[
    {
        "title": "Alternative pathway of complement: recruitment of precursor properdin by the labile C3/C5 convertase and the potentiation of the pathway.",
        "journal": "The Journal of experimental medicine",
        "date": "1976",
        "authors": "Medicus RG, Gotze O, Muller-Eberhard HJ",
        "reference": {
            "type": "PubMed",
            "id": "978134",
            "url": "https://pubmed.ncbi.nlm.nih.gov/978134"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P01700-1",
                "protein_name": "Immunoglobulin lambda variable 1-47",
                "gene_name": "IGLV1-47",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01714-1",
                "protein_name": "Immunoglobulin lambda variable 3-19",
                "gene_name": "IGLV3-19",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P80748-1",
                "protein_name": "Immunoglobulin lambda variable 3-21",
                "gene_name": "IGLV3-21",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A075B6P5-1",
                "protein_name": "Immunoglobulin kappa variable 2-28",
                "gene_name": "IGKV2-28",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A075B6S6-1",
                "protein_name": "Immunoglobulin kappa variable 2D-30",
                "gene_name": "IGKV2D-30",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "A0A0C4DH25-1",
                "protein_name": "Immunoglobulin kappa variable 3D-20",
                "gene_name": "IGKV3D-20",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01593-1",
                "protein_name": "Immunoglobulin kappa variable 1D-33",
                "gene_name": "IGKV1D-33",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01599-1",
                "protein_name": "Immunoglobulin kappa variable 1-17",
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                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01601-1",
                "protein_name": "Immunoglobulin kappa variable 1D-16",
                "gene_name": "IGKV1D-16",
                "tax_name": "Human"
            },
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                "uniprot_canonical_ac": "P01611-1",
                "protein_name": "Immunoglobulin kappa variable 1D-12",
                "gene_name": "IGKV1D-12",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01615-1",
                "protein_name": "Immunoglobulin kappa variable 2D-28",
                "gene_name": "IGKV2D-28",
                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01619-1",
                "protein_name": "Immunoglobulin kappa variable 3-20",
                "gene_name": "IGKV3-20",
                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01624-1",
                "protein_name": "Immunoglobulin kappa variable 3-15",
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                "tax_name": "Human"
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                "uniprot_canonical_ac": "P04433-1",
                "protein_name": "Immunoglobulin kappa variable 3-11",
                "gene_name": "IGKV3-11",
                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01602-1",
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                "gene_name": "IGKV1-5",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P00734-1",
                "protein_name": "Prothrombin",
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                "protein_name": "Clusterin",
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                "uniprot_canonical_ac": "P06681-1",
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                "protein_name": "B-lymphocyte antigen CD19",
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                "uniprot_canonical_ac": "P08246-1",
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                "protein_name": "Immunoglobulin heavy variable 3-53",
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                "protein_name": "Immunoglobulin heavy variable 4-34",
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                "uniprot_canonical_ac": "P01597-1",
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                "uniprot_canonical_ac": "P06310-1",
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                "uniprot_canonical_ac": "P06312-1",
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                "uniprot_canonical_ac": "P08603-1",
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                "uniprot_canonical_ac": "P05156-1",
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                "uniprot_canonical_ac": "Q16581-1",
                "protein_name": "C3a anaphylatoxin chemotactic receptor",
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                "uniprot_canonical_ac": "P00736-1",
                "protein_name": "Complement C1r subcomponent",
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                "protein_name": "Complement C1s subcomponent",
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                "protein_name": "C4b-binding protein alpha chain",
                "gene_name": "C4BPA",
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                "uniprot_canonical_ac": "P02747-1",
                "protein_name": "Complement C1q subcomponent subunit C",
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            {
                "uniprot_canonical_ac": "P20851-1",
                "protein_name": "C4b-binding protein beta chain",
                "gene_name": "C4BPB",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "Q96IY4-1",
                "protein_name": "Carboxypeptidase B2",
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                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P00746-1",
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                "gene_name": "CFD",
                "tax_name": "Human"
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                "uniprot_canonical_ac": "P0C0L5-1",
                "protein_name": "Complement C4-B",
                "gene_name": "C4B_2; C4B",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P0C0L4-1",
                "protein_name": "Complement C4-A",
                "gene_name": "C4A",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P07360-1",
                "protein_name": "Complement component C8 gamma chain",
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            {
                "uniprot_canonical_ac": "P13671-1",
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                "gene_name": "C6",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01031-1",
                "protein_name": "Complement C5",
                "gene_name": "C5",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P02748-1",
                "protein_name": "Complement component C9",
                "gene_name": "C9",
                "tax_name": "Human"
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                "uniprot_canonical_ac": "P07357-1",
                "protein_name": "Complement component C8 alpha chain",
                "gene_name": "C8A",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P08174-1",
                "protein_name": "Complement decay-accelerating factor",
                "gene_name": "CD55",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15529-1",
                "protein_name": "Membrane cofactor protein",
                "gene_name": "CD46",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P04432-1",
                "protein_name": "Immunoglobulin kappa variable 1D-39",
                "gene_name": "IGKV1D-39",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P06315-1",
                "protein_name": "Immunoglobulin kappa variable 5-2",
                "gene_name": "IGKV5-2",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01699-1",
                "protein_name": "Immunoglobulin lambda variable 1-44",
                "gene_name": "IGLV1-44",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01701-1",
                "protein_name": "Immunoglobulin lambda variable 1-51",
                "gene_name": "IGLV1-51",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01704-1",
                "protein_name": "Immunoglobulin lambda variable 2-14",
                "gene_name": "IGLV2-14",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01706-1",
                "protein_name": "Immunoglobulin lambda variable 2-11",
                "gene_name": "IGLV2-11",
                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01709-1",
                "protein_name": "Immunoglobulin lambda variable 2-8",
                "gene_name": "IGLV2-8",
                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01717-1",
                "protein_name": "Immunoglobulin lambda variable 3-25",
                "gene_name": "IGLV3-25",
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            {
                "uniprot_canonical_ac": "P01721-1",
                "protein_name": "Immunoglobulin lambda variable 6-57",
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                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01703-1",
                "protein_name": "Immunoglobulin lambda variable 1-40",
                "gene_name": "IGLV1-40",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01705-1",
                "protein_name": "Immunoglobulin lambda variable 2-23",
                "gene_name": "IGLV2-23",
                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01715-1",
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                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01718-1",
                "protein_name": "Immunoglobulin lambda variable 3-27",
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                "tax_name": "Human"
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                "uniprot_canonical_ac": "P04211-1",
                "protein_name": "Immunoglobulin lambda variable 7-43",
                "gene_name": "IGLV7-43",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P05155-1",
                "protein_name": "Plasma protease C1 inhibitor",
                "gene_name": "SERPING1",
                "tax_name": "Human"
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                "uniprot_canonical_ac": "P22792-1",
                "protein_name": "Carboxypeptidase N subunit 2",
                "gene_name": "CPN2",
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                "uniprot_canonical_ac": "P20023-1",
                "protein_name": "Complement receptor type 2",
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                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01860-2",
                "protein_name": "Immunoglobulin heavy constant gamma 3",
                "gene_name": "IGHG3",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01861-2",
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                "gene_name": "IGHG4",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P0CF74-1",
                "protein_name": "Immunoglobulin lambda constant 6",
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                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P17927-1",
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                "tax_name": "Human"
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                "uniprot_canonical_ac": "P10643-1",
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                "gene_name": "C7",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P07358-1",
                "protein_name": "Complement component C8 beta chain",
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                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BXR6-1",
                "protein_name": "Complement factor H-related protein 5",
                "gene_name": "CFHR5",
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                "uniprot_canonical_ac": "P36980-1",
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                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "Q02985-1",
                "protein_name": "Complement factor H-related protein 3",
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                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P02746-1",
                "protein_name": "Complement C1q subcomponent subunit B",
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                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "Q9P296-1",
                "protein_name": "C5a anaphylatoxin chemotactic receptor 2",
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            {
                "uniprot_canonical_ac": "P02745-1",
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                "uniprot_canonical_ac": "P04004-1",
                "protein_name": "Vitronectin",
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                "uniprot_canonical_ac": "P51124-1",
                "protein_name": "Granzyme M",
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            {
                "uniprot_canonical_ac": "P01825-1",
                "protein_name": "Immunoglobulin heavy variable 4-59",
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                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01817-1",
                "protein_name": "Immunoglobulin heavy variable 2-5",
                "gene_name": "IGHV2-5",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01824-1",
                "protein_name": "Immunoglobulin heavy variable 4-39",
                "gene_name": "IGHV4-39",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P23083-1",
                "protein_name": "Immunoglobulin heavy variable 1-2",
                "gene_name": "IGHV1-2",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P07225-1",
                "protein_name": "Vitamin K-dependent protein S",
                "gene_name": "PROS1",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01742-1",
                "protein_name": "Immunoglobulin heavy variable 1-69",
                "gene_name": "IGHV1-69",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01768-1",
                "protein_name": "Immunoglobulin heavy variable 3-30",
                "gene_name": "IGHV3-30",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01814-1",
                "protein_name": "Immunoglobulin heavy variable 2-70",
                "gene_name": "IGHV2-70",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "Q92496-1",
                "protein_name": "Complement factor H-related protein 4",
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                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01772-1",
                "protein_name": "Immunoglobulin heavy variable 3-33",
                "gene_name": "IGHV3-33",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01762-1",
                "protein_name": "Immunoglobulin heavy variable 3-11",
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                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01763-1",
                "protein_name": "Immunoglobulin heavy variable 3-48",
                "gene_name": "IGHV3-48",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01764-1",
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                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "P01766-1",
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                "gene_name": "IGHV3-13",
                "tax_name": "Human"
            },
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                "uniprot_canonical_ac": "P01780-1",
                "protein_name": "Immunoglobulin heavy variable 3-7",
                "gene_name": "IGHV3-7",
                "tax_name": "Human"
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                "uniprot_canonical_ac": "P01782-1",
                "protein_name": "Immunoglobulin heavy variable 3-9",
                "gene_name": "IGHV3-9",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "A0M8Q6-1",
                "protein_name": "Immunoglobulin lambda constant 7",
                "gene_name": "IGLC7",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01834-1",
                "protein_name": "Immunoglobulin kappa constant",
                "gene_name": "IGKC",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01859-2",
                "protein_name": "Immunoglobulin heavy constant gamma 2",
                "gene_name": "IGHG2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P0CG04-1",
                "protein_name": "Immunoglobulin lambda constant 1",
                "gene_name": "IGLC1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P0DOY3-1",
                "protein_name": "Immunoglobulin lambda constant 3",
                "gene_name": "IGLC3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P13987-1",
                "protein_name": "CD59 glycoprotein",
                "gene_name": "CD59",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P60033-1",
                "protein_name": "CD81 antigen",
                "gene_name": "CD81",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P21730-1",
                "protein_name": "C5a anaphylatoxin chemotactic receptor 1",
                "gene_name": "C5AR1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15169-1",
                "protein_name": "Carboxypeptidase N catalytic chain",
                "gene_name": "CPN1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01024-1",
                "protein_name": "Complement C3",
                "gene_name": "C3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P00751-1",
                "protein_name": "Complement factor B",
                "gene_name": "CFB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01743-1",
                "protein_name": "Immunoglobulin heavy variable 1-46",
                "gene_name": "IGHV1-46",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P27918-1",
                "protein_name": "Properdin",
                "gene_name": "CFP",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A0C4DH73-1",
                "protein_name": "Immunoglobulin kappa variable 1-12",
                "gene_name": "IGKV1-12",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A2NJV5-1",
                "protein_name": "Immunoglobulin kappa variable 2-29",
                "gene_name": "IGKV2-29",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01594-1",
                "protein_name": "Immunoglobulin kappa variable 1-33",
                "gene_name": "IGKV1-33",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P04430-1",
                "protein_name": "Immunoglobulin kappa variable 1-16",
                "gene_name": "IGKV1-16",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01857-2",
                "protein_name": "Immunoglobulin heavy constant gamma 1",
                "gene_name": "IGHG1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q03591-1",
                "protein_name": "Complement factor H-related protein 1",
                "gene_name": "CFHR1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P01700",
                        "url": "https://www.uniprot.org/uniprotkb/P01700"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.978134",
        "abstract": "",
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    {
        "title": "Cbl-mediated negative regulation of the Syk tyrosine kinase. A critical role for Cbl phosphotyrosine-binding domain binding to Syk phosphotyrosine 323.",
        "journal": "The Journal of biological chemistry",
        "date": "1998",
        "authors": "Lupher ML Jr, Rao N, Lill NL, Andoniou CE, Miyake S, Clark EA, Druker B, Band H",
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    {
        "title": "Definition of the sites of interaction between the protein tyrosine phosphatase SHP-1 and CD22.",
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        "title": "Mechanism of activation of Pak1 kinase by membrane localization.",
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    {
        "title": "Molecular cloning and expression of Galbeta1,3GalNAc alpha2, 3-sialyltransferase from human fetal liver.",
        "journal": "European journal of biochemistry",
        "date": "1999",
        "authors": "Shang J, Qiu R, Wang J, Liu J, Zhou R, Ding H, Yang S, Zhang S, Jin C",
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    {
        "title": "Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene.",
        "journal": "Nature genetics",
        "date": "2000",
        "authors": "Akama TO, Nishida K, Nakayama J, Watanabe H, Ozaki K, Nakamura T, Dota A, Kawasaki S, Inoue Y, Maeda N, Yamamoto S, Fujiwara T, Thonar EJ, Shimomura Y, Kinoshita S, Tanigami A, Fukuda MN",
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    {
        "title": "Functional expression and genomic structure of human N-acetylglucosamine-6-O-sulfotransferase that transfers sulfate to beta-N-acetylglucosamine at the nonreducing end of an N-acetyllactosamine sequence.",
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        ],
        "species": [
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                "name": "Homo sapiens",
                "taxid": 9606,
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        ],
        "record_id": "pubmed.11042394",
        "abstract": "",
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    {
        "title": "Molecular cloning and characterization of UDP-GlcNAc:lactosylceramide beta 1,3-N-acetylglucosaminyltransferase (beta 3Gn-T5), an essential enzyme for the expression of HNK-1 and Lewis X epitopes on glycolipids.",
        "journal": "The Journal of biological chemistry",
        "date": "2001",
        "authors": "Togayachi A, Akashima T, Ookubo R, Kudo T, Nishihara S, Iwasaki H, Natsume A, Mio H, Inokuchi J, Irimura T, Sasaki K, Narimatsu H",
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    {
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                    {
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                "table_id": "glycosylation_automatic_literature_mining",
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        ]
    },
    {
        "title": "Molecular cloning and characterization of a novel UDP-GlcNAc:GalNAc-peptide beta1,3-N-acetylglucosaminyltransferase (beta 3Gn-T6), an enzyme synthesizing the core 3 structure of O-glycans.",
        "journal": "The Journal of biological chemistry",
        "date": "2002",
        "authors": "Iwai T, Inaba N, Naundorf A, Zhang Y, Gotoh M, Iwasaki H, Kudo T, Togayachi A, Ishizuka Y, Nakanishi H, Narimatsu H",
        "reference": {
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            "id": "11821425",
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                "uniprot_canonical_ac": "Q9H195-1",
                "protein_name": "Mucin-3B",
                "gene_name": "MUC3B",
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                "uniprot_canonical_ac": "Q14435-1",
                "protein_name": "Polypeptide N-acetylgalactosaminyltransferase 3",
                "gene_name": "GALNT3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q06828-1",
                "protein_name": "Fibromodulin",
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            },
            {
                "uniprot_canonical_ac": "Q6P9A2-1",
                "protein_name": "Polypeptide N-acetylgalactosaminyltransferase 18",
                "gene_name": "GALNT18",
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            },
            {
                "uniprot_canonical_ac": "Q86SR1-1",
                "protein_name": "Polypeptide N-acetylgalactosaminyltransferase 10",
                "gene_name": "GALNT10",
                "tax_name": "Human"
            },
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                "protein_name": "Polypeptide N-acetylgalactosaminyltransferase 12",
                "gene_name": "GALNT12",
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            },
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                "uniprot_canonical_ac": "Q8N428-1",
                "protein_name": "Polypeptide N-acetylgalactosaminyltransferase 16",
                "gene_name": "GALNT16",
                "tax_name": "Human"
            },
            {
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            },
            {
                "uniprot_canonical_ac": "Q8NCG5-1",
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            },
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                "uniprot_canonical_ac": "Q76EJ3-1",
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        ],
        "species": [
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                "name": "Homo sapiens",
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        ],
        "record_id": "pubmed.11821425",
        "abstract": "",
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    {
        "title": "Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.",
        "journal": "The Journal of clinical investigation",
        "date": "2002",
        "authors": "Hansske B, Thiel C, Lubke T, Hasilik M, Honing S, Peters V, Heidemann PH, Hoffmann GF, Berger EG, von Figura K, Korner C",
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        ],
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                ],
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                                "description": "B4GALT1-CDG is a congenital disorder of glycosylation characterized by macrocephaly due to Dandy-Walker malformation, hydrocephaly, hypotonia, myopathy and coagulation anomalies. To date, only one case has been reported. The syndrome is associated with mutations in the GALT1 gene (localized to region q13 of chromosome 9) leading to a deficiency in the Golgi apparatus enzyme beta-1,4-galactosyl transferase."
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                            {
                                "id": "MONDO:0011772",
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                                "id": "MIM:607091",
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                                "url": "https://www.omim.org/entry/607091",
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                                "url": "https://www.omim.org/entry/607091"
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                                "id": "2683",
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        "title": "Screening for N-glycosylated proteins by liquid chromatography mass spectrometry.",
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        "abstract": "",
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    {
        "title": "Characterization of a cDNA encoding a protein with limited similarity to beta1, 3-N-acetylglucosaminyltransferase.",
        "journal": "Molecular biology reports",
        "date": "2004",
        "authors": "Zheng H, Li Y, Ji C, Li J, Zhang J, Yin G, Xu J, Ye X, Wu M, Zou X, Gu S, Xie Y, Mao Y",
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    {
        "title": "A novel beta1,3-N-acetylglucosaminyltransferase (beta3Gn-T8), which synthesizes poly-N-acetyllactosamine, is dramatically upregulated in colon cancer.",
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        "authors": "Ishida H, Togayachi A, Sakai T, Iwai T, Hiruma T, Sato T, Okubo R, Inaba N, Kudo T, Gotoh M, Shoda J, Tanaka N, Narimatsu H",
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    {
        "title": "Transition of galactosyltransferase 1 from trans-Golgi cisterna to the trans-Golgi network is signal mediated.",
        "journal": "Molecular biology of the cell",
        "date": "2006",
        "authors": "Schaub BE, Berger B, Berger EG, Rohrer J",
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        "title": "West syndrome caused by ST3Gal-III deficiency.",
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        "title": "Human glucosamine-6-sulfatase cDNA reveals homology with steroid sulfatase.",
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        "authors": "Robertson DA, Freeman C, Nelson PV, Morris CP, Hopwood JJ",
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    {
        "title": "Cloning and expression of human Gal beta 1,3(4)GlcNAc alpha 2,3-sialyltransferase.",
        "journal": "Biochemical and biophysical research communications",
        "date": "1993",
        "authors": "Kitagawa H, Paulson JC",
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        "species": [
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                "name": "Homo sapiens",
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        "record_id": "pubmed.8333853",
        "abstract": "",
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                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "table_stats": [
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                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
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                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
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                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Characterization of two glycolipid: alpha 2-3sialyltransferases, SAT-3 (CMP-NeuAc:nLcOse4Cer alpha 2-3sialyltransferase) and SAT-4 (CMP-NeuAc:GgOse4Cer alpha 2-3sialyltransferase), from human colon carcinoma (Colo 205) cell line.",
        "journal": "Biochemistry",
        "date": "1996",
        "authors": "Basu SS, Basu M, Li Z, Basu S",
        "reference": {
            "type": "PubMed",
            "id": "8611500",
            "url": "https://pubmed.ncbi.nlm.nih.gov/8611500"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P51884-1",
                "protein_name": "Lumican",
                "gene_name": "LUM",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P78382-1",
                "protein_name": "CMP-sialic acid transporter",
                "gene_name": "SLC35A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O15466-1",
                "protein_name": "Alpha-2,8-sialyltransferase 8E",
                "gene_name": "ST8SIA5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BXD5-1",
                "protein_name": "N-acetylneuraminate lyase",
                "gene_name": "NPL",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9H195-1",
                "protein_name": "Mucin-3B",
                "gene_name": "MUC3B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43916-1",
                "protein_name": "Carbohydrate sulfotransferase 1",
                "gene_name": "CHST1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q06828-1",
                "protein_name": "Fibromodulin",
                "gene_name": "FMOD",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y4C5-1",
                "protein_name": "Carbohydrate sulfotransferase 2",
                "gene_name": "CHST2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NRA2-1",
                "protein_name": "Sialin",
                "gene_name": "SLC17A5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9GZS9-1",
                "protein_name": "Carbohydrate sulfotransferase 5",
                "gene_name": "CHST5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9GZX3-1",
                "protein_name": "Carbohydrate sulfotransferase 6",
                "gene_name": "CHST6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P16112-1",
                "protein_name": "Aggrecan core protein",
                "gene_name": "ACAN",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8TBE9-1",
                "protein_name": "N-acylneuraminate-9-phosphatase",
                "gene_name": "NANP",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UQ49-1",
                "protein_name": "Sialidase-3",
                "gene_name": "NEU3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y3R4-1",
                "protein_name": "Sialidase-2",
                "gene_name": "NEU2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q99983-1",
                "protein_name": "Osteomodulin",
                "gene_name": "OMD",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P10619-1",
                "protein_name": "Lysosomal protective protein",
                "gene_name": "CTSA",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q76EJ3-1",
                "protein_name": "Nucleotide sugar transporter SLC35D2",
                "gene_name": "SLC35D2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q11201-1",
                "protein_name": "CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1",
                "gene_name": "ST3GAL1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NSC7-1",
                "protein_name": "Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1",
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                "tax_name": "Human"
            },
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                "protein_name": "Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3",
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                "tax_name": "Human"
            },
            {
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                "protein_name": "CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 2",
                "gene_name": "ST3GAL2",
                "tax_name": "Human"
            },
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                "uniprot_canonical_ac": "Q9UJ37-1",
                "protein_name": "Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2",
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                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15907-1",
                "protein_name": "Beta-galactoside alpha-2,6-sialyltransferase 1",
                "gene_name": "ST6GAL1",
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            },
            {
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                "protein_name": "Lactosylceramide alpha-2,3-sialyltransferase",
                "gene_name": "ST3GAL5",
                "tax_name": "Human"
            },
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                "uniprot_canonical_ac": "Q92185-1",
                "protein_name": "Alpha-N-acetylneuraminide alpha-2,8-sialyltransferase",
                "gene_name": "ST8SIA1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q92186-1",
                "protein_name": "Alpha-2,8-sialyltransferase 8B",
                "gene_name": "ST8SIA2",
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            },
            {
                "uniprot_canonical_ac": "Q9BVH7-1",
                "protein_name": "Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 5",
                "gene_name": "ST6GALNAC5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q11203-1",
                "protein_name": "CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase",
                "gene_name": "ST3GAL3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q969X2-1",
                "protein_name": "Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6",
                "gene_name": "ST6GALNAC6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96JF0-1",
                "protein_name": "Beta-galactoside alpha-2,6-sialyltransferase 2",
                "gene_name": "ST6GAL2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9H4F1-1",
                "protein_name": "Alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase",
                "gene_name": "ST6GALNAC4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43505-1",
                "protein_name": "Beta-1,4-glucuronyltransferase 1",
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                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P16278-1",
                "protein_name": "Beta-galactosidase",
                "gene_name": "GLB1",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "Q9NY97-1",
                "protein_name": "N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2",
                "gene_name": "B3GNT2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O60513-1",
                "protein_name": "Beta-1,4-galactosyltransferase 4",
                "gene_name": "B4GALT4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43286-1",
                "protein_name": "Beta-1,4-galactosyltransferase 5",
                "gene_name": "B4GALT5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q7LGC8-1",
                "protein_name": "Carbohydrate sulfotransferase 3",
                "gene_name": "CHST3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q99102-1",
                "protein_name": "Mucin-4",
                "gene_name": "MUC4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96DR8-1",
                "protein_name": "Mucin-like protein 1",
                "gene_name": "MUCL1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P98088-1",
                "protein_name": "Mucin-5AC",
                "gene_name": "MUC5AC",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9HC84-1",
                "protein_name": "Mucin-5B",
                "gene_name": "MUC5B",
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            },
            {
                "uniprot_canonical_ac": "O60938-1",
                "protein_name": "Keratocan",
                "gene_name": "KERA",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y274-1",
                "protein_name": "Type 2 lactosamine alpha-2,3-sialyltransferase",
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                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P61647-1",
                "protein_name": "Alpha-2,8-sialyltransferase 8F",
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            },
            {
                "uniprot_canonical_ac": "Q92187-1",
                "protein_name": "CMP-N-acetylneuraminate-poly-alpha-2,8-sialyltransferase",
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            {
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            },
            {
                "uniprot_canonical_ac": "Q9NR45-1",
                "protein_name": "N-acetylneuraminate-9-phosphate synthase",
                "gene_name": "NANS",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P20774-1",
                "protein_name": "Mimecan",
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                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q99519-1",
                "protein_name": "Sialidase-1",
                "gene_name": "NEU1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8WWR8-1",
                "protein_name": "Sialidase-4",
                "gene_name": "NEU4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q02817-1",
                "protein_name": "Mucin-2",
                "gene_name": "MUC2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8TAX7-1",
                "protein_name": "Mucin-7",
                "gene_name": "MUC7",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O60909-1",
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            },
            {
                "uniprot_canonical_ac": "Q9Y223-1",
                "protein_name": "Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase",
                "gene_name": "GNE",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UBX8-1",
                "protein_name": "Beta-1,4-galactosyltransferase 6",
                "gene_name": "B4GALT6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O60512-1",
                "protein_name": "Beta-1,4-galactosyltransferase 3",
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            },
            {
                "uniprot_canonical_ac": "P15291-1",
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            },
            {
                "uniprot_canonical_ac": "Q8NFL0-1",
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            },
            {
                "uniprot_canonical_ac": "Q9Y2A9-1",
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            },
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            },
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            },
            {
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            {
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            {
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            },
            {
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                "protein_name": "Mucin-1",
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                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P51884",
                        "url": "https://www.uniprot.org/uniprotkb/P51884"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.8611500",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
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        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
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                        "count": 75
                    }
                ],
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                    {
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                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Molecular cloning and expression of human Gal beta 1,3GalNAc alpha 2,3-sialytransferase (hST3Gal II).",
        "journal": "Biochemical and biophysical research communications",
        "date": "1996",
        "authors": "Kim YJ, Kim KS, Kim SH, Kim CH, Ko JH, Choe IS, Tsuji S, Lee YC",
        "reference": {
            "type": "PubMed",
            "id": "8920913",
            "url": "https://pubmed.ncbi.nlm.nih.gov/8920913"
        },
        "referenced_glycans": [],
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                "uniprot_canonical_ac": "P51884-1",
                "protein_name": "Lumican",
                "gene_name": "LUM",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P78382-1",
                "protein_name": "CMP-sialic acid transporter",
                "gene_name": "SLC35A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O15466-1",
                "protein_name": "Alpha-2,8-sialyltransferase 8E",
                "gene_name": "ST8SIA5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BXD5-1",
                "protein_name": "N-acetylneuraminate lyase",
                "gene_name": "NPL",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9H195-1",
                "protein_name": "Mucin-3B",
                "gene_name": "MUC3B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43916-1",
                "protein_name": "Carbohydrate sulfotransferase 1",
                "gene_name": "CHST1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q06828-1",
                "protein_name": "Fibromodulin",
                "gene_name": "FMOD",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y4C5-1",
                "protein_name": "Carbohydrate sulfotransferase 2",
                "gene_name": "CHST2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NRA2-1",
                "protein_name": "Sialin",
                "gene_name": "SLC17A5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9GZS9-1",
                "protein_name": "Carbohydrate sulfotransferase 5",
                "gene_name": "CHST5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9GZX3-1",
                "protein_name": "Carbohydrate sulfotransferase 6",
                "gene_name": "CHST6",
                "tax_name": "Human"
            },
            {
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                "protein_name": "Aggrecan core protein",
                "gene_name": "ACAN",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8TBE9-1",
                "protein_name": "N-acylneuraminate-9-phosphatase",
                "gene_name": "NANP",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UQ49-1",
                "protein_name": "Sialidase-3",
                "gene_name": "NEU3",
                "tax_name": "Human"
            },
            {
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                "protein_name": "Sialidase-2",
                "gene_name": "NEU2",
                "tax_name": "Human"
            },
            {
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                "tax_name": "Human"
            },
            {
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                "protein_name": "Lysosomal protective protein",
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                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q76EJ3-1",
                "protein_name": "Nucleotide sugar transporter SLC35D2",
                "gene_name": "SLC35D2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q11201-1",
                "protein_name": "CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1",
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                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NSC7-1",
                "protein_name": "Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1",
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            },
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                "protein_name": "Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3",
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            {
                "uniprot_canonical_ac": "Q9UJ37-1",
                "protein_name": "Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2",
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            },
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                "uniprot_canonical_ac": "Q969X2-1",
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                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96JF0-1",
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                "uniprot_canonical_ac": "Q9H4F1-1",
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                "gene_name": "ST6GALNAC4",
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            {
                "uniprot_canonical_ac": "Q9NY97-1",
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                "gene_name": "B3GNT2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O60513-1",
                "protein_name": "Beta-1,4-galactosyltransferase 4",
                "gene_name": "B4GALT4",
                "tax_name": "Human"
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            {
                "uniprot_canonical_ac": "O43286-1",
                "protein_name": "Beta-1,4-galactosyltransferase 5",
                "gene_name": "B4GALT5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q16880-1",
                "protein_name": "2-hydroxyacylsphingosine 1-beta-galactosyltransferase",
                "gene_name": "UGT8",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q16739-1",
                "protein_name": "Ceramide glucosyltransferase",
                "gene_name": "UGCG",
                "tax_name": "Human"
            },
            {
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                "protein_name": "Carbohydrate sulfotransferase 3",
                "gene_name": "CHST3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8TCT0-1",
                "protein_name": "Ceramide kinase",
                "gene_name": "CERK",
                "tax_name": "Human"
            },
            {
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            },
            {
                "uniprot_canonical_ac": "Q96DR8-1",
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            {
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            },
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            },
            {
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                "tax_name": "Human"
            },
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            },
            {
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                "gene_name": "GAL3ST1",
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            },
            {
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            {
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                "uniprot_canonical_ac": "O60909-1",
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            },
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            },
            {
                "uniprot_canonical_ac": "Q9Y223-1",
                "protein_name": "Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase",
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            },
            {
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                "protein_name": "Beta-1,4-galactosyltransferase 6",
                "gene_name": "B4GALT6",
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            },
            {
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            },
            {
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                "gene_name": "B4GALT1",
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            },
            {
                "uniprot_canonical_ac": "Q8NFL0-1",
                "protein_name": "UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7",
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            },
            {
                "uniprot_canonical_ac": "Q9Y2A9-1",
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            },
            {
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            {
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        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "P51884",
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                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
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        ],
        "record_id": "pubmed.8920913",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
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        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
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                        "count": 86
                    }
                ],
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    {
        "title": "The expanding beta 4-galactosyltransferase gene family: messages from the databanks.",
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        "authors": "Lo NW, Shaper JH, Pevsner J, Shaper NL",
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                        "count": 0
                    },
                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
                    },
                    {
                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            }
        ]
    },
    {
        "title": "Analysis of protein-coding genetic variation in 60,706 humans.",
        "journal": "Nature",
        "date": "2016",
        "authors": "Lek M, Karczewski KJ, Minikel EV, Samocha KE, Banks E, Fennell T, O'Donnell-Luria AH, Ware JS, Hill AJ, Cummings BB, Tukiainen T, Birnbaum DP, Kosmicki JA, Duncan LE, Estrada K, Zhao F, Zou J, Pierce-Hoffman E, Berghout J, Cooper DN, Deflaux N, DePristo M, Do R, Flannick J, Fromer M, Gauthier L, Goldstein J, Gupta N, Howrigan D, Kiezun A, Kurki MI, Moonshine AL, Natarajan P, Orozco L, Peloso GM, Poplin R, Rivas MA, Ruano-Rubio V, Rose SA, Ruderfer DM, Shakir K, Stenson PD, Stevens C, Thomas BP, Tiao G, Tusie-Luna MT, Weisburd B, Won HH, Yu D, Altshuler DM, Ardissino D, Boehnke M, Danesh J, Donnelly S, Elosua R, Florez JC, Gabriel SB, Getz G, Glatt SJ, Hultman CM, Kathiresan S, Laakso M, McCarroll S, McCarthy MI, McGovern D, McPherson R, Neale BM, Palotie A, Purcell SM, Saleheen D, Scharf JM, Sklar P, Sullivan PF, Tuomilehto J, Tsuang MT, Watkins HC, Wilson JG, Daly MJ, MacArthur DG",
        "reference": {
            "type": "PubMed",
            "id": "27535533",
            "url": "https://pubmed.ncbi.nlm.nih.gov/27535533"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "Q03252-1",
                "protein_name": "Lamin-B2",
                "gene_name": "LMNB2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P35499-1",
                "protein_name": "Sodium channel protein type 4 subunit alpha",
                "gene_name": "SCN4A",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9HC10-1",
                "protein_name": "Otoferlin",
                "gene_name": "OTOF",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q02094-1",
                "protein_name": "Ammonium transporter Rh type A",
                "gene_name": "RHAG",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P43694-1",
                "protein_name": "Transcription factor GATA-4",
                "gene_name": "GATA4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O14832-1",
                "protein_name": "Phytanoyl-CoA dioxygenase, peroxisomal",
                "gene_name": "PHYH",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O60243-1",
                "protein_name": "Heparan-sulfate 6-O-sulfotransferase 1",
                "gene_name": "HS6ST1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9HAZ2-1",
                "protein_name": "Histone-lysine N-methyltransferase PRDM16",
                "gene_name": "PRDM16",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43511-1",
                "protein_name": "Pendrin",
                "gene_name": "SLC26A4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q16518-1",
                "protein_name": "Retinoid isomerohydrolase",
                "gene_name": "RPE65",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NPF0-1",
                "protein_name": "CD320 antigen",
                "gene_name": "CD320",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P19235-1",
                "protein_name": "Erythropoietin receptor",
                "gene_name": "EPOR",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8IZT6-1",
                "protein_name": "Abnormal spindle-like microcephaly-associated protein",
                "gene_name": "ASPM",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q92851-1",
                "protein_name": "Caspase-10",
                "gene_name": "CASP10",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P12110-1",
                "protein_name": "Collagen alpha-2(VI) chain",
                "gene_name": "COL6A2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NWW5-1",
                "protein_name": "Ceroid-lipofuscinosis neuronal protein 6",
                "gene_name": "CLN6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15313-1",
                "protein_name": "V-type proton ATPase subunit B, kidney isoform",
                "gene_name": "ATP6V1B1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P41220-1",
                "protein_name": "Regulator of G protein signaling 2",
                "gene_name": "RGS2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P31327-1",
                "protein_name": "Carbamoyl-phosphate synthase [ammonia], mitochondrial",
                "gene_name": "CPS1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q3T906-1",
                "protein_name": "N-acetylglucosamine-1-phosphotransferase subunits alpha/beta",
                "gene_name": "GNPTAB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O60260-1",
                "protein_name": "E3 ubiquitin-protein ligase parkin",
                "gene_name": "PRKN",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UBY8-1",
                "protein_name": "Protein CLN8",
                "gene_name": "CLN8",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P51993-1",
                "protein_name": "4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT6",
                "gene_name": "FUT6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P11413-1",
                "protein_name": "Glucose-6-phosphate 1-dehydrogenase",
                "gene_name": "G6PD",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P16930-1",
                "protein_name": "Fumarylacetoacetase",
                "gene_name": "FAH",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y223-1",
                "protein_name": "Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase",
                "gene_name": "GNE",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43464-1",
                "protein_name": "Serine protease HTRA2, mitochondrial",
                "gene_name": "HTRA2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P14138-1",
                "protein_name": "Endothelin-3",
                "gene_name": "EDN3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6ZVD7-1",
                "protein_name": "Storkhead-box protein 1",
                "gene_name": "STOX1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q86TC9-1",
                "protein_name": "Myopalladin",
                "gene_name": "MYPN",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q86W24-1",
                "protein_name": "NACHT, LRR and PYD domains-containing protein 14",
                "gene_name": "NLRP14",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P07225-1",
                "protein_name": "Vitamin K-dependent protein S",
                "gene_name": "PROS1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q969X6-1",
                "protein_name": "U3 small nucleolar RNA-associated protein 4 homolog",
                "gene_name": "UTP4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O75695-1",
                "protein_name": "Protein XRP2",
                "gene_name": "RP2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P19878-1",
                "protein_name": "Neutrophil cytosol factor 2",
                "gene_name": "NCF2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P10070-5",
                "protein_name": "Transcription activator GLI2",
                "gene_name": "GLI2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O95477-1",
                "protein_name": "Phospholipid-transporting ATPase ABCA1",
                "gene_name": "ABCA1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43186-1",
                "protein_name": "Cone-rod homeobox protein",
                "gene_name": "CRX",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P10275-1",
                "protein_name": "Androgen receptor",
                "gene_name": "AR",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q03252",
                        "url": "https://www.uniprot.org/uniprotkb/Q03252"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "O60243",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/O60243"
                    },
                    {
                        "id": "rs199538589",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs199538589"
                    },
                    {
                        "id": "rs199538589",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs199538589"
                    },
                    {
                        "id": "rs199538589",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs199538589"
                    },
                    {
                        "id": "rs199538589",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs199538589#frequency_tab"
                    },
                    {
                        "id": "rs199538589",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs199538589"
                    },
                    {
                        "id": "21700882",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/21700882"
                    },
                    {
                        "id": "27535533",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/27535533"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 382,
                "end_pos": 382,
                "subjects_tested": "4177",
                "subjects_positive": "1",
                "frequency": "0.0",
                "sequence_org": "R",
                "sequence_mut": "W",
                "comment": "Somatic mutation passed 1 filters: protein-of-interest(glycogene, sulfotransferase).",
                "chr_id": "2",
                "chr_pos": "128268254",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R382",
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                    {
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                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:10283",
                            "name": "prostate cancer",
                            "description": "A male reproductive organ cancer that is located_in the prostate."
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                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "NGP - new growth of prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "hereditary prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "malignant tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
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                                "description": ""
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                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostate neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "prostatic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:10283",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:10283",
                                "name": "tumor of the prostate",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "HPCX1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010257",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                                "name": "prostate cancer, hereditary, X-linked 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "HPCX2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010405",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010405",
                                "name": "prostate cancer, hereditary, X-linked 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the RNASEL gene."
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "RNASEL familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "familial prostate cancer caused by mutation in RNASEL",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "prostate cancer, hereditary, type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011098",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                                "name": "HPC1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "prostate cancer, hereditary, type 8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011270",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                                "name": "HPC8",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, hereditary, type 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "prostate cancer, susceptibility to, 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012093",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012093",
                                "name": "HPC3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, hereditary, type 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "prostate cancer, susceptibility to, 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012094",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                                "name": "HPC4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "prostate cancer, hereditary, type 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012244",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012244",
                                "name": "HPC5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "prostate cancer, hereditary, type 6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012300",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                                "name": "HPC6",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "HPC7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012470",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                                "name": "prostate cancer, hereditary, 7",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "prostate cancer, hereditary, type 9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012597",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012597",
                                "name": "HPC9",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "HPC10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012620",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012620",
                                "name": "prostate cancer, hereditary, 10",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the EHBP1 gene."
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "EHBP1 familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "familial prostate cancer caused by mutation in EHBP1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "prostate cancer, hereditary, type 12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012741",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012741",
                                "name": "HPC12",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": "Any familial prostate cancer in which the cause of the disease is a mutation in the MSMB gene."
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "MSMB familial prostate cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "familial prostate cancer caused by mutation in MSMB",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "prostate cancer, hereditary, type 13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012758",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012758",
                                "name": "HPC13",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "HPC11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012768",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012768",
                                "name": "prostate cancer, hereditary, 11",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "HPC14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012769",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012769",
                                "name": "prostate cancer, hereditary, 14",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "HPC15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012770",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012770",
                                "name": "prostate cancer, hereditary, 15",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0700275",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0700275",
                                "name": "prostate cancer, hereditary",
                                "description": "An instance of prostate cancer that is caused by an inherited genomic modification in an individual. Familial prostate cancer (FPC) is a malignant tumor of the prostate with an early onset. FPC is either asymptomatic or causes mictionary symptoms, erectile dysfunction, bone pain, venous compression and infectious or inflammatory syndrome (for the metastatic forms). It is also characterized by familial antecedents."
                            },
                            {
                                "id": "MIM:601518",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/601518",
                                "name": "Prostate cancer, hereditary, 1",
                                "description": "Prostate cancer, hereditary, 1"
                            },
                            {
                                "id": "MIM:610997",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/610997",
                                "name": "Prostate cancer, hereditary, 9",
                                "description": "Prostate cancer, hereditary, 9"
                            },
                            {
                                "id": "MIM:611868",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611868",
                                "name": "Prostate cancer, hereditary, 12",
                                "description": "Prostate cancer, hereditary, 12"
                            },
                            {
                                "id": "MIM:611928",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611928",
                                "name": "Prostate cancer, hereditary, 13",
                                "description": "Prostate cancer, hereditary, 13"
                            },
                            {
                                "id": "MIM:611955",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/611955",
                                "name": "Prostate cancer, hereditary, 11",
                                "description": "Prostate cancer, hereditary, 11"
                            },
                            {
                                "id": "MIM:176807",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/176807",
                                "name": "Prostate cancer",
                                "description": "Prostate cancer"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "10283",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:10283"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090075",
                        "recommended_name": {
                            "id": "DOID:0090075",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090075",
                            "name": "hypogonadotropic hypogonadism 15 with or without anosmia",
                            "description": "A hypogonadotropic hypogonadism that has_material_basis_in mutation in the HS6ST1 gene on chromosome 2q14, sometimes in association with mutations in other genes."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0013946",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013946",
                                "name": "hypogonadotropic hypogonadism 15 with or without anosmia",
                                "description": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the HS6ST1 gene."
                            },
                            {
                                "id": "MONDO:0013946",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013946",
                                "name": "HS6ST1 hypogonadotropic hypogonadism",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013946",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013946",
                                "name": "hypogonadotropic hypogonadism 15 with or without anosmia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013946",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013946",
                                "name": "hypogonadotropic hypogonadism caused by mutation in HS6ST1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013946",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013946",
                                "name": "HH15",
                                "description": ""
                            },
                            {
                                "id": "MIM:614880",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/614880",
                                "name": "Hypogonadotropic hypogonadism 15 with or without anosmia",
                                "description": "Hypogonadotropic hypogonadism 15 with or without anosmia"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "614880",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/614880"
                            },
                            {
                                "id": "0090075",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090075"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090078",
                        "recommended_name": {
                            "id": "DOID:0090078",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090078",
                            "name": "hypogonadotropic hypogonadism 7 with or without anosmia",
                            "description": "A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0007794",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007794",
                                "name": "hypogonadotropic hypogonadism 7 with or without anosmia",
                                "description": "A hypogonadotropic hypogonadism that has material basis in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported."
                            },
                            {
                                "id": "MONDO:0007794",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007794",
                                "name": "hypogonadotropic hypogonadism 7 with or without anosmia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007794",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007794",
                                "name": "hypogonadotropic hypogonadism 7 without anosmia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007794",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007794",
                                "name": "HH7",
                                "description": ""
                            },
                            {
                                "id": "MIM:146110",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/146110",
                                "name": "Hypogonadotropic hypogonadism 7 with or without anosmia",
                                "description": "Hypogonadotropic hypogonadism 7 with or without anosmia"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090078",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090078"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ],
                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "O60243-1"
            },
            {
                "evidence": [
                    {
                        "id": "rs121908627",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs121908627"
                    },
                    {
                        "id": "rs121908627",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs121908627"
                    },
                    {
                        "id": "rs121908627",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs121908627"
                    },
                    {
                        "id": "rs121908627",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs121908627#frequency_tab"
                    },
                    {
                        "id": "rs121908627",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs121908627"
                    },
                    {
                        "id": "11528398",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11528398"
                    },
                    {
                        "id": "27535533",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/27535533"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 696,
                "end_pos": 696,
                "sequence_org": "V",
                "sequence_mut": "M",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/nucleotide synthesis.",
                "chr_id": "9",
                "chr_pos": "36217448",
                "ref_nt": "T",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "V696",
                "disease": [
                    {
                        "disease_id": "DOID:0080718",
                        "recommended_name": {
                            "id": "DOID:0080718",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0080718",
                            "name": "GNE myopathy",
                            "description": "A myopathy that is characterized by progressive skeletal muscle atrophy, distal muscle weakness and bilateral foot drop caused by weakness of the anterior tibialis muscles with onset in early adulthood, and that has_material_basis_in mutations in the GNE gene which encodes the rate-limiting enzyme of sialic acid biosynthesis."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0080718",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0080718",
                                "name": "Distal myopathy, Nonaka type",
                                "description": ""
                            },
                            {
                                "id": "DOID:0080718",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0080718",
                                "name": "Hereditary Inclusion Body Myopathy",
                                "description": ""
                            },
                            {
                                "id": "DOID:0080718",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0080718",
                                "name": "Nonaka myopathy",
                                "description": ""
                            },
                            {
                                "id": "DOID:0080718",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0080718",
                                "name": "inclusion body myopathy 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "GNE myopathy",
                                "description": "Nonaka distal myopathy (described in Japan) and the quadriceps-sparing autosomal recessive inclusion body myopathy type 2 (IBM2; independently described in Iranian Jews and later in other Jewish and non-Jewish populations) constitute the same pathological entity, distinguished by the sparing of quadriceps."
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "DMRV",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "HIBM2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "IBM2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "Nonaka myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "distal myopathy with rimmed vacuoles",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "distal myopathy, Nonaka type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "hereditary inclusion body myopathy type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "inclusion body myopathy autosomal recessive",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "inclusion body myopathy type 2",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "quadriceps-sparing myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "NM",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "QSM",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "inclusion body myopathy 2, autosomal recessive",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "inclusion body myopathy, autosomal recessive",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "inclusion body myopathy, quadriceps-sparing",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "quadriceps sparing myopathy",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011603",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603",
                                "name": "rimmed vacuole myopathy",
                                "description": ""
                            },
                            {
                                "id": "MIM:605820",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/605820",
                                "name": "Nonaka myopathy",
                                "description": "Nonaka myopathy"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0011603",
                                "database": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011603"
                            },
                            {
                                "id": "605820",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/605820"
                            },
                            {
                                "id": "GNE",
                                "database": "Genomics England",
                                "url": "https://panelapp.genomicsengland.co.uk/panels/25/gene/GNE/#!details"
                            },
                            {
                                "id": "10020",
                                "database": "GlyCosmos",
                                "url": "https://glycosmos.org/glycogenes/show/10020#disease"
                            },
                            {
                                "id": "0080718",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0080718"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:3659",
                        "recommended_name": {
                            "id": "DOID:3659",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:3659",
                            "name": "sialuria",
                            "description": "A lysosomal storage disease characterized by increased sialic acid in the urine."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0010028",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010028",
                                "name": "sialuria",
                                "description": "Sialuria is an extremely rare metabolic disorder described in fewer than 10 patients to date and characterized by variable signs and symptoms, mostly in infancy, including transient failure to thrive, slightly prolonged neonatal jaundice, equivocal or mild hepatomegaly, microcytic anemia, frequent upper respiratory infections, gastroenteritis, dehydration and flat and coarse facies. Learning difficulties and seizures may occur in childhood."
                            },
                            {
                                "id": "MONDO:0010028",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010028",
                                "name": "sialuria",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0010028",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0010028",
                                "name": "sialuria, French type",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011449",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011449",
                                "name": "Salla disease",
                                "description": "Salla disease is the mildest form of the free sialic acid storage disorders, which primarily affect the nervous system. Infants with Salla disease typically begin to experience poor muscle tone (hypotonia) during the first year of life,followed by slowly progressive neurological problems. Signs and symptoms include intellectual disability and developmental delay; seizures ; ataxia ; muscle spasticity; and involuntary slow movements of the limbs (athetosis). About one-third of affected children learn to walk. It is caused by mutations in the SLC17A5 gene and is inherited in an autosomal recessive manner. Treatment is generally symptomatic and supportive."
                            },
                            {
                                "id": "MONDO:0011449",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011449",
                                "name": "Salla disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011449",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011449",
                                "name": "sialic acid storage disease",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011449",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011449",
                                "name": "SD",
                                "description": ""
                            },
                            {
                                "id": "MIM:269921",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/269921",
                                "name": "Sialuria",
                                "description": "Sialuria"
                            },
                            {
                                "id": "MIM:604369",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/604369",
                                "name": "Salla disease",
                                "description": "Salla disease"
                            }
                        ],
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                        "evidence": [
                            {
                                "id": "269921",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/269921"
                            },
                            {
                                "id": "3659",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:3659"
                            },
                            {
                                "id": "3659",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:3659"
                            }
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    {
        "title": "Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy.",
        "journal": "Genetics in medicine : official journal of the American College of Medical Genetics",
        "date": "2021",
        "authors": "Parry DA, Martin CA, Greene P, Marsh JA, Blyth M, Cox H, Donnelly D, Greenhalgh L, Greville-Heygate S, Harrison V, Lachlan K, McKenna C, Quigley AJ, Rea G, Robertson L, Suri M, Jackson AP",
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        "title": "Lamin B2 contributes to the proliferation of bladder cancer cells via activating the expression of cell division cycle\u2011associated protein 3.",
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    {
        "title": "Characterization and mapping to human chromosome 8q24.3 of Ly-6-related gene 9804 encoding an apparent homologue of mouse TSA-1.",
        "journal": "J. Immunol.",
        "date": "1998",
        "authors": "Shan X, Bourdeau A, Rhoton A, Wells D E, Cohen E H, Landgraf B E, Palfree R G",
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    {
        "title": "Adaptor signalling proteins Grb2 and Grb7 are recruited by human G6f, a novel member of the immunoglobulin superfamily encoded in the MHC.",
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        "date": "2003",
        "authors": "De Vet EC, Aguado B, Campbell RD",
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    {
        "title": "Elucidation of N-glycosylation sites on human platelet proteins: a glycoproteomic approach.",
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        "date": "2006",
        "authors": "Lewandrowski U, Moebius J, Walter U, Sickmann A",
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