[
    {
        "uniprot_canonical_ac": "Q5RI55-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI55",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI55"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 276,
        "chemical_mass": 31998.0,
        "gene_names": "ccdc3a;ccdc3a;ccdc3;si:ch211-220p15.9",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI55",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI55"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "negative regulation of gene expression",
                "id": "GO:0010629",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010629",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI55",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI55"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q5RI55-1"
    },
    {
        "uniprot_canonical_ac": "Q5RI65-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI65",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI65"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 366,
        "chemical_mass": 41776.0,
        "gene_names": "lmx1a;lmx1a;si:ch211-260g14.3",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0110591",
                "name": "autosomal dominant nonsyndromic deafness 7",
                "description": "An autosomal dominant nonsyndromic deafness that is characterized by progressive high-tone hearing loss and has_material_basis_in variation in the chromosome region 1q21-q23.",
                "url": "https://disease-ontology.org/term/DOID:0110591",
                "evidence": [
                    {
                        "id": "0110591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110591"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI65",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI65"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI65",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI65"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
                "id": "GO:0006357",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006357",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI65",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI65"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron differentiation",
                "id": "GO:0030182",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030182",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI65",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI65"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI65",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI65"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase II transcription regulatory region sequence-specific DNA binding",
                "id": "GO:0000977",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000977",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI65",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI65"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-binding transcription factor activity, RNA polymerase II-specific",
                "id": "GO:0000981",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000981",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI65",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI65"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI65",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI65"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q5RI65-1"
    },
    {
        "uniprot_canonical_ac": "Q5RI92-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI92",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI92"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 341,
        "chemical_mass": 38790.0,
        "gene_names": "ptger2b;ptger2b;si:ch211-13n20.1;si:dkey-29m11.3;zgc:136608",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0080822",
                "name": "aspirin-induced respiratory disease",
                "description": "An intrinsic asthma that is characterized by severe and prolonged airway obstruction after the ingestion of aspirin or other non-steroidal anti-inflammatory drugs.",
                "url": "https://disease-ontology.org/term/DOID:0080822",
                "evidence": [
                    {
                        "id": "0080822",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080822"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111579",
                "name": "asthma, nasal polyps, and aspirin intolerance",
                "description": "A respiratory system disease characterized by asthma, aspirin-induced bronchoconstriction, and nasal polyps.",
                "url": "https://disease-ontology.org/term/DOID:0111579",
                "evidence": [
                    {
                        "id": "0111579",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111579"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2876",
                "name": "laryngeal squamous cell carcinoma",
                "description": "A laryngeal carcinoma that has_material_basis_in squamous cells.",
                "url": "https://disease-ontology.org/term/DOID:2876",
                "evidence": [
                    {
                        "id": "2876",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2876"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3907",
                "name": "lung squamous cell carcinoma",
                "description": "A non-small cell lung carcinoma that has_material_basis_in the squamous cell.",
                "url": "https://disease-ontology.org/term/DOID:3907",
                "evidence": [
                    {
                        "id": "3907",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3907"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI92",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI92"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "inflammatory response",
                "id": "GO:0006954",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006954",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI92",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI92"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adenylate cyclase-activating G protein-coupled receptor signaling pathway",
                "id": "GO:0007189",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007189",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI92",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI92"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of cytosolic calcium ion concentration",
                "id": "GO:0007204",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007204",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI92",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI92"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular response to prostaglandin E stimulus",
                "id": "GO:0071380",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071380",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI92",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI92"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "prostaglandin E receptor activity",
                "id": "GO:0004957",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004957",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RI92",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RI92"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q5RI92-1"
    },
    {
        "uniprot_canonical_ac": "Q5RIH2-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RIH2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RIH2"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 919,
        "chemical_mass": 99167.0,
        "gene_names": "mthfd1a;mthfd1a",
        "protein_name": "C-1-tetrahydrofolate synthase, cytoplasmic",
        "disease": [
            {
                "disease_id": "DOID:0080016",
                "name": "spina bifida",
                "description": "A neural tube defect that is characterized by incomplete closing of the spine and membranes around the spinal cord during early development.",
                "url": "https://disease-ontology.org/term/DOID:0080016",
                "evidence": [
                    {
                        "id": "0080016",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080016"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080074",
                "name": "neural tube defect",
                "description": "A physical disorder characterized by incomplete closure of the neural tube.",
                "url": "https://disease-ontology.org/term/DOID:0080074",
                "evidence": [
                    {
                        "id": "0080074",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080074"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080633",
                "name": "developmental cardiac valvular defect",
                "description": "A physical disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PLD1 gene on chromosome 3q26.",
                "url": "https://disease-ontology.org/term/DOID:0080633",
                "evidence": [
                    {
                        "id": "0080633",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080633"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14250",
                "name": "Down syndrome",
                "description": "A chromosomal duplication syndrome that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability.",
                "url": "https://disease-ontology.org/term/DOID:14250",
                "evidence": [
                    {
                        "id": "14250",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14250"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6419",
                "name": "tetralogy of Fallot",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:6419",
                "evidence": [
                    {
                        "id": "6419",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6419"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:674",
                "name": "cleft palate",
                "description": "An orofacial cleft characterized by a fissure of the soft and/or hard palate, due to faulty fusion of the two plates of the skull that form the hard palate.",
                "url": "https://disease-ontology.org/term/DOID:674",
                "evidence": [
                    {
                        "id": "674",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:674"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7693",
                "name": "abdominal aortic aneurysm",
                "description": "An aortic aneurysm that is located_in the abdominal aorta.",
                "url": "https://disease-ontology.org/term/DOID:7693",
                "evidence": [
                    {
                        "id": "7693",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7693"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9296",
                "name": "cleft lip",
                "description": "An orofacial cleft that is characterized by a congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences.",
                "url": "https://disease-ontology.org/term/DOID:9296",
                "evidence": [
                    {
                        "id": "9296",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9296"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RIH2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RIH2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "formate-tetrahydrofolate ligase activity",
                "id": "GO:0004329",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004329",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RIH2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RIH2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "methenyltetrahydrofolate cyclohydrolase activity",
                "id": "GO:0004477",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004477",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RIH2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RIH2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "methylenetetrahydrofolate dehydrogenase (NADP+) activity",
                "id": "GO:0004488",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004488",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RIH2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RIH2"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RIH2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RIH2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "tetrahydrofolate interconversion",
                "id": "GO:0035999",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035999",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RIH2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RIH2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "one-carbon metabolic process",
                "id": "GO:0006730",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006730",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RIH2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RIH2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "tetrahydrofolate metabolic process",
                "id": "GO:0046653",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046653",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RIH2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RIH2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q5RIH2-1"
    },
    {
        "uniprot_canonical_ac": "Q5RII3-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RII3",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RII3"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 352,
        "chemical_mass": 39274.0,
        "gene_names": "ginm1;ginm1;si:ch211-87e4.1;si:dkey-15j16.2",
        "protein_name": "Glycoprotein integral membrane protein 1",
        "disease": [],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5RII3",
                        "url": "https://www.uniprot.org/uniprotkb/Q5RII3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q5RII3-1",
                "start_pos": "109",
                "end_pos": "109",
                "site_lbl": "Asn109",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "N-linked",
                        "subtype": "",
                        "prediction_tool_list": [],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "N",
                        "relation": "attached",
                        "comment": "N-linked (GlcNAc...) asparagine",
                        "icn3d_view": {},
                        "start_pos": 109,
                        "start_aa": "Asn",
                        "end_pos": 109,
                        "end_aa": "Asn",
                        "residue": "Asn",
                        "site_lbl": "Asn109",
                        "evidence": [
                            {
                                "id": "Q5RII3",
                                "database": "UniProtKB",
                                "url": "https://www.uniprot.org/uniprotkb/Q5RII3#ptm_processing"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q5RII3-1",
                "start_pos": "151",
                "end_pos": "151",
                "site_lbl": "Asn151",
                "weight": 0.0,
                "glycosylation": [
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                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1457,
                        "start_aa": "Thr",
                        "end_pos": 1457,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1457",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q5SNV1-1",
                "start_pos": "1991",
                "end_pos": "1991",
                "site_lbl": "Thr1991",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1991,
                        "start_aa": "Thr",
                        "end_pos": 1991,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1991",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "Q5SNV1-1",
                "start_pos": "1993",
                "end_pos": "1993",
                "site_lbl": "Thr1993",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
                        "start_pos": 1993,
                        "start_aa": "Thr",
                        "end_pos": 1993,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1993",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "Q5SNV1-1"
    },
    {
        "uniprot_canonical_ac": "Q5SP48-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
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                    {
                        "database": "UniProtKB",
                        "id": "Q5SP48",
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                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 184,
        "chemical_mass": 20553.0,
        "gene_names": "yaf2;si:ch211-155a11.5;yaf2;zgc:136577",
        "protein_name": "",
        "disease": [],
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            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
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                    {
                        "database": "UniProtKB",
                        "id": "Q5SP48",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SP48",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SP48"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription coregulator activity",
                "id": "GO:0003712",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003712",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SP48",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SP48"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
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                    {
                        "database": "UniProtKB",
                        "id": "Q5SP48",
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                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
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                    {
                        "database": "UniProtKB",
                        "id": "Q5SP48",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "forebrain development",
                "id": "GO:0030900",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030900",
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                    {
                        "database": "UniProtKB",
                        "id": "Q5SP48",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SP48"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of apoptotic process",
                "id": "GO:0043066",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043066",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SP48",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of DNA-templated transcription",
                "id": "GO:0006355",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "apoptotic process",
                "id": "GO:0006915",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006915",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SP48",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SP48"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of DNA-templated transcription",
                "id": "GO:0045893",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045893",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SP48",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SP48"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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    },
    {
        "uniprot_canonical_ac": "Q5SPH9-1",
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            {
                "name": "Danio rerio",
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                    {
                        "database": "UniProtKB",
                        "id": "Q5SPH9",
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                ],
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                "glygen_name": "Zebrafish",
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        ],
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        "chemical_mass": 21308.0,
        "gene_names": "mrps10;im:6911513;si:ch211-51e12.6",
        "protein_name": "Small ribosomal subunit protein uS10m",
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            {
                "name": "mitochondrial small ribosomal subunit",
                "id": "GO:0005763",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005763",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SPH9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SPH9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SPH9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SPH9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "translation",
                "id": "GO:0006412",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006412",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SPH9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SPH9"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "structural constituent of ribosome",
                "id": "GO:0003735",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003735",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SPH9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SPH9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "Q5SPH9-1"
    },
    {
        "uniprot_canonical_ac": "Q5SPN9-1",
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            {
                "name": "Danio rerio",
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                    {
                        "database": "UniProtKB",
                        "id": "Q5SPN9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SPN9"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 76,
        "chemical_mass": 7576.0,
        "gene_names": "pkib;im:7054531;pkib;si:dkey-150h13.1",
        "protein_name": "cAMP-dependent protein kinase inhibitor",
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        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SPN9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SPN9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SPN9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SPN9"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "cAMP-dependent protein kinase inhibitor activity",
                "id": "GO:0004862",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004862",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5SPN9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5SPN9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q5SPN9-1"
    },
    {
        "uniprot_canonical_ac": "Q5TKT2-1",
        "species": [
            {
                "name": "Danio rerio",
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                    {
                        "database": "UniProtKB",
                        "id": "Q5TKT2",
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                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
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        "chemical_mass": 19140.0,
        "gene_names": "il17c;il17-3;il17c",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular region",
                "id": "GO:0005576",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5TKT2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5TKT2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cellular response to lipopolysaccharide",
                "id": "GO:0071222",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071222",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5TKT2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5TKT2"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "cytokine activity",
                "id": "GO:0005125",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005125",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5TKT2",
                        "url": "https://www.uniprot.org/uniprotkb/Q5TKT2"
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                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "Q5TKT4-1",
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                "name": "Danio rerio",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
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        ],
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        "chemical_mass": 17219.0,
        "gene_names": "f1;il17-1;il17a/f1",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050169",
                "name": "cutaneous lupus erythematosus",
                "description": "A lupus erythematosus that causes skin lesions on parts of the body that are exposed to sunlight.",
                "url": "https://disease-ontology.org/term/DOID:0050169",
                "evidence": [
                    {
                        "id": "0050169",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050169"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060180",
                "name": "colitis",
                "description": "An inflammatory bowel disease that involves inflammation located_in colon.",
                "url": "https://disease-ontology.org/term/DOID:0060180",
                "evidence": [
                    {
                        "id": "0060180",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060180"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060189",
                "name": "ileitis",
                "description": "An inflammatory bowel disease characterized by inflammation located_in ileum, has_symptom diarrhea, has_symptom abdominal pain, often in the right lower quadrant, has_symptom weight loss.",
                "url": "https://disease-ontology.org/term/DOID:0060189",
                "evidence": [
                    {
                        "id": "0060189",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060189"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080600",
                "name": "COVID-19",
                "description": "A Coronavirus infectious disease that is characterized by fever, cough and shortness of breath and that has_material_basis_in Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a subtype of Betacoronavirus pandemicum.",
                "url": "https://disease-ontology.org/term/DOID:0080600",
                "evidence": [
                    {
                        "id": "0080600",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080600"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080815",
                "name": "childhood-onset asthma",
                "description": "A chronic asthma that is characterized by first presentation in early childhood.",
                "url": "https://disease-ontology.org/term/DOID:0080815",
                "evidence": [
                    {
                        "id": "0080815",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080815"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080998",
                "name": "acute necrotizing pancreatitis",
                "description": "An acute pancreatitis that is characterized by one or more areas of necrosis in the pancreas with varying degree of involvement of the surrounding tissues or organ systems.",
                "url": "https://disease-ontology.org/term/DOID:0080998",
                "evidence": [
                    {
                        "id": "0080998",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080998"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1024",
                "name": "leprosy",
                "description": "A primary bacterial infectious disease that results_in infection located_in superficial peripheral nerves, located_in skin, located_in mucous membranes of the upper respiratory tract, located_in anterior chamber of the eyes, or located_in testes, has_material_basis_in Mycobacterium leprae, which is transmitted_by aerosol spread from infected nasal secretions to exposed nasal and oral mucosa. The infection has_symptom skin lesions, has_symptom sensory loss, has_symptom motor loss and has_symptom eye damage.",
                "url": "https://disease-ontology.org/term/DOID:1024",
                "evidence": [
                    {
                        "id": "1024",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1024"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10247",
                "name": "pleurisy",
                "description": "A pleural disease that is characterized by inflammation of the pleura, the lining of the pleural cavity surrounding the lungs.",
                "url": "https://disease-ontology.org/term/DOID:10247",
                "evidence": [
                    {
                        "id": "10247",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10247"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1025",
                "name": "tuberculoid leprosy",
                "description": "A leprosy that results in one erythematous large plaque with well-defined borders that are elevated and that slope down into an atrophic center.",
                "url": "https://disease-ontology.org/term/DOID:1025",
                "evidence": [
                    {
                        "id": "1025",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1025"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10316",
                "name": "pneumoconiosis",
                "description": "An interstitial lung disease that is caused by the inhalation of dust.",
                "url": "https://disease-ontology.org/term/DOID:10316",
                "evidence": [
                    {
                        "id": "10316",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10316"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10325",
                "name": "silicosis",
                "description": "A pneumoconiosis that is an inflammation and scarring of the upper lobes of the lungs causing nodular lesions resulting from inhalation of silica, quartz or slate particles.",
                "url": "https://disease-ontology.org/term/DOID:10325",
                "evidence": [
                    {
                        "id": "10325",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10325"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10887",
                "name": "lepromatous leprosy",
                "description": "A leprosy that results in early cutaneous lesions which consist of pale macules that are small, diffuse, and symmetric. This form of leprosy is characterized by hypoesthesia over extensor surfaces of the distal extremities, alopecia affecting lateral aspects of the eyebrows, saddle-nose deformity and oral lepromas.",
                "url": "https://disease-ontology.org/term/DOID:10887",
                "evidence": [
                    {
                        "id": "10887",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10887"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10966",
                "name": "lipoid nephrosis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:10966",
                "evidence": [
                    {
                        "id": "10966",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10966"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11265",
                "name": "trachoma",
                "description": "A commensal bacterial infectious disease that results_in infection located_in eye, has_material_basis_in Chlamydia trachomatis (A, B, Ba and C serovars), which is transmitted_by contact with eye discharge from the infected person and transmitted_by congenital method. The infection causes eyelid to turn inward which makes eyelashes to scratch the cornea.",
                "url": "https://disease-ontology.org/term/DOID:11265",
                "evidence": [
                    {
                        "id": "11265",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11265"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12306",
                "name": "vitiligo",
                "description": "An autoimmune disease that causes depigmentation of patches of skin resulting from loss of function or death of melanoctyes.",
                "url": "https://disease-ontology.org/term/DOID:12306",
                "evidence": [
                    {
                        "id": "12306",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12306"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12361",
                "name": "Graves' disease",
                "description": "An autoimmune disease of endocrine system that involves production of excessive amount of thyroid hormones, located_in thyroid gland.",
                "url": "https://disease-ontology.org/term/DOID:12361",
                "evidence": [
                    {
                        "id": "12361",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12361"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1273",
                "name": "respiratory syncytial virus infectious disease",
                "description": "A viral infectious disease that results_in infection located_in upper respiratory tract or located_in lower respiratory tract, has_material_basis_in Human respiratory syncytial virus (Orthopneumovirus hominis), which is transmitted_by droplet spread of nasal secretions from an infected person while coughing or sneezing, or transmitted_by contaminated fomites. The infection has_symptom runny nose, has_symptom fever, has_symptom cough, has_symptom wheezing, and has_symptom respiratory distress.",
                "url": "https://disease-ontology.org/term/DOID:1273",
                "evidence": [
                    {
                        "id": "1273",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1273"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13141",
                "name": "uveitis",
                "description": "An uveal disease is characterized by inflammation of any of the layers of the uvea of the eye, which includes the iris, ciliary body, and choroid.",
                "url": "https://disease-ontology.org/term/DOID:13141",
                "evidence": [
                    {
                        "id": "13141",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13141"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13241",
                "name": "Behcet's disease",
                "description": "An autoimmune disease that is characterized by mucocutaneous manifestations, including recurrent oral and genital ulcerations, ocular manifestations, especially chronic relapsing uveitis, and systemic vasculitis involving arteries and veins of all sizes.",
                "url": "https://disease-ontology.org/term/DOID:13241",
                "evidence": [
                    {
                        "id": "13241",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13241"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13375",
                "name": "temporal arteritis",
                "description": "A central nervous system vasculitis that is characterized by inflammation of the lining of arteries, often arteries in the head.",
                "url": "https://disease-ontology.org/term/DOID:13375",
                "evidence": [
                    {
                        "id": "13375",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13375"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1485",
                "name": "cystic fibrosis",
                "description": "A syndrome that is characterized by the buildup of thick, sticky mucus that can damage many organs.",
                "url": "https://disease-ontology.org/term/DOID:1485",
                "evidence": [
                    {
                        "id": "1485",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1485"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1580",
                "name": "diffuse scleroderma",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:1580",
                "evidence": [
                    {
                        "id": "1580",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1580"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2058",
                "name": "chronic mucocutaneous candidiasis",
                "description": "A candidiasis that refers to a heterogeneous group of disorders characterized by recurrent or persistent superficial fungal infections located_in skin, located_in mucous membrane, or located_in nail due to T-cell defects, has-agent Candida species and has_symptom scaling of skin lesions, has_symptom thickening of nails, has_symptom swollen periungal tissue, and has_symptom scarring of the scalp.",
                "url": "https://disease-ontology.org/term/DOID:2058",
                "evidence": [
                    {
                        "id": "2058",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2058"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2316",
                "name": "brain ischemia",
                "description": "An ischemia that is characterized by insufficient blood flow to the brain to meet metabolic demand.",
                "url": "https://disease-ontology.org/term/DOID:2316",
                "evidence": [
                    {
                        "id": "2316",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2316"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2377",
                "name": "multiple sclerosis",
                "description": "A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring.",
                "url": "https://disease-ontology.org/term/DOID:2377",
                "evidence": [
                    {
                        "id": "2377",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2377"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2755",
                "name": "Mycobacterium avium complex disease",
                "description": "A primary bacterial infectious disease that results_in infection, has_material_basis_in Mycobacterium avium complex (MAC), which is transmitted_by inhalation or transmitted_by ingestion of via the respiratory or gastrointestinal tract respectively. The bacteria cause disseminated infection in HIV infected people, while pulmonary disease in immunocompetent persons.",
                "url": "https://disease-ontology.org/term/DOID:2755",
                "evidence": [
                    {
                        "id": "2755",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2755"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2841",
                "name": "asthma",
                "description": "A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors. The disease has_symptom recurring periods of wheezing (a whistling sound while breathing), has_symptom chest tightness, has_symptom shortness of breath, has_symptom mucus production and has_symptom coughing.",
                "url": "https://disease-ontology.org/term/DOID:2841",
                "evidence": [
                    {
                        "id": "2841",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2841"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2942",
                "name": "bronchiolitis",
                "description": "A lung disease that is an inflammation of the bronchioles, the smallest air passages of the lungs. It is caused by viruses and bacteria. The disease has_symptom cough, has_symptom wheezing, has_symptom shortness of breath, has_symptom fever, has_symptom nasal flaring in infants and has_symptom bluish skin due to lack of oxygen.",
                "url": "https://disease-ontology.org/term/DOID:2942",
                "evidence": [
                    {
                        "id": "2942",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2942"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2957",
                "name": "pulmonary tuberculosis",
                "description": "A tuberculosis that is a contagious disease located_in lungs. The infection has_symptom fever, has_symptom cough, has_symptom difficulty in breathing, has_symptom inflammatory infiltrations, has_symptom formation of tubercles, has_symptom caseation, has_symptom pleural effusion, and has_symptom fibrosis.",
                "url": "https://disease-ontology.org/term/DOID:2957",
                "evidence": [
                    {
                        "id": "2957",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2957"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3083",
                "name": "chronic obstructive pulmonary disease",
                "description": "An obstructive lung disease that is a chronic and progressive disorder of small airways in the lungs and that is characterized by irreversible airflow obstruction, typically identified by reductions in quantitative spirometric indices, induced forced expiratory volume at 1 second (FEV1) and the ratio of FEV1 to forced vital capacity (less than 0.7 is diagnostic of COPD). Lung volume is increased and pulmonary hypertension may occur. The pathologic changes result in the disruption of the airflow in the bronchial airways. Signs and symptoms include shortness of breath, wheezing, productive cough and chest tightness. COPD is a consequence (an end result) of chronic bronchitis, emphysema or both.",
                "url": "https://disease-ontology.org/term/DOID:3083",
                "evidence": [
                    {
                        "id": "3083",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3083"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3310",
                "name": "atopic dermatitis",
                "description": "An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking.",
                "url": "https://disease-ontology.org/term/DOID:3310",
                "evidence": [
                    {
                        "id": "3310",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3310"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3388",
                "name": "periodontal disease",
                "description": "A mouth disease that is relating to or affecting the structures surrounding and supporting the teeth.",
                "url": "https://disease-ontology.org/term/DOID:3388",
                "evidence": [
                    {
                        "id": "3388",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3388"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3482",
                "name": "plague",
                "description": "A primary bacterial infectious disease that results_in infection, located_in lymph node, located_in vasculature or located_in lungs, has_material_basis_in Yersinia pestis, which is transmitted_by oriental rat flea (Xenopsylla cheopis) infected by feeding on rodents and other mammals, transmitted_by air, transmitted_by direct contact or transmitted_by ingestion of contaminated undercooked food.",
                "url": "https://disease-ontology.org/term/DOID:3482",
                "evidence": [
                    {
                        "id": "3482",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3482"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3770",
                "name": "pulmonary fibrosis",
                "description": "An interstitial lung disease that is characterized by destruction, scarring, and thickening of the interstitial lung tissues and progressive pulmonary function loss in a restrictive pattern, has_symptom progressive shortness of breath, fatigue, and chronic cough, possibly has_material_basis_in exposure to certain chemicals, autoimmune conditions, and radiation. It can be caused by inhaling hazardous chemicals, certain diseases, medication and genetics or unknown causes.",
                "url": "https://disease-ontology.org/term/DOID:3770",
                "evidence": [
                    {
                        "id": "3770",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3770"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:418",
                "name": "systemic scleroderma",
                "description": "A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies.",
                "url": "https://disease-ontology.org/term/DOID:418",
                "evidence": [
                    {
                        "id": "418",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:418"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4448",
                "name": "macular degeneration",
                "description": "A retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye and has_symptom vision loss.",
                "url": "https://disease-ontology.org/term/DOID:4448",
                "evidence": [
                    {
                        "id": "4448",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4448"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4481",
                "name": "allergic rhinitis",
                "description": "A rhinitis that is an allergic inflammation and irritation of the nasal airways involving sneezing, runny nose, nasal congestion, itching and tearing of the eyes caused by exposure to an allergen such as pollen, dust, mold, animal dander and droppings of cockroaches or house dust mites.",
                "url": "https://disease-ontology.org/term/DOID:4481",
                "evidence": [
                    {
                        "id": "4481",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4481"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4483",
                "name": "rhinitis",
                "description": "A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip.",
                "url": "https://disease-ontology.org/term/DOID:4483",
                "evidence": [
                    {
                        "id": "4483",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4483"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4780",
                "name": "anti-basement membrane glomerulonephritis",
                "description": "A Goodpasture syndrome that is characterized by damage to only kidney capillaries.",
                "url": "https://disease-ontology.org/term/DOID:4780",
                "evidence": [
                    {
                        "id": "4780",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4780"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body.",
                "url": "https://disease-ontology.org/term/DOID:6000",
                "evidence": [
                    {
                        "id": "6000",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6000"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6543",
                "name": "acne",
                "description": "A sebaceous gland disease characterized by areas of blackheads, whiteheads, pimples, greasy skin, and possibly scarring.",
                "url": "https://disease-ontology.org/term/DOID:6543",
                "evidence": [
                    {
                        "id": "6543",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:6543"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7147",
                "name": "ankylosing spondylitis",
                "description": "An arthritis that results_in inflammation in the joints of the spine and pelvis. The disease has_symptom pain, has_symptom stiffness in the spine, has_symptom stiffness in the neck, has_symptom stiffness in the hips, has_symptom stiffness in the jaw and has_symptom stiffness in the rib cage.",
                "url": "https://disease-ontology.org/term/DOID:7147",
                "evidence": [
                    {
                        "id": "7147",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7147"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:7148",
                "name": "rheumatoid arthritis",
                "description": "An arthritis that is an autoimmune disease which attacks healthy cells and tissue located_in joint.",
                "url": "https://disease-ontology.org/term/DOID:7148",
                "evidence": [
                    {
                        "id": "7148",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:7148"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:820",
                "name": "myocarditis",
                "description": "An extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle.",
                "url": "https://disease-ontology.org/term/DOID:820",
                "evidence": [
                    {
                        "id": "820",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:820"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:823",
                "name": "periapical periodontitis",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:823",
                "evidence": [
                    {
                        "id": "823",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:823"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8893",
                "name": "psoriasis",
                "description": "A skin disease that is characterized by patches of thick red skin and silvery scales.",
                "url": "https://disease-ontology.org/term/DOID:8893",
                "evidence": [
                    {
                        "id": "8893",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8893"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9008",
                "name": "psoriatic arthritis",
                "description": "An arthritis that is characterized by joint inflammation that usually occurs in combination with psoriasis.",
                "url": "https://disease-ontology.org/term/DOID:9008",
                "evidence": [
                    {
                        "id": "9008",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9008"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9074",
                "name": "systemic lupus erythematosus",
                "description": "A lupus erythematosus that is an inflammation of connective tissue marked by skin rashes, joint pain and swelling, inflammation of the kidneys and inflammation of the tissue surrounding the heart.",
                "url": "https://disease-ontology.org/term/DOID:9074",
                "evidence": [
                    {
                        "id": "9074",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9074"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9111",
                "name": "cutaneous leishmaniasis",
                "description": "A leishmaniasis that involves skin infection caused by Leishmania species, resulting in one or more cutaneous lesions.",
                "url": "https://disease-ontology.org/term/DOID:9111",
                "evidence": [
                    {
                        "id": "9111",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9111"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9408",
                "name": "acute myocardial infarction",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:9408",
                "evidence": [
                    {
                        "id": "9408",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9408"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9415",
                "name": "allergic asthma",
                "description": "An extrinsic asthma that is characterized by symptoms that are triggered by an allergic reaction caused by inhaled allergens such as dust mite allergen, pet dander, pollen and mold. The disease has_symptom coughing, has_symptom wheezing, has_symptom shortness of breath or has_symptom rapid breathing, and has_symptom chest tightness.",
                "url": "https://disease-ontology.org/term/DOID:9415",
                "evidence": [
                    {
                        "id": "9415",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9415"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5TKT4",
                        "url": "https://www.uniprot.org/uniprotkb/Q5TKT4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "inflammatory response",
                "id": "GO:0006954",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006954",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5TKT4",
                        "url": "https://www.uniprot.org/uniprotkb/Q5TKT4"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "cytokine activity",
                "id": "GO:0005125",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005125",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5TKT4",
                        "url": "https://www.uniprot.org/uniprotkb/Q5TKT4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q5TKT4-1"
    },
    {
        "uniprot_canonical_ac": "Q5TYP9-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5TYP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5TYP9"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 101,
        "chemical_mass": 11381.0,
        "gene_names": "ccl38a.4;ccl38a.4;si:dkeyp-59a8.3;zgc:171266",
        "protein_name": "C-C motif chemokine",
        "disease": [],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5TYP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5TYP9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "immune response",
                "id": "GO:0006955",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006955",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5TYP9",
                        "url": "https://www.uniprot.org/uniprotkb/Q5TYP9"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
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                ],
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                ],
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            }
        ],
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            {
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            {
                "name": "actin binding",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "actin cytoskeleton organization",
                "id": "GO:0030036",
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                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
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    },
    {
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        "protein_name": "",
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            {
                "name": "signaling receptor binding",
                "id": "GO:0005102",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005102",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9P0E4",
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                ],
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            },
            {
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9P0E4",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "junctional sarcoplasmic reticulum membrane",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0014701",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9P0E4",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "sarcoplasmic reticulum membrane",
                "id": "GO:0033017",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033017",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9P0E4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9P0E4"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "heart contraction",
                "id": "GO:0060047",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060047",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9P0E4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9P0E4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum",
                "id": "GO:0010880",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010880",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9P0E4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9P0E4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of cardiac muscle cell membrane potential",
                "id": "GO:0086036",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0086036",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9P0E4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9P0E4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "release of sequestered calcium ion into cytosol by sarcoplasmic reticulum",
                "id": "GO:0014808",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0014808",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9P0E4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9P0E4"
                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A8M9P0E4-1",
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                "end_pos": "2030",
                "site_lbl": "Thr2030",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
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                        "end_aa": "Thr",
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                        "site_lbl": "Thr2030",
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                                "id": "",
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                        ]
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                ]
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        ],
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    },
    {
        "uniprot_canonical_ac": "A0A8M9P0S1-1",
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            {
                "name": "Danio rerio",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9P0S1",
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                ],
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                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
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        ],
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        "chemical_mass": 38845.0,
        "gene_names": "fosaa;fosaa",
        "protein_name": "",
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            {
                "disease_id": "DOID:0050328",
                "name": "congenital hypothyroidism",
                "description": "A hypothyroidism that is present at birth.",
                "url": "https://disease-ontology.org/term/DOID:0050328",
                "evidence": [
                    {
                        "id": "0050328",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050328"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0050741",
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                "url": "https://disease-ontology.org/term/DOID:0050741",
                "evidence": [
                    {
                        "id": "0050741",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050741"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0050742",
                "name": "nicotine dependence",
                "description": "A substance dependence that is characterized by a physical dependence on nicotine.",
                "url": "https://disease-ontology.org/term/DOID:0050742",
                "evidence": [
                    {
                        "id": "0050742",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050742"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0050860",
                "name": "colorectal adenoma",
                "description": "An intestinal benign neoplasm that has_material_basis_in epithelial tissue of glandular origin and is located_in colon and located_in rectum.",
                "url": "https://disease-ontology.org/term/DOID:0050860",
                "evidence": [
                    {
                        "id": "0050860",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050860"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050861",
                "name": "colorectal adenocarcinoma",
                "description": "A colorectal carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:0050861",
                "evidence": [
                    {
                        "id": "0050861",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050861"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050865",
                "name": "tongue squamous cell carcinoma",
                "description": "A head and neck squamous cell carcinoma that is located_in the tongue.",
                "url": "https://disease-ontology.org/term/DOID:0050865",
                "evidence": [
                    {
                        "id": "0050865",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050865"
                    }
                ],
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            },
            {
                "disease_id": "DOID:10112",
                "name": "sleeping sickness",
                "description": "A trypanosomiasis that results from infection by Trypanosoma brucei and gambiense, which is transmitted by the bite of an infected tsetse fly (Glossina spp). The symptoms include fever, headache, joint pain, itching, confusion, sensory disturbances, poor coordination and sleep disturbances.",
                "url": "https://disease-ontology.org/term/DOID:10112",
                "evidence": [
                    {
                        "id": "10112",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10112"
                    }
                ],
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            },
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                "disease_id": "DOID:10763",
                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
                "url": "https://disease-ontology.org/term/DOID:10763",
                "evidence": [
                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10808",
                "name": "gastric ulcer",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:10808",
                "evidence": [
                    {
                        "id": "10808",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10808"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10892",
                "name": "hypospadias",
                "description": "A physical disorder characterized by an abnormally placed urethral opening on the underside of the penis or on the perineum.",
                "url": "https://disease-ontology.org/term/DOID:10892",
                "evidence": [
                    {
                        "id": "10892",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10892"
                    }
                ],
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            },
            {
                "disease_id": "DOID:11371",
                "name": "functional diarrhea",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11371",
                "evidence": [
                    {
                        "id": "11371",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11371"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11870",
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                "description": "A frontotemporal dementia that is characterized by a spectrum of neuropsychiatric symptoms ranging from those that affect the patient's personality to those that cause a decline in cognitive function.",
                "url": "https://disease-ontology.org/term/DOID:11870",
                "evidence": [
                    {
                        "id": "11870",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11870"
                    }
                ],
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            },
            {
                "disease_id": "DOID:1574",
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                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
                    {
                        "id": "1574",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1574"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1596",
                "name": "depressive disorder",
                "description": "A mood disorder characterized by persistent sadness, emptiness, or irritability and decreased ability to function.",
                "url": "https://disease-ontology.org/term/DOID:1596",
                "evidence": [
                    {
                        "id": "1596",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1596"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1826",
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                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions.",
                "url": "https://disease-ontology.org/term/DOID:1826",
                "evidence": [
                    {
                        "id": "1826",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1826"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1984",
                "name": "rectal benign neoplasm",
                "description": "An intestinal benign neoplasm located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:1984",
                "evidence": [
                    {
                        "id": "1984",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1984"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2384",
                "name": "Wernicke encephalopathy",
                "description": "A brain disease that is characterized by the presence of neurological symptoms of ophthalmoplegia, ataxia, and confusion caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves, in particular thiamine (vitamin B1).",
                "url": "https://disease-ontology.org/term/DOID:2384",
                "evidence": [
                    {
                        "id": "2384",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2384"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2560",
                "name": "morphine dependence",
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                "url": "https://disease-ontology.org/term/DOID:2560",
                "evidence": [
                    {
                        "id": "2560",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2560"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2921",
                "name": "glomerulonephritis",
                "description": "A nephritis that causes inflammation of the glomeruli located_in kidney.",
                "url": "https://disease-ontology.org/term/DOID:2921",
                "evidence": [
                    {
                        "id": "2921",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2921"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3328",
                "name": "temporal lobe epilepsy",
                "description": "A focal epilepsy that is characterized by recurrent, unprovoked focal seizures that originate in the temporal lobe of the brain and last about one or two minutes.",
                "url": "https://disease-ontology.org/term/DOID:3328",
                "evidence": [
                    {
                        "id": "3328",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3328"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3744",
                "name": "cervical squamous cell carcinoma",
                "description": "A cervix carcinoma that has_material_basis_in squamous cells of the cervix.",
                "url": "https://disease-ontology.org/term/DOID:3744",
                "evidence": [
                    {
                        "id": "3744",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3744"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia.",
                "url": "https://disease-ontology.org/term/DOID:5844",
                "evidence": [
                    {
                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:6000",
                "name": "congestive heart failure",
                "description": "A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body.",
                "url": "https://disease-ontology.org/term/DOID:6000",
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                        "database": "AGR",
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                "disease_id": "DOID:6364",
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                "description": "A brain disease that is characterized by moderate to severe headaches, nausea, extreme sensitivity to light and sound and intense unilaterial throbbing or pulsing.",
                "url": "https://disease-ontology.org/term/DOID:6364",
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                        "id": "6364",
                        "database": "AGR",
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                        "database": "AGR",
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                        "id": "898",
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                        "id": "90",
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                        "id": "9408",
                        "database": "AGR",
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                ],
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                    {
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                "pmid": ""
            },
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                "name": "homophilic cell adhesion via plasma membrane adhesion molecules",
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                "pmid": ""
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                ],
                "pmid": ""
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            {
                "name": "cell-cell adhesion mediated by cadherin",
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                    {
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                "name": "calcium ion binding",
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                    {
                        "database": "UniProtKB",
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                "pmid": ""
            },
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                    {
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                ],
                "pmid": ""
            },
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                "name": "beta-catenin binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008013",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                "pmid": ""
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        ],
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                "pmid": ""
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        ],
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                "name": "cell-cell adhesion",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098609",
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                "pmid": ""
            },
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        "protein_name": "",
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                "name": "cytoplasm",
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                ],
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        ],
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        "gene_names": "LOC108179272;LOC108179272",
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                "name": "skeletal muscle contraction",
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                        "database": "UniProtKB",
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                "name": "sarcoplasmic reticulum",
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                "pmid": ""
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                ],
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                "glygen_name": "Zebrafish",
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        "length": 530,
        "chemical_mass": 60023.0,
        "gene_names": "LOC110438168;LOC110438168",
        "protein_name": "",
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        "record_id": "A0A8M9P2T4-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9P2V8-1",
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                "name": "Danio rerio",
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                ],
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        ],
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        "chemical_mass": 42586.0,
        "gene_names": "htr1e;htr1e",
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                "name": "plasma membrane",
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                ],
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            {
                "name": "membrane",
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                "name": "extracellular space",
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        ],
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        "gene_names": "LOC110438207;LOC110438207",
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    },
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                ],
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        "protein_name": "C2H2-type domain-containing protein",
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                "name": "cytoplasm",
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                "name": "ubiquitin-like ligase-substrate adaptor activity",
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                "name": "Cul3-RING ubiquitin ligase complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031463",
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                    {
                        "database": "UniProtKB",
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                "pmid": ""
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                "name": "proteasome-mediated ubiquitin-dependent protein catabolic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043161",
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                    {
                        "database": "UniProtKB",
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                        "start_aa": "Thr",
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                "description": "An aspergillosis that is a serious fungal infection of the lung with pneumonia caused by Aspergillus, which spreads to other parts of the body through bloodstream in patients with acute leukemia and recipients of tissue transplants. Clinical symptoms include pulmonary nodules and hemorrhage.",
                "url": "https://disease-ontology.org/term/DOID:0050073",
                "evidence": [
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:0050153",
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                "url": "https://disease-ontology.org/term/DOID:1883",
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                        "id": "1883",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1883"
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                ],
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                "name": "immune response",
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                        "database": "UniProtKB",
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                "name": "complement component C1q complex binding",
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        ],
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        ],
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                "name": "negative regulation of insulin receptor signaling pathway",
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                        "database": "UniProtKB",
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                ],
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                ],
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            }
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                "name": "ubiquitin protein ligase activity",
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                ],
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        ],
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        "gene_names": "LOC101886833;LOC101886833",
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                "name": "extracellular space",
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                ],
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                "name": "immune response",
                "id": "GO:0006955",
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                "pmid": ""
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                ],
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        ],
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                        "site_category_dict": {
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                "name": "heterochromatin formation",
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        "gene_names": "olfcq10;olfcq10;si:ch211-127a20.6;v2rh7",
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            {
                "name": "G protein-coupled receptor activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004930",
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        "uniprot_canonical_ac": "A3KQN9-1",
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                ],
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        ],
        "length": 996,
        "chemical_mass": 113637.0,
        "gene_names": "ints8;ints8;zgc:111823",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "chromosome",
                "id": "GO:0005694",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005694",
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                "name": "integrator complex",
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        "uniprot_canonical_ac": "A3KQR6-1",
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            }
        ],
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    },
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                "pmid": ""
            },
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