{
    "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"
        }
    ],
    "protein_names": [
        {
            "name": "Coiled coil domain containing 28B",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A0G2K7D0"
        }
    ],
    "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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                    "url": "https://www.alliancegenome.org/disease/DOID:0110123"
                }
            ]
        },
        {
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            "recommended_name": {
                "id": "DOID:1935",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1935",
                "name": "Bardet-Biedl syndrome",
                "description": "A syndrome that results from mutations in multiple BBS genes affecting cellular cilia structure or function (ciliopathy) resulting in variable presentation and characterized principally by obesity, retinitis pigmentosa,vision loss, polydactyly, mental retardation, hypogonadism, and renal failure in some cases."
            },
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                {
                    "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."
                },
                {
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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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                    "description": "Bardet-Biedl syndrome"
                }
            ],
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                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1935"
                }
            ]
        }
    ],
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    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
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        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
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                    "id": "A0A0G2K7D0",
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            ],
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                        "id": "ENSRNOG00000047578",
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        }
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            "url": "https://www.ebi.ac.uk/interpro/entry/IPR025271",
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            "categories": [
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        },
        {
            "id": "PHKEKAR",
            "url": "https://omabrowser.org/oma/group/PHKEKAR/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR13400",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR13400",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR13400:SF2",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR13400:SF2",
            "database": "PANTHER",
            "categories": [
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            ]
        },
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            "id": "PF13270",
            "url": "http://pfam.xfam.org/family/PF13270",
            "database": "Pfam",
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        },
        {
            "id": "1583447",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1583447",
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        },
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            "id": "M0R957",
            "url": "https://www.uniprot.org/uniprot/M0R957",
            "database": "UniProtKB",
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            ]
        },
        {
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            "url": "https://www.uniprot.org/uniprot/M0R957-1",
            "database": "UniProtKB",
            "categories": [
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        }
    ],
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    },
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            "isoform_ac": "A0A0G2K7D0-1",
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            },
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                        "id": "ENSRNOT00000083369.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000083369.2"
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                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000074154.2",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000074154.2"
                    }
                ]
            }
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            },
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                        "id": "ENSRNOT00000075659.2",
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                    },
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                        "database": "Ensembl Peptide",
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        {
            "name": "isoformset.uniprotkb",
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