{
    "uniprot_canonical_ac": "A0A8I5ZSX2-1",
    "uniprot_ac": "A0A8I5ZSX2",
    "uniprot_id": "A0A8I5ZSX2_RAT",
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        "chemical_mass": 58106.0,
        "monoisotopic_mass": 58106.0
    },
    "refseq": {},
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            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A8I5ZSX2"
        }
    ],
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            "disease_id": "DOID:11723",
            "recommended_name": {
                "id": "DOID:11723",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:11723",
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                "description": "A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy."
            },
            "synonyms": [
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                    "id": "DOID:11723",
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                    "url": "http://disease-ontology.org/term/DOID:11723",
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                    "description": ""
                },
                {
                    "id": "MONDO:0010679",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010679",
                    "name": "Duchenne muscular dystrophy",
                    "description": "Duchenne muscular dystrophy (DMD) is a neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle."
                },
                {
                    "id": "MONDO:0010679",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010679",
                    "name": "DMD",
                    "description": ""
                },
                {
                    "id": "MONDO:0010679",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010679",
                    "name": "Duchenne muscular dystrophy",
                    "description": ""
                },
                {
                    "id": "MONDO:0010679",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010679",
                    "name": "Duchenne muscular dystrophy, X-linked recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0010679",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010679",
                    "name": "muscular dystrophy, Duchenne",
                    "description": ""
                },
                {
                    "id": "MONDO:0010679",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010679",
                    "name": "severe dystrophinopathy, Duchenne type",
                    "description": ""
                },
                {
                    "id": "MONDO:0010679",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010679",
                    "name": "muscular dystrophy, Duchenne type",
                    "description": ""
                },
                {
                    "id": "MONDO:0010679",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010679",
                    "name": "muscular dystrophy, pseudohypertrophic progressive, Duchenne type",
                    "description": ""
                },
                {
                    "id": "MIM:310200",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/310200",
                    "name": "Duchenne muscular dystrophy",
                    "description": "Duchenne muscular dystrophy"
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                }
            ]
        }
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    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
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            "name": "Rattus norvegicus",
            "taxid": 10116,
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            "id": "cd00992",
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            "id": "IPR001478",
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            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001849",
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            "id": "IPR011993",
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            "id": "IPR015482",
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            "id": "IPR036034",
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            "id": "YVTRYLW",
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            "id": "PTHR10554",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10554",
            "database": "PANTHER",
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        },
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            "id": "PF00595",
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        },
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            "id": "1560290",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1560290",
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        },
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            "id": "F1M2M1-1",
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            "database": "UniProtKB",
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    },
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                        "url": "https://www.ensembl.org/id/ENSRNOP00000081625.1"
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                "length": 519,
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            },
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                    {
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                        "id": "ENSRNOP00000009679.8",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000009679.8"
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            "name": "isoformset.uniprotkb",
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