                "site_category": "reported_with_glycan",
                "site_category_dict": {
                    "reported_with_glycan": true
                },
                "site_seq": "",
                "relation": "attached",
                "comment": "",
                "icn3d_view": {},
                "evidence": [
                    {
                        "id": "2271582",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/2271582"
                    },
                    {
                        "id": "573",
                        "database": "GlyConnect",
                        "url": "https://glyconnect.expasy.org/browser/proteins/573"
                    }
                ],
                "filter_code": "000000000000000000000.0000000.00010000000000.0100000.1100000000.110111100001111110.00010.01000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.2271582",
        "abstract": "",
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 10
                    }
                ],
                "sort_fields": [
                    "glytoucan_ac"
                ]
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    },
                    {
                        "field": "total_sites",
                        "count": 1
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 1
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 1
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 2
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "exact_sites",
                        "count": 0
                    },
                    {
                        "field": "fuzzy_sites",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_n_linked_sites",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_n_linked_glycan_sites",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_n_linked_glycans",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "glytoucan_ac",
                    "type",
                    "subtype",
                    "site_category",
                    "site_seq",
                    "relation",
                    "comment",
                    "filter_code",
                    "uniprot_canonical_ac"
                ]
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    },
                    {
                        "field": "total_sites",
                        "count": 1
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 1
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 1
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 2
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "exact_sites",
                        "count": 0
                    },
                    {
                        "field": "fuzzy_sites",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_n_linked_sites",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_n_linked_glycan_sites",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_n_linked_glycans",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "glytoucan_ac",
                    "type",
                    "subtype",
                    "site_category",
                    "site_seq",
                    "relation",
                    "comment",
                    "filter_code",
                    "uniprot_canonical_ac"
                ]
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.",
        "journal": "Annals of neurology",
        "date": "2012",
        "authors": "Arsov T, Mullen SA, Rogers S, Phillips AM, Lawrence KM, Damiano JA, Goldberg-Stern H, Afawi Z, Kivity S, Trager C, Petrou S, Berkovic SF, Scheffer IE",
        "reference": {
            "type": "PubMed",
            "id": "23280796",
            "url": "https://pubmed.ncbi.nlm.nih.gov/23280796"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs398123069",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs398123069"
                    },
                    {
                        "id": "rs398123069",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs398123069"
                    },
                    {
                        "id": "23280796",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/23280796"
                    }
                ],
                "glycoeffect": [
                    "n-glyco-sequon-loss"
                ],
                "start_pos": 411,
                "end_pos": 411,
                "sequence_org": "N",
                "sequence_mut": "S",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42927651",
                "ref_nt": "C",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "N411",
                "disease": [
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111313",
                        "recommended_name": {
                            "id": "DOID:0111313",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111313",
                            "name": "obsolete idiopathic generalized epilepsy 12",
                            "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC2A1 on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111313",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111313",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "susceptibility to idiopathic generalised epilepsy 12",
                                "description": ""
                            },
                            {
                                "id": "MIM:614847",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614847",
                                "name": "Epilepsy, idiopathic generalized 12",
                                "description": "Epilepsy, idiopathic generalized 12"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "614847",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/614847"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "001000000000000000000.00000000000000.000000000001000000.00001.10.000.010",
                "uniprot_canonical_ac": "P11166-1"
            },
            {
                "evidence": [
                    {
                        "id": "P11166",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P11166"
                    },
                    {
                        "id": "rs13306758",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs13306758"
                    },
                    {
                        "id": "rs13306758",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs13306758"
                    },
                    {
                        "id": "rs13306758",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs13306758"
                    },
                    {
                        "id": "rs13306758",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs13306758#frequency_tab"
                    },
                    {
                        "id": "rs13306758",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs13306758"
                    },
                    {
                        "id": "23280796",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/23280796"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 458,
                "end_pos": 458,
                "subjects_tested": "2670",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Somatic mutation passed 1 filters: protein-of-interest(glycogene, carbohydrate synthesis and metabolism/transporter).",
                "chr_id": "1",
                "chr_pos": "42927148",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R458",
                "disease": [
                    {
                        "disease_id": "DOID:1319",
                        "recommended_name": {
                            "id": "DOID:1319",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1319",
                            "name": "brain cancer",
                            "description": "A central nervous system cancer that is characterized by the growth of abnormal cells in the tissues of the brain."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "BT - Brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "adult malignant brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "brain neoplasm, adult",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant brain tumour",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of Brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "malignant tumor of adult brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary brain tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "primary malignant neoplasm of brain",
                                "description": ""
                            },
                            {
                                "id": "DOID:1319",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1319",
                                "name": "tumor of the Brain",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4203",
                            "DOID:3541",
                            "DOID:4706",
                            "DOID:1659",
                            "DOID:368"
                        ],
                        "evidence": [
                            {
                                "id": "1319",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1319"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090045",
                        "recommended_name": {
                            "id": "DOID:0090045",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090045",
                            "name": "glucose transporter type 1 deficiency syndrome 2",
                            "description": "A dystonia characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs that has_material_basis_in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "childhood-onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090045",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090045",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": "A form of paroxysmal dyskinesia, characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities."
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2, childhood onset",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PED",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "PxMD-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "childhood onset GLUT1 deficiency syndrome type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "dystonia 18",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dystonia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "DYT-SLC2A1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "GLUT1DS2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012805",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012805",
                                "name": "ped with or without epilepsy and/or hemolytic Anaemia",
                                "description": ""
                            },
                            {
                                "id": "MIM:612126",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/612126",
                                "name": "GLUT1 deficiency syndrome 2",
                                "description": "GLUT1 deficiency syndrome 2"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            },
                            {
                                "id": "0090045",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090045"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090044",
                        "recommended_name": {
                            "id": "DOID:0090044",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090044",
                            "name": "dystonia 9",
                            "description": "A dystonia that is characterized by paroxysmal choreoathetosis and progressive spastic paraplegia, with episodes often precipitated by alcohol, fatigue, or emotional stress, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090044",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090044",
                                "name": "paroxysmal choreoathetosis with spasticity",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": "A dystonia characterized by autosomal dominant inheritance of paroxysmal choreoathetosis and progressive spastic paraplegia, episodes are often precipitated by alcohol, fatigue, or emotional stress that has material basis in heterozygous mutation in the SLC2A1 gene on chromosome 1p34."
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "DYT9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "dystonia type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010983",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010983",
                                "name": "episodic choreoathetosis/spasticity",
                                "description": ""
                            },
                            {
                                "id": "MIM:601042",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601042",
                                "name": "Dystonia 9",
                                "description": "Dystonia 9"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            },
                            {
                                "id": "0090044",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090044"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0111313",
                        "recommended_name": {
                            "id": "DOID:0111313",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0111313",
                            "name": "obsolete idiopathic generalized epilepsy 12",
                            "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC2A1 on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0111313",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0111313",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "EIG12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "epilepsy, idiopathic generalized, susceptibility to, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013919",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013919",
                                "name": "susceptibility to idiopathic generalised epilepsy 12",
                                "description": ""
                            },
                            {
                                "id": "MIM:614847",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614847",
                                "name": "Epilepsy, idiopathic generalized 12",
                                "description": "Epilepsy, idiopathic generalized 12"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "614847",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/614847"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.23280796",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Crystal structure of the human glucose transporter GLUT1.",
        "journal": "Nature",
        "date": "2014",
        "authors": "Deng D, Xu C, Sun P, Wu J, Yan C, Hu M, Yan N",
        "reference": {
            "type": "PubMed",
            "id": "24847886",
            "url": "https://pubmed.ncbi.nlm.nih.gov/24847886"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "mutagenesis": [
            {
                "start_pos": 45,
                "end_pos": 45,
                "sequence_org": "N",
                "sequence_mut": "T",
                "comment": "Loss of glycosylation site.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    },
                    {
                        "database": "PubMed",
                        "id": "24847886",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/24847886"
                    }
                ],
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs80359828",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs80359828"
                    },
                    {
                        "id": "rs80359828",
                        "database": "ENSEMBL",
                        "url": "https://www.ensembl.org/id/rs80359828"
                    },
                    {
                        "id": "24847886",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/24847886"
                    },
                    {
                        "id": "9462754",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/9462754"
                    }
                ],
                "glycoeffect": [
                    "o-glyco-site-loss"
                ],
                "start_pos": 449,
                "end_pos": 449,
                "sequence_org": "Y",
                "sequence_mut": "*",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "1",
                "chr_pos": "42927173",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Y449",
                "disease": [
                    {
                        "disease_id": "DOID:0070560",
                        "recommended_name": {
                            "id": "DOID:0070560",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070560",
                            "name": "glucose transporter type 1 deficiency syndrome",
                            "description": "A glucose metabolism disease characterized by deficient glucose transport over the blood-brain barrier and reduced glucose availability in the central nervous system that has_material_basis_in mutation in the SLC2A1 gene on chromosome 1p34.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070560",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070560",
                                "name": "GLUT1DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            },
                            {
                                "id": "0070560",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070560"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0070561",
                        "recommended_name": {
                            "id": "DOID:0070561",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070561",
                            "name": "glucose transporter type 1 deficiency syndrome 1",
                            "description": "A glucose transporter type 1 deficiency syndrome characterized by infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, and complex movement disorders."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070561",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070561",
                                "name": "classic glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": "Glucose transporter type 1 (GLUT1) deficiency syndrome is characterized by an encephalopathy marked by childhood epilepsy that is refractory to treatment, deceleration of cranial growth leading to microcephaly, psychomotor retardation, spasticity, ataxia, dysarthria and other paroxysmal neurological phenomena often occurring before meals. Symptoms appear between the age of 1 and 4 months, following a normal birth and gestation."
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "De Vivo disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1, infantile onset, severe",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1-DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "Glucose Transporter Type 1 Deficiency Syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "encephalopathy due to GLUT1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glut-1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "G1D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 DS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "GLUT1DS1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transport defect, blood-brain barrier",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter Protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter protein syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type 1 deficiency syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011724",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011724",
                                "name": "glucose transporter type1 (glut-1) deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:606777",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/606777",
                                "name": "GLUT1 deficiency syndrome 1",
                                "description": "GLUT1 deficiency syndrome 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            },
                            {
                                "id": "0070561",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070561"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000000000000000100.00000000000000.000000000001000000.00001.10.000.001",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.24847886",
        "abstract": "",
        "glycosylation": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Role of GLUT1 in regulation of reactive oxygen species.",
        "journal": "Redox biology",
        "date": "2014",
        "authors": "Andrisse S, Koehler RM, Chen JE, Patel GD, Vallurupalli VR, Ratliff BA, Warren DE, Fisher JS",
        "reference": {
            "type": "PubMed",
            "id": "25101238",
            "url": "https://pubmed.ncbi.nlm.nih.gov/25101238"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "phosphorylation": [
            {
                "start_pos": 490,
                "end_pos": 490,
                "kinase_uniprot_canonical_ac": "",
                "kinase_gene_name": "",
                "residue": "Ser",
                "comment": "Phosphoserine",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    },
                    {
                        "database": "PubMed",
                        "id": "24275569",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/24275569"
                    },
                    {
                        "database": "PubMed",
                        "id": "21406692",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/21406692"
                    },
                    {
                        "database": "PubMed",
                        "id": "23186163",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/23186163"
                    },
                    {
                        "database": "iPTMnet",
                        "id": "P11166",
                        "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P11166"
                    },
                    {
                        "database": "PubMed",
                        "id": "17525332",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/17525332"
                    },
                    {
                        "database": "PubMed",
                        "id": "18578522",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18578522"
                    },
                    {
                        "database": "PubMed",
                        "id": "19651622",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19651622"
                    },
                    {
                        "database": "PubMed",
                        "id": "19664994",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19664994"
                    },
                    {
                        "database": "PubMed",
                        "id": "25101238",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/25101238"
                    },
                    {
                        "database": "PubMed",
                        "id": "30799198",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30799198"
                    }
                ],
                "site_lbl": "Ser490",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.25101238",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    },
                    {
                        "field": "total_sites",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "start_pos",
                    "end_pos",
                    "kinase_uniprot_canonical_ac",
                    "kinase_gene_name",
                    "residue",
                    "comment",
                    "site_lbl",
                    "uniprot_canonical_ac"
                ]
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Mechanism of inhibition of human glucose transporter GLUT1 is conserved between cytochalasin B and phenylalanine amides.",
        "journal": "Proceedings of the National Academy of Sciences of the United States of America",
        "date": "2016",
        "authors": "Kapoor K, Finer-Moore JS, Pedersen BP, Caboni L, Waight A, Hillig RC, Bringmann P, Heisler I, Muller T, Siebeneicher H, Stroud RM",
        "reference": {
            "type": "PubMed",
            "id": "27078104",
            "url": "https://pubmed.ncbi.nlm.nih.gov/27078104"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.27078104",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Characterization and expression of human HepG2/erythrocyte glucose-transporter gene.",
        "journal": "Diabetes",
        "date": "1988",
        "authors": "Fukumoto H, Seino S, Imura H, Seino Y, Bell G I",
        "reference": {
            "type": "PubMed",
            "id": "2834252",
            "url": "https://pubmed.ncbi.nlm.nih.gov/2834252"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.2834252",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Oxidized ATM-mediated glycolysis enhancement in breast cancer-associated fibroblasts contributes to tumor invasion through lactate as metabolic coupling.",
        "journal": "EBioMedicine",
        "date": "2019",
        "authors": "Sun K, Tang S, Hou Y, Xi L, Chen Y, Yin J, Peng M, Zhao M, Cui X, Liu M",
        "reference": {
            "type": "PubMed",
            "id": "30799198",
            "url": "https://pubmed.ncbi.nlm.nih.gov/30799198"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "phosphorylation": [
            {
                "start_pos": 490,
                "end_pos": 490,
                "kinase_uniprot_canonical_ac": "",
                "kinase_gene_name": "",
                "residue": "Ser",
                "comment": "Phosphoserine",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    },
                    {
                        "database": "PubMed",
                        "id": "24275569",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/24275569"
                    },
                    {
                        "database": "PubMed",
                        "id": "21406692",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/21406692"
                    },
                    {
                        "database": "PubMed",
                        "id": "23186163",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/23186163"
                    },
                    {
                        "database": "iPTMnet",
                        "id": "P11166",
                        "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P11166"
                    },
                    {
                        "database": "PubMed",
                        "id": "17525332",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/17525332"
                    },
                    {
                        "database": "PubMed",
                        "id": "18578522",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18578522"
                    },
                    {
                        "database": "PubMed",
                        "id": "19651622",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19651622"
                    },
                    {
                        "database": "PubMed",
                        "id": "19664994",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19664994"
                    },
                    {
                        "database": "PubMed",
                        "id": "25101238",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/25101238"
                    },
                    {
                        "database": "PubMed",
                        "id": "30799198",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30799198"
                    }
                ],
                "site_lbl": "Ser490",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "record_id": "pubmed.30799198",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    },
                    {
                        "field": "total_sites",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "start_pos",
                    "end_pos",
                    "kinase_uniprot_canonical_ac",
                    "kinase_gene_name",
                    "residue",
                    "comment",
                    "site_lbl",
                    "uniprot_canonical_ac"
                ]
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Structural Basis for Blocking Sugar Uptake into the Malaria Parasite Plasmodium falciparum.",
        "journal": "Cell",
        "date": "2020-10-01",
        "authors": "Jiang Xin, Yuan Yafei, Huang Jian, Zhang Shuo, Luo Shuchen, Wang Nan, Pu Debing, Zhao Na, Tang Qingxuan, Hirata Kunio, Yang Xikang, Jiao Yaqing, Sakata-Kato Tomoyo, Wu Jia-Wei, Yan Chuangye, Kato Nobutaka, Yin Hang, Yan Nieng",
        "reference": {
            "type": "PubMed",
            "id": "32860739",
            "url": "https://pubmed.ncbi.nlm.nih.gov/32860739"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P11169-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 3",
                "gene_name": "SLC2A3",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.32860739",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "A Nodal enhanced micropeptide NEMEP regulates glucose uptake during mesendoderm differentiation of embryonic stem cells.",
        "journal": "Nat. Commun.",
        "date": "2022",
        "authors": "Fu Haipeng, Wang Tingyu, Kong Xiaohui, Yan Kun, Yang Yang, Cao Jingyi, Yuan Yafei, Wang Nan, Kee Kehkooi, Lu Zhi John, Xi Qiaoran",
        "reference": {
            "type": "PubMed",
            "id": "35810171",
            "url": "https://pubmed.ncbi.nlm.nih.gov/35810171"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P32037-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 3",
                "gene_name": "Slc2a3",
                "tax_name": "Mouse"
            },
            {
                "uniprot_canonical_ac": "Q4W5P6-1",
                "protein_name": "Small integral membrane protein 43",
                "gene_name": "SMIM43; TMEM155",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A286YD83-1",
                "protein_name": "Small integral membrane protein 43",
                "gene_name": "Smim43",
                "tax_name": "Mouse"
            },
            {
                "uniprot_canonical_ac": "P11169-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 3",
                "gene_name": "SLC2A3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P17809-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "Slc2a1",
                "tax_name": "Mouse"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.35810171",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 6
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Sequence and structure of a human glucose transporter.",
        "journal": "Science (New York, N.Y.)",
        "date": "1985",
        "authors": "Mueckler M, Caruso C, Baldwin SA, Panico M, Blench I, Morris HR, Allard WJ, Lienhard GE, Lodish HF",
        "reference": {
            "type": "PubMed",
            "id": "3839598",
            "url": "https://pubmed.ncbi.nlm.nih.gov/3839598"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P11168-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 2",
                "gene_name": "SLC2A2",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "glycosylation": [
            {
                "glytoucan_ac": "",
                "type": "N-linked",
                "subtype": "other",
                "prediction_tool_list": [],
                "site_category": "reported",
                "site_category_dict": {
                    "reported": true
                },
                "site_seq": "N",
                "relation": "attached",
                "comment": "N-linked (GlcNAc...) asparagine",
                "icn3d_view": {},
                "start_pos": 45,
                "start_aa": "Asn",
                "end_pos": 45,
                "end_aa": "Asn",
                "residue": "Asn",
                "site_lbl": "Asn45",
                "evidence": [
                    {
                        "id": "P11166",
                        "database": "UniProtKB",
                        "url": "https://www.uniprot.org/uniprotkb/P11166#ptm_processing"
                    },
                    {
                        "id": "19349973",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19349973"
                    },
                    {
                        "id": "3839598",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/3839598"
                    },
                    {
                        "id": "24190977",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/24190977"
                    },
                    {
                        "id": "GLY_000143",
                        "database": "GlyGen",
                        "url": "https://data.glygen.org/GLY_000143"
                    }
                ],
                "filter_code": "001000000000000000000.00010000000000.00.01101",
                "uniprot_canonical_ac": "P11166-1"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs2473916930",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs2473916930"
                    },
                    {
                        "id": "15397919",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/15397919"
                    },
                    {
                        "id": "3839598",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/3839598"
                    },
                    {
                        "id": "9266402",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/9266402"
                    },
                    {
                        "id": "9354798",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/9354798"
                    },
                    {
                        "id": "9686354",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/9686354"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 46,
                "end_pos": 46,
                "sequence_org": "L",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "3",
                "chr_pos": "171014706",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "L46",
                "disease": [
                    {
                        "disease_id": "DOID:0070562",
                        "recommended_name": {
                            "id": "DOID:0070562",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070562",
                            "name": "Fanconi-Bickel syndrome",
                            "description": "A glucose metabolism disease characterized by hepatorenal glycogen accumulation, proximal renal tubular dysfunction, and impaired utilization of glucose and galactose that has_material_basis_in homozygous or compound heterozygous mutations in the SLC2A2 gene on chromosome 3q26.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070562",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070562",
                                "name": "FBS",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070562",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070562",
                                "name": "glycogen storage disease XI",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070562",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070562",
                                "name": "glycogenosis type XI",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070562",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070562",
                                "name": "glycogenosis, Fanconi type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "glycogen storage disease due to GLUT2 deficiency",
                                "description": "Fanconi-Bickel glycogenosis (FBG) is a rare glycogen storage disease characterized by hepatorenal glycogen accumulation, severe renal tubular dysfunction and impaired glucose and galactose metabolism."
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "Bickel-Fanconi glycogenosis",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "FBS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "Fanconi Bickel syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "Fanconi syndrome with intestinal malabsorption and galactose intolerance",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "Fanconi-Bickel disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "Fanconi-Bickel syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "GSD due to GLUT2 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "glycogen storage disease due to GLUT2 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "glycogenosis due to GLUT2 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "GLUT2 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "GSD type 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "GSD type XI",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "glycogen storage disease 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "glycogen storage disease XI",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "glycogen storage disease type 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "glycogen storage disease type XI",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "glycogenosis Fanconi EXACT",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "hepatic glycogenosis with amino aciduria and glucosuria",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "hepatorenal glycogenosis with renal Fanconi syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "hepatorenal glycogenosis with renal fanconi syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009216",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009216",
                                "name": "pseudo-phlorizin diabetes",
                                "description": ""
                            },
                            {
                                "id": "MIM:227810",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/227810",
                                "name": "Fanconi-Bickel syndrome",
                                "description": "Fanconi-Bickel syndrome"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0070562",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070562"
                            },
                            {
                                "id": "0070562",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070562"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000000010000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P11168-1"
            }
        ],
        "record_id": "pubmed.3839598",
        "abstract": "",
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    },
                    {
                        "field": "total_sites",
                        "count": 1
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 1
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "exact_sites",
                        "count": 1
                    },
                    {
                        "field": "exact_n_linked_sites",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_sites",
                        "count": 0
                    }
                ],
                "sort_fields": [
                    "glytoucan_ac",
                    "type",
                    "subtype",
                    "site_category",
                    "site_seq",
                    "relation",
                    "comment",
                    "start_pos",
                    "start_aa",
                    "end_pos",
                    "end_aa",
                    "residue",
                    "site_lbl",
                    "filter_code",
                    "uniprot_canonical_ac"
                ]
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    },
                    {
                        "field": "total_sites",
                        "count": 1
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 1
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "exact_sites",
                        "count": 1
                    },
                    {
                        "field": "exact_n_linked_sites",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_sites",
                        "count": 0
                    }
                ],
                "sort_fields": [
                    "glytoucan_ac",
                    "type",
                    "subtype",
                    "site_category",
                    "site_seq",
                    "relation",
                    "comment",
                    "start_pos",
                    "start_aa",
                    "end_pos",
                    "end_aa",
                    "residue",
                    "site_lbl",
                    "filter_code",
                    "uniprot_canonical_ac"
                ]
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variant.",
        "journal": "European journal of neurology",
        "date": "2024-08",
        "authors": "Giugno Alessia, Falcone Elena, Fortunato Francesco, Sammarra Ilaria, Procopio Radha, Gagliardi Monica, Bauleo Alessia, de Stefano Laura, Martino Iolanda, Gambardella Antonio",
        "reference": {
            "type": "PubMed",
            "id": "38803061",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38803061"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38803061",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "GLUT1 promotes cell proliferation via binds and stabilizes phosphorylated EGFR in lung adenocarcinoma.",
        "journal": "Cell communication and signaling : CCS",
        "date": "2024-06-03",
        "authors": "Zhou Zhiqing, Li Yu, Chen Sijie, Xie Zhangrong, Du Yuhui, Liu Yue, Shi Yuxuan, Lin Xiangyi, Zeng Xiaofei, Zhao Huijie, Chen Guoan",
        "reference": {
            "type": "PubMed",
            "id": "38831321",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38831321"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38831321",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Stroke and Stroke-Like Episodes: Recurrent Manifestations in GLUT1 Deficiency Syndrome.",
        "journal": "Pediatric neurology",
        "date": "2024-08",
        "authors": "Olivotto Sara, Freddi Anna, Previtali Roberto, Mauri Alessia, Cereda Cristina, De Amicis Ramona, Bertoli Simona, Doneda Chiara, Veggiotti Pierangelo",
        "reference": {
            "type": "PubMed",
            "id": "38914025",
            "url": "https://pubmed.ncbi.nlm.nih.gov/38914025"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.38914025",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Dysregulated GLUT1 results in the pathogenesis of preeclampsia by impairing the function of trophoblast cells.",
        "journal": "Scientific reports",
        "date": "2024-10-10",
        "authors": "Pei Jingyuan, Liao Yangyou, Bai Xiaoxian, Li Min, Wang Jing, Li Xiaotong, Zhang Hongshuo, Sui Linlin, Kong Ying",
        "reference": {
            "type": "PubMed",
            "id": "39390043",
            "url": "https://pubmed.ncbi.nlm.nih.gov/39390043"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.39390043",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "O-GlcNAcylation of epidermal growth factor receptor and glucose transporter 1 prevents their intrinsic down regulation in breast cancer cells.",
        "journal": "Biochemistry and cell biology = Biochimie et biologie cellulaire",
        "date": "2025-05-14",
        "authors": "Padilla-Meier G Pauline, Bhatia Yeshika, Mishra Suresh",
        "reference": {
            "type": "PubMed",
            "id": "40367522",
            "url": "https://pubmed.ncbi.nlm.nih.gov/40367522"
        },
        "referenced_glycans": [
            {
                "glytoucan_ac": "G49108TO"
            }
        ],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P00533-1",
                "protein_name": "Epidermal growth factor receptor",
                "gene_name": "EGFR",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "glycosylation": [
            {
                "glytoucan_ac": "G49108TO",
                "type": "O-linked",
                "subtype": "O-GlcNAcylation",
                "prediction_tool_list": [],
                "site_category": "reported_with_glycan",
                "site_category_dict": {
                    "reported_with_glycan": true
                },
                "site_seq": "S",
                "relation": "attached",
                "comment": "O-GlcNAcylation",
                "icn3d_view": {},
                "start_pos": 465,
                "start_aa": "Ser",
                "end_pos": 465,
                "end_aa": "Ser",
                "residue": "Ser",
                "site_lbl": "Ser465",
                "evidence": [
                    {
                        "id": "34019948",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/34019948"
                    },
                    {
                        "id": "P11166",
                        "database": "O-GlcNAc Database",
                        "url": "https://www.oglcnac.mcw.edu/search/?query_protein=P11166"
                    },
                    {
                        "id": "40596516",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/40596516"
                    },
                    {
                        "id": "18984734",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18984734"
                    },
                    {
                        "id": "35083852",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/35083852"
                    },
                    {
                        "id": "41018975",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/41018975"
                    },
                    {
                        "id": "40367522",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/40367522"
                    },
                    {
                        "id": "34725712",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/34725712"
                    },
                    {
                        "id": "P11166",
                        "database": "O-GlcNAc Atlas",
                        "url": "https://oglcnac.org/atlas/detail/P11166"
                    },
                    {
                        "id": "573",
                        "database": "GlyConnect",
                        "url": "https://glyconnect.expasy.org/browser/proteins/573"
                    }
                ],
                "filter_code": "000000000000000100000.xxxxxxx.00000001000000.xxxxxxx.xxxxxxxxxx.xxxxxxxxxxxxxxxxxx.xxxxx.01011",
                "uniprot_canonical_ac": "P11166-1"
            },
            {
                "glytoucan_ac": "G49108TO",
                "type": "O-linked",
                "subtype": "O-GlcNAcylation",
                "prediction_tool_list": [],
                "site_category": "reported_with_glycan",
                "site_category_dict": {
                    "reported_with_glycan": true
                },
                "site_seq": "S",
                "relation": "attached",
                "comment": "O-GlcNAcylation",
                "icn3d_view": {},
                "start_pos": 1096,
                "start_aa": "Ser",
                "end_pos": 1096,
                "end_aa": "Ser",
                "residue": "Ser",
                "site_lbl": "Ser1096",
                "evidence": [
                    {
                        "id": "33465208",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33465208"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Database",
                        "url": "https://www.oglcnac.mcw.edu/search/?query_protein=P00533"
                    },
                    {
                        "id": "30962710",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30962710"
                    },
                    {
                        "id": "33214551",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33214551"
                    },
                    {
                        "id": "34019948",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/34019948"
                    },
                    {
                        "id": "31492838",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/31492838"
                    },
                    {
                        "id": "30059200",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30059200"
                    },
                    {
                        "id": "38665916",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/38665916"
                    },
                    {
                        "id": "28510447",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/28510447"
                    },
                    {
                        "id": "26108188",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/26108188"
                    },
                    {
                        "id": "40367522",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/40367522"
                    },
                    {
                        "id": "35289036",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/35289036"
                    },
                    {
                        "id": "29237092",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/29237092"
                    },
                    {
                        "id": "39534244",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/39534244"
                    }
                ],
                "filter_code": "000000000000000100000.xxxxxxx.00000001000000.xxxxxxx.xxxxxxxxxx.xxxxxxxxxxxxxxxxxx.xxxxx.01000",
                "uniprot_canonical_ac": "P00533-1"
            },
            {
                "glytoucan_ac": "G49108TO",
                "type": "O-linked",
                "subtype": "O-GlcNAcylation",
                "prediction_tool_list": [],
                "site_category": "reported_with_glycan",
                "site_category_dict": {
                    "reported_with_glycan": true
                },
                "site_seq": "S",
                "relation": "attached",
                "comment": "O-GlcNAcylation",
                "icn3d_view": {},
                "start_pos": 364,
                "start_aa": "Ser",
                "end_pos": 364,
                "end_aa": "Ser",
                "residue": "Ser",
                "site_lbl": "Ser364",
                "evidence": [
                    {
                        "id": "33465208",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33465208"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Database",
                        "url": "https://www.oglcnac.mcw.edu/search/?query_protein=P00533"
                    },
                    {
                        "id": "30962710",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30962710"
                    },
                    {
                        "id": "33214551",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33214551"
                    },
                    {
                        "id": "34019948",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/34019948"
                    },
                    {
                        "id": "31492838",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/31492838"
                    },
                    {
                        "id": "30059200",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30059200"
                    },
                    {
                        "id": "38665916",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/38665916"
                    },
                    {
                        "id": "28510447",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/28510447"
                    },
                    {
                        "id": "26108188",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/26108188"
                    },
                    {
                        "id": "40367522",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/40367522"
                    },
                    {
                        "id": "35289036",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/35289036"
                    },
                    {
                        "id": "29237092",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/29237092"
                    },
                    {
                        "id": "39534244",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/39534244"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Atlas",
                        "url": "https://oglcnac.org/atlas/detail/P00533"
                    }
                ],
                "filter_code": "000000000000000100000.xxxxxxx.00000001000000.xxxxxxx.xxxxxxxxxx.xxxxxxxxxxxxxxxxxx.xxxxx.01000",
                "uniprot_canonical_ac": "P00533-1"
            },
            {
                "glytoucan_ac": "G49108TO",
                "type": "O-linked",
                "subtype": "O-GlcNAcylation",
                "prediction_tool_list": [],
                "site_category": "reported_with_glycan",
                "site_category_dict": {
                    "reported_with_glycan": true
                },
                "site_seq": "S",
                "relation": "attached",
                "comment": "O-GlcNAcylation",
                "icn3d_view": {},
                "start_pos": 380,
                "start_aa": "Ser",
                "end_pos": 380,
                "end_aa": "Ser",
                "residue": "Ser",
                "site_lbl": "Ser380",
                "evidence": [
                    {
                        "id": "33465208",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33465208"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Database",
                        "url": "https://www.oglcnac.mcw.edu/search/?query_protein=P00533"
                    },
                    {
                        "id": "30962710",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30962710"
                    },
                    {
                        "id": "33214551",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33214551"
                    },
                    {
                        "id": "34019948",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/34019948"
                    },
                    {
                        "id": "31492838",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/31492838"
                    },
                    {
                        "id": "30059200",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30059200"
                    },
                    {
                        "id": "38665916",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/38665916"
                    },
                    {
                        "id": "28510447",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/28510447"
                    },
                    {
                        "id": "26108188",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/26108188"
                    },
                    {
                        "id": "40367522",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/40367522"
                    },
                    {
                        "id": "35289036",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/35289036"
                    },
                    {
                        "id": "29237092",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/29237092"
                    },
                    {
                        "id": "39534244",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/39534244"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Atlas",
                        "url": "https://oglcnac.org/atlas/detail/P00533"
                    }
                ],
                "filter_code": "000000000000000100000.xxxxxxx.00000001000000.xxxxxxx.xxxxxxxxxx.xxxxxxxxxxxxxxxxxx.xxxxx.01000",
                "uniprot_canonical_ac": "P00533-1"
            },
            {
                "glytoucan_ac": "G49108TO",
                "type": "O-linked",
                "subtype": "O-GlcNAcylation",
                "prediction_tool_list": [],
                "site_category": "reported_with_glycan",
                "site_category_dict": {
                    "reported_with_glycan": true
                },
                "site_seq": "T",
                "relation": "attached",
                "comment": "O-GlcNAcylation",
                "icn3d_view": {},
                "start_pos": 384,
                "start_aa": "Thr",
                "end_pos": 384,
                "end_aa": "Thr",
                "residue": "Thr",
                "site_lbl": "Thr384",
                "evidence": [
                    {
                        "id": "33465208",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33465208"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Database",
                        "url": "https://www.oglcnac.mcw.edu/search/?query_protein=P00533"
                    },
                    {
                        "id": "30962710",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30962710"
                    },
                    {
                        "id": "33214551",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33214551"
                    },
                    {
                        "id": "34019948",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/34019948"
                    },
                    {
                        "id": "31492838",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/31492838"
                    },
                    {
                        "id": "30059200",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30059200"
                    },
                    {
                        "id": "38665916",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/38665916"
                    },
                    {
                        "id": "28510447",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/28510447"
                    },
                    {
                        "id": "26108188",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/26108188"
                    },
                    {
                        "id": "40367522",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/40367522"
                    },
                    {
                        "id": "35289036",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/35289036"
                    },
                    {
                        "id": "29237092",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/29237092"
                    },
                    {
                        "id": "39534244",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/39534244"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Atlas",
                        "url": "https://oglcnac.org/atlas/detail/P00533"
                    }
                ],
                "filter_code": "000000000000000010000.xxxxxxx.00000001000000.xxxxxxx.xxxxxxxxxx.xxxxxxxxxxxxxxxxxx.xxxxx.01000",
                "uniprot_canonical_ac": "P00533-1"
            },
            {
                "glytoucan_ac": "G49108TO",
                "type": "O-linked",
                "subtype": "O-GlcNAcylation",
                "prediction_tool_list": [],
                "site_category": "reported_with_glycan",
                "site_category_dict": {
                    "reported_with_glycan": true
                },
                "site_seq": "T",
                "relation": "attached",
                "comment": "O-GlcNAcylation",
                "icn3d_view": {},
                "start_pos": 430,
                "start_aa": "Thr",
                "end_pos": 430,
                "end_aa": "Thr",
                "residue": "Thr",
                "site_lbl": "Thr430",
                "evidence": [
                    {
                        "id": "33465208",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33465208"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Database",
                        "url": "https://www.oglcnac.mcw.edu/search/?query_protein=P00533"
                    },
                    {
                        "id": "30962710",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30962710"
                    },
                    {
                        "id": "33214551",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33214551"
                    },
                    {
                        "id": "34019948",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/34019948"
                    },
                    {
                        "id": "31492838",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/31492838"
                    },
                    {
                        "id": "30059200",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30059200"
                    },
                    {
                        "id": "38665916",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/38665916"
                    },
                    {
                        "id": "28510447",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/28510447"
                    },
                    {
                        "id": "26108188",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/26108188"
                    },
                    {
                        "id": "40367522",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/40367522"
                    },
                    {
                        "id": "35289036",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/35289036"
                    },
                    {
                        "id": "29237092",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/29237092"
                    },
                    {
                        "id": "39534244",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/39534244"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Atlas",
                        "url": "https://oglcnac.org/atlas/detail/P00533"
                    }
                ],
                "filter_code": "000000000000000010000.xxxxxxx.00000001000000.xxxxxxx.xxxxxxxxxx.xxxxxxxxxxxxxxxxxx.xxxxx.01000",
                "uniprot_canonical_ac": "P00533-1"
            },
            {
                "glytoucan_ac": "G49108TO",
                "type": "O-linked",
                "subtype": "O-GlcNAcylation",
                "prediction_tool_list": [],
                "site_category": "reported_with_glycan",
                "site_category_dict": {
                    "reported_with_glycan": true
                },
                "site_seq": "T",
                "relation": "attached",
                "comment": "O-GlcNAcylation",
                "icn3d_view": {},
                "start_pos": 474,
                "start_aa": "Thr",
                "end_pos": 474,
                "end_aa": "Thr",
                "residue": "Thr",
                "site_lbl": "Thr474",
                "evidence": [
                    {
                        "id": "33465208",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33465208"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Database",
                        "url": "https://www.oglcnac.mcw.edu/search/?query_protein=P00533"
                    },
                    {
                        "id": "30962710",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30962710"
                    },
                    {
                        "id": "33214551",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/33214551"
                    },
                    {
                        "id": "34019948",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/34019948"
                    },
                    {
                        "id": "31492838",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/31492838"
                    },
                    {
                        "id": "30059200",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/30059200"
                    },
                    {
                        "id": "38665916",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/38665916"
                    },
                    {
                        "id": "28510447",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/28510447"
                    },
                    {
                        "id": "26108188",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/26108188"
                    },
                    {
                        "id": "40367522",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/40367522"
                    },
                    {
                        "id": "35289036",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/35289036"
                    },
                    {
                        "id": "29237092",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/29237092"
                    },
                    {
                        "id": "39534244",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/39534244"
                    },
                    {
                        "id": "P00533",
                        "database": "O-GlcNAc Atlas",
                        "url": "https://oglcnac.org/atlas/detail/P00533"
                    }
                ],
                "filter_code": "000000000000000010000.xxxxxxx.00000001000000.xxxxxxx.xxxxxxxxxx.xxxxxxxxxxxxxxxxxx.xxxxx.01000",
                "uniprot_canonical_ac": "P00533-1"
            }
        ],
        "record_id": "pubmed.40367522",
        "abstract": "",
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 2
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "glytoucan_ac"
                ]
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 7
                    },
                    {
                        "field": "total_sites",
                        "count": 7
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 7
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 7
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 1
                    },
                    {
                        "field": "exact_sites",
                        "count": 7
                    },
                    {
                        "field": "exact_o_linked_sites",
                        "count": 7
                    },
                    {
                        "field": "exact_o_linked_glycan_sites",
                        "count": 7
                    },
                    {
                        "field": "exact_o_linked_glycans",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_sites",
                        "count": 0
                    }
                ],
                "sort_fields": [
                    "glytoucan_ac",
                    "type",
                    "subtype",
                    "site_category",
                    "site_seq",
                    "relation",
                    "comment",
                    "start_pos",
                    "start_aa",
                    "end_pos",
                    "end_aa",
                    "residue",
                    "site_lbl",
                    "filter_code",
                    "uniprot_canonical_ac"
                ]
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 7
                    },
                    {
                        "field": "total_sites",
                        "count": 7
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 7
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 7
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 1
                    },
                    {
                        "field": "exact_sites",
                        "count": 7
                    },
                    {
                        "field": "exact_o_linked_sites",
                        "count": 7
                    },
                    {
                        "field": "exact_o_linked_glycan_sites",
                        "count": 7
                    },
                    {
                        "field": "exact_o_linked_glycans",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_sites",
                        "count": 0
                    }
                ],
                "sort_fields": [
                    "glytoucan_ac",
                    "type",
                    "subtype",
                    "site_category",
                    "site_seq",
                    "relation",
                    "comment",
                    "start_pos",
                    "start_aa",
                    "end_pos",
                    "end_aa",
                    "residue",
                    "site_lbl",
                    "filter_code",
                    "uniprot_canonical_ac"
                ]
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Lactose biosynthesis.",
        "journal": "Reviews of physiology, biochemistry and pharmacology",
        "date": "1975",
        "authors": "Brew K, Hill RL",
        "reference": {
            "type": "PubMed",
            "id": "806951",
            "url": "https://pubmed.ncbi.nlm.nih.gov/806951"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P00709-1",
                "protein_name": "Alpha-lactalbumin",
                "gene_name": "LALBA",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15291-1",
                "protein_name": "Beta-1,4-galactosyltransferase 1",
                "gene_name": "B4GALT1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P11166",
                        "url": "https://www.uniprot.org/uniprotkb/P11166"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.806951",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 3
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    }
]
