[
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                "name": "Danio rerio",
                "taxid": 7955,
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                "pmid": ""
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            {
                "name": "early endosome membrane",
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                "pmid": ""
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            {
                "name": "phagophore assembly site",
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                "pmid": ""
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                "name": "protein transport",
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                ],
                "pmid": ""
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            {
                "name": "endocytic recycling",
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                        "id": "Q566W7",
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                "pmid": ""
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            {
                "name": "piecemeal microautophagy of the nucleus",
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                ],
                "pmid": ""
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                "name": "reticulophagy",
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                        "id": "Q566W7",
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                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of autophagosome assembly",
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                        "id": "Q566W7",
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                ],
                "pmid": ""
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                "name": "phosphatidylinositol binding",
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                "pmid": ""
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                "name": "RNA binding",
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                "pmid": ""
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        ],
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                "name": "cytoplasm",
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                "pmid": ""
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            {
                "name": "nuclear speck",
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                "pmid": ""
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            {
                "name": "catalytic step 2 spliceosome",
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                "pmid": ""
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            {
                "name": "exon-exon junction complex",
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                "evidence": [
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                "pmid": ""
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        ],
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                "name": "mRNA processing",
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                        "url": "https://www.uniprot.org/uniprotkb/Q566Y8"
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                ],
                "pmid": ""
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            {
                "name": "regulation of translation",
                "id": "GO:0006417",
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                ],
                "pmid": ""
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            {
                "name": "RNA splicing",
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                ],
                "pmid": ""
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            {
                "name": "nuclear-transcribed mRNA catabolic process, nonsense-mediated decay",
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                "pmid": ""
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                "name": "regulation of gene expression",
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                "pmid": ""
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                "name": "mRNA transport",
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                "pmid": ""
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            {
                "name": "regulation of alternative mRNA splicing, via spliceosome",
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                "name": "manganese ion binding",
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                "pmid": ""
            },
            {
                "name": "GPI-mannose ethanolamine phosphate phosphodiesterase activity",
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                        "id": "Q566Y9",
                        "url": "https://www.uniprot.org/uniprotkb/Q566Y9"
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                "pmid": ""
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        ],
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                "name": "endoplasmic reticulum to Golgi vesicle-mediated transport",
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                ],
                "pmid": ""
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            {
                "name": "GPI anchor biosynthetic process",
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                "pmid": ""
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                "name": "endoplasmic reticulum-Golgi intermediate compartment membrane",
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                "name": "endoplasmic reticulum exit site",
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                "url": "https://disease-ontology.org/term/DOID:0060364",
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            {
                "name": "spindle pole",
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                ],
                "pmid": ""
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                "name": "cytoplasm",
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                        "url": "https://www.uniprot.org/uniprotkb/Q567G2"
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                ],
                "pmid": ""
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            {
                "name": "cleavage furrow",
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                "name": "protein-macromolecule adaptor activity",
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                "pmid": ""
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                "name": "cerebellar Purkinje cell differentiation",
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                ],
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            {
                "name": "cytoplasmic microtubule organization",
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            {
                "name": "midbrain development",
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                ],
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                "url": "https://disease-ontology.org/term/DOID:9074",
                "evidence": [
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                        "url": "https://www.uniprot.org/uniprotkb/Q567V5"
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                "pmid": ""
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            {
                "name": "cytosol",
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                "pmid": ""
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            {
                "name": "spliceosomal snRNP complex",
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                "pmid": ""
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            {
                "name": "U12-type spliceosomal complex",
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                "pmid": ""
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        ],
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                "name": "mRNA splicing, via spliceosome",
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                "pmid": ""
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                ],
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                "pmid": ""
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                "pmid": ""
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            {
                "name": "sterol biosynthetic process",
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                "pmid": ""
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                ],
                "pmid": ""
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            {
                "name": "spliceosomal complex",
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                "pmid": ""
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                "name": "mRNA processing",
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            {
                "name": "RNA splicing",
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                ],
                "pmid": ""
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            {
                "name": "protein kinase inhibitor activity",
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                    }
                ],
                "pmid": ""
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            {
                "name": "double-stranded RNA binding",
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                ],
                "pmid": ""
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                ],
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                ],
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            {
                "name": "DNA-binding transcription activator activity, RNA polymerase II-specific",
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                "url": "https://disease-ontology.org/term/DOID:0111080",
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            {
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                "name": "zeta DNA polymerase complex",
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                "name": "DNA repair",
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                "name": "positive regulation of peptidyl-serine phosphorylation",
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                "name": "negative regulation of protein catabolic process",
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                "name": "protein serine/threonine phosphatase inhibitor activity",
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                "name": "ubiquitin protein ligase activity",
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            {
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                ],
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                "name": "nucleus",
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                    }
                ],
                "pmid": ""
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        ],
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            {
                "name": "defense response to Gram-positive bacterium",
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                "evidence": [
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                ],
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                ],
                "pmid": ""
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            {
                "name": "histone H2A acetyltransferase activity",
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                "pmid": ""
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            {
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            {
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            {
                "name": "SCF-dependent proteasomal ubiquitin-dependent protein catabolic process",
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            {
                "name": "L-valine catabolic process",
                "id": "GO:0006574",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006574",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EB4",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EB4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q58EB4-1"
    },
    {
        "uniprot_canonical_ac": "Q58EE9-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EE9",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EE9"
                    }
                ],
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                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 444,
        "chemical_mass": 51249.0,
        "gene_names": "gfap;cb345;etID36982.3;gfapl;gfap;wu:fb34h11;wu:fk42c12;xx:af506734;zgc:110485",
        "protein_name": "Glial fibrillary acidic protein",
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            {
                "disease_id": "DOID:0051061",
                "name": "stroke",
                "description": "A cerebrovascular disease that is characterized by disruption of blood flow to the brain resulting in damage to brain cells due to a lack of oxygen.",
                "url": "https://disease-ontology.org/term/DOID:0051061",
                "evidence": [
                    {
                        "id": "0051061",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0051061"
                    }
                ],
                "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:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "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:4252",
                "name": "Alexander disease",
                "description": "A leukodystrophy that is characterized by the destruction of white matter and the formation of Rosenthal fibers consisting of abnormal clumps of protein that accumulate in astrocytes.",
                "url": "https://disease-ontology.org/term/DOID:4252",
                "evidence": [
                    {
                        "id": "4252",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4252"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4724",
                "name": "brain edema",
                "description": "A brain disease that is characterized by excess accumulation of fluid in the intracellular and/or extracellular spaces of the brain, has_symptom nausea, has_symptom vomiting, has_symptom blurred vision, has_symptom seizure, has_symptom coma.",
                "url": "https://disease-ontology.org/term/DOID:4724",
                "evidence": [
                    {
                        "id": "4724",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4724"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5679",
                "name": "retinal disease",
                "description": "An eye disease that is located_in the retina.",
                "url": "https://disease-ontology.org/term/DOID:5679",
                "evidence": [
                    {
                        "id": "5679",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5679"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "structural constituent of cytoskeleton",
                "id": "GO:0005200",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005200",
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                    {
                        "database": "UniProtKB",
                        "id": "Q58EE9",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EE9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                    {
                        "database": "UniProtKB",
                        "id": "Q58EE9",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EE9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intermediate filament",
                "id": "GO:0005882",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005882",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EE9",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EE9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell projection",
                "id": "GO:0042995",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042995",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EE9",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EE9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "type III intermediate filament",
                "id": "GO:0045098",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045098",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EE9",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EE9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "intermediate filament organization",
                "id": "GO:0045109",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045109",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EE9",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EE9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of chaperone-mediated autophagy",
                "id": "GO:1904714",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904714",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EE9",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EE9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q58EE9-1"
    },
    {
        "uniprot_canonical_ac": "Q58EG2-1",
        "species": [
            {
                "name": "Danio rerio",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EG2",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EG2"
                    }
                ],
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                "glygen_name": "Zebrafish",
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            }
        ],
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        "chemical_mass": 38319.0,
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        "protein_name": "Erlin-1",
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            {
                "disease_id": "DOID:0110813",
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                "evidence": [
                    {
                        "id": "0110813",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110813"
                    }
                ],
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            },
            {
                "disease_id": "DOID:2476",
                "name": "hereditary spastic paraplegia",
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                "url": "https://disease-ontology.org/term/DOID:2476",
                "evidence": [
                    {
                        "id": "2476",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2476"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "cholesterol metabolic process",
                "id": "GO:0008203",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008203",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EG2",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EG2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of fatty acid biosynthetic process",
                "id": "GO:0045717",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045717",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EG2",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EG2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of cholesterol biosynthetic process",
                "id": "GO:0045541",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045541",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EG2",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EG2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "SREBP signaling pathway",
                "id": "GO:0032933",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032933",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EG2",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EG2"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "endoplasmic reticulum membrane",
                "id": "GO:0005789",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005789",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EG2",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EG2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein-containing complex",
                "id": "GO:0032991",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032991",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EG2",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EG2"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "ubiquitin protein ligase binding",
                "id": "GO:0031625",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031625",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EG2",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EG2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cholesterol binding",
                "id": "GO:0015485",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015485",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EG2",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EG2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "Q58EG2-1",
                "start_pos": "106",
                "end_pos": "106",
                "site_lbl": "Asn106",
                "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": 106,
                        "start_aa": "Asn",
                        "end_pos": 106,
                        "end_aa": "Asn",
                        "residue": "Asn",
                        "site_lbl": "Asn106",
                        "evidence": [
                            {
                                "id": "Q58EG2",
                                "database": "UniProtKB",
                                "url": "https://www.uniprot.org/uniprotkb/Q58EG2#ptm_processing"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "Q58EG2-1"
    },
    {
        "uniprot_canonical_ac": "Q58EK4-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EK4",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EK4"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 383,
        "chemical_mass": 42409.0,
        "gene_names": "parla;parla;parl;zgc:112986",
        "protein_name": "Presenilin-associated rhomboid-like protein A, mitochondrial",
        "disease": [
            {
                "disease_id": "DOID:11830",
                "name": "myopia",
                "description": "A refractive error characterized by the inability to see farther objects clearly.",
                "url": "https://disease-ontology.org/term/DOID:11830",
                "evidence": [
                    {
                        "id": "11830",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11830"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2018",
                "name": "hyperinsulinism",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:2018",
                "evidence": [
                    {
                        "id": "2018",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2018"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3393",
                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.",
                "url": "https://disease-ontology.org/term/DOID:3393",
                "evidence": [
                    {
                        "id": "3393",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3393"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3459",
                "name": "breast carcinoma",
                "description": "A breast cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.",
                "url": "https://disease-ontology.org/term/DOID:3459",
                "evidence": [
                    {
                        "id": "3459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3459"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3652",
                "name": "Leigh disease",
                "description": "A cytochrome-c oxidase deficiency disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity.",
                "url": "https://disease-ontology.org/term/DOID:3652",
                "evidence": [
                    {
                        "id": "3652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:705",
                "name": "Leber hereditary optic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:705",
                "evidence": [
                    {
                        "id": "705",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:705"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "serine-type endopeptidase activity",
                "id": "GO:0004252",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004252",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EK4",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EK4"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "mitochondrion",
                "id": "GO:0005739",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005739",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EK4",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "mitochondrial inner membrane",
                "id": "GO:0005743",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005743",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EK4",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EK4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein processing",
                "id": "GO:0016485",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016485",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EK4",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EK4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mitochondrion organization",
                "id": "GO:0010821",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010821",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EK4",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EK4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "Q58EK4-1"
    },
    {
        "uniprot_canonical_ac": "Q58EN8-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q58EN8",
                        "url": "https://www.uniprot.org/uniprotkb/Q58EN8"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 617,
        "chemical_mass": 70429.0,
        "gene_names": "vps33b;vps33b;zgc:110803",
        "protein_name": "Vacuolar protein sorting-associated protein 33B",
        "disease": [
            {
                "disease_id": "DOID:0050763",
                "name": "ARC syndrome",
                "description": "A syndrome that is characterized by congenital joint contractures, renal tubular dysfunction, cholestasis, severe failure to thrive, ichthyosis and a defect in platelet alpha-granule biogenesis and that has_material_basis_in homozygous or compound heterozygous mutation in the VPS33B gene or homozygous or compound heterozygous mutation in the VIPAR gene on chromosome 14q24.3.",
                "url": "https://disease-ontology.org/term/DOID:0050763",
                "evidence": [
                    {
                        "id": "0050763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070221",
                "name": "progressive familial intrahepatic cholestasis",
                "description": "An intrahepatic cholestasis characterized by early onset of chronic unremitting cholestasis of hepatocellular origin that progresses to hepatic fibrosis, cirrhosis, and end-stage liver disease before adulthood.",
                "url": "https://disease-ontology.org/term/DOID:0070221",
                "evidence": [
                    {
                        "id": "0070221",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070221"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080954",
                "name": "arthrogryposis multiplex congenita",
                "description": "A nervous system disease that is characterized by development of multiple joint contractures affecting two or more areas of the body prior to birth.",
                "url": "https://disease-ontology.org/term/DOID:0080954",
                "evidence": [
                    {
                        "id": "0080954",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080954"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111353",
                "name": "arthrogryposis, renal dysfunction, and cholestasis 1",
                "description": "An arthrogryposis, renal dysfunction, and cholestasis that has_material_basis_in homozygous or compound heterozygous mutation in VPS33B on 15q26.1.",
                "url": "https://disease-ontology.org/term/DOID:0111353",
                "evidence": [
                    {
                        "id": "0111353",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111353"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13580",
                "name": "cholestasis",
                "description": "A bile duct disease that is characterized by where bile cannot flow from the liver to the duodenum.",
                "url": "https://disease-ontology.org/term/DOID:13580",
                "evidence": [
                    {
                        "id": "13580",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13580"
                    }
                ],
                "weight": 0.0
            },
            {
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            },
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                ],
                "pmid": ""
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        ],
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            {
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                "disease_id": "DOID:9620",
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                "id": "GO:0005615",
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                "pmid": ""
            },
            {
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        ],
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            {
                "name": "regulation of cell adhesion",
                "id": "GO:0030155",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030155",
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            {
                "name": "neuron projection development",
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                        "glytoucan_ac": "",
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                        },
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                        "relation": "attached",
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                        "start_aa": "Thr",
                        "end_pos": 1499,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1499",
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                                "id": "",
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                        ]
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                ]
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                "name": "peptidyl-prolyl cis-trans isomerase activity",
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                ],
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            {
                "name": "RNA splicing",
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                "name": "retina development in camera-type eye",
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                ],
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            },
            {
                "name": "cell-cell adhesion mediated by cadherin",
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                ],
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        ],
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                "name": "plasma membrane",
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                        "type": "O-linked",
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                        "site_category_dict": {
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                        "relation": "attached",
                        "comment": "",
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                ],
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        ],
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            {
                "name": "intracellular vesicle",
                "id": "GO:0097708",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097708",
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                "pmid": ""
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            {
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                ],
                "pmid": ""
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            {
                "name": "plasma membrane",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PBV5"
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                ],
                "pmid": ""
            },
            {
                "name": "cell projection",
                "id": "GO:0042995",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042995",
                "evidence": [
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                ],
                "pmid": ""
            },
            {
                "name": "presynapse",
                "id": "GO:0098793",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098793",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "synapse",
                "id": "GO:0045202",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045202",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PBV5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PBV5"
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                ],
                "pmid": ""
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            {
                "name": "protein-macromolecule adaptor activity",
                "id": "GO:0030674",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PBV5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PBV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "calcium ion binding",
                "id": "GO:0005509",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005509",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PBV5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PBV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "guanyl-nucleotide exchange factor activity",
                "id": "GO:0005085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PBV5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PBV5"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "intracellular signal transduction",
                "id": "GO:0035556",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035556",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PBV5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PBV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endosomal transport",
                "id": "GO:0016197",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016197",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PBV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "clathrin-dependent synaptic vesicle endocytosis",
                "id": "GO:0150007",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0150007",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PBV5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PBV5"
                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A8M9PBV5-1",
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                "end_pos": "172",
                "site_lbl": "Thr172",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
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                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
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                        "start_aa": "Thr",
                        "end_pos": 172,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr172",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A0A8M9PBV5-1",
                "start_pos": "867",
                "end_pos": "867",
                "site_lbl": "Thr867",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
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                            {
                                "label": "isoglyp",
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                        ],
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                        "site_category_dict": {
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                        },
                        "site_seq": "",
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                        "comment": "",
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                        "start_pos": 867,
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                        "site_lbl": "Thr867",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "A0A8M9PC12-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PC12",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PC12"
                    }
                ],
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                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 512,
        "chemical_mass": 58415.0,
        "gene_names": "frk;frk",
        "protein_name": "Tyrosine-protein kinase",
        "disease": [
            {
                "disease_id": "DOID:10155",
                "name": "intestinal cancer",
                "description": "A gastrointestinal system cancer that is located_in the intestine.",
                "url": "https://disease-ontology.org/term/DOID:10155",
                "evidence": [
                    {
                        "id": "10155",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10155"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2907",
                "name": "Goldenhar syndrome",
                "description": "A syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch.",
                "url": "https://disease-ontology.org/term/DOID:2907",
                "evidence": [
                    {
                        "id": "2907",
                        "database": "AGR",
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                    }
                ],
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            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "cranial skeletal system development",
                "id": "GO:1904888",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904888",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PC12"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell surface receptor protein tyrosine kinase signaling pathway",
                "id": "GO:0007169",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007169",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PC12",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell differentiation",
                "id": "GO:0030154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PC12",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PC12"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "non-membrane spanning protein tyrosine kinase activity",
                "id": "GO:0004715",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004715",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
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                "name": "signaling receptor binding",
                "id": "GO:0005102",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005102",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PC12",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PC12",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PC12",
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                    }
                ],
                "pmid": ""
            },
            {
                "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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                    }
                ],
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            }
        ],
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        "uniprot_canonical_ac": "A0A8M9PC75-1",
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        ],
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                    {
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                        "database": "AGR",
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                ],
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            {
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                "evidence": [
                    {
                        "id": "0070249",
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                ],
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            },
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                        "id": "0080954",
                        "database": "AGR",
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                ],
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            },
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                "url": "https://disease-ontology.org/term/DOID:0080979",
                "evidence": [
                    {
                        "id": "0080979",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080979"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111618",
                "name": "autosomal recessive spinocerebellar ataxia 8",
                "description": "An autosomal recessive cerebellar ataxia characterized by slowly progressive neurodegeneration resulting in gait ataxia and other cerebellar signs, spasticity, secondary musculoskeletal abnormalities, and ocular movement anomalies that has_material_basis_in homozygous or compound heterozygous mutation in SYNE1 on chromosome 6q25.2.",
                "url": "https://disease-ontology.org/term/DOID:0111618",
                "evidence": [
                    {
                        "id": "0111618",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111618"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11726",
                "name": "Emery-Dreifuss muscular dystrophy",
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                "url": "https://disease-ontology.org/term/DOID:11726",
                "evidence": [
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                        "id": "11726",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11726"
                    }
                ],
                "weight": 0.0
            },
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                "evidence": [
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                        "id": "3312",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3312"
                    }
                ],
                "weight": 0.0
            },
            {
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                "evidence": [
                    {
                        "id": "9884",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9884"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "actin binding",
                "id": "GO:0003779",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PC75",
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                ],
                "pmid": ""
            },
            {
                "name": "cytoskeleton-nuclear membrane anchor activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140444",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
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        ],
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            {
                "name": "cytoskeleton",
                "id": "GO:0005856",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005856",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            },
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                "name": "nuclear membrane",
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                    }
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        ],
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                ],
                "pmid": ""
            },
            {
                "name": "dendrite",
                "id": "GO:0030425",
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                "pmid": ""
            },
            {
                "name": "neuronal cell body",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043025",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "postsynapse",
                "id": "GO:0098794",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098794",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PC77"
                    }
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                "id": "GO:0045332",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045332",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDL2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDL2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Golgi organization",
                "id": "GO:0007030",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007030",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDL2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDL2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PDL2-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PDN1-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDN1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDN1"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 581,
        "chemical_mass": 64957.0,
        "gene_names": "pimr211;pimr211",
        "protein_name": "non-specific serine/threonine protein kinase",
        "disease": [],
        "molecular_function": [
            {
                "name": "protein serine/threonine kinase activity",
                "id": "GO:0004674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004674",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDN1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDN1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDN1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDN1"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDN1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDN1"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "negative regulation of apoptotic process",
                "id": "GO:0043066",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043066",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDN1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDN1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mitotic cell cycle",
                "id": "GO:0007346",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007346",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDN1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDN1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PDN1-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PDP8-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDP8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDP8"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 219,
        "chemical_mass": 24837.0,
        "gene_names": "si:dkey-40m6.14;gstk1;zgc:92763",
        "protein_name": "Glutathione S-transferase kappa",
        "disease": [
            {
                "disease_id": "DOID:0080208",
                "name": "metabolic dysfunction-associated steatotic liver disease",
                "description": "A steatotic liver disease characterized by at least one of five specified cardiometabolic risk factors and no other discernible cause with normal to no alcohol use. The five cardiometabolic risk factors are: (1) higher than normal body mass index or waist circumference; (2) higher than normal serum glucose or glycated hemoglobin level, or type 2 diabetes; (3) higher than normal blood pressure or hypertensive treatment; (4) higher than normal plasma triglycerides or lipid lowering treatment; and (5) lower than normal plasma high-density lipoprotein cholesterol.",
                "url": "https://disease-ontology.org/term/DOID:0080208",
                "evidence": [
                    {
                        "id": "0080208",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080208"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:234",
                "name": "colon adenocarcinoma",
                "description": "A colon carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:234",
                "evidence": [
                    {
                        "id": "234",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:234"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "glutathione transferase activity",
                "id": "GO:0004364",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004364",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDP8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDP8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "oxidoreductase activity",
                "id": "GO:0016491",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016491",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDP8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDP8"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDP8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDP8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PDP8-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PDQ2-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 2280,
        "chemical_mass": 245512.0,
        "gene_names": "arid1aa;arid1aa",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050934",
                "name": "ovarian clear cell carcinoma",
                "description": "An ovarian carcinoma that has_material_basis_in cells with clear cytoplasm and glycogen secreting hob nail cells.",
                "url": "https://disease-ontology.org/term/DOID:0050934",
                "evidence": [
                    {
                        "id": "0050934",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050934"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070042",
                "name": "Coffin-Siris syndrome 1",
                "description": "A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the ARID1B gene on chromosome 6q25.3.",
                "url": "https://disease-ontology.org/term/DOID:0070042",
                "evidence": [
                    {
                        "id": "0070042",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070042"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070044",
                "name": "Coffin-Siris syndrome 2",
                "description": "A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the ARID1A gene on chromosome 1p36.11.",
                "url": "https://disease-ontology.org/term/DOID:0070044",
                "evidence": [
                    {
                        "id": "0070044",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070044"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10591",
                "name": "pre-eclampsia",
                "description": "A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:10591",
                "evidence": [
                    {
                        "id": "10591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "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:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:162",
                "name": "cancer",
                "description": "A disease of cellular proliferation that is malignant and primary, characterized by uncontrolled cellular proliferation, local cell invasion and metastasis.",
                "url": "https://disease-ontology.org/term/DOID:162",
                "evidence": [
                    {
                        "id": "162",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:162"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1925",
                "name": "Coffin-Siris syndrome",
                "description": "An autosomal dominant intellectual developmental disorder that is characterized by mental retardation associated with coarse facial features, hypertrichosis, sparse scalp hair, and hypoplastic or absent fifth fingernails or toenails.",
                "url": "https://disease-ontology.org/term/DOID:1925",
                "evidence": [
                    {
                        "id": "1925",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1925"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon.",
                "url": "https://disease-ontology.org/term/DOID:219",
                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2870",
                "name": "endometrial adenocarcinoma",
                "description": "An endometrial carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:2870",
                "evidence": [
                    {
                        "id": "2870",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2870"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3717",
                "name": "gastric adenocarcinoma",
                "description": "A stomach carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3717",
                "evidence": [
                    {
                        "id": "3717",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3717"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4914",
                "name": "esophagus adenocarcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:4914",
                "evidence": [
                    {
                        "id": "4914",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4914"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4927",
                "name": "Klatskin's tumor",
                "description": "An intrahepatic cholangiocarcinoma arising near or at the confluence of the right and left hepatic ducts.",
                "url": "https://disease-ontology.org/term/DOID:4927",
                "evidence": [
                    {
                        "id": "4927",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4927"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4928",
                "name": "intrahepatic cholangiocarcinoma",
                "description": "A cholangiocarcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree.",
                "url": "https://disease-ontology.org/term/DOID:4928",
                "evidence": [
                    {
                        "id": "4928",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4928"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:769",
                "name": "neuroblastoma",
                "description": "An autonomic nervous system neoplasm that derives_from immature nerve cells.",
                "url": "https://disease-ontology.org/term/DOID:769",
                "evidence": [
                    {
                        "id": "769",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:769"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9261",
                "name": "nasopharynx carcinoma",
                "description": "A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract.",
                "url": "https://disease-ontology.org/term/DOID:9261",
                "evidence": [
                    {
                        "id": "9261",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9261"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleoplasm",
                "id": "GO:0005654",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "SWI/SNF complex",
                "id": "GO:0016514",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016514",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nBAF complex",
                "id": "GO:0071565",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071565",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "brahma complex",
                "id": "GO:0035060",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035060",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "chromatin remodeling",
                "id": "GO:0006338",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006338",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "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": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nervous system development",
                "id": "GO:0007399",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007399",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "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": "A0A8M9PDQ2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PDQ2"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A8M9PDQ2-1",
                "start_pos": "1363",
                "end_pos": "1363",
                "site_lbl": "Thr1363",
                "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": 1363,
                        "start_aa": "Thr",
                        "end_pos": 1363,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1363",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            },
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                "uniprot_canonical_ac": "A0A8M9PDQ2-1",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008188",
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            },
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                "name": "neuromedin U receptor activity",
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                "evidence": [
                    {
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                    }
                ],
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            }
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    },
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                    }
                ],
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        ],
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "external side of plasma membrane",
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                    {
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                    }
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            }
        ],
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                "name": "immune response",
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                    }
                ],
                "pmid": ""
            },
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                "name": "positive regulation of cytosolic calcium ion concentration",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007204",
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                    {
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                "pmid": ""
            },
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                "name": "calcium-mediated signaling",
                "id": "GO:0019722",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019722",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell chemotaxis",
                "id": "GO:0060326",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060326",
                "evidence": [
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                "name": "C-C chemokine receptor activity",
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                ],
                "pmid": ""
            }
        ],
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                ],
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            }
        ],
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                "name": "cytoplasm",
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                    {
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                ],
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            },
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                "name": "plasma membrane",
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                ],
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            },
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                "name": "synapse",
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                    {
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            }
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            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "synaptic signaling",
                "id": "GO:0099536",
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                    {
                        "database": "UniProtKB",
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                ],
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            }
        ],
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                        "glytoucan_ac": "",
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                        "start_aa": "Thr",
                        "end_pos": 355,
                        "end_aa": "Thr",
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                        "site_lbl": "Thr355",
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                                "database": "GlyGen",
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                ]
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                "site_lbl": "Thr438",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
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    {
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        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
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                ],
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                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 322,
        "chemical_mass": 33914.0,
        "gene_names": "sdsl;sdsl;si:ch73-9j13.2",
        "protein_name": "L-serine ammonia-lyase",
        "disease": [
            {
                "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": [
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                        "id": "14250",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14250"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
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                    {
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "gluconeogenesis",
                "id": "GO:0006094",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PEB6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PEB6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "L-threonine catabolic process",
                "id": "GO:0006567",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006567",
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                ],
                "pmid": ""
            },
            {
                "name": "L-serine catabolic process",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006565",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "L-serine ammonia-lyase activity",
                "id": "GO:0003941",
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                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "threonine deaminase activity",
                "id": "GO:0004794",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004794",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
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            }
        ],
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        "uniprot_canonical_ac": "A0A8M9PED3-1",
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                        "id": "A0A8M9PED3",
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            }
        ],
        "length": 441,
        "chemical_mass": 49004.0,
        "gene_names": "foxn3;foxn3;zgc:136571",
        "protein_name": "Forkhead box protein N3",
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            {
                "name": "DNA-binding transcription factor activity",
                "id": "GO:0003700",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PED3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PED3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cis-regulatory region sequence-specific DNA binding",
                "id": "GO:0000987",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000987",
                "evidence": [
                    {
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                ],
                "pmid": ""
            }
        ],
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                "name": "nucleus",
                "id": "GO:0005634",
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            }
        ],
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                "name": "DNA-templated transcription",
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            },
            {
                "name": "regulation of DNA-templated transcription",
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                "evidence": [
                    {
                        "database": "UniProtKB",
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        ],
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        "species": [
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        "protein_name": "carnitine O-palmitoyltransferase",
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                "disease_id": "DOID:0090129",
                "name": "carnitine palmitoyltransferase I deficiency",
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                "url": "https://disease-ontology.org/term/DOID:0090129",
                "evidence": [
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                ],
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            },
            {
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                "name": "lipid metabolism disorder",
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                "evidence": [
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                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3319",
                "name": "lymphangioleiomyomatosis",
                "description": "A lung disease that is characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas.",
                "url": "https://disease-ontology.org/term/DOID:3319",
                "evidence": [
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                        "id": "3319",
                        "database": "AGR",
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                ],
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            }
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                "name": "carnitine O-palmitoyltransferase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004095",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PEG9",
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                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "mitochondrial outer membrane",
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                    }
                ],
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        ],
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                "name": "fatty acid beta-oxidation",
                "id": "GO:0006635",
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                "evidence": [
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            },
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                "name": "regulation of fatty acid beta-oxidation",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031998",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                "name": "calcium ion regulated lysosome exocytosis",
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                "name": "acetylcholine-gated monoatomic cation-selective channel activity",
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                "name": "serotonin-gated monoatomic cation channel activity",
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
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                "name": "transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1904315",
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                        "database": "UniProtKB",
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                "name": "excitatory extracellular ligand-gated monoatomic ion channel activity",
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            {
                "name": "cytoplasm",
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                "name": "MAP kinase tyrosine/serine/threonine phosphatase activity",
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                "pmid": ""
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                        "database": "UniProtKB",
                        "id": "A0A8M9PJ26",
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                        "id": "11729",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11729"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1564",
                "name": "fungal infectious disease",
                "description": "A disease by infectious agent that results_in infection, has_material_basis_in Fungi, which pass the resistance barriers of the human or animal body.",
                "url": "https://disease-ontology.org/term/DOID:1564",
                "evidence": [
                    {
                        "id": "1564",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1564"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2722",
                "name": "acrodermatitis",
                "description": "A dermatitis that selectively affects the hands and feet.",
                "url": "https://disease-ontology.org/term/DOID:2722",
                "evidence": [
                    {
                        "id": "2722",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2722"
                    }
                ],
                "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:2986",
                "name": "IgA glomerulonephritis",
                "description": "A glomerulonephritis characterized by build up of IgA antibody in the glomerulus.",
                "url": "https://disease-ontology.org/term/DOID:2986",
                "evidence": [
                    {
                        "id": "2986",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2986"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3178",
                "name": "skin papilloma",
                "description": "A skin benign neoplasm that is composed of epithelial cells and a fibrous stalk.",
                "url": "https://disease-ontology.org/term/DOID:3178",
                "evidence": [
                    {
                        "id": "3178",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3178"
                    }
                ],
                "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: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: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
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJ26",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJ26"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "inflammatory response",
                "id": "GO:0006954",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006954",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJ26",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJ26"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "immune response",
                "id": "GO:0006955",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006955",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJ26",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJ26"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "chemokine activity",
                "id": "GO:0008009",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008009",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJ26",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJ26"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PJ26-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PJ89-1",
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            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJ89",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJ89"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 904,
        "chemical_mass": 100414.0,
        "gene_names": "fnip2;fnip2;si:ch211-42i9.8",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJ89",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJ89"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "lysosomal membrane",
                "id": "GO:0005765",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005765",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJ89",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJ89"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "protein-folding chaperone binding",
                "id": "GO:0051087",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051087",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJ89",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJ89"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATPase inhibitor activity",
                "id": "GO:0042030",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042030",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJ89",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJ89"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PJ89-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PJB1-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 1873,
        "chemical_mass": 209389.0,
        "gene_names": "nsd1b;nsd1b",
        "protein_name": "Histone-lysine N-methyltransferase, H3 lysine-36 specific",
        "disease": [
            {
                "disease_id": "DOID:0112103",
                "name": "Sotos syndrome 1",
                "description": "A Sotos syndrome that has_material_basis_in heterozygous mutation in the NSD1 gene or deletion in the chromosome region 5q35 that includes the NSD1 gene.",
                "url": "https://disease-ontology.org/term/DOID:0112103",
                "evidence": [
                    {
                        "id": "0112103",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112103"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10907",
                "name": "microcephaly",
                "description": "A congenital nervous system abnormality that is characterized by a significantly smaller than normal head in infants.",
                "url": "https://disease-ontology.org/term/DOID:10907",
                "evidence": [
                    {
                        "id": "10907",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10907"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14748",
                "name": "Sotos syndrome",
                "description": "A syndrome that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life.",
                "url": "https://disease-ontology.org/term/DOID:14748",
                "evidence": [
                    {
                        "id": "14748",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14748"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:225",
                "name": "syndrome",
                "description": "A disease characterized by a group of signs and symptoms that occur together and characterize a particular abnormality.",
                "url": "https://disease-ontology.org/term/DOID:225",
                "evidence": [
                    {
                        "id": "225",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:225"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:769",
                "name": "neuroblastoma",
                "description": "An autonomic nervous system neoplasm that derives_from immature nerve cells.",
                "url": "https://disease-ontology.org/term/DOID:769",
                "evidence": [
                    {
                        "id": "769",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:769"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9119",
                "name": "acute myeloid leukemia",
                "description": "A myeloid leukemia that is characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells.",
                "url": "https://disease-ontology.org/term/DOID:9119",
                "evidence": [
                    {
                        "id": "9119",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9119"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nucleoplasm",
                "id": "GO:0005654",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chromatin",
                "id": "GO:0000785",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000785",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chromosome",
                "id": "GO:0005694",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005694",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of DNA-templated transcription",
                "id": "GO:0006355",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006355",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "methylation",
                "id": "GO:0032259",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032259",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "heterochromatin formation",
                "id": "GO:0031507",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031507",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transcription coregulator activity",
                "id": "GO:0003712",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003712",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear receptor binding",
                "id": "GO:0016922",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016922",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H3K36 methyltransferase activity",
                "id": "GO:0046975",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046975",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone H3K36 dimethyltransferase activity",
                "id": "GO:0140954",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140954",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJB1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJB1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A8M9PJB1-1",
                "start_pos": "583",
                "end_pos": "583",
                "site_lbl": "Thr583",
                "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": 583,
                        "start_aa": "Thr",
                        "end_pos": 583,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr583",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "A0A8M9PJB1-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PJD6-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJD6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJD6"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 596,
        "chemical_mass": 66896.0,
        "gene_names": "LOC563925;LOC563925",
        "protein_name": "non-specific serine/threonine protein kinase",
        "disease": [],
        "molecular_function": [
            {
                "name": "protein serine/threonine kinase activity",
                "id": "GO:0004674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004674",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJD6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJD6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJD6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJD6"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJD6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJD6"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "negative regulation of apoptotic process",
                "id": "GO:0043066",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043066",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJD6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJD6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mitotic cell cycle",
                "id": "GO:0007346",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007346",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJD6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJD6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A8M9PJD6-1",
                "start_pos": "44",
                "end_pos": "44",
                "site_lbl": "Thr44",
                "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": 44,
                        "start_aa": "Thr",
                        "end_pos": 44,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr44",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "A0A8M9PJD6-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PJE3-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJE3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJE3"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 549,
        "chemical_mass": 61373.0,
        "gene_names": "slc22a5;slc22a5",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050700",
                "name": "cardiomyopathy",
                "description": "A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle.",
                "url": "https://disease-ontology.org/term/DOID:0050700",
                "evidence": [
                    {
                        "id": "0050700",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050700"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050908",
                "name": "myelodysplastic syndrome",
                "description": "A bone marrow cancer that is characterized by under production of white blood cells, red blood cells and platelets.",
                "url": "https://disease-ontology.org/term/DOID:0050908",
                "evidence": [
                    {
                        "id": "0050908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080208",
                "name": "metabolic dysfunction-associated steatotic liver disease",
                "description": "A steatotic liver disease characterized by at least one of five specified cardiometabolic risk factors and no other discernible cause with normal to no alcohol use. The five cardiometabolic risk factors are: (1) higher than normal body mass index or waist circumference; (2) higher than normal serum glucose or glycated hemoglobin level, or type 2 diabetes; (3) higher than normal blood pressure or hypertensive treatment; (4) higher than normal plasma triglycerides or lipid lowering treatment; and (5) lower than normal plasma high-density lipoprotein cholesterol.",
                "url": "https://disease-ontology.org/term/DOID:0080208",
                "evidence": [
                    {
                        "id": "0080208",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080208"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14365",
                "name": "systemic primary carnitine deficiency disease",
                "description": "An amino acid metabolic disorder that involves defective proteins called carnitine transporters, which bring carnitine into cells and prevent its escape from the body preventing the body cannot utilize fats for energy.",
                "url": "https://disease-ontology.org/term/DOID:14365",
                "evidence": [
                    {
                        "id": "14365",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14365"
                    }
                ],
                "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: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:655",
                "name": "inherited metabolic disorder",
                "description": "A disease of metabolism that is characterized by enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to inherited enzyme abnormality.",
                "url": "https://disease-ontology.org/term/DOID:655",
                "evidence": [
                    {
                        "id": "655",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:655"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8778",
                "name": "Crohn's disease",
                "description": "An intestinal disease that involves inflammation located_in intestine.",
                "url": "https://disease-ontology.org/term/DOID:8778",
                "evidence": [
                    {
                        "id": "8778",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8778"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "quaternary ammonium group transmembrane transporter activity",
                "id": "GO:0015651",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015651",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJE3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJE3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJE3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJE3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "carnitine transmembrane transporter activity",
                "id": "GO:0015226",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015226",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJE3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJE3"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "quaternary ammonium group transport",
                "id": "GO:0015697",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015697",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJE3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJE3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoatomic ion transport",
                "id": "GO:0006811",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006811",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJE3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJE3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "heme biosynthetic process",
                "id": "GO:0006783",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006783",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJE3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJE3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "carnitine transport",
                "id": "GO:0015879",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015879",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJE3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJE3"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJE3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJE3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PJE3-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PJH5-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJH5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJH5"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 576,
        "chemical_mass": 64707.0,
        "gene_names": "mmp25a;mmp25a;si:ch73-248e21.6",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "metalloendopeptidase activity",
                "id": "GO:0004222",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004222",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJH5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJH5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJH5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJH5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metallopeptidase activity",
                "id": "GO:0008237",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008237",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJH5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJH5"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJH5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJH5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular matrix",
                "id": "GO:0031012",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031012",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJH5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJH5"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJH5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJH5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular matrix organization",
                "id": "GO:0030198",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030198",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJH5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJH5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "collagen catabolic process",
                "id": "GO:0030574",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030574",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJH5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJH5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A8M9PJH5-1",
                "start_pos": "536",
                "end_pos": "536",
                "site_lbl": "Thr536",
                "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": 536,
                        "start_aa": "Thr",
                        "end_pos": 536,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr536",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A0A8M9PJH5-1",
                "start_pos": "415",
                "end_pos": "415",
                "site_lbl": "Tyr415",
                "weight": 0.0,
                "phosphorylation": [
                    {
                        "kinase_uniprot_canonical_ac": "",
                        "kinase_gene_name": "",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A8M9PJH5",
                                "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJH5"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "A0A8M9PJH5-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PJP1-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJP1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJP1"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 1068,
        "chemical_mass": 117078.0,
        "gene_names": "si:ch211-13f8.1;si:ch211-13f8.1",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "regulation of cellular localization",
                "id": "GO:0060341",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060341",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJP1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJP1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "centrosome cycle",
                "id": "GO:0007098",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007098",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJP1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJP1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "establishment or maintenance of cell polarity",
                "id": "GO:0007163",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007163",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJP1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJP1"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJP1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJP1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell cortex",
                "id": "GO:0005938",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005938",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJP1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJP1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "apical plasma membrane",
                "id": "GO:0016324",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016324",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJP1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJP1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PJP1-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PJQ9-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJQ9"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 687,
        "chemical_mass": 77162.0,
        "gene_names": "tars2;tars2",
        "protein_name": "threonine--tRNA ligase",
        "disease": [
            {
                "disease_id": "DOID:0111465",
                "name": "combined oxidative phosphorylation deficiency 21",
                "description": "A combined oxidative phosphorylation deficiency characterized either by onset within the first months of life of severe hypotonia, failure to thrive, epilepsy, and early death or by onset after 6 months of life with a milder course and longer survival that has_material_basis_in homozygous or compound heterozygous mutation in the TARS2 gene on chromosome 1q21.2.",
                "url": "https://disease-ontology.org/term/DOID:0111465",
                "evidence": [
                    {
                        "id": "0111465",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111465"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111867",
                "name": "nonphotosensitive trichothiodystrophy",
                "description": "A trichothiodystrophy characterized by absence of extreme sensitivity to UV radiation.",
                "url": "https://disease-ontology.org/term/DOID:0111867",
                "evidence": [
                    {
                        "id": "0111867",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111867"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9252",
                "name": "amino acid metabolic disorder",
                "description": "An inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids.",
                "url": "https://disease-ontology.org/term/DOID:9252",
                "evidence": [
                    {
                        "id": "9252",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9252"
                    }
                ],
                "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": "A0A8M9PJQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJQ9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "threonine-tRNA ligase activity",
                "id": "GO:0004829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004829",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJQ9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ligase activity",
                "id": "GO:0016874",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016874",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJQ9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJQ9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "skeletal muscle fiber development",
                "id": "GO:0048741",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048741",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJQ9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cerebellum development",
                "id": "GO:0021549",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0021549",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJQ9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "threonyl-tRNA aminoacylation",
                "id": "GO:0006435",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006435",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJQ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJQ9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PJQ9-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PJW6-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJW6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJW6"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 1936,
        "chemical_mass": 221612.0,
        "gene_names": "myhz1.1l;myhz1.1l",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050646",
                "name": "distal arthrogryposis",
                "description": "A muscle tissue disease characterized by congenital joint contractures of hand and feet.",
                "url": "https://disease-ontology.org/term/DOID:0050646",
                "evidence": [
                    {
                        "id": "0050646",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050646"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050700",
                "name": "cardiomyopathy",
                "description": "A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle.",
                "url": "https://disease-ontology.org/term/DOID:0050700",
                "evidence": [
                    {
                        "id": "0050700",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050700"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080326",
                "name": "familial hypertrophic cardiomyopathy",
                "description": "A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations.",
                "url": "https://disease-ontology.org/term/DOID:0080326",
                "evidence": [
                    {
                        "id": "0080326",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080326"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080719",
                "name": "congenital myopathy 6",
                "description": "A congenital myopathy that is characterized by childhood onset of congenital joint contractures, external ophthalmoplegia, and proximal muscle weakness, and that has_material_basis_in heterozygous, compound heterozygous, or homozygous mutation in the gene encoding myosin heavy chain IIa ( (MYHC2A or MYH2) on chromosome 17p13.",
                "url": "https://disease-ontology.org/term/DOID:0080719",
                "evidence": [
                    {
                        "id": "0080719",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080719"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110454",
                "name": "dilated cardiomyopathy 1S",
                "description": "A dilated cardiomyopathy that has_material_basis_in mutation in the MYH7 gene on chromosome 14q12.",
                "url": "https://disease-ontology.org/term/DOID:0110454",
                "evidence": [
                    {
                        "id": "0110454",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110454"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111269",
                "name": "autosomal dominant hyaline body myopathy",
                "description": "A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2.",
                "url": "https://disease-ontology.org/term/DOID:0111269",
                "evidence": [
                    {
                        "id": "0111269",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111269"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111596",
                "name": "distal arthrogryposis type 1",
                "description": "A distal arthrogryposis characterized by autosomal domiant inheritance of contractures of the distal regions of the hands and feet with no facial involvement or other anomalies.",
                "url": "https://disease-ontology.org/term/DOID:0111596",
                "evidence": [
                    {
                        "id": "0111596",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111596"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111602",
                "name": "distal arthrogryposis type 2B3",
                "description": "A distal arthrogryposis type 2B that has_material_basis_in heterozygous mutation in the MYH3 gene on chromosome 17p13.1.",
                "url": "https://disease-ontology.org/term/DOID:0111602",
                "evidence": [
                    {
                        "id": "0111602",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111602"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0111605",
                "name": "distal arthrogryposis type 2A",
                "description": "A Freeman-Sheldon syndrome that has_material_basis_in heterozygous mutation in the MYH3 gene on chromosome 17p13.1.",
                "url": "https://disease-ontology.org/term/DOID:0111605",
                "evidence": [
                    {
                        "id": "0111605",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0111605"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11446",
                "name": "sciatic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11446",
                "evidence": [
                    {
                        "id": "11446",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11446"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11720",
                "name": "distal myopathy",
                "description": "A muscular dystrophy that is characterized by predominant weakness and atrophy beginning in the feet and/or hands.",
                "url": "https://disease-ontology.org/term/DOID:11720",
                "evidence": [
                    {
                        "id": "11720",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11720"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12930",
                "name": "dilated cardiomyopathy",
                "description": "An intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently.",
                "url": "https://disease-ontology.org/term/DOID:12930",
                "evidence": [
                    {
                        "id": "12930",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12930"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:2106",
                "name": "myotonia congenita",
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                "url": "https://disease-ontology.org/term/DOID:2106",
                "evidence": [
                    {
                        "id": "2106",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2106"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3429",
                "name": "inclusion body myositis",
                "description": "A myositis that is characterized by late onset of skeletal muscle inflammation, weakness, and atrophy with cytoplasmic granules and vacuoles in the muscle.",
                "url": "https://disease-ontology.org/term/DOID:3429",
                "evidence": [
                    {
                        "id": "3429",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3429"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:397",
                "name": "restrictive cardiomyopathy",
                "description": "An intrinsic cardiomyopathy characterized by impaired ventricular filling, with normal or decreased diastolic volume of either or both ventricles typically resulting from increased stiffness of the myocardium.",
                "url": "https://disease-ontology.org/term/DOID:397",
                "evidence": [
                    {
                        "id": "397",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:397"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:423",
                "name": "myopathy",
                "description": "A muscular disease in which the muscle fibers do not function resulting in muscular weakness.",
                "url": "https://disease-ontology.org/term/DOID:423",
                "evidence": [
                    {
                        "id": "423",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:423"
                    }
                ],
                "weight": 0.0
            }
        ],
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            {
                "name": "system development",
                "id": "GO:0048731",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048731",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJW6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJW6"
                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJW6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJW6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin filament binding",
                "id": "GO:0051015",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051015",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJW6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJW6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microfilament motor activity",
                "id": "GO:0000146",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000146",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJW6",
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                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJW6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJW6"
                    }
                ],
                "pmid": ""
            },
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                "name": "myosin filament",
                "id": "GO:0032982",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032982",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJW6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJW6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "myofibril",
                "id": "GO:0030016",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030016",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJW6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJW6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "myosin II complex",
                "id": "GO:0016460",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016460",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PJW6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PJW6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PJW6-1"
    },
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        "uniprot_canonical_ac": "A0A8M9PN97-1",
        "species": [
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                "name": "Danio rerio",
                "taxid": 7955,
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PN97",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PN97"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
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        "chemical_mass": 143826.0,
        "gene_names": "slc4a7;slc4a7",
        "protein_name": "Anion exchange protein",
        "disease": [
            {
                "disease_id": "DOID:0110839",
                "name": "Usher syndrome type 2C",
                "description": "An Usher syndrome type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the ADGRV1 gene on chromosome 5q14.",
                "url": "https://disease-ontology.org/term/DOID:0110839",
                "evidence": [
                    {
                        "id": "0110839",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110839"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2355",
                "name": "anemia",
                "description": "A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells.",
                "url": "https://disease-ontology.org/term/DOID:2355",
                "evidence": [
                    {
                        "id": "2355",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2355"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "basolateral plasma membrane",
                "id": "GO:0016323",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016323",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PN97",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PN97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "apical plasma membrane",
                "id": "GO:0016324",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016324",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
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                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "monoatomic anion transmembrane transporter activity",
                "id": "GO:0008509",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008509",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PN97",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PN97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium ion transmembrane transporter activity",
                "id": "GO:0015081",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015081",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PN97",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PN97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "solute:inorganic anion antiporter activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005452",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PN97",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PN97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "bicarbonate transmembrane transporter activity",
                "id": "GO:0015106",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015106",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PN97",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PN97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium:bicarbonate symporter activity",
                "id": "GO:0008510",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008510",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PN97",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PN97"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "transmembrane transport",
                "id": "GO:0055085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PN97",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PN97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "bicarbonate transport",
                "id": "GO:0015701",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015701",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PN97",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PN97"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of intracellular pH",
                "id": "GO:0051453",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051453",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PN97",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PN97"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A8M9PN97-1",
                "start_pos": "309",
                "end_pos": "309",
                "site_lbl": "Thr309",
                "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": 309,
                        "start_aa": "Thr",
                        "end_pos": 309,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr309",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "A0A8M9PN97-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PKB0-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PKB0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PKB0"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 275,
        "chemical_mass": 31540.0,
        "gene_names": "si:ch211-151m7.3;si:ch211-151m7.3",
        "protein_name": "non-specific serine/threonine protein kinase",
        "disease": [],
        "molecular_function": [
            {
                "name": "protein serine/threonine kinase activity",
                "id": "GO:0004674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004674",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PKB0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PKB0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PKB0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PKB0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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                "name": "nuclear import signal receptor activity",
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                "name": "protein import into nucleus",
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                "pmid": ""
            }
        ],
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                "name": "negative regulation of apoptotic process",
                "id": "GO:0043066",
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                "name": "GTP binding",
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        ],
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                "name": "nucleus",
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        ],
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                "evidence": [
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                        "id": "10591",
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                ],
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                    {
                        "id": "10763",
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                ],
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            },
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                ],
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            },
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                        "glytoucan_ac": "",
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                        "site_category_dict": {
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        ],
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        "uniprot_canonical_ac": "A0A8M9PR98-1",
        "species": [
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                "name": "Danio rerio",
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        "chemical_mass": 35907.0,
        "gene_names": "mtx1b;mtx1b;mtx1;zgc:101675",
        "protein_name": "Metaxin",
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                "name": "SAM complex",
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        "uniprot_canonical_ac": "A0A8M9PSC1-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSC1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSC1"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 2261,
        "chemical_mass": 242994.0,
        "gene_names": "arid1ab;arid1ab",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050934",
                "name": "ovarian clear cell carcinoma",
                "description": "An ovarian carcinoma that has_material_basis_in cells with clear cytoplasm and glycogen secreting hob nail cells.",
                "url": "https://disease-ontology.org/term/DOID:0050934",
                "evidence": [
                    {
                        "id": "0050934",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050934"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070042",
                "name": "Coffin-Siris syndrome 1",
                "description": "A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the ARID1B gene on chromosome 6q25.3.",
                "url": "https://disease-ontology.org/term/DOID:0070042",
                "evidence": [
                    {
                        "id": "0070042",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070042"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0070044",
                "name": "Coffin-Siris syndrome 2",
                "description": "A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the ARID1A gene on chromosome 1p36.11.",
                "url": "https://disease-ontology.org/term/DOID:0070044",
                "evidence": [
                    {
                        "id": "0070044",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070044"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10534",
                "name": "stomach cancer",
                "description": "A gastrointestinal system cancer that is located_in the stomach.",
                "url": "https://disease-ontology.org/term/DOID:10534",
                "evidence": [
                    {
                        "id": "10534",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10534"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10591",
                "name": "pre-eclampsia",
                "description": "A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy.",
                "url": "https://disease-ontology.org/term/DOID:10591",
                "evidence": [
                    {
                        "id": "10591",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10591"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "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:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:162",
                "name": "cancer",
                "description": "A disease of cellular proliferation that is malignant and primary, characterized by uncontrolled cellular proliferation, local cell invasion and metastasis.",
                "url": "https://disease-ontology.org/term/DOID:162",
                "evidence": [
                    {
                        "id": "162",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:162"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1925",
                "name": "Coffin-Siris syndrome",
                "description": "An autosomal dominant intellectual developmental disorder that is characterized by mental retardation associated with coarse facial features, hypertrichosis, sparse scalp hair, and hypoplastic or absent fifth fingernails or toenails.",
                "url": "https://disease-ontology.org/term/DOID:1925",
                "evidence": [
                    {
                        "id": "1925",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1925"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:219",
                "name": "colon cancer",
                "description": "A colorectal cancer that is located_in the colon.",
                "url": "https://disease-ontology.org/term/DOID:219",
                "evidence": [
                    {
                        "id": "219",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:219"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2870",
                "name": "endometrial adenocarcinoma",
                "description": "An endometrial carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:2870",
                "evidence": [
                    {
                        "id": "2870",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2870"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3717",
                "name": "gastric adenocarcinoma",
                "description": "A stomach carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:3717",
                "evidence": [
                    {
                        "id": "3717",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3717"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3908",
                "name": "lung non-small cell carcinoma",
                "description": "A lung carcinoma that is characterized as any type of epithelial lung cancer other than small cell lung carcinoma.",
                "url": "https://disease-ontology.org/term/DOID:3908",
                "evidence": [
                    {
                        "id": "3908",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3908"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4914",
                "name": "esophagus adenocarcinoma",
                "description": "An esophageal carcinoma that derives_from epithelial cells of glandular origin.",
                "url": "https://disease-ontology.org/term/DOID:4914",
                "evidence": [
                    {
                        "id": "4914",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4914"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4927",
                "name": "Klatskin's tumor",
                "description": "An intrahepatic cholangiocarcinoma arising near or at the confluence of the right and left hepatic ducts.",
                "url": "https://disease-ontology.org/term/DOID:4927",
                "evidence": [
                    {
                        "id": "4927",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4927"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4928",
                "name": "intrahepatic cholangiocarcinoma",
                "description": "A cholangiocarcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree.",
                "url": "https://disease-ontology.org/term/DOID:4928",
                "evidence": [
                    {
                        "id": "4928",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4928"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:684",
                "name": "hepatocellular carcinoma",
                "description": "A liver carcinoma that has_material_basis_in undifferentiated hepatocytes and located_in the liver.",
                "url": "https://disease-ontology.org/term/DOID:684",
                "evidence": [
                    {
                        "id": "684",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:684"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:769",
                "name": "neuroblastoma",
                "description": "An autonomic nervous system neoplasm that derives_from immature nerve cells.",
                "url": "https://disease-ontology.org/term/DOID:769",
                "evidence": [
                    {
                        "id": "769",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:769"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9256",
                "name": "colorectal cancer",
                "description": "A large intestine cancer that is located_in the colon and/or located_in the rectum.",
                "url": "https://disease-ontology.org/term/DOID:9256",
                "evidence": [
                    {
                        "id": "9256",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9256"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9261",
                "name": "nasopharynx carcinoma",
                "description": "A pharynx cancer that is located in the nasopharynx, the uppermost region of the pharynx or throat, where the nasal passages and auditory tubes join the remainder of the upper respiratory tract.",
                "url": "https://disease-ontology.org/term/DOID:9261",
                "evidence": [
                    {
                        "id": "9261",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9261"
                    }
                ],
                "weight": 0.0
            }
        ],
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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": "A0A8M9PSC1",
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                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleoplasm",
                "id": "GO:0005654",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "SWI/SNF complex",
                "id": "GO:0016514",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "nBAF complex",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071565",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "brahma complex",
                "id": "GO:0035060",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035060",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSC1"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "chromatin remodeling",
                "id": "GO:0006338",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
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                "id": "GO:0006351",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of transcription by RNA polymerase II",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSC1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSC1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nervous system development",
                "id": "GO:0007399",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007399",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSC1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSC1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of DNA-templated transcription",
                "id": "GO:0045893",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045893",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSC1"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PSC1-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PSE6-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSE6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSE6"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 760,
        "chemical_mass": 83983.0,
        "gene_names": "adam23b;adam23b",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "metalloendopeptidase activity",
                "id": "GO:0004222",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004222",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSE6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metallopeptidase activity",
                "id": "GO:0008237",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008237",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSE6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSE6"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSE6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSE6"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "endomembrane system",
                "id": "GO:0012505",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0012505",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSE6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSE6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "presynaptic membrane",
                "id": "GO:0042734",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042734",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSE6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSE6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PSE6-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PSI8-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSI8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSI8"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 491,
        "chemical_mass": 55163.0,
        "gene_names": "acvr1c;acvr1c",
        "protein_name": "Activin receptor type-1C",
        "disease": [],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSI8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSI8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSI8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSI8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "activin receptor activity, type I",
                "id": "GO:0016361",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016361",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSI8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSI8"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSI8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSI8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "activin receptor complex",
                "id": "GO:0048179",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048179",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSI8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSI8"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "nervous system development",
                "id": "GO:0007399",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007399",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSI8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSI8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "apoptotic process",
                "id": "GO:0006915",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006915",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSI8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSI8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cellular response to growth factor stimulus",
                "id": "GO:0071363",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071363",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSI8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSI8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "activin receptor signaling pathway",
                "id": "GO:0032924",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032924",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSI8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSI8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PSI8-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PST9-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PST9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PST9"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 739,
        "chemical_mass": 80644.0,
        "gene_names": "LOC110438304;LOC110438304",
        "protein_name": "non-specific serine/threonine protein kinase",
        "disease": [],
        "molecular_function": [
            {
                "name": "protein serine/threonine kinase activity",
                "id": "GO:0004674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004674",
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                    {
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                        "id": "A0A8M9PST9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PST9"
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                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
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                        "database": "UniProtKB",
                        "id": "A0A8M9PST9",
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                "pmid": ""
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                "name": "endoplasmic reticulum",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "endoplasmic reticulum membrane",
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                "evidence": [
                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein transport",
                "id": "GO:0015031",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015031",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSV5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSV5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "GPI anchor biosynthetic process",
                "id": "GO:0006506",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006506",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSV5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSV5"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "hydrolase activity, acting on ester bonds",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016788",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSV5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSV5"
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                ],
                "pmid": ""
            },
            {
                "name": "deacylase activity",
                "id": "GO:0160215",
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                "evidence": [
                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSV5"
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                ],
                "pmid": ""
            }
        ],
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            {
                "uniprot_canonical_ac": "A0A8M9PSV5-1",
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                "glycosylation": [
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                        "glytoucan_ac": "",
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                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
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                        ],
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                        "site_category_dict": {
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                        },
                        "site_seq": "",
                        "relation": "attached",
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                        "icn3d_view": {},
                        "start_pos": 539,
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                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            }
        ],
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    },
    {
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                    }
                ],
                "common_name": "Zebrafish",
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        ],
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        "chemical_mass": 55420.0,
        "gene_names": "camk1gb;camk1gb;fk61c03;wu:fk61c03;zgc:73155",
        "protein_name": "",
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            {
                "name": "calmodulin binding",
                "id": "GO:0005516",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005516",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSZ5",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSZ5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSZ5"
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                ],
                "pmid": ""
            },
            {
                "name": "calcium/calmodulin-dependent protein kinase activity",
                "id": "GO:0004683",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004683",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSZ5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSZ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "kinase activity",
                "id": "GO:0016301",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016301",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSZ5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSZ5"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSZ5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSZ5"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "signal transduction",
                "id": "GO:0007165",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007165",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSZ5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSZ5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "locomotor rhythm",
                "id": "GO:0045475",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045475",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PSZ5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PSZ5"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "A0A8M9PT00-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT00",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PT00"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 365,
        "chemical_mass": 42950.0,
        "gene_names": "fbxo25;fbxo25;zgc:100907",
        "protein_name": "F-box only protein 25",
        "disease": [
            {
                "disease_id": "DOID:1094",
                "name": "attention deficit hyperactivity disorder",
                "description": "A specific developmental disorder that is characterized by co-existence of attentional problems and hyperactivity, with each behavior occurring infrequently alone and symptoms starting before seven years of age.",
                "url": "https://disease-ontology.org/term/DOID:1094",
                "evidence": [
                    {
                        "id": "1094",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1094"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT00",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PT00"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT00",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PT00"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "SCF ubiquitin ligase complex",
                "id": "GO:0019005",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019005",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT00",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PT00"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein ubiquitination",
                "id": "GO:0016567",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016567",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT00",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PT00"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PT00-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PT37-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT37",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PT37"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 1830,
        "chemical_mass": 199317.0,
        "gene_names": "tns1b;tns1b",
        "protein_name": "",
        "disease": [
            {
                "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
            }
        ],
        "cellular_component": [
            {
                "name": "focal adhesion",
                "id": "GO:0005925",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005925",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT37",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PT37"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT37",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PT37"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phosphoprotein phosphatase activity",
                "id": "GO:0004721",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004721",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT37",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PT37"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "fibroblast migration",
                "id": "GO:0010761",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010761",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT37",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PT37"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A8M9PT37-1",
                "start_pos": "1232",
                "end_pos": "1232",
                "site_lbl": "Thr1232",
                "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": 1232,
                        "start_aa": "Thr",
                        "end_pos": 1232,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1232",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A0A8M9PT37-1",
                "start_pos": "1267",
                "end_pos": "1267",
                "site_lbl": "Thr1267",
                "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": "reported site T1231 is on non-canonical isoform A0AC58GHN6-1 which maps to canonical isoform site A0A8M9PT37-1:1267",
                        "icn3d_view": {},
                        "start_pos": 1267,
                        "start_aa": "Thr",
                        "end_pos": 1267,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1267",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A0A8M9PT37-1",
                "start_pos": "1451",
                "end_pos": "1451",
                "site_lbl": "Thr1451",
                "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": 1451,
                        "start_aa": "Thr",
                        "end_pos": 1451,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1451",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A0A8M9PT37-1",
                "start_pos": "1513",
                "end_pos": "1513",
                "site_lbl": "Thr1513",
                "weight": 0.0,
                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
                        "prediction_tool_list": [
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            },
                            {
                                "label": "isoglyp",
                                "url": "https://github.com/jonmohl/ISOGlyP"
                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "reported site T1450 is on non-canonical isoform A0AC58GHP0-1 which maps to canonical isoform site A0A8M9PT37-1:1513",
                        "icn3d_view": {},
                        "start_pos": 1513,
                        "start_aa": "Thr",
                        "end_pos": 1513,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1513",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            },
            {
                "uniprot_canonical_ac": "A0A8M9PT37-1",
                "start_pos": "1619",
                "end_pos": "1619",
                "site_lbl": "Thr1619",
                "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": "reported site T1512 is on non-canonical isoform A0AC58GHN7-1 which maps to canonical isoform site A0A8M9PT37-1:1619",
                        "icn3d_view": {},
                        "start_pos": 1619,
                        "start_aa": "Thr",
                        "end_pos": 1619,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr1619",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "A0A8M9PT37-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PT54-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PT54",
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                "pmid": ""
            }
        ],
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        "biomarkers": [],
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    },
    {
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        ],
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        "chemical_mass": 129686.0,
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        "disease": [],
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            {
                "name": "integrin-mediated signaling pathway",
                "id": "GO:0007229",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "cell-cell adhesion",
                "id": "GO:0098609",
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "cell surface",
                "id": "GO:0009986",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "integrin alpha2-beta1 complex",
                "id": "GO:0034666",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0034666",
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                    {
                        "database": "UniProtKB",
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                ],
                "pmid": ""
            }
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            {
                "name": "metal ion binding",
                "id": "GO:0046872",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "signaling receptor activity",
                "id": "GO:0038023",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0038023",
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                    {
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                ],
                "pmid": ""
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        ],
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        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "A0A8M9PTZ0-1",
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                ],
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        "chemical_mass": 47966.0,
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                        "database": "AGR",
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                "name": "hypertension",
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries.",
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                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
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                "evidence": [
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                        "id": "11612",
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                "description": "",
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                        "id": "13948",
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                        "url": "https://www.alliancegenome.org/disease/DOID:13948"
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                        "id": "1574",
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                        "url": "https://www.alliancegenome.org/disease/DOID:1574"
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                ],
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                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9976"
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                ],
                "weight": 0.0
            }
        ],
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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": ""
            }
        ],
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            {
                "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": "A0A8M9PTZ0",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell-cell signaling",
                "id": "GO:0007267",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007267",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PTZ0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PTZ0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "positive regulation of MAPK cascade",
                "id": "GO:0043410",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043410",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PTZ0",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "adenylate cyclase-activating adrenergic receptor signaling pathway",
                "id": "GO:0071880",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071880",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PTZ0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PTZ0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "adenylate cyclase-inhibiting adrenergic receptor signaling pathway",
                "id": "GO:0071881",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071881",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PTZ0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PTZ0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "phospholipase C-activating G protein-coupled receptor signaling pathway",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007200",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PTZ0",
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                    }
                ],
                "pmid": ""
            }
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
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                "name": "alpha1-adrenergic receptor activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004937",
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                    {
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                        "id": "A0A8M9PTZ0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PTZ0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "A0A8M9PU00-1",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PU00",
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                ],
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        ],
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        "chemical_mass": 85867.0,
        "gene_names": "tacc1;tacc1",
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        "disease": [],
        "cellular_component": [
            {
                "name": "cytosol",
                "id": "GO:0005829",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PU00",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PU00"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoskeleton",
                "id": "GO:0005856",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005856",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PU00",
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                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cerebral cortex development",
                "id": "GO:0021987",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0021987",
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                    {
                        "database": "UniProtKB",
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                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PU00"
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                "pmid": ""
            },
            {
                "name": "mitotic spindle organization",
                "id": "GO:0007052",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007052",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PU00",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "nuclear migration",
                "id": "GO:0007097",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007097",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PU00",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PU00"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "astral microtubule organization",
                "id": "GO:0030953",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030953",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PU00",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PU00"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "A0A8M9PUK6-1",
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                "name": "Danio rerio",
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                        "database": "UniProtKB",
                        "id": "A0A8M9PUK6",
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                ],
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        ],
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        "chemical_mass": 80169.0,
        "gene_names": "nefla;nefla",
        "protein_name": "",
        "disease": [
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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"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0050433",
                "name": "fatal familial insomnia",
                "description": "A prion disease that is characterized by insomnia, hallucinations, dementia and death, located_in the brain.",
                "url": "https://disease-ontology.org/term/DOID:0050433",
                "evidence": [
                    {
                        "id": "0050433",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050433"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0051061",
                "name": "stroke",
                "description": "A cerebrovascular disease that is characterized by disruption of blood flow to the brain resulting in damage to brain cells due to a lack of oxygen.",
                "url": "https://disease-ontology.org/term/DOID:0051061",
                "evidence": [
                    {
                        "id": "0051061",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0051061"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080294",
                "name": "Charcot-Marie-Tooth disease dominant intermediate G",
                "description": "A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the NEFL gene on chromosome 8p21.",
                "url": "https://disease-ontology.org/term/DOID:0080294",
                "evidence": [
                    {
                        "id": "0080294",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080294"
                    }
                ],
                "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:0080832",
                "name": "mild cognitive impairment",
                "description": "A cognitive disorder that is characterized by objective impairment in cognition with minimal impairment of their capacity to undertake the instrumental activities of daily living.",
                "url": "https://disease-ontology.org/term/DOID:0080832",
                "evidence": [
                    {
                        "id": "0080832",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080832"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110149",
                "name": "Charcot-Marie-Tooth disease type 1F",
                "description": "A Charcot-Marie-Tooth disease type 1 that has_material_basis_in mutation in the NEFL gene.",
                "url": "https://disease-ontology.org/term/DOID:0110149",
                "evidence": [
                    {
                        "id": "0110149",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110149"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0110165",
                "name": "Charcot-Marie-Tooth disease type 2E",
                "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the light polypeptide neurofilament protein gene (NEFL) on chromosome 8p21.",
                "url": "https://disease-ontology.org/term/DOID:0110165",
                "evidence": [
                    {
                        "id": "0110165",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0110165"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10595",
                "name": "Charcot-Marie-Tooth disease",
                "description": "A neuromuscular disease that is characterized by a slowly progressive degeneration of the muscles of the foot, lower leg, hand and forearm.",
                "url": "https://disease-ontology.org/term/DOID:10595",
                "evidence": [
                    {
                        "id": "10595",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10595"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
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                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
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                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11446",
                "name": "sciatic neuropathy",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11446",
                "evidence": [
                    {
                        "id": "11446",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11446"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11949",
                "name": "Creutzfeldt-Jakob disease",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:11949",
                "evidence": [
                    {
                        "id": "11949",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11949"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12217",
                "name": "Lewy body dementia",
                "description": "A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities that has_material_basis_in accumulation of alpha-synuclein, SCNA, (protein). The causal mutation might be in SCNA or SCNB or some other gene(s) but the end result is always accumulation of SCNA in Lewy bodies.",
                "url": "https://disease-ontology.org/term/DOID:12217",
                "evidence": [
                    {
                        "id": "12217",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12217"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12894",
                "name": "Sjogren's syndrome",
                "description": "An autoimmune disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva.",
                "url": "https://disease-ontology.org/term/DOID:12894",
                "evidence": [
                    {
                        "id": "12894",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12894"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14330",
                "name": "Parkinson's disease",
                "description": "A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.",
                "url": "https://disease-ontology.org/term/DOID:14330",
                "evidence": [
                    {
                        "id": "14330",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14330"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1459",
                "name": "hypothyroidism",
                "description": "A thyroid gland disease which involves an underproduction of thyroid hormone.",
                "url": "https://disease-ontology.org/term/DOID:1459",
                "evidence": [
                    {
                        "id": "1459",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1459"
                    }
                ],
                "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"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "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:2378",
                "name": "relapsing-remitting multiple sclerosis",
                "description": "A multiple sclerosis that is characterized by relapse (attacks of symptom flare-ups) followed by remission (periods of recovery). Symptoms may vary from mild to severe, and relapses and remissions may last for days or months. More than 80 percent of people who have MS begin with relapsing-remitting cycles.",
                "url": "https://disease-ontology.org/term/DOID:2378",
                "evidence": [
                    {
                        "id": "2378",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2378"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3008",
                "name": "invasive ductal carcinoma",
                "description": "A breast ductal carcinoma that is characterized by infiltration into the fibrous or fatty tissue of the breast outside of the duct where it originated.",
                "url": "https://disease-ontology.org/term/DOID:3008",
                "evidence": [
                    {
                        "id": "3008",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3008"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3213",
                "name": "demyelinating disease",
                "description": "A central nervous system disease that is characterized by damage to the myelin sheath present around nerve axons.",
                "url": "https://disease-ontology.org/term/DOID:3213",
                "evidence": [
                    {
                        "id": "3213",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3213"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:332",
                "name": "amyotrophic lateral sclerosis",
                "description": "A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.",
                "url": "https://disease-ontology.org/term/DOID:332",
                "evidence": [
                    {
                        "id": "332",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:332"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:4166",
                "name": "syphilis",
                "description": "A primary bacterial infectious disease that is a sexually transmitted systemic disease, has_material_basis_in Treponema pallidum subsp pallidum, which is transmitted_by sexual contact, transmitted_by blood product transfusion, transmitted_by congenital method from mother to fetus or transmitted_by contact with infectious lesions. If left untreated, produces chancres, rashes, and systemic lesions in a clinical course with three stages continued over many years.",
                "url": "https://disease-ontology.org/term/DOID:4166",
                "evidence": [
                    {
                        "id": "4166",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:4166"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:526",
                "name": "human immunodeficiency virus infectious disease",
                "description": "A viral infectious disease that results in destruction of immune system, leading to life-threatening opportunistic infections and cancers, has_material_basis_in Human immunodeficiency virus 1 (Lentivirus humimdef1) or Human immunodeficiency virus 2 (Lentivirus humimdef2), which are transmitted by sexual contact, transmitted by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted by congenital method, and transmitted by contaminated needles. The virus infects helper T cells (CD4+ T cells) which are directly or indirectly destroyed, macrophages, and dendritic cells. The infection has symptom diarrhea, has symptom fatigue, has symptom fever, has symptom vaginal yeast infection, has symptom headache, has symptom mouth sores, has symptom muscle aches, has symptom sore throat, and has symptom swollen lymph glands.",
                "url": "https://disease-ontology.org/term/DOID:526",
                "evidence": [
                    {
                        "id": "526",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:526"
                    }
                ],
                "weight": 0.0
            },
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                "disease_id": "DOID:639",
                "name": "acute disseminated encephalomyelitis",
                "description": "An encephalomyelitis characterized by inflammation located in brain and located in spinal cord that damages myelin. It usually occurs after viral infection, but also following vaccination, bacterial or parasitic infection.",
                "url": "https://disease-ontology.org/term/DOID:639",
                "evidence": [
                    {
                        "id": "639",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:639"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:643",
                "name": "progressive multifocal leukoencephalopathy",
                "description": "A viral infectious disease that involves reactivation of JC polyomavirus (Betapolyomavirus secuhominis) in immune-compromised individuals which causes the loss of white matter (which is made up of myelin, a substance the surrounds and protects nerve fibers) in multiple areas of the brain. The symptoms include hemiparesis, aphasia, dysarthria, hemianopia, cognitive impairment and coma.",
                "url": "https://disease-ontology.org/term/DOID:643",
                "evidence": [
                    {
                        "id": "643",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:643"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8725",
                "name": "vascular dementia",
                "description": "A dementia that involves impairments in cognitive function caused by problems in blood vessels that feed the brain.",
                "url": "https://disease-ontology.org/term/DOID:8725",
                "evidence": [
                    {
                        "id": "8725",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8725"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8869",
                "name": "neuromyelitis optica",
                "description": "A central nervous system disease characterized by inflammation of the optic nerve (optic neuritis) and inflammation of the spinal cord (myelitis).",
                "url": "https://disease-ontology.org/term/DOID:8869",
                "evidence": [
                    {
                        "id": "8869",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8869"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9255",
                "name": "frontotemporal dementia",
                "description": "A dementia characterized by progressive neuronal loss predominantly involving the frontal and/or temporal lobes of the brain resulting in a gradual and progressive decline in behavior or language.",
                "url": "https://disease-ontology.org/term/DOID:9255",
                "evidence": [
                    {
                        "id": "9255",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9255"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "axon",
                "id": "GO:0030424",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030424",
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                    {
                        "database": "UniProtKB",
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                "pmid": ""
            },
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                "id": "GO:0005882",
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                    }
                ],
                "pmid": ""
            },
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                "name": "postsynaptic intermediate filament cytoskeleton",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0099160",
                "evidence": [
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            }
        ],
        "molecular_function": [
            {
                "name": "structural constituent of postsynaptic intermediate filament cytoskeleton",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0099184",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "neurofilament bundle assembly",
                "id": "GO:0033693",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033693",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
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        "record_id": "A0A8M9PUK6-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PUK7-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUK7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUK7"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 607,
        "chemical_mass": 68881.0,
        "gene_names": "si:ch211-203d1.3;si:ch211-203d1.3",
        "protein_name": "Protein phosphatase Slingshot homolog 1",
        "disease": [
            {
                "disease_id": "DOID:1574",
                "name": "alcohol use disorder",
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.",
                "url": "https://disease-ontology.org/term/DOID:1574",
                "evidence": [
                    {
                        "id": "1574",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1574"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "actin binding",
                "id": "GO:0003779",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003779",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUK7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUK7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein serine/threonine phosphatase activity",
                "id": "GO:0004722",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004722",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUK7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUK7"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoskeleton",
                "id": "GO:0005856",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005856",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUK7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUK7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cleavage furrow",
                "id": "GO:0032154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUK7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUK7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "midbody",
                "id": "GO:0030496",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030496",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUK7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUK7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "negative regulation of actin filament polymerization",
                "id": "GO:0030837",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030837",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUK7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUK7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PUK7-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PUN0-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUN0"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 263,
        "chemical_mass": 29949.0,
        "gene_names": "caln2;caln2",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUN0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "trans-Golgi network membrane",
                "id": "GO:0032588",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032588",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUN0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "perinuclear region of cytoplasm",
                "id": "GO:0048471",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048471",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUN0"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "calcium ion binding",
                "id": "GO:0005509",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005509",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUN0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PUN0-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PUP4-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUP4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUP4"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 375,
        "chemical_mass": 41019.0,
        "gene_names": "ndrg3a;fc04h03;ndr3;ndrg3a;ndrg3;wu:fc04h03;zgc:63551",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUP4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUP4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "signal transduction",
                "id": "GO:0007165",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007165",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUP4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUP4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "nervous system development",
                "id": "GO:0007399",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007399",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUP4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUP4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cell differentiation",
                "id": "GO:0030154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUP4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUP4"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "Wnt signaling pathway",
                "id": "GO:0016055",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016055",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUP4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUP4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PUP4-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PUQ6-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "A0A8M9PUQ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUQ6"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 956,
        "chemical_mass": 106738.0,
        "gene_names": "snx19b;snx19b",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "phosphatidylinositol binding",
                "id": "GO:0035091",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035091",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUQ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUQ6"
                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
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        "record_id": "A0A8M9PUQ6-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PUR8-1",
        "species": [
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                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "A0A8M9PUR8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUR8"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 492,
        "chemical_mass": 55085.0,
        "gene_names": "znf276;zgc:158366;znf276",
        "protein_name": "Zinc finger protein 276",
        "disease": [],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PUR8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PUR8"
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                ],
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        ],
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    {
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        "protein_name": "Collagen alpha-2(VI) chain",
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                "url": "https://disease-ontology.org/term/DOID:0060942",
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                ],
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                        "id": "0061198",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0061198"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0061199",
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                        "id": "0061199",
                        "database": "AGR",
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                    }
                ],
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            },
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                "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",
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                        "id": "5844",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5844"
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                ],
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            }
        ],
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            {
                "name": "cell adhesion",
                "id": "GO:0007155",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007155",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVL2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PVL2"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axonogenesis",
                "id": "GO:0007409",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007409",
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                    {
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "muscle organ development",
                "id": "GO:0007517",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007517",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "muscle cell development",
                "id": "GO:0055001",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055001",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVL2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PVL2"
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "extracellular matrix",
                "id": "GO:0031012",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031012",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVL2",
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                ],
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            }
        ],
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            {
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                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
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                                "label": "isoglyp",
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                        ],
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                        },
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                        "relation": "attached",
                        "comment": "",
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                        "end_aa": "Thr",
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                                "id": "",
                                "database": "GlyGen",
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                        ]
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                ]
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        ],
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    },
    {
        "uniprot_canonical_ac": "A0A8M9PVN0-1",
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                "name": "Danio rerio",
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                ],
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                "reference_species": "Danio rerio [7955]"
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        ],
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        "gene_names": "LOC100537594;LOC100537594",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "system development",
                "id": "GO:0048731",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048731",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVN0",
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                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "ATP binding",
                "id": "GO:0005524",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PVN0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "actin filament binding",
                "id": "GO:0051015",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051015",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PVN0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "microfilament motor activity",
                "id": "GO:0000146",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000146",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PVN0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PVN0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "myosin filament",
                "id": "GO:0032982",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032982",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PVN0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "myofibril",
                "id": "GO:0030016",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030016",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PVN0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "myosin II complex",
                "id": "GO:0016460",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016460",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PVN0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PVN0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PVN0-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PW15-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PW15",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PW15"
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                ],
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                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
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        ],
        "length": 1841,
        "chemical_mass": 203896.0,
        "gene_names": "tsc2;fc16b02;tsc2;tuberin;wu:fc16b02",
        "protein_name": "Tuberin",
        "disease": [
            {
                "disease_id": "DOID:0050902",
                "name": "medulloblastoma",
                "description": "An infratentorial cancer that is located_in the lower part of the brain and is a type of primitive neuroectodermal tumor.",
                "url": "https://disease-ontology.org/term/DOID:0050902",
                "evidence": [
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                        "id": "0050902",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050902"
                    }
                ],
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            },
            {
                "disease_id": "DOID:0060041",
                "name": "autism spectrum disorder",
                "description": "A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior.",
                "url": "https://disease-ontology.org/term/DOID:0060041",
                "evidence": [
                    {
                        "id": "0060041",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060041"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0080325",
                "name": "tuberous sclerosis 2",
                "description": "A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the TSC2 gene, which encodes tuberin, on chromosome 16p13.",
                "url": "https://disease-ontology.org/term/DOID:0080325",
                "evidence": [
                    {
                        "id": "0080325",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0080325"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:127",
                "name": "leiomyoma",
                "description": "A cell type benign neoplasm that is a benign tumor of smooth muscle cells.",
                "url": "https://disease-ontology.org/term/DOID:127",
                "evidence": [
                    {
                        "id": "127",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:127"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13223",
                "name": "uterine fibroid",
                "description": "An uterine benign neoplasm derived from the smooth muscle layer of the uterus.",
                "url": "https://disease-ontology.org/term/DOID:13223",
                "evidence": [
                    {
                        "id": "13223",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13223"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:13515",
                "name": "tuberous sclerosis",
                "description": "A hamartoma syndrome that is characterized by the growth of numerous noncancerous tumors in many parts of the body.",
                "url": "https://disease-ontology.org/term/DOID:13515",
                "evidence": [
                    {
                        "id": "13515",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:13515"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:2030",
                "name": "anxiety disorder",
                "description": "A cognitive disorder that involves an excessive, irrational dread of everyday situations.",
                "url": "https://disease-ontology.org/term/DOID:2030",
                "evidence": [
                    {
                        "id": "2030",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2030"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3314",
                "name": "angiomyolipoma",
                "description": "A cell type benign neoplasm that is primarily located in the kidneys but may be found in the lungs, liver or other organs and is derived from perivascular epithelioid cells.",
                "url": "https://disease-ontology.org/term/DOID:3314",
                "evidence": [
                    {
                        "id": "3314",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3314"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3317",
                "name": "hepatic angiomyolipoma",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:3317",
                "evidence": [
                    {
                        "id": "3317",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3317"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3319",
                "name": "lymphangioleiomyomatosis",
                "description": "A lung disease that is characterized by progressive cystic destruction of the lung and lymphatic abnormalities, frequently associated with renal angiomyolipomas.",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0060193"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:10652",
                "name": "Alzheimer's disease",
                "description": "A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.",
                "url": "https://disease-ontology.org/term/DOID:10652",
                "evidence": [
                    {
                        "id": "10652",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10652"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:12217",
                "name": "Lewy body dementia",
                "description": "A dementia that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities that has_material_basis_in accumulation of alpha-synuclein, SCNA, (protein). The causal mutation might be in SCNA or SCNB or some other gene(s) but the end result is always accumulation of SCNA in Lewy bodies.",
                "url": "https://disease-ontology.org/term/DOID:12217",
                "evidence": [
                    {
                        "id": "12217",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:12217"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14330",
                "name": "Parkinson's disease",
                "description": "A synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.",
                "url": "https://disease-ontology.org/term/DOID:14330",
                "evidence": [
                    {
                        "id": "14330",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14330"
                    }
                ],
                "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"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1612",
                "name": "breast cancer",
                "description": "An organ system cancer that originates in the mammary gland.",
                "url": "https://disease-ontology.org/term/DOID:1612",
                "evidence": [
                    {
                        "id": "1612",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1612"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1686",
                "name": "glaucoma",
                "description": "An eye disease that is characterized by an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function.",
                "url": "https://disease-ontology.org/term/DOID:1686",
                "evidence": [
                    {
                        "id": "1686",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1686"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3981",
                "name": "pantothenate kinase-associated neurodegeneration",
                "description": "A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13.",
                "url": "https://disease-ontology.org/term/DOID:3981",
                "evidence": [
                    {
                        "id": "3981",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3981"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:768",
                "name": "retinoblastoma",
                "description": "A retinal cell cancer and malignant neoplasm of retina and neuroblastoma and neuroendocrine tumors that derives_from the tissues of the retina.",
                "url": "https://disease-ontology.org/term/DOID:768",
                "evidence": [
                    {
                        "id": "768",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:768"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:8725",
                "name": "vascular dementia",
                "description": "A dementia that involves impairments in cognitive function caused by problems in blood vessels that feed the brain.",
                "url": "https://disease-ontology.org/term/DOID:8725",
                "evidence": [
                    {
                        "id": "8725",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8725"
                    }
                ],
                "weight": 0.0
            }
        ],
        "cellular_component": [
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWC8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWC8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuronal cell body",
                "id": "GO:0043025",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043025",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWC8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWC8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "axon terminus",
                "id": "GO:0043679",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043679",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWC8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWC8"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "synapse organization",
                "id": "GO:0050808",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050808",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWC8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWC8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "chemical synaptic transmission",
                "id": "GO:0007268",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007268",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWC8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWC8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "synaptic vesicle endocytosis",
                "id": "GO:0048488",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048488",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWC8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWC8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "dopaminergic neuron differentiation",
                "id": "GO:0071542",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071542",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWC8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWC8"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "larval locomotory behavior",
                "id": "GO:0008345",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008345",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWC8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWC8"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "cuprous ion binding",
                "id": "GO:1903136",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1903136",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWC8",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWC8"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PWC8-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PWI3-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWI3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWI3"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 1402,
        "chemical_mass": 157082.0,
        "gene_names": "polr3a;fb81e09;im:7139382;polr3a;wu:fb81e09",
        "protein_name": "DNA-directed RNA polymerase subunit",
        "disease": [
            {
                "disease_id": "DOID:0060786",
                "name": "hypomyelinating leukodystrophy",
                "description": "A leukodystrophy characterized by improper formation of the myelin sheath in the central nervous system resulting in T2 hyperintensity and variable T1 signal on magnetic resonance imaging.",
                "url": "https://disease-ontology.org/term/DOID:0060786",
                "evidence": [
                    {
                        "id": "0060786",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060786"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060794",
                "name": "hypomyelinating leukodystrophy 7",
                "description": "A hypomyelinating leukodystrophy characterized by autosomal recessive inheritance of hildhood onset of progressive motor decline manifest as spasticity, ataxia, tremor, and cerebellar signs, as well as mild cognitive regression that has_material_basis_in homozygous or compound heterozygous mutation in the POLR3A gene on chromosome 10q22.",
                "url": "https://disease-ontology.org/term/DOID:0060794",
                "evidence": [
                    {
                        "id": "0060794",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060794"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0081333",
                "name": "Wiedemann-Rautenstrauch syndrome",
                "description": "A progeroid syndrome that is characterized by intrauterine growth retardation, failure to thrive, short stature, a progeroid appearance, hypotonia, and variable mental impairment and that has_material_basis_in compound heterozygous mutation in the POLR3A gene on chromosome 10q22.",
                "url": "https://disease-ontology.org/term/DOID:0081333",
                "evidence": [
                    {
                        "id": "0081333",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0081333"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "tRNA transcription by RNA polymerase III",
                "id": "GO:0042797",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042797",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWI3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWI3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006351",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWI3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWI3"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWI3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWI3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWI3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWI3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-directed RNA polymerase activity",
                "id": "GO:0003899",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003899",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWI3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWI3"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleoplasm",
                "id": "GO:0005654",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005654",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWI3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWI3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "RNA polymerase III complex",
                "id": "GO:0005666",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005666",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWI3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWI3"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "DNA-directed RNA polymerase complex",
                "id": "GO:0000428",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000428",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWI3",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWI3"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9PWI3-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PWJ6-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 661,
        "chemical_mass": 75544.0,
        "gene_names": "rgs9b;rgs9b;rgs9;zC147H1.2;zgc:73189",
        "protein_name": "Regulator of G-protein signaling 9",
        "disease": [
            {
                "disease_id": "DOID:0070363",
                "name": "bradyopsia 1",
                "description": "A braydopsia that has_material_basis_in homozygous or compound heterozygous mutation in the RGS9 gene on chromosome 17q24.",
                "url": "https://disease-ontology.org/term/DOID:0070363",
                "evidence": [
                    {
                        "id": "0070363",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0070363"
                    }
                ],
                "weight": 0.0
            }
        ],
        "biological_process": [
            {
                "name": "G protein-coupled receptor signaling pathway",
                "id": "GO:0007186",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007186",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular signal transduction",
                "id": "GO:0035556",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035556",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "visual perception",
                "id": "GO:0007601",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007601",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "negative regulation of signal transduction",
                "id": "GO:0009968",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009968",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of G protein-coupled receptor signaling pathway",
                "id": "GO:0008277",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008277",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "G protein-coupled dopamine receptor signaling pathway",
                "id": "GO:0007212",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007212",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "neuron projection",
                "id": "GO:0043005",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043005",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "GTPase activator activity",
                "id": "GO:0005096",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005096",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWJ6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWJ6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A8M9PWJ6-1",
                "start_pos": "518",
                "end_pos": "518",
                "site_lbl": "Thr518",
                "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": 518,
                        "start_aa": "Thr",
                        "end_pos": 518,
                        "end_aa": "Thr",
                        "residue": "Thr",
                        "site_lbl": "Thr518",
                        "evidence": [
                            {
                                "id": "",
                                "database": "GlyGen",
                                "url": "https://data.glygen.org/"
                            }
                        ]
                    }
                ]
            }
        ],
        "record_id": "A0A8M9PWJ6-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PWP2-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWP2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWP2"
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                ],
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            }
        ],
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            {
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                ],
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        ],
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                    {
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                            {
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                ]
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        ],
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    {
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            {
                "name": "cytoplasm",
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                ],
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            },
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                ],
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            },
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "G protein-coupled receptor signaling pathway",
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                    {
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        ],
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            {
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                    {
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                    }
                ],
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            },
            {
                "name": "guanyl-nucleotide exchange factor activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005085",
                "evidence": [
                    {
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                ],
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        ],
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    {
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                ],
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        ],
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            {
                "name": "plasma membrane",
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                    {
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                ],
                "pmid": ""
            },
            {
                "name": "early endosome membrane",
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                    {
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                ],
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            }
        ],
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    {
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                ],
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        ],
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                ],
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                ],
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                ],
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                ],
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                ],
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                "url": "https://disease-ontology.org/term/DOID:1470",
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                ],
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                ],
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                "url": "https://disease-ontology.org/term/DOID:9970",
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                ],
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            },
            {
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                ],
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            }
        ],
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            {
                "name": "G protein-coupled receptor activity",
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                        "database": "UniProtKB",
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                ],
                "pmid": ""
            },
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                "name": "neuropeptide binding",
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                    {
                        "database": "UniProtKB",
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            },
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                ],
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        ],
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            {
                "name": "plasma membrane",
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                    {
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            {
                "name": "membrane",
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                "name": "adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway",
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                ],
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        ],
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        "protein_name": "protein-tyrosine-phosphatase",
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                "disease_id": "DOID:0050425",
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                "url": "https://disease-ontology.org/term/DOID:0050425",
                "evidence": [
                    {
                        "id": "0050425",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0050425"
                    }
                ],
                "weight": 0.0
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            {
                "disease_id": "DOID:10763",
                "name": "hypertension",
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                    {
                        "id": "10763",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:10763"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:14227",
                "name": "azoospermia",
                "description": "A male infertility disease characterized by the absence of any measurable level of sperm in semen.",
                "url": "https://disease-ontology.org/term/DOID:14227",
                "evidence": [
                    {
                        "id": "14227",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:14227"
                    }
                ],
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            },
            {
                "disease_id": "DOID:3393",
                "name": "coronary artery disease",
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                "url": "https://disease-ontology.org/term/DOID:3393",
                "evidence": [
                    {
                        "id": "3393",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3393"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9351",
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                "description": "A glucose metabolism disease that is characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both.",
                "url": "https://disease-ontology.org/term/DOID:9351",
                "evidence": [
                    {
                        "id": "9351",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9351"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.",
                "url": "https://disease-ontology.org/term/DOID:9352",
                "evidence": [
                    {
                        "id": "9352",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:9352"
                    }
                ],
                "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": "A0A8M9Q0T4",
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                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "synapse organization",
                "id": "GO:0050808",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050808",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q0T4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q0T4"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "protein tyrosine phosphatase activity",
                "id": "GO:0004725",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004725",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q0T4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q0T4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [
            {
                "uniprot_canonical_ac": "A0A8M9Q0T4-1",
                "start_pos": "411",
                "end_pos": "411",
                "site_lbl": "Thr411",
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                "glycosylation": [
                    {
                        "glytoucan_ac": "",
                        "type": "O-linked",
                        "subtype": "",
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                            {
                                "label": "isoglyp",
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                            }
                        ],
                        "site_category": "predicted",
                        "site_category_dict": {
                            "predicted": true
                        },
                        "site_seq": "",
                        "relation": "attached",
                        "comment": "",
                        "icn3d_view": {},
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                        "start_aa": "Thr",
                        "end_pos": 411,
                        "end_aa": "Thr",
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                        "evidence": [
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                                "id": "",
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                        ]
                    }
                ]
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "A0A8M9PYJ9-1",
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            {
                "name": "Danio rerio",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PYJ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PYJ9"
                    }
                ],
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        ],
        "length": 817,
        "chemical_mass": 92149.0,
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        "protein_name": "non-specific serine/threonine protein kinase",
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            {
                "name": "protein serine/threonine kinase activity",
                "id": "GO:0004674",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004674",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PYJ9",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "ATP binding",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005524",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PYJ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PYJ9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "kinase activity",
                "id": "GO:0016301",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016301",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PYJ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PYJ9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PYJ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PYJ9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "cytoplasm",
                "id": "GO:0005737",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PYJ9",
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                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cell differentiation",
                "id": "GO:0030154",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030154",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PYJ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PYJ9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "intracellular signal transduction",
                "id": "GO:0035556",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035556",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PYJ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PYJ9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "spliceosomal complex assembly",
                "id": "GO:0000245",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000245",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PYJ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PYJ9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "regulation of mRNA processing",
                "id": "GO:0050684",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050684",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PYJ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PYJ9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "A0A8M9PYJ9-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PWS6-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWS6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWS6"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 619,
        "chemical_mass": 72027.0,
        "gene_names": "sp100.1;sp100.1",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0112254",
                "name": "hepatic venoocclusive disease with immunodeficiency",
                "description": "A syndrome characterized by severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells, hepatic vascular occlusion, and fibrosis that has_material_basis_in homozygous or compound heterozygous mutation in the SP110 gene on chromosome 2q37.1.",
                "url": "https://disease-ontology.org/term/DOID:0112254",
                "evidence": [
                    {
                        "id": "0112254",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0112254"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:399",
                "name": "tuberculosis",
                "description": "A primary bacterial infectious disease that is located_in lungs, located_in lymph nodes, located_in pericardium, located_in brain, located_in pleura or located_in gastrointestinal tract, has_material_basis_in Mycobacterium tuberculosis, which is transmitted_by droplets released into the air when an infected person coughs or sneezes.",
                "url": "https://disease-ontology.org/term/DOID:399",
                "evidence": [
                    {
                        "id": "399",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:399"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWS6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWS6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWS6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWS6"
                    }
                ],
                "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": "A0A8M9PWS6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWS6"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWS6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWS6"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "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": "A0A8M9PWS6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWS6"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "A0A8M9PWV9-1",
        "species": [
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                "name": "Danio rerio",
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                        "id": "A0A8M9PWV9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWV9"
                    }
                ],
                "common_name": "Zebrafish",
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        ],
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        "chemical_mass": 112489.0,
        "gene_names": "adamts1;adamts1",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:1826",
                "name": "epilepsy",
                "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"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
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                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "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:5199",
                "name": "ureteral obstruction",
                "description": "An urinary tract obstruction that is characterized by a blockage in one or both of the tubes (ureters) that carry urine from the kidneys to the bladder.",
                "url": "https://disease-ontology.org/term/DOID:5199",
                "evidence": [
                    {
                        "id": "5199",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5199"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:5200",
                "name": "urinary tract obstruction",
                "description": "",
                "url": "https://disease-ontology.org/term/DOID:5200",
                "evidence": [
                    {
                        "id": "5200",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:5200"
                    }
                ],
                "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
            }
        ],
        "molecular_function": [
            {
                "name": "metalloendopeptidase activity",
                "id": "GO:0004222",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004222",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWV9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWV9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metallopeptidase activity",
                "id": "GO:0008237",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008237",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWV9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWV9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "metal ion binding",
                "id": "GO:0046872",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046872",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWV9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWV9"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "proteolysis",
                "id": "GO:0006508",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWV9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWV9"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "extracellular matrix organization",
                "id": "GO:0030198",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030198",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWV9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWV9"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular matrix",
                "id": "GO:0031012",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031012",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "A0A8M9PWV9-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9PWY6-1",
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                "name": "Danio rerio",
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                ],
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        ],
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        "chemical_mass": 58129.0,
        "gene_names": "slc29a4b;slc29a4b",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWY6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWY6"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "nucleoside transmembrane transporter activity",
                "id": "GO:0005337",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005337",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWY6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWY6"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "monoamine transmembrane transporter activity",
                "id": "GO:0008504",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008504",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9PWY6",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9PWY6"
                    }
                ],
                "pmid": ""
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                ],
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        ],
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            {
                "name": "plasma membrane",
                "id": "GO:0005886",
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                ],
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                ],
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        ],
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                ],
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            {
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                ],
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            },
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                "name": "intermediate filament organization",
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                    {
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            }
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                    {
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                ],
                "pmid": ""
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            {
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            }
        ],
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                "name": "cardiac muscle cell development",
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                ],
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        ],
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                ],
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        ],
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        "gene_names": "vps37d;vps37d",
        "protein_name": "",
        "disease": [],
        "biological_process": [
            {
                "name": "protein targeting to membrane",
                "id": "GO:0006612",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006612",
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                ],
                "pmid": ""
            },
            {
                "name": "protein targeting to vacuole",
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                "evidence": [
                    {
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                "name": "autism spectrum disorder",
                "description": "A pervasive developmental disorder that is a spectrum of psychological conditions. The disease has_symptom widespread abnormalities of social interactions and communication, has_symptom severely restricted interests and has_symptom highly repetitive behavior.",
                "url": "https://disease-ontology.org/term/DOID:0060041",
                "evidence": [
                    {
                        "id": "0060041",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060041"
                    }
                ],
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            },
            {
                "disease_id": "DOID:11161",
                "name": "neonatal respiratory failure",
                "description": "A respiratory failure that is characterized by inadequate gas exchange by the respiratory system in neonates.",
                "url": "https://disease-ontology.org/term/DOID:11161",
                "evidence": [
                    {
                        "id": "11161",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11161"
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                ],
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            },
            {
                "disease_id": "DOID:11162",
                "name": "respiratory failure",
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                ],
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            },
            {
                "disease_id": "DOID:12120",
                "name": "pulmonary alveolar proteinosis",
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                "url": "https://disease-ontology.org/term/DOID:12120",
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                        "id": "12120",
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                        "url": "https://www.alliancegenome.org/disease/DOID:12120"
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                ],
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                "url": "https://disease-ontology.org/term/DOID:12716",
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                ],
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                        "id": "3082",
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            },
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                    {
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                        "id": "A0A8M9Q293",
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            },
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042626",
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            },
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                "name": "ATP hydrolysis activity",
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                ],
                "pmid": ""
            },
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                "name": "ABC-type transporter activity",
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                ],
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            }
        ],
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            {
                "name": "cytoplasm",
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                    {
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                "pmid": ""
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                "pmid": ""
            },
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                "name": "endomembrane system",
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "lipid transport",
                "id": "GO:0006869",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006869",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
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                "name": "Danio rerio",
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                ],
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            }
        ],
        "length": 518,
        "chemical_mass": 60877.0,
        "gene_names": "chst15a;chst15",
        "protein_name": "Sulfotransferase",
        "disease": [],
        "molecular_function": [
            {
                "name": "sulfotransferase activity",
                "id": "GO:0008146",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008146",
                "evidence": [
                    {
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                        "id": "A0A8M9Q298",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q298"
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                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9Q298-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9Q2B9-1",
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                        "database": "UniProtKB",
                        "id": "A0A8M9Q2B9",
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                ],
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            }
        ],
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        "chemical_mass": 40211.0,
        "gene_names": "si:dkey-183c6.7;si:dkey-183c6.7",
        "protein_name": "Urea transporter",
        "disease": [],
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            {
                "name": "urea transmembrane transport",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071918",
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                    {
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                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2B9"
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                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2B9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2B9"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "urea transmembrane transporter activity",
                "id": "GO:0015204",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015204",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2B9",
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                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
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        "record_id": "A0A8M9Q2B9-1"
    },
    {
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        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
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                        "id": "A0A8M9Q2C4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2C4"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 444,
        "chemical_mass": 49940.0,
        "gene_names": "si:dkeyp-75h12.7;si:dkeyp-75h12.7",
        "protein_name": "",
        "disease": [],
        "cellular_component": [
            {
                "name": "plasma membrane",
                "id": "GO:0005886",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2C4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2C4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "cytokine-mediated signaling pathway",
                "id": "GO:0019221",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019221",
                "evidence": [
                    {
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                        "id": "A0A8M9Q2C4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2C4"
                    }
                ],
                "pmid": ""
            }
        ],
        "molecular_function": [
            {
                "name": "cytokine receptor activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0004896",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2C4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2C4"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "A0A8M9Q2C4-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9Q2I0-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
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                        "database": "UniProtKB",
                        "id": "A0A8M9Q2I0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2I0"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 355,
        "chemical_mass": 39376.0,
        "gene_names": "LOC100535100;LOC100535100",
        "protein_name": "Na(+)/H(+) exchange regulatory cofactor NHE-RF",
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        "molecular_function": [
            {
                "name": "signaling receptor binding",
                "id": "GO:0005102",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005102",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2I0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2I0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "protein-membrane adaptor activity",
                "id": "GO:0043495",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043495",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2I0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2I0"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "protein localization to plasma membrane",
                "id": "GO:0072659",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072659",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2I0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2I0"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "endomembrane system",
                "id": "GO:0012505",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0012505",
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                    {
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                        "id": "A0A8M9Q2I0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2I0"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "apical plasma membrane",
                "id": "GO:0016324",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016324",
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "A0A8M9Q2I0",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2I0"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M9Q2I0-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M9Q2R5-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2R5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2R5"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 690,
        "chemical_mass": 74116.0,
        "gene_names": "slco3a1b;slco3a1b",
        "protein_name": "Solute carrier organic anion transporter family member",
        "disease": [],
        "biological_process": [
            {
                "name": "monoatomic ion transport",
                "id": "GO:0006811",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006811",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2R5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2R5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "transmembrane transport",
                "id": "GO:0055085",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055085",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2R5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2R5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "sodium-independent organic anion transport",
                "id": "GO:0043252",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043252",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2R5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2R5"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "prostaglandin transport",
                "id": "GO:0015732",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015732",
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                        "id": "A0A8M9Q2R5",
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                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "basolateral plasma membrane",
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                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
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    },
    {
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                        "id": "A0A8M9Q2X1",
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                    }
                ],
                "common_name": "Zebrafish",
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            }
        ],
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        "gene_names": "LOC141374989;LOC141374989",
        "protein_name": "NAD(P)(+)--arginine ADP-ribosyltransferase",
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            {
                "name": "nucleotidyltransferase activity",
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                        "id": "A0A8M9Q2X1",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M9Q2X1"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "NAD+ poly-ADP-ribosyltransferase activity",
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                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003950",
                "evidence": [
                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "NAD+-protein-arginine ADP-ribosyltransferase activity",
                "id": "GO:0106274",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M9Q2X1",
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                    }
                ],
                "pmid": ""
            }
        ],
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                        "id": "A0A8M9Q381",
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                ],
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        ],
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        "gene_names": "si:ch211-127i16.2;si:ch211-127i16.2",
        "protein_name": "Amine oxidase",
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            {
                "name": "monoamine oxidase activity",
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                "evidence": [
                    {
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        "gene_names": "si:ch73-40a17.4;si:ch73-40a17.4",
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            {
                "name": "nucleus",
                "id": "GO:0005634",
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                    {
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                "pmid": ""
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                "name": "chromosome",
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                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "DNA-templated transcription",
                "id": "GO:0006351",
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                    {
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                "pmid": ""
            },
            {
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                    {
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            }
        ],
        "molecular_function": [
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
                "pmid": ""
            },
            {
                "name": "identical protein binding",
                "id": "GO:0042802",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042802",
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                    {
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                        "id": "A0A8M2BIG9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M2BIG9"
                    }
                ],
                "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": "A0A8M2BIG9",
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                    }
                ],
                "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": "A0A8M2BIG9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M2BIG9"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
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        "record_id": "A0A8M2BIG9-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M2BII2-1",
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            {
                "name": "Danio rerio",
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                "evidence": [
                    {
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                        "id": "A0A8M2BII2",
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                    }
                ],
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                "reference_species": "Danio rerio [7955]"
            }
        ],
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        "chemical_mass": 22329.0,
        "gene_names": "pebp4;pebp4",
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                "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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                                "database": "GlyGen",
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    },
    {
        "uniprot_canonical_ac": "A0A8M2BIJ9-1",
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            {
                "name": "Danio rerio",
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                "evidence": [
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                ],
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                "reference_species": "Danio rerio [7955]"
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        ],
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        "gene_names": "acin1a;acin1a",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "nucleic acid binding",
                "id": "GO:0003676",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003676",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M2BIJ9",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M2BIJ9"
                    }
                ],
                "pmid": ""
            }
        ],
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        "biomarkers": [],
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    },
    {
        "uniprot_canonical_ac": "A0A8M2BIR4-1",
        "species": [
            {
                "name": "Danio rerio",
                "taxid": 7955,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M2BIR4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M2BIR4"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 1432,
        "chemical_mass": 160372.0,
        "gene_names": "rasal2;rasal2",
        "protein_name": "",
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            {
                "disease_id": "DOID:0060037",
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                "url": "https://disease-ontology.org/term/DOID:0060037",
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                    {
                        "id": "0060037",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060037"
                    }
                ],
                "weight": 0.0
            }
        ],
        "molecular_function": [
            {
                "name": "GTPase activator activity",
                "id": "GO:0005096",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005096",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M2BIR4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M2BIR4"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "regulation of intracellular signal transduction",
                "id": "GO:1902531",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902531",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M2BIR4",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M2BIR4"
                    }
                ],
                "pmid": ""
            }
        ],
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    },
    {
        "uniprot_canonical_ac": "A0A8M3AQB7-1",
        "species": [
            {
                "name": "Danio rerio",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M3AQB7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M3AQB7"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
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        "chemical_mass": 96581.0,
        "gene_names": "phc3;phc3a;phc3;si:dkey-127k13.2",
        "protein_name": "",
        "disease": [],
        "molecular_function": [
            {
                "name": "DNA binding",
                "id": "GO:0003677",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003677",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M3AQB7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M3AQB7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "zinc ion binding",
                "id": "GO:0008270",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M3AQB7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M3AQB7"
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                ],
                "pmid": ""
            },
            {
                "name": "chromatin binding",
                "id": "GO:0003682",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003682",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M3AQB7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M3AQB7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "histone binding",
                "id": "GO:0042393",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042393",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M3AQB7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M3AQB7"
                    }
                ],
                "pmid": ""
            }
        ],
        "cellular_component": [
            {
                "name": "nucleus",
                "id": "GO:0005634",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M3AQB7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M3AQB7"
                    }
                ],
                "pmid": ""
            },
            {
                "name": "PRC1 complex",
                "id": "GO:0035102",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035102",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M3AQB7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M3AQB7"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
                "name": "negative regulation of DNA-templated transcription",
                "id": "GO:0045892",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045892",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M3AQB7",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M3AQB7"
                    }
                ],
                "pmid": ""
            }
        ],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M3AQB7-1"
    },
    {
        "uniprot_canonical_ac": "A0A8M2BIN2-1",
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            {
                "name": "Danio rerio",
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                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M2BIN2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M2BIN2"
                    }
                ],
                "common_name": "Zebrafish",
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            }
        ],
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        "chemical_mass": 13145.0,
        "gene_names": "ccl20l;ccl20l",
        "protein_name": "",
        "disease": [
            {
                "disease_id": "DOID:0050486",
                "name": "exanthem",
                "description": "A skin disease that is characterized by a rash that results from a variety of causes including bacteria, viruses, toxins, drugs and autoimmune disorders.",
                "url": "https://disease-ontology.org/term/DOID:0050486",
                "evidence": [
                    {
                        "id": "0050486",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0050486"
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                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:0060061",
                "name": "primary cutaneous T-cell non-Hodgkin lymphoma",
                "description": "A peripheral T-cell lymphoma that has_material_basis_in a mutation of T cells.",
                "url": "https://disease-ontology.org/term/DOID:0060061",
                "evidence": [
                    {
                        "id": "0060061",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:0060061"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11168",
                "name": "anogenital venereal wart",
                "description": "A viral infectious disease that results_in infection located_in skin of vagina, cervix, uterus, anus, penis, scrotum, mouth, or throat, has_material_basis_in human papillomaviruses (types 6 and 11), which are transmitted_by direct contact with the skin during oral, genital, or anal sex with an infected partner. The infection has_symptom anogenital warts.",
                "url": "https://disease-ontology.org/term/DOID:11168",
                "evidence": [
                    {
                        "id": "11168",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11168"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:11729",
                "name": "Lyme disease",
                "description": "A primary bacterial infectious disease that results_in infection, has_material_basis_in Borrelia burgdorferi, which is transmitted_by blacklegged tick (Ixodes scapularis) or transmitted_by western blacklegged tick (Ixodes pacificus). The infection has_symptom fever, has_symptom headache, has_symptom fatigue, and has_symptom skin rash called erythema migrans. If left untreated, infection can spread to joints, the heart, and the nervous system.",
                "url": "https://disease-ontology.org/term/DOID:11729",
                "evidence": [
                    {
                        "id": "11729",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:11729"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1564",
                "name": "fungal infectious disease",
                "description": "A disease by infectious agent that results_in infection, has_material_basis_in Fungi, which pass the resistance barriers of the human or animal body.",
                "url": "https://disease-ontology.org/term/DOID:1564",
                "evidence": [
                    {
                        "id": "1564",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1564"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas.",
                "url": "https://disease-ontology.org/term/DOID:1793",
                "evidence": [
                    {
                        "id": "1793",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:1793"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:224",
                "name": "transient cerebral ischemia",
                "description": "A brain ischemia that is characterized by ischemia of brief duration and without resultant tissue death.",
                "url": "https://disease-ontology.org/term/DOID:224",
                "evidence": [
                    {
                        "id": "224",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:224"
                    }
                ],
                "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:2722",
                "name": "acrodermatitis",
                "description": "A dermatitis that selectively affects the hands and feet.",
                "url": "https://disease-ontology.org/term/DOID:2722",
                "evidence": [
                    {
                        "id": "2722",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2722"
                    }
                ],
                "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:2986",
                "name": "IgA glomerulonephritis",
                "description": "A glomerulonephritis characterized by build up of IgA antibody in the glomerulus.",
                "url": "https://disease-ontology.org/term/DOID:2986",
                "evidence": [
                    {
                        "id": "2986",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:2986"
                    }
                ],
                "weight": 0.0
            },
            {
                "disease_id": "DOID:3178",
                "name": "skin papilloma",
                "description": "A skin benign neoplasm that is composed of epithelial cells and a fibrous stalk.",
                "url": "https://disease-ontology.org/term/DOID:3178",
                "evidence": [
                    {
                        "id": "3178",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:3178"
                    }
                ],
                "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: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:8577",
                "name": "ulcerative colitis",
                "description": "A colitis that is predominantly confined to the mucosa located_in colon and includes characteristic ulcers, or open sores.",
                "url": "https://disease-ontology.org/term/DOID:8577",
                "evidence": [
                    {
                        "id": "8577",
                        "database": "AGR",
                        "url": "https://www.alliancegenome.org/disease/DOID:8577"
                    }
                ],
                "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
            }
        ],
        "cellular_component": [
            {
                "name": "extracellular space",
                "id": "GO:0005615",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "A0A8M2BIN2",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M2BIN2"
                    }
                ],
                "pmid": ""
            }
        ],
        "biological_process": [
            {
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                    }
                ],
                "pmid": ""
            }
        ],
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            {
                "name": "nucleus",
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            {
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                    {
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                ],
                "pmid": ""
            }
        ],
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            {
                "name": "signal transduction",
                "id": "GO:0007165",
                "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007165",
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                    {
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                ],
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            }
        ],
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            {
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                    {
                        "glytoucan_ac": "",
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                        "site_category_dict": {
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                        },
                        "site_seq": "",
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                        "icn3d_view": {},
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                ]
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        ],
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    },
    {
        "uniprot_canonical_ac": "A0A8M3BEL9-1",
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                "name": "Danio rerio",
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                    {
                        "database": "UniProtKB",
                        "id": "A0A8M3BEL9",
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        ],
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            {
                "name": "adherens junction",
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                ],
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        ],
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        "uniprot_canonical_ac": "A0A8M6YSJ2-1",
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                "name": "Danio rerio",
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                    {
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                        "id": "A0A8M6YSJ2",
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                ],
                "common_name": "Zebrafish",
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        ],
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        "chemical_mass": 43553.0,
        "gene_names": "LOC100330563;LOC100330563",
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        "cellular_component": [
            {
                "name": "membrane",
                "id": "GO:0016020",
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                    {
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                ],
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                        "id": "A0A8M6YSM0",
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                ],
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                "glygen_name": "Zebrafish",
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        ],
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        "chemical_mass": 120740.0,
        "gene_names": "si:ch211-181d7.2;si:ch211-181d7.1;si:ch211-181d7.2",
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                "url": "https://disease-ontology.org/term/DOID:0080208",
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                "url": "https://disease-ontology.org/term/DOID:0080270",
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                        "id": "0080270",
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                "url": "https://disease-ontology.org/term/DOID:0090062",
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                        "url": "https://www.alliancegenome.org/disease/DOID:0090062"
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                ],
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                "url": "https://disease-ontology.org/term/DOID:3590",
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                        "id": "9452",
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                ],
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        ],
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                    }
                ],
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            }
        ],
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        "protein_name": "",
        "disease": [],
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            {
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                ],
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            }
        ],
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            {
                "name": "growth factor activity",
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                    {
                        "database": "UniProtKB",
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                    }
                ],
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        ],
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    },
    {
        "uniprot_canonical_ac": "A0A8M6YT64-1",
        "species": [
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                "name": "Danio rerio",
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                ],
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        ],
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        "gene_names": "gnly;gnly",
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                "name": "defense response to bacterium",
                "id": "GO:0042742",
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                ],
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                ],
                "weight": 0.0
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        ],
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            {
                "name": "sperm flagellum",
                "id": "GO:0036126",
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                        "id": "A0A8M6YU94",
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                    {
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                ],
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        ],
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            {
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                        "database": "UniProtKB",
                        "id": "A0A8M6YVV5",
                        "url": "https://www.uniprot.org/uniprotkb/A0A8M6YVV5"
                    }
                ],
                "common_name": "Zebrafish",
                "glygen_name": "Zebrafish",
                "reference_species": "Danio rerio [7955]"
            }
        ],
        "length": 748,
        "chemical_mass": 83405.0,
        "gene_names": "LOC101885876;LOC101885876",
        "protein_name": "",
        "disease": [],
        "binding_glycans": [],
        "biomarkers": [],
        "sites": [],
        "record_id": "A0A8M6YVV5-1"
    }
]
