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        "title": "Crystal structure of N-glycosylated human glypican-1 core protein: structure of two loops evolutionarily conserved in vertebrate glypican-1.",
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        "authors": "Svensson G, Awad W, Hakansson M, Mani K, Logan DT",
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        "title": "Attenuation of cancer proliferation by suppression of glypican-1 and its pleiotropic effects in neoplastic behavior.",
        "journal": "Oncotarget",
        "date": "2023-03-21",
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                        "count": 0
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                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
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                    {
                        "field": "total",
                        "count": 0
                    },
                    {
                        "field": "total_sites",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported",
                "table_stats": [
                    {
                        "field": "total",
                        "count": 0
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                    {
                        "field": "total_sites",
                        "count": 0
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                    {
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                    {
                        "field": "o_linked_sites",
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                    {
                        "field": "n_linked_glycan_sites",
                        "count": 0
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                    {
                        "field": "o_linked_glycan_sites",
                        "count": 0
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                    {
                        "field": "n_linked_glycans",
                        "count": 0
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                    {
                        "field": "o_linked_glycans",
                        "count": 0
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                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
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                    {
                        "field": "total",
                        "count": 0
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                    {
                        "field": "total_sites",
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                    {
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                    {
                        "field": "o_linked_sites",
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                    {
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                        "count": 0
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                    {
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                ],
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            {
                "table_id": "glycosylation_predicted",
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                    {
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                    {
                        "field": "o_linked_glycans",
                        "count": 0
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                ],
                "sort_fields": []
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            {
                "table_id": "glycosylation_automatic_literature_mining",
                "table_stats": [
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                        "field": "total",
                        "count": 0
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                    {
                        "field": "total_sites",
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                        "count": 0
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                    {
                        "field": "o_linked_glycans",
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                ],
                "sort_fields": []
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        ]
    },
    {
        "title": "A study of the hexose-6-phosphate dehydrogenase gene R453Q and 11beta-hydroxysteroid dehydrogenase type 1 gene 83557insA polymorphisms in the polycystic ovary syndrome.",
        "journal": "The Journal of clinical endocrinology and metabolism",
        "date": "2005-07",
        "authors": "San Mill\u00e1n Jos\u00e9 L, Botella-Carretero Jos\u00e9 I, Alvarez-Blasco Francisco, Luque-Ram\u00edrez Manuel, Sancho Jos\u00e9, Moghetti Paolo, Escobar-Morreale H\u00e9ctor F",
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            "type": "PubMed",
            "id": "15827106",
            "url": "https://pubmed.ncbi.nlm.nih.gov/15827106"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "O95479-1",
                "protein_name": "GDH/6PGL endoplasmic bifunctional protein",
                "gene_name": "H6PD",
                "tax_name": "Human"
            }
        ],
        "species": [
            {
                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
                    {
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                        "id": "O95479",
                        "url": "https://www.uniprot.org/uniprotkb/O95479"
                    }
                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
            }
        ],
        "snv": [
            {
                "evidence": [
                    {
                        "id": "O95479",
                        "database": "BioMuta",
                        "url": "https://hivelab.biochemistry.gwu.edu/biomuta/proteinview/O95479"
                    },
                    {
                        "id": "rs6688832",
                        "database": "dbSNP",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs6688832"
                    },
                    {
                        "id": "rs6688832",
                        "database": "1000Genomes",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs6688832"
                    },
                    {
                        "id": "rs6688832",
                        "database": "ExAC",
                        "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs6688832"
                    },
                    {
                        "id": "rs6688832",
                        "database": "TOPMed",
                        "url": "https://www.ncbi.nlm.nih.gov/snp/rs6688832#frequency_tab"
                    },
                    {
                        "id": "rs6688832",
                        "database": "gnomAD",
                        "url": "http://gnomad.broadinstitute.org/awesome?query=rs6688832"
                    },
                    {
                        "id": "12858176",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/12858176"
                    },
                    {
                        "id": "15827106",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/15827106"
                    },
                    {
                        "id": "16091483",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/16091483"
                    },
                    {
                        "id": "16817821",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/16817821"
                    },
                    {
                        "id": "17062770",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/17062770"
                    },
                    {
                        "id": "18628520",
                        "database": "PubMed",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18628520"
                    },
                    {
                        "id": "rs6688832",
                        "database": "COSMIC",
                        "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs6688832"
                    }
                ],
                "glycoeffect": [],
                "start_pos": 453,
                "end_pos": 453,
                "subjects_tested": "4799",
                "subjects_positive": "4",
                "frequency": "0.1",
                "sequence_org": "R",
                "sequence_mut": "Q",
                "comment": "Somatic mutation passed 1 filters: protein-of-interest(glycogene, carbohydrate synthesis and metabolism/metabolic enzymes).",
                "chr_id": "1",
                "chr_pos": "9263851",
                "ref_nt": "G",
                "alt_nt": "A",
                "minor_allelic_frequency": "",
                "site_lbl": "R453",
                "disease": [
                    {
                        "disease_id": "DOID:1324",
                        "recommended_name": {
                            "id": "DOID:1324",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:1324",
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                            "description": "A respiratory system cancer that is located_in the lung."
                        },
                        "synonyms": [
                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
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                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "adenocarcinoma of lung, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "cancer of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, protection against, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, resistance to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
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                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumor",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant lung tumour",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant neoplasm of the lung",
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                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumor of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "malignant tumour of the lung",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, somatic",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0008903",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                                "name": "nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "LNCR1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012159",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012159",
                                "name": "lung cancer susceptibility 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "LNCR3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012942",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                                "name": "lung cancer susceptibility 3",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "LNCR4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0012955",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0012955",
                                "name": "lung cancer susceptibility 4",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "LNCR5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0013631",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0013631",
                                "name": "lung cancer susceptibility 5",
                                "description": ""
                            },
                            {
                                "id": "MIM:211980",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/211980",
                                "name": "Lung cancer",
                                "description": "Lung cancer"
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:4765"
                        ],
                        "evidence": [
                            {
                                "id": "1324",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:1324"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:2531",
                        "recommended_name": {
                            "id": "DOID:2531",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:2531",
                            "name": "hematologic cancer",
                            "description": "An organ system cancer located in the hematological system that is characterized by uncontrolled cellular proliferation in blood, bone marrow and lymph nodes."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "Hematologic malignancy",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "Hematologic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "Hematological tumors",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "blood cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "hematopoietic and lymphoid system tumor",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "hematopoietic cancer",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "hematopoietic neoplasm",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "hematopoietic tumors",
                                "description": ""
                            },
                            {
                                "id": "DOID:2531",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:2531",
                                "name": "malignant hematopoietic neoplasm",
                                "description": ""
                            }
                        ],
                        "unlinked_id_list": [
                            "DOID:0081452",
                            "DOID:706",
                            "DOID:1039",
                            "DOID:5604",
                            "DOID:6536",
                            "DOID:0080638",
                            "DOID:7757",
                            "DOID:0050743",
                            "DOID:4960",
                            "DOID:8527",
                            "DOID:1036",
                            "DOID:5772"
                        ],
                        "evidence": [
                            {
                                "id": "2531",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:2531"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090139",
                        "recommended_name": {
                            "id": "DOID:0090139",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090139",
                            "name": "cortisone reductase deficiency",
                            "description": "An endocrine system disease characterized by failure to regenerate the active glucocorticoid cortisol from cortisone resulting in adrenal hyperandrogenism."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090139",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090139",
                                "name": "CORTRD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "cortisone reductase deficiency 1",
                                "description": "Decreased activity of hexose-6-phosphatase due to autosomal recessive mutation(s) in the H6PD gene. This enzyme is necessary to generate NADPH, a cofactor in the 11-beta-hydroxysteroid dehydrogenase pathway required for conversion of cortisone to cortisol. The condition is characterized by hyperandrogenism as a result of increased adrenocorticotropic hormone stimulation of the adrenal gland due to failure of cortisol-mediated down-regulation, and is clinically indistinguishable from 11-beta HSD type 1 deficiency."
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "CORTRD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "H6PD cortisone reductase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "apparent cortisone reductase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "cortisone reductase deficiency 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "cortisone reductase deficiency caused by mutation in H6PD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "cortisone reductase deficiency type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "hexose-6-phosphate dehydrogenase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:604931",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/604931",
                                "name": "Cortisone reductase deficiency 1",
                                "description": "Cortisone reductase deficiency 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "0090139",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090139"
                            },
                            {
                                "id": "0090139",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090139"
                            }
                        ]
                    },
                    {
                        "disease_id": "DOID:0090141",
                        "recommended_name": {
                            "id": "DOID:0090141",
                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090141",
                            "name": "cortisone reductase deficiency 1",
                            "description": "A cortisone reductase deficiency that is characterized by failure to regenerate cortisol via the enzyme 11-beta-hydroxysteroid dehydrogenase which requires NADPH regeneration by hexose-6-phosphate dehydrogenase, resulting in ACTH-mediated adrenal hyperandrogenism. It has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the hexose-6-phosphate dehydrogenase gene (H6PD) on chromosome 1p36."
                        },
                        "synonyms": [
                            {
                                "id": "DOID:0090141",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090141",
                                "name": "CORTRD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "cortisone reductase deficiency 1",
                                "description": "Decreased activity of hexose-6-phosphatase due to autosomal recessive mutation(s) in the H6PD gene. This enzyme is necessary to generate NADPH, a cofactor in the 11-beta-hydroxysteroid dehydrogenase pathway required for conversion of cortisone to cortisol. The condition is characterized by hyperandrogenism as a result of increased adrenocorticotropic hormone stimulation of the adrenal gland due to failure of cortisol-mediated down-regulation, and is clinically indistinguishable from 11-beta HSD type 1 deficiency."
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "CORTRD1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "H6PD cortisone reductase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "apparent cortisone reductase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "cortisone reductase deficiency 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "cortisone reductase deficiency caused by mutation in H6PD",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "cortisone reductase deficiency type 1",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0011503",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0011503",
                                "name": "hexose-6-phosphate dehydrogenase deficiency",
                                "description": ""
                            },
                            {
                                "id": "MIM:604931",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/604931",
                                "name": "Cortisone reductase deficiency 1",
                                "description": "Cortisone reductase deficiency 1"
                            }
                        ],
                        "unlinked_id_list": [],
                        "evidence": [
                            {
                                "id": "604931",
                                "database": "MIM",
                                "url": "https://www.omim.org/entry/604931"
                            },
                            {
                                "id": "0090141",
                                "database": "AGR",
                                "url": "https://www.alliancegenome.org/disease/DOID:0090141"
                            }
                        ]
                    }
                ],
                "keywords": [
                    "biomuta",
                    "somatic",
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                "filter_code": "010000000000000000000.00000000000000.000000000001000000.00001.11.000.000",
                "uniprot_canonical_ac": "O95479-1"
            }
        ],
        "record_id": "pubmed.15827106",
        "abstract": "",
        "glycosylation": [],
        "mutagenesis": [],
        "phosphorylation": [],
        "glycation": [],
        "section_stats": [
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