{
    "uniprot_canonical_ac": "A0A0G2K7D0-1",
    "uniprot_ac": "A0A0G2K7D0",
    "uniprot_id": "A0A0G2K7D0_RAT",
    "mass": {
        "chemical_mass": 23323.0,
        "monoisotopic_mass": 23323.0
    },
    "refseq": {},
    "gene_names": [
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            "name": "Ccdc28b",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0G2K7D0",
            "id": "A0A0G2K7D0"
        }
    ],
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            "resource": "UniProtKB",
            "type": "synonym",
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            "id": "A0A0G2K7D0"
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    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0110123",
            "recommended_name": {
                "id": "DOID:0110123",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110123",
                "name": "Bardet-Biedl syndrome 1",
                "description": "A Bardet-Biedl syndrome that has_material_basis_in homozygous mutation in the BBS1 gene on chromosome 11q13."
            },
            "synonyms": [
                {
                    "id": "DOID:0110123",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110123",
                    "name": "BBS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008854",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008854",
                    "name": "Bardet-Biedl syndrome 1",
                    "description": "A Bardet-Biedl syndrome that has material basis in homozygous mutation in the BBS1 gene on chromosome 11q13."
                },
                {
                    "id": "MONDO:0008854",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008854",
                    "name": "BBS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008854",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008854",
                    "name": "Bardet-Biedl syndrome 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0008854",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008854",
                    "name": "Bardet-Biedl syndrome 1, modifier of",
                    "description": ""
                },
                {
                    "id": "MONDO:0008854",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008854",
                    "name": "Bardet-Biedl syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MIM:209900",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/209900",
                    "name": "Bardet-Biedl syndrome",
                    "description": "Bardet-Biedl syndrome"
                }
            ],
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                }
            ]
        },
        {
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                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1935",
                "name": "Bardet-Biedl syndrome",
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                },
                {
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                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008854",
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                },
                {
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                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0008854",
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                    "description": ""
                },
                {
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                    "description": ""
                },
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                    "description": ""
                },
                {
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                }
            ]
        }
    ],
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    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
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            "name": "Rattus norvegicus",
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                    "database": "UniProtKB",
                    "id": "A0A0G2K7D0",
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                        "id": "ENSRNOG00000047578",
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                    }
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            }
        }
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        {
            "id": "IPR025271",
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        },
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            "id": "PHKEKAR",
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            ]
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            "id": "PTHR13400",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR13400",
            "database": "PANTHER",
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                "Protein Classification"
            ]
        },
        {
            "id": "PTHR13400:SF2",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR13400:SF2",
            "database": "PANTHER",
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            ]
        },
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            "id": "PF13270",
            "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF13270",
            "database": "Pfam",
            "categories": [
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            ]
        },
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            "id": "1583447",
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            ]
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            ]
        },
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            ]
        },
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            "id": "M0R957",
            "url": "https://www.uniprot.org/uniprot/M0R957",
            "database": "UniProtKB",
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                "Protein"
            ]
        },
        {
            "id": "M0R957-1",
            "url": "https://www.uniprot.org/uniprot/M0R957-1",
            "database": "UniProtKB",
            "categories": [
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            ]
        }
    ],
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    },
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            },
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                        "id": "ENSRNOT00000083369.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000083369.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000074154.2",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000074154.2"
                    }
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                "header": "tr|M0R957-1|M0R957_RAT Computationally mapped isoform of Coiled coil domain containing 28B  OS=Rattus norvegicus OX=10116 GN=Ccdc28b PE=4 SV=1 CANONICAL=A0A0G2K7D0-1"
            },
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                        "id": "ENSRNOT00000075659.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000075659.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000066019.2",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000066019.2"
                    }
                ]
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        }
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                }
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            "gene_name": "CCDC28B",
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            },
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                    "id": "A0A0G2K7D0",
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                }
            ],
            "glygen_name": "Bovine",
            "common_name": "Bovine"
        },
        {
            "uniprot_canonical_ac": "Q8CEG5-1",
            "protein_name": "Coiled-coil domain-containing protein 28B",
            "gene_name": "Ccdc28b",
            "tax_id": 10090,
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                "sequence": "MEDKKKKRSPKPCLTQPAQAPGTLRRVPVPTSHSGSLALGLPHLPSPKQRAKFKRAGKEKCRPVLAGGGGGSAGTPLQHSFLTEVTDVYEMEGGLLNLLNDFHSGRLQAFGKECSFEQLEHVREMQEKLARLHFSLDVCGEEEDEEEEEDGVTEGLPEEQKKTMADRNLDQLLSNLEDLSNSIQKLHLAENAEPEDQPAA",
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            },
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                    "id": "A0A0G2K7D0",
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                    "database": "OMA"
                }
            ],
            "glygen_name": "Mouse",
            "common_name": "Mouse"
        },
        {
            "uniprot_canonical_ac": "Q9BUN5-1",
            "protein_name": "Coiled-coil domain-containing protein 28B",
            "gene_name": "CCDC28B",
            "tax_id": 9606,
            "organism": "Homo sapiens",
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                "sequence": "MDDKKKKRSPKPCLAQPAQAPGTLRRVPVPTSHSGSLALGLPHLPSPKQRAKFKRVGKEKCRPVLAGGGSGSAGTPLQHSFLTEVTDVYEMEGGLLNLLNDFHSGRLQAFGKECSFEQLEHVREMQEKLARLHFSLDVCGEEEDDEEEEDGVTEGLPEEQKKTMADRNLDQLLSNLEDLSNSIQKLHLAENAEPEEQSAA",
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            },
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                    "database": "OMA"
                }
            ],
            "glygen_name": "Human",
            "common_name": "Human"
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    ],
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                "name": "Cellular Component",
                "total": 1,
                "go_terms": [
                    {
                        "name": "centrosome",
                        "id": "GO:0005813",
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                        "name": "cilium assembly",
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    "interactions": [],
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    "reaction_participants": [],
    "reaction_enzymes": [],
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    "synthesized_glycans": [],
    "enzyme_annotation": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
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        {
            "name": "homologset.oma",
            "label": "OMA Homologs"
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    "sequence_features": {
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        "sequon_annotation_sites": []
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