{
    "uniprot_canonical_ac": "A0A8I5ZPA3-1",
    "uniprot_ac": "A0A8I5ZPA3",
    "uniprot_id": "A0A8I5ZPA3_RAT",
    "mass": {
        "chemical_mass": 39016.0,
        "monoisotopic_mass": 39016.0
    },
    "refseq": {},
    "gene_names": [
        {
            "name": "Abo2",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZPA3",
            "id": "A0A8I5ZPA3"
        }
    ],
    "protein_names": [
        {
            "name": "Uncharacterized protein",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A8I5ZPA3"
        }
    ],
    "function": [],
    "disease": [
        {
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            "recommended_name": {
                "id": "DOID:0080600",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0080600",
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            },
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0080600",
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                    "description": ""
                },
                {
                    "id": "DOID:0080600",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0080600",
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                    "description": ""
                },
                {
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0080600",
                    "name": "Wuhan coronavirus infection",
                    "description": ""
                },
                {
                    "id": "DOID:0080600",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0080600",
                    "name": "Wuhan seafood market pneumonia virus infection",
                    "description": ""
                },
                {
                    "id": "DOID:0080600",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0080600",
                    "name": "COVID19",
                    "description": ""
                },
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                    "id": "DOID:0080600",
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                    "url": "http://disease-ontology.org/term/DOID:0080600",
                    "name": "SARS-CoV-2 infection",
                    "description": ""
                }
            ],
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                    "database": "Alliance of Genome Resources",
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                }
            ]
        },
        {
            "disease_id": "DOID:0081267",
            "recommended_name": {
                "id": "DOID:0081267",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0081267",
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                "description": "An immune system disease that is characterized by recognition by mature donor T cells, that contaminate the allogeneic bone marrow, of the recipient's tissue as foreign, causing a severe inflammatory disease characterized by rashes, diarrhea, and liver disease, and that has_material_basis_in an associated with variation in the interleukin-10 gene (IL10) on chromosome 1q32."
            },
            "synonyms": [
                {
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0081267",
                    "name": "GvHD",
                    "description": ""
                },
                {
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0081267",
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                    "description": ""
                },
                {
                    "id": "MONDO:0100048",
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                {
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                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100048",
                    "name": "GVHDS",
                    "description": ""
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            "evidence": [
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                    "id": "0081267",
                    "database": "Alliance of Genome Resources",
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        {
            "disease_id": "DOID:10763",
            "recommended_name": {
                "id": "DOID:10763",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10763",
                "name": "hypertension",
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            },
            "synonyms": [
                {
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10763",
                    "name": "HTN",
                    "description": ""
                },
                {
                    "id": "DOID:10763",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10763",
                    "name": "hyperpiesia",
                    "description": ""
                },
                {
                    "id": "DOID:10763",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10763",
                    "name": "vascular hypertensive disorder",
                    "description": ""
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            ],
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                    "database": "Alliance of Genome Resources",
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                }
            ]
        },
        {
            "disease_id": "DOID:1240",
            "recommended_name": {
                "id": "DOID:1240",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1240",
                "name": "leukemia",
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            },
            "synonyms": [],
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                    "id": "1240",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1240"
                }
            ]
        },
        {
            "disease_id": "DOID:13406",
            "recommended_name": {
                "id": "DOID:13406",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:13406",
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                "description": "A sarcoidosis that is characterized by noncaseating granulomatous infiltration of the lungs and supporting lymph nodes, bilateral hilar adenopathy, and pulmonary issues, has_symptom shortness of breath, fatigue, wheezing, and chronic cough, and develops_from a type IV hypersensitivity reaction."
            },
            "synonyms": [
                {
                    "id": "DOID:13406",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:13406",
                    "name": "lung Sarcoidosis",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "13406",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:13406"
                }
            ]
        },
        {
            "disease_id": "DOID:14067",
            "recommended_name": {
                "id": "DOID:14067",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:14067",
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                "description": "A malaria described as a severe form of the disease caused by a parasite Plasmodium falciparum, which is marked by irrregular recurrence of paroxysms and prolonged or continuous fever."
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            "synonyms": [
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:14067",
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                    "description": ""
                },
                {
                    "id": "DOID:14067",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:14067",
                    "name": "malignant tertian fever",
                    "description": ""
                },
                {
                    "id": "DOID:14067",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:14067",
                    "name": "falciparum malaria",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "14067",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:14067"
                }
            ]
        },
        {
            "disease_id": "DOID:1496",
            "recommended_name": {
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                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1496",
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                "description": "A parasitic helminthiasis infectious disease that involves parasitic infection of humans and domestic animals caused by the larval stages of tapeworms of the genus Echinococcus in the liver, lungs, spleen, brain, heart and kidneys."
            },
            "synonyms": [
                {
                    "id": "DOID:1496",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1496",
                    "name": "Echinococcosis of liver",
                    "description": ""
                },
                {
                    "id": "DOID:1496",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1496",
                    "name": "echinococcal disease",
                    "description": ""
                },
                {
                    "id": "DOID:1496",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1496",
                    "name": "hepatic echinococcosis",
                    "description": ""
                },
                {
                    "id": "DOID:1496",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1496",
                    "name": "hydatid disease",
                    "description": ""
                },
                {
                    "id": "DOID:1496",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1496",
                    "name": "hydatidosis",
                    "description": ""
                },
                {
                    "id": "DOID:1496",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1496",
                    "name": "liver echinococcus",
                    "description": ""
                },
                {
                    "id": "DOID:1496",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1496",
                    "name": "pulmonary echinococcosis",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1496",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1496"
                }
            ]
        },
        {
            "disease_id": "DOID:1793",
            "recommended_name": {
                "id": "DOID:1793",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1793",
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                "description": "An endocrine gland cancer located_in the pancreas."
            },
            "synonyms": [
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "Ca body of pancreas",
                    "description": ""
                },
                {
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                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "Ca head of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "Ca tail of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "malignant neoplasm of body of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "malignant neoplasm of head of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "malignant neoplasm of tail of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "pancreas neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "pancreatic neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "pancreatic tumor",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1793",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1793"
                }
            ]
        },
        {
            "disease_id": "DOID:2237",
            "recommended_name": {
                "id": "DOID:2237",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2237",
                "name": "hepatitis",
                "description": ""
            },
            "synonyms": [
                {
                    "id": "DOID:2237",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2237",
                    "name": "acute and subacute liver necrosis",
                    "description": ""
                },
                {
                    "id": "DOID:2237",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2237",
                    "name": "acute hepatitis",
                    "description": ""
                },
                {
                    "id": "DOID:2237",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2237",
                    "name": "acute/subac. necrosis of liver",
                    "description": ""
                },
                {
                    "id": "DOID:2237",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2237",
                    "name": "animal hepatitis",
                    "description": ""
                },
                {
                    "id": "DOID:2237",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2237",
                    "name": "chronic hepatitis",
                    "description": ""
                },
                {
                    "id": "DOID:2237",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2237",
                    "name": "chronic persistent hepatitis",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "2237",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2237"
                }
            ]
        },
        {
            "disease_id": "DOID:2841",
            "recommended_name": {
                "id": "DOID:2841",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/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."
            },
            "synonyms": [
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "Exercise induced asthma",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "bronchial hyperreactivity",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "chronic obstructive asthma",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "chronic obstructive asthma with acute exacerbation",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "chronic obstructive asthma with status asthmaticus",
                    "description": ""
                },
                {
                    "id": "DOID:2841",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2841",
                    "name": "exercise-induced asthma",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "inherited susceptibility to asthma",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, nocturnal, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, bronchial",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, diminished response to Antileukotriene treatment 1N",
                    "description": ""
                },
                {
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                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, protection against",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0010940",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010940",
                    "name": "asthma-related traits, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MIM:600807",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/600807",
                    "name": "Asthma",
                    "description": "Asthma"
                }
            ],
            "evidence": [
                {
                    "id": "2841",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2841"
                }
            ]
        },
        {
            "disease_id": "DOID:2945",
            "recommended_name": {
                "id": "DOID:2945",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2945",
                "name": "severe acute respiratory syndrome",
                "description": "A Coronavirus infection that results_in infection located_in respiratory tract, has_material_basis_in SARS coronavirus (SARS-CoV), which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia."
            },
            "synonyms": [
                {
                    "id": "DOID:2945",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2945",
                    "name": "SARS",
                    "description": ""
                },
                {
                    "id": "DOID:2945",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2945",
                    "name": "SARS-CoV infection",
                    "description": ""
                },
                {
                    "id": "MONDO:0005091",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005091",
                    "name": "severe acute respiratory syndrome",
                    "description": "A viral respiratory infection caused by the SARS coronavirus. It is transmitted through close person-to-person contact. It is manifested with high fever, headache, dry cough and myalgias. It may progress to pneumonia and cause death."
                },
                {
                    "id": "MONDO:0005091",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005091",
                    "name": "SARS",
                    "description": ""
                },
                {
                    "id": "MONDO:0005091",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005091",
                    "name": "SARS coronavirus caused disease or disorder",
                    "description": ""
                },
                {
                    "id": "MONDO:0005091",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005091",
                    "name": "SARS coronavirus disease or disorder",
                    "description": ""
                },
                {
                    "id": "MONDO:0005091",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005091",
                    "name": "SARS coronavirus infectious disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0005091",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005091",
                    "name": "SARS-CoV infection",
                    "description": ""
                },
                {
                    "id": "MONDO:0005091",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0005091",
                    "name": "acute respiratory coronavirus infection",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "2945",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2945"
                }
            ]
        },
        {
            "disease_id": "DOID:4948",
            "recommended_name": {
                "id": "DOID:4948",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:4948",
                "name": "gallbladder carcinoma",
                "description": "A gallbladder cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells."
            },
            "synonyms": [
                {
                    "id": "DOID:4948",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:4948",
                    "name": "cancer of the gallbladder",
                    "description": ""
                },
                {
                    "id": "DOID:4948",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:4948",
                    "name": "carcinoma gallbladder",
                    "description": ""
                },
                {
                    "id": "DOID:4948",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:4948",
                    "name": "carcinoma of gallbladder",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "4948",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:4948"
                }
            ]
        },
        {
            "disease_id": "DOID:552",
            "recommended_name": {
                "id": "DOID:552",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:552",
                "name": "pneumonia",
                "description": "A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing."
            },
            "synonyms": [
                {
                    "id": "DOID:552",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:552",
                    "name": "acute pneumonia",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "552",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:552"
                }
            ]
        },
        {
            "disease_id": "DOID:583",
            "recommended_name": {
                "id": "DOID:583",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:583",
                "name": "hemolytic anemia",
                "description": ""
            },
            "synonyms": [
                {
                    "id": "DOID:583",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:583",
                    "name": "ANEMIA HEMOLYTIC",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "hemolytic anemia due to pyrimidine 5' nucleotidase deficiency",
                    "description": "Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency is a rare, hereditary, hemolytic anemia due to an erythrocyte nucleotide metabolism disorder characterized by mild to moderate hemolytic anemia associated with basophilic stippling and the accumulation of high concentrations of pyrimidine nucleotides within the erythrocyte. Patients present with variable features of jaundice, splenomegaly, hepatomegaly, gallstones, and sometimes require transfusions. Rare cases of mild development delay and learning difficulties are reported."
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "P5N deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "UMPH1 deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "anemia, hemolytic, due to UMPH1 deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "uridine 5'-monophosphate hydrolase deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "Umph1 deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "hemolytic Anaemia due to P5N deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "hemolytic Anaemia due to Umph1 deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "hemolytic Anemia due to P5N deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "hemolytic Anemia due to Umph1 deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "pyrimidine 5-prime Nucleotidase deficiency, hemolytic Anaemia due to",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "pyrimidine 5-prime Nucleotidase deficiency, hemolytic Anemia due to",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "uridine 5-prime monophosphate hydrolase deficiency, hemolytic anaemia due to",
                    "description": ""
                },
                {
                    "id": "MONDO:0009946",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009946",
                    "name": "uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to",
                    "description": ""
                },
                {
                    "id": "MONDO:0012967",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012967",
                    "name": "hemolytic anemia due to adenylate kinase deficiency",
                    "description": "Hemolytic anemia due to adenylate kinase deficiency is a rare hemolytic anemia due to an erythrocyte nucleotide metabolism disorder characterized by moderate to severe chronic nonspherocytic hemolytic anemia that may require regular blood transfusions and/or splenectomy and may be associated with psychomotor impairment."
                },
                {
                    "id": "MONDO:0012967",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012967",
                    "name": "ADENYLATE KINASE deficiency, hemolytic anaemia due to",
                    "description": ""
                },
                {
                    "id": "MONDO:0012967",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012967",
                    "name": "ADENYLATE KINASE deficiency, hemolytic anemia due to",
                    "description": ""
                },
                {
                    "id": "MIM:266120",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/266120",
                    "name": "P5N deficiency",
                    "description": "P5N deficiency"
                },
                {
                    "id": "MIM:612631",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/612631",
                    "name": "Hemolytic anemia due to adenylate kinase deficiency",
                    "description": "Hemolytic anemia due to adenylate kinase deficiency"
                }
            ],
            "evidence": [
                {
                    "id": "583",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:583"
                }
            ]
        },
        {
            "disease_id": "DOID:9952",
            "recommended_name": {
                "id": "DOID:9952",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9952",
                "name": "acute lymphoblastic leukemia",
                "description": "A acute leukemia that is characterized by over production of lymphoblasts."
            },
            "synonyms": [
                {
                    "id": "DOID:9952",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9952",
                    "name": "ALL",
                    "description": ""
                },
                {
                    "id": "DOID:9952",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9952",
                    "name": "precursor lymphoblastic lymphoma/leukemia",
                    "description": ""
                },
                {
                    "id": "DOID:9952",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9952",
                    "name": "acute lymphoblastic leukaemia",
                    "description": ""
                },
                {
                    "id": "DOID:9952",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9952",
                    "name": "acute lymphocytic leukaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0009539",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009539",
                    "name": "lymphoblastic leukemia, acute, with lymphomatous features",
                    "description": ""
                },
                {
                    "id": "MONDO:0009539",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009539",
                    "name": "leukemia, acute lymphoblastic",
                    "description": ""
                },
                {
                    "id": "MONDO:0009539",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009539",
                    "name": "lymphoblastic leukemia, acute, with lymphomatous features",
                    "description": ""
                },
                {
                    "id": "MONDO:0009539",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009539",
                    "name": "lall",
                    "description": ""
                },
                {
                    "id": "MONDO:0009539",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009539",
                    "name": "lymphomatous All",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, acute lymphocytic, susceptibility to, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "T-cell acute lymphoblastic leukemia, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, T-cell acute lymphoblastic, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, T-cell acute lymphocytic, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, acute lymphoblastic, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, acute lymphocytic, Philadelphia chromosome positive, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, acute lymphocytic, susceptibility to, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "ALL",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "All1",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, B-cell acute lymphoblastic, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, T-cell acute lymphoblastic, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, acute lymphoblastic",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, acute lymphoblastic, B-Hyperdiploid, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0013108",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108",
                    "name": "leukemia, acute lymphoblastic, susceptibility to, 1",
                    "description": ""
                },
                {
                    "id": "MIM:613065",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/613065",
                    "name": "Leukemia, acute lymphoblastic",
                    "description": "Leukemia, acute lymphoblastic"
                }
            ],
            "evidence": [
                {
                    "id": "9952",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:9952"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A8I5ZPA3",
                    "url": "https://www.uniprot.org/uniprot/A0A8I5ZPA3"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Abo2",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZPA3",
            "locus": {}
        }
    ],
    "crossref": [
        {
            "id": "ENSRNOG00000045801",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000045801",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "cd02515",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd02515",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR005076",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR005076",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR029044",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR029044",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "TGKPKCY",
            "url": "https://omabrowser.org/oma/group/TGKPKCY/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "4223357at2759",
            "url": "http://www.orthodb.org/?query=4223357at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10462",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10462",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10462:SF29",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10462:SF29",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF03414",
            "url": "http://pfam.xfam.org/family/PF03414",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "R-RNO-9033807",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-9033807",
            "database": "Reactome",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "1311152",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1311152",
            "database": "RGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "A0A8I5ZPA3",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZPA3",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I5ZPA3-1",
            "url": "https://www.uniprot.org/uniprot/A0A8I5ZPA3-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I6ADA3",
            "url": "https://www.uniprot.org/uniprot/A0A8I6ADA3",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A8I6ADA3-1",
            "url": "https://www.uniprot.org/uniprot/A0A8I6ADA3-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "D4A7T1",
            "url": "https://www.uniprot.org/uniprot/D4A7T1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "D4A7T1-1",
            "url": "https://www.uniprot.org/uniprot/D4A7T1-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "LNLRTGRLKCYSLHLGILPLTVLVLVFFCQGRASHNLPVNLGSAVFFFRKAYPQPRVLTPTRTDVLVLTPWLAPIIWEGTFNIDILNEQFRLRNTTIGLTVFAIKKYVVFLKLFLETAEQHFMVGHKVIYYVFTDRPADVPQVPLGAGRRLVVLAVRNYTRWQDVSMHRMEIISHFSEQRFWHEVDYLVCGDVDMKFRDHVGVEILSALFGTLHPGFYRSRRESFTYERRPQSQAYIPWDQGDFYYMGAFFGGSVVEVHHLTKACHQAMVEDQDNGIEAVWHDESHLNKYLLYHKPTKVLSPEYMWDQQLLGWPSIMKKLRYVAVPKNHQAIRN",
        "length": 334,
        "header": "tr|A0A8I5ZPA3-1|A0A8I5ZPA3_RAT Isoform 1 of Uncharacterized protein  OS=Rattus norvegicus OX=10116 GN=Abo2 PE=3 SV=1 CANONICAL=A0A8I5ZPA3-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A8I5ZPA3-1",
            "url": "",
            "sequence": {
                "sequence": "LNLRTGRLKCYSLHLGILPLTVLVLVFFCQGRASHNLPVNLGSAVFFFRKAYPQPRVLTPTRTDVLVLTPWLAPIIWEGTFNIDILNEQFRLRNTTIGLTVFAIKKYVVFLKLFLETAEQHFMVGHKVIYYVFTDRPADVPQVPLGAGRRLVVLAVRNYTRWQDVSMHRMEIISHFSEQRFWHEVDYLVCGDVDMKFRDHVGVEILSALFGTLHPGFYRSRRESFTYERRPQSQAYIPWDQGDFYYMGAFFGGSVVEVHHLTKACHQAMVEDQDNGIEAVWHDESHLNKYLLYHKPTKVLSPEYMWDQQLLGWPSIMKKLRYVAVPKNHQAIRN",
                "length": 334,
                "header": "tr|A0A8I5ZPA3-1|A0A8I5ZPA3_RAT Isoform 1 of Uncharacterized protein  OS=Rattus norvegicus OX=10116 GN=Abo2 PE=3 SV=1 CANONICAL=A0A8I5ZPA3-1"
            },
            "locus": {
                "chromosome": "3",
                "start_pos": 10027908,
                "end_pos": 10021572,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000106649.1",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000106649.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000079782.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000079782.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8I6ADA3-1",
            "url": "",
            "sequence": {
                "sequence": "MNLRGRLKCYSLHLGILPLTVLVLVFFCFVCLSLRSQEWGHPGAVNRKAYPQPRVLTPTRTDVLVLTPWLAPIIWEGTFNIDILNEQFRLRNTTIGLTVFAIKKYVVFLKLFLETAEQHFMVGHKVIYYVFTDRPADVPQVPLGAGRRLVVLAVRNYTRWQDVSMHRMEIISHFSEQRFWHEVDYLVCGDVDMKFRDHVGVEILSALFGTLHPGFYRSRRESFTYERRPQSQAYIPWDQGDFYYMGAFFGGSVVEVHHLTKACHQAMVEDQDNGIEAVWHDESHLNKYLLYHKPTKVLSPEYMWDQQLLGWPSIMKKLRYVAVPKNHQAIRN",
                "length": 332,
                "header": "tr|A0A8I6ADA3-1|A0A8I6ADA3_RAT Computationally mapped isoform of Uncharacterized protein  OS=Rattus norvegicus OX=10116 GN=Abo2 PE=3 SV=1 CANONICAL=A0A8I5ZPA3-1"
            },
            "locus": {
                "chromosome": "3",
                "start_pos": 10027908,
                "end_pos": 10003110,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000099183.1",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000099183.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000091204.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000091204.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "D4A7T1-1",
            "url": "",
            "sequence": {
                "sequence": "MKDLRLGRLKCYSLHLGILPLTVLVLVFFCFVCLSLRSQEWGHPGAVNRKAYPQPRVLTPTRTDVLVLTPWLAPIIWEGTFNIDILNEQFRLRNTTIGLTVFAIKKYVVFLKLFLETAEQHFMVGHKVIYYVFTDRPADVPQVPLGAGRRLVVLAVRNYTRWQDVSMHRMEIISHFSEQRFWHEVDYLVCGDVDMKFRDHVGVEILSALFGTLHPGFYRSRRESFTYERRPQSQAYIPWDQGDFYYMGAFFGGSVVEVHHLTKACHQAMVEDQDNGIEAVWHDESHLNKYLLYHKPTKVLSPEYMWDQQLLGWPSIMKKLRYVAVPKNHQAIRN",
                "length": 334,
                "header": "tr|D4A7T1-1|A0A8I5ZPA3_RAT Computationally mapped isoform of Uncharacterized protein  OS=Rattus norvegicus OX=10116 GN=Abo2 PE=3 SV=3 CANONICAL=A0A8I5ZPA3-1"
            },
            "locus": {
                "chromosome": "3",
                "start_pos": 10027908,
                "end_pos": 10011564,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000061276.5",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000061276.5"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000057988.3",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000057988.3"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "R-RNO-9033807",
            "name": "ABO blood group biosynthesis",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-9033807",
            "resource": "Reactome",
            "description": "ABO blood group biosynthesis"
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                "name": "Cellular Component",
                "total": 3,
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                        "id": "GO:0005794",
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                        "pmid": ""
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                        "pmid": ""
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                        "pmid": ""
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                        "name": "glycoprotein-fucosylgalactoside alpha-N-acetylgalactosaminyltransferase activity",
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                                "url": "https://www.uniprot.org/uniprot/A0A8I5ZPA3"
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                        "pmid": ""
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            "end_pos": 160,
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            "end_pos": 96,
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    "ptm_annotation": [],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
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