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                            "url": "https://glyconnect.expasy.org/browser/proteins/1177"
                        }
                    ],
                    "protein_name": "Dipeptidyl peptidase 4",
                    "gene_name": "DPP4",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 766,
                    "chemical_mass": 88279.0
                }
            ]
        },
        {
            "start_pos": "2767",
            "site_seq": "N",
            "site_lbl": "Asn2767",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P35555-1",
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                    "end_pos": 2767,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29391424",
                            "url": "https://glygen.org/publication/PubMed/29391424"
                        },
                        {
                            "database": "GlyConnect",
                            "id": "1235",
                            "url": "https://glyconnect.expasy.org/browser/proteins/1235"
                        }
                    ],
                    "protein_name": "Fibrillin-1",
                    "gene_name": "FBN1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 2871,
                    "chemical_mass": 312298.0
                }
            ]
        },
        {
            "start_pos": "2767",
            "site_seq": "TAIFAFnISHVSNK",
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            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P35555-1",
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                    "end_pos": 2767,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29391424",
                            "url": "https://glygen.org/publication/PubMed/29391424"
                        },
                        {
                            "database": "GlyConnect",
                            "id": "1235",
                            "url": "https://glyconnect.expasy.org/browser/proteins/1235"
                        }
                    ],
                    "protein_name": "Fibrillin-1",
                    "gene_name": "FBN1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 2871,
                    "chemical_mass": 312298.0
                }
            ]
        },
        {
            "start_pos": "2767",
            "site_seq": "TAIFAFNISHVSNK",
            "site_lbl": "Asn2767",
            "residue": "Asn",
            "glycoprotein": [
                {
                    "uniprot_canonical_ac": "P35555-1",
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                    "end_pos": 2767,
                    "residue": "Asn",
                    "evidence": [
                        {
                            "database": "PubMed",
                            "id": "29391424",
                            "url": "https://glygen.org/publication/PubMed/29391424"
                        },
                        {
                            "database": "GlyConnect",
                            "id": "1235",
                            "url": "https://glyconnect.expasy.org/browser/proteins/1235"
                        }
                    ],
                    "protein_name": "Fibrillin-1",
                    "gene_name": "FBN1",
                    "tax_id": 9606,
                    "tax_name": "Homo sapiens",
                    "tax_common_name": "Human",
                    "length": 2871,
                    "chemical_mass": 312298.0
                }
            ]
        },
        {
            "start_pos": "2767",
            "site_seq": "",
            "site_lbl": "N2767",
            "residue": "",
            "snv": [
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "D",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NIS->DIS).",
                    "chr_id": "15",
                    "chr_pos": "48411307",
                    "evidence": [
                        {
                            "id": "rs771437236",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771437236"
                        },
                        {
                            "id": "rs771437236",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs771437236"
                        },
                        {
                            "id": "rs771437236",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs771437236#frequency_tab"
                        },
                        {
                            "id": "rs771437236",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs771437236"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111243",
                            "evidence": [
                                {
                                    "id": "102370",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/102370"
                                },
                                {
                                    "id": "0111243",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111243",
                            "evidence": [
                                {
                                    "id": "102370",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/102370"
                                },
                                {
                                    "id": "0111243",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111243",
                            "evidence": [
                                {
                                    "id": "102370",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/102370"
                                },
                                {
                                    "id": "0111243",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111243",
                            "evidence": [
                                {
                                    "id": "102370",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/102370"
                                },
                                {
                                    "id": "0111243",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.",
                            "url": "http://disease-ontology.org/term/DOID:0111150",
                            "evidence": [
                                {
                                    "id": "129600",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/129600"
                                },
                                {
                                    "id": "0111150",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.",
                            "url": "http://disease-ontology.org/term/DOID:0111150",
                            "evidence": [
                                {
                                    "id": "129600",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/129600"
                                },
                                {
                                    "id": "0111150",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.",
                            "url": "http://disease-ontology.org/term/DOID:0111150",
                            "evidence": [
                                {
                                    "id": "129600",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/129600"
                                },
                                {
                                    "id": "0111150",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.",
                            "url": "http://disease-ontology.org/term/DOID:0111150",
                            "evidence": [
                                {
                                    "id": "129600",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/129600"
                                },
                                {
                                    "id": "0111150",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111726",
                            "evidence": [
                                {
                                    "id": "614185",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/614185"
                                },
                                {
                                    "id": "0111726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111726",
                            "evidence": [
                                {
                                    "id": "614185",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/614185"
                                },
                                {
                                    "id": "0111726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111726",
                            "evidence": [
                                {
                                    "id": "614185",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/614185"
                                },
                                {
                                    "id": "0111726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111726",
                            "evidence": [
                                {
                                    "id": "614185",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/614185"
                                },
                                {
                                    "id": "0111726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens.",
                            "url": "http://disease-ontology.org/term/DOID:14323",
                            "evidence": [
                                {
                                    "id": "14323",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14323"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens.",
                            "url": "http://disease-ontology.org/term/DOID:14323",
                            "evidence": [
                                {
                                    "id": "14323",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14323"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens.",
                            "url": "http://disease-ontology.org/term/DOID:14323",
                            "evidence": [
                                {
                                    "id": "14323",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14323"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens.",
                            "url": "http://disease-ontology.org/term/DOID:14323",
                            "evidence": [
                                {
                                    "id": "14323",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14323"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111561",
                            "evidence": [
                                {
                                    "id": "184900",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/184900"
                                },
                                {
                                    "id": "0111561",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111561",
                            "evidence": [
                                {
                                    "id": "184900",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/184900"
                                },
                                {
                                    "id": "0111561",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111561",
                            "evidence": [
                                {
                                    "id": "184900",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/184900"
                                },
                                {
                                    "id": "0111561",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111561",
                            "evidence": [
                                {
                                    "id": "184900",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/184900"
                                },
                                {
                                    "id": "0111561",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050475",
                            "name": "Weill-Marchesani syndrome",
                            "description": "A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.",
                            "url": "http://disease-ontology.org/term/DOID:0050475",
                            "evidence": [
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050475",
                            "name": "Weill-Marchesani syndrome",
                            "description": "A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.",
                            "url": "http://disease-ontology.org/term/DOID:0050475",
                            "evidence": [
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050475",
                            "name": "Weill-Marchesani syndrome",
                            "description": "A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.",
                            "url": "http://disease-ontology.org/term/DOID:0050475",
                            "evidence": [
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050475",
                            "name": "Weill-Marchesani syndrome",
                            "description": "A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.",
                            "url": "http://disease-ontology.org/term/DOID:0050475",
                            "evidence": [
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                }
                            ]
                        }
                    ]
                },
                {
                    "weight": 100,
                    "sequence_org": "N",
                    "sequence_mut": "S",
                    "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NIS->SIS).",
                    "chr_id": "15",
                    "chr_pos": "48411306",
                    "evidence": [
                        {
                            "id": "rs536503540",
                            "database": "dbSNP",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs536503540"
                        },
                        {
                            "id": "rs536503540",
                            "database": "1000Genomes",
                            "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs536503540"
                        },
                        {
                            "id": "rs536503540",
                            "database": "ExAC",
                            "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs536503540"
                        },
                        {
                            "id": "rs536503540",
                            "database": "TOPMed",
                            "url": "https://www.ncbi.nlm.nih.gov/snp/rs536503540#frequency_tab"
                        },
                        {
                            "id": "rs536503540",
                            "database": "gnomAD",
                            "url": "http://gnomad.broadinstitute.org/awesome?query=rs536503540"
                        }
                    ],
                    "disease": [
                        {
                            "disease_id": "DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111243",
                            "evidence": [
                                {
                                    "id": "102370",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/102370"
                                },
                                {
                                    "id": "0111243",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111243",
                            "evidence": [
                                {
                                    "id": "102370",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/102370"
                                },
                                {
                                    "id": "0111243",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111243",
                            "evidence": [
                                {
                                    "id": "102370",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/102370"
                                },
                                {
                                    "id": "0111243",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111243",
                            "evidence": [
                                {
                                    "id": "102370",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/102370"
                                },
                                {
                                    "id": "0111243",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111243",
                            "name": "acromicric dysplasia",
                            "description": "An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111243",
                            "evidence": [
                                {
                                    "id": "102370",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/102370"
                                },
                                {
                                    "id": "0111243",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111243"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.",
                            "url": "http://disease-ontology.org/term/DOID:0111150",
                            "evidence": [
                                {
                                    "id": "129600",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/129600"
                                },
                                {
                                    "id": "0111150",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.",
                            "url": "http://disease-ontology.org/term/DOID:0111150",
                            "evidence": [
                                {
                                    "id": "129600",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/129600"
                                },
                                {
                                    "id": "0111150",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.",
                            "url": "http://disease-ontology.org/term/DOID:0111150",
                            "evidence": [
                                {
                                    "id": "129600",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/129600"
                                },
                                {
                                    "id": "0111150",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.",
                            "url": "http://disease-ontology.org/term/DOID:0111150",
                            "evidence": [
                                {
                                    "id": "129600",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/129600"
                                },
                                {
                                    "id": "0111150",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111150",
                            "name": "autosomal dominant isolated ectopia lentis 1",
                            "description": "An isolated ectopia lentis that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.",
                            "url": "http://disease-ontology.org/term/DOID:0111150",
                            "evidence": [
                                {
                                    "id": "129600",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/129600"
                                },
                                {
                                    "id": "0111150",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111150"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111726",
                            "evidence": [
                                {
                                    "id": "614185",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/614185"
                                },
                                {
                                    "id": "0111726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111726",
                            "evidence": [
                                {
                                    "id": "614185",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/614185"
                                },
                                {
                                    "id": "0111726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111726",
                            "evidence": [
                                {
                                    "id": "614185",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/614185"
                                },
                                {
                                    "id": "0111726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111726",
                            "evidence": [
                                {
                                    "id": "614185",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/614185"
                                },
                                {
                                    "id": "0111726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111726",
                            "name": "geleophysic dysplasia 2",
                            "description": "A geleophysic dysplasia that has_material_basis_in heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111726",
                            "evidence": [
                                {
                                    "id": "614185",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/614185"
                                },
                                {
                                    "id": "0111726",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111726"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens.",
                            "url": "http://disease-ontology.org/term/DOID:14323",
                            "evidence": [
                                {
                                    "id": "14323",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14323"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens.",
                            "url": "http://disease-ontology.org/term/DOID:14323",
                            "evidence": [
                                {
                                    "id": "14323",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14323"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens.",
                            "url": "http://disease-ontology.org/term/DOID:14323",
                            "evidence": [
                                {
                                    "id": "14323",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14323"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens.",
                            "url": "http://disease-ontology.org/term/DOID:14323",
                            "evidence": [
                                {
                                    "id": "14323",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14323"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:14323",
                            "name": "Marfan syndrome",
                            "description": "A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens.",
                            "url": "http://disease-ontology.org/term/DOID:14323",
                            "evidence": [
                                {
                                    "id": "14323",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:14323"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111561",
                            "evidence": [
                                {
                                    "id": "184900",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/184900"
                                },
                                {
                                    "id": "0111561",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111561",
                            "evidence": [
                                {
                                    "id": "184900",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/184900"
                                },
                                {
                                    "id": "0111561",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111561",
                            "evidence": [
                                {
                                    "id": "184900",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/184900"
                                },
                                {
                                    "id": "0111561",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111561",
                            "evidence": [
                                {
                                    "id": "184900",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/184900"
                                },
                                {
                                    "id": "0111561",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0111561",
                            "name": "stiff skin syndrome",
                            "description": "A skin disease characterized by hard, thick skin, usually over the entire body, limiting joint mobility and causing flexion contractures that has_material_basis_in heterozygous mutation in the FBN1 gene on chromosome 15q21.1.",
                            "url": "http://disease-ontology.org/term/DOID:0111561",
                            "evidence": [
                                {
                                    "id": "184900",
                                    "database": "MIM",
                                    "url": "https://www.omim.org/entry/184900"
                                },
                                {
                                    "id": "0111561",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0111561"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050475",
                            "name": "Weill-Marchesani syndrome",
                            "description": "A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.",
                            "url": "http://disease-ontology.org/term/DOID:0050475",
                            "evidence": [
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050475",
                            "name": "Weill-Marchesani syndrome",
                            "description": "A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.",
                            "url": "http://disease-ontology.org/term/DOID:0050475",
                            "evidence": [
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050475",
                            "name": "Weill-Marchesani syndrome",
                            "description": "A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.",
                            "url": "http://disease-ontology.org/term/DOID:0050475",
                            "evidence": [
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050475",
                            "name": "Weill-Marchesani syndrome",
                            "description": "A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.",
                            "url": "http://disease-ontology.org/term/DOID:0050475",
                            "evidence": [
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                }
                            ]
                        },
                        {
                            "disease_id": "DOID:0050475",
                            "name": "Weill-Marchesani syndrome",
                            "description": "A syndrome characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities.",
                            "url": "http://disease-ontology.org/term/DOID:0050475",
                            "evidence": [
                                {
                                    "id": "0050475",
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                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
                                },
                                {
                                    "id": "0050475",
                                    "database": "AGR",
                                    "url": "https://www.alliancegenome.org/disease/DOID:0050475"
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                            ]
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                    ]
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                {
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                            "url": "https://glygen.org/publication/PubMed/29391424"
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                        {
                            "database": "GlyConnect",
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                            "url": "https://glyconnect.expasy.org/browser/proteins/1235"
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                    ],
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            ]
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                        {
                            "database": "GlyConnect",
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                            "url": "https://glyconnect.expasy.org/browser/proteins/1256"
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                    ],
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            ]
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        {
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                        {
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                            "url": "https://glyconnect.expasy.org/browser/proteins/1256"
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                    ],
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            ]
        },
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                            "id": "rs923974095",
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                        {
                            "id": "rs923974095",
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                        {
                            "id": "rs923974095",
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                    ]
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            ],
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                        {
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                    ],
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            ]
        },
        {
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                        {
                            "database": "GlyConnect",
                            "id": "137",
                            "url": "https://glyconnect.expasy.org/browser/proteins/137"
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                    ],
                    "protein_name": "Epidermal growth factor receptor",
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            ]
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                        {
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                            "id": "1439",
                            "url": "https://glyconnect.expasy.org/browser/proteins/1439"
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                    ],
                    "protein_name": "Laminin subunit alpha-2",
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                        {
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                            "url": "https://glyconnect.expasy.org/browser/proteins/1439"
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                    ],
                    "protein_name": "Laminin subunit alpha-2",
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            ]
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                        {
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                        {
                            "id": "rs1476993127",
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                    ]
                },
                {
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                        {
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                        {
                            "id": "rs1476993127",
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                    ]
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                        {
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                    ],
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                        {
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                    ],
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            ]
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        {
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                        {
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                    ],
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            ]
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                        {
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            ]
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                        {
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                    ],
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                                {
                                    "id": "4159",
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                },
                {
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            ]
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                        {
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                        {
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                        {
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            ]
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        {
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                            "url": "https://glygen.org/publication/PubMed/29391424"
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                        {
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                            "url": "https://glyconnect.expasy.org/browser/proteins/1709"
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                    ],
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            ]
        },
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                    ],
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            ]
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                    ],
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            ]
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                        {
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                    ],
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            ]
        },
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                        {
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                    ],
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            ]
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            ]
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                        {
                            "id": "rs781474959",
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                        {
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                    ]
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            ],
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                    ],
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            ]
        },
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                {
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                        {
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                    ],
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            ]
        },
        {
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                        {
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                    ],
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            ]
        },
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            ]
        },
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                        {
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                        {
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                        {
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            ],
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            ]
        },
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            ]
        },
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            ]
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                        {
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                    ]
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                    ],
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            ]
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        {
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                    ],
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            ]
        },
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                    ],
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        },
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            ]
        },
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                        {
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                            "url": "https://glyconnect.expasy.org/browser/proteins/1983"
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                    ],
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                        {
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                    ],
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                        {
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                    ],
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                                {
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                            ]
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                    ],
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                        {
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                    ]
                },
                {
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                    ],
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                },
                {
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                        {
                            "id": "rs1245775900",
                            "database": "TOPMed",
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                        {
                            "id": "rs1245775900",
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                        {
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                    ],
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                        {
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                    ],
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                        {
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            ]
        },
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                        {
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                        {
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                        {
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                    ],
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                            ]
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                    ]
                },
                {
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                },
                {
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                        {
                            "id": "rs2117048285",
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                    ]
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                            "url": "https://glyconnect.expasy.org/browser/proteins/518"
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            ]
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            ]
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                        {
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                            "url": "https://glyconnect.expasy.org/browser/proteins/613"
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                    ],
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                            "url": "https://glyconnect.expasy.org/browser/proteins/613"
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                    ],
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            ]
        },
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                    ],
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            ]
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                        {
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                        {
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                                    "id": "363",
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                    ],
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            ]
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        {
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                        {
                            "database": "GlyConnect",
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                        {
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                    ],
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                        {
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                        {
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                    ],
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            ]
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                        {
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                            "url": "https://glyconnect.expasy.org/browser/proteins/79"
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                    ],
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            ]
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        {
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                        {
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            ]
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                    ]
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                            "url": "https://glyconnect.expasy.org/browser/proteins/20"
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                    ],
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            ]
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    ],
    "record_id": "G12793SR"
}
