{
    "uniprot_canonical_ac": "A0A0G2JSV6-1",
    "uniprot_ac": "A0A0G2JSV6",
    "uniprot_id": "A0A0G2JSV6_RAT",
    "mass": {
        "chemical_mass": 15285.0,
        "monoisotopic_mass": 15285.0
    },
    "refseq": {
        "ac": "NP_001007723",
        "name": "hemoglobin alpha, adult chain 2",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001007723"
    },
    "gene_names": [
        {
            "name": "Hba-a2",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6",
            "id": "A0A0G2JSV6"
        },
        {
            "name": "Glnc2; Glnc3; Hba-a1; Hba1; Hba2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001007723",
            "id": "NP_001007723"
        },
        {
            "name": "Glnc2",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6",
            "id": "A0A0G2JSV6"
        },
        {
            "name": "Hba-a2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001007723",
            "id": "NP_001007723"
        },
        {
            "name": "Hba2",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6",
            "id": "A0A0G2JSV6"
        },
        {
            "name": "rCG_34342",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6",
            "id": "A0A0G2JSV6"
        }
    ],
    "protein_names": [
        {
            "name": "2-alpha-1 globin; 2-alpha globin; hemoglobin alpha 2 chain; globin c2; globin c3; Hemoglobin subunit alpha-1/2; Alpha-1/2-globin; Hemoglobin alpha-1/2 chain; hemoglobin, alpha 2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001007723",
            "id": "NP_001007723"
        },
        {
            "name": "Globin c2",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6#names_and_taxonomy",
            "id": "A0A0G2JSV6"
        },
        {
            "name": "Hemoglobin alpha, adult chain 2",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6#names_and_taxonomy",
            "id": "A0A0G2JSV6"
        },
        {
            "name": "RCG34342, isoform CRA_a",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6#names_and_taxonomy",
            "id": "A0A0G2JSV6"
        },
        {
            "name": "hemoglobin alpha, adult chain 2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001007723",
            "id": "NP_001007723"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0110031",
            "recommended_name": {
                "id": "DOID:0110031",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110031",
                "name": "hemoglobin H disease",
                "description": "An alpha thalassemia that has_material_basis_in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other."
            },
            "synonyms": [
                {
                    "id": "DOID:0110031",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110031",
                    "name": "HBH",
                    "description": ""
                },
                {
                    "id": "DOID:0110031",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110031",
                    "name": "alpha thalassemia, haemoglobin H type",
                    "description": ""
                },
                {
                    "id": "DOID:0110031",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110031",
                    "name": "alpha thalassemia, hemoglobin H type",
                    "description": ""
                },
                {
                    "id": "DOID:0110031",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110031",
                    "name": "alpha-thalassemia intermedia",
                    "description": ""
                },
                {
                    "id": "DOID:0110031",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110031",
                    "name": "haemoglobin H disease",
                    "description": ""
                },
                {
                    "id": "DOID:0110031",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110031",
                    "name": "haemoglobin H disease, deletional",
                    "description": ""
                },
                {
                    "id": "DOID:0110031",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110031",
                    "name": "hemoglobin H disease, deletional",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "hemoglobin H disease",
                    "description": "Hemoglobin H (HbH) disease is a moderate to severe form of alpha-thalassemia (see this term) characterized by pronounced microcytic hypochromic hemolytic anemia."
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "Hemoglobin H disease, Deletional",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "HbH disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "alpha-thalassemia intermedia",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "HEMOGLOBIN H disease; HbH",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "alpha thalassemia, hemoglobin H type",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "Alpha-thalassemia intermedia",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "hemoglobin H disease, deletional",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "Hemoglobin H disease, Nondeletional",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "HbH",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "Alpha-thalassemia, Hemoglobin H type",
                    "description": ""
                },
                {
                    "id": "MONDO:0013512",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013512",
                    "name": "hemoglobin H disease",
                    "description": ""
                },
                {
                    "id": "MIM:613978",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/613978",
                    "name": "Hemoglobin H disease",
                    "description": "Hemoglobin H disease"
                }
            ],
            "evidence": [
                {
                    "id": "0110031",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110031"
                }
            ]
        },
        {
            "disease_id": "DOID:0111363",
            "recommended_name": {
                "id": "DOID:0111363",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0111363",
                "name": "Heinz body anemia",
                "description": "A congenital nonspherocytic hemolytic anemia characterized by nonspherocytic hemolytic anemia of Dacie type I with Heinz bodies seen in erythrocytes after splenectomy that has_material_basis_in heterozygous mutation in HBA1, HBA2 or HBB on chromosome 11p15.4, 16p13.3, and 16p13.3, respectively."
            },
            "synonyms": [
                {
                    "id": "MONDO:0007705",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007705",
                    "name": "Heinz body anemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0007705",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007705",
                    "name": "Heinz body anemias",
                    "description": ""
                },
                {
                    "id": "MIM:140700",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/140700",
                    "name": "Heinz body anemias",
                    "description": "Heinz body anemias"
                }
            ],
            "evidence": [
                {
                    "id": "0111363",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111363"
                }
            ]
        },
        {
            "disease_id": "DOID:0111631",
            "recommended_name": {
                "id": "DOID:0111631",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0111631",
                "name": "familial erythrocytosis 7",
                "description": "A primary polycythemia characterized by high oxygen affinity hemoglobin and compensatory polycythemia that has_material_basis_in heterozygous mutation in either HBA2 or HBA1 on chromosome 16p13.3."
            },
            "synonyms": [
                {
                    "id": "DOID:0111631",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111631",
                    "name": "ECYT7",
                    "description": ""
                },
                {
                    "id": "DOID:0111631",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111631",
                    "name": "alpha-globin type erythrocytosis",
                    "description": ""
                },
                {
                    "id": "DOID:0111631",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111631",
                    "name": "alpha-globin type polycythemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0054802",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0054802",
                    "name": "erythrocytosis, familial, 7",
                    "description": ""
                },
                {
                    "id": "MONDO:0054802",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0054802",
                    "name": "erythrocytosis, Alpha-globin type",
                    "description": ""
                },
                {
                    "id": "MONDO:0054802",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0054802",
                    "name": "erythrocytosis, FAMILIAL, 7; ECYT7",
                    "description": ""
                },
                {
                    "id": "MONDO:0054802",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0054802",
                    "name": "polycythemia, Alpha-globin type",
                    "description": ""
                },
                {
                    "id": "MONDO:0054802",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0054802",
                    "name": "ECYT7",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "0111631",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111631"
                }
            ]
        },
        {
            "disease_id": "DOID:1099",
            "recommended_name": {
                "id": "DOID:1099",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1099",
                "name": "alpha thalassemia",
                "description": "Alpha thalassemia is a thalassemia involving the genes HBA1and HBA2 hemoglobin genes."
            },
            "synonyms": [
                {
                    "id": "DOID:1099",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1099",
                    "name": "Alpha thalassaemia",
                    "description": ""
                },
                {
                    "id": "DOID:1099",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1099",
                    "name": "alpha-Thalassemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0011399",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011399",
                    "name": "alpha thalassemia",
                    "description": "Alpha-thalassemia is an inherited hemoglobinopathy characterized by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles."
                },
                {
                    "id": "MONDO:0011399",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011399",
                    "name": "A-thalassemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0011399",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011399",
                    "name": "alpha-thalassemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0011399",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011399",
                    "name": "Alpha thalassaemia",
                    "description": ""
                },
                {
                    "id": "MIM:604131",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/604131",
                    "name": "Alpha-thalassemia",
                    "description": "Alpha-thalassemia"
                }
            ],
            "evidence": [
                {
                    "id": "1099",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1099"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0G2JSV6",
                    "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Hba-a2",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6",
            "locus": {
                "chromosome": "10",
                "start_pos": 15590220,
                "end_pos": 15589364,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSRNOG00000047321",
                        "url": "https://www.ensembl.org/id/ENSRNOG00000047321"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "ENSRNOG00000047321",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000047321",
            "database": "Bgee"
        },
        {
            "id": "cd08927",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd08927",
            "database": "CDD"
        },
        {
            "id": "360504",
            "url": "https://www.ncbi.nlm.nih.gov/gene/360504",
            "database": "GeneID"
        },
        {
            "id": "IPR000971",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR000971",
            "database": "InterPro"
        },
        {
            "id": "IPR002338",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR002338",
            "database": "InterPro"
        },
        {
            "id": "IPR002339",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR002339",
            "database": "InterPro"
        },
        {
            "id": "IPR009050",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR009050",
            "database": "InterPro"
        },
        {
            "id": "IPR012292",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR012292",
            "database": "InterPro"
        },
        {
            "id": "rno:360504",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:360504",
            "database": "KEGG Pathway"
        },
        {
            "id": "TTKTYFH",
            "url": "https://omabrowser.org/oma/group/TTKTYFH/",
            "database": "OMA"
        },
        {
            "id": "1398217at2759",
            "url": "http://www.orthodb.org/?query=1398217at2759",
            "database": "OrthoDB"
        },
        {
            "id": "PF00042",
            "url": "http://pfam.xfam.org/family/PF00042",
            "database": "Pfam"
        },
        {
            "id": "R-RNO-1237044",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-1237044",
            "database": "Reactome"
        },
        {
            "id": "R-RNO-1247673",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-1247673",
            "database": "Reactome"
        },
        {
            "id": "R-RNO-2168880",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-2168880",
            "database": "Reactome"
        },
        {
            "id": "R-RNO-9707564",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-9707564",
            "database": "Reactome"
        },
        {
            "id": "R-RNO-9707616",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-9707616",
            "database": "Reactome"
        },
        {
            "id": "NP_001007723",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001007723",
            "database": "RefSeq"
        },
        {
            "id": "1359364",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1359364",
            "database": "RGD"
        },
        {
            "id": "A0A0G2JSV6",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6",
            "database": "UniProtKB"
        },
        {
            "id": "A0A0G2JSV6-1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6-1",
            "database": "UniProtKB"
        }
    ],
    "sequence": {
        "sequence": "MVLSAADKTNIKNCWGKIGGHGGEYGEEALQRMFAAFPTTKTYFSHIDVSPGSAQVKAHGKKVADALAKAADHVEDLPGALSTLSDLHAHKLRVDPVNFKFLSHCLLVTLACHHPGDFTPAMHASLDKFLASVSTVLTSKYR",
        "length": 142,
        "header": "tr|A0A0G2JSV6-1|A0A0G2JSV6_RAT Isoform 1 of Globin c2  OS=Rattus norvegicus OX=10116 GN=Hba-a2 PE=1 SV=1 CANONICAL=A0A0G2JSV6-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A0A0G2JSV6-1",
            "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6#A0A0G2JSV6-1",
            "sequence": {
                "sequence": "MVLSAADKTNIKNCWGKIGGHGGEYGEEALQRMFAAFPTTKTYFSHIDVSPGSAQVKAHGKKVADALAKAADHVEDLPGALSTLSDLHAHKLRVDPVNFKFLSHCLLVTLACHHPGDFTPAMHASLDKFLASVSTVLTSKYR",
                "length": 142,
                "header": "tr|A0A0G2JSV6-1|A0A0G2JSV6_RAT Isoform 1 of Globin c2  OS=Rattus norvegicus OX=10116 GN=Hba-a2 PE=1 SV=1 CANONICAL=A0A0G2JSV6-1"
            },
            "locus": {
                "chromosome": "10",
                "start_pos": 15590174,
                "end_pos": 15589449,
                "strand": "+",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000048977",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000048977"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000044081",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000044081"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "rno:360504",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:360504",
            "resource": "KEGG Pathway"
        },
        {
            "id": "R-RNO-1237044",
            "name": "Erythrocytes take up carbon dioxide and release oxygen",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-1237044",
            "resource": "Reactome",
            "description": "Erythrocytes take up carbon dioxide and release oxygen"
        },
        {
            "id": "R-RNO-1247673",
            "name": "Erythrocytes take up oxygen and release carbon dioxide",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-1247673",
            "resource": "Reactome",
            "description": "Erythrocytes take up oxygen and release carbon dioxide"
        },
        {
            "id": "R-RNO-2168880",
            "name": "Scavenging of heme from plasma",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-2168880",
            "resource": "Reactome",
            "description": "Scavenging of heme from plasma"
        },
        {
            "id": "R-RNO-9707564",
            "name": "Cytoprotection by HMOX1",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-9707564",
            "resource": "Reactome",
            "description": "Cytoprotection by HMOX1"
        },
        {
            "id": "R-RNO-9707616",
            "name": "Heme signaling",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-9707616",
            "resource": "Reactome",
            "description": "Heme signaling"
        }
    ],
    "orthologs": [
        {
            "uniprot_canonical_ac": "P01946-1",
            "protein_name": "Hemoglobin subunit alpha-1/2",
            "gene_name": "Hba1",
            "tax_id": 10116,
            "organism": "Rattus norvegicus",
            "sequence": {
                "sequence": "MVLSADDKTNIKNCWGKIGGHGGEYGEEALQRMFAAFPTTKTYFSHIDVSPGSAQVKAHGKKVADALAKAADHVEDLPGALSTLSDLHAHKLRVDPVNFKFLSHCLLVTLACHHPGDFTPAMHASLDKFLASVSTVLTSKYR",
                "length": 142
            },
            "evidence": [
                {
                    "id": "133979",
                    "url": "http://www.informatics.jax.org/homology/133979",
                    "database": "MGI"
                }
            ],
            "common_name": "Rat"
        },
        {
            "uniprot_canonical_ac": "P69905-1",
            "protein_name": "Hemoglobin subunit alpha",
            "gene_name": "HBA2",
            "tax_id": 9606,
            "organism": "Homo sapiens",
            "sequence": {
                "sequence": "MVLSPADKTNVKAAWGKVGAHAGEYGAEALERMFLSFPTTKTYFPHFDLSHGSAQVKGHGKKVADALTNAVAHVDDMPNALSALSDLHAHKLRVDPVNFKLLSHCLLVTLAAHLPAEFTPAVHASLDKFLASVSTVLTSKYR",
                "length": 142
            },
            "evidence": [
                {
                    "id": "A0A0G2JSV6",
                    "url": "https://omabrowser.org/oma/group/A0A0G2JSV6/",
                    "database": "OMA"
                }
            ],
            "common_name": "Human"
        }
    ],
    "go_annotation": {
        "categories": [
            {
                "name": "Molecular Function",
                "total": 5,
                "go_terms": [
                    {
                        "name": "organic acid binding",
                        "id": "GO:0043177",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043177",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": "21873635"
                    },
                    {
                        "name": "iron ion binding",
                        "id": "GO:0005506",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005506",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "heme binding",
                        "id": "GO:0020037",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0020037",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": "21873635"
                    },
                    {
                        "name": "oxygen binding",
                        "id": "GO:0019825",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0019825",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": "21873635"
                    },
                    {
                        "name": "oxygen carrier activity",
                        "id": "GO:0005344",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005344",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": "21873635"
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 8,
                "go_terms": [
                    {
                        "name": "in utero embryonic development",
                        "id": "GO:0001701",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001701",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to bacterium",
                        "id": "GO:0009617",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009617",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to hydrogen peroxide",
                        "id": "GO:0042542",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042542",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "positive regulation of cell death",
                        "id": "GO:0010942",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010942",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to estradiol",
                        "id": "GO:0032355",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0032355",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": "20534718"
                    },
                    {
                        "name": "hydrogen peroxide catabolic process",
                        "id": "GO:0042744",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042744",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "erythrocyte development",
                        "id": "GO:0048821",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048821",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cellular oxidant detoxification",
                        "id": "GO:0098869",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098869",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 4,
                "go_terms": [
                    {
                        "name": "extracellular space",
                        "id": "GO:0005615",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005615",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "hemoglobin complex",
                        "id": "GO:0005833",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005833",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "haptoglobin-hemoglobin complex",
                        "id": "GO:0031838",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031838",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cytosolic small ribosomal subunit",
                        "id": "GO:0022627",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022627",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0G2JSV6",
                                "url": "https://www.uniprot.org/uniprot/A0A0G2JSV6"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "homologset.mgi",
            "label": "MGI Homologs"
        },
        {
            "name": "homologset.oma",
            "label": "OMA Homologs"
        }
    ]
}