{
    "uniprot_canonical_ac": "A0A499JF18-1",
    "uniprot_ac": "A0A499JF18",
    "uniprot_id": "A0A499JF18_DROME",
    "mass": {
        "chemical_mass": 133714.0,
        "monoisotopic_mass": 133714.0
    },
    "refseq": {
        "ac": "NP_727173",
        "name": "uncharacterized protein, isoform I",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_727173"
    },
    "gene_names": [
        {
            "name": "Cph",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A499JF18",
            "id": "A0A499JF18"
        },
        {
            "name": "Bcl11; Dmel\\CG9650",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572385",
            "id": "NP_572385"
        },
        {
            "name": "CG9650",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572385",
            "id": "NP_572385"
        },
        {
            "name": "CG9650",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A499JF18",
            "id": "A0A499JF18"
        },
        {
            "name": "Dmel\\CG9650",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A499JF18",
            "id": "A0A499JF18"
        },
        {
            "name": "Dmel_CG9650",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A499JF18",
            "id": "A0A499JF18"
        }
    ],
    "protein_names": [
        {
            "name": "CG9650-PG",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001096899",
            "id": "NP_001096899"
        },
        {
            "name": "CG9650-PI",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_727173",
            "id": "NP_727173"
        },
        {
            "name": "CG9650-PJ",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572385",
            "id": "NP_572385"
        },
        {
            "name": "CG9650-PL",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001096900",
            "id": "NP_001096900"
        },
        {
            "name": "Uncharacterized protein, isoform K",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A499JF18"
        },
        {
            "name": "uncharacterized protein, isoform G",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001096899",
            "id": "NP_001096899"
        },
        {
            "name": "uncharacterized protein, isoform I",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_727173",
            "id": "NP_727173"
        },
        {
            "name": "uncharacterized protein, isoform J",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_572385",
            "id": "NP_572385"
        },
        {
            "name": "uncharacterized protein, isoform L",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001096900",
            "id": "NP_001096900"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0060041",
            "recommended_name": {
                "id": "DOID:0060041",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/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."
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "0060041",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0060041"
                }
            ]
        },
        {
            "disease_id": "DOID:0111979",
            "recommended_name": {
                "id": "DOID:0111979",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0111979",
                "name": "immunodeficiency 49",
                "description": "A T cell deficiency characterized by T cell lymphopenia, low T-cell receptor excision circles, impaired T-cell proliferative responses, dysmorphic facial features, hypotonia and severe global developmental delay that has_material_basis_in heterozygous mutation in the BCL11B gene on chromosome 14q32.2."
            },
            "synonyms": [
                {
                    "id": "DOID:0111979",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111979",
                    "name": "IMD49",
                    "description": ""
                },
                {
                    "id": "DOID:0111979",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111979",
                    "name": "severe combined immunodeficiency, T-cell negative, B-cell positive, NK cell positive, with intellectual disability, spasticity, and craniofacial abnormalities",
                    "description": ""
                },
                {
                    "id": "DOID:0111979",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111979",
                    "name": "SCID, T-cell negative, B-cell positive, NK cell positive, with intellectual disability, spasticity, and craniofacial abnormalities",
                    "description": ""
                },
                {
                    "id": "MONDO:0014981",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014981",
                    "name": "immunodeficiency 49",
                    "description": "Any primary immunodeficiency disease in which the cause of the disease is a mutation in the BCL11B gene."
                },
                {
                    "id": "MONDO:0014981",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014981",
                    "name": "BCL11B primary immunodeficiency disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0014981",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014981",
                    "name": "IMD49",
                    "description": ""
                },
                {
                    "id": "MONDO:0014981",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014981",
                    "name": "immunodeficiency 49",
                    "description": ""
                },
                {
                    "id": "MONDO:0014981",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014981",
                    "name": "immunodeficiency 49; IMD49",
                    "description": ""
                },
                {
                    "id": "MONDO:0014981",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014981",
                    "name": "immunodeficiency type 49",
                    "description": ""
                },
                {
                    "id": "MONDO:0014981",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014981",
                    "name": "primary immunodeficiency disease caused by mutation in BCL11B",
                    "description": ""
                },
                {
                    "id": "MONDO:0014981",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014981",
                    "name": "SCID, T cell-Negative, B cell-Positive, Nk cell-Positive, with intellectual disability, spasticity, and craniofacial abnormalities",
                    "description": ""
                },
                {
                    "id": "MONDO:0014981",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014981",
                    "name": "severe combined immunodeficiency, T cell-Negative, B cell-Positive, Nk cell-Positive, with intellectual disability, spasticity, and craniofacial abnormalities",
                    "description": ""
                },
                {
                    "id": "MIM:617237",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/617237",
                    "name": "Immunodeficiency 49",
                    "description": "Immunodeficiency 49"
                }
            ],
            "evidence": [
                {
                    "id": "0111979",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111979"
                }
            ]
        },
        {
            "disease_id": "DOID:10923",
            "recommended_name": {
                "id": "DOID:10923",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10923",
                "name": "sickle cell anemia",
                "description": "A blood protein disease that is characterized by low number of red blood cells, repeated infections, and periodic episodes of pain, resulting from atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape."
            },
            "synonyms": [
                {
                    "id": "DOID:10923",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10923",
                    "name": "Hb SC disease",
                    "description": ""
                },
                {
                    "id": "DOID:10923",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10923",
                    "name": "Hb-S/Hb-C disease",
                    "description": ""
                },
                {
                    "id": "DOID:10923",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10923",
                    "name": "Hb-SS disease without crisis",
                    "description": ""
                },
                {
                    "id": "DOID:10923",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10923",
                    "name": "Hemoglobin S disease without crisis",
                    "description": ""
                },
                {
                    "id": "DOID:10923",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10923",
                    "name": "Sickle-cell/Hb-C disease without crisis",
                    "description": ""
                },
                {
                    "id": "DOID:10923",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10923",
                    "name": "drepanocytosis",
                    "description": ""
                },
                {
                    "id": "DOID:10923",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10923",
                    "name": "haemoglobin SC disease",
                    "description": ""
                },
                {
                    "id": "DOID:10923",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10923",
                    "name": "hemoglobin SC disease",
                    "description": ""
                },
                {
                    "id": "DOID:10923",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10923",
                    "name": "sickle cell anaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "sickle cell anemia",
                    "description": "Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur."
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "Haemoglobin S disease without crisis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "Hb SC disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "Hb-S/Hb-C disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "Hb-SS disease without crisis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "Hemoglobin S disease without crisis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "drepanocytosis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "haemoglobin SC disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "hemoglobin SC disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "sickle cell anemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "sickle cell disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "sickle-cell/Hb-C disease without crisis",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "sickling disorder due to Haemoglobin S",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "sickling disorder due to Hemoglobin S",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "Haemoglobin S disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "HbS disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011382",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011382",
                    "name": "Hemoglobin S disease",
                    "description": ""
                },
                {
                    "id": "MIM:603903",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/603903",
                    "name": "Sickle cell disease",
                    "description": "Sickle cell disease"
                }
            ],
            "evidence": [
                {
                    "id": "10923",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10923"
                }
            ]
        },
        {
            "disease_id": "DOID:12241",
            "recommended_name": {
                "id": "DOID:12241",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:12241",
                "name": "beta thalassemia",
                "description": "A thalassemia characterized by the reduced or absent synthesis of the beta globin chains of hemoglobin."
            },
            "synonyms": [
                {
                    "id": "MONDO:0013517",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013517",
                    "name": "beta-thalassemia HBB/LCRB",
                    "description": "Abnormal clinical manifestations of beta thalassemia that are as a result of the underlying genotype."
                },
                {
                    "id": "MONDO:0013517",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013517",
                    "name": "thalassemia, beta",
                    "description": ""
                },
                {
                    "id": "MONDO:0013517",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013517",
                    "name": "thalassemia, hispanic gamma-delta-beta",
                    "description": ""
                },
                {
                    "id": "MONDO:0013517",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013517",
                    "name": "beta-thalassemia",
                    "description": ""
                },
                {
                    "id": "MIM:613985",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/613985",
                    "name": "Beta-thalassemia",
                    "description": "Beta-thalassemia"
                }
            ],
            "evidence": [
                {
                    "id": "12241",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:12241"
                }
            ]
        },
        {
            "disease_id": "DOID:1289",
            "recommended_name": {
                "id": "DOID:1289",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1289",
                "name": "neurodegenerative disease",
                "description": "A central nervous system disease that results in the progressive deterioration of function or structure of neurons."
            },
            "synonyms": [
                {
                    "id": "DOID:1289",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1289",
                    "name": "degenerative disease",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1289",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1289"
                }
            ]
        },
        {
            "disease_id": "DOID:3908",
            "recommended_name": {
                "id": "DOID:3908",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/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."
            },
            "synonyms": [
                {
                    "id": "DOID:3908",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3908",
                    "name": "NSCLC",
                    "description": ""
                },
                {
                    "id": "DOID:3908",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3908",
                    "name": "Non-small cell lung cancer",
                    "description": ""
                },
                {
                    "id": "DOID:3908",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3908",
                    "name": "non-small cell lung carcinoma",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "3908",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3908"
                }
            ]
        },
        {
            "disease_id": "DOID:5419",
            "recommended_name": {
                "id": "DOID:5419",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:5419",
                "name": "schizophrenia",
                "description": "A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness."
            },
            "synonyms": [
                {
                    "id": "DOID:5419",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5419",
                    "name": "schizophrenia-1",
                    "description": ""
                },
                {
                    "id": "MONDO:0005090",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005090",
                    "name": "schizophrenia",
                    "description": "A major psychotic disorder characterized by abnormalities in the perception or expression of reality. It affects the cognitive and psychomotor functions. Common clinical signs and symptoms include delusions, hallucinations, disorganized thinking, and retreat from reality."
                },
                {
                    "id": "MONDO:0005090",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005090",
                    "name": "schizophrenia 12",
                    "description": ""
                },
                {
                    "id": "MONDO:0005090",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005090",
                    "name": "schizophrenia",
                    "description": ""
                },
                {
                    "id": "MONDO:0005090",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005090",
                    "name": "schizophrenia (disease)",
                    "description": ""
                },
                {
                    "id": "MONDO:0005090",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005090",
                    "name": "schizophrenia-1",
                    "description": ""
                },
                {
                    "id": "MONDO:0005090",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005090",
                    "name": "SCZD",
                    "description": ""
                },
                {
                    "id": "MONDO:0005090",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005090",
                    "name": "schizoaffective disorder",
                    "description": ""
                },
                {
                    "id": "MONDO:0005090",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005090",
                    "name": "schizophrenia with or without an affective disorder",
                    "description": ""
                },
                {
                    "id": "MONDO:0005090",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005090",
                    "name": "schizophrenia, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MIM:181500",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/181500",
                    "name": "Schizophrenia",
                    "description": "Schizophrenia"
                }
            ],
            "evidence": [
                {
                    "id": "5419",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:5419"
                }
            ]
        },
        {
            "disease_id": "DOID:9352",
            "recommended_name": {
                "id": "DOID:9352",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9352",
                "name": "type 2 diabetes mellitus",
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin."
            },
            "synonyms": [
                {
                    "id": "DOID:9352",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9352",
                    "name": "NIDDM",
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                {
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                {
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                {
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                    "resource": "Disease Ontology",
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                },
                {
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9352",
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                },
                {
                    "id": "MONDO:0011955",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011955",
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                    "description": ""
                },
                {
                    "id": "MONDO:0011955",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011955",
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                    "description": ""
                },
                {
                    "id": "MONDO:0011955",
                    "resource": "MONDO",
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                    "description": ""
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                {
                    "id": "MONDO:0011955",
                    "resource": "MONDO",
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                {
                    "id": "MONDO:0011955",
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                {
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                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
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                {
                    "id": "MONDO:0005148",
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                {
                    "id": "MONDO:0005148",
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                    "url": "https://monarchinitiative.org/disease/MONDO:0005148",
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                {
                    "id": "MONDO:0005148",
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                {
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                {
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                {
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    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
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            "name": "Drosophila melanogaster",
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            "id": "IPR036236",
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        {
            "id": "dme:Dmel_CG9650",
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            "database": "KEGG Pathway",
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        {
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        {
            "id": "5351439at2759",
            "url": "http://www.orthodb.org/?query=5351439at2759",
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        "length": 1254,
        "header": "tr|A0A499JF18-1|A0A499JF18_DROME Isoform 1 of Uncharacterized protein, isoform K  OS=Drosophila melanogaster OX=7227 GN=Cph PE=4 SV=1 CANONICAL=A0A499JF18-1"
    },
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        {
            "isoform_ac": "A0A023GPJ3-1",
            "url": "",
            "sequence": {
                "sequence": "MDRDAEEGRPLSLVNRRPSISAPISGRKSAPASAAAAVAAAAAAAAAAAAASSTASGSRIHTPPPSPADLLADGASSTPKRLVDENDNTTPKDSETGATTLDSNAAPSSPAAIERQSSGDSSCEMEEQQDRQDKQSQPKQAKVKQEPYDEEGVNHHQNQDDDDDEEMEERSLAKRPKMELVDAEANTVHTEPSNYTCSTCKTRYTSAWRLIQHVQHSHGVKIYVESPGGGATLTVATPAALNNSALALAAAAAAASASGLASPQPAVSPNPAVTSSAKRSSPLGAAGSTILSTSVSSTCSNSLVNTSGGSISNTSSIGSPQQQQLQLQQQQAQQQQQRVQQQQRENLASAMAAGMRHHPLLPPPEAMHANPFQLLRMPLPPALAQAGNVVPTVAPLFGRPSPADHYRMEQLVSEQFRHHGFNLAAAAAAAQAQFNANGQVVGGVVSGSGEPRPPSSSSSGSQRGSVPPAALPPPSLSSQQQQQQQQAVQQQQQQGAQQQLQSAQQQQQSQQQSQQQQQITPGLVGGAGGSLKLEPQQMDFYSQRLRQLAGTTSPGAGSTVNSSSPSPRQKQSPHFASPSPSQQQQQQLATIPRPHSLTPPEKLGDASSENGSLGLILASTPRSASTPPSKTGDVSLQEPIAHCYSCSYCDKKFRFENNLIIHQRTHTGEKPYKCTACDFECSHIQKLMKHMRVHRSPADDQDNQDNQDDGSNADSLETNEADNDEDPNPDESEEELGDGDNDPDGDGDLDGEDEDEDELEECEDMDYKAEDLSVSNRIDGKSQSPKTTSSGATSLVGELMDKFGLSNIAQYSEAYKQALQESGRKEAAAAAAAAAAAADNNNRGGAGAPLSDKLNGLPVAALRLRDEFAKNCNMFQQPQDGGAPSQVPLFNPFPNPFELSKRMKMDGGDWWGMSQALHRNEALFENLKLKPLGLGGANSLIQGPLLKKESRQRNDTCEFCGKVFKNCSNLTVHRRSHTGEKPYKCELCSYACAQSSKLTRHMKTHGRTGKDVYRCRFCDMPFSVPSTLEKHMRKCVVNQGKAAAAANAVAAAQAAQAAAQHIQAAAQQAQAVQAQAVQAQAAQQSQQQQQQLSPMGVVGYPPQFVSGHNLSLPGSVSGDNDSNASSSMTGVHPISLKEEA",
                "length": 1140,
                "header": "tr|A0A023GPJ3-1|A0A499JF18_DROME Computationally mapped isoform of Uncharacterized protein, isoform K  OS=Drosophila melanogaster OX=7227 GN=Cph PE=4 SV=1 CANONICAL=A0A499JF18-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 7239899,
                "end_pos": 7232528,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0339815",
                        "url": "https://www.ensembl.org/id/FBtr0339815"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0308848",
                        "url": "https://www.ensembl.org/id/FBpp0308848"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A499JF18-1",
            "url": "",
            "sequence": {
                "sequence": "MYNKMLSISEDHGFRSLSHSDSTENDAVATQDILTCGACQKAFALSDIVKFIQHKVLQCNKENYGQCATQNPQMDRDAEEGRPLSLVNRRPSISAPISGRKSAPASAAAAVAAAAAAAAAAAAASSTASGSRIHTPPPSPADLLADGASSTPKRLVDENDNTTPKDSETGATTLDSNAAPSSPAAIERQSSGDSSCEMEEQQDRQDKQSQPKQAKVKQEPYDEEGVNHHQNQDDDDDEEMEERSLAKRPKMELVDAEANTVHTEPSNYTCSTCKTRYTSAWRLIQHVQHSHGVKIYVESPGGGATLTVATPAALNNSALALAAAAAAASASGLASPQPAVSPNPAVTSSAKRSSPLGAAGSTILSTSVSSTCSNSLVNTSGGSISNTSSIGSPQQQQLQLQQQQAQQQQQRVQQQQRENLASAMAAGMRHHPLLPPPEAMHANPFQLLRMPLPPALAQAGNVVPTVAPLFGRPSPADHYRMEQLVSEQFRHHGFNLAAAAAAAQAQFNANGQVVGGVVSGSGEPRPPSSSSSGSQRGSVPPAALPPPSLSSQQQQQQQQAVQQQQQQGAQQQLQSAQQQQQSQQQSQQQQQITPGLVGGAGGSLKLEPQQMDFYSQRLRQLAGTTSPGAGSTVNSSSPSPRQKQSPHFASPSPSQQQQQQLATIPRPHSLTPPEKLGDASSENGSLGLILASTPRSASTPPSKTGDVSLQEPIAHCYSCSYCDKKFRFENNLIIHQRTHTGEKPYKCTACDFECSHIQKLMKHMRVHRSPADDQDNQDNQDDGSNADSLETNEADNDEDPNPDESEEELGDGDNDPDGDGDLDGEDEDEDELEECEDMDYKAEDLSVSNRIDGKSQSPKTTSSGATSLVGELMDKFGLSNIAQYSEAYKQALQESGRKEAAAAAAAAAAAADNNNRGGAGAPLSDKLNGLPVAALRLRDEFAKNCNMFQQPQDGGAPSQVPLFNPFPNPFELSKRMKMDGGDWWGMSQALHRNEALFENLKLKPLGLGGANSLIQGPLLKKESRQRNDTCEFCGKVFKNCSNLTVHRRSHTGEKPYKCELCSYACAQSSKLTRHMKTHGRTGKDVYRCRFCDMPFSVPSTLEKHMRKCVVNQGKAAAAANAVAAAQAAQAAAQHIQAAAQQAQAVQAQAVQAQAAQQSQQQQQQLSPMGVVGYPPQFVSGHNLSLPGSVSGDNDSNASSSMTGVHPISLKEEAXLFSGFPVPLAPPPPLQQHQPHLQQPQQQQTSRSRIMSRIF",
                "length": 1254,
                "header": "tr|A0A499JF18-1|A0A499JF18_DROME Isoform 1 of Uncharacterized protein, isoform K  OS=Drosophila melanogaster OX=7227 GN=Cph PE=4 SV=1 CANONICAL=A0A499JF18-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 7240022,
                "end_pos": 7226932,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0474234",
                        "url": "https://www.ensembl.org/id/FBtr0474234"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0423187",
                        "url": "https://www.ensembl.org/id/FBpp0423187"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A8JV11-1",
            "url": "",
            "sequence": {
                "sequence": "MYNKMLSISEDHGFRSLSHSDSTENDAVATQDILTCGACQKAFALSDIVKFIQHKVLQCNKENYGQCATQNPQMDRDAEEGRPLSLVNRRPSISAPISGRKSAPASAAAAVAAAAAAAAAAAAASSTASGSRIHTPPPSPADLLADGASSTPKRLVDENDNTTPKDSETGATTLDSNAAPSSPAAIERQSSGDSSCEMEEQQDRQDKQSQPKQAKVKQEPYDEEGVNHHQNQDDDDDEEMEERSLAKRPKMELVDAEANTVHTEPSNYTCSTCKTRYTSAWRLIQHVQHSHGVKIYVESPGGGATLTVATPAALNNSALALAAAAAAASASGLASPQPAVSPNPAVTSSAKRSSPLGAAGSTILSTSVSSTCSNSLVNTSGGSISNTSSIGSPQQQQLQLQQQQAQQQQQRVQQQQRENLASAMAAGMRHHPLLPPPEAMHANPFQLLRMPLPPALAQAGNVVPTVAPLFGRPSPADHYRMEQLVSEQFRHHGFNLAAAAAAAQAQFNANGQVVGGVVSGSGEPRPPSSSSSGSQRGSVPPAALPPPSLSSQQQQQQQQAVQQQQQQGAQQQLQSAQQQQQSQQQSQQQQQITPGLVGGAGGSLKLEPQQMDFYSQRLRQLAGTTSPGAGSTVNSSSPSPRQKQSPHFASPSPSQQQQQQLATIPRPHSLTPPEKLGDASSENGSLGLILASTPRSASTPPSKTGDVSLQEPIAHCYSCSYCDKKFRFENNLIIHQRTHTGEKPYKCTACDFECSHIQKLMKHMRVHRSPADDQDNQDNQDDGSNADSLETNEADNDEDPNPDESEEELGDGDNDPDGDGDLDGEDEDEDELEECEDMDYKAEDLSVSNRIDGKSQSPKTTSSGATSLVGELMDKFGLSNIAQYSEAYKQALQESGRKEAAAAAAAAAAAADNNNRGGAGAPLSDKLNGLPVAALRLRDEFAKNCNMFQQPQDGGAPSQVPLFNPFPNPFELSKRMKMDGGDWWGMSQALHRNEALFENLKLKPLGLGGANSLIQGPLLKKESRQRNDTCEFCGKVFKNCSNLTVHRRSHTGEKPYKCELCSYACAQSSKLTRHMKTHGRTGKDVYRCRFCDMPFSVPSTLEKHMRKCVVNQGKAAAAANAVAAAQAAQAAAQHIQAAAQQAQAVQAQAVQAQAAQQSQQQQQQLSPMGVVGYPPQFVSGHNLSLPGSVSGDNDSNASSSMTGVHPISLKEEA",
                "length": 1213,
                "header": "tr|A8JV11-1|A0A499JF18_DROME Computationally mapped isoform of Uncharacterized protein, isoform K  OS=Drosophila melanogaster OX=7227 GN=Cph PE=4 SV=3 CANONICAL=A0A499JF18-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 7239899,
                "end_pos": 7226932,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0474235",
                        "url": "https://www.ensembl.org/id/FBtr0474235"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0423188",
                        "url": "https://www.ensembl.org/id/FBpp0423188"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A8JV12-1",
            "url": "",
            "sequence": {
                "sequence": "MFPGNMISPKVRGTNSDSTENDAVATQDILTCGACQKAFALSDIVKFIQHKVLQCNKENYGQCATQNPQMDRDAEEGRPLSLVNRRPSISAPISGRKSAPASAAAAVAAAAAAAAAAAAASSTASGSRIHTPPPSPADLLADGASSTPKRLVDENDNTTPKDSETGATTLDSNAAPSSPAAIERQSSGDSSCEMEEQQDRQDKQSQPKQAKVKQEPYDEEGVNHHQNQDDDDDEEMEERSLAKRPKMELVDAEANTVHTEPSNYTCSTCKTRYTSAWRLIQHVQHSHGVKIYVESPGGGATLTVATPAALNNSALALAAAAAAASASGLASPQPAVSPNPAVTSSAKRSSPLGAAGSTILSTSVSSTCSNSLVNTSGGSISNTSSIGSPQQQQLQLQQQQAQQQQQRVQQQQRENLASAMAAGMRHHPLLPPPEAMHANPFQLLRMPLPPALAQAGNVVPTVAPLFGRPSPADHYRMEQLVSEQFRHHGFNLAAAAAAAQAQFNANGQVVGGVVSGSGEPRPPSSSSSGSQRGSVPPAALPPPSLSSQQQQQQQQAVQQQQQQGAQQQLQSAQQQQQSQQQSQQQQQITPGLVGGAGGSLKLEPQQMDFYSQRLRQLAGTTSPGAGSTVNSSSPSPRQKQSPHFASPSPSQQQQQQLATIPRPHSLTPPEKLGDASSENGSLGLILASTPRSASTPPSKTGDVSLQEPIAHCYSCSYCDKKFRFENNLIIHQRTHTGEKPYKCTACDFECSHIQKLMKHMRVHRSPADDQDNQDNQDDGSNADSLETNEADNDEDPNPDESEEELGDGDNDPDGDGDLDGEDEDEDELEECEDMDYKAEDLSVSNRIDGKSQSPKTTSSGATSLVGELMDKFGLSNIAQYSEAYKQALQESGRKEAAAAAAAAAAAADNNNRGGAGAPLSDKLNGLPVAALRLRDEFAKNCNMFQQPQDGGAPSQVPLFNPFPNPFELSKRMKMDGGDWWGMSQALHRNEALFENLKLKPLGLGGANSLIQGPLLKKESRQRNDTCEFCGKVFKNCSNLTVHRRSHTGEKPYKCELCSYACAQSSKLTRHMKTHGRTGKDVYRCRFCDMPFSVPSTLEKHMRKCVVNQGKAAAAANAVAAAQAAQAAAQHIQAAAQQAQAVQAQAVQAQAAQQSQQQQQQLSPMGVVGYPPQFVSGHNLSLPGSVSGDNDSNASSSMTGVHPISLKEEA",
                "length": 1209,
                "header": "tr|A8JV12-1|A0A499JF18_DROME Computationally mapped isoform of Uncharacterized protein, isoform K  OS=Drosophila melanogaster OX=7227 GN=Cph PE=4 SV=2 CANONICAL=A0A499JF18-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 7239899,
                "end_pos": 7217846,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0301240",
                        "url": "https://www.ensembl.org/id/FBtr0301240"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0290458",
                        "url": "https://www.ensembl.org/id/FBpp0290458"
                    }
                ]
            }
        },
        {
            "isoform_ac": "R9PY46-1",
            "url": "",
            "sequence": {
                "sequence": "MRIKMPAVRIAQDSDSTENDAVATQDILTCGACQKAFALSDIVKFIQHKVLQCNKENYGQCATQNPQMDRDAEEGRPLSLVNRRPSISAPISGRKSAPASAAAAVAAAAAAAAAAAAASSTASGSRIHTPPPSPADLLADGASSTPKRLVDENDNTTPKDSETGATTLDSNAAPSSPAAIERQSSGDSSCEMEEQQDRQDKQSQPKQAKVKQEPYDEEGVNHHQNQDDDDDEEMEERSLAKRPKMELVDAEANTVHTEPSNYTCSTCKTRYTSAWRLIQHVQHSHGVKIYVESPGGGATLTVATPAALNNSALALAAAAAAASASGLASPQPAVSPNPAVTSSAKRSSPLGAAGSTILSTSVSSTCSNSLVNTSGGSISNTSSIGSPQQQQLQLQQQQAQQQQQRVQQQQRENLASAMAAGMRHHPLLPPPEAMHANPFQLLRMPLPPALAQAGNVVPTVAPLFGRPSPADHYRMEQLVSEQFRHHGFNLAAAAAAAQAQFNANGQVVGGVVSGSGEPRPPSSSSSGSQRGSVPPAALPPPSLSSQQQQQQQQAVQQQQQQGAQQQLQSAQQQQQSQQQSQQQQQITPGLVGGAGGSLKLEPQQMDFYSQRLRQLAGTTSPGAGSTVNSSSPSPRQKQSPHFASPSPSQQQQQQLATIPRPHSLTPPEKLGDASSENGSLGLILASTPRSASTPPSKTGDVSLQEPIAHCYSCSYCDKKFRFENNLIIHQRTHTGEKPYKCTACDFECSHIQKLMKHMRVHRSPADDQDNQDNQDDGSNADSLETNEADNDEDPNPDESEEELGDGDNDPDGDGDLDGEDEDEDELEECEDMDYKAEDLSVSNRIDGKSQSPKTTSSGATSLVGELMDKFGLSNIAQYSEAYKQALQESGRKEAAAAAAAAAAAADNNNRGGAGAPLSDKLNGLPVAALRLRDEFAKNCNMFQQPQDGGAPSQVPLFNPFPNPFELSKRMKMDGGDWWGMSQALHRNEALFENLKLKPLGLGGANSLIQGPLLKKESRQRNDTCEFCGKVFKNCSNLTVHRRSHTGEKPYKCELCSYACAQSSKLTRHMKTHGRTGKDVYRCRFCDMPFSVPSTLEKHMRKCVVNQGKAAAAANAVAAAQAAQAAAQHIQAAAQQAQAVQAQAVQAQAAQQSQQQQQQLSPMGVVGYPPQFVSGHNLSLPGSVSGDNDSNASSSMTGVHPISLKEEA",
                "length": 1207,
                "header": "tr|R9PY46-1|A0A499JF18_DROME Computationally mapped isoform of Uncharacterized protein, isoform K  OS=Drosophila melanogaster OX=7227 GN=Cph PE=4 SV=1 CANONICAL=A0A499JF18-1"
            },
            "locus": {
                "chromosome": "X",
                "start_pos": 7239899,
                "end_pos": 7197309,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0309030",
                        "url": "https://www.ensembl.org/id/FBtr0309030"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0301059",
                        "url": "https://www.ensembl.org/id/FBpp0301059"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "dme:Dmel_CG9650",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG9650",
            "resource": "KEGG Pathway"
        }
    ],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Molecular Function",
                "total": 3,
                "go_terms": [
                    {
                        "name": "DNA-binding transcription factor activity",
                        "id": "GO:0003700",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003700",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A499JF18",
                                "url": "https://www.uniprot.org/uniprot/A0A499JF18"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "RNA polymerase II cis-regulatory region sequence-specific DNA binding",
                        "id": "GO:0000978",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000978",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A499JF18",
                                "url": "https://www.uniprot.org/uniprot/A0A499JF18"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "DNA-binding transcription factor binding",
                        "id": "GO:0140297",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0140297",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A499JF18",
                                "url": "https://www.uniprot.org/uniprot/A0A499JF18"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 2,
                "go_terms": [
                    {
                        "name": "nucleus",
                        "id": "GO:0005634",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A499JF18",
                                "url": "https://www.uniprot.org/uniprot/A0A499JF18"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cytosol",
                        "id": "GO:0005829",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A499JF18",
                                "url": "https://www.uniprot.org/uniprot/A0A499JF18"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 4,
                "go_terms": [
                    {
                        "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": "A0A499JF18",
                                "url": "https://www.uniprot.org/uniprot/A0A499JF18"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "negative regulation of peptide hormone secretion",
                        "id": "GO:0090278",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090278",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A499JF18",
                                "url": "https://www.uniprot.org/uniprot/A0A499JF18"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of gene expression",
                        "id": "GO:0010628",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010628",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A499JF18",
                                "url": "https://www.uniprot.org/uniprot/A0A499JF18"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "neuroblast fate specification",
                        "id": "GO:0014018",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0014018",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A499JF18",
                                "url": "https://www.uniprot.org/uniprot/A0A499JF18"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 1027,
            "end_pos": 1029,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1039,
            "end_pos": 1041,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1042,
            "end_pos": 1044,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1182,
            "end_pos": 1184,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1193,
            "end_pos": 1195,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1196,
            "end_pos": 1198,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 161,
            "end_pos": 163,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 267,
            "end_pos": 269,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 315,
            "end_pos": 317,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 378,
            "end_pos": 380,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 386,
            "end_pos": 388,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 634,
            "end_pos": 636,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 683,
            "end_pos": 685,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
        }
    ],
    "section_stats": [
        {
            "table_id": "glycosylation",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported_with_glycan",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_predicted",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
                    "count": 0
                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_automatic_literature_mining",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
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