{
    "uniprot_canonical_ac": "P24090-1",
    "uniprot_ac": "P24090",
    "uniprot_id": "FETUA_RAT",
    "mass": {
        "chemical_mass": 37982.0,
        "monoisotopic_mass": 37982.0
    },
    "refseq": {
        "ac": "NP_037030",
        "name": "alpha-2-HS-glycoprotein precursor",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_037030"
    },
    "gene_names": [
        {
            "name": "Ahsg",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/P24090",
            "id": "P24090"
        },
        {
            "name": "AABR07034632.1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/P24090",
            "id": "P24090"
        },
        {
            "name": "Aa2-066; BSP; pp63",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_037030",
            "id": "NP_037030"
        },
        {
            "name": "Ahsg",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_037030",
            "id": "NP_037030"
        },
        {
            "name": "Fetua",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/P24090",
            "id": "P24090"
        }
    ],
    "protein_names": [
        {
            "name": "Alpha-2-HS-glycoprotein",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "P24090"
        },
        {
            "name": "59 kDa bone sialic acid-containing protein",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P24090"
        },
        {
            "name": "BSP",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P24090"
        },
        {
            "name": "Fetuin-A",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P24090"
        },
        {
            "name": "Glycoprotein PP63",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P24090"
        },
        {
            "name": "alpha-2-HS-glycoprotein precursor",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_037030",
            "id": "NP_037030"
        },
        {
            "name": "fetuin-A; glycoprotein PP63; 59 kDa bone sialic acid-containing protein; alpha 2 HS-glycoprotein alpha 2 (fetuin); phosphorylated N-glycoprotein pp63",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_037030",
            "id": "NP_037030"
        }
    ],
    "function": [
        {
            "annotation": "Could inhibit both insulin-receptor tyrosine kinase activity and insulin-stimulated receptor autophosphorylation and, concomitantly, antagonize the mitogenic effect of the hormone in cultured rat hepatoma cells.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P24090",
                    "url": "https://www.uniprot.org/uniprot/P24090#function"
                }
            ]
        },
        {
            "annotation": "Fetuin-A Deficiency but Not Pentraxin 3, FGF-21, or Irisin, Predisposes to More Serious COVID-19 Course. Publication Status: Online-Only",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_037030",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_037030"
                },
                {
                    "database": "PubMed",
                    "id": "34680053",
                    "url": "https://glygen.org/publication/PubMed/34680053"
                }
            ]
        },
        {
            "annotation": "Fetuin-A exerts the stimulatory effects on inflammatory responses in HUVECs, macrophage foam cell formation, and proliferation and collagen production in HASMCs, leading to the development of atherosclerosis. Erratum:[Atherosclerosis. 2016 Oct;253:346. PMID: 27184817]",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_037030",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_037030"
                },
                {
                    "database": "PubMed",
                    "id": "26828753",
                    "url": "https://glygen.org/publication/PubMed/26828753"
                }
            ]
        },
        {
            "annotation": "The protective effects of pioglitazone on lipotoxicity in beta cells may involve the inhibition of the activation of the Fetuin A and TLR4 signaling pathway.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_037030",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_037030"
                },
                {
                    "database": "PubMed",
                    "id": "25986658",
                    "url": "https://glygen.org/publication/PubMed/25986658"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0080628",
            "recommended_name": {
                "id": "DOID:0080628",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0080628",
                "name": "alopecia-mental retardation syndrome 1",
                "description": "An alopecia-mental retardation syndrome that has_material_basis_in homozygous mutation in the AHSG gene on chromosome 3q27."
            },
            "synonyms": [
                {
                    "id": "MONDO:0021035",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0021035",
                    "name": "alopecia-intellectual disability syndrome 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0021035",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0021035",
                    "name": "APMR",
                    "description": ""
                },
                {
                    "id": "MONDO:0021035",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0021035",
                    "name": "APMR1",
                    "description": ""
                },
                {
                    "id": "MONDO:0021035",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0021035",
                    "name": "alopecia-intellectual disability syndrome 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0021035",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0021035",
                    "name": "alopecia-mental retardation syndrome 1",
                    "description": ""
                },
                {
                    "id": "MIM:203650",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/203650",
                    "name": "Alopecia-intellectual disability syndrome 1",
                    "description": "Alopecia-intellectual disability syndrome 1"
                }
            ],
            "evidence": [
                {
                    "id": "0080628",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0080628"
                }
            ]
        },
        {
            "disease_id": "DOID:11714",
            "recommended_name": {
                "id": "DOID:11714",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:11714",
                "name": "gestational diabetes",
                "description": "A diabetes mellitus that manifests during pregnancy."
            },
            "synonyms": [
                {
                    "id": "DOID:11714",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11714",
                    "name": "GDM",
                    "description": ""
                },
                {
                    "id": "DOID:11714",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11714",
                    "name": "Gestational diabetes mellitus",
                    "description": ""
                },
                {
                    "id": "DOID:11714",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11714",
                    "name": "Maternal gestational diabetes mellitus",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "11714",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:11714"
                }
            ]
        },
        {
            "disease_id": "DOID:3393",
            "recommended_name": {
                "id": "DOID:3393",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:3393",
                "name": "coronary artery disease",
                "description": "An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles."
            },
            "synonyms": [
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "CHD",
                    "description": ""
                },
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "Coronary disease",
                    "description": ""
                },
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "coronary arteriosclerosis",
                    "description": ""
                },
                {
                    "id": "DOID:3393",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:3393",
                    "name": "coronary heart disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "coronary heart disease, susceptibility to, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "coronary heart disease, susceptibility to, 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "coronary heart disease, susceptibility to, type 4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012010",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012010",
                    "name": "Chds4",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "coronary heart disease, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "coronary heart disease, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "coronary heart disease, susceptibility to, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012009",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012009",
                    "name": "Chds2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform mole, recurrent, 2",
                    "description": "Any complete hydatidiform mole in which the cause of the disease is a mutation in the KHDC3L gene."
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "KHDC3L complete hydatidiform mole",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "complete hydatidiform mole caused by mutation in KHDC3L",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform Mole, recurrent, type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform mole, recurrent, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "HYDM2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform MOLE, recurrent, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013671",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013671",
                    "name": "hydatidiform Mole, complete",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to, 1",
                    "description": "Any coronary artery disease in which the cause of the disease is a mutation in the CX3CR1 gene."
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "CX3CR1 coronary artery disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary artery disease caused by mutation in CX3CR1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary artery disease, resistance to",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "coronary heart disease, susceptibility to, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0011817",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011817",
                    "name": "Chds1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease, autosomal dominant, 1",
                    "description": "Any coronary artery disease in which the cause of the disease is a mutation in the MEF2A gene."
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "MEF2A coronary artery disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease caused by mutation in MEF2A",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease, autosomal dominant, 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease, autosomal dominant, type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "ADCAD1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012011",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012011",
                    "name": "coronary artery disease with myocardial infarction",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant 2",
                    "description": "Any coronary artery disease in which the cause of the disease is a mutation in the LRP6 gene."
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "LRP6 coronary artery disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease caused by mutation in LRP6",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "coronary artery disease, autosomal dominant, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012586",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012586",
                    "name": "ADCAD2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012788",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012788",
                    "name": "coronary heart disease, susceptibility to, 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012788",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012788",
                    "name": "CHDS9",
                    "description": ""
                },
                {
                    "id": "MONDO:0012788",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012788",
                    "name": "coronary heart disease, susceptibility to, 9",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "coronary heart disease, susceptibility to, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "coronary heart disease, susceptibility to, 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "coronary heart disease, susceptibility to, type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0010331",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0010331",
                    "name": "Chds3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012628",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012628",
                    "name": "coronary heart disease, susceptibility to, 8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012628",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012628",
                    "name": "CHDS8",
                    "description": ""
                },
                {
                    "id": "MONDO:0012628",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012628",
                    "name": "coronary heart disease, susceptibility to, 8",
                    "description": ""
                },
                {
                    "id": "MIM:614293",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/614293",
                    "name": "Hydatidiform mole, recurrent, 2",
                    "description": "Hydatidiform mole, recurrent, 2"
                },
                {
                    "id": "MIM:608320",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/608320",
                    "name": "Coronary artery disease, autosomal dominant, 1",
                    "description": "Coronary artery disease, autosomal dominant, 1"
                },
                {
                    "id": "MIM:610947",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/610947",
                    "name": "Coronary artery disease, autosomal dominant, 2",
                    "description": "Coronary artery disease, autosomal dominant, 2"
                }
            ],
            "evidence": [
                {
                    "id": "3393",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:3393"
                }
            ]
        },
        {
            "disease_id": "DOID:5844",
            "recommended_name": {
                "id": "DOID:5844",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:5844",
                "name": "myocardial infarction",
                "description": "A coronary artery disease characterized by myocardial cell death (myocardial necrosis) due to prolonged ischaemia."
            },
            "synonyms": [
                {
                    "id": "DOID:5844",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5844",
                    "name": "Myocardial infarct",
                    "description": ""
                },
                {
                    "id": "DOID:5844",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:5844",
                    "name": "heart attack",
                    "description": ""
                },
                {
                    "id": "MONDO:0012058",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012058",
                    "name": "myocardial infarction, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012058",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012058",
                    "name": "myocardial infarction, susceptibility to, 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012058",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012058",
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                    "id": "MONDO:0012058",
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                "url": "http://disease-ontology.org/term/DOID:9352",
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            "id": "R-RNO-114608",
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            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "R-RNO-381426",
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            "database": "Reactome",
            "categories": [
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            ]
        },
        {
            "id": "R-RNO-6798695",
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            "database": "Reactome",
            "categories": [
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        {
            "id": "R-RNO-8957275",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-8957275",
            "database": "Reactome",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "NP_037030",
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            "database": "RefSeq",
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            ]
        },
        {
            "id": "15004297",
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            "database": "RGD",
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            ]
        },
        {
            "id": "2075",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=2075",
            "database": "RGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "P24090",
            "url": "DISABLED",
            "database": "UniCarbKB",
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        },
        {
            "id": "A0A8I5Y586",
            "url": "https://www.uniprot.org/uniprot/A0A8I5Y586",
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        },
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            ]
        },
        {
            "id": "A0A8I5ZY55-1",
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            ]
        },
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            "id": "F1LM19-1",
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        },
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        }
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        "length": 352,
        "header": "sp|P24090-1|FETUA_RAT Isoform 1 of Alpha-2-HS-glycoprotein  OS=Rattus norvegicus OX=10116 GN=Ahsg PE=1 SV=2 CANONICAL=P24090-1"
    },
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                "length": 301,
                "header": "tr|A0A8I5Y586-1|A0A8I5Y586_RAT Computationally mapped isoform of Alpha-2-HS-glycoprotein  OS=Rattus norvegicus OX=10116 GN=Ahsg PE=1 SV=1 CANONICAL=P24090-1"
            },
            "locus": {
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                    {
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                        "id": "ENSRNOT00000108250.1",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000108250.1"
                    },
                    {
                        "database": "Ensembl Peptide",
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                    }
                ]
            }
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                "length": 557,
                "header": "tr|A0A8I5ZY55-1|FETUA_RAT Computationally mapped isoform of Alpha-2-HS-glycoprotein  OS=Rattus norvegicus OX=10116 GN=Ahsg PE=1 SV=1 CANONICAL=P24090-1"
            },
            "locus": {
                "chromosome": "11",
                "start_pos": 78129328,
                "end_pos": 78121750,
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                        "id": "ENSRNOT00000103458.1",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000103458.1"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000082555.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000082555.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "F1LM19-1",
            "url": "",
            "sequence": {
                "sequence": "MKSLVLLLCFAQLWSCQSAPQGAGLGFRELACDDPETEHVALIAVDYLNKHLLQGFRQILNQIDKVKVWSRRPFGEVYELEIDTLETTCHALDPTPLANCSVRQQAEHAVEGDCDFHILKQDGQFRVLHAQCHSTPDSAEDVRKFCPRCPILIRFNDTNVVHTVKTALAAFNAQNNGTYFKLVEISRAQNVPIGCSVLFSLYFSARDVTEKKRKQEAKIFLLQKQQYGFCKATLIHRLGGEEVSVACKLFQTQPQPANANPAGPAPTVGQAAPVAPPAGPPESVVVGPVAVPLGLPDHRTHHDLRHAFSPVASVESASGEVLHSPKVGQPGDAGAAGPVAPLCPGRVRYFKI",
                "length": 352,
                "header": "tr|F1LM19-1|F1LM19_RAT Computationally mapped isoform of Alpha-2-HS-glycoprotein  OS=Rattus norvegicus OX=10116 GN=Ahsg PE=1 SV=3 CANONICAL=P24090-1"
            },
            "locus": {
                "chromosome": "11",
                "start_pos": 78127926,
                "end_pos": 78121750,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000058422",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000058422"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000055223",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000055223"
                    }
                ]
            }
        },
        {
            "isoform_ac": "P24090-1",
            "url": "",
            "sequence": {
                "sequence": "MKSLVLLLCFAQLWSCQSAPQGAGLGFRELACDDPETEHVALIAVDYLNKHLLQGFRQILNQIDKVKVWSRRPFGEVYELEIDTLETTCHALDPTPLANCSVRQQAEHAVEGDCDFHILKQDGQFRVLHAQCHSTPDSAEDVRKFCPRCPILIRFNDTNVVHTVKTALAAFNAQNNGTYFKLVEISRAQNVPFPVSTLVEFVIAATDCTGQEVTDPAKCNLLAEKQYGFCKATLIHRLGGEEVSVACKLFQTQPQPANANPAGPAPTVGQAAPVAPPAGPPESVVVGPVAVPLGLPDHRTHHDLRHAFSPVASVESASGEVLHSPKVGQPGDAGAAGPVAPLCPGRVRYFKI",
                "length": 352,
                "header": "sp|P24090-1|FETUA_RAT Isoform 1 of Alpha-2-HS-glycoprotein  OS=Rattus norvegicus OX=10116 GN=Ahsg PE=1 SV=2 CANONICAL=P24090-1"
            },
            "locus": {
                "chromosome": "11",
                "start_pos": 78127926,
                "end_pos": 78121750,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000058422",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000058422"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000055223",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000055223"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q7TP75-1",
            "url": "",
            "sequence": {
                "sequence": "MPSGPGGEVFGEEGEVFREEGEIFREEGEVFREEGEVFREEGEVCREEGEVCREEGEVCMEEGEVCMEEGEVCMEEGEVCREEGEVFREEGEVCMEEGEVFREEGEVCREEGEVCRKEGEVCREEGDVFREEGEVFREVGEVCMEEGEVFREEGEVLKEEGEIFREEGEVLKEEGEVCMEEGEVFREEGEVCMEEGEIFREEGEYLEGDQSTTLEESGLSGAAMKSLVLLLCFAQLWSCQSAPQGAGLGFRELACDDPETEHVALIAVDYLNKHLLQGFRQILNQIDKVKVWSRRPFGEVYELEIDTLETTCHALDPTPLANCSVRQQAEHAVEGDCDFHILKQDGQFRVLHAQCHSTPDSAEDVRKFCPRCPILIRFNDTNVVHTVKTALAAFNAQNNGTYFKLVEISRAQNVQYGFCKATLIHRLGGEEVSVACKLFQTQPQPANANPAGPAPTVGQAAPVAPPAGPPESVVVGPVAVPLGLPDHRTHHDLRHAFSPVASVESASGEVLHSPKNFFMSILSDIFYLLLLLLLLLLLLLLLLLAVVIVIVLV",
                "length": 553,
                "header": "tr|Q7TP75-1|Q7TP75_RAT Computationally mapped isoform of Alpha-2-HS-glycoprotein  OS=Rattus norvegicus OX=10116 GN=Ahsg PE=1 SV=1 CANONICAL=P24090-1"
            },
            "locus": {
                "chromosome": "11",
                "start_pos": 78145956,
                "end_pos": 78117921,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000078203.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000078203.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000073898.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000073898.1"
                    }
                ]
            }
        }
    ],
    "glycosylation": [
        {
            "glytoucan_ac": "G00912UN",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported_with_glycan",
            "site_seq": "N",
            "relation": "attached",
            "comment": "",
            "start_pos": 156,
            "start_aa": "Asn",
            "end_pos": 156,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn156",
            "evidence": [
                {
                    "id": "P24090",
                    "database": "UniCarbKB",
                    "url": ""
                },
                {
                    "id": "34106099",
                    "database": "PubMed",
                    "url": "https://glygen.org/publication/PubMed/34106099"
                },
                {
                    "id": "10.1039/D0MO00044B",
                    "database": "DOI",
                    "url": "https://glygen.org/publication/DOI/10.1039/D0MO00044B"
                }
            ]
        },
        {
            "glytoucan_ac": "",
            "type": "N-linked",
            "subtype": "",
            "site_category": "reported",
            "site_seq": "N",
            "relation": "attached",
            "comment": "N-linked (GlcNAc...) asparagine",
            "start_pos": 156,
            "start_aa": "Asn",
            "end_pos": 156,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn156",
            "evidence": [
                {
                    "id": "P24090",
                    "database": "UniProtKB",
                    "url": "https://www.uniprot.org/uniprot/P24090#ptm_processing"
                }
            ]
        },
        {
            "glytoucan_ac": "",
            "type": "N-linked",
            "subtype": "",
            "site_category": "predicted",
            "site_seq": "N",
            "relation": "attached",
            "comment": "N-linked (GlcNAc...) asparagine",
            "start_pos": 176,
            "start_aa": "Asn",
            "end_pos": 176,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn176",
            "evidence": [
                {
                    "id": "P24090",
                    "database": "UniProtKB",
                    "url": "https://www.uniprot.org/uniprot/P24090#ptm_processing"
                }
            ]
        },
        {
            "glytoucan_ac": "",
            "type": "N-linked",
            "subtype": "",
            "site_category": "predicted",
            "site_seq": "N",
            "relation": "attached",
            "comment": "N-linked (GlcNAc...) asparagine",
            "start_pos": 99,
            "start_aa": "Asn",
            "end_pos": 99,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn99",
            "evidence": [
                {
                    "id": "P24090",
                    "database": "UniProtKB",
                    "url": "https://www.uniprot.org/uniprot/P24090#ptm_processing"
                }
            ]
        }
    ],
    "phosphorylation": [
        {
            "start_pos": 134,
            "end_pos": 134,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P24090",
                    "url": "https://www.uniprot.org/uniprot/P24090"
                }
            ],
            "site_lbl": "Ser134"
        },
        {
            "start_pos": 135,
            "end_pos": 135,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Thr",
            "comment": "Phosphothreonine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P24090",
                    "url": "https://www.uniprot.org/uniprot/P24090"
                }
            ],
            "site_lbl": "Thr135"
        },
        {
            "start_pos": 138,
            "end_pos": 138,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P24090",
                    "url": "https://www.uniprot.org/uniprot/P24090"
                },
                {
                    "database": "PubMed",
                    "id": "16641100",
                    "url": "https://glygen.org/publication/PubMed/16641100"
                },
                {
                    "database": "PubMed",
                    "id": "22673903",
                    "url": "https://glygen.org/publication/PubMed/22673903"
                },
                {
                    "database": "iPTMnet",
                    "id": "P24090",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P24090"
                }
            ],
            "site_lbl": "Ser138"
        },
        {
            "start_pos": 309,
            "end_pos": 309,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P24090",
                    "url": "https://www.uniprot.org/uniprot/P24090"
                },
                {
                    "database": "PubMed",
                    "id": "22673903",
                    "url": "https://glygen.org/publication/PubMed/22673903"
                },
                {
                    "database": "iPTMnet",
                    "id": "P24090",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P24090"
                }
            ],
            "site_lbl": "Ser309"
        },
        {
            "start_pos": 313,
            "end_pos": 313,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P24090",
                    "url": "https://www.uniprot.org/uniprot/P24090"
                },
                {
                    "database": "PubMed",
                    "id": "22673903",
                    "url": "https://glygen.org/publication/PubMed/22673903"
                },
                {
                    "database": "phospho.ELM",
                    "id": "P24090",
                    "url": "http://phospho.elm.eu.org/byAccession/P24090.html"
                },
                {
                    "database": "iPTMnet",
                    "id": "P24090",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P24090"
                },
                {
                    "database": "PubMed",
                    "id": "16396499",
                    "url": "https://glygen.org/publication/PubMed/16396499"
                }
            ],
            "site_lbl": "Ser313"
        },
        {
            "start_pos": 316,
            "end_pos": 316,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P24090",
                    "url": "https://www.uniprot.org/uniprot/P24090"
                },
                {
                    "database": "PubMed",
                    "id": "22673903",
                    "url": "https://glygen.org/publication/PubMed/22673903"
                },
                {
                    "database": "phospho.ELM",
                    "id": "P24090",
                    "url": "http://phospho.elm.eu.org/byAccession/P24090.html"
                },
                {
                    "database": "iPTMnet",
                    "id": "P24090",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P24090"
                },
                {
                    "database": "PubMed",
                    "id": "16396499",
                    "url": "https://glygen.org/publication/PubMed/16396499"
                }
            ],
            "site_lbl": "Ser316"
        },
        {
            "start_pos": 318,
            "end_pos": 318,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P24090",
                    "url": "https://www.uniprot.org/uniprot/P24090"
                },
                {
                    "database": "PubMed",
                    "id": "22673903",
                    "url": "https://glygen.org/publication/PubMed/22673903"
                },
                {
                    "database": "phospho.ELM",
                    "id": "P24090",
                    "url": "http://phospho.elm.eu.org/byAccession/P24090.html"
                },
                {
                    "database": "iPTMnet",
                    "id": "P24090",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P24090"
                },
                {
                    "database": "PubMed",
                    "id": "16396499",
                    "url": "https://glygen.org/publication/PubMed/16396499"
                }
            ],
            "site_lbl": "Ser318"
        }
    ],
    "glycation": [],
    "keywords": [
        "glycoprotein",
        "glycoprotein_reported_with_glycan",
        "glycoprotein_reported",
        "glycoprotein_predicted"
    ],
    "publication": [
        {
            "title": "N-Glycosylation in isolated rat nerve terminals",
            "journal": "Molecular Omics",
            "date": "2021",
            "authors": "Matthies I., Abrahams J.L., Jensen P., Oliveira T., Kolarich D., Larsen M.R.",
            "evidence": [
                {
                    "database": "UniCarbKB",
                    "id": "P24090",
                    "url": ""
                }
            ],
            "reference": [
                {
                    "type": "DOI",
                    "id": "10.1039/D0MO00044B",
                    "url": "https://glygen.org/publication/DOI/10.1039/D0MO00044B"
                }
            ]
        },
        {
            "title": "The rat protein encoded by clone pp63 is a fetuin/alpha 2-HS glycoprotein-like molecule, but is it the tyrosine kinase inhibitor pp63?",
            "journal": "Cell",
            "date": "1992",
            "authors": "Brown WM, Christie DL, Dziegielewska KM, Saunders NR, Yang F",
            "evidence": [
                {
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            "title": "Quantitative phosphoproteomics of vasopressin-sensitive renal cells: regulation of aquaporin-2 phosphorylation at two sites.",
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