{
    "uniprot_canonical_ac": "A0A096MJH9-1",
    "uniprot_ac": "A0A096MJH9",
    "uniprot_id": "A0A096MJH9_RAT",
    "mass": {
        "chemical_mass": 33571.0,
        "monoisotopic_mass": 33571.0
    },
    "refseq": {
        "ac": "NP_001032446",
        "name": "popeye domain-containing protein 3 isoform 2",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001032446"
    },
    "gene_names": [
        {
            "name": "Popdc3",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A096MJH9",
            "id": "A0A096MJH9"
        },
        {
            "name": "LOC641520",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A096MJH9",
            "id": "A0A096MJH9"
        }
    ],
    "protein_names": [
        {
            "name": "Popeye domain containing 3",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A096MJH9"
        },
        {
            "name": "popeye domain-containing protein 3 isoform 2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001032446",
            "id": "NP_001032446"
        },
        {
            "name": "popeye domain-containing protein 3",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001032446",
            "id": "NP_001032446"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0110274",
            "recommended_name": {
                "id": "DOID:0110274",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110274",
                "name": "autosomal recessive limb-girdle muscular dystrophy",
                "description": "A limb-girdle muscular dystrophy has_material_basis_in autosomal recessive inheritance."
            },
            "synonyms": [
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "autosomal recessive limb-girdle muscular dystrophy type 2A",
                    "description": "Autosomal recessive limb-girdle muscular dystrophy type 2A (LGMD2A) is a subtype of autosomal recessive limb girdle muscular dystrophy characterized by a variable age of onset of progressive, typically symmetrical and selective weakness and atrophy of proximal shoulder- and pelvic-girdle muscles (gluteus maximus, thigh adductors, and muscles of the posterior compartment of the limbs are most commonly affected) without cardiac or facial involvement. Clinical manifestations include exercise intolerance, a waddling gait, scapular winging and calf pseudo-hypertrophy."
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "CAPN3 autosomal recessive limb-girdle muscular dystrophy",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "LGMD2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "Leyden-Moebius muscular dystrophy",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in CAPN3",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "autosomal recessive limb-girdle muscular dystrophy type 2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "calpainopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "limb-girdle muscular dystrophy due to calpain deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "limb-girdle muscular dystrophy type 2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "muscular dystrophy, limb-girdle, autosomal recessive 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "muscular dystrophy, limb-girdle, type 2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "pelvofemoral muscular dystrophy",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "primary calpainopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "LGMD2",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "limb-girdle muscular dystrophy type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "muscular dystrophy limb girdle type 2A, erb type",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "muscular dystrophy, Pelvofemoral",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "muscular dystrophy, limb-girdle, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0009675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009675",
                    "name": "myositis, eosinophilic",
                    "description": ""
                },
                {
                    "id": "MIM:253600",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/253600",
                    "name": "Muscular dystrophy, limb-girdle, autosomal recessive 1",
                    "description": "Muscular dystrophy, limb-girdle, autosomal recessive 1"
                }
            ],
            "evidence": [
                {
                    "id": "0110274",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110274"
                }
            ]
        },
        {
            "disease_id": "DOID:9884",
            "recommended_name": {
                "id": "DOID:9884",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9884",
                "name": "muscular dystrophy",
                "description": "A myopathy is characterized by progressive skeletal muscle weakness degeneration."
            },
            "synonyms": [
                {
                    "id": "MONDO:0010678",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010678",
                    "name": "muscular dystrophy, progressive Pectorodorsal",
                    "description": ""
                },
                {
                    "id": "MONDO:0010678",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010678",
                    "name": "muscular dystrophy, progressive Pectorodorsal",
                    "description": ""
                },
                {
                    "id": "MONDO:0010678",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010678",
                    "name": "muscular dystrophy, progressive, involving shoulder girdle and back",
                    "description": ""
                },
                {
                    "id": "MONDO:0010884",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010884",
                    "name": "muscular dystrophy, scapulohumeral",
                    "description": ""
                },
                {
                    "id": "MONDO:0010884",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010884",
                    "name": "muscular dystrophy, scapulohumeral",
                    "description": ""
                },
                {
                    "id": "MONDO:0010676",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010676",
                    "name": "muscular dystrophy, Hemizygous lethal type",
                    "description": ""
                },
                {
                    "id": "MONDO:0010676",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010676",
                    "name": "muscular dystrophy, Hemizygous lethal type",
                    "description": ""
                },
                {
                    "id": "MONDO:0010675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010675",
                    "name": "muscular dystrophy, cardiac type",
                    "description": ""
                },
                {
                    "id": "MONDO:0010675",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010675",
                    "name": "muscular dystrophy, cardiac type",
                    "description": ""
                },
                {
                    "id": "MONDO:0010677",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010677",
                    "name": "muscular dystrophy, Mabry type",
                    "description": ""
                },
                {
                    "id": "MONDO:0010677",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010677",
                    "name": "muscular dystrophy, Mabry type",
                    "description": ""
                },
                {
                    "id": "MONDO:0008028",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008028",
                    "name": "muscular dystrophy, Barnes type",
                    "description": ""
                },
                {
                    "id": "MONDO:0008028",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008028",
                    "name": "muscular dystrophy, Barnes type",
                    "description": ""
                },
                {
                    "id": "MONDO:0008034",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008034",
                    "name": "muscular dystrophy, pseudohypertrophic, with Internalized capillaries",
                    "description": ""
                },
                {
                    "id": "MONDO:0008034",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008034",
                    "name": "muscular dystrophy, pseudohypertrophic, with Internalized capillaries",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "9884",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:9884"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A096MJH9",
                    "url": "https://www.uniprot.org/uniprot/A0A096MJH9"
                }
            ],
            "common_name": "Rat"
        }
    ],
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            "name": "Popdc3",
            "url": "https://www.uniprot.org/uniprot/A0A096MJH9",
            "locus": {
                "chromosome": "20",
                "start_pos": 48800593,
                "end_pos": 48772462,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSRNOG00000047102",
                        "url": "https://www.ensembl.org/id/ENSRNOG00000047102"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "ENSRNOG00000047102",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000047102",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "641520",
            "url": "https://www.ncbi.nlm.nih.gov/gene/641520",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "IPR006916",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR006916",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR018490",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR018490",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "rno:641520",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:641520",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "HMPGTEL",
            "url": "https://omabrowser.org/oma/group/HMPGTEL/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "5385961at2759",
            "url": "http://www.orthodb.org/?query=5385961at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR12101",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR12101",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR12101:SF18",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR12101:SF18",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF04831",
            "url": "http://pfam.xfam.org/family/PF04831",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "XP_006256661",
            "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006256661",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "1590760",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1590760",
            "database": "RGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "A0A096MJH9",
            "url": "https://www.uniprot.org/uniprot/A0A096MJH9",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A096MJH9-1",
            "url": "https://www.uniprot.org/uniprot/A0A096MJH9-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q3KRE1",
            "url": "https://www.uniprot.org/uniprot/Q3KRE1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q3KRE1-1",
            "url": "https://www.uniprot.org/uniprot/Q3KRE1-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MEKNSSLWKSLVTEHPLCTTWKQEAEGAIFHLASILFVVGFMGGSGFFGLLYVFSLLGLGFLCSAVWAWVDVCAADIFSWNFVLFVICFMQFVHIAYQVHSITFAREFHVLYSSLFKPLGIPLPVFRTIALSSEVVTLEKEHCYAMQGKTSIDRLSVLVSGRIRVTVDGEFLHYISPFQFLDSPEWDSLRPTEEGIFQVTLTADTDCRYVSWRRKKLYLLFAQHRYISRLFSVLIGSDIADKLYALNDRVYIGKKHHYDIRLPNYYQLSSPDLSRSPLTEQFRNSRQHCNK",
        "length": 291,
        "header": "tr|A0A096MJH9-1|A0A096MJH9_RAT Isoform 1 of Popeye domain containing 3  OS=Rattus norvegicus OX=10116 GN=Popdc3 PE=1 SV=1 CANONICAL=A0A096MJH9-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A096MJH9-1",
            "url": "",
            "sequence": {
                "sequence": "MEKNSSLWKSLVTEHPLCTTWKQEAEGAIFHLASILFVVGFMGGSGFFGLLYVFSLLGLGFLCSAVWAWVDVCAADIFSWNFVLFVICFMQFVHIAYQVHSITFAREFHVLYSSLFKPLGIPLPVFRTIALSSEVVTLEKEHCYAMQGKTSIDRLSVLVSGRIRVTVDGEFLHYISPFQFLDSPEWDSLRPTEEGIFQVTLTADTDCRYVSWRRKKLYLLFAQHRYISRLFSVLIGSDIADKLYALNDRVYIGKKHHYDIRLPNYYQLSSPDLSRSPLTEQFRNSRQHCNK",
                "length": 291,
                "header": "tr|A0A096MJH9-1|A0A096MJH9_RAT Isoform 1 of Popeye domain containing 3  OS=Rattus norvegicus OX=10116 GN=Popdc3 PE=1 SV=1 CANONICAL=A0A096MJH9-1"
            },
            "locus": {
                "chromosome": "20",
                "start_pos": 48800175,
                "end_pos": 48797116,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000077065.3",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000077065.3"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000068135.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000068135.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q3KRE1-1",
            "url": "",
            "sequence": {
                "sequence": "MEKNSSLWKSLVTEHPLCTTWKQEAEGAIFHLASILFVFVHIAYQVHSITFAREFHVLYSSLFKPLGIPLPVFRTIALSSEVVTLEKEHCYAMQGKTSIDRLSVLVSGRIRVTVDGEFLHYISPFQFLDSPEWDSLRPTEEGIFQVTLTADTDCRYVSWRRKKLYLLFAQHRYISRLFSVLIGSDIADKLYALNDRVYIGKKHHYDIRLPNYYQLSSPDLSRSPLTEQFRNSRQHCNK",
                "length": 238,
                "header": "tr|Q3KRE1-1|Q3KRE1_RAT Computationally mapped isoform of Popeye domain-containing 3  OS=Rattus norvegicus OX=10116 GN=Popdc3 PE=1 SV=1 CANONICAL=A0A096MJH9-1"
            },
            "locus": {
                "chromosome": "20",
                "start_pos": 48800175,
                "end_pos": 48797116,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000073259.3",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000073259.3"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000066864.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000066864.1"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "rno:641520",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:641520",
            "resource": "KEGG Pathway"
        }
    ],
    "orthologs": [
        {
            "uniprot_canonical_ac": "Q9ES81-1",
            "protein_name": "Popeye domain-containing protein 3",
            "gene_name": "Popdc3",
            "tax_id": 10090,
            "organism": "Mus musculus",
            "sequence": {
                "sequence": "MEKNSSLWKSLVTEHPLCTTWKQEAEGAIYHLASILFVVGFMGGSGFFGLLYVFSLLGLGFLSSAVWAWVDICAADIFSWNFVLFVICFMQFVHIAYQVHSITFARDFHVLYSSLFKPLGIPLPVFRTIALSSEVVSLEKEHCYAMQGKTSIDRLSVLISGRIRVTVDGEFLHYISPFQFLDSPEWDSLRPTEEGIFQVTLTADTDCRYVSWRRKKLYLLFAQHRYISRLFSVLIGSDIADKLYALNDRVYIGKKHHYDIRLPNYYHMSTPDLSRSPLTEQFRNSRQHCNK",
                "length": 291
            },
            "evidence": [
                {
                    "id": "45226270",
                    "url": "http://www.informatics.jax.org/homology/45226270",
                    "database": "MGI"
                }
            ],
            "common_name": "Mouse"
        },
        {
            "uniprot_canonical_ac": "Q9HBV1-1",
            "protein_name": "Popeye domain-containing protein 3",
            "gene_name": "POPDC3",
            "tax_id": 9606,
            "organism": "Homo sapiens",
            "sequence": {
                "sequence": "MERNSSLWKNLIDEHPVCTTWKQEAEGAIYHLASILFVVGFMGGSGFFGLLYVFSLLGLGFLCSAVWAWVDVCAADIFSWNFVLFVICFMQFVHIAYQVRSITFAREFQVLYSSLFQPLGISLPVFRTIALSSEVVTLEKEHCYAMQGKTSIDKLSLLVSGRIRVTVDGEFLHYIFPLQFLDSPEWDSLRPTEEGIFQVTLTAETDCRYVSWRRKKLYLLFAQHRYISRLFSVLIGSDIADKLYALNDRVYIGKRYHYDIRLPNFYQMSTPEIRRSPLTQHFQNSRRYCDK",
                "length": 291
            },
            "evidence": [
                {
                    "id": "45226270",
                    "url": "http://www.informatics.jax.org/homology/45226270",
                    "database": "MGI"
                }
            ],
            "common_name": "Human"
        }
    ],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 4,
                "go_terms": [
                    {
                        "name": "heart development",
                        "id": "GO:0007507",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007507",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A096MJH9",
                                "url": "https://www.uniprot.org/uniprot/A0A096MJH9"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "regulation of membrane potential",
                        "id": "GO:0042391",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042391",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A096MJH9",
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