[
    {
        "title": "DJBP: a novel DJ-1-binding protein, negatively regulates the androgen receptor by recruiting histone deacetylase complex, and DJ-1 antagonizes this inhibition by abrogation of this complex.",
        "journal": "Molecular cancer research : MCR",
        "date": "2003",
        "authors": "Niki T, Takahashi-Niki K, Taira T, Iguchi-Ariga SM, Ariga H",
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        "abstract": "",
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    {
        "title": "Finishing the finished human chromosome 22 sequence.",
        "journal": "Genome Biol.",
        "date": "2008",
        "authors": "Cole Charlotte G, McCann Owen T, Collins John E, Oliver Karen, Willey David, Gribble Susan M, Yang Fengtang, McLaren Karen, Rogers Jane, Ning Zemin, Beare David M, Dunham Ian",
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                "uniprot_canonical_ac": "Q9UGU0-1",
                "protein_name": "Transcription factor 20",
                "gene_name": "TCF20",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43435-1",
                "protein_name": "T-box transcription factor TBX1",
                "gene_name": "TBX1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P85298-1",
                "protein_name": "Rho GTPase-activating protein 8",
                "gene_name": "ARHGAP8",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q10587-1",
                "protein_name": "Thyrotroph embryonic factor",
                "gene_name": "TEF",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6ICL7-1",
                "protein_name": "Solute carrier family 35 member E4",
                "gene_name": "SLC35E4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UDX4-1",
                "protein_name": "SEC14-like protein 3",
                "gene_name": "SEC14L3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q2NKQ1-1",
                "protein_name": "Small G protein signaling modulator 1",
                "gene_name": "SGSM1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8IWY4-1",
                "protein_name": "Signal peptide, CUB and EGF-like domain-containing protein 1",
                "gene_name": "SCUBE1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9H4I8-1",
                "protein_name": "Serine hydrolase-like protein 2",
                "gene_name": "SERHL2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96HU1-1",
                "protein_name": "Small G protein signaling modulator 3",
                "gene_name": "SGSM3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O00192-1",
                "protein_name": "Splicing regulator ARVCF",
                "gene_name": "ARVCF",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "B8ZZ34-1",
                "protein_name": "Protein shisa-8",
                "gene_name": "SHISA8",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q15735-1",
                "protein_name": "Phosphatidylinositol 4,5-bisphosphate 5-phosphatase A",
                "gene_name": "INPP5J",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6UXY1-1",
                "protein_name": "BAR/IMD domain-containing adapter protein 2-like 2",
                "gene_name": "BAIAP2L2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UBB4-1",
                "protein_name": "Ataxin-10",
                "gene_name": "ATXN10",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6UXH1-1",
                "protein_name": "Protein disulfide isomerase CRELD2",
                "gene_name": "CRELD2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96DF8-1",
                "protein_name": "Splicing factor ESS-2 homolog",
                "gene_name": "ESS2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O75791-1",
                "protein_name": "GRB2-related adapter protein 2",
                "gene_name": "GRAP2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8IWL3-1",
                "protein_name": "Iron-sulfur cluster co-chaperone protein HscB",
                "gene_name": "HSCB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15289-1",
                "protein_name": "Arylsulfatase A",
                "gene_name": "ARSA",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NQG6-1",
                "protein_name": "Mitochondrial dynamics protein MIEF1",
                "gene_name": "MIEF1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q7L3V2-1",
                "protein_name": "Protein Bop",
                "gene_name": "RTL10",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q00587-1",
                "protein_name": "Cdc42 effector protein 1",
                "gene_name": "CDC42EP1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O15371-1",
                "protein_name": "Eukaryotic translation initiation factor 3 subunit D",
                "gene_name": "EIF3D",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P11274-1",
                "protein_name": "Breakpoint cluster region protein",
                "gene_name": "BCR",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UJY5-1",
                "protein_name": "ADP-ribosylation factor-binding protein GGA1",
                "gene_name": "GGA1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UBR1-1",
                "protein_name": "Beta-ureidopropionase",
                "gene_name": "UPB1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BWT7-1",
                "protein_name": "Caspase recruitment domain-containing protein 10",
                "gene_name": "CARD10",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A8K8P3-1",
                "protein_name": "Protein SFI1 homolog",
                "gene_name": "SFI1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8IWD4-1",
                "protein_name": "Coiled-coil domain-containing protein 117",
                "gene_name": "CCDC117",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q12772-1",
                "protein_name": "Sterol regulatory element-binding protein 2",
                "gene_name": "SREBF2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q569K6-1",
                "protein_name": "Coiled-coil domain-containing protein 157",
                "gene_name": "CCDC157",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8WTX7-1",
                "protein_name": "Cytosolic arginine sensor for mTORC1 subunit 1",
                "gene_name": "CASTOR1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8WYQ3-1",
                "protein_name": "Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial",
                "gene_name": "CHCHD10",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8TCT0-1",
                "protein_name": "Ceramide kinase",
                "gene_name": "CERK",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A0A0MT92-1",
                "protein_name": "Immunoglobulin lambda joining 7",
                "gene_name": "IGLJ7",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O75419-1",
                "protein_name": "Cell division control protein 45 homolog",
                "gene_name": "CDC45",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6IBW4-1",
                "protein_name": "Condensin-2 complex subunit H2",
                "gene_name": "NCAPH2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q69YQ0-1",
                "protein_name": "Cytospin-A",
                "gene_name": "SPECC1L",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P35579-1",
                "protein_name": "Myosin-9",
                "gene_name": "MYH9",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q53GT1-1",
                "protein_name": "Kelch-like protein 22",
                "gene_name": "KLHL22",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P05162-1",
                "protein_name": "Galectin-2",
                "gene_name": "LGALS2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q969R2-1",
                "protein_name": "Oxysterol-binding protein 2",
                "gene_name": "OSBP2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96MU8-1",
                "protein_name": "Kremen protein 1",
                "gene_name": "KREMEN1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O00587-1",
                "protein_name": "Beta-1,3-N-acetylglucosaminyltransferase manic fringe",
                "gene_name": "MFNG",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q7RTP6-1",
                "protein_name": "[F-actin]-monooxygenase MICAL3",
                "gene_name": "MICAL3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P53778-1",
                "protein_name": "Mitogen-activated protein kinase 12",
                "gene_name": "MAPK12",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P24347-1",
                "protein_name": "Stromelysin-3",
                "gene_name": "MMP11",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O75648-1",
                "protein_name": "Mitochondrial tRNA-specific 2-thiouridylase 1",
                "gene_name": "TRMU",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BZR6-1",
                "protein_name": "Reticulon-4 receptor",
                "gene_name": "RTN4R",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O75600-1",
                "protein_name": "2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial",
                "gene_name": "GCAT",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96G42-1",
                "protein_name": "Kelch domain-containing protein 7B",
                "gene_name": "KLHDC7B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O95461-1",
                "protein_name": "Xylosyl- and glucuronyltransferase LARGE1",
                "gene_name": "LARGE1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P42356-1",
                "protein_name": "Phosphatidylinositol 4-kinase alpha",
                "gene_name": "PI4KA",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43808-1",
                "protein_name": "Peroxisomal membrane protein PMP34",
                "gene_name": "SLC25A17",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P56556-1",
                "protein_name": "NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6",
                "gene_name": "NDUFA6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P78395-1",
                "protein_name": "Melanoma antigen preferentially expressed in tumors",
                "gene_name": "PRAME",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P53814-1",
                "protein_name": "Smoothelin",
                "gene_name": "SMTN",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q13356-1",
                "protein_name": "RING-type E3 ubiquitin-protein ligase PPIL2",
                "gene_name": "PPIL2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q5THK1-1",
                "protein_name": "Protein PRR14L",
                "gene_name": "PRR14L",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P56706-1",
                "protein_name": "Protein Wnt-7b",
                "gene_name": "WNT7B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P32927-1",
                "protein_name": "Cytokine receptor common subunit beta",
                "gene_name": "CSF2RB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8IVS2-1",
                "protein_name": "Malonyl-CoA-acyl carrier protein transacylase, mitochondrial",
                "gene_name": "MCAT",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q2WGN9-1",
                "protein_name": "GRB2-associated-binding protein 4",
                "gene_name": "GAB4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UMW8-1",
                "protein_name": "Ubl carboxyl-terminal hydrolase 18",
                "gene_name": "USP18",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15814-1",
                "protein_name": "Immunoglobulin lambda-like polypeptide 1",
                "gene_name": "IGLL1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "B9A064-1",
                "protein_name": "Immunoglobulin lambda-like polypeptide 5",
                "gene_name": "IGLL5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9HBI1-1",
                "protein_name": "Beta-parvin",
                "gene_name": "PARVB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BXT6-1",
                "protein_name": "RNA helicase Mov10l1",
                "gene_name": "MOV10L1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6ICL3-1",
                "protein_name": "Transport and Golgi organization protein 2 homolog",
                "gene_name": "TANGO2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O60784-1",
                "protein_name": "Target of Myb1 membrane trafficking protein",
                "gene_name": "TOM1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P53007-1",
                "protein_name": "Tricarboxylate transport protein, mitochondrial",
                "gene_name": "SLC25A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A0A0MTA1-1",
                "protein_name": "Immunoglobulin lambda joining 4 (non-functional)",
                "gene_name": "IGLJ4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y262-1",
                "protein_name": "Eukaryotic translation initiation factor 3 subunit L",
                "gene_name": "EIF3L",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q14166-1",
                "protein_name": "Tubulin--tyrosine ligase-like protein 12",
                "gene_name": "TTLL12",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UNF0-1",
                "protein_name": "Protein kinase C and casein kinase substrate in neurons protein 2",
                "gene_name": "PACSIN2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O96015-1",
                "protein_name": "Dynein axonemal light chain 4",
                "gene_name": "DNAL4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96A84-1",
                "protein_name": "EMI domain-containing protein 1",
                "gene_name": "EMID1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P30046-1",
                "protein_name": "D-dopachrome decarboxylase",
                "gene_name": "DDT",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UHP6-1",
                "protein_name": "Radial spoke head 14 homolog",
                "gene_name": "RSPH14",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UH17-1",
                "protein_name": "DNA dC->dU-editing enzyme APOBEC-3B",
                "gene_name": "APOBEC3B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6NTF7-1",
                "protein_name": "DNA dC->dU-editing enzyme APOBEC-3H",
                "gene_name": "APOBEC3H",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96AK3-1",
                "protein_name": "DNA dC->dU-editing enzyme APOBEC-3D",
                "gene_name": "APOBEC3D",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y534-1",
                "protein_name": "Cold shock domain-containing protein C2",
                "gene_name": "CSDC2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NRA8-1",
                "protein_name": "Eukaryotic translation initiation factor 4E transporter",
                "gene_name": "EIF4ENIF1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q01844-1",
                "protein_name": "RNA-binding protein EWS",
                "gene_name": "EWSR1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6NXT1-1",
                "protein_name": "Ankyrin repeat domain-containing protein 54",
                "gene_name": "ANKRD54",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P49674-1",
                "protein_name": "Casein kinase I isoform epsilon",
                "gene_name": "CSNK1E",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P35240-1",
                "protein_name": "Merlin",
                "gene_name": "NF2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q09472-1",
                "protein_name": "Histone acetyltransferase p300",
                "gene_name": "EP300",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O95236-1",
                "protein_name": "Apolipoprotein L3",
                "gene_name": "APOL3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P35626-1",
                "protein_name": "G protein-coupled receptor kinase 3",
                "gene_name": "GRK3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q99757-1",
                "protein_name": "Thioredoxin, mitochondrial",
                "gene_name": "TXN2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NP61-1",
                "protein_name": "ADP-ribosylation factor GTPase-activating protein 3",
                "gene_name": "ARFGAP3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9HBI0-1",
                "protein_name": "Gamma-parvin",
                "gene_name": "PARVG",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NRD5-1",
                "protein_name": "PRKCA-binding protein",
                "gene_name": "PICK1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q92523-1",
                "protein_name": "Carnitine O-palmitoyltransferase 1, muscle isoform",
                "gene_name": "CPT1B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P30536-1",
                "protein_name": "Translocator protein",
                "gene_name": "TSPO",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43246-1",
                "protein_name": "Cationic amino acid transporter 4",
                "gene_name": "SLC7A4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8WYQ4-1",
                "protein_name": "Uncharacterized protein C22orf15",
                "gene_name": "C22orf15",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y3I1-1",
                "protein_name": "F-box only protein 7",
                "gene_name": "FBXO7",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q99999-1",
                "protein_name": "Galactosylceramide sulfotransferase",
                "gene_name": "GAL3ST1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q99501-1",
                "protein_name": "GAS2-like protein 1",
                "gene_name": "GAS2L1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BYB0-1",
                "protein_name": "SH3 and multiple ankyrin repeat domains protein 3",
                "gene_name": "SHANK3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P19440-1",
                "protein_name": "Glutathione hydrolase 1 proenzyme",
                "gene_name": "GGT1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P36269-1",
                "protein_name": "Glutathione hydrolase 5 proenzyme",
                "gene_name": "GGT5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q14390-1",
                "protein_name": "Glutathione hydrolase light chain 2",
                "gene_name": "GGTLC2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96RT7-1",
                "protein_name": "Gamma-tubulin complex component 6",
                "gene_name": "TUBGCP6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NNW7-1",
                "protein_name": "Thioredoxin reductase 2, mitochondrial",
                "gene_name": "TXNRD2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q5R3I4-1",
                "protein_name": "Tetratricopeptide repeat protein 38",
                "gene_name": "TTC38",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P19971-1",
                "protein_name": "Thymidine phosphorylase",
                "gene_name": "TYMP",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9ULC8-1",
                "protein_name": "Palmitoyltransferase ZDHHC8",
                "gene_name": "ZDHHC8",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q86YH2-1",
                "protein_name": "Zinc finger protein 280B",
                "gene_name": "ZNF280B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A0A0MT93-1",
                "protein_name": "Immunoglobulin lambda joining 6",
                "gene_name": "IGLJ6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A994J5G1-1",
                "protein_name": "Tubulin alpha 3f pseudogene",
                "gene_name": "TUBA3FP",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P17861-1",
                "protein_name": "X-box-binding protein 1",
                "gene_name": "XBP1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6P5X5-1",
                "protein_name": "Synaptic plasticity regulator PANTS",
                "gene_name": "C22orf39",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6NVV7-1",
                "protein_name": "Cysteine-rich DPF motif domain-containing protein 1",
                "gene_name": "CDPF1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q14106-1",
                "protein_name": "Protein Tob2",
                "gene_name": "TOB2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43251-1",
                "protein_name": "RNA binding protein fox-1 homolog 2",
                "gene_name": "RBFOX2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O00541-1",
                "protein_name": "Pescadillo homolog",
                "gene_name": "PES1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O95503-1",
                "protein_name": "Chromobox protein homolog 6",
                "gene_name": "CBX6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O95696-1",
                "protein_name": "Bromodomain-containing protein 1",
                "gene_name": "BRD1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8NFQ6-1",
                "protein_name": "BPI fold-containing family C protein",
                "gene_name": "BPIFC",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O95931-1",
                "protein_name": "Chromobox protein homolog 7",
                "gene_name": "CBX7",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8N5Z5-1",
                "protein_name": "BTB/POZ domain-containing protein KCTD17",
                "gene_name": "KCTD17",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y6J0-1",
                "protein_name": "Calcineurin-binding protein cabin-1",
                "gene_name": "CABIN1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UDX3-1",
                "protein_name": "SEC14-like protein 4",
                "gene_name": "SEC14L4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P49593-1",
                "protein_name": "Protein phosphatase 1F",
                "gene_name": "PPM1F",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8N3F8-1",
                "protein_name": "MICAL-like protein 1",
                "gene_name": "MICALL1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8NEG7-1",
                "protein_name": "Protein DENND6B",
                "gene_name": "DENND6B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8WYQ5-1",
                "protein_name": "Microprocessor complex subunit DGCR8",
                "gene_name": "DGCR8",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q15049-1",
                "protein_name": "Membrane protein MLC1",
                "gene_name": "MLC1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q13615-1",
                "protein_name": "Phosphatidylinositol-3,5-bisphosphate 3-phosphatase MTMR3",
                "gene_name": "MTMR3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q15459-1",
                "protein_name": "Splicing factor 3A subunit 1",
                "gene_name": "SF3A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y6X9-1",
                "protein_name": "ATPase MORC2",
                "gene_name": "MORC2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9H4I9-1",
                "protein_name": "Essential MCU regulator, mitochondrial",
                "gene_name": "SMDT1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BYW1-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 11",
                "gene_name": "SLC2A11",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O00178-1",
                "protein_name": "GTP-binding protein 1",
                "gene_name": "GTPBP1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P00387-1",
                "protein_name": "NADH-cytochrome b5 reductase 3",
                "gene_name": "CYB5R3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P33992-1",
                "protein_name": "DNA replication licensing factor MCM5",
                "gene_name": "MCM5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BXW7-1",
                "protein_name": "Haloacid dehalogenase-like hydrolase domain-containing 5",
                "gene_name": "HDHD5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q15080-1",
                "protein_name": "Neutrophil cytosol factor 4",
                "gene_name": "NCF4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BY77-1",
                "protein_name": "Polymerase delta-interacting protein 3",
                "gene_name": "POLDIP3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8NG94-1",
                "protein_name": "Olfactory receptor 11H1",
                "gene_name": "OR11H1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P48739-1",
                "protein_name": "Phosphatidylinositol transfer protein beta isoform",
                "gene_name": "PITPNB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q92871-1",
                "protein_name": "Phosphomannomutase 1",
                "gene_name": "PMM1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O60733-1",
                "protein_name": "85/88 kDa calcium-independent phospholipase A2",
                "gene_name": "PLA2G6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96EK2-1",
                "protein_name": "PHD finger protein 21B",
                "gene_name": "PHF21B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NST1-1",
                "protein_name": "1-acylglycerol-3-phosphate O-acyltransferase PNPLA3",
                "gene_name": "PNPLA3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q7Z3Z3-1",
                "protein_name": "Piwi-like protein 3",
                "gene_name": "PIWIL3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q7Z6Z6-1",
                "protein_name": "Patatin-like phospholipase domain-containing protein 5",
                "gene_name": "PNPLA5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15153-1",
                "protein_name": "Ras-related C3 botulinum toxin substrate 2",
                "gene_name": "RAC2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P43487-1",
                "protein_name": "Ran-specific GTPase-activating protein",
                "gene_name": "RANBP1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P20472-1",
                "protein_name": "Parvalbumin alpha",
                "gene_name": "PVALB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P30566-1",
                "protein_name": "Adenylosuccinate lyase",
                "gene_name": "ADSL",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6S545-1",
                "protein_name": "POTE ankyrin domain family member H",
                "gene_name": "POTEH",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P46060-1",
                "protein_name": "Ran GTPase-activating protein 1",
                "gene_name": "RANGAP1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O76054-1",
                "protein_name": "SEC14-like protein 2",
                "gene_name": "SEC14L2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96RN5-1",
                "protein_name": "Mediator of RNA polymerase II transcription subunit 15",
                "gene_name": "MED15",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P53671-1",
                "protein_name": "LIM domain kinase 2",
                "gene_name": "LIMK2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q969S8-1",
                "protein_name": "Polyamine deacetylase HDAC10",
                "gene_name": "HDAC10",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8N7B1-1",
                "protein_name": "HORMA domain-containing protein 2",
                "gene_name": "HORMAD2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01127-1",
                "protein_name": "Platelet-derived growth factor subunit B",
                "gene_name": "PDGFB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0M8Q6-1",
                "protein_name": "Immunoglobulin lambda constant 7",
                "gene_name": "IGLC7",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P0CG04-1",
                "protein_name": "Immunoglobulin lambda constant 1",
                "gene_name": "IGLC1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UNT1-1",
                "protein_name": "Rab-like protein 2B",
                "gene_name": "RABL2B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8WUA7-1",
                "protein_name": "TBC1 domain family member 22A",
                "gene_name": "TBC1D22A",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P20062-1",
                "protein_name": "Transcobalamin-2",
                "gene_name": "TCN2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q13769-1",
                "protein_name": "THO complex subunit 5",
                "gene_name": "THOC5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9H4I3-1",
                "protein_name": "TraB domain-containing protein",
                "gene_name": "TRABD",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96AY4-1",
                "protein_name": "Tetratricopeptide repeat protein 28",
                "gene_name": "TTC28",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "B5MCN3-1",
                "protein_name": "SEC14-like protein 6",
                "gene_name": "SEC14L6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O95502-1",
                "protein_name": "Neuronal pentraxin receptor",
                "gene_name": "NPTXR",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6ICG8-1",
                "protein_name": "Postacrosomal sheath WW domain-binding protein",
                "gene_name": "WBP2NL",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q16587-1",
                "protein_name": "Zinc finger protein 74",
                "gene_name": "ZNF74",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UKI3-1",
                "protein_name": "Pre-B lymphocyte protein 3",
                "gene_name": "VPREB3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P12018-1",
                "protein_name": "Immunoglobulin iota chain",
                "gene_name": "VPREB1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P09382-1",
                "protein_name": "Galectin-1",
                "gene_name": "LGALS1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q14565-1",
                "protein_name": "Meiotic recombination protein DMC1 homolog",
                "gene_name": "DMC1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9H6E4-1",
                "protein_name": "Coiled-coil domain-containing protein 134",
                "gene_name": "CCDC134",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BXF3-1",
                "protein_name": "Chromatin remodeling regulator CECR2",
                "gene_name": "CECR2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BZE7-1",
                "protein_name": "UPF0193 protein EVG1",
                "gene_name": "C22orf23",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UH03-1",
                "protein_name": "Neuronal-specific septin-3",
                "gene_name": "SEPTIN3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BY27-1",
                "protein_name": "Protein DGCR6L",
                "gene_name": "DGCR6L",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8NEJ0-1",
                "protein_name": "Dual specificity protein phosphatase 18",
                "gene_name": "DUSP18",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UIA0-1",
                "protein_name": "Cytohesin-4",
                "gene_name": "CYTH4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8IWF2-1",
                "protein_name": "FAD-dependent oxidoreductase domain-containing protein 2",
                "gene_name": "FOXRED2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O43759-1",
                "protein_name": "Synaptogyrin-1",
                "gene_name": "SYNGR1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "F5H4B4-1",
                "protein_name": "Protein FAM227A",
                "gene_name": "FAM227A",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6IC98-1",
                "protein_name": "GRAM domain-containing protein 4",
                "gene_name": "GRAMD4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96F46-1",
                "protein_name": "Interleukin-17 receptor A",
                "gene_name": "IL17RA",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6ZVW7-1",
                "protein_name": "Interleukin-17 receptor E-like protein",
                "gene_name": "IL17REL",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8N653-1",
                "protein_name": "Leucine-zipper-like transcriptional regulator 1",
                "gene_name": "LZTR1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O15031-1",
                "protein_name": "Plexin-B2",
                "gene_name": "PLXNB2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9ULX9-1",
                "protein_name": "Transcription factor MafF",
                "gene_name": "MAFF",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q2VPJ9-1",
                "protein_name": "Leucine-rich repeat-containing protein 75B",
                "gene_name": "LRRC75B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q5TIA1-1",
                "protein_name": "Meiosis inhibitor protein 1",
                "gene_name": "MEI1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q99719-1",
                "protein_name": "Septin-5",
                "gene_name": "SEPTIN5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q10571-1",
                "protein_name": "Transcriptional activator MN1",
                "gene_name": "MN1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UGB7-1",
                "protein_name": "Inositol oxygenase",
                "gene_name": "MIOX",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q15759-1",
                "protein_name": "Mitogen-activated protein kinase 11",
                "gene_name": "MAPK11",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q99705-1",
                "protein_name": "Melanin-concentrating hormone receptor 1",
                "gene_name": "MCHR1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BPW8-1",
                "protein_name": "Protein NipSnap homolog 1",
                "gene_name": "NIPSNAP1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8IUG5-1",
                "protein_name": "Unconventional myosin-XVIIIb",
                "gene_name": "MYO18B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P02144-1",
                "protein_name": "Myoglobin",
                "gene_name": "MB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NY65-1",
                "protein_name": "Tubulin alpha-8 chain",
                "gene_name": "TUBA8",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A0A0MT99-1",
                "protein_name": "Immunoglobulin lambda joining 3",
                "gene_name": "IGLJ3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P23142-1",
                "protein_name": "Fibulin-1",
                "gene_name": "FBLN1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q7Z5A7-1",
                "protein_name": "Chemokine-like protein TAFA-5",
                "gene_name": "TAFA5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O60704-1",
                "protein_name": "Protein-tyrosine sulfotransferase 2",
                "gene_name": "TPST2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8IZ69-1",
                "protein_name": "tRNA (uracil-5-)-methyltransferase homolog A",
                "gene_name": "TRMT2A",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q16762-1",
                "protein_name": "Thiosulfate sulfurtransferase",
                "gene_name": "TST",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P25325-1",
                "protein_name": "3-mercaptopyruvate sulfurtransferase",
                "gene_name": "MPST",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A6PVC2-1",
                "protein_name": "Protein monoglycylase TTLL8",
                "gene_name": "TTLL8",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P36543-1",
                "protein_name": "V-type proton ATPase subunit E 1",
                "gene_name": "ATP6V1E1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6ICI0-1",
                "protein_name": "LHFPL tetraspan subfamily member 7 protein",
                "gene_name": "LHFPL7",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A1W2PR19-1",
                "protein_name": "Glutathione S-transferase theta-4",
                "gene_name": "GSTT4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0A0A0MT82-1",
                "protein_name": "Immunoglobulin lambda joining 2",
                "gene_name": "IGLJ2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P29274-1",
                "protein_name": "Adenosine receptor A2a",
                "gene_name": "ADORA2A",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q04917-1",
                "protein_name": "14-3-3 protein eta",
                "gene_name": "YWHAH",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y3L3-1",
                "protein_name": "SH3 domain-binding protein 1",
                "gene_name": "SH3BP1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q99798-1",
                "protein_name": "Aconitate hydratase, mitochondrial",
                "gene_name": "ACO2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O96017-1",
                "protein_name": "Serine/threonine-protein kinase Chk2",
                "gene_name": "CHEK2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NRW3-1",
                "protein_name": "DNA dC->dU-editing enzyme APOBEC-3C",
                "gene_name": "APOBEC3C",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y3M2-1",
                "protein_name": "Protein chibby homolog 1",
                "gene_name": "CBY1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BXI6-1",
                "protein_name": "TBC1 domain family member 10A",
                "gene_name": "TBC1D10A",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UBB9-1",
                "protein_name": "Tuftelin-interacting protein 11",
                "gene_name": "TFIP11",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "Q5THR3",
                        "url": "https://www.uniprot.org/uniprotkb/Q5THR3"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.18477386",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
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    {
        "title": "A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity.",
        "journal": "Human genetics",
        "date": "1999",
        "authors": "Burwinkel B, Sanjad SA, Al-Sabban E, Al-Abbad A, Kilimann MW",
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    {
        "title": "Renal Na(+)-glucose cotransporters.",
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                "sort_fields": []
            },
            {
                "table_id": "glycosylation_predicted",
                "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_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    },
                    {
                        "field": "total_sites",
                        "count": 1
                    },
                    {
                        "field": "n_linked_sites",
                        "count": 1
                    },
                    {
                        "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
                    },
                    {
                        "field": "exact_sites",
                        "count": 1
                    },
                    {
                        "field": "exact_n_linked_sites",
                        "count": 1
                    },
                    {
                        "field": "fuzzy_sites",
                        "count": 0
                    }
                ],
                "sort_fields": [
                    "glytoucan_ac",
                    "type",
                    "subtype",
                    "site_category",
                    "site_seq",
                    "relation",
                    "comment",
                    "start_pos",
                    "start_aa",
                    "end_pos",
                    "end_aa",
                    "residue",
                    "site_lbl",
                    "mining_tool",
                    "filter_code",
                    "uniprot_canonical_ac"
                ]
            }
        ]
    },
    {
        "title": "Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria.",
        "journal": "Human genetics",
        "date": "2004",
        "authors": "Calado J, Soto K, Clemente C, Correia P, Rueff J",
        "reference": {
            "type": "PubMed",
            "id": "14614622",
            "url": "https://pubmed.ncbi.nlm.nih.gov/14614622"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P13866-1",
                "protein_name": "Sodium/glucose cotransporter 1",
                "gene_name": "SLC5A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P31639-1",
                "protein_name": "Sodium/glucose cotransporter 2",
                "gene_name": "SLC5A2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q5TF39-1",
                "protein_name": "Solute carrier family 60 member 2",
                "gene_name": "SLC60A2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q2M3M2-1",
                "protein_name": "Sodium/glucose cotransporter 4",
                "gene_name": "SLC5A9",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NY91-1",
                "protein_name": "Probable glucose sensor protein SLC5A4",
                "gene_name": "SLC5A4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "A0PJK1-1",
                "protein_name": "Sodium/mannose cotransporter SLC5A10",
                "gene_name": "SLC5A10",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BRV3-1",
                "protein_name": "Sugar transporter SWEET1",
                "gene_name": "SLC50A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P14672-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 4",
                "gene_name": "SLC2A4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P11166-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 1",
                "gene_name": "SLC2A1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8TDB8-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 14",
                "gene_name": "SLC2A14",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8TD20-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 12",
                "gene_name": "SLC2A12",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9UGQ3-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 6",
                "gene_name": "SLC2A6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BYW1-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 11",
                "gene_name": "SLC2A11",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NRM0-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 9",
                "gene_name": "SLC2A9",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "O95528-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 10",
                "gene_name": "SLC2A10",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NSA1-1",
                "protein_name": "Fibroblast growth factor 21",
                "gene_name": "FGF21",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q96JT2-1",
                "protein_name": "Solute carrier family 45 member 3",
                "gene_name": "SLC45A3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P11169-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 3",
                "gene_name": "SLC2A3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P11168-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 2",
                "gene_name": "SLC2A2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9NY64-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 8",
                "gene_name": "SLC2A8",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6PXP3-1",
                "protein_name": "Solute carrier family 2, facilitated glucose transporter member 7",
                "gene_name": "SLC2A7",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P13866",
                        "url": "https://www.uniprot.org/uniprotkb/P13866"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "rs267607067",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs267607067"
                    },
                    {
                        "id": "14614622",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/14614622"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 167,
                "end_pos": 167,
                "sequence_org": "Q",
                "sequence_mut": "null",
                "comment": "Germline mutation passed 1 filters: glycogene of type=glycogene, carbohydrate synthesis and metabolism/transporter.",
                "chr_id": "16",
                "chr_pos": "31486201",
                "ref_nt": "l",
                "alt_nt": "null",
                "minor_allelic_frequency": "",
                "site_lbl": "Q167",
                "disease": [
                    {
                        "disease_id": "DOID:0070613",
                        "recommended_name": {
                            "id": "DOID:0070613",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070613",
                            "name": "familial renal glucosuria",
                            "description": "A renal glycosuria that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the SLC5A2 gene on chromosome 16p11.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070613",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070613",
                                "name": "FRG",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070613",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070613",
                                "name": "SGLT2 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070613",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070613",
                                "name": "familial renal glycosuria",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070613",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070613",
                                "name": "hereditary renal glycosuria",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "familial renal glucosuria",
                                "description": "Familial Renal Glucosuria (FRG) is characterized by the presence of persistent isolated glucosuria in the absence of both generalized proximal tubular dysfunction and hyperglycemia. FRG is usually considered a benign entity as most patients are not affected by severe clinical consequences. Polyuria and enuresis and later a mild growth and pubertal maturation delay are the only manifestations that have been reported during a follow-up period of 30 years. Episodic dehydration and ketosis during pregnancy and starvation and an increased incidence of urinary tract infections have occasionally been reported in severe cases. FRG is caused by loss-of-function mutations in the gene SLC5A2 (16p11.2)."
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "Renal Glycosuria",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "SGLT2 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "familial renal glucosuria",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "GLYS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "renal glucosuria",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "renal glycosuria",
                                "description": ""
                            },
                            {
                                "id": "MIM:233100",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/233100",
                                "name": "Renal glucosuria",
                                "description": "Renal glucosuria"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "233100",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/233100"
                            },
                            {
                                "id": "0070613",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070613"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "ebi",
                    "germline",
                    "disease"
                ],
                "filter_code": "000000100000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P31639-1"
            },
            {
                "evidence": [
                    {
                        "id": "P31639",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/P31639"
                    },
                    {
                        "id": "rs61742739",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs61742739"
                    },
                    {
                        "id": "rs61742739",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs61742739"
                    },
                    {
                        "id": "rs61742739",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs61742739"
                    },
                    {
                        "id": "rs61742739",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs61742739#frequency_tab"
                    },
                    {
                        "id": "rs61742739",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs61742739"
                    },
                    {
                        "id": "14614622",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/14614622"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 654,
                "end_pos": 654,
                "subjects_tested": "4177",
                "subjects_positive": "2",
                "frequency": "0.0",
                "sequence_org": "N",
                "sequence_mut": "S",
                "comment": "Somatic mutation passed 1 filters: protein-of-interest(glycogene, carbohydrate synthesis and metabolism/transporter).",
                "chr_id": "16",
                "chr_pos": "31490477",
                "ref_nt": "A",
                "alt_nt": "G",
                "minor_allelic_frequency": "",
                "site_lbl": "N654",
                "disease": [
                    {
                        "disease_id": "DOID:10283",
                        "recommended_name": {
                            "id": "DOID:10283",
                            "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."
                        },
                        "synonyms": [
                            {
                                "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",
                                "name": "prostate cancer, familial",
                                "description": ""
                            },
                            {
                                "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:0070613",
                        "recommended_name": {
                            "id": "DOID:0070613",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0070613",
                            "name": "familial renal glucosuria",
                            "description": "A renal glycosuria that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the SLC5A2 gene on chromosome 16p11.2."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0070613",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070613",
                                "name": "FRG",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070613",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070613",
                                "name": "SGLT2 deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070613",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070613",
                                "name": "familial renal glycosuria",
                                "description": ""
                            },
                            {
                                "id": "DOID:0070613",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0070613",
                                "name": "hereditary renal glycosuria",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "familial renal glucosuria",
                                "description": "Familial Renal Glucosuria (FRG) is characterized by the presence of persistent isolated glucosuria in the absence of both generalized proximal tubular dysfunction and hyperglycemia. FRG is usually considered a benign entity as most patients are not affected by severe clinical consequences. Polyuria and enuresis and later a mild growth and pubertal maturation delay are the only manifestations that have been reported during a follow-up period of 30 years. Episodic dehydration and ketosis during pregnancy and starvation and an increased incidence of urinary tract infections have occasionally been reported in severe cases. FRG is caused by loss-of-function mutations in the gene SLC5A2 (16p11.2)."
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "Renal Glycosuria",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "SGLT2 deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "familial renal glucosuria",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "GLYS",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "renal glucosuria",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0009297",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0009297",
                                "name": "renal glycosuria",
                                "description": ""
                            },
                            {
                                "id": "MIM:233100",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/233100",
                                "name": "Renal glucosuria",
                                "description": "Renal glucosuria"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "233100",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/233100"
                            },
                            {
                                "id": "0070613",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0070613"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
                    "cancer",
                    "disease",
                    "ebi",
                    "germline"
                ],
                "filter_code": "001000000000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "P31639-1"
            }
        ],
        "record_id": "pubmed.14614622",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 21
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
                    "gene_name",
                    "tax_name"
                ]
            },
            {
                "table_id": "referenced_glycans",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation",
                "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": "phosphorylation",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "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_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": [
                    {
                        "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_automatic_literature_mining",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    },
                    {
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                        "count": 0
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                    {
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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": "Glucose accumulation can account for the initial water flux triggered by Na+/glucose cotransport.",
        "journal": "Biophysical journal",
        "date": "2004-01",
        "authors": "Gagnon Maril\u00e8ne P, Bissonnette Pierre, Deslandes Louis-Martin, Wallendorff Bernadette, Lapointe Jean-Yves",
        "reference": {
            "type": "PubMed",
            "id": "14695256",
            "url": "https://pubmed.ncbi.nlm.nih.gov/14695256"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P13866-1",
                "protein_name": "Sodium/glucose cotransporter 1",
                "gene_name": "SLC5A1",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P13866",
                        "url": "https://www.uniprot.org/uniprotkb/P13866"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "record_id": "pubmed.14695256",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "snv": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
            {
                "table_id": "referenced_proteins",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 1
                    }
                ],
                "sort_fields": [
                    "uniprot_canonical_ac",
                    "protein_name",
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        "authors": "Vitart V, Rudan I, Hayward C, Gray NK, Floyd J, Palmer CN, Knott SA, Kolcic I, Polasek O, Graessler J, Wilson JF, Marinaki A, Riches PL, Shu X, Janicijevic B, Smolej-Narancic N, Gorgoni B, Morgan J, Campbell S, Biloglav Z, Barac-Lauc L, Pericic M, Klaric IM, Zgaga L, Skaric-Juric T, Wild SH, Richardson WA, Hohenstein P, Kimber CH, Tenesa A, Donnelly LA, Fairbanks LD, Aringer M, McKeigue PM, Ralston SH, Morris AD, Rudan P, Hastie ND, Campbell H, Wright AF",
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                            "url": "https://disease-ontology.org/term/DOID:10283",
                            "name": "prostate cancer",
                            "description": "A male reproductive organ cancer that is located_in the prostate."
                        },
                        "synonyms": [
                            {
                                "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",
                                "name": "prostate cancer, familial",
                                "description": ""
                            },
                            {
                                "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:9352",
                        "recommended_name": {
                            "id": "DOID:9352",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:9352",
                            "name": "type 2 diabetes mellitus",
                            "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "NIDDM",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "non-insulin-dependent diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "type 2 diabetes",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "type II diabetes mellitus",
                                "description": ""
                            },
                            {
                                "id": "DOID:9352",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:9352",
                                "name": "insulin resistance",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "type 2 diabetes mellitus",
                                "description": "A type of diabetes mellitus that is characterized by insulin resistance or desensitization and increased blood glucose levels. This is a chronic disease that can develop gradually over the life of a patient and can be linked to both environmental factors and heredity."
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "NIDDM",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "T2D",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0005148",
                                "name": "T2DM",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0005148",
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                            {
                                "id": "MONDO:0005148",
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                            {
                                "id": "MONDO:0005148",
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                            {
                                "id": "MONDO:0005148",
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                            {
                                "id": "MONDO:0005148",
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                            {
                                "id": "MONDO:0005148",
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                                "id": "MONDO:0005148",
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                            {
                                "id": "MONDO:0005148",
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                                "name": "diabetes mellitus, noninsulin-dependent, late onset",
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                            {
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                            {
                                "id": "MONDO:0005148",
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                            {
                                "id": "MONDO:0005148",
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                                "id": "MONDO:0005148",
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                                "id": "MONDO:0005148",
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                            {
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                            {
                                "id": "MONDO:0005148",
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                            {
                                "id": "MONDO:0005148",
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                            {
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                            {
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                            {
                                "id": "MONDO:0011027",
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                                "name": "diabetes mellitus, noninsulin-dependent, 1",
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                            {
                                "id": "MONDO:0011027",
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                            {
                                "id": "MONDO:0011027",
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                            {
                                "id": "MONDO:0011072",
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                            {
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                                "id": "MONDO:0011072",
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                            {
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                            {
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                                "id": "MONDO:0011955",
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                            {
                                "id": "MONDO:0011955",
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                                "id": "MONDO:0011955",
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                            {
                                "id": "MIM:125853",
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                            {
                                "id": "MIM:601283",
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                                "url": "https://www.omim.org/entry/601283",
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                        ],
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                            {
                                "id": "9352",
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                ],
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    {
        "title": "Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter.",
        "journal": "Nature",
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        "authors": "Turk E, Zabel B, Mundlos S, Dyer J, Wright EM",
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                "sequence_org": "D",
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                "chr_pos": "32043363",
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                            "description": "A female reproductive organ cancer that is located_in the uterus."
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                                "id": "DOID:363",
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                                "name": "malignant neoplasm of uterus",
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                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
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                                "name": "malignant uterine tumor",
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                            {
                                "id": "DOID:363",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:363",
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                            {
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        "title": "Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish.",
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]
