[
    {
        "uniprot_canonical_ac": "P98160-1",
        "uniprot_ac": "P98160",
        "uniprot_id": "PGBM_HUMAN",
        "mass": {
            "chemical_mass": 468830.0,
            "monoisotopic_mass": 468830.0
        },
        "refseq": {
            "ac": "NP_001278789",
            "name": "basement membrane-specific heparan sulfate proteoglycan core protein isoform a precursor",
            "summary": "This gene encodes the perlecan protein, which consists of a core protein to which three long chains of glycosaminoglycans (heparan sulfate or chondroitin sulfate) are attached. The perlecan protein is a large multidomain proteoglycan that binds to and cross-links many extracellular matrix components and cell-surface molecules. It has been shown that this protein interacts with laminin, prolargin, collagen type IV, FGFBP1, FBLN2, FGF7 and transthyretin, etc., and it plays essential roles in multiple biological activities. Perlecan is a key component of the vascular extracellular matrix, where it helps to maintain the endothelial barrier function. It is a potent inhibitor of smooth muscle cell proliferation and is thus thought to help maintain vascular homeostasis. It can also promote growth factor (e.g., FGF2) activity and thus stimulate endothelial growth and re-generation. It is a major component of basement membranes, where it is involved in the stabilization of other molecules as well as being involved with glomerular permeability to macromolecules and cell adhesion. Mutations in this gene cause Schwartz-Jampel syndrome type 1, Silverman-Handmaker type of dyssegmental dysplasia, and tardive dyskinesia. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014].",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
        },
        "gene_names": [
            {
                "name": "HSPG2",
                "type": "recommended",
                "evidence": [
                    {
                        "id": "P98160",
                        "database": "UniProtKB",
                        "url": "https://www.uniprot.org/uniprotkb/P98160"
                    }
                ]
            },
            {
                "name": "HSPG2",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            },
            {
                "name": "HSPG",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            },
            {
                "name": "PLC",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            },
            {
                "name": "PRCAN",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            },
            {
                "name": "SJA",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            },
            {
                "name": "SJS1",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            },
            {
                "name": "SJS",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            }
        ],
        "protein_names": [
            {
                "name": "Basement membrane-specific heparan sulfate proteoglycan core protein",
                "type": "recommended",
                "evidence": [
                    {
                        "id": "P98160",
                        "database": "UniProtKB",
                        "url": "https://www.uniprot.org/uniprotkb/P98160/entry#names_and_taxonomy"
                    }
                ]
            },
            {
                "name": "HSPG",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "P98160",
                        "database": "UniProtKB",
                        "url": "https://www.uniprot.org/uniprotkb/P98160/entry#names_and_taxonomy"
                    }
                ]
            },
            {
                "name": "PLC",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "P98160",
                        "database": "UniProtKB",
                        "url": "https://www.uniprot.org/uniprotkb/P98160/entry#names_and_taxonomy"
                    }
                ]
            },
            {
                "name": "Perlecan",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "P98160",
                        "database": "UniProtKB",
                        "url": "https://www.uniprot.org/uniprotkb/P98160/entry#names_and_taxonomy"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein isoform a precursor",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            },
            {
                "name": "endorepellin (domain V region)",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            },
            {
                "name": "perlecan proteoglycan",
                "type": "synonym",
                "evidence": [
                    {
                        "id": "NP_001278789",
                        "database": "RefSeq",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            }
        ],
        "function": [
            {
                "annotation": "Anti-angiogenic and anti-tumor peptide that inhibits endothelial cell migration, collagen-induced endothelial tube morphogenesis and blood vessel growth in the chorioallantoic membrane. Blocks endothelial cell adhesion to fibronectin and type I collagen. Anti-tumor agent in neovascularization. Interaction with its ligand, integrin alpha2/beta1, is required for the anti-angiogenic properties. Evokes a reduction in phosphorylation of receptor tyrosine kinases via alpha2/beta1 integrin-mediated activation of the tyrosine phosphatase, PTPN6.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P98160",
                        "url": "https://www.uniprot.org/uniprotkb/P98160#function"
                    }
                ]
            },
            {
                "annotation": "Dyssegmental dysplasia Rolland-Desbuquois type is caused by pathogenic variants in HSPG2 - a founder haplotype shared in five patients.",
                "evidence": [
                    {
                        "database": "RefSeq",
                        "id": "NP_001278789",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    },
                    {
                        "database": "PubMed",
                        "id": "38424183",
                        "url": "https://glygen.org/publication/PubMed/38424183"
                    }
                ]
            },
            {
                "annotation": "Has anti-angiogenic properties that require binding of calcium ions for full activity.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P98160",
                        "url": "https://www.uniprot.org/uniprotkb/P98160#function"
                    }
                ]
            },
            {
                "annotation": "Identification of B-cell-related HSPG2 and CDSN as susceptibility loci for Kawasaki disease.",
                "evidence": [
                    {
                        "database": "RefSeq",
                        "id": "NP_001278789",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    },
                    {
                        "database": "PubMed",
                        "id": "37453912",
                        "url": "https://glygen.org/publication/PubMed/37453912"
                    }
                ]
            },
            {
                "annotation": "Integral component of basement membranes. Component of the glomerular basement membrane (GBM), responsible for the fixed negative electrostatic membrane charge, and which provides a barrier which is both size- and charge-selective. It serves as an attachment substrate for cells. Plays essential roles in vascularization. Critical for normal heart development and for regulating the vascular response to injury. Also required for avascular cartilage development (PubMed:12435733, PubMed:15591058, PubMed:19789387). In muscle, it is essential for localizing acetylcholinesterase (AChE) at the neuromuscular junctions (NMJ), most probably acting as an adapter that links the acetylcholinesterase collagenic tail peptide (COLQ) to alpha-dystroglycan, and is therefore involved in the down-regulation of colinergic synaptic transmission (By similarity).",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P98160",
                        "url": "https://www.uniprot.org/uniprotkb/P98160#function"
                    },
                    {
                        "database": "PubMed",
                        "id": "12435733",
                        "url": "https://glygen.org/publication/PubMed/12435733"
                    },
                    {
                        "database": "PubMed",
                        "id": "15591058",
                        "url": "https://glygen.org/publication/PubMed/15591058"
                    },
                    {
                        "database": "UniProtKB",
                        "id": "Q05793",
                        "url": "https://www.uniprot.org/uniprotkb/Q05793#function"
                    },
                    {
                        "database": "PubMed",
                        "id": "19789387",
                        "url": "https://glygen.org/publication/PubMed/19789387"
                    }
                ]
            },
            {
                "annotation": "Perlecan (HSPG2) promotes structural, contractile, and metabolic development of human cardiomyocytes.",
                "evidence": [
                    {
                        "database": "RefSeq",
                        "id": "NP_001278789",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    },
                    {
                        "database": "PubMed",
                        "id": "38198277",
                        "url": "https://glygen.org/publication/PubMed/38198277"
                    }
                ]
            },
            {
                "annotation": "Perlecan: Roles in osteoarthritis and potential treating target. Review article",
                "evidence": [
                    {
                        "database": "RefSeq",
                        "id": "NP_001278789",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    },
                    {
                        "database": "PubMed",
                        "id": "36379311",
                        "url": "https://glygen.org/publication/PubMed/36379311"
                    }
                ]
            },
            {
                "annotation": "This gene encodes the perlecan protein, which consists of a core protein to which three long chains of glycosaminoglycans (heparan sulfate or chondroitin sulfate) are attached. The perlecan protein is a large multidomain proteoglycan that binds to and cross-links many extracellular matrix components and cell-surface molecules. It has been shown that this protein interacts with laminin, prolargin, collagen type IV, FGFBP1, FBLN2, FGF7 and transthyretin, etc., and it plays essential roles in multiple biological activities. Perlecan is a key component of the vascular extracellular matrix, where it helps to maintain the endothelial barrier function. It is a potent inhibitor of smooth muscle cell proliferation and is thus thought to help maintain vascular homeostasis. It can also promote growth factor (e.g., FGF2) activity and thus stimulate endothelial growth and re-generation. It is a major component of basement membranes, where it is involved in the stabilization of other molecules as well as being involved with glomerular permeability to macromolecules and cell adhesion. Mutations in this gene cause Schwartz-Jampel syndrome type 1, Silverman-Handmaker type of dyssegmental dysplasia, and tardive dyskinesia. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014].",
                "evidence": [
                    {
                        "database": "RefSeq",
                        "id": "NP_001278789",
                        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001278789"
                    }
                ]
            }
        ],
        "disease": [
            {
                "disease_id": "DOID:0060770",
                "recommended_name": {
                    "id": "DOID:0060770",
                    "resource": "Disease Ontology",
                    "url": "https://disease-ontology.org/term/DOID:0060770",
                    "name": "dextro-looped transposition of the great arteries",
                    "description": "A congenital heart disease characterized by complete inversion of the great vessels where the aorta incorrectly arises from the right ventricle and the pulmonary artery incorrectly arises from the left ventricle."
                },
                "synonyms": [
                    {
                        "id": "DOID:0060770",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0060770",
                        "name": "congenitally uncorrected transposition of the great vessels",
                        "description": ""
                    },
                    {
                        "id": "DOID:0060770",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0060770",
                        "name": "ventriculoarterial discordance with atrioventricular concordance",
                        "description": ""
                    },
                    {
                        "id": "DOID:0060770",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0060770",
                        "name": "D-TGA",
                        "description": ""
                    },
                    {
                        "id": "DOID:0060770",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0060770",
                        "name": "DTGA1",
                        "description": ""
                    },
                    {
                        "id": "DOID:0060770",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0060770",
                        "name": "isolated ventriculoarterial discordance",
                        "description": ""
                    },
                    {
                        "id": "DOID:0060770",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0060770",
                        "name": "congenitally uncorrected transposition of the great arteries",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0012128",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0012128",
                        "name": "obsolete transposition of the great arteries, dextro-looped",
                        "description": "OBSOLETE. Any dextro-looped transposition of the great arteries in which the cause of the disease is a mutation in the MED13L gene."
                    },
                    {
                        "id": "MONDO:0012128",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0012128",
                        "name": "DTGA",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0012128",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0012128",
                        "name": "DTGA1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0012128",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0012128",
                        "name": "MED13L dextro-looped transposition of the great arteries",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0012128",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0012128",
                        "name": "dextro-looped transposition of the great arteries 1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0012128",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0012128",
                        "name": "dextro-looped transposition of the great arteries caused by mutation in MED13L",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0012128",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0012128",
                        "name": "dextro-looped transposition of the great arteries type 1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0012128",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0012128",
                        "name": "transposition of the great arteries, dextro-looped type 1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0012128",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0012128",
                        "name": "transposition of the great arteries, dextro-looped 1",
                        "description": ""
                    }
                ],
                "unlinked_id_list": [],
                "evidence": [
                    {
                        "id": "0060770",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060770"
                    }
                ]
            },
            {
                "disease_id": "DOID:0090005",
                "recommended_name": {
                    "id": "DOID:0090005",
                    "resource": "Disease Ontology",
                    "url": "https://disease-ontology.org/term/DOID:0090005",
                    "name": "Schwartz-Jampel syndrome 1",
                    "description": "A syndrome characterized by neuromyotonia and chondrodysplasia that has_material_basis_in hypomorphic mutations in the HSPG2 gene on chromosome 1p36."
                },
                "synonyms": [
                    {
                        "id": "DOID:0090005",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0090005",
                        "name": "Aberfeld syndrome",
                        "description": ""
                    },
                    {
                        "id": "DOID:0090005",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0090005",
                        "name": "Burton skeletal dysplasia",
                        "description": ""
                    },
                    {
                        "id": "DOID:0090005",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0090005",
                        "name": "Burton syndrome",
                        "description": ""
                    },
                    {
                        "id": "DOID:0090005",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0090005",
                        "name": "Catel-Hempel syndrome",
                        "description": ""
                    },
                    {
                        "id": "DOID:0090005",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0090005",
                        "name": "Schwartz-Jampel syndrome type 1",
                        "description": ""
                    },
                    {
                        "id": "DOID:0090005",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0090005",
                        "name": "Schwartz-Jampel-Aberfeld syndrome",
                        "description": ""
                    },
                    {
                        "id": "DOID:0090005",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0090005",
                        "name": "Catel-Hempel type dysostosis enchondralis metaepiphysaria",
                        "description": ""
                    },
                    {
                        "id": "DOID:0090005",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0090005",
                        "name": "myotonic chondrodystrophy",
                        "description": ""
                    },
                    {
                        "id": "DOID:0090005",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0090005",
                        "name": "osteochondromuscular dystrophy",
                        "description": ""
                    },
                    {
                        "id": "DOID:0090005",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:0090005",
                        "name": "myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0100435",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0100435",
                        "name": "Schwartz-Jampel syndrome type 1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0100435",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0100435",
                        "name": "SJA syndrome",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0100435",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0100435",
                        "name": "SJS1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0100435",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0100435",
                        "name": "Schwartz-Jampel syndrome type 1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0100435",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0100435",
                        "name": "Schwartz-Jampel syndrome, type 1",
                        "description": ""
                    },
                    {
                        "id": "MIM:255800",
                        "resource": "MIM",
                        "url": "https://www.omim.org/entry/255800",
                        "name": "Schwartz-Jampel syndrome",
                        "description": "Schwartz-Jampel syndrome"
                    }
                ],
                "unlinked_id_list": [],
                "evidence": [
                    {
                        "id": "255800",
                        "database": "MIM",
                        "url": "https://www.omim.org/entry/255800"
                    },
                    {
                        "id": "0090005",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090005"
                    }
                ]
            },
            {
                "disease_id": "DOID:0090032",
                "recommended_name": {
                    "id": "DOID:0090032",
                    "resource": "Disease Ontology",
                    "url": "https://disease-ontology.org/term/DOID:0090032",
                    "name": "Silverman-Handmaker type dyssegmental dysplasia",
                    "description": "An osteochondrodysplasia characterized by short-limbed dwarfism, anisospondyly, and neonatal lethality that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding perlecan (HSPG2) on chromosome 1p36."
                },
                "synonyms": [
                    {
                        "id": "MONDO:0009140",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0009140",
                        "name": "Silverman-Handmaker type dyssegmental dysplasia",
                        "description": "Dyssegmental dysplasia, Silverman-Handmaker type is a rare, genetic, primary bone dysplasia, and lethal form of neonatal short-limbed dwarfism, characterized by anisospondyly, severe short stature and limb shortening, metaphyseal flaring and distinct dysmorphic features (i.e. flat facial appearance, abnormal ears, short neck, narrow thorax). Additional features may include other skeletal findings (e.g. joint contractures, bowed limbs, talipes equinovarus) and urogenital and cardiovascular abnormalities."
                    },
                    {
                        "id": "MONDO:0009140",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0009140",
                        "name": "Anisospondylic camptomicromelic dwarfism Silverman-Handmaker type",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0009140",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0009140",
                        "name": "DDSH",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0009140",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0009140",
                        "name": "dyssegmental dwarfism Silverman-Handmaker type",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0009140",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0009140",
                        "name": "dyssegmental dysplasia Silverman-Handmaker type",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0009140",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0009140",
                        "name": "dyssegmental dysplasia, Silverman-Handmaker type",
                        "description": ""
                    },
                    {
                        "id": "MIM:224410",
                        "resource": "MIM",
                        "url": "https://www.omim.org/entry/224410",
                        "name": "Dyssegmental dysplasia Silverman-Handmaker type",
                        "description": "Dyssegmental dysplasia Silverman-Handmaker type"
                    }
                ],
                "unlinked_id_list": [],
                "evidence": [
                    {
                        "id": "224410",
                        "database": "MIM",
                        "url": "https://www.omim.org/entry/224410"
                    },
                    {
                        "id": "0090032",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0090032"
                    }
                ]
            },
            {
                "disease_id": "DOID:10763",
                "recommended_name": {
                    "id": "DOID:10763",
                    "resource": "Disease Ontology",
                    "url": "https://disease-ontology.org/term/DOID:10763",
                    "name": "hypertension",
                    "description": "An artery disease characterized by chronic elevated blood pressure in the arteries."
                },
                "synonyms": [
                    {
                        "id": "DOID:10763",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:10763",
                        "name": "HTN",
                        "description": ""
                    },
                    {
                        "id": "DOID:10763",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:10763",
                        "name": "hyperpiesia",
                        "description": ""
                    },
                    {
                        "id": "DOID:10763",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:10763",
                        "name": "vascular hypertensive disorder",
                        "description": ""
                    }
                ],
                "unlinked_id_list": [
                    "DOID:13731",
                    "DOID:11130"
                ],
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ]
            },
            {
                "disease_id": "DOID:13481",
                "recommended_name": {
                    "id": "DOID:13481",
                    "resource": "Disease Ontology",
                    "url": "https://disease-ontology.org/term/DOID:13481",
                    "name": "thanatophoric dysplasia",
                    "description": "An osteochondrodysplasia that results_in short arms and legs with excess folds of skin."
                },
                "synonyms": [
                    {
                        "id": "MONDO:0008546",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008546",
                        "name": "thanatophoric dysplasia type 1",
                        "description": "Thanatophoric dysplasia type 1 (TD1) is a form of TD characterized by short, bowed femurs, micromelia, narrow thorax, and brachydactyly."
                    },
                    {
                        "id": "MONDO:0008546",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008546",
                        "name": "TD1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008546",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008546",
                        "name": "thanatophoric dwarfism type 1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008546",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008546",
                        "name": "thanatophoric dysplasia, type 1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008546",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008546",
                        "name": "type 1 thanatophoric dysplasia",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008546",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008546",
                        "name": "PLSD San Diego type",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008546",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008546",
                        "name": "thanatophoric dwarfism 1",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008546",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008546",
                        "name": "thanatophoric dysplasia type I",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008546",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008546",
                        "name": "thanatophoric dysplasia, type I",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008547",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008547",
                        "name": "thanatophoric dysplasia type 2",
                        "description": "Thanatophoric dysplasia characterized by a cloverleaf-like skull and straight femurs."
                    },
                    {
                        "id": "MONDO:0008547",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008547",
                        "name": "TD2",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008547",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008547",
                        "name": "cloverleaf skull-micromelic bone dysplasia syndrome",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008547",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008547",
                        "name": "thanatophoric dwarfism type 2",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008547",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008547",
                        "name": "thanatophoric dwarfism-cloverleaf skull syndrome",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008547",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008547",
                        "name": "thanatophoric dysplasia, type 2",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008547",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008547",
                        "name": "type 2 thanatophoric dysplasia",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008547",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008547",
                        "name": "thanatophoric dwarfism - cloverleaf skull",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008547",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008547",
                        "name": "thanatophoric dysplasia type II",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0008547",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0008547",
                        "name": "thanatophoric dysplasia, type II",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0010114",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0010114",
                        "name": "thanatophoric dysplasia, Glasgow variant",
                        "description": ""
                    },
                    {
                        "id": "MONDO:0010114",
                        "resource": "MONDO",
                        "url": "https://monarchinitiative.org/disease/MONDO:0010114",
                        "name": "thanatophoric dysplasia, Glasgow variant",
                        "description": ""
                    },
                    {
                        "id": "MIM:187600",
                        "resource": "MIM",
                        "url": "https://www.omim.org/entry/187600",
                        "name": "Thanatophoric dysplasia 1",
                        "description": "Thanatophoric dysplasia 1"
                    },
                    {
                        "id": "MIM:187601",
                        "resource": "MIM",
                        "url": "https://www.omim.org/entry/187601",
                        "name": "Thanatophoric dysplasia 2",
                        "description": "Thanatophoric dysplasia 2"
                    }
                ],
                "unlinked_id_list": [],
                "evidence": [
                    {
                        "id": "13481",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13481"
                    }
                ]
            },
            {
                "disease_id": "DOID:2256",
                "recommended_name": {
                    "id": "DOID:2256",
                    "resource": "Disease Ontology",
                    "url": "https://disease-ontology.org/term/DOID:2256",
                    "name": "osteochondrodysplasia",
                    "description": "A bone development disease that results_in defective development of cartilage or bone."
                },
                "synonyms": [
                    {
                        "id": "DOID:2256",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:2256",
                        "name": "Cartilage Development disorder",
                        "description": ""
                    },
                    {
                        "id": "DOID:2256",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:2256",
                        "name": "Congenital anomaly of cartilage",
                        "description": ""
                    },
                    {
                        "id": "DOID:2256",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:2256",
                        "name": "Osteochondrodysplasia syndrome",
                        "description": ""
                    },
                    {
                        "id": "DOID:2256",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:2256",
                        "name": "chondrodystrophy",
                        "description": ""
                    },
                    {
                        "id": "DOID:2256",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:2256",
                        "name": "skeletal dysplasia",
                        "description": ""
                    }
                ],
                "unlinked_id_list": [
                    "DOID:0112284",
                    "DOID:0070305",
                    "DOID:0080049",
                    "DOID:0080942",
                    "DOID:0112280"
                ],
                "evidence": [
                    {
                        "id": "2256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2256"
                    }
                ]
            },
            {
                "disease_id": "DOID:3407",
                "recommended_name": {
                    "id": "DOID:3407",
                    "resource": "Disease Ontology",
                    "url": "https://disease-ontology.org/term/DOID:3407",
                    "name": "carotid artery disease",
                    "description": ""
                },
                "synonyms": [
                    {
                        "id": "DOID:3407",
                        "resource": "Disease Ontology",
                        "url": "https://disease-ontology.org/term/DOID:3407",
                        "name": "disorder of carotid artery",
                        "description": ""
                    }
                ],
                "unlinked_id_list": [],
                "evidence": [
                    {
                        "id": "3407",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3407"
                    }
                ]
            },
            {
                "disease_id": "DOID:4195",
                "recommended_name": {
                    "id": "DOID:4195",
                    "resource": "Disease Ontology",
                    "url": "https://disease-ontology.org/term/DOID:4195",
                    "name": "hyperglycemia",
                    "description": ""
                },
                "synonyms": [],
                "unlinked_id_list": [],
                "evidence": [
                    {
                        "id": "4195",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4195"
                    }
                ]
            }
        ],
        "snv": [],
        "mutagenesis": [
            {
                "start_pos": 4197,
                "end_pos": 4197,
                "sequence_org": "D",
                "sequence_mut": "I",
                "comment": "Abolishes BMP1-mediated cleavage of endorepellin.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P98160",
                        "url": "https://www.uniprot.org/uniprotkb/P98160"
                    },
                    {
                        "database": "PubMed",
                        "id": "15591058",
                        "url": "https://glygen.org/publication/PubMed/15591058"
                    }
                ]
            },
            {
                "start_pos": 4258,
                "end_pos": 4258,
                "sequence_org": "D",
                "sequence_mut": "A",
                "comment": "Retains proper folding. Reduced calcium ion binding.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P98160",
                        "url": "https://www.uniprot.org/uniprotkb/P98160"
                    },
                    {
                        "database": "PubMed",
                        "id": "15591058",
                        "url": "https://glygen.org/publication/PubMed/15591058"
                    }
                ]
            },
            {
                "start_pos": 4327,
                "end_pos": 4327,
                "sequence_org": "N",
                "sequence_mut": "A",
                "comment": "Retains proper folding. Reduced calcium ion binding.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P98160",
                        "url": "https://www.uniprot.org/uniprotkb/P98160"
                    },
                    {
                        "database": "PubMed",
                        "id": "15591058",
                        "url": "https://glygen.org/publication/PubMed/15591058"
                    }
                ]
            }
        ],
        "expression_tissue": [
            {
                "tissue": {
                    "name": "Adult mammalian kidney",
                    "namespace": "UBERON",
                    "id": "0000082",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0000082"
                },
                "score": "86.77",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Oral cavity",
                    "namespace": "UBERON",
                    "id": "0000167",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0000167"
                },
                "score": "85.24",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Stomach",
                    "namespace": "UBERON",
                    "id": "0000945",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0000945"
                },
                "score": "95.96",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Uterus",
                    "namespace": "UBERON",
                    "id": "0000995",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0000995"
                },
                "score": "97.31",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Esophagus",
                    "namespace": "UBERON",
                    "id": "0001043",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0001043"
                },
                "score": "98.83",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Rectum",
                    "namespace": "UBERON",
                    "id": "0001052",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0001052"
                },
                "score": "87.31",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Colon",
                    "namespace": "UBERON",
                    "id": "0001155",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0001155"
                },
                "score": "93.18",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Urinary bladder",
                    "namespace": "UBERON",
                    "id": "0001255",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0001255"
                },
                "score": "94.36",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Thyroid gland",
                    "namespace": "UBERON",
                    "id": "0002046",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0002046"
                },
                "score": "98.46",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Lung",
                    "namespace": "UBERON",
                    "id": "0002048",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0002048"
                },
                "score": "93.82",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Liver",
                    "namespace": "UBERON",
                    "id": "0002107",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0002107"
                },
                "score": "89.07",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Prostate gland",
                    "namespace": "UBERON",
                    "id": "0002367",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0002367"
                },
                "score": "98.15",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            },
            {
                "tissue": {
                    "name": "Thoracic mammary gland",
                    "namespace": "UBERON",
                    "id": "0005200",
                    "url": "http://purl.obolibrary.org/obo/UBERON_0005200"
                },
                "score": "96.31",
                "present": "HIGH",
                "evidence": [
                    {
                        "database": "Bgee",
                        "id": "ENSG00000142798",
                        "url": "https://bgee.org/?page=gene&gene_id=ENSG00000142798"
                    }
                ]
            }
        ],
        "expression_disease": [
            {
                "significant": "Yes",
                "trend": "down",
                "name": "Prostate cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:10283",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "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"
                            }
                        ]
                    }
                ]
            },
            {
                "significant": "No",
                "trend": "up",
                "name": "Stomach cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "disease": [
                    {
                        "disease_id": "DOID:10534",
                        "recommended_name": {
                            "id": "DOID:10534",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:10534",
                            "name": "stomach cancer",
                            "description": "A gastrointestinal system cancer that is located_in the stomach."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:10534",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10534",
                                "name": "gastric cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10534",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10534",
                                "name": "gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer",
                                "description": "A primary or metastatic malignant neoplasm involving the stomach."
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "Ca lesser curvature - stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "GC",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "cancer of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer risk after h. pylori infection",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "gastric cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant gastric tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant stomach neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of greater curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumor of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of greater curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of lesser curve of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant tumour of the stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "stomach cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "Ca body - stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "ca greater curvature of stomach",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001056",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                                "name": "malignant neoplasm of body of stomach",
                                "description": ""
                            },
                            {
                                "id": "MIM:613659",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/613659",
                                "name": "Gastric cancer",
                                "description": "Gastric cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10534",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10534"
                            },
                            {
                                "id": "10534",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10534"
                            }
                        ]
                    }
                ]
            },
            {
                "significant": "Yes",
                "trend": "down",
                "name": "Urinary bladder cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:11054",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "disease": [
                    {
                        "disease_id": "DOID:11054",
                        "recommended_name": {
                            "id": "DOID:11054",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:11054",
                            "name": "urinary bladder cancer",
                            "description": "An urinary system cancer that results_in malignant growth located_in the urinary bladder."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:11054",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:11054",
                                "name": "bladder cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:11054",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:11054",
                                "name": "tumor of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "urinary bladder cancer",
                                "description": "A primary or metastatic malignant neoplasm involving the bladder."
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "tumor of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "tumour of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "bladder cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "cancer of urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant bladder neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant bladder tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant bladder tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm of bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm of the urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm of urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm, bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant neoplasm, urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumor of bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumor of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumor of the urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumor of urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumor, urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumour of bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumour of the bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumour of the urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant tumour of urinary bladder",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant urinary bladder neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant urinary bladder tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "malignant urinary bladder tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "urinary bladder cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "urinary bladder malignant neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "urinary bladder malignant tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0001187",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                                "name": "urinary bladder malignant tumour",
                                "description": ""
                            },
                            {
                                "id": "MIM:109800",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/109800",
                                "name": "Bladder cancer",
                                "description": "Bladder cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "11054",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:11054"
                            }
                        ]
                    }
                ]
            },
            {
                "significant": "Yes",
                "trend": "up",
                "name": "Head and neck cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:11934",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "disease": [
                    {
                        "disease_id": "DOID:11934",
                        "recommended_name": {
                            "id": "DOID:11934",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:11934",
                            "name": "head and neck cancer",
                            "description": "An organ system cancer that arises in the head or neck region. This region includes the nasal cavity, sinuses, lips, mouth, salivary glands, throat, or larynx."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:11934",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:11934",
                                "name": "head and neck neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:11934",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:11934",
                                "name": "head and neck tumours",
                                "description": ""
                            },
                            {
                                "id": "DOID:11934",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:11934",
                                "name": "head/neck neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:11934",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:11934",
                                "name": "tumor of head and neck",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:1542"
                        ],
                        "evidence": [
                            {
                                "id": "11934",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:11934"
                            }
                        ]
                    }
                ]
            },
            {
                "significant": "Yes",
                "trend": "down",
                "name": "Lung cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:1324",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "disease": [
                    {
                        "disease_id": "DOID:1324",
                        "recommended_name": {
                            "id": "DOID:1324",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1324",
                            "name": "lung cancer",
                            "description": "A respiratory system cancer that is located_in the lung."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": "A malignant neoplasm involving the lung."
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "cancer of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, resistance to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung neoplasm",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "LNCR1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "LNCR3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "LNCR4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "LNCR5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MIM:211980",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/211980",
                                "name": "Lung cancer",
                                "description": "Lung cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4765"
                        ],
                        "evidence": [
                            {
                                "id": "1324",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1324"
                            }
                        ]
                    }
                ]
            },
            {
                "significant": "Yes",
                "trend": "down",
                "name": "Breast cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "disease": [
                    {
                        "disease_id": "DOID:1612",
                        "recommended_name": {
                            "id": "DOID:1612",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1612",
                            "name": "breast cancer",
                            "description": "An organ system cancer that originates in the mammary gland."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "breast tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "malignant neoplasm of breast",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "malignant tumor of the breast",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "mammary cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "mammary tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:1612",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1612",
                                "name": "primary breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "hereditary breast carcinoma",
                                "description": "Breast carcinoma that has developed in relatives of patients with history of breast carcinoma."
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer susceptibility, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, early-onset, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, invasive ductal, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, lobular, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, male, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "breast cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial breast carcinoma",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial cancer of breast",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "familial cancer of the breast",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "hereditary breast cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0016419",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                                "name": "hereditary breast carcinoma",
                                "description": ""
                            },
                            {
                                "id": "MIM:114480",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/114480",
                                "name": "Breast cancer",
                                "description": "Breast cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3017",
                            "DOID:0050938"
                        ],
                        "evidence": [
                            {
                                "id": "1612",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1612"
                            }
                        ]
                    }
                ]
            },
            {
                "significant": "Yes",
                "trend": "up",
                "name": "Thyroid cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:1781",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "disease": [
                    {
                        "disease_id": "DOID:1781",
                        "recommended_name": {
                            "id": "DOID:1781",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1781",
                            "name": "thyroid cancer",
                            "description": "An endocrine gland cancer located in the thyroid gland located in the neck below the thyroid cartilage."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:1781",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1781",
                                "name": "Thyroid gland neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1781",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1781",
                                "name": "malignant neoplasm of thyroid gland",
                                "description": ""
                            },
                            {
                                "id": "DOID:1781",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1781",
                                "name": "malignant tumour of thyroid gland",
                                "description": ""
                            },
                            {
                                "id": "DOID:1781",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1781",
                                "name": "neoplasm of thyroid gland",
                                "description": ""
                            },
                            {
                                "id": "DOID:1781",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1781",
                                "name": "thyroid neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:1781",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:1781",
                                "name": "thyroid gland cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3973",
                            "DOID:0080524",
                            "DOID:0080525"
                        ],
                        "evidence": [
                            {
                                "id": "1781",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1781"
                            }
                        ]
                    }
                ]
            },
            {
                "significant": "Yes",
                "trend": "up",
                "name": "Kidney cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:263",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "disease": [
                    {
                        "disease_id": "DOID:263",
                        "recommended_name": {
                            "id": "DOID:263",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:263",
                            "name": "kidney cancer",
                            "description": "A urinary system cancer that is located_in the kidney."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:263",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:263",
                                "name": "malignant neoplasm of kidney except pelvis",
                                "description": ""
                            },
                            {
                                "id": "DOID:263",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:263",
                                "name": "malignant tumour of kidney",
                                "description": ""
                            },
                            {
                                "id": "DOID:263",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:263",
                                "name": "renal cancer",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:3675",
                            "DOID:4455"
                        ],
                        "evidence": [
                            {
                                "id": "263",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:263"
                            }
                        ]
                    }
                ]
            },
            {
                "significant": "Yes",
                "trend": "up",
                "name": "Liver cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:3571",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "disease": [
                    {
                        "disease_id": "DOID:3571",
                        "recommended_name": {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:3571",
                            "name": "liver cancer",
                            "description": "A hepatobiliary system cancer that is located_in the liver."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "Ca liver - primary",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "Resectable malignant neoplasm of Liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "hepatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "hepatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant hepato-biliary neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver, primary",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant tumor of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "non-resectable primary hepatic malignant neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "primary liver cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "primary malignant neoplasm of liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "resectable malignant neoplasm of the liver",
                                "description": ""
                            },
                            {
                                "id": "DOID:3571",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:3571",
                                "name": "malignant neoplasm of liver, not specified as primary or secondary",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "3571",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:3571"
                            }
                        ]
                    }
                ]
            },
            {
                "significant": "Yes",
                "trend": "down",
                "name": "Uterine cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:363",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "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"
                            }
                        ]
                    }
                ]
            },
            {
                "significant": "No",
                "trend": "down",
                "name": "Esophageal cancer [DO disease name]",
                "url": "https://disease-ontology.org/term/DOID:5041",
                "evidence": [
                    {
                        "database": "BioXpress",
                        "id": "P98160",
                        "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P98160"
                    }
                ],
                "disease": [
                    {
                        "disease_id": "DOID:5041",
                        "recommended_name": {
                            "id": "DOID:5041",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:5041",
                            "name": "esophageal cancer",
                            "description": "A gastrointestinal system cancer that is located_in the esophagus."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "Ca lower third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "Ca middle third oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "esophagus cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of distal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of lower third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of middle third of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of proximal third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant neoplasm of upper third esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of Distal Third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of Proximal Third of esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of abdominal esophagus",
                                "description": ""
                            },
                            {
                                "id": "DOID:5041",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:5041",
                                "name": "malignant tumor of the middle Third of the esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer",
                                "description": "A primary or metastatic malignant neoplasm involving the esophagus."
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "cancer of esophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "cancer of oesophagus",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007576",
                                "name": "esophageal cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
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                                "description": ""
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                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
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                                "name": "esophageal squamous cell carcinoma, somatic",
                                "description": ""
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                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
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                                "description": ""
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                            {
                                "id": "MONDO:0007576",
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                            {
                                "id": "MONDO:0007576",
                                "resource": "MONDO",
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                                "name": "malignant esophageal tumor",
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                            },
                            {
                                "id": "MONDO:0007576",
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                            {
                                "id": "MONDO:0007576",
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                            {
                                "id": "MONDO:0007576",
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                            {
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            {
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            {
                "id": "R-HSA-9694614",
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                "database": "Reactome",
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                "id": "R-HSA-975634",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-975634",
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                "id": "R-HSA-9769735",
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                "id": "R-HSA-9769739",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9769739",
                "database": "Reactome",
                "categories": [
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            {
                "id": "R-HSA-977225",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-977225",
                "database": "Reactome",
                "categories": [
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                "id": "R-HSA-9820960",
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            {
                "id": "R-HSA-9833110",
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                "database": "Reactome",
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                "id": "R-HSA-9913351",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9913351",
                "database": "Reactome",
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            {
                "id": "R-HSA-9918481",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9918481",
                "database": "Reactome",
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                "id": "NP_001278789",
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            },
            {
                "id": "GLY_000040",
                "url": "http://data.glygen.org/GLY_000040",
                "database": "UniCarbKB",
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            {
                "id": "A0A0U1RQT3",
                "url": "https://www.uniprot.org/uniprotkb/A0A0U1RQT3",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
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            {
                "id": "A0A0U1RQT3-1",
                "url": "https://www.uniprot.org/uniprotkb/A0A0U1RQT3-1",
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                "categories": [
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            },
            {
                "id": "A0A2R8YH07",
                "url": "https://www.uniprot.org/uniprotkb/A0A2R8YH07",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
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            },
            {
                "id": "A0A2R8YH07-1",
                "url": "https://www.uniprot.org/uniprotkb/A0A2R8YH07-1",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
                ]
            },
            {
                "id": "A0A3B3IT11",
                "url": "https://www.uniprot.org/uniprotkb/A0A3B3IT11",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
                ]
            },
            {
                "id": "A0A3B3IT11-1",
                "url": "https://www.uniprot.org/uniprotkb/A0A3B3IT11-1",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
                ]
            },
            {
                "id": "H0Y5A9",
                "url": "https://www.uniprot.org/uniprotkb/H0Y5A9",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
                ]
            },
            {
                "id": "H0Y5A9-1",
                "url": "https://www.uniprot.org/uniprotkb/H0Y5A9-1",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
                ]
            },
            {
                "id": "H7BYA5",
                "url": "https://www.uniprot.org/uniprotkb/H7BYA5",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
                ]
            },
            {
                "id": "H7BYA5-1",
                "url": "https://www.uniprot.org/uniprotkb/H7BYA5-1",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
                ]
            },
            {
                "id": "P98160",
                "url": "https://www.uniprot.org/uniprotkb/P98160",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
                ]
            },
            {
                "id": "P98160-1",
                "url": "https://www.uniprot.org/uniprotkb/P98160-1",
                "database": "UniProtKB",
                "categories": [
                    "Protein"
                ]
            }
        ],
        "sequence": {
            "sequence": "MGWRAAGALLLALLLHGRLLAVTHGLRAYDGLSLPEDIETVTASQMRWTHSYLSDDEDMLADSISGDDLGSGDLGSGDFQMVYFRALVNFTRSIEYSPQLEDAGSREFREVSEAVVDTLESEYLKIPGDQVVSVVFIKELDGWVFVELDVGSEGNADGAQIQEMLLRVISSGSVASYVTSPQGFQFRRLGTVPQFPRACTEAEFACHSYNECVALEYRCDRRPDCRDMSDELNCEEPVLGISPTFSLLVETTSLPPRPETTIMRQPPVTHAPQPLLPGSVRPLPCGPQEAACRNGHCIPRDYLCDGQEDCEDGSDELDCGPPPPCEPNEFPCGNGHCALKLWRCDGDFDCEDRTDEANCPTKRPEEVCGPTQFRCVSTNMCIPASFHCDEESDCPDRSDEFGCMPPQVVTPPRESIQASRGQTVTFTCVAIGVPTPIINWRLNWGHIPSHPRVTVTSEGGRGTLIIRDVKESDQGAYTCEAMNARGMVFGIPDGVLELVPQRGPCPDGHFYLEHSAACLPCFCFGITSVCQSTRRFRDQIRLRFDQPDDFKGVNVTMPAQPGTPPLSSTQLQIDPSLHEFQLVDLSRRFLVHDSFWALPEQFLGNKVDSYGGSLRYNVRYELARGMLEPVQRPDVVLMGAGYRLLSRGHTPTQPGALNQRQVQFSEEHWVHESGRPVQRAELLQVLQSLEAVLIQTVYNTKMASVGLSDIAMDTTVTHATSHGRAHSVEECRCPIGYSGLSCESCDAHFTRVPGGPYLGTCSGCNCNGHASSCDPVYGHCLNCQHNTEGPQCNKCKAGFFGDAMKATATSCRPCPCPYIDASRRFSDTCFLDTDGQATCDACAPGYTGRRCESCAPGYEGNPIQPGGKCRPVNQEIVRCDERGSMGTSGEACRCKNNVVGRLCNECADGSFHLSTRNPDGCLKCFCMGVSRHCTSSSWSRAQLHGASEEPGHFSLTNAASTHTTNEGIFSPTPGELGFSSFHRLLSGPYFWSLPSRFLGDKVTSYGGELRFTVTQRSQPGSTPLHGQPLVVLQGNNIILEHHVAQEPSPGQPSTFIVPFREQAWQRPDGQPATREHLLMALAGIDTLLIRASYAQQPAESRVSGISMDVAVPEETGQDPALEVEQCSCPPGYRGPSCQDCDTGYTRTPSGLYLGTCERCSCHGHSEACEPETGACQGCQHHTEGPRCEQCQPGYYGDAQRGTPQDCQLCPCYGDPAAGQAAHTCFLDTDGHPTCDACSPGHSGRHCERCAPGYYGNPSQGQPCQRDSQVPGPIGCNCDPQGSVSSQCDAAGQCQCKAQVEGLTCSHCRPHHFHLSASNPDGCLPCFCMGITQQCASSAYTRHLISTHFAPGDFQGFALVNPQRNSRLTGEFTVEPVPEGAQLSFGNFAQLGHESFYWQLPETYQGDKVAAYGGKLRYTLSYTAGPQGSPLSDPDVQITGNNIMLVASQPALQGPERRSYEIMFREEFWRRPDGQPATREHLLMALADLDELLIRATFSSVPLAASISAVSLEVAQPGPSNRPRALEVEECRCPPGYIGLSCQDCAPGYTRTGSGLYLGHCELCECNGHSDLCHPETGACSQCQHNAAGEFCELCAPGYYGDATAGTPEDCQPCACPLTNPENMFSRTCESLGAGGYRCTACEPGYTGQYCEQCGPGYVGNPSVQGGQCLPETNQAPLVVEVHPARSIVPQGGSHSLRCQVSGSPPHYFYWSREDGRPVPSGTQQRHQGSELHFPSVQPSDAGVYICTCRNLHQSNTSRAELLVTEAPSKPITVTVEEQRSQSVRPGADVTFICTAKSKSPAYTLVWTRLHNGKLPTRAMDFNGILTIRNVQLSDAGTYVCTGSNMFAMDQGTATLHVQASGTLSAPVVSIHPPQLTVQPGQLAEFRCSATGSPTPTLEWTGGPGGQLPAKAQIHGGILRLPAVEPTDQAQYLCRAHSSAGQQVARAVLHVHGGGGPRVQVSPERTQVHAGRTVRLYCRAAGVPSATITWRKEGGSLPPQARSERTDIATLLIPAITTADAGFYLCVATSPAGTAQARIQVVVLSASDASPPPVKIESSSPSVTEGQTLDLNCVVAGSAHAQVTWYRRGGSLPPHTQVHGSRLRLPQVSPADSGEYVCRVENGSGPKEASITVSVLHGTHSGPSYTPVPGSTRPIRIEPSSSHVAEGQTLDLNCVVPGQAHAQVTWHKRGGSLPARHQTHGSLLRLHQVTPADSGEYVCHVVGTSGPLEASVLVTIEASVIPGPIPPVRIESSSSTVAEGQTLDLSCVVAGQAHAQVTWYKRGGSLPARHQVRGSRLYIFQASPADAGQYVCRASNGMEASITVTVTGTQGANLAYPAGSTQPIRIEPSSSQVAEGQTLDLNCVVPGQSHAQVTWHKRGGSLPVRHQTHGSLLRLYQASPADSGEYVCRVLGSSVPLEASVLVTIEPAGSVPALGVTPTVRIESSSSQVAEGQTLDLNCLVAGQAHAQVTWHKRGGSLPARHQVHGSRLRLLQVTPADSGEYVCRVVGSSGTQEASVLVTIQQRLSGSHSQGVAYPVRIESSSASLANGHTLDLNCLVASQAPHTITWYKRGGSLPSRHQIVGSRLRIPQVTPADSGEYVCHVSNGAGSRETSLIVTIQGSGSSHVPSVSPPIRIESSSPTVVEGQTLDLNCVVARQPQAIITWYKRGGSLPSRHQTHGSHLRLHQMSVADSGEYVCRANNNIDALEASIVISVSPSAGSPSAPGSSMPIRIESSSSHVAEGETLDLNCVVPGQAHAQVTWHKRGGSLPSHHQTRGSRLRLHHVSPADSGEYVCRVMGSSGPLEASVLVTIEASGSSAVHVPAPGGAPPIRIEPSSSRVAEGQTLDLKCVVPGQAHAQVTWHKRGGNLPARHQVHGPLLRLNQVSPADSGEYSCQVTGSSGTLEASVLVTIEPSSPGPIPAPGLAQPIYIEASSSHVTEGQTLDLNCVVPGQAHAQVTWYKRGGSLPARHQTHGSQLRLHLVSPADSGEYVCRAASGPGPEQEASFTVTVPPSEGSSYRLRSPVISIDPPSSTVQQGQDASFKCLIHDGAAPISLEWKTRNQELEDNVHISPNGSIITIVGTRPSNHGTYRCVASNAYGVAQSVVNLSVHGPPTVSVLPEGPVWVKVGKAVTLECVSAGEPRSSARWTRISSTPAKLEQRTYGLMDSHAVLQISSAKPSDAGTYVCLAQNALGTAQKQVEVIVDTGAMAPGAPQVQAEEAELTVEAGHTATLRCSATGSPAPTIHWSKLRSPLPWQHRLEGDTLIIPRVAQQDSGQYICNATSPAGHAEATIILHVESPPYATTVPEHASVQAGETVQLQCLAHGTPPLTFQWSRVGSSLPGRATARNELLHFERAAPEDSGRYRCRVTNKVGSAEAFAQLLVQGPPGSLPATSIPAGSTPTVQVTPQLETKSIGASVEFHCAVPSDRGTQLRWFKEGGQLPPGHSVQDGVLRIQNLDQSCQGTYICQAHGPWGKAQASAQLVIQALPSVLINIRTSVQTVVVGHAVEFECLALGDPKPQVTWSKVGGHLRPGIVQSGGVVRIAHVELADAGQYRCTATNAAGTTQSHVLLLVQALPQISMPQEVRVPAGSAAVFPCIASGYPTPDISWSKLDGSLPPDSRLENNMLMLPSVRPQDAGTYVCTATNRQGKVKAFAHLQVPERVVPYFTQTPYSFLPLPTIKDAYRKFEIKITFRPDSADGMLLYNGQKRVPGSPTNLANRQPDFISFGLVGGRPEFRFDAGSGMATIRHPTPLALGHFHTVTLLRSLTQGSLIVGDLAPVNGTSQGKFQGLDLNEELYLGGYPDYGAIPKAGLSSGFIGCVRELRIQGEEIVFHDLNLTAHGISHCPTCRDRPCQNGGQCHDSESSSYVCVCPAGFTGSRCEHSQALHCHPEACGPDATCVNRPDGRGYTCRCHLGRSGLRCEEGVTVTTPSLSGAGSYLALPALTNTHHELRLDVEFKPLAPDGVLLFSGGKSGPVEDFVSLAMVGGHLEFRYELGSGLAVLRSAEPLALGRWHRVSAERLNKDGSLRVNGGRPVLRSSPGKSQGLNLHTLLYLGGVEPSVPLSPATNMSAHFRGCVGEVSVNGKRLDLTYSFLGSQGIGQCYDSSPCERQPCQHGATCMPAGEYEFQCLCRDGFKGDLCEHEENPCQLREPCLHGGTCQGTRCLCLPGFSGPRCQQGSGHGIAESDWHLEGSGGNDAPGQYGAYFHDDGFLAFPGHVFSRSLPEVPETIELEVRTSTASGLLLWQGVEVGEAGQGKDFISLGLQDGHLVFRYQLGSGEARLVSEDPINDGEWHRVTALREGRRGSIQVDGEELVSGRSPGPNVAVNAKGSVYIGGAPDVATLTGGRFSSGITGCVKNLVLHSARPGAPPPQPLDLQHRAQAGANTRPCPS",
            "length": 4391,
            "header": "sp|P98160-1|PGBM_HUMAN Isoform 1 of Basement membrane-specific heparan sulfate proteoglycan core protein  OS=Homo sapiens OX=9606 GN=HSPG2 PE=1 SV=4 CANONICAL=P98160-1"
        },
        "isoforms": [
            {
                "isoform_ac": "A0A0U1RQT3-1",
                "url": "https://www.uniprot.org/uniprotkb/A0A0U1RQT3/entry",
                "sequence": {
                    "sequence": "XNMLMLPSVRPQDAGTYVCTATNRQGKVKAFAHLQVPERVVPYFTQTPYSFLPLPTIKDAYRKFEIKITFRPDSADGLLLYSGMLLYNGQKRVPGSPTNLANRQPDFISFGLVGGRPEFRFDAGSGMATIRHPTPLALGHFHTVTLLRSLTQGSLIVGDLAPVNGTSQGKFQGLDLNEELYLGGYPDYGAIPKAGLSSGFIGCVRELRIQGEEIVFHDLNLTAHGISHCPTCRDRPCQNGGQCHDSESSSYVCVCPAGFTGSRCEHSQALHCHPEACGPDATCVNRPDGRGYTCRCHLGRSGLRCEE",
                    "length": 307,
                    "header": "tr|A0A0U1RQT3-1|A0A0U1RQT3_HUMAN Computationally mapped isoform of Heparan sulfate proteoglycan 2  OS=Homo sapiens OX=9606 GN=HSPG2 PE=1 SV=1 CANONICAL=P98160-1"
                },
                "locus": {
                    "chromosome": "1",
                    "start_pos": 21833577,
                    "end_pos": 21829993,
                    "strand": "+",
                    "evidence": [
                        {
                            "database": "Ensembl Transcript",
                            "id": "ENST00000635682.1",
                            "url": "https://www.ensembl.org/id/ENST00000635682.1"
                        },
                        {
                            "database": "Ensembl Peptide",
                            "id": "ENSP00000489161.1",
                            "url": "https://www.ensembl.org/id/ENSP00000489161.1"
                        }
                    ]
                }
            },
            {
                "isoform_ac": "A0A2R8YH07-1",
                "url": "https://www.uniprot.org/uniprotkb/A0A2R8YH07/entry",
                "sequence": {
                    "sequence": "ISTHFAPGDFQGFALVNPQRNSRLTGEFTVEPVPEGAQLSFGNFAQLGHESFYWQLPETYQGDKGEAYFARMRRAHQNRTSLSEEQLRAAVTAGRIPEPPEGRDWAQRASQVDEAQRRMDAEIWQLLSSFAAQPQPPPQGLSPHPQPAAALRAAPPPSSSSSSSSSSASLSFSPGSQFSLSYEGFSLLPGSLYYWQLPRAFLGDKVAAYGGKLRYTLSYTAGPQGSPLSDPDVQIT",
                    "length": 236,
                    "header": "tr|A0A2R8YH07-1|A0A2R8YH07_HUMAN Computationally mapped isoform of Heparan sulfate proteoglycan 2  OS=Homo sapiens OX=9606 GN=HSPG2 PE=1 SV=1 CANONICAL=P98160-1"
                },
                "locus": {
                    "chromosome": "1",
                    "start_pos": 21872377,
                    "end_pos": 21865717,
                    "strand": "+",
                    "evidence": [
                        {
                            "database": "Ensembl Transcript",
                            "id": "ENST00000644714.1",
                            "url": "https://www.ensembl.org/id/ENST00000644714.1"
                        },
                        {
                            "database": "Ensembl Peptide",
                            "id": "ENSP00000496473.1",
                            "url": "https://www.ensembl.org/id/ENSP00000496473.1"
                        }
                    ]
                }
            },
            {
                "isoform_ac": "A0A3B3IT11-1",
                "url": "https://www.uniprot.org/uniprotkb/A0A3B3IT11/entry",
                "sequence": {
                    "sequence": "XYFRALVNFTRSIEYSPQLEDAGSREFREVSEAVVDTLESEYLKIPGDQVVSVVFIKELDGWVFVELDVGSEGNADGAQIQEMLLRVISSGSVASYVTSPQGFQFRRLGTAQTPPPPPAAVAVAVTPVPQFPRACTEAEFACHSYNECVALEYRCDRRPDCRDMSDELNCEEPVLGISPTFSLLVETTSLPPRPETTIMRQPPVTHAPQPLLPGSVRPLPCGPQEAACRNGHCIPRDYLCDGQEDCEDGSDELDCGPPPPCEPNEFPCGNGHCALKLWRCDGDFDCED",
                    "length": 288,
                    "header": "tr|A0A3B3IT11-1|A0A3B3IT11_HUMAN Computationally mapped isoform of Heparan sulfate proteoglycan 2  OS=Homo sapiens OX=9606 GN=HSPG2 PE=1 SV=1 CANONICAL=P98160-1"
                },
                "locus": {
                    "chromosome": "1",
                    "start_pos": 21890694,
                    "end_pos": 21887236,
                    "strand": "+",
                    "evidence": [
                        {
                            "database": "Ensembl Transcript",
                            "id": "ENST00000374673.4",
                            "url": "https://www.ensembl.org/id/ENST00000374673.4"
                        },
                        {
                            "database": "Ensembl Peptide",
                            "id": "ENSP00000497688.1",
                            "url": "https://www.ensembl.org/id/ENSP00000497688.1"
                        }
                    ]
                }
            },
            {
                "isoform_ac": "H0Y5A9-1",
                "url": "https://www.uniprot.org/uniprotkb/H0Y5A9/entry",
                "sequence": {
                    "sequence": "XTPSGLYLGTCERCSCHGHSEACEPETGACQGCQHHTEGPRCEQCQPGYYGDAQRGTPQDCQLCPCYGDPAAGQAAHTCFLDTDGHPTCDACSPGHSGRHCERCAPGYYGNPSQGQPCQRDSQVPGPIGCNCDPQGSVSSQCDAAGQCQCKVSPNPCPCGACSAPLPRPCGEIRQHLVEAETWAWGAGHGGQGRGCP",
                    "length": 197,
                    "header": "tr|H0Y5A9-1|PGBM_HUMAN Computationally mapped isoform of Basement membrane-specific heparan sulfate proteoglycan core protein  OS=Homo sapiens OX=9606 GN=HSPG2 PE=1 SV=1 CANONICAL=P98160-1"
                },
                "locus": {
                    "chromosome": "1",
                    "start_pos": 21874706,
                    "end_pos": 21872859,
                    "strand": "+",
                    "evidence": [
                        {
                            "database": "Ensembl Transcript",
                            "id": "ENST00000427897.1",
                            "url": "https://www.ensembl.org/id/ENST00000427897.1"
                        },
                        {
                            "database": "Ensembl Peptide",
                            "id": "ENSP00000397573.1",
                            "url": "https://www.ensembl.org/id/ENSP00000397573.1"
                        }
                    ]
                }
            },
            {
                "isoform_ac": "H7BYA5-1",
                "url": "https://www.uniprot.org/uniprotkb/H7BYA5/entry",
                "sequence": {
                    "sequence": "XGTPPLTFQWSRVGSSLPGRATARNELLHFERAAPEDSGRYRCRVTNKVGSAEAFAQLLVQESRTWTRAAKGRIYARPMDLGGRPRPVPSWLSKVGGWLQASAKSREQR",
                    "length": 109,
                    "header": "tr|H7BYA5-1|H7BYA5_HUMAN Computationally mapped isoform of Heparan sulfate proteoglycan 2  OS=Homo sapiens OX=9606 GN=HSPG2 PE=1 SV=2 CANONICAL=P98160-1"
                },
                "locus": {
                    "chromosome": "1",
                    "start_pos": 21839006,
                    "end_pos": 21835493,
                    "strand": "+",
                    "evidence": [
                        {
                            "database": "Ensembl Transcript",
                            "id": "ENST00000374676.4",
                            "url": "https://www.ensembl.org/id/ENST00000374676.4"
                        },
                        {
                            "database": "Ensembl Peptide",
                            "id": "ENSP00000363808.5",
                            "url": "https://www.ensembl.org/id/ENSP00000363808.5"
                        }
                    ]
                }
            },
            {
                "isoform_ac": "P98160-1",
                "url": "https://www.uniprot.org/uniprotkb/P98160/entry#P98160-1",
                "sequence": {
                    "sequence": "MGWRAAGALLLALLLHGRLLAVTHGLRAYDGLSLPEDIETVTASQMRWTHSYLSDDEDMLADSISGDDLGSGDLGSGDFQMVYFRALVNFTRSIEYSPQLEDAGSREFREVSEAVVDTLESEYLKIPGDQVVSVVFIKELDGWVFVELDVGSEGNADGAQIQEMLLRVISSGSVASYVTSPQGFQFRRLGTVPQFPRACTEAEFACHSYNECVALEYRCDRRPDCRDMSDELNCEEPVLGISPTFSLLVETTSLPPRPETTIMRQPPVTHAPQPLLPGSVRPLPCGPQEAACRNGHCIPRDYLCDGQEDCEDGSDELDCGPPPPCEPNEFPCGNGHCALKLWRCDGDFDCEDRTDEANCPTKRPEEVCGPTQFRCVSTNMCIPASFHCDEESDCPDRSDEFGCMPPQVVTPPRESIQASRGQTVTFTCVAIGVPTPIINWRLNWGHIPSHPRVTVTSEGGRGTLIIRDVKESDQGAYTCEAMNARGMVFGIPDGVLELVPQRGPCPDGHFYLEHSAACLPCFCFGITSVCQSTRRFRDQIRLRFDQPDDFKGVNVTMPAQPGTPPLSSTQLQIDPSLHEFQLVDLSRRFLVHDSFWALPEQFLGNKVDSYGGSLRYNVRYELARGMLEPVQRPDVVLMGAGYRLLSRGHTPTQPGALNQRQVQFSEEHWVHESGRPVQRAELLQVLQSLEAVLIQTVYNTKMASVGLSDIAMDTTVTHATSHGRAHSVEECRCPIGYSGLSCESCDAHFTRVPGGPYLGTCSGCNCNGHASSCDPVYGHCLNCQHNTEGPQCNKCKAGFFGDAMKATATSCRPCPCPYIDASRRFSDTCFLDTDGQATCDACAPGYTGRRCESCAPGYEGNPIQPGGKCRPVNQEIVRCDERGSMGTSGEACRCKNNVVGRLCNECADGSFHLSTRNPDGCLKCFCMGVSRHCTSSSWSRAQLHGASEEPGHFSLTNAASTHTTNEGIFSPTPGELGFSSFHRLLSGPYFWSLPSRFLGDKVTSYGGELRFTVTQRSQPGSTPLHGQPLVVLQGNNIILEHHVAQEPSPGQPSTFIVPFREQAWQRPDGQPATREHLLMALAGIDTLLIRASYAQQPAESRVSGISMDVAVPEETGQDPALEVEQCSCPPGYRGPSCQDCDTGYTRTPSGLYLGTCERCSCHGHSEACEPETGACQGCQHHTEGPRCEQCQPGYYGDAQRGTPQDCQLCPCYGDPAAGQAAHTCFLDTDGHPTCDACSPGHSGRHCERCAPGYYGNPSQGQPCQRDSQVPGPIGCNCDPQGSVSSQCDAAGQCQCKAQVEGLTCSHCRPHHFHLSASNPDGCLPCFCMGITQQCASSAYTRHLISTHFAPGDFQGFALVNPQRNSRLTGEFTVEPVPEGAQLSFGNFAQLGHESFYWQLPETYQGDKVAAYGGKLRYTLSYTAGPQGSPLSDPDVQITGNNIMLVASQPALQGPERRSYEIMFREEFWRRPDGQPATREHLLMALADLDELLIRATFSSVPLAASISAVSLEVAQPGPSNRPRALEVEECRCPPGYIGLSCQDCAPGYTRTGSGLYLGHCELCECNGHSDLCHPETGACSQCQHNAAGEFCELCAPGYYGDATAGTPEDCQPCACPLTNPENMFSRTCESLGAGGYRCTACEPGYTGQYCEQCGPGYVGNPSVQGGQCLPETNQAPLVVEVHPARSIVPQGGSHSLRCQVSGSPPHYFYWSREDGRPVPSGTQQRHQGSELHFPSVQPSDAGVYICTCRNLHQSNTSRAELLVTEAPSKPITVTVEEQRSQSVRPGADVTFICTAKSKSPAYTLVWTRLHNGKLPTRAMDFNGILTIRNVQLSDAGTYVCTGSNMFAMDQGTATLHVQASGTLSAPVVSIHPPQLTVQPGQLAEFRCSATGSPTPTLEWTGGPGGQLPAKAQIHGGILRLPAVEPTDQAQYLCRAHSSAGQQVARAVLHVHGGGGPRVQVSPERTQVHAGRTVRLYCRAAGVPSATITWRKEGGSLPPQARSERTDIATLLIPAITTADAGFYLCVATSPAGTAQARIQVVVLSASDASPPPVKIESSSPSVTEGQTLDLNCVVAGSAHAQVTWYRRGGSLPPHTQVHGSRLRLPQVSPADSGEYVCRVENGSGPKEASITVSVLHGTHSGPSYTPVPGSTRPIRIEPSSSHVAEGQTLDLNCVVPGQAHAQVTWHKRGGSLPARHQTHGSLLRLHQVTPADSGEYVCHVVGTSGPLEASVLVTIEASVIPGPIPPVRIESSSSTVAEGQTLDLSCVVAGQAHAQVTWYKRGGSLPARHQVRGSRLYIFQASPADAGQYVCRASNGMEASITVTVTGTQGANLAYPAGSTQPIRIEPSSSQVAEGQTLDLNCVVPGQSHAQVTWHKRGGSLPVRHQTHGSLLRLYQASPADSGEYVCRVLGSSVPLEASVLVTIEPAGSVPALGVTPTVRIESSSSQVAEGQTLDLNCLVAGQAHAQVTWHKRGGSLPARHQVHGSRLRLLQVTPADSGEYVCRVVGSSGTQEASVLVTIQQRLSGSHSQGVAYPVRIESSSASLANGHTLDLNCLVASQAPHTITWYKRGGSLPSRHQIVGSRLRIPQVTPADSGEYVCHVSNGAGSRETSLIVTIQGSGSSHVPSVSPPIRIESSSPTVVEGQTLDLNCVVARQPQAIITWYKRGGSLPSRHQTHGSHLRLHQMSVADSGEYVCRANNNIDALEASIVISVSPSAGSPSAPGSSMPIRIESSSSHVAEGETLDLNCVVPGQAHAQVTWHKRGGSLPSHHQTRGSRLRLHHVSPADSGEYVCRVMGSSGPLEASVLVTIEASGSSAVHVPAPGGAPPIRIEPSSSRVAEGQTLDLKCVVPGQAHAQVTWHKRGGNLPARHQVHGPLLRLNQVSPADSGEYSCQVTGSSGTLEASVLVTIEPSSPGPIPAPGLAQPIYIEASSSHVTEGQTLDLNCVVPGQAHAQVTWYKRGGSLPARHQTHGSQLRLHLVSPADSGEYVCRAASGPGPEQEASFTVTVPPSEGSSYRLRSPVISIDPPSSTVQQGQDASFKCLIHDGAAPISLEWKTRNQELEDNVHISPNGSIITIVGTRPSNHGTYRCVASNAYGVAQSVVNLSVHGPPTVSVLPEGPVWVKVGKAVTLECVSAGEPRSSARWTRISSTPAKLEQRTYGLMDSHAVLQISSAKPSDAGTYVCLAQNALGTAQKQVEVIVDTGAMAPGAPQVQAEEAELTVEAGHTATLRCSATGSPAPTIHWSKLRSPLPWQHRLEGDTLIIPRVAQQDSGQYICNATSPAGHAEATIILHVESPPYATTVPEHASVQAGETVQLQCLAHGTPPLTFQWSRVGSSLPGRATARNELLHFERAAPEDSGRYRCRVTNKVGSAEAFAQLLVQGPPGSLPATSIPAGSTPTVQVTPQLETKSIGASVEFHCAVPSDRGTQLRWFKEGGQLPPGHSVQDGVLRIQNLDQSCQGTYICQAHGPWGKAQASAQLVIQALPSVLINIRTSVQTVVVGHAVEFECLALGDPKPQVTWSKVGGHLRPGIVQSGGVVRIAHVELADAGQYRCTATNAAGTTQSHVLLLVQALPQISMPQEVRVPAGSAAVFPCIASGYPTPDISWSKLDGSLPPDSRLENNMLMLPSVRPQDAGTYVCTATNRQGKVKAFAHLQVPERVVPYFTQTPYSFLPLPTIKDAYRKFEIKITFRPDSADGMLLYNGQKRVPGSPTNLANRQPDFISFGLVGGRPEFRFDAGSGMATIRHPTPLALGHFHTVTLLRSLTQGSLIVGDLAPVNGTSQGKFQGLDLNEELYLGGYPDYGAIPKAGLSSGFIGCVRELRIQGEEIVFHDLNLTAHGISHCPTCRDRPCQNGGQCHDSESSSYVCVCPAGFTGSRCEHSQALHCHPEACGPDATCVNRPDGRGYTCRCHLGRSGLRCEEGVTVTTPSLSGAGSYLALPALTNTHHELRLDVEFKPLAPDGVLLFSGGKSGPVEDFVSLAMVGGHLEFRYELGSGLAVLRSAEPLALGRWHRVSAERLNKDGSLRVNGGRPVLRSSPGKSQGLNLHTLLYLGGVEPSVPLSPATNMSAHFRGCVGEVSVNGKRLDLTYSFLGSQGIGQCYDSSPCERQPCQHGATCMPAGEYEFQCLCRDGFKGDLCEHEENPCQLREPCLHGGTCQGTRCLCLPGFSGPRCQQGSGHGIAESDWHLEGSGGNDAPGQYGAYFHDDGFLAFPGHVFSRSLPEVPETIELEVRTSTASGLLLWQGVEVGEAGQGKDFISLGLQDGHLVFRYQLGSGEARLVSEDPINDGEWHRVTALREGRRGSIQVDGEELVSGRSPGPNVAVNAKGSVYIGGAPDVATLTGGRFSSGITGCVKNLVLHSARPGAPPPQPLDLQHRAQAGANTRPCPS",
                    "length": 4391,
                    "header": "sp|P98160-1|PGBM_HUMAN Isoform 1 of Basement membrane-specific heparan sulfate proteoglycan core protein  OS=Homo sapiens OX=9606 GN=HSPG2 PE=1 SV=4 CANONICAL=P98160-1"
                },
                "locus": {
                    "chromosome": "1",
                    "start_pos": 21937217,
                    "end_pos": 21823319,
                    "strand": "+",
                    "evidence": [
                        {
                            "database": "Ensembl Transcript",
                            "id": "ENST00000374695.8",
                            "url": "https://www.ensembl.org/id/ENST00000374695.8"
                        },
                        {
                            "database": "Ensembl Peptide",
                            "id": "ENSP00000363827.3",
                            "url": "https://www.ensembl.org/id/ENSP00000363827.3"
                        }
                    ]
                }
            }
        ],
        "glycosylation": [
            {
                "glytoucan_ac": "G43417UB",
                "type": "O-linked",
                "subtype": "other",
                "prediction_tool_list": [],
                "site_category": "reported_with_glycan",
                "site_category_dict": {
                    "reported_with_glycan": true
                },
                "site_seq": "T",
                "relation": "attached",
                "comment": "",
                "icn3d_view": {},
                "start_pos": 1145,
                "start_aa": "Thr",
                "end_pos": 1145,
                "end_aa": "Thr",
                "residue": "Thr",
                "site_lbl": "Thr1145",
                "evidence": [
                    {
                        "id": "30459171",
                        "database": "PubMed",
                        "url": "https://glygen.org/publication/PubMed/30459171"
                    },
                    {
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            {
                "id": "R-HSA-975634",
                "name": "",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-975634",
                "resource": "Reactome",
                "description": "Retinoid metabolism and transport"
            },
            {
                "id": "R-HSA-9769735",
                "name": "",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9769735",
                "resource": "Reactome",
                "description": "Initiation of coagulation cascade"
            },
            {
                "id": "R-HSA-9769739",
                "name": "",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9769739",
                "resource": "Reactome",
                "description": "Regulation of clotting cascade"
            },
            {
                "id": "R-HSA-977225",
                "name": "",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-977225",
                "resource": "Reactome",
                "description": "Amyloid fiber formation"
            },
            {
                "id": "R-HSA-9820960",
                "name": "",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9820960",
                "resource": "Reactome",
                "description": "Respiratory syncytial virus (RSV) attachment and entry"
            },
            {
                "id": "R-HSA-9833110",
                "name": "",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9833110",
                "resource": "Reactome",
                "description": "RSV-host interactions"
            },
            {
                "id": "R-HSA-9856532",
                "name": "",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9856532",
                "resource": "Reactome",
                "description": "Mechanical load activates signaling by PIEZO1 and integrins in osteocytes"
            },
            {
                "id": "R-HSA-9913351",
                "name": "",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9913351",
                "resource": "Reactome",
                "description": "Formation of the dystrophin-glycoprotein complex (DGC)"
            },
            {
                "id": "R-HSA-9918481",
                "name": "",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9918481",
                "resource": "Reactome",
                "description": "Dengue Virus-Host Interactions"
            },
            {
                "id": "R-HSA-9918485",
                "name": "",
                "url": "https://www.reactome.org/PathwayBrowser/#R-HSA-9918485",
                "resource": "Reactome",
                "description": "Dengue Virus Attachment and Entry"
            }
        ],
        "orthologs": [
            {
                "uniprot_canonical_ac": "A0A8I6ASH2-1",
                "protein_name": "Basement membrane-specific heparan sulfate proteoglycan core protein",
                "gene_name": "Hspg2",
                "tax_id": 10116,
                "organism": "Rattus norvegicus",
                "sequence": {
                    "sequence": "MGQRAVGSLLLGLLLHARLLAVTQGLRAYDGLSLPEDTETVTASRYGWTYSYLSDDEDLLADDASGDGLGSGDLGSGDFQMVYFRALVNFTRSIEYSPQLEDANAKEFREVSEAVVEKLETEYVKIPGDQIVSVVFIKELDGWVFVELDVGSEGNADGSQIQEVLHTVVSSGSIGPYVTSPWGFKFRRLGTVPQFPRVCTETEFACHSYNECVALEYRCDRRPDCRDMSDELNCEEAVSEISSLPSAVVKVSPLPLWPEAATLPPPVMHGPQFLLPNVPGPTACGPQEASCHSGHCIPRDYLCDGQEDCRDGSDELGCGPPPPCEPNEFSCENGHCALKLWRCDGDFDCEDHTDEANCPVKHPGEVCGPTQFQCVSTNRCIPASFHCDEETDCPDRSDEFGCMPPQVVTPPQQSIQASRGQTVTFTCVATGVPTPIINWRLNWGHIPVNPRVTMTSEGGRGTLIIRDVKEADQGAYTCEAMNSRGMVFGIPDGVLELVPQRGPCPDGHFYLEDSASCLPCFCFGVTNLCQSSRRFRDQIRLNFDQPSDFKGVNVTMPSQPGVPPLSSTQLQIDPTLQEFQLVDLSRRFLVHDAFWALPKQFLGNKVDSYGGFLRYKVRYELARGMLEPVQKPDVILVGAGYRLHSRGHTPTHPGALNQRQVQLSEEHWVHESGRPVQRAEMLQALASLEAVLLQTVYNTKMTSVGLSDIVMDTTVTYTTIHGRAHSVEECRCPIGYSGLSCESCDAHFTRVPGGPYLGTCSGCNCNGHASSCDPVYGHCLNCQHNTEGPQCDKCKPGFFGDATKATATACRPCPCPYIDASQRFSDTCFLDTDGQATCDACAPGYTGRRCESCAPGYEGNPIQPGGKCRPSNQELVRCDERGSLSATGEACRCKNNVVGRSCNECSEGSFHLSKQNPDGCLKCFCMGVSRQCSSSSWSRAQVLGASVQPSQFTLTNAAGTHTTSEGVSSPAPGELLFSSFHNLLSEPYFWSLPASFRGDKVTSYGGELRFTVTQRPRPGSAPLHRQPLVVLQGNNIVLEHHASREPSPGQPSNFIVPFQEQVWQRPDGQPATREHLLMALAGIDALLIQASHTQQPAESRLSGISMDVAVPENTGQDPAREVEHCTCPPGYRGPSCQDCDTGYTRVASGLYLGTCERCNCHGHSETCEPETGACQSCQHHTEGASCEQCQPGYYGDPQRGTPQDCQPCPCYGTPAAGQASHTCFLDTDGHPTCDSCSPGHSGRHCERCAPGYHGNPSQGQPCHRDGQVPEVPGCDCDPHGSISSQCDATGQCQCKAQVEGRTCSHCRPHHFHLSASNPEGCLPCFCMGVTQQCTSSSYSRQLISTHFAPGDFQGFALVNPQRNSQLTGGFTVEPVPDGARLSFSNFAHLGQESFYWQLPETYQGDKVAAYGGKLRYTLSYTSGPQGSPLSDPDIQITGNNIMLVASQPALQGPERRSYEIIFREEFWRRPDGQPATREHLLMALADLDELLVRATFSSVPRAASISAVSLEVAQPGPSGGPQALEVEECRCPPGYVGLSCQDCAPGYTRTGSGLYLGQCELCECNGHSEVCHPETGACTGCQHNTVGEFCETCATGYYGDATAGTPEDCQPCACPLTNPENMFSRTCESLGAGGYRCTACEPGYTGQYCEQCAPGYEGNPNVQGGRCQPLTKESLEVQIHPSRSVVPQGGPHSLRCQVNGSPPHYFYWSREDGRPLPSGAQQRHQGSELHFPSVQPSDAGVYICTCRNLIHTSNSRAELLVAEAPSKPITVTVEEQRSQSVRPGADVTFICTAKSKSPAYTLVWTRLHNGKLPSRAMDFNGILTIRNVQPSDAGTYVCTGSNMFAMDQGTATLHVQVSGTSTAPVASIHPPQLTVQPGQLAEFRCSATGNPTPTLEWIGGPSGQLPTKAQIHNGILRLPAIEPSDQGQYLCRALSSAGQHVVRAMLQVHGGSGPRVQVSPERTQVHEGRTVRLYCRAAGVPSASITWRKEGGSLPPQARSENTDIPTLLIPAIRVADSGFYLCVATSPTGTAQARIQVVVLSASGASSVPVRIESSSPSVTEGQTLDLNCAVMGLTYTQVTWYKRGGSLPPHAQVHGSRLRLPQVSPADSGEYVCRVESDLGPKEASIVVSVLHSPHSGPSYTPATSSTPPIRIESSSSHVAEGQTLDLNCVVPGQAQVTWRKRGGSLPARHQTHGSLLRLHQVSPADSGEYVCHVLLGSEHIETSVLVAIEPAVSIPAPGPVPPVRIESSSPTVAEGQTLDLNCVVAGQAHAQVTWYKRGSSLPARHQVRGSRLYIFQASPADAGEYVCRAGNGQEATITVKVTGNQGANIAYPPGSTPTIRIESSSSHVAEGQTLDLNCVVQGQAHAQVTWHKRGGSLPARHQTHGSLLRLHQVSPVDSGEYVCRVEGGPVPLESSVLVAIEPAGSVPALGVTPPVRIESSSSHVSEGQSLDLNCLVAGQTHPQISWHKRGGSLPARHQVHGSRLRLLQVTPADSGEYVCRVVSGSGTHEASVLVTIQQHLSPSHPQSVVHPVRIESSSPSLANGHTLDLNCLVASLTPHTITWYKRGGSLPSRHQIVGSRLRIPQVTPADSGEYVCHVSNGVGSQETSLIVTIESRGPSHVPSVSPPMRIETSSPTVTEGQTLDLNCVVVGRPQATITWYKRGGSLPFRHQAHGSRLRLHQMSVADSGEYVCRANNNIDAQETSIMISVSPNTNAPSASASPVPIRIESSSSHVAEGQTLDLNCVVPGQAHAQVTWHKRGGSLPAHHQAHGSRLRLYQVSPADSGEYVCRVLSSSGPLEASVLVSITASASNVHVPGENPFPPIRIETSSSQVAEGQTLDLTCVVPGQAHAQVTWHKRGGSLPAGHQVHGHILRLNRVSPADSGEYSCQVTGSSGTLEASVLVTIEASQPSPIPAPGLAQPIYIESSSSHLAEGQTVDLNCVVPGQAHAQVTWHKRGSSLPARHQTHGSLLRLYHISPADSGEYVCQVAGSSHPEHEASFKITVPASEGSSYRLRSPVISIEPPSSTVQQGQDASFKCLIHEGATPISLEWKTRNQELEDNVHISPNGSIMTIVGARPSNHGAYRCVASNVYGVAQSVVNLIVHGPPTVSVLPEGPVHVKMGKDITLECVSSGEPRSSPRWTRLGIPVKLEPRMFGLMNSHAMLKIASVKPSDAGTYVCQAQNALGTAQKQVELIVDTGTVAPGAPQVQVEEAELTLEAGHTATLHCSATGNPPPTIHWSKLRAPLPWQHRIEGNTLVIPRVAQQDSGQYICNATNSAGHTEATVVLHVESHPYATIIPEHTSVQPGKLVQLQCLAHGTPPLTYQWSRVGGILPEKAVARNQLLRLEPAGRADSGRYRCQVSNKVGSAEAFAQVLVQGSSGDVPDTSTPVGSTPTVQVTPQQETKSIGASVEFHCAVPNEHGTHLRWLKEGGQLPPGHSVQDGVLRIQNLDQSCQGTYICQAHGPWGQAQATAQLIVQALPSVLINVRTSVHSVVVGHSVEFECLALGDPKPQVTWSKVGGRLRSGIVQSGSVIRIAHVELADAGQYRCAATNAAGTTQSHVLLLVQALPQISTPPEVRVPAGSAAVFPCMASGYPTPAITWSKVDGDLPPDSRLENNMLMLPSVRPEDAGTYVCTATNRQGKVKAFAYLQVPERVVPYFTQTPYSFLPLPTIKDAYRKFEIKITFRPDSADGMLLYNGQKHTPGSPTNLANRQPDFISFGLVGGRPEFRFDAGSGMATIRHPTPLALGQFHTVTLLRSLTQGSMIVGNLAPVNGTSQGKFQGLDLNEELYLGGYPDYRAIPKAGLSSGFVGCVRELRIQGEEIVFHDVNLTTHGISHCPTCQDRPCQNGGQCHDSESSSYTCVCPAGFTGSRCEHSQALHCHPEACGPDATCVNRPDGRGYNCRCHLGRSGMRCEEGVTVTTPSMSGAGSYLVLPALTNTHHELRLDVEFKPLEPDGILLFSGGKSGPVEDFVSLAMVGGHLEFRYELGSGLAVLRSLEPLALGRWHRVSAERLNKDGSLQVDGGRPVLRSSPGKSQGLNLHTLLYLGGVEPSVQLSPATNMSAHFRGCVGEVSVNGKRLDLTYSFLGSRGVGQCYDSSPCERQPCRNGATCMPAGEYEFQCLCQDGFKGDLCEHEENPCQLQEPCLNGGTCRGTRCLCLPGFSGPRCQQGAGYGVVESDWHPEGSGGNDAPGQYGAYFHDNGFLALPGNSFSRSLPEVPETIEFEVRTSTANGLLLWQGVVKESSRSKDFISLGLQDGHLVFNYQLGSGEARLVSEDPINDGEWHRVTALREGQRGSIQVDGEELVIGRSPGPNVAVNTKDIIYIGGAPDVATLTRGKFSSGITGCLKNLVLHSARPGAPPPQPLDLQHRAQAGANTRPCPS",
                    "length": 4387
                },
                "evidence": [
                    {
                        "id": "HGNC:5273",
                        "url": "https://alliancegenome.org/gene/HGNC:5273#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "ZFIN:ZDB-GENE-080807-4",
                        "url": "https://alliancegenome.org/gene/ZFIN:ZDB-GENE-080807-4#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "MGI:96257",
                        "url": "https://alliancegenome.org/gene/MGI:96257#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "RGD:621770",
                        "url": "https://alliancegenome.org/gene/RGD:621770#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "FB:FBgn0284408",
                        "url": "https://alliancegenome.org/gene/FB:FBgn0284408#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "P98160",
                        "url": "https://omabrowser.org/oma/group/P98160/",
                        "database": "OMA"
                    }
                ],
                "glygen_name": "Rat",
                "common_name": "Rat"
            },
            {
                "uniprot_canonical_ac": "A0A8M9PWV8-1",
                "protein_name": "Basement membrane-specific heparan sulfate proteoglycan core protein isoform X1",
                "gene_name": "hspg2",
                "tax_id": 7955,
                "organism": "Danio rerio",
                "sequence": {
                    "sequence": "MGARIRAHKFTLFILPLVFTSHLFNVALSSKVWDEVPFPEDLEEENEQLGDYVDDEGYDPSGDISGEEDGSTPEPSSTDPGPTVTIYYRALVNFTNSFQYVPELDDIYSNAFNEISSAVVDTLESDYNRIPGQQTVNVVLIKKIGKDVFVELDVGSDNNSNETQIREVLFSVVKEGTIASYDTSVVGFQFRRLGEADTLPPVESIFISVKPSPRECTSNEFSCQDGLACIPREYVCDKRPDCNDLSDEIDCGVGVAPLRPTQPTPPRPRPPPGPGPCRADQATCQNGQCISREYLCDGESDCTDGSDESRCGTPSPCEPNEFKCQNGRCALKLWRCDGDNDCQDNSDEMNCPTKRPGAACAPEQFVCLSDRKCIPASYQCDEEPDCADRSDEFGCAPPTVTVSPEESITASRGDTVTFTCSAIGVPVPIITWRLNWGHIPANNRITMISENGQGTLTIRDVKEGDQGAYTCEAINAKGLVFAIPDGVLSLSQKPNPVVSSSPFILAGNCRDGHFSVGGHCMPCFCFGITKKCQSTGRYRNQITLRFTEEEDFKGVNVSFPSRPGLPQPLSSTQMLINPETEEFQLVDLSRRFLDQDSFWSLPRQFLGNKVDSYGGYLKFKVSYSLQRGGSEPKVRPDVVLTGSGQKFIYRRGEPTFPDTFNSREIRFTEENWEHSNGRAVTRDDLMMTLANLESIHIRTIYDNRMASVGLSDISMDTTTKEFSQHGNPREVEECRCPAGYSGLSCESCSPGFERVPGPYLGICAGCNCNGHASACDPVSGHCLSCQHKTEGAQCEKCKPGFFGDPSRGQYDDCKPCPCPYTETSRRFSDTCFLDHDNQATCDACREGYTGRRCEKCAPGYVGNPLQPNGKCIPAASPISKCDNRGTINPISKPCYCKSNVAGALCDECKTGAFHLTADNPEGCLQCFCMGVTKQCASSTWSRDQVRGGVNGQLFTLSNAANTRTISEGITQRGSTEVVYRSFTNIHNDIFYWVLPQNFRGDKVTAYGGELKYRVRYEPHARSMVIDGQPDVVLQGSGIFLEHYSQIKPLPRVPATITVTFRESAWRRADGQPCTREHLLMALADINVFMIRATYADNMAETSLSNIQMDIAVPHSTGNERAMEVEECACPQGYSGPSCQDCDVGYTRTPGLYLGTCEKCECHGHASSCDSETGDCLNCLHNTIGRRCENCISGYYGNPKTGDPQACRPCPCLGQTSNQPSSCYLGSDGQPVCECPAGYTGRRCERCAPGYIGNPQLGQRCTPGSNNGDCYRCDQSGSEGCSGTGVCRCKMNVEGPTCSSCKQGTFHLSPANKDGCLSCFCMGVTQQCTSSRHYRDVVSTMFSPGNYQGFALVNRQRTNRIDNGFSVELSTEGTQLSYTNFNYLGQEPHYWQLPKAYQGDKKASSARTRRANQYPADEARKLDDEIWEIITNFSNGQSSFPFSSSSQSSHSSSFEAQNSLSLSSVRDPSFHSGLTSPLKASESHSSDPAHSSHPDSTQQVEQEKNIIGVVRGPRPVPSNKYVLVYNGFSLHPDDVLFWQLPEPFKGEKVGAYGGKLKYTISYVPGPRGSPIEDADVQIIGNDITLVARQIWQRGHGARESQDFEIVFREEHWQRPDGMPATREHLMMVLADLDDILIRASYHTEMRSSSISGVHMDVAVPEYTSLAQALEVEQCQCPPGYSGLSCQDCASGYTRTGGGLYLGHCEPCECNGHSDTCHPETGICTNCQHNTKGELCEQCVDGFFGDPTAGTPEDCQPCACPGTDPENQFSRTCESLGNGGYQCTACQPGYLGQYCERCAPGYVGNPQARVPCRSDAAFLVVKVYPERVQVAQGLPVTLRCQVSGSPPHYFQWSREDGRPISSSAERRRQGEELHFPGIQSNDAGVYICTCRDQRSSNRSKAEIVVATLPSKPIEVFIEEPKAQSVRVGSTVSFICTAKSKLPAYTLVWTRKGNGKLPNRAMDFNGILTIQNVQPEDAGIYVCTGSNMLGMDEGSAVLYVPEASQSQMFYTAYEMFEGHRKPAEGVQPVATLSPPVQTVKEGDVAQFRCTVTGNPTPAVEWIGGSGKRISSKAVIRNGQLTISSVDRSDEGEYICKALNTHGEHTARGVLHVQSTGQPNGLPHVQVSPQRVEIYEGETLRLYCRAIGSPTPSLKWNKRGGSLPPQAIPSHGFHQFKSNSLDVLQRRIEELQARMDRTDIGTLVVPNIRLSDAGTYLCVGTNAAGSSEAHIDVSVTKGENILSGVIIQPPSASVIEGEALDLNCLVPGTSTGSVKWSRAGGLLSSNHQVLETRLRILRASADDTGDYICTVENGPSPQKATVSVSVTSSASLGLQTPIISIEPHSAVVKQGESASFRCKVHNGAQPVRLEWKLTNNLPLPDNVKVGPDSSIMTVTNAQAKNQGTYRCVASNLYGMTHSIVSLIVRESPKAVVTPAGPVRVRVGDPINLECQAAGEPRPSVRWHRLDNNRKTMLSSTVPVDSSAIIQVLVARPEDSGTYVCSAQNNQGTTETRVEVFVEGGPQVPTVPRASVREPMIIVVEGSTATLHCDAHGFPKPTITWFKERSSLPWRHKIVDNSLILPNVGRQDSGQYVCNATNHLGTSEVTIMLEVDTPPYATSLPNDVSVRVGEVIRLQCLAHGTPPLRYEWTKINGSLPSTAQLQGGDLQINLAKENDAGTYRCVASNKVGKSEALAKVSVRSSLSVKVSPQVEVKALGSAVEFTCAAKGGLQIEWLKEGGVLPPNHHIKDGILRIENLEQSNEGIYTCRVTSQFEHAQDSAKLLIQALPKVKINVRTSVQTVMVGNSVEFECHAIGDPEPTVRWSKVGAPLPDHVEIRGNILRIDQVFESDSGQYRCTATNDVGSEHSHVVLNIQSLPQIAALPESKEVTIGSDAVLPCIASGYPVPTITWSKVENDLPPKCRQDGHALTVPVVTESDAGTYVCTAANKQGKVEAFTRLNVHERVMPYFTQEPLSYLTLPTIKNSYKAFSIKITFRPDNVDGLILYAGMIIYNGQKKTTGADFISFGLLGGRPEFRFDVGSGMATIRYPTPIKLGEFHTVHLYRNQTQGSLVVDGQAPVNGTSQGKFKGLDLNEELFVGGYPNYSMLAKTAGLKTGFVGCIKQLIIQGDEVIFKDLDKSSTGVSNCPTCKDRPCQNDGTCEDSVASLYKCTCKRGFTGSNCQHHSSLHCHTEACGPDATCINRPSGLGYDCRCHLGKSGNKCMDGTLITTPLFDGEDSYIAYPPLTNIHNDLRIEMEFKPMDPDGLMFFSGGKKMKVEDFVAVSMVNGHVEFRYELGTGQAVLRSQEPVSLDQWHRVVAERLNKDGSLTVDHAKEITRSSPGKAQGLNIHTPMYLGGVPSMDILPKPANVSMLFDGCIGEVFINGKKVDLSYSFTESRAISQCNDDSPCDRRPCLHAGTCMATAEYEYQCFCAEGYEGDRCEIVKESCRHSSQCQNGGSCVNNHCVCPAGYSGRHCEKGQESSFSEAMWSLEGSGGNDSPIEYSAYFHDNGYLALPKPMFPRSAPDSPETIELEINTASKDGLILWQGVESAGALNLHKKHANIKELGDQGKGKDFISLGLQNGHLVFSYQLGSGEAQIVSGEPVNDRQWHKITAVRTGKHGYLQIDGGSVQRGQSQGKSIMVNTKGNIYLGGAPDMQALTGGKYSSGMTGCVKNLSLMNARPGEQPARPIDLQVHAEEGINVERCLT",
                    "length": 3701
                },
                "evidence": [
                    {
                        "id": "HGNC:5273",
                        "url": "https://alliancegenome.org/gene/HGNC:5273#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "ZFIN:ZDB-GENE-080807-4",
                        "url": "https://alliancegenome.org/gene/ZFIN:ZDB-GENE-080807-4#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "MGI:96257",
                        "url": "https://alliancegenome.org/gene/MGI:96257#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "RGD:621770",
                        "url": "https://alliancegenome.org/gene/RGD:621770#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "FB:FBgn0284408",
                        "url": "https://alliancegenome.org/gene/FB:FBgn0284408#orthology",
                        "database": "AGR"
                    }
                ],
                "glygen_name": "Zebrafish",
                "common_name": "Zebrafish"
            },
            {
                "uniprot_canonical_ac": "A0ACD4DAU3-1",
                "protein_name": "Terribly reduced optic lobes, isoform BD",
                "gene_name": "trol",
                "tax_id": 7227,
                "organism": "Drosophila melanogaster",
                "sequence": {
                    "sequence": "MMGSPGSQASAIATSVGIRSGRRGQAGGSLLLRLLAVTFVLAACHAPLLTNAKQISNLGDDQDFMLADDESLQGINDSEWQLMGDDIDDGLLDDVDETLKPMETKSEEEDLPTGNWFSQSVHRVRRSINRLFGSDDNQERGRRQQRERSQRNRDAINRQKELRRRQKEDHNRWKQMRMERQLEKQRLVKRTNHVVFNRATDPRKRASDLYDENEASGYHEEDTTLYRTYFVVNEPYDNEYRDRESVQFQNLQKLLDDDLRNFFHSNYEGNDDEEQEIRSTLERVEPTNDNFKIRVQLRIELPTSVNDFGSKLQQQLNVYNRIENLSAATDGVFSFTESSVTEESVRHLDVGFVEPHITLFHEQNTGYDDFDRKPTTETQDIEEEAIDVTLPQEEVEGSGSDDSSCRGDATFTCPRSGKTICDEMRCDREIQCPDGEDEEYCNYPNVCTEDQFKCDDKCLELKKRCDGSIDCLDQTDEAGCINAPEPEPEPEPEPEPEPESEPEAEPEPEPEPEPESEPEQEPEPQVPEANECQANEFRCNNGDCIDARKRCNNVSDCSEGEDENEECPAACSGMEYQCRDGTRCISVSQQCDGHSDCSDGDDEEHCDGSGYDSEECRFDEFHCGTGECIPMRQVCDNIYDCNDYSDEVNCVEGEEEDRVGIPIGHQPWRPASKHDDWLHEMDTSEYQVYQPSNVYEKANSQNPCASNQFRCTTSNVCIPLHLRCDGFYHCNDMSDEKSCEQYQRHTTTRRPLTLATPTSRITTQGPGLLERRNTTTATEASRWPWATKTTTIATTTSNPITTVGVANSPPQTCLENIEFACHNRDCISIESVCDGIPDCGRNEDEDDALCKCSGDKYKCQRGGGCIPKSQVCDGKPQCHDRSDESACHLHGRLNKTRLGVKCLESQYQCGDGSCISGYKRCNGIHDCADASDEYNCIYDYEDTYDTDPNNNPLNECDILEFECDYSQCLPLEKKCDGYADCEDMSDELECQSYTDHCLESEFECDSYCLPRDQLCNGIPNCQDGSDERNCTFCREDAYLCNTGECVADNQRCNGIADCADGSDERHCARIYCPPNKLACNGTCVSRRIKCDGIRDCLDGYDEMYCPETNNHYPTQNVNVIRPKLGPNPIPKSCRPHEWQCANLECIDSSLQCNEIKDCSDGSDEELSVCFGTATTRLKPSDCSPEQFYCDESCYNRSVRCNGHVDCSDGSDEVGCSLPCPQHQCPSGRCYTESERCDRHRHCEDGSDEANCCYANQFRCNNGDCVSGSAPCNGYSECSDHSDELNCGGTQECLPNQFRCNSGQCVSSSVRCNGRTDCQDSSDEQNCAADSNDRRPNQLNLKTYPDSQIIKESREVIFRCRDEGPARAKVKWSRPGGRPLPPGFTDRNGRLEIPNIRVEDAGTYVCEAVGYASYIPGQQVTVNLNVERYNDVGSRPESACTEYQATCMNGECIDKSSICDGNPDCSDASDEQSCSLGLKCQPNQFMCSNSKCVDRTWRCDGENDCGDNSDETSCDPEPSGAPCRYNEFQCRSGHCIPKSFQCDNVPDCTDGTDEVGCMAPLPIRPPPQSVSLLEYEVLELTCVATGTPTPTIVWRLNWGHVPDKCESKSYGGTGTLRCPDMRPQDSGAYSCEIINTRGTHFVNPDTIVTVRPVRTDVCEAGFFNMLARKAEECVQCFCFGVAKACDSANLFTYAIHPPILSHRVVSVELSPLRQIVINEAAPGQDLLTLLHGVQFRATNVHFSGRETPYLALPADYMGNQLKSYGGNLRYEVNYRGSGRPVNGPDVIITGNRFTLTYRVRTQPGQNNRVSIPFVPGGWQKPDGRKASREEIMMILANVDNILIRLGYLDSTAREVDLINIALDSAGTADKGLGSASLVEKCQCPPGYVGDSCESCASGYVRQPGGPWLGHCVPFIPDSCPSGTYGDPRRGVPCKECPCPLTGSNNFASGCQQSPDGDVVCRCNEGYTGRRCEQCAAGYQGNPLAAGGICRRIPDTSCNVDGTYSVHSNGTCQCKDSVIGEQCDTCKSKSFHLNSFTYTGCIECFCSGVGLDCDSSTWYRDQVTSTFGRSRVDHGFVLVTNYMQPTPDTVPVSMAAEPNALSFIGSADQSGNTLYWSLPAAFLGNKLSSYGGKLTYTLSYSPLPNGIMSRNSAPDVVIKSGEDLRLIHYRKSQVVPSVANTYSVEIKESAWQRGDEVVANREHVLMALSDITAIYIKATYTTSTKEASLRQVTLDVATPTNLGTPRAVEVEQCRCPEGYLGLSCEQCAPGYARDPEGGIYLGLCRPCECNGHSKYCNSDTGDCEECSDNTEGPSCERCAAGYVGDATRGTIYDCQPDEGYPIPSPPAPGNQTLECTAYCQIEGIYDCRGNECLCKRNVIGDQCDQCRPGTYGLSAQNQDGCKECYCSGLASQCRSAALYRQLIPVDFILNAPLITDESGAVQDTENLIPDISRNMYTYTHTSYLPKYWSLRGSVLGNQLFSYGGRLSYSLIVESYGNYERGHDIVLIGNGLKLIWSRPDGNENQEEYNVRLHEDEQWTRQDRESARPASRSDFMTVLSDLQHILIRATPRVPTQSTSIGNVILESAVTTRTPGATHASDIELCQCPSGYVGTSCESCAPLHYRDASGSCSLCPCDVSNTESCDLVSGGYVECRCKARWKGDRCREIDTNDPTDIGTEDPVLTQIIVSIQKPEITIVPVGGSMTLSCSGRMRWSNSPVIVNWYKENSRLPENVEVQGGNLYLYDLQVSDSGVYICQAVNNETASVFKDTVSITITRYAQEMLARYEKDQLSPAEIVNLPSHVTFEEYVNNEIICEVLGNPAPRVTWARVDGHADAQSTRTYDNRLIFDSPRKSDEGRYRCQAENDQNRDEKYVIVYVQSNPPQPPPQQDRLYITPEEINGLAGESFQLNCQFTSVASLRYDWSHNGRSLSSSPARNVEIRGNTLEVRDASESDSGVYTCVAYDVRTRRNFTESARVNIDRREEQPFGNKPIIESLEQNILIIQGEDYSITCEASGSPYPSIKWAKVHDFMPENVHISGNVLTIYGARFENRGVYSCVAENDHGSDLSSTSIDIEPRERPSVKIVSAPLQTFSVGAPASLYCTVEGIPDPTVEWVRVDGQPLSPRHKIQSPGYMVIDDIQLEDSGDYECRAKNIVGEATGVATITVQEPTLVQIIPDNRDLRLTEGDELSLTCVGSGVPNPEVEWVNEMALKRDLYSPPSNTAILKIYRVTKADAGIYTCHGKNEAGSDEAHVRVEVQERRGDIGGVDDDSDRDPINYNPPQQQNPGIHQPGSNQLLATDIGDNVTLTCDMFQPLNTRWERVDGAPLPRNAYTIKNRLEIVRVEQQNLGQYRCNGIGRDGNVKTYFVKELVLMPLPRIRFYPNIPLTVEAGQNLDVHCQVENVRPEDVHWSTDNNRPLPSSVRIVGSVLRFVSITQAAAGEYRCSAFNQYGNRSQIARVAVKKPADFHQVPQSQLQRHREGENIQLQCTVTDQYGVRAQDNVEFNWFRDDRRPLPNNARTDSQILVLTNLRPEDAGRYICNSYDVDRGQQLPEVSIDLQVLRAPQYPYNRFKGGVSLKDTPCMVLYICAAATPPPNSPIYLPPQLPAKSRDYSLKLDDQSSNLRAGESTDVECYSSDDTYTDVVWERSDGAPLSNNVRQVGNRLVISNVSPSDAGNYVCKCKTDEGDLYTTSYKLEVEDQPHELKSSKIVYAKVGANADLQCGADESRQPTYRWSRQYGQLQAGRSLMNEKLSLDSVQANDAGTYICTAQYADGETADFPNILVVTGAIPQFRQEPRSYMSFPTLPNSSFKFNFELTFRPENGDGLLLFNGQTRGSGDYIALSLKDRYAEFRFDFGGKPMLVRAEEPLALNEWHTVRVSRFKRDGYIQVDEQHPVAFPTLQQIPQLDLIEDLYIGGVPNWELLPADAVSQQVGFVGCISRLTLQGRTVELIREAKYKEGITDCRPCAQGPCQNKGVCLESQTEQAYTCICQPGWTGRDCAIEGTQCTPGVCGAGRCENTENDMECLCPLNRSGDRCQYNEILNEHSLNFKGNSFAAYGTPKVTKVNITLSVRPASLEDSVILYTAESTLPSGDYLALVLRGGHAELLINTAARLDPVVVRSAEPLPLNRWTRIEIRRRLGEGILRVGDGPERKAKAPGSDRILSLKTHLYVGGYDRSTVKVNRDVNITKGFDGCISRLYNFQKPVNLLADIKDAANIQSCGETNMIGGDEDSDNEPPVPPPTPDVHENELQPYAMAPCASDPCENGGSCSEQEDVAVCSCPFGFSGKHCQEHLQLGFNASFRGDGYVELNRSHFQPALEQSYTSMGIVFTTNKPNGLLFWWGQEAGEEYTGQDFIAAAVVDGYVEYSMRLDGEEAVIRNSDIRVDNGERHIVIAKRDENTAILEVDRMLHSGETRPTSKKSMKLPGNVFVGGAPDLEVFTGFRYKHNLNGCIVVVEGETVGQINLSSAAVNGVNANVCPANDDPLGGTEPPVV",
                    "length": 4489
                },
                "evidence": [
                    {
                        "id": "HGNC:5273",
                        "url": "https://alliancegenome.org/gene/HGNC:5273#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "ZFIN:ZDB-GENE-080807-4",
                        "url": "https://alliancegenome.org/gene/ZFIN:ZDB-GENE-080807-4#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "MGI:96257",
                        "url": "https://alliancegenome.org/gene/MGI:96257#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "RGD:621770",
                        "url": "https://alliancegenome.org/gene/RGD:621770#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "FB:FBgn0284408",
                        "url": "https://alliancegenome.org/gene/FB:FBgn0284408#orthology",
                        "database": "AGR"
                    }
                ],
                "glygen_name": "Fruit fly",
                "common_name": "Fruit fly"
            },
            {
                "uniprot_canonical_ac": "Q05793-1",
                "protein_name": "Basement membrane-specific heparan sulfate proteoglycan core protein",
                "gene_name": "Hspg2",
                "tax_id": 10090,
                "organism": "Mus musculus",
                "sequence": {
                    "sequence": "MGQRAVGSLLLGLLLHARLLAVTHGLRAYDGLSLPEDTETVTASRYGWTYSYLSDDEDLLADDASGDGLGSGDVGSGDFQMVYFRALVNFTRSIEYSPQLEDASAKEFREVSEAVVEKLEPEYRKIPGDQIVSVVFIKELDGWVFVELDVGSEGNADGSQIQEVLHTVVSSGSIGPYVTSPWGFKFRRLGTVPQFPRVCTETEFACHSYNECVALEYRCDRRPDCRDMSDELNCEEPVPELSSSTPAVGKVSPLPLWPEAATTPPPPVTHGPQFLLPSVPGPSACGPQEASCHSGHCIPRDYLCDGQEDCRDGSDELGCASPPPCEPNEFACENGHCALKLWRCDGDFDCEDRTDEANCSVKQPGEVCGPTHFQCVSTNRCIPASFHCDEESDCPDRSDEFGCMPPQVVTPPQQSIQASRGQTVTFTCVATGVPTPIINWRLNWGHIPAHPRVTMTSEGGRGTLIIRDVKEADQGAYTCEAMNSRGMVFGIPDGVLELVPQRGPCPDGHFYLEDSASCLPCFCFGVTNVCQSSLRFRDQIRLSFDQPNDFKGVNVTMPSQPGVPPLSSTQLQIDPALQEFQLVDLSRRFLVHDAFWALPKQFLGNKVDSYGGFLRYKVRYELARGMLEPVQKPDVILVGAGYRLHSRGHTPTHPGTLNQRQVQLSEEHWVHESGRPVQRAEMLQALASLEAVLLQTVYNTKMASVGLSDIVMDTTVTHTTIHGRAHSVEECRCPIGYSGLSCESCDAHFTRVPGGPYLGTCSGCNCNGHASSCDPVYGHCLNCQHNTEGPQCDKCKPGFFGDATKATATACRPCPCPYIDASRRFSDTCFLDTDGQATCDACAPGYTGRRCESCAPGYEGNPIQPGGKCRPTTQEIVRCDERGSLGTSGETCRCKNNVVGRLCNECSDGSFHLSKQNPDGCLKCFCMGVSRQCSSSSWSRAQVLGASEQPSQFSLSNAAGTHTTSEGVSSPAPGELSFSSFHNLLSEPYFWSLPASFRGDKVTSYGGELRFTVMQRPRPSSAPLHRQPLVVLQGNNIVLEHHASRDPSPGQPSNFIVPFQEQAWQRPDGQPATREHLLMALAGIDALLIQASYTQQPAESRLSGISMDVAVPENTGQDSAREVEQCTCPPGYRGPSCQDCDTGYTRVPSGLYLGTCERCNCHGHSETCEPETGACQSCQHHTEGASCEQCQPGYYGDAQRGTPQDCQPCPCYGAPAAGQAAHTCFLDTDGHPTCDSCSPGHSGRHCERCAPGYYGNPSQGQPCHRDGQVPEVLGCGCDPHGSISSQCDAAGQCQCKAQVEGRSCSHCRPHHFHLSASNPEGCLPCFCMGVTQQCASSSYSRQLISTHFAPGDFQGFALVNPQRNSQLTGGFTVEPVHDGARLSFSNFAHLGQESFYWQLPEIYQGDKVAAYGGKLRYTLSYTAGPQGSPLLDPDIQITGNNIMLVASQPALQGPERRSYEIIFREEFWRRPDGQPATREHLLMALADLDELLVRATFSSVPRAASISAVSLEGAQPGPSSGPRALEVEECRCPPGYVGLSCQDCAPGYTRTGSGLYLGQCELCECNGHSDLCHPETGACSRCQHNTAGEFCELCATGYYGDATAGTPEDCQPCACPLTNPENMFSRTCESLGAGGYRCTACEPGYTGQYCEQCAPGYEGDPNVQGGRCQPLTKESLEVQIHPSRSVVPQGGPHSLRCQVSGSPPHYFYWSREDGRPLPSSAQQRHQGSELHFPSVQPSDAGVYICTCRNLIHTSNSRAELLVAEAPSKPIMVTVEEQRSQSVRPGADVTFICTAKSKSPAYTLVWTRLHNGKLPSRAMDFNGILTIRNVQPSDAGTYVCTGSNMFAMDQGTATLHVQVSGTSTAPVASIHPPQLTVQPGQQAEFRCSATGNPTPMLEWIGGPSGQLPAKAQIHNGILRLPAIEPSDQGQYLCRALSSAGQHVARAMLQVHGGSGPRVQVSPERTQVHEGRTVRLYCRAAGVPSASITWRKEGGSLPFRHQAHGSRLRLHHMSVADSGEYVCRANNNIDAQETSIMISVSPSTNSPPAPASPAPIRIESSSSRVAEGQTLDLNCVVPGHAHAQVTWHKRGGSLPTHHQTHGSRLRLYQVSSADSGEYVCSVLSSSGPLEASVLVSITPAAANVHIPGVVPPIRIETSSSRVAEGQTLDLSCVVPGQAHAQVTWHKRGGSLPAGHQVHGHMLRLNRVSPADSGEYSCQVTGSSGTLEASVLVTIEASEPSPIPAPGLAQPVYIESSSSHLTEGQTVDLKCVVPGQAHAQVTWHKRGSSLPARHQTHGSLLRLYQLSPADSGEYVCQVAGSSHPEHEASFKLTVPSSQNSSFRLRSPVISIEPPSSTVQQGQDASFKCLIHEGAMPIKVEWKIRDQELEDNVHISPNGSIITIVAPGPATMEPTACVASNVYGMAQSVVNLSVHGPPTVSVLPEGPVHVKMGKDITLECISSGEPRSSPRWTRLGIPVKLEPRMFGLMNSHAMLKIASVKPSDAGTYVCQAQNALGTAQKQVELIVDTGTVAPGTPQVQVEESELTLEAGHTATLHCSATGNPPPTIHWSKLRAPLPWQHRIEGNTLVIPRVAQQDSGQYICNATNSAGHTEATVVLHVESPPYATIIPEHTSAQPGNLVQLQCLAHGTPPLTYQWSLVGGVLPEKAVVRNQLLRLEPTVPEDSGRYRCQVSNRVGSAEAFAQVLVQGSSSNLPDTSIPGGSTPTVQVTPQLETRNIGASVEFHCAVPNERGTHLRWLKEGGQLPPGHSVQDGVLRIQNLDQNCQGTYVCQAHGPWGQAQATAQLIVQALPSVLINVRTSVHSVVVGHSVEFECLALGDPKPQVTWSKVGGHLRPGIVQSGTIIRIAHVELADAGQYRCAATNAAGTTQSHVLLLVQALPQISTPPEIRVPAGSAAVFPCMASGYPTPAITWSKVDGDLPPDSRLENNMLMLPSVRPEDAGTYVCTATNRQGKVKAFAYLQVPERVIPYFTQTPYSFLPLPTIKDAYRKFEIKITFRPDSADGMLLYNGQKRSPTNLANRQPDFISFGLVGGRPEFRFDAGSGMATIRHPTPLALGQFHTVTLLRSLTQGSLIVGNLAPVNGTSQGKFQGLDLNEELYLGGYPDYGAIPKAGLSSGFVGCVRELRIQGEEIVFHDVNLTTHGISHCPTCQDRPCQNGGQCQDSESSSYTCVCPAGFTAAAVNIRKPCTATPSLWADATCVNRPDGRGYTCRCHLGRSGVRCEEGVTVTTPSMSGAGSYLALPALTNTHHELRLDVEFKPLEPNGILLFSGGKSGPVEDFVSLAMVGGHLEFRYELGSGLAVLRSHEPLALGRWHRVSAERLNKDGSLRVDGGRPVLRSSPGKSQGLNLHTLLYLGGVEPSVQLSPATNMSAHFHGCVGEVSVNGKRLDLTYSFLGSQGVGQCYDSSPCERQPCRNGATCMPAGEYEFQCLCQDGFKGDLCEHEENPCQLHEPCLNGGTCRGARCLCLPGFSGPRCQQGAGYGVVESDWHPEGSGGNDAPGQYGAYFYDNGFLGLPGNSFSRSLPEVPETIEFEVRTSTADGLLLWQGVVREASRSKDFISLGLQDGHLVFSYQLGSGEARLVSGDPINDGEWHRITALREGQRGSIQVDGEDLVTGRSPGPNVAVNTKDIIYIGGAPDVATLTRGKFSSGITGCIKNLVLHTARPGAPPPQPLDLQHRAQAGANTRPCPS",
                    "length": 3707
                },
                "evidence": [
                    {
                        "id": "HGNC:5273",
                        "url": "https://alliancegenome.org/gene/HGNC:5273#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "ZFIN:ZDB-GENE-080807-4",
                        "url": "https://alliancegenome.org/gene/ZFIN:ZDB-GENE-080807-4#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "MGI:96257",
                        "url": "https://alliancegenome.org/gene/MGI:96257#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "RGD:621770",
                        "url": "https://alliancegenome.org/gene/RGD:621770#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "FB:FBgn0284408",
                        "url": "https://alliancegenome.org/gene/FB:FBgn0284408#orthology",
                        "database": "AGR"
                    },
                    {
                        "id": "P98160",
                        "url": "https://omabrowser.org/oma/group/P98160/",
                        "database": "OMA"
                    }
                ],
                "glygen_name": "Mouse",
                "common_name": "Mouse"
            }
        ],
        "go_annotation": {
            "categories": [
                {
                    "name": "Biological Process",
                    "total": 11,
                    "go_terms": [
                        {
                            "name": "circulatory system development",
                            "id": "GO:0072359",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072359",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "angiogenesis",
                            "id": "GO:0001525",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001525",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "lipid metabolic process",
                            "id": "GO:0006629",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006629",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "inflammatory response",
                            "id": "GO:0006954",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006954",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "cell differentiation",
                            "id": "GO:0030154",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "brain development",
                            "id": "GO:0007420",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007420",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "negative regulation of synaptic transmission, cholinergic",
                            "id": "GO:0032223",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032223",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "receptor-mediated endocytosis",
                            "id": "GO:0006898",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006898",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "negative regulation of angiogenesis",
                            "id": "GO:0016525",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016525",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "protein localization to synapse",
                            "id": "GO:0035418",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035418",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "vesicle-mediated transport",
                            "id": "GO:0016192",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016192",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        }
                    ]
                },
                {
                    "name": "Molecular Function",
                    "total": 5,
                    "go_terms": [
                        {
                            "name": "molecular adaptor activity",
                            "id": "GO:0060090",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060090",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "low-density lipoprotein particle receptor binding",
                            "id": "GO:0050750",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050750",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "amyloid-beta binding",
                            "id": "GO:0001540",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001540",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "calcium ion binding",
                            "id": "GO:0005509",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005509",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "extracellular matrix structural constituent conferring compression resistance",
                            "id": "GO:0030021",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030021",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        }
                    ]
                },
                {
                    "name": "Cellular Component",
                    "total": 19,
                    "go_terms": [
                        {
                            "name": "extracellular region",
                            "id": "GO:0005576",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "extracellular space",
                            "id": "GO:0005615",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "Golgi lumen",
                            "id": "GO:0005796",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005796",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "plasma membrane",
                            "id": "GO:0005886",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "focal adhesion",
                            "id": "GO:0005925",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005925",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "extracellular matrix",
                            "id": "GO:0031012",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031012",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "neuromuscular junction",
                            "id": "GO:0031594",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031594",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "extracellular exosome",
                            "id": "GO:0070062",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070062",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "neuron projection",
                            "id": "GO:0043005",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043005",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "basement membrane",
                            "id": "GO:0005604",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005604",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "lysosomal lumen",
                            "id": "GO:0043202",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043202",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "microfibril",
                            "id": "GO:0001527",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001527",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "elastic fiber",
                            "id": "GO:0071953",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071953",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "plasma membrane protein complex",
                            "id": "GO:0098797",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098797",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "gel phase of basement membrane",
                            "id": "GO:0140148",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140148",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "cell periphery",
                            "id": "GO:0071944",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071944",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "cytoplasm",
                            "id": "GO:0005737",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "membrane",
                            "id": "GO:0016020",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        },
                        {
                            "name": "endomembrane system",
                            "id": "GO:0012505",
                            "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0012505",
                            "evidence": [
                                {
                                    "database": "UniProtKB",
                                    "id": "P98160",
                                    "url": "https://www.uniprot.org/uniprotkb/P98160"
                                }
                            ],
                            "pmid": ""
                        }
                    ]
                }
            ]
        },
        "pro_annotation": [
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein N-glycosylated 1 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been N-glycosylated at the residue equivalent to Asn-3780 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G09197ZW. Example: UniProtKB:P98160-1, Asn-3780, MOD:00160~GNO:G09197ZW. [PRO:DNx, PMID:29741879]",
                "evidence": [
                    {
                        "id": "PR:000056734",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056734"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 1 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-1869 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-1869, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056735",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056735"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 2 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2140 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-2140, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056736",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056736"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 3 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2429 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G29068FM. Example: UniProtKB:P98160-1, Ser-2429, MOD:00002~GNO:G29068FM. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056737",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056737"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 4 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2429 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-2429, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056738",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056738"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 5 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2429 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G58001LT. Example: UniProtKB:P98160-1, Ser-2429, MOD:00002~GNO:G58001LT. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056739",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056739"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 6 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2559 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-2559, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056740",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056740"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 7 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2637 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-2637, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056741",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056741"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 8 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2638 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-2638, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056742",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056742"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 9 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2716 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-2716, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056743",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056743"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 10 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2719 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G29068FM. Example: UniProtKB:P98160-1, Ser-2719, MOD:00002~GNO:G29068FM. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056744",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056744"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 11 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2719 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-2719, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056745",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056745"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 12 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2721 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-2721, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056746",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056746"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 13 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-279 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G29068FM. Example: UniProtKB:P98160-1, Ser-279, MOD:00002~GNO:G29068FM. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056747",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056747"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 14 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-279 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-279, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056748",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056748"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 15 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2815 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-2815, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056749",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056749"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 16 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-2816 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-2816, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056750",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056750"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 17 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-3393 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-3393, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056751",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056751"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 18 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-3398 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-3398, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056752",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056752"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 19 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-3398 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G53434XO. Example: UniProtKB:P98160-1, Ser-3398, MOD:00002~GNO:G53434XO. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056753",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056753"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 20 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-3398 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G58001LT. Example: UniProtKB:P98160-1, Ser-3398, MOD:00002~GNO:G58001LT. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056754",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056754"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 21 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-3398 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G73004SD. Example: UniProtKB:P98160-1, Ser-3398, MOD:00002~GNO:G73004SD. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056755",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056755"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 22 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Ser-3630 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Ser-3630, MOD:00002~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056756",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056756"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 23 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-1145 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-1145, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056757",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056757"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 24 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-1147 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-1147, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056758",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056758"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 25 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-1862 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G29068FM. Example: UniProtKB:P98160-1, Thr-1862, MOD:00005~GNO:G29068FM. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056759",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056759"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 26 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-1862 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-1862, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056760",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056760"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 27 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-1862 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G58001LT. Example: UniProtKB:P98160-1, Thr-1862, MOD:00005~GNO:G58001LT. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056761",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056761"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 28 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-1876 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G29068FM. Example: UniProtKB:P98160-1, Thr-1876, MOD:00005~GNO:G29068FM. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056762",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056762"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 29 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-1876 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-1876, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056763",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056763"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 30 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-1926 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-1926, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056764",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056764"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 31 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-2145 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G29068FM. Example: UniProtKB:P98160-1, Thr-2145, MOD:00005~GNO:G29068FM. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056765",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056765"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 32 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-2145 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-2145, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056766",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056766"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 33 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-251 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G73004SD. Example: UniProtKB:P98160-1, Thr-251, MOD:00005~GNO:G73004SD. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056767",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056767"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 34 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-260 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G40740AD. Example: UniProtKB:P98160-1, Thr-260, MOD:00005~GNO:G40740AD. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056768",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056768"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 35 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-260 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G57317CE. Example: UniProtKB:P98160-1, Thr-260, MOD:00005~GNO:G57317CE. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056769",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056769"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 36 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-2646 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-2646, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056770",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056770"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 37 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-269 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G29068FM. Example: UniProtKB:P98160-1, Thr-269, MOD:00005~GNO:G29068FM. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056771",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056771"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 38 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-269 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-269, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056772",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056772"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 39 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-269 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G53434XO. Example: UniProtKB:P98160-1, Thr-269, MOD:00005~GNO:G53434XO. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056773",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056773"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 40 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-269 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G58001LT. Example: UniProtKB:P98160-1, Thr-269, MOD:00005~GNO:G58001LT. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056774",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056774"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 41 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-3032 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-3032, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056775",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056775"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 42 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-3392 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-3392, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056776",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056776"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 43 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-3399 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-3399, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056777",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056777"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 44 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-3401 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-3401, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056778",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056778"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 45 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-3405 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-3405, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056779",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056779"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 46 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-361 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-361, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056780",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056780"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 47 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-42 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-42, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:22171320]",
                "evidence": [
                    {
                        "id": "PR:000056781",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056781"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 48 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-563 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-563, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056782",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056782"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 49 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-915 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G29068FM. Example: UniProtKB:P98160-1, Thr-915, MOD:00005~GNO:G29068FM. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056783",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056783"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 50 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-915 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-915, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056784",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056784"
                    }
                ]
            },
            {
                "name": "basement membrane-specific heparan sulfate proteoglycan core protein O-glycosylated 51 (human)",
                "definition": "A basement membrane-specific heparan sulfate proteoglycan core protein (human) that has been O-glycosylated at the residue equivalent to Thr-972 of the amino acid sequence represented by UniProtKB:P98160-1, in which the glycan composition is represented by GlyTouCan:G43417UB. Example: UniProtKB:P98160-1, Thr-972, MOD:00005~GNO:G43417UB. [PRO:DNx, PMID:30459171]",
                "evidence": [
                    {
                        "id": "PR:000056785",
                        "database": "PRO",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=PR:000056785"
                    }
                ]
            }
        ],
        "site_annotation": [
            {
                "start_pos": 1755,
                "end_pos": 1757,
                "annotation": "n_glycosylation_sequon"
            },
            {
                "start_pos": 2121,
                "end_pos": 2123,
                "annotation": "n_glycosylation_sequon"
            },
            {
                "start_pos": 3072,
                "end_pos": 3074,
                "annotation": "n_glycosylation_sequon"
            },
            {
                "start_pos": 3105,
                "end_pos": 3107,
                "annotation": "n_glycosylation_sequon"
            },
            {
                "start_pos": 3279,
                "end_pos": 3281,
                "annotation": "n_glycosylation_sequon"
            },
            {
                "start_pos": 3780,
                "end_pos": 3782,
                "annotation": "n_glycosylation_sequon"
            },
            {
                "start_pos": 3836,
                "end_pos": 3838,
                "annotation": "n_glycosylation_sequon"
            },
            {
                "start_pos": 4068,
                "end_pos": 4070,
                "annotation": "n_glycosylation_sequon"
            },
            {
                "start_pos": 554,
                "end_pos": 556,
                "annotation": "n_glycosylation_sequon"
            },
            {
                "start_pos": 89,
                "end_pos": 91,
                "annotation": "n_glycosylation_sequon"
            }
        ],
        "ptm_annotation": [
            {
                "annotation": "O-glycosylated with core 1 or possibly core 8 glycans. Contains three heparan sulfate chains. Also contains chondroitin sulfate.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P98160",
                        "url": "https://www.uniprot.org/uniprotkb/P98160"
                    },
                    {
                        "database": "PubMed",
                        "id": "25326458",
                        "url": "https://glygen.org/publication/PubMed/25326458"
                    },
                    {
                        "database": "PubMed",
                        "id": "15591058",
                        "url": "https://glygen.org/publication/PubMed/15591058"
                    },
                    {
                        "database": "PubMed",
                        "id": "22171320",
                        "url": "https://glygen.org/publication/PubMed/22171320"
                    }
                ]
            },
            {
                "annotation": "Proteolytic processing produces the C-terminal angiogenic peptide, endorepellin. This peptide can be further processed to produce the LG3 peptide.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P98160",
                        "url": "https://www.uniprot.org/uniprotkb/P98160"
                    },
                    {
                        "database": "PubMed",
                        "id": "12435733",
                        "url": "https://glygen.org/publication/PubMed/12435733"
                    },
                    {
                        "database": "PubMed",
                        "id": "15591058",
                        "url": "https://glygen.org/publication/PubMed/15591058"
                    }
                ]
            }
        ],
        "interactions": [],
        "reactions": [],
        "reaction_participants": [],
        "reaction_enzymes": [],
        "biomarkers": [],
        "structures": [
            {
                "pdb_id": "3sh4",
                "pdb_chain": "a",
                "start_pos": 4197,
                "end_pos": 4391,
                "overlap": "1.0",
                "method": "X-Ray_Crystallography",
                "type": "experimental",
                "resolution": -1.0,
                "url": "https://data.glygen.org/ln2downloads/pdb/current/3sh4.pdb",
                "url_external": "https://www.rcsb.org/structure/3sh4"
            }
        ],
        "lectin_list": [
            {
                "lectin_class": "Laminin G-like",
                "evidence": [
                    {
                        "id": "21996443",
                        "database": "PubMed",
                        "url": "https://glygen.org/publication/PubMed/21996443"
                    },
                    {
                        "id": "10.1016/j.jmb.2011.09.048",
                        "database": "DOI",
                        "url": "https://glygen.org/publication/DOI/10.1016/j.jmb.2011.09.048"
                    }
                ]
            }
        ],
        "domain_list": [
            {
                "evidence": [
                    {
                        "id": "P98160",
                        "database": "UniProtKB",
                        "url": "https://www.uniprot.org/uniprotkb/P98160"
                    },
                    {
                        "id": "PRU00076",
                        "database": "PROSITE",
                        "url": "https://prosite.expasy.org/PRU00076"
                    }
                ],
                "ann_type": "Domain_Extent_Annotation",
                "uniprotkb_annotation": "EGF-like 1",
                "eco_id": "ECO_0000255",
                "start_pos": 3844,
                "end_pos": 3881,
                "start_aa": "His",
                "end_aa": "Glu",
                "glycosite_overlap": [
                    {
                        "position": 3847,
                        "amino_acid": "Thr"
                    }
                ]
            },
            {
                "evidence": [
                    {
                        "id": "P98160",
                        "database": "UniProtKB",
                        "url": "https://www.uniprot.org/uniprotkb/P98160"
                    },
                    {
                        "id": "PRU00076",
                        "database": "PROSITE",
                        "url": "https://prosite.expasy.org/PRU00076"
                    }
                ],
                "ann_type": "Domain_Extent_Annotation",
                "uniprotkb_annotation": "EGF-like 2",
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]
