{
    "uniprot_canonical_ac": "P08603-1",
    "uniprot_ac": "P08603",
    "uniprot_id": "CFAH_HUMAN",
    "mass": {
        "chemical_mass": 139096.0,
        "monoisotopic_mass": 139096.0
    },
    "refseq": {
        "ac": "NP_000177",
        "name": "complement factor H isoform a precursor",
        "summary": "This gene is a member of the Regulator of Complement Activation (RCA) gene cluster and encodes a protein with twenty short consensus repeat (SCR) domains. This protein is secreted into the bloodstream and has an essential role in the regulation of complement activation, restricting this innate defense mechanism to microbial infections. Mutations in this gene have been associated with hemolytic-uremic syndrome (HUS) and chronic hypocomplementemic nephropathy. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Oct 2011].",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_000177"
    },
    "gene_names": [
        {
            "name": "CFH",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/P08603",
            "id": "P08603"
        },
        {
            "name": "AHUS1; AMBP1; ARMD4; ARMS1; CFHL3; FH; FHL1; HF; HF1; HF2; HUS",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_000177",
            "id": "NP_000177"
        },
        {
            "name": "CFH",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_000177",
            "id": "NP_000177"
        },
        {
            "name": "HF1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/P08603",
            "id": "P08603"
        },
        {
            "name": "HF2",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/P08603",
            "id": "P08603"
        },
        {
            "name": "HF",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/P08603",
            "id": "P08603"
        }
    ],
    "protein_names": [
        {
            "name": "Complement factor H",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "P08603"
        },
        {
            "name": "H factor 1 (complement); H factor 2 (complement); beta-1H; age-related maculopathy susceptibility 1; beta-1-H-globulin; factor H-like 1; adrenomedullin binding protein",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_000177",
            "id": "NP_000177"
        },
        {
            "name": "H factor 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P08603"
        },
        {
            "name": "complement factor H isoform a precursor",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_000177",
            "id": "NP_000177"
        }
    ],
    "function": [
        {
            "annotation": "(Microbial infection) In the mosquito midgut, binds to the surface of parasite P.falciparum gametocytes and protects the parasite from alternative complement pathway-mediated elimination.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P08603",
                    "url": "https://www.uniprot.org/uniprot/P08603#function"
                },
                {
                    "database": "PubMed",
                    "id": "23332154",
                    "url": "https://glygen.org/publication/PubMed/23332154"
                }
            ]
        },
        {
            "annotation": "Complement factor H attenuates TNF-alpha-induced inflammation by upregulating EIF3C in rheumatoid arthritis. Publication Status: Online-Only",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_000177",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_000177"
                },
                {
                    "database": "PubMed",
                    "id": "37996918",
                    "url": "https://glygen.org/publication/PubMed/37996918"
                }
            ]
        },
        {
            "annotation": "Glycoprotein that plays an essential role in maintaining a well-balanced immune response by modulating complement activation. Acts as a soluble inhibitor of complement, where its binding to self markers such as glycan structures prevents complement activation and amplification on cell surfaces (PubMed:21285368, PubMed:25402769). Accelerates the decay of the complement alternative pathway (AP) C3 convertase C3bBb, thus preventing local formation of more C3b, the central player of the complement amplification loop (PubMed:19503104, PubMed:26700768). As a cofactor of the serine protease factor I, CFH also regulates proteolytic degradation of already-deposited C3b (PubMed:23332154, PubMed:18252712, PubMed:28671664). In addition, mediates several cellular responses through interaction with specific receptors. For example, interacts with CR3/ITGAM receptor and thereby mediates the adhesion of human neutrophils to different pathogens. In turn, these pathogens are phagocytosed and destroyed (PubMed:9558116, PubMed:20008295).",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P08603",
                    "url": "https://www.uniprot.org/uniprot/P08603#function"
                },
                {
                    "database": "PubMed",
                    "id": "23332154",
                    "url": "https://glygen.org/publication/PubMed/23332154"
                },
                {
                    "database": "PubMed",
                    "id": "26700768",
                    "url": "https://glygen.org/publication/PubMed/26700768"
                },
                {
                    "database": "PubMed",
                    "id": "21285368",
                    "url": "https://glygen.org/publication/PubMed/21285368"
                },
                {
                    "database": "PubMed",
                    "id": "9558116",
                    "url": "https://glygen.org/publication/PubMed/9558116"
                },
                {
                    "database": "PubMed",
                    "id": "19503104",
                    "url": "https://glygen.org/publication/PubMed/19503104"
                },
                {
                    "database": "PubMed",
                    "id": "28671664",
                    "url": "https://glygen.org/publication/PubMed/28671664"
                },
                {
                    "database": "PubMed",
                    "id": "20008295",
                    "url": "https://glygen.org/publication/PubMed/20008295"
                },
                {
                    "database": "PubMed",
                    "id": "25402769",
                    "url": "https://glygen.org/publication/PubMed/25402769"
                },
                {
                    "database": "PubMed",
                    "id": "18252712",
                    "url": "https://glygen.org/publication/PubMed/18252712"
                }
            ]
        },
        {
            "annotation": "Identification of complement factor H variants that predispose to pre-eclampsia: A genetic and functional study.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_000177",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_000177"
                },
                {
                    "database": "PubMed",
                    "id": "37156755",
                    "url": "https://glygen.org/publication/PubMed/37156755"
                }
            ]
        },
        {
            "annotation": "Mesangial C3 Deposition, Complement-Associated Variant, and Disease Progression in IgA Nephropathy.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_000177",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_000177"
                },
                {
                    "database": "PubMed",
                    "id": "37651123",
                    "url": "https://glygen.org/publication/PubMed/37651123"
                }
            ]
        },
        {
            "annotation": "This gene is a member of the Regulator of Complement Activation (RCA) gene cluster and encodes a protein with twenty short consensus repeat (SCR) domains. This protein is secreted into the bloodstream and has an essential role in the regulation of complement activation, restricting this innate defense mechanism to microbial infections. Mutations in this gene have been associated with hemolytic-uremic syndrome (HUS) and chronic hypocomplementemic nephropathy. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Oct 2011].",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_000177",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_000177"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0060746",
            "recommended_name": {
                "id": "DOID:0060746",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0060746",
                "name": "basal laminar drusen",
                "description": "A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium on Bruch membrane and that has_material_basis_in mutations in the CFH gene on chromosome 1q31.3."
            },
            "synonyms": [
                {
                    "id": "DOID:0060746",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060746",
                    "name": "cuticular drusen",
                    "description": ""
                },
                {
                    "id": "DOID:0060746",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060746",
                    "name": "drusen of bruch membrane",
                    "description": ""
                },
                {
                    "id": "DOID:0060746",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0060746",
                    "name": "early adult-onset grouped drusen",
                    "description": ""
                },
                {
                    "id": "MONDO:0007472",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007472",
                    "name": "basal laminar drusen",
                    "description": "A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium on Bruch membrane and that has material basis in mutations in the CFH gene on chromosome 1q31.3."
                },
                {
                    "id": "MONDO:0007472",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007472",
                    "name": "basal laminar drusen",
                    "description": ""
                },
                {
                    "id": "MONDO:0007472",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007472",
                    "name": "cuticular drusen",
                    "description": ""
                },
                {
                    "id": "MONDO:0007472",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007472",
                    "name": "drusen of Bruch membrane",
                    "description": ""
                },
                {
                    "id": "MONDO:0007472",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007472",
                    "name": "early adult-onset grouped drusen",
                    "description": ""
                },
                {
                    "id": "MONDO:0007472",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007472",
                    "name": "drusen, cuticular",
                    "description": ""
                },
                {
                    "id": "MONDO:0007472",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007472",
                    "name": "drusen, early adult-onset, grouped",
                    "description": ""
                },
                {
                    "id": "MIM:126700",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/126700",
                    "name": "Basal laminar drusen",
                    "description": "Basal laminar drusen"
                }
            ],
            "evidence": [
                {
                    "id": "126700",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/126700"
                }
            ]
        },
        {
            "disease_id": "DOID:0110017",
            "recommended_name": {
                "id": "DOID:0110017",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110017",
                "name": "age related macular degeneration 4",
                "description": "An age related macular degeneration conferred by variation in the CFH gene on chromosome 1q31."
            },
            "synonyms": [
                {
                    "id": "DOID:0110017",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110017",
                    "name": "ARMD4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012540",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012540",
                    "name": "age related macular degeneration 4",
                    "description": "Any age-related macular degeneration in which the cause of the disease is a mutation in the CFH gene."
                },
                {
                    "id": "MONDO:0012540",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012540",
                    "name": "ARMD4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012540",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012540",
                    "name": "CFH age-related macular degeneration",
                    "description": ""
                },
                {
                    "id": "MONDO:0012540",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012540",
                    "name": "age related macular degeneration type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012540",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012540",
                    "name": "age-related macular degeneration caused by mutation in CFH",
                    "description": ""
                },
                {
                    "id": "MONDO:0012540",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012540",
                    "name": "macular Degeneration, age-related, type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012540",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012540",
                    "name": "macular degeneration, age-related, 4",
                    "description": ""
                },
                {
                    "id": "MIM:610698",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/610698",
                    "name": "Macular degeneration, age-related, 4",
                    "description": "Macular degeneration, age-related, 4"
                }
            ],
            "evidence": [
                {
                    "id": "610698",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/610698"
                }
            ]
        },
        {
            "disease_id": "MONDO:0009335",
            "recommended_name": {
                "id": "MONDO:0009335",
                "resource": "MONDO",
                "url": "https://monarchinitiative.org/disease/MONDO:0009335",
                "name": "hemolytic uremic syndrome, atypical, susceptibility to, 1",
                "description": ""
            },
            "synonyms": [
                {
                    "id": "MONDO:0009335",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009335",
                    "name": "hemolytic uremic syndrome, atypical, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0009335",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009335",
                    "name": "hemolytic uremic syndrome, atypical, susceptibility to, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009335",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009335",
                    "name": "hemolytic uremic syndrome, atypical, susceptibility to, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009335",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009335",
                    "name": "AHUS1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009335",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009335",
                    "name": "Ahus, susceptibility to, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0009335",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009335",
                    "name": "hemolytic uremic syndrome, typical",
                    "description": ""
                },
                {
                    "id": "MONDO:0009335",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0009335",
                    "name": "susceptibility to atypical hemolytic uremic syndrome 1",
                    "description": ""
                },
                {
                    "id": "MIM:235400",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/235400",
                    "name": "Hemolytic uremic syndrome atypical 1",
                    "description": "Hemolytic uremic syndrome atypical 1"
                }
            ],
            "evidence": [
                {
                    "id": "235400",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/235400"
                }
            ]
        },
        {
            "disease_id": "MONDO:0012350",
            "recommended_name": {
                "id": "MONDO:0012350",
                "resource": "MONDO",
                "url": "https://monarchinitiative.org/disease/MONDO:0012350",
                "name": "complement factor H deficiency",
                "description": ""
            },
            "synonyms": [
                {
                    "id": "MONDO:0012350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012350",
                    "name": "complement factor H deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0012350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012350",
                    "name": "CFHD",
                    "description": ""
                },
                {
                    "id": "MONDO:0012350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012350",
                    "name": "Cfh deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0012350",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012350",
                    "name": "factor H deficiency",
                    "description": ""
                },
                {
                    "id": "MIM:609814",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/609814",
                    "name": "Complement factor H deficiency",
                    "description": "Complement factor H deficiency"
                }
            ],
            "evidence": [
                {
                    "id": "609814",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/609814"
                }
            ]
        }
    ],
    "snv": [
        {
            "evidence": [
                {
                    "id": "rs779431195",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779431195"
                },
                {
                    "id": "rs779431195",
                    "database": "ExAC",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs779431195"
                },
                {
                    "id": "rs779431195",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs779431195"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-loss",
                "o-glyco-site-loss"
            ],
            "start_pos": 1031,
            "end_pos": 1031,
            "sequence_org": "T",
            "sequence_mut": "A",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVT->NVA).",
            "chr_id": "1",
            "chr_pos": "196742009",
            "ref_nt": "G",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "T1031",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs1283447296",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1283447296"
                },
                {
                    "id": "rs1283447296",
                    "database": "TOPMed",
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs1283447296#frequency_tab"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-loss",
                "o-glyco-site-loss"
            ],
            "start_pos": 1031,
            "end_pos": 1031,
            "sequence_org": "T",
            "sequence_mut": "K",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVT->NVK).",
            "chr_id": "1",
            "chr_pos": "196742010",
            "ref_nt": "A",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "T1031",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs377051240",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs377051240"
                },
                {
                    "id": "rs377051240",
                    "database": "ExAC",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs377051240"
                },
                {
                    "id": "rs377051240",
                    "database": "TOPMed",
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs377051240#frequency_tab"
                },
                {
                    "id": "rs377051240",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs377051240"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-loss",
                "o-glyco-site-loss"
            ],
            "start_pos": 1031,
            "end_pos": 1031,
            "sequence_org": "T",
            "sequence_mut": "R",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NVT->NVR).",
            "chr_id": "1",
            "chr_pos": "196742031",
            "ref_nt": "G",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "T1031",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs1160757371",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1160757371"
                },
                {
                    "id": "rs1160757371",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1160757371"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ],
            "start_pos": 1036,
            "end_pos": 1036,
            "sequence_org": "R",
            "sequence_mut": "T",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (NSR->NST).",
            "chr_id": "1",
            "chr_pos": "196742025",
            "ref_nt": "C",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "R1036",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs932614951",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs932614951"
                },
                {
                    "id": "rs932614951",
                    "database": "TOPMed",
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs932614951#frequency_tab"
                },
                {
                    "id": "rs932614951",
                    "database": "gnomAD",
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                {
                    "id": "rs770185390",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs770185390"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-loss"
            ],
            "start_pos": 822,
            "end_pos": 822,
            "sequence_org": "N",
            "sequence_mut": "I",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NMT->IMT).",
            "chr_id": "1",
            "chr_pos": "196736875",
            "ref_nt": "T",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "N822",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs770185390",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs770185390"
                },
                {
                    "id": "rs770185390",
                    "database": "ExAC",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs770185390"
                },
                {
                    "id": "rs770185390",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs770185390"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-loss"
            ],
            "start_pos": 822,
            "end_pos": 822,
            "sequence_org": "N",
            "sequence_mut": "S",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NMT->SMT).",
            "chr_id": "1",
            "chr_pos": "196736875",
            "ref_nt": "G",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "N822",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs894673509",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs894673509"
                },
                {
                    "id": "rs894673509",
                    "database": "TOPMed",
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs894673509#frequency_tab"
                },
                {
                    "id": "rs894673509",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs894673509"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-loss",
                "o-glyco-site-loss"
            ],
            "start_pos": 824,
            "end_pos": 824,
            "sequence_org": "T",
            "sequence_mut": "K",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NMT->NMK).",
            "chr_id": "1",
            "chr_pos": "196736881",
            "ref_nt": "A",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "T824",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs1379860048",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1379860048"
                },
                {
                    "id": "rs1379860048",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1379860048"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-gain",
                "o-glyco-site-loss"
            ],
            "start_pos": 834,
            "end_pos": 834,
            "sequence_org": "K",
            "sequence_mut": "N",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (KVS->NVS).",
            "chr_id": "1",
            "chr_pos": "196736912",
            "ref_nt": "C",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "K834",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs114743644",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs114743644"
                },
                {
                    "id": "rs114743644",
                    "database": "1000Genomes",
                    "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs114743644"
                },
                {
                    "id": "rs114743644",
                    "database": "ExAC",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs114743644"
                },
                {
                    "id": "rs114743644",
                    "database": "TOPMed",
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs114743644#frequency_tab"
                },
                {
                    "id": "rs114743644",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs114743644"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-loss",
                "o-glyco-site-loss"
            ],
            "start_pos": 884,
            "end_pos": 884,
            "sequence_org": "S",
            "sequence_mut": "F",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NSS->NSF).",
            "chr_id": "1",
            "chr_pos": "196737529",
            "ref_nt": "T",
            "alt_nt": "null",
            "minor_allelic_frequency": "0.000799",
            "site_lbl": "S884",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs763377571",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763377571"
                },
                {
                    "id": "rs763377571",
                    "database": "ExAC",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs763377571"
                },
                {
                    "id": "rs763377571",
                    "database": "TOPMed",
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs763377571#frequency_tab"
                },
                {
                    "id": "rs763377571",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs763377571"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-loss",
                "o-glyco-site-loss"
            ],
            "start_pos": 884,
            "end_pos": 884,
            "sequence_org": "S",
            "sequence_mut": "P",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NSS->NSP).",
            "chr_id": "1",
            "chr_pos": "196737528",
            "ref_nt": "C",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "S884",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs114743644",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs114743644"
                },
                {
                    "id": "rs114743644",
                    "database": "1000Genomes",
                    "url": "https://www.ensembl.org/homo_sapiens/Variation/Explore?v=rs114743644"
                },
                {
                    "id": "rs114743644",
                    "database": "ExAC",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs114743644"
                },
                {
                    "id": "rs114743644",
                    "database": "TOPMed",
                    "url": "https://www.ncbi.nlm.nih.gov/snp/rs114743644#frequency_tab"
                },
                {
                    "id": "rs114743644",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs114743644"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-loss",
                "o-glyco-site-loss"
            ],
            "start_pos": 884,
            "end_pos": 884,
            "sequence_org": "S",
            "sequence_mut": "Y",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NSS->NSY).",
            "chr_id": "1",
            "chr_pos": "196737529",
            "ref_nt": "A",
            "alt_nt": "null",
            "minor_allelic_frequency": "0.000799",
            "site_lbl": "S884",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs1316683858",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1316683858"
                },
                {
                    "id": "rs1316683858",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1316683858"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-gain"
            ],
            "start_pos": 893,
            "end_pos": 893,
            "sequence_org": "H",
            "sequence_mut": "N",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (HGT->NGT).",
            "chr_id": "1",
            "chr_pos": "196737555",
            "ref_nt": "A",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "H893",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs1361345512",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1361345512"
                },
                {
                    "id": "rs1361345512",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1361345512"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-gain",
                "o-glyco-site-loss"
            ],
            "start_pos": 898,
            "end_pos": 898,
            "sequence_org": "S",
            "sequence_mut": "N",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-gain (SYT->NYT).",
            "chr_id": "1",
            "chr_pos": "196737571",
            "ref_nt": "A",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "S898",
            "keywords": [
                "ebi",
                "germline"
            ]
        },
        {
            "evidence": [
                {
                    "id": "rs1240893783",
                    "database": "dbSNP",
                    "url": "https://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?type=rs&rs=rs1240893783"
                },
                {
                    "id": "rs1240893783",
                    "database": "gnomAD",
                    "url": "http://gnomad.broadinstitute.org/awesome?query=rs1240893783"
                }
            ],
            "glycoeffect": [
                "n-glyco-sequon-loss"
            ],
            "start_pos": 911,
            "end_pos": 911,
            "sequence_org": "N",
            "sequence_mut": "S",
            "comment": "Germline mutation passed 1 out of 1 filters: n-glyco-sequon-loss (NET->SET).",
            "chr_id": "1",
            "chr_pos": "196737610",
            "ref_nt": "G",
            "alt_nt": "null",
            "minor_allelic_frequency": "",
            "site_lbl": "N911",
            "keywords": [
                "ebi",
                "germline"
            ]
        }
    ],
    "mutagenesis": [
        {
            "start_pos": 1182,
            "end_pos": 1182,
            "sequence_org": "R",
            "sequence_mut": "A",
            "comment": "About 50% loss of C3b binding.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P08603",
                    "url": "https://www.uniprot.org/uniprot/P08603"
                },
                {
                    "database": "PubMed",
                    "id": "16601698",
                    "url": "https://glygen.org/publication/PubMed/16601698"
                }
            ]
        },
        {
            "start_pos": 1183,
            "end_pos": 1183,
            "sequence_org": "W",
            "sequence_mut": "L",
            "comment": "About 40% loss of C3b binding.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P08603",
                    "url": "https://www.uniprot.org/uniprot/P08603"
                },
                {
                    "database": "PubMed",
                    "id": "16601698",
                    "url": "https://glygen.org/publication/PubMed/16601698"
                }
            ]
        },
        {
            "start_pos": 1186,
            "end_pos": 1186,
            "sequence_org": "K",
            "sequence_mut": "A",
            "comment": "About 20% loss of C3b binding.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P08603",
                    "url": "https://www.uniprot.org/uniprot/P08603"
                },
                {
                    "database": "PubMed",
                    "id": "16601698",
                    "url": "https://glygen.org/publication/PubMed/16601698"
                }
            ]
        },
        {
            "start_pos": 1188,
            "end_pos": 1188,
            "sequence_org": "K",
            "sequence_mut": "A",
            "comment": "About 50% loss of C3b binding.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P08603",
                    "url": "https://www.uniprot.org/uniprot/P08603"
                },
                {
                    "database": "PubMed",
                    "id": "16601698",
                    "url": "https://glygen.org/publication/PubMed/16601698"
                }
            ]
        },
        {
            "start_pos": 1198,
            "end_pos": 1198,
            "sequence_org": "E",
            "sequence_mut": "A",
            "comment": "About 30% loss of C3b binding.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P08603",
                    "url": "https://www.uniprot.org/uniprot/P08603"
                },
                {
                    "database": "PubMed",
                    "id": "16601698",
                    "url": "https://glygen.org/publication/PubMed/16601698"
                }
            ]
        },
        {
            "start_pos": 337,
            "end_pos": 337,
            "sequence_org": "H",
            "sequence_mut": "A",
            "comment": "About 10% loss of heparin-binding.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P08603",
                    "url": "https://www.uniprot.org/uniprot/P08603"
                },
                {
                    "database": "PubMed",
                    "id": "17893204",
                    "url": "https://glygen.org/publication/PubMed/17893204"
                }
            ]
        },
        {
            "start_pos": 341,
            "end_pos": 341,
            "sequence_org": "R",
            "sequence_mut": "A",
            "comment": "About 20% loss of heparin-binding.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P08603",
                    "url": "https://www.uniprot.org/uniprot/P08603"
                },
                {
                    "database": "PubMed",
                    "id": "17893204",
                    "url": "https://glygen.org/publication/PubMed/17893204"
                }
            ]
        }
    ],
    "expression_tissue": [
        {
            "tissue": {
                "name": "Adult mammalian kidney",
                "namespace": "UBERON",
                "id": "0000082",
                "url": "http://purl.obolibrary.org/obo/UBERON_0000082"
            },
            "score": "75.16",
            "present": "MEDIUM",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Oral cavity",
                "namespace": "UBERON",
                "id": "0000167",
                "url": "http://purl.obolibrary.org/obo/UBERON_0000167"
            },
            "score": "91.44",
            "present": "HIGH",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Stomach",
                "namespace": "UBERON",
                "id": "0000945",
                "url": "http://purl.obolibrary.org/obo/UBERON_0000945"
            },
            "score": "89.02",
            "present": "HIGH",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Uterus",
                "namespace": "UBERON",
                "id": "0000995",
                "url": "http://purl.obolibrary.org/obo/UBERON_0000995"
            },
            "score": "58.11",
            "present": "LOW",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Esophagus",
                "namespace": "UBERON",
                "id": "0001043",
                "url": "http://purl.obolibrary.org/obo/UBERON_0001043"
            },
            "score": "98.01",
            "present": "HIGH",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Rectum",
                "namespace": "UBERON",
                "id": "0001052",
                "url": "http://purl.obolibrary.org/obo/UBERON_0001052"
            },
            "score": "97.46",
            "present": "HIGH",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Colon",
                "namespace": "UBERON",
                "id": "0001155",
                "url": "http://purl.obolibrary.org/obo/UBERON_0001155"
            },
            "score": "71.12",
            "present": "MEDIUM",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Urinary bladder",
                "namespace": "UBERON",
                "id": "0001255",
                "url": "http://purl.obolibrary.org/obo/UBERON_0001255"
            },
            "score": "97.1",
            "present": "HIGH",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Thyroid gland",
                "namespace": "UBERON",
                "id": "0002046",
                "url": "http://purl.obolibrary.org/obo/UBERON_0002046"
            },
            "score": "96.55",
            "present": "HIGH",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Lung",
                "namespace": "UBERON",
                "id": "0002048",
                "url": "http://purl.obolibrary.org/obo/UBERON_0002048"
            },
            "score": "83.38",
            "present": "HIGH",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Liver",
                "namespace": "UBERON",
                "id": "0002107",
                "url": "http://purl.obolibrary.org/obo/UBERON_0002107"
            },
            "score": "99.63",
            "present": "HIGH",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Prostate gland",
                "namespace": "UBERON",
                "id": "0002367",
                "url": "http://purl.obolibrary.org/obo/UBERON_0002367"
            },
            "score": "85.99",
            "present": "HIGH",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        },
        {
            "tissue": {
                "name": "Thoracic mammary gland",
                "namespace": "UBERON",
                "id": "0005200",
                "url": "http://purl.obolibrary.org/obo/UBERON_0005200"
            },
            "score": "90.91",
            "present": "HIGH",
            "evidence": [
                {
                    "database": "Bgee",
                    "id": "ENSG00000000971",
                    "url": "https://bgee.org/?page=gene&gene_id=ENSG00000000971"
                }
            ]
        }
    ],
    "expression_disease": [
        {
            "significant": "Yes",
            "trend": "down",
            "name": "Prostate cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:10283",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:10283",
                    "recommended_name": {
                        "id": "DOID:10283",
                        "resource": "Disease Ontology",
                        "url": "http://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": "http://disease-ontology.org/term/DOID:10283",
                            "name": "NGP - new growth of prostate",
                            "description": ""
                        },
                        {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10283",
                            "name": "hereditary prostate cancer",
                            "description": ""
                        },
                        {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10283",
                            "name": "malignant tumor of the prostate",
                            "description": ""
                        },
                        {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10283",
                            "name": "prostate cancer, familial",
                            "description": ""
                        },
                        {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10283",
                            "name": "prostate neoplasm",
                            "description": ""
                        },
                        {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10283",
                            "name": "prostatic cancer",
                            "description": ""
                        },
                        {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10283",
                            "name": "prostatic neoplasm",
                            "description": ""
                        },
                        {
                            "id": "DOID:10283",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10283",
                            "name": "tumor of the prostate",
                            "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: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: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: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:0012094",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0012094",
                            "name": "prostate cancer, hereditary, on chromosome 7",
                            "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: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:0011270",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                            "name": "predisposing for prostate cancer",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0011270",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0011270",
                            "name": "prostate cancer, susceptibility to",
                            "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:0012300",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0012300",
                            "name": "prostate cancer, susceptibility to",
                            "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:0023122",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                            "name": "familial prostate carcinoma",
                            "description": "Prostate carcinoma that has developed in relatives of patients with a history of prostate carcinoma."
                        },
                        {
                            "id": "MONDO:0023122",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                            "name": "familial prostate cancer",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0023122",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                            "name": "hereditary prostate cancer",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0023122",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                            "name": "hereditary prostate carcinoma",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0023122",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                            "name": "prostate cancer, autosomal dominant, somatic mutation",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0023122",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                            "name": "prostate cancer, familial, susceptibility to, autosomal dominant, somatic mutation",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0023122",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                            "name": "prostate cancer, somatic",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0023122",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                            "name": "prostate cancer, susceptibility to, autosomal dominant, somatic mutation",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0023122",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                            "name": "prostate cancer, familial",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0023122",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0023122",
                            "name": "prostate cancer, hereditary",
                            "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:0012470",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0012470",
                            "name": "prostate cancer aggressiveness",
                            "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:0011098",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0011098",
                            "name": "Prca1",
                            "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: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:0010257",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0010257",
                            "name": "prostate cancer susceptibility, X-linked",
                            "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": "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:176807",
                            "resource": "MIM",
                            "url": "https://www.omim.org/entry/176807",
                            "name": "Prostate cancer",
                            "description": "Prostate cancer"
                        },
                        {
                            "id": "MIM:601518",
                            "resource": "MIM",
                            "url": "https://www.omim.org/entry/601518",
                            "name": "Prostate cancer, hereditary, 1",
                            "description": "Prostate cancer, hereditary, 1"
                        },
                        {
                            "id": "MIM:611955",
                            "resource": "MIM",
                            "url": "https://www.omim.org/entry/611955",
                            "name": "Prostate cancer, hereditary, 11",
                            "description": "Prostate cancer, hereditary, 11"
                        }
                    ]
                }
            ]
        },
        {
            "significant": "No",
            "trend": "down",
            "name": "Stomach cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:10534",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:10534",
                    "recommended_name": {
                        "id": "DOID:10534",
                        "resource": "Disease Ontology",
                        "url": "http://disease-ontology.org/term/DOID:10534",
                        "name": "stomach cancer",
                        "description": "A gastrointestinal system cancer that is located_in the stomach."
                    },
                    "synonyms": [
                        {
                            "id": "DOID:10534",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "name": "gastric cancer",
                            "description": ""
                        },
                        {
                            "id": "DOID:10534",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:10534",
                            "name": "gastric neoplasm",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "gastric cancer",
                            "description": "A primary or metastatic malignant neoplasm involving the stomach."
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "gastric neoplasm",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "Ca lesser curvature - stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "cancer of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "gastric cancer",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "gastric cancer risk after h. pylori infection",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "gastric cancer, somatic",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant gastric neoplasm",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant gastric tumor",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant gastric tumour",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant neoplasm of lesser curve of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant neoplasm of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant neoplasm of the stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant stomach neoplasm",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant tumor of body of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant tumor of greater curve of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant tumor of lesser curve of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant tumor of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant tumor of the stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant tumour of body of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant tumour of greater curve of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant tumour of lesser curve of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant tumour of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant tumour of the stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "stomach cancer",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "Ca body - stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "ca greater curvature of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "malignant neoplasm of body of stomach",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001056",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001056",
                            "name": "gastric cancer, intestinal",
                            "description": ""
                        },
                        {
                            "id": "MIM:613659",
                            "resource": "MIM",
                            "url": "https://www.omim.org/entry/613659",
                            "name": "Gastric cancer",
                            "description": "Gastric cancer"
                        }
                    ]
                }
            ]
        },
        {
            "significant": "Yes",
            "trend": "down",
            "name": "Urinary bladder cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:11054",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:11054",
                    "recommended_name": {
                        "id": "DOID:11054",
                        "resource": "Disease Ontology",
                        "url": "http://disease-ontology.org/term/DOID:11054",
                        "name": "urinary bladder cancer",
                        "description": "An urinary system cancer that results_in malignant growth located_in the urinary bladder."
                    },
                    "synonyms": [
                        {
                            "id": "DOID:11054",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:11054",
                            "name": "bladder cancer",
                            "description": ""
                        },
                        {
                            "id": "DOID:11054",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:11054",
                            "name": "tumor of the bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "urinary bladder cancer",
                            "description": "A primary or metastatic malignant neoplasm involving the bladder."
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "tumor of the bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "tumour of the bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "bladder cancer, somatic",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "cancer of urinary bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant bladder neoplasm",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant bladder tumor",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant bladder tumour",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant neoplasm of bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant neoplasm of the bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant neoplasm of the urinary bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant neoplasm of urinary bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant neoplasm, bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant neoplasm, urinary bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant tumor of bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant tumor of the bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant tumor of the urinary bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant tumor of urinary bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant tumor, urinary bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant tumour of bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant tumour of the bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant tumour of the urinary bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant tumour of urinary bladder",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant urinary bladder neoplasm",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant urinary bladder tumor",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "malignant urinary bladder tumour",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "urinary bladder cancer",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "urinary bladder malignant neoplasm",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "urinary bladder malignant tumor",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0001187",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                            "name": "urinary bladder malignant tumour",
                            "description": ""
                        },
                        {
                            "id": "MIM:109800",
                            "resource": "MIM",
                            "url": "https://www.omim.org/entry/109800",
                            "name": "Bladder cancer",
                            "description": "Bladder cancer"
                        }
                    ]
                }
            ]
        },
        {
            "significant": "Yes",
            "trend": "down",
            "name": "Head and neck cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:11934",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:11934",
                    "recommended_name": {
                        "id": "DOID:11934",
                        "resource": "Disease Ontology",
                        "url": "http://disease-ontology.org/term/DOID:11934",
                        "name": "head and neck cancer",
                        "description": "An organ system cancer that arises in the head or neck region. This region includes the nasal cavity, sinuses, lips, mouth, salivary glands, throat, or larynx."
                    },
                    "synonyms": [
                        {
                            "id": "DOID:11934",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:11934",
                            "name": "head and neck neoplasm",
                            "description": ""
                        },
                        {
                            "id": "DOID:11934",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:11934",
                            "name": "head and neck tumours",
                            "description": ""
                        },
                        {
                            "id": "DOID:11934",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:11934",
                            "name": "head/neck neoplasm",
                            "description": ""
                        },
                        {
                            "id": "DOID:11934",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:11934",
                            "name": "tumor of head and neck",
                            "description": ""
                        }
                    ]
                }
            ]
        },
        {
            "significant": "Yes",
            "trend": "down",
            "name": "Lung cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:1324",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:1324",
                    "recommended_name": {
                        "id": "DOID:1324",
                        "resource": "Disease Ontology",
                        "url": "http://disease-ontology.org/term/DOID:1324",
                        "name": "lung cancer",
                        "description": "A respiratory system cancer that is located_in the lung."
                    },
                    "synonyms": [
                        {
                            "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:0012942",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0012942",
                            "name": "adenocarcinoma of lung, susceptibility to",
                            "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": "MONDO:0008903",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                            "name": "lung cancer",
                            "description": "A malignant neoplasm involving the lung."
                        },
                        {
                            "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",
                            "name": "malignant lung neoplasm",
                            "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",
                            "description": ""
                        },
                        {
                            "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:0008903",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                            "name": "Nonsmall cell lung cancer",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0008903",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                            "name": "alveolar cell carcinoma",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0008903",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                            "name": "lung cancer, protection against",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0008903",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0008903",
                            "name": "lung neoplasm",
                            "description": ""
                        },
                        {
                            "id": "MIM:211980",
                            "resource": "MIM",
                            "url": "https://www.omim.org/entry/211980",
                            "name": "Lung cancer",
                            "description": "Lung cancer"
                        }
                    ]
                }
            ]
        },
        {
            "significant": "Yes",
            "trend": "down",
            "name": "Breast cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:1612",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:1612",
                    "recommended_name": {
                        "id": "DOID:1612",
                        "resource": "Disease Ontology",
                        "url": "http://disease-ontology.org/term/DOID:1612",
                        "name": "breast cancer",
                        "description": "A thoracic cancer that originates in the mammary gland."
                    },
                    "synonyms": [
                        {
                            "id": "DOID:1612",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1612",
                            "name": "breast tumor",
                            "description": ""
                        },
                        {
                            "id": "DOID:1612",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1612",
                            "name": "malignant neoplasm of breast",
                            "description": ""
                        },
                        {
                            "id": "DOID:1612",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1612",
                            "name": "malignant tumor of the breast",
                            "description": ""
                        },
                        {
                            "id": "DOID:1612",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1612",
                            "name": "mammary cancer",
                            "description": ""
                        },
                        {
                            "id": "DOID:1612",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1612",
                            "name": "mammary tumor",
                            "description": ""
                        },
                        {
                            "id": "DOID:1612",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1612",
                            "name": "primary breast cancer",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "hereditary breast carcinoma",
                            "description": "Breast carcinoma that has developed in relatives of patients with history of breast carcinoma."
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "breast cancer susceptibility, autosomal dominant, somatic mutation",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "breast cancer, early-onset, susceptibility to, autosomal dominant, somatic mutation",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "breast cancer, invasive ductal, autosomal dominant, somatic mutation",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "breast cancer, lobular, somatic",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "breast cancer, male, susceptibility to, autosomal dominant, somatic mutation",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "breast cancer, protection against, autosomal dominant, somatic mutation",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "breast cancer, somatic",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "breast cancer, susceptibility to, autosomal dominant, somatic mutation",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "familial breast cancer",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "familial breast carcinoma",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "familial cancer of breast",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "familial cancer of the breast",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "hereditary breast cancer",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "hereditary breast carcinoma",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "breast cancer, familial",
                            "description": ""
                        },
                        {
                            "id": "MONDO:0016419",
                            "resource": "MONDO",
                            "url": "https://monarchinitiative.org/disease/MONDO:0016419",
                            "name": "breast cancer, familial Male",
                            "description": ""
                        },
                        {
                            "id": "MIM:114480",
                            "resource": "MIM",
                            "url": "https://www.omim.org/entry/114480",
                            "name": "Breast cancer",
                            "description": "Breast cancer"
                        }
                    ]
                }
            ]
        },
        {
            "significant": "No",
            "trend": "up",
            "name": "Thyroid cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:1781",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:1781",
                    "recommended_name": {
                        "id": "DOID:1781",
                        "resource": "Disease Ontology",
                        "url": "http://disease-ontology.org/term/DOID:1781",
                        "name": "thyroid cancer",
                        "description": "An endocrine gland cancer located in the thryoid gland located in the neck below the thyroid cartilage."
                    },
                    "synonyms": [
                        {
                            "id": "DOID:1781",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1781",
                            "name": "thyroid gland cancer",
                            "description": ""
                        },
                        {
                            "id": "DOID:1781",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1781",
                            "name": "Thyroid gland neoplasm",
                            "description": ""
                        },
                        {
                            "id": "DOID:1781",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1781",
                            "name": "malignant neoplasm of thyroid gland",
                            "description": ""
                        },
                        {
                            "id": "DOID:1781",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1781",
                            "name": "malignant tumour of thyroid gland",
                            "description": ""
                        },
                        {
                            "id": "DOID:1781",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1781",
                            "name": "neoplasm of thyroid gland",
                            "description": ""
                        },
                        {
                            "id": "DOID:1781",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:1781",
                            "name": "thyroid neoplasm",
                            "description": ""
                        }
                    ]
                }
            ]
        },
        {
            "significant": "Yes",
            "trend": "up",
            "name": "Kidney cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:263",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:263",
                    "recommended_name": {
                        "id": "DOID:263",
                        "resource": "Disease Ontology",
                        "url": "http://disease-ontology.org/term/DOID:263",
                        "name": "kidney cancer",
                        "description": "A urinary system cancer that is located_in the kidney."
                    },
                    "synonyms": [
                        {
                            "id": "DOID:263",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:263",
                            "name": "malignant neoplasm of kidney except pelvis",
                            "description": ""
                        },
                        {
                            "id": "DOID:263",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:263",
                            "name": "malignant tumour of kidney",
                            "description": ""
                        },
                        {
                            "id": "DOID:263",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:263",
                            "name": "renal cancer",
                            "description": ""
                        }
                    ]
                }
            ]
        },
        {
            "significant": "Yes",
            "trend": "down",
            "name": "Liver cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:3571",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:3571",
                    "recommended_name": {
                        "id": "DOID:3571",
                        "resource": "Disease Ontology",
                        "url": "http://disease-ontology.org/term/DOID:3571",
                        "name": "liver cancer",
                        "description": "A hepatobiliary system cancer that is located_in the liver."
                    },
                    "synonyms": [
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "Ca liver - primary",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "Resectable malignant neoplasm of Liver",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "hepatic cancer",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "hepatic neoplasm",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "malignant hepato-biliary neoplasm",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "malignant neoplasm of liver",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "malignant neoplasm of liver, primary",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "malignant tumor of liver",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "neoplasm of liver",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "non-resectable primary hepatic malignant neoplasm",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "primary liver cancer",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "primary malignant neoplasm of liver",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "resectable malignant neoplasm of the liver",
                            "description": ""
                        },
                        {
                            "id": "DOID:3571",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:3571",
                            "name": "malignant neoplasm of liver, not specified as primary or secondary",
                            "description": ""
                        }
                    ]
                }
            ]
        },
        {
            "significant": "No",
            "trend": "up",
            "name": "Uterine cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:363",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:363",
                    "recommended_name": {
                        "id": "DOID:363",
                        "resource": "Disease Ontology",
                        "url": "http://disease-ontology.org/term/DOID:363",
                        "name": "uterine cancer",
                        "description": "A female reproductive organ cancer that is located_in the uterus."
                    },
                    "synonyms": [
                        {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "CA - cancer of uterus",
                            "description": ""
                        },
                        {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "Tumour of uterus",
                            "description": ""
                        },
                        {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "malignant neoplasm of uterus",
                            "description": ""
                        },
                        {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "malignant uterine tumor",
                            "description": ""
                        },
                        {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "neoplasm of uterus",
                            "description": ""
                        },
                        {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "uterine tumor",
                            "description": ""
                        },
                        {
                            "id": "DOID:363",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:363",
                            "name": "uterus neoplasm",
                            "description": ""
                        }
                    ]
                }
            ]
        },
        {
            "significant": "No",
            "trend": "up",
            "name": "Esophageal cancer [DO disease name]",
            "url": "http://disease-ontology.org/term/DOID:5041",
            "evidence": [
                {
                    "database": "BioXpress",
                    "id": "P08603",
                    "url": "https://hive.biochemistry.gwu.edu/bioxpress/transcriptview/P08603"
                }
            ],
            "disease": [
                {
                    "disease_id": "DOID:5041",
                    "recommended_name": {
                        "id": "DOID:5041",
                        "resource": "Disease Ontology",
                        "url": "http://disease-ontology.org/term/DOID:5041",
                        "name": "esophageal cancer",
                        "description": "A gastrointestinal system cancer that is located_in the esophagus."
                    },
                    "synonyms": [
                        {
                            "id": "DOID:5041",
                            "resource": "Disease Ontology",
                            "url": "http://disease-ontology.org/term/DOID:5041",
                            "name": "Ca lower third oesophagus",
                            "description": ""
                        },
                        {
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        "length": 1231,
        "header": "sp|P08603-1|CFAH_HUMAN Isoform 1 of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=4 CANONICAL=P08603-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0D9SG88-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVSFTL",
                "length": 449,
                "header": "tr|A0A0D9SG88-1|A0A0D9SG88_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196701328,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000630130.2",
                        "url": "https://www.ensembl.org/id/ENST00000630130.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000487250.1",
                        "url": "https://www.ensembl.org/id/ENSP00000487250.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SI55-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQIVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVSFTL",
                "length": 388,
                "header": "tr|A0A8Q3SI55-1|A0A8Q3SI55_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=4 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196701328,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695968.1",
                        "url": "https://www.ensembl.org/id/ENST00000695968.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512295.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512295.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SI73-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVD",
                "length": 207,
                "header": "tr|A0A8Q3SI73-1|CFAH_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196678946,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000696031.1",
                        "url": "https://www.ensembl.org/id/ENST00000696031.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512340.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512340.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SI76-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVSFTL",
                "length": 424,
                "header": "tr|A0A8Q3SI76-1|A0A8Q3SI76_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=4 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196701328,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000696030.1",
                        "url": "https://www.ensembl.org/id/ENST00000696030.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512339.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512339.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SI78-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVAIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEG",
                "length": 928,
                "header": "tr|A0A8Q3SI78-1|A0A8Q3SI78_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196737662,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695969.1",
                        "url": "https://www.ensembl.org/id/ENST00000695969.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512296.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512296.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SI99-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEGLPCKSPPEISHGVVAHMSDSYQYGEEVTYKCFEGFGIDGPAIAKCLGEKWSHPPSCIKTDCLSLPSFENAIPMGEKKDVYKAGEQVTYTCATYYKMDGASNVTCINSRWTGRPTCRDTSCVNPPTVQNAYIVSRQMSKYPSGERVRYQCRSPYEMFGDEEVMCLNGNWTEPPQCKDSTGKCGPPPPIDNGDITSFPLSVYAPASSVEYQCQNLYQLEGNKRITCRNGQWSEPPKCLHPCVISREIMENYNIALRWTAKQKLYSRTGESVEFVCKRGYRLSSRSHTLRTTCWDGKLEYPTCAKR",
                "length": 1229,
                "header": "tr|A0A8Q3SI99-1|A0A8Q3SI99_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196747310,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000696027.1",
                        "url": "https://www.ensembl.org/id/ENST00000696027.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512336.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512336.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SIB6-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVAIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEETDCLSLPSFENAIPMGEKKDVYKAGEQVTYTCATYYKMDGASNVTCINSRWTGRPTCRDTSCVNPPTVQNAYIVSRQMSKYPSGERVRYQCRSPYEMFGDEEVMCLNGNWTEPPQCKDSTGKCGPPPPIDNGDITSFPLSVYAPASSVEYQCQNLYQLEGNKRITCRNGQWSEPPKCLHPCVISREIMENYNIALRWTAKQKLYSRTGESVEFVCKRGYRLSSRSHTLRTTCWDGKLEYPTCAKR",
                "length": 1173,
                "header": "tr|A0A8Q3SIB6-1|A0A8Q3SIB6_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196747310,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695970.1",
                        "url": "https://www.ensembl.org/id/ENST00000695970.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512297.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512297.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SIC3-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVAIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEGLPCKSPPEISHGVVAHMSDSYQYGEEVTYKCFEETDCLSLPSFENAIPMGEKKDVYKAGEQVTYTCATYYKMDGASNVTCINSRWTGRPTCRDTSCVNPPTVQNAYIVSRQMSKYPSGERVRYQCRSPYEMFGDEEVMCLNGNWTEPPQCKDSTGKCGPPPPIDNGDITSFPLSVYAPASSVEYQCQNLYQLEGNKRITCRNGQWSEPPKCLHPCVISREIMENYNIALRWTAKQKLYSRTGESVEFVCKRGYRLSSRSHTLRTTCWDGKLEYPTCAKR",
                "length": 1207,
                "header": "tr|A0A8Q3SIC3-1|A0A8Q3SIC3_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196747310,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000696028.1",
                        "url": "https://www.ensembl.org/id/ENST00000696028.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512337.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512337.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SID7-1",
            "url": "",
            "sequence": {
                "sequence": "MVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVSFTL",
                "length": 386,
                "header": "tr|A0A8Q3SID7-1|A0A8Q3SID7_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=4 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196701328,
                "end_pos": 196673109,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695987.1",
                        "url": "https://www.ensembl.org/id/ENST00000695987.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512312.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512312.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SID8-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVAIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEGLPCKSPPEISHGVVAHMSDSYQYGEEVTYKCFEGFGIDGPAIAKCLGEKWSHPPSCINCLSLPSFENAIPMGEKKDVYKAGEQVTYTCATYYKMDGASNVTCINSRWTGRPTCRDTSCVNPPTVQNAYIVSRQMSKYPSGERVRYQCRSPYEMFGDEEVMCLNGNWTEPPQCKDSTGKCGPPPPIDNGDITSFPLSVYAPASSVEYQCQNLYQLEGNKRITCRNGQWSEPPKCLHPCVISREIMENYNIALRWTAKQKLYSRTGESVEFVCKRGYRLSSRSHTLRTTCWDGKLEYPTCAKR",
                "length": 1229,
                "header": "tr|A0A8Q3SID8-1|A0A8Q3SID8_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196747310,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000696029.1",
                        "url": "https://www.ensembl.org/id/ENST00000696029.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512338.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512338.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SIE0-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTYIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVAIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEGLPCKSPPEISHGVVAHMSDSYQYGEEVTYKCFEGFGIDGPAIAKCLGEKWSHPPSCIKTDCLSLPSFENAIPMGEKKDVYKAGEQVTYTCATYYKMDGASNVTCINSRWTGRPTCRDTSCVNPPTVQNAYIVSRQMSKYPSGERVRYQCRSPYEMFGDEEVMCLNGNWTEPPQCKDSTGKCGPPPPIDNGDITSFPLSVYAPASSVEYQCQNLYQLEGNKRITCRNGQWSEPPKCLHPCVISREIMENYNIALRWTAKQKLYSRTGESVEFVCKRGYRLSSRSHTLRTTCWDGKLEYPTCAKR",
                "length": 1224,
                "header": "tr|A0A8Q3SIE0-1|A0A8Q3SIE0_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196747310,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695971.1",
                        "url": "https://www.ensembl.org/id/ENST00000695971.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512298.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512298.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SIE8-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYGKMRTS",
                "length": 571,
                "header": "tr|A0A8Q3SIE8-1|A0A8Q3SIE8_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=4 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196725139,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000696026.1",
                        "url": "https://www.ensembl.org/id/ENST00000696026.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512335.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512335.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3SJ41-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCLTCQTVISMEKKLRTNVLKVLELMGLQLQNA",
                "length": 775,
                "header": "tr|A0A8Q3SJ41-1|A0A8Q3SJ41_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=4 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196740756,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695972.1",
                        "url": "https://www.ensembl.org/id/ENST00000695972.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512299.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512299.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WKW2-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVSKAVLTFSTQPCLQQRNHFWSQKKSQALPSELLIEGHPSPA",
                "length": 486,
                "header": "tr|A0A8Q3WKW2-1|A0A8Q3WKW2_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=4 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196701362,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695978.1",
                        "url": "https://www.ensembl.org/id/ENST00000695978.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512304.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512304.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WKW3-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVAIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEGLPCKSPPEISHGVVAHMSDSYQYGEEVTYKCFEGFGIDGPAIAKCLGEKWSHPPSCIKTDCLSLPSFENAIPMGEKKDVYKAGEQVTYTCATYYKMDGASNVTCINSRWTGRPTCRDTSCVNPPTVQNAYIVSRQMSKYPSGERVRYQCRSPYEMFGDEEVMCLNGNWTEPPQCKDSTGKCGPPPPIDNGDITSFPLSVYAPASSVEYQCQNLYQLEGNKRITCRNGQWSEPPKCLHPCVISREIMENYNIALRWTAKQKLYSRTELN",
                "length": 1196,
                "header": "tr|A0A8Q3WKW3-1|A0A8Q3WKW3_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196752079,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695981.1",
                        "url": "https://www.ensembl.org/id/ENST00000695981.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512306.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512306.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WKW6-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKVFLL",
                "length": 628,
                "header": "tr|A0A8Q3WKW6-1|A0A8Q3WKW6_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=4 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196726466,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695975.1",
                        "url": "https://www.ensembl.org/id/ENST00000695975.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512302.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512302.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WKW7-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVAIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEGLPCKSPPEISHGVVAHMSDSYQYGEEVTYKCFEGFGIDGPAIAKCLGEKWSHPPSCIKTDCLSLPSFENAIPMGEKKDVYKAGEQVTYTCATYYKMDGASNVTCINSRWTGRPTCRDTSCVNPPTVQNAYIVSRQMSKYPSGERVRYQCRSPYEMFGDEEVMCLNGNWTEPPQCKDSTGKCGPPPPIDNGDITSFPLSVYAPASSVEYQCQNLYQLEGNKRITCRNGQWSEPPKCLHPCVISREIMENYNIALRWTAKQKLYSRTGESVEFVCKRGYRLSSRSHTLRTTCWDGKLEYPTCAKR",
                "length": 1172,
                "header": "tr|A0A8Q3WKW7-1|A0A8Q3WKW7_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196747310,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695974.1",
                        "url": "https://www.ensembl.org/id/ENST00000695974.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512301.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512301.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WKX0-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYDGPNAVLLHGYIA",
                "length": 578,
                "header": "tr|A0A8Q3WKX0-1|A0A8Q3WKX0_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=4 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196720344,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695973.1",
                        "url": "https://www.ensembl.org/id/ENST00000695973.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512300.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512300.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WKX4-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQTIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEGLPCKSPPEISHGVVAHMSDSYQYGEEVTYKCFEGFGIDGPAIAKCLGEKWSHPPSCIKTDCLSLPSFENAIPMGEKKDVYKAGEQVTYTCATYYKMDGASNVTCINSRWTGRPTCRDTSCVNPPTVQNAYIVSRQMSKYPSGERVRYQCRSPYEMFGDEEVMCLNGNWTEPPQCKDSTGKCGPPPPIDNGDITSFPLSVYAPASSVEYQCQNLYQLEGNKRITCRNGQWSEPPKCLHPCVISREIMENYNIALRWTAKQKLYSRTGESVEFVCKRGYRLSSRSHTLRTTCWDGKLEYPTCAKR",
                "length": 567,
                "header": "tr|A0A8Q3WKX4-1|A0A8Q3WKX4_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196747310,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695984.1",
                        "url": "https://www.ensembl.org/id/ENST00000695984.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512309.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512309.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WL05-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTYIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVSFTL",
                "length": 442,
                "header": "tr|A0A8Q3WL05-1|CFAH_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196701328,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695979.1",
                        "url": "https://www.ensembl.org/id/ENST00000695979.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512305.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512305.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WLF7-1",
            "url": "",
            "sequence": {
                "sequence": "MVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVAIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEGLPCKSPPEISHGVVAHMSDSYQYGEEVTYKCFEGFGIDGPAIAKCLGEKWSHPPSCIKTDCLSLPSFENAIPMGEKKDVYKAGEQVTYTCATYYKMDGASNVTCINSRWTGRPTCRDTSCVNPPTVQNAYIVSRQMSKYPSGERVRYQCRSPYEMFGDEEVMCLNGNWTEPPQCKDSTGKCGPPPPIDNGDITSFPLSVYAPASSVEYQCQNLYQLEGNKRITCRNGQWSEPPKCLHPCVISREIMENYNIALRWTAKQKLYSRTGESVEFVCKRGYRLSSRSHTLRTTCWDGKLEYPTCAKR",
                "length": 1168,
                "header": "tr|A0A8Q3WLF7-1|A0A8Q3WLF7_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196747310,
                "end_pos": 196673109,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695976.1",
                        "url": "https://www.ensembl.org/id/ENST00000695976.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512303.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512303.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WLY2-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVAIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEGLPCKSPPEISHGVVAHMSDSYQYGEEKQIVSVYLALKMPYPWERRRMC",
                "length": 976,
                "header": "tr|A0A8Q3WLY2-1|A0A8Q3WLY2_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196741940,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695983.1",
                        "url": "https://www.ensembl.org/id/ENST00000695983.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512308.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512308.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WM65-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGNPKVFRKYQNHGGQKYGLRLEERET",
                "length": 142,
                "header": "tr|A0A8Q3WM65-1|A0A8Q3WM65_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=4 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196675525,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000695986.1",
                        "url": "https://www.ensembl.org/id/ENST00000695986.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512311.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512311.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A8Q3WM71-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVSKYTTLKS",
                "length": 453,
                "header": "tr|A0A8Q3WM71-1|A0A8Q3WM71_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=4 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196690262,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000696023.1",
                        "url": "https://www.ensembl.org/id/ENST00000696023.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000512334.1",
                        "url": "https://www.ensembl.org/id/ENSP00000512334.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "P08603-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNYGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVKTCSKSSIDIENGFISESQYTYALKEKAKYQCKLGYVTADGETSGSITCGKDGWSAQPTCIKSCDIPVFMNARTKNDFTWFKLNDTLDYECHDGYESNTGSTTGSIVCGYNGWSDLPICYERECELPKIDVHLVPDRKKDQYKVGEVLKFSCKPGFTIVGPNSVQCYHFGLSPDLPICKEQVQSCGPPPELLNGNVKEKTKEEYGHSEVVEYYCNPRFLMKGPNKIQCVDGEWTTLPVCIVEESTCGDIPELEHGWAQLSSPPYYYGDSVEFNCSESFTMIGHRSITCIHGVWTQLPQCVAIDKLKKCKSSNLIILEEHLKNKKEFDHNSNIRYRCRGKEGWIHTVCINGRWDPEVNCSMAQIQLCPPPPQIPNSHNMTTTLNYRDGEKVSVLCQENYLIQEGEEITCKDGRWQSIPLCVEKIPCSQPPQIEHGTINSSRSSQESYAHGTKLSYTCEGGFRISEENETTCYMGKWSSPPQCEGLPCKSPPEISHGVVAHMSDSYQYGEEVTYKCFEGFGIDGPAIAKCLGEKWSHPPSCIKTDCLSLPSFENAIPMGEKKDVYKAGEQVTYTCATYYKMDGASNVTCINSRWTGRPTCRDTSCVNPPTVQNAYIVSRQMSKYPSGERVRYQCRSPYEMFGDEEVMCLNGNWTEPPQCKDSTGKCGPPPPIDNGDITSFPLSVYAPASSVEYQCQNLYQLEGNKRITCRNGQWSEPPKCLHPCVISREIMENYNIALRWTAKQKLYSRTGESVEFVCKRGYRLSSRSHTLRTTCWDGKLEYPTCAKR",
                "length": 1231,
                "header": "sp|P08603-1|CFAH_HUMAN Isoform 1 of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=4 CANONICAL=P08603-1"
            },
            "locus": {}
        },
        {
            "isoform_ac": "P08603-2",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEVVKCLPVTAPENGKIVSSAMEPDREYHFGQAVRFVCNSGYKIEGDEEMHCSDDGFWSKEKPKCVEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNYGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVSFTL",
                "length": 449,
                "header": "sp|P08603-2|CFAH_HUMAN Isoform 2 of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=4 CANONICAL=P08603-1"
            },
            "locus": {}
        },
        {
            "isoform_ac": "Q5TFM2-1",
            "url": "",
            "sequence": {
                "sequence": "MRLLAKIICLMLWAICVAEDCNELPPRRNTEILTGSWSDQTYPEGTQAIYKCRPGYRSLGNVIMVCRKGEWVALNPLRKCQKRPCGHPGDTPFGTFTLTGGNVFEYGVKAVYTCNEGYQLLGEINYRECDTDGWTNDIPICEEISCKSPDVINGSPISQKIIYKENERFQYKCNMGYEYSERGDAVCTESGWRPLPSCEEKSCDNPYIPNGDYSPLRIKHRTGDEITYQCRNGFYPATRGNTAKCTSTGWIPAPRCTLKPCDYPDIKHGGLYHENMRRPYFPVAVGKYYSYYCDEHFETPSGSYWDHIHCTQDGWSPAVPCLRKCYFPYLENGYNQNHGRKFVQGKSIDVACHPGYALPKAQTTVTCMENGWSPTPRCIRVSFTL",
                "length": 385,
                "header": "tr|Q5TFM2-1|Q5TFM2_HUMAN Computationally mapped isoform of Complement factor H  OS=Homo sapiens OX=9606 GN=CFH PE=1 SV=1 CANONICAL=P08603-1"
            },
            "locus": {
                "chromosome": "1",
                "start_pos": 196701328,
                "end_pos": 196652118,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENST00000359637.3",
                        "url": "https://www.ensembl.org/id/ENST00000359637.3"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSP00000352658.2",
                        "url": "https://www.ensembl.org/id/ENSP00000352658.2"
                    }
                ]
            }
        }
    ],
    "glycosylation": [
        {
            "glytoucan_ac": "G00875VP",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 1029,
            "start_aa": "Asn",
            "end_pos": 1029,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn1029",
            "evidence": [
                {
                    "id": "722",
                    "database": "GlyConnect",
                    "url": "https://glyconnect.expasy.org/browser/proteins/722"
                },
                {
                    "id": "24279413",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/24279413"
                }
            ]
        },
        {
            "glytoucan_ac": "G00912UN",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 1029,
            "start_aa": "Asn",
            "end_pos": 1029,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn1029",
            "evidence": [
                {
                    "id": "P08603",
                    "database": "UniCarbKB",
                    "url": ""
                },
                {
                    "id": "29671580",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/29671580"
                },
                {
                    "id": "P08603@N1029",
                    "database": "GPTwiki",
                    "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/P08603@N1029"
                }
            ]
        },
        {
            "glytoucan_ac": "G04909DG",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 1029,
            "start_aa": "Asn",
            "end_pos": 1029,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn1029",
            "evidence": [
                {
                    "id": "P08603",
                    "database": "UniCarbKB",
                    "url": ""
                },
                {
                    "id": "17591618",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/17591618"
                }
            ]
        },
        {
            "glytoucan_ac": "G06247RL",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 1029,
            "start_aa": "Asn",
            "end_pos": 1029,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn1029",
            "evidence": [
                {
                    "id": "P08603@N1029",
                    "database": "GPTwiki",
                    "url": "https://edwardslab.bmcb.georgetown.edu/gptwiki/P08603@N1029"
                }
            ]
        },
        {
            "glytoucan_ac": "G06356OH",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 1029,
            "start_aa": "Asn",
            "end_pos": 1029,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn1029",
            "evidence": [
                {
                    "id": "722",
                    "database": "GlyConnect",
                    "url": "https://glyconnect.expasy.org/browser/proteins/722"
                },
                {
                    "id": "29741879",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/29741879"
                },
                {
                    "id": "29391424",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/29391424"
                },
                {
                    "id": "29671580",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/29671580"
                },
                {
                    "id": "32125861",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/32125861"
                }
            ]
        },
        {
            "glytoucan_ac": "G08146BT",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 1029,
            "start_aa": "Asn",
            "end_pos": 1029,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn1029",
            "evidence": [
                {
                    "id": "P08603",
                    "database": "UniCarbKB",
                    "url": ""
                },
                {
                    "id": "17591618",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/17591618"
                }
            ]
        },
        {
            "glytoucan_ac": "G08293MJ",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 1029,
            "start_aa": "Asn",
            "end_pos": 1029,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn1029",
            "evidence": [
                {
                    "id": "P08603",
                    "database": "UniCarbKB",
                    "url": ""
                },
                {
                    "id": "29671580",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/29671580"
                }
            ]
        },
        {
            "glytoucan_ac": "G22140GZ",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 1029,
            "start_aa": "Asn",
            "end_pos": 1029,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn1029",
            "evidence": [
                {
                    "id": "722",
                    "database": "GlyConnect",
                    "url": "https://glyconnect.expasy.org/browser/proteins/722"
                },
                {
                    "id": "25265424",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/25265424"
                }
            ]
        },
        {
            "glytoucan_ac": "G22310AV",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 1029,
            "start_aa": "Asn",
            "end_pos": 1029,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn1029",
            "evidence": [
                {
                    "id": "722",
                    "database": "GlyConnect",
                    "url": "https://glyconnect.expasy.org/browser/proteins/722"
                },
                {
                    "id": "29391424",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/29391424"
                }
            ]
        },
        {
            "glytoucan_ac": "G23863VK",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 1029,
            "start_aa": "Asn",
            "end_pos": 1029,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn1029",
            "evidence": [
                {
                    "id": "722",
                    "database": "GlyConnect",
                    "url": "https://glyconnect.expasy.org/browser/proteins/722"
                },
                {
                    "id": "25265424",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/25265424"
                },
                {
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    "phosphorylation": [],
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    "keywords": [
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        {
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            ]
        },
        {
            "title": "Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.",
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            "organism": "Mus musculus",
            "sequence": {
                "sequence": "MRLSARIIWLILWTVCAAEDCKGPPPRENSEILSGSWSEQLYPEGTQATYKCRPGYRTLGTIVKVCKNGKWVASNPSRICRKKPCGHPGDTPFGSFRLAVGSQFEFGAKVVYTCDDGYQLLGEIDYRECGADGWINDIPLCEVVKCLPVTELENGRIVSGAAETDQEYYFGQVVRFECNSGFKIEGHKEIHCSENGLWSNEKPRCVEILCTPPRVENGDGINVKPVYKENERYHYKCKHGYVPKERGDAVCTGSGWSSQPFCEEKRCSPPYILNGIYTPHRIIHRSDDEIRYECNYGFYPVTGSTVSKCTPTGWIPVPRCTLKPCEFPQFKYGRLYYEESLRPNFPVSIGNKYSYKCDNGFSPPSGYSWDYLRCTAQGWEPEVPCVRKCVFHYVENGDSAYWEKVYVQGQSLKVQCYNGYSLQNGQDTMTCTENGWSPPPKCIRIKTCSASDIHIDNGFLSESSSIYALNRETSYRCKQGYVTNTGEISGSITCLQNGWSPQPSCIKSCDMPVFENSITKNTRTWFKLNDKLDYECLVGFENEYKHTKGSITCTYYGWSDTPSCYERECSVPTLDRKLVVSPRKEKYRVGDLLEFSCHSGHRVGPDSVQCYHFGWSPGFPTCKGQVASCAPPLEILNGEINGAKKVEYSHGEVVKYDCKPRFLLKGPNKIQCVDGNWTTLPVCIEEERTCGDIPELEHGSAKCSVPPYHHGDSVEFICEENFTMIGHGSVSCISGKWTQLPKCVATDQLEKCRVLKSTGIEAIKPKLTEFTHNSTMDYKCRDKQEYERSICINGKWDPEPNCTSKTSCPPPPQIPNTQVIETTVKYLDGEKLSVLCQDNYLTQDSEEMVCKDGRWQSLPRCIEKIPCSQPPTIEHGSINLPRSSEERRDSIESSSHEHGTTFSYVCDDGFRIPEENRITCYMGKWSTPPRCVGLPCGPPPSIPLGTVSLELESYQHGEEVTYHCSTGFGIDGPAFIICEGGKWSDPPKCIKTDCDVLPTVKNAIIRGKSKKSYRTGEQVTFRCQSPYQMNGSDTVTCVNSRWIGQPVCKDNSCVDPPHVPNATIVTRTKNKYLHGDRVRYECNKPLELFGQVEVMCENGIWTEKPKCRDSTGKCGPPPPIDNGDITSLSLPVYEPLSSVEYQCQKYYLLKGKKTITCRNGKWSEPPTCLHACVIPENIMESHNIILKWRHTEKIYSHSGEDIEFGCKYGYYKARDSPPFRTKCINGTINYPTCV",
                "length": 1234
            },
            "evidence": [
                {
                    "id": "45923124",
                    "url": "http://www.informatics.jax.org/homology/45923124",
                    "database": "MGI"
                }
            ],
            "common_name": "Mouse"
        }
    ],
    "go_annotation": {
        "categories": [
            {
                "name": "Cellular Component",
                "total": 6,
                "go_terms": [
                    {
                        "name": "extracellular region",
                        "id": "GO:0005576",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005576",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "extracellular space",
                        "id": "GO:0005615",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "extracellular exosome",
                        "id": "GO:0070062",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0070062",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "blood microparticle",
                        "id": "GO:0072562",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0072562",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "serine-type endopeptidase complex",
                        "id": "GO:1905370",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905370",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "symbiont cell surface",
                        "id": "GO:0106139",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0106139",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 6,
                "go_terms": [
                    {
                        "name": "proteolysis",
                        "id": "GO:0006508",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006508",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "regulation of complement activation",
                        "id": "GO:0030449",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030449",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "complement activation",
                        "id": "GO:0006956",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006956",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "complement activation, alternative pathway",
                        "id": "GO:0006957",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006957",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "regulation of complement-dependent cytotoxicity",
                        "id": "GO:1903659",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1903659",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "regulation of complement activation, alternative pathway",
                        "id": "GO:0030451",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030451",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 4,
                "go_terms": [
                    {
                        "name": "heparin binding",
                        "id": "GO:0008201",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008201",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "identical protein binding",
                        "id": "GO:0042802",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042802",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "heparan sulfate proteoglycan binding",
                        "id": "GO:0043395",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043395",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "complement component C3b binding",
                        "id": "GO:0001851",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001851",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P08603",
                                "url": "https://www.uniprot.org/uniprot/P08603"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [
        {
            "name": "complement factor H N-glycosylated 1 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1029 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G00912UN. Example: UniProtKB:P08603-1, Asn-1029, MOD:00160~GNO:G00912UN. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054493",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054493"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 2 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1029 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G04909DG. Example: UniProtKB:P08603-1, Asn-1029, MOD:00160~GNO:G04909DG. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054494",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054494"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 3 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1029 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G08146BT. Example: UniProtKB:P08603-1, Asn-1029, MOD:00160~GNO:G08146BT. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054495",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054495"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 4 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1029 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G08293MJ. Example: UniProtKB:P08603-1, Asn-1029, MOD:00160~GNO:G08293MJ. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054496",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054496"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 5 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1029 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G42358LZ. Example: UniProtKB:P08603-1, Asn-1029, MOD:00160~GNO:G42358LZ. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054497",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054497"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 6 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1029 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G51941GC. Example: UniProtKB:P08603-1, Asn-1029, MOD:00160~GNO:G51941GC. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054498",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054498"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 7 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1029 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G59626AS. Example: UniProtKB:P08603-1, Asn-1029, MOD:00160~GNO:G59626AS. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054499",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054499"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 8 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1029 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G93860XO. Example: UniProtKB:P08603-1, Asn-1029, MOD:00160~GNO:G93860XO. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054500",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054500"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 9 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1095 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G00912UN. Example: UniProtKB:P08603-1, Asn-1095, MOD:00160~GNO:G00912UN. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054501",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054501"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 10 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1095 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G04909DG. Example: UniProtKB:P08603-1, Asn-1095, MOD:00160~GNO:G04909DG. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054502",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054502"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 11 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1095 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G08146BT. Example: UniProtKB:P08603-1, Asn-1095, MOD:00160~GNO:G08146BT. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054503",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054503"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 12 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1095 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G42358LZ. Example: UniProtKB:P08603-1, Asn-1095, MOD:00160~GNO:G42358LZ. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054504",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054504"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 13 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1095 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G75221WP. Example: UniProtKB:P08603-1, Asn-1095, MOD:00160~GNO:G75221WP. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054505",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054505"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 14 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-1095 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G93860XO. Example: UniProtKB:P08603-1, Asn-1095, MOD:00160~GNO:G93860XO. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054506",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054506"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 15 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-217 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G00912UN. Example: UniProtKB:P08603-1, Asn-217, MOD:00160~GNO:G00912UN. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054507",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054507"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 16 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-802 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G04909DG. Example: UniProtKB:P08603-1, Asn-802, MOD:00160~GNO:G04909DG. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054508",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054508"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 17 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-802 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G08146BT. Example: UniProtKB:P08603-1, Asn-802, MOD:00160~GNO:G08146BT. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054509",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054509"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 18 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-802 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G22140GZ. Example: UniProtKB:P08603-1, Asn-802, MOD:00160~GNO:G22140GZ. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054510",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054510"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 19 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-802 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G37399XV. Example: UniProtKB:P08603-1, Asn-802, MOD:00160~GNO:G37399XV. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054511",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054511"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 20 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-802 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G42358LZ. Example: UniProtKB:P08603-1, Asn-802, MOD:00160~GNO:G42358LZ. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054512",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054512"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 21 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-802 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G57818FI. Example: UniProtKB:P08603-1, Asn-802, MOD:00160~GNO:G57818FI. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054513",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054513"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 22 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-802 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G75221WP. Example: UniProtKB:P08603-1, Asn-802, MOD:00160~GNO:G75221WP. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054514",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054514"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 23 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-822 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G00912UN. Example: UniProtKB:P08603-1, Asn-822, MOD:00160~GNO:G00912UN. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054515",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054515"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 24 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-822 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G04909DG. Example: UniProtKB:P08603-1, Asn-822, MOD:00160~GNO:G04909DG. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054516",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054516"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 25 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-822 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G06247RL. Example: UniProtKB:P08603-1, Asn-822, MOD:00160~GNO:G06247RL. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054517",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054517"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 26 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-822 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G08146BT. Example: UniProtKB:P08603-1, Asn-822, MOD:00160~GNO:G08146BT. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054518",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054518"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 27 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-822 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G42358LZ. Example: UniProtKB:P08603-1, Asn-822, MOD:00160~GNO:G42358LZ. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054519",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054519"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 28 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-822 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G51941GC. Example: UniProtKB:P08603-1, Asn-822, MOD:00160~GNO:G51941GC. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054520",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054520"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 29 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-822 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G75221WP. Example: UniProtKB:P08603-1, Asn-822, MOD:00160~GNO:G75221WP. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054521",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054521"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 30 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-822 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G88374WZ. Example: UniProtKB:P08603-1, Asn-822, MOD:00160~GNO:G88374WZ. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054522",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054522"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 31 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-822 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G93860XO. Example: UniProtKB:P08603-1, Asn-822, MOD:00160~GNO:G93860XO. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054523",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054523"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 32 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G00912UN. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G00912UN. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054524",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054524"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 33 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G04909DG. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G04909DG. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054525",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054525"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 34 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G06247RL. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G06247RL. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054526",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054526"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 35 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G08146BT. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G08146BT. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054527",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054527"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 36 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G22140GZ. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G22140GZ. [PRO:DNx, PMID:19838169]",
            "evidence": [
                {
                    "id": "PR:000054528",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054528"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 37 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G27947YN. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G27947YN. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054529",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054529"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 38 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G42358LZ. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G42358LZ. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054530",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054530"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 39 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G51941GC. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G51941GC. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054531",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054531"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 40 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G59626AS. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G59626AS. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054532",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054532"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 41 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G75221WP. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G75221WP. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054533",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054533"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 42 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G85144OK. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G85144OK. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054534",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054534"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 43 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G88374WZ. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G88374WZ. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054535",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054535"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 44 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G93860XO. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G93860XO. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054536",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054536"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 45 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G94917XT. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G94917XT. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054537",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054537"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 46 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-882 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G95865ZB. Example: UniProtKB:P08603-1, Asn-882, MOD:00160~GNO:G95865ZB. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054538",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054538"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 47 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-911 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G00912UN. Example: UniProtKB:P08603-1, Asn-911, MOD:00160~GNO:G00912UN. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054539",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054539"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 48 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-911 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G04909DG. Example: UniProtKB:P08603-1, Asn-911, MOD:00160~GNO:G04909DG. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054540",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054540"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 49 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-911 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G06247RL. Example: UniProtKB:P08603-1, Asn-911, MOD:00160~GNO:G06247RL. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054541",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054541"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 50 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-911 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G08146BT. Example: UniProtKB:P08603-1, Asn-911, MOD:00160~GNO:G08146BT. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054542",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054542"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 51 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-911 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G27947YN. Example: UniProtKB:P08603-1, Asn-911, MOD:00160~GNO:G27947YN. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054543",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054543"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 52 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-911 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G42358LZ. Example: UniProtKB:P08603-1, Asn-911, MOD:00160~GNO:G42358LZ. [PRO:DNx, PMID:17591618, PMID:24279413]",
            "evidence": [
                {
                    "id": "PR:000054544",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054544"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 53 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-911 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G51941GC. Example: UniProtKB:P08603-1, Asn-911, MOD:00160~GNO:G51941GC. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054545",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054545"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 54 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-911 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan composition is represented by GlyTouCan:G59626AS. Example: UniProtKB:P08603-1, Asn-911, MOD:00160~GNO:G59626AS. [PRO:DNx, PMID:29671580]",
            "evidence": [
                {
                    "id": "PR:000054546",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054546"
                }
            ]
        },
        {
            "name": "complement factor H N-glycosylated 55 (human)",
            "definition": "A complement factor H (human) that has been N-glycosylated at the residue equivalent to Asn-911 of the amino acid sequence represented by UniProtKB:P08603-1, in which the glycan structure is represented by GlyTouCan:G93860XO. Example: UniProtKB:P08603-1, Asn-911, MOD:00160~GNO:G93860XO. [PRO:DNx, PMID:17591618]",
            "evidence": [
                {
                    "id": "PR:000054547",
                    "database": "PRO",
                    "url": "https://proconsortium.org/app/entry/PR:000054547"
                }
            ]
        }
    ],
    "site_annotation": [
        {
            "start_pos": 1029,
            "end_pos": 1031,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 1095,
            "end_pos": 1097,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 217,
            "end_pos": 219,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 529,
            "end_pos": 531,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 718,
            "end_pos": 720,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 802,
            "end_pos": 804,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 822,
            "end_pos": 824,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 882,
            "end_pos": 884,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 911,
            "end_pos": 913,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [
        {
            "annotation": "Sulfated on tyrosine residues.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P08603",
                    "url": "https://www.uniprot.org/uniprot/P08603"
                },
                {
                    "database": "PubMed",
                    "id": "25136834",
                    "url": "https://glygen.org/publication/PubMed/25136834"
                }
            ]
        }
    ],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
        },
        {
            "name": "homologset.mgi",
            "label": "MGI Homologs"
        }
    ],
    "sequence_features": {
        "n_linked_sites": [
            217,
            529,
            718,
            802,
            822,
            882,
            911,
            1029,
            1095
        ],
        "o_linked_sites": [],
        "snv_sites": [
            39,
            217,
            232,
            240,
            307,
            308,
            518,
            531,
            542,
            671,
            718,
            776,
            778,
            802,
            822,
            824,
            834,
            884,
            893,
            898,
            911,
            1031,
            1036,
            1045,
            1095,
            1097,
            1104
        ],
        "glycation_sites": [],
        "phosphorylation_sites": [],
        "sequon_annotation_sites": [
            {
                "start_pos": 1029,
                "end_pos": 1031
            },
            {
                "start_pos": 1095,
                "end_pos": 1097
            },
            {
                "start_pos": 217,
                "end_pos": 219
            },
            {
                "start_pos": 529,
                "end_pos": 531
            },
            {
                "start_pos": 718,
                "end_pos": 720
            },
            {
                "start_pos": 802,
                "end_pos": 804
            },
            {
                "start_pos": 822,
                "end_pos": 824
            },
            {
                "start_pos": 882,
                "end_pos": 884
            },
            {
                "start_pos": 911,
                "end_pos": 913
            }
        ]
    },
    "section_stats": [
        {
            "table_id": "glycosylation",
            "table_stats": [
                {
                    "field": "total",
                    "count": 202
                },
                {
                    "field": "total_sites",
                    "count": 9
                },
                {
                    "field": "n_linked_glycans",
                    "count": 66
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 18
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_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"
            ]
        },
        {
            "table_id": "glycosylation_reported",
            "table_stats": [
                {
                    "field": "total",
                    "count": 9
                },
                {
                    "field": "total_sites",
                    "count": 9
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 9
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