{
    "uniprot_canonical_ac": "O08962-1",
    "uniprot_ac": "O08962",
    "uniprot_id": "KCNH2_RAT",
    "mass": {
        "chemical_mass": 126952.0,
        "monoisotopic_mass": 126952.0
    },
    "refseq": {
        "ac": "XP_008760852",
        "name": "potassium voltage-gated channel subfamily H member 2 isoform X3",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/XP_008760852"
    },
    "gene_names": [
        {
            "name": "Kcnh2",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/O08962",
            "id": "O08962"
        },
        {
            "name": "ERG1",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/XP_008760852",
            "id": "XP_008760852"
        },
        {
            "name": "Erg",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/O08962",
            "id": "O08962"
        },
        {
            "name": "Kcnh2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/XP_008760852",
            "id": "XP_008760852"
        }
    ],
    "protein_names": [
        {
            "name": "Potassium voltage-gated channel subfamily H member 2",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "O08962"
        },
        {
            "name": "ERG-1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "O08962"
        },
        {
            "name": "Eag-related protein 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "O08962"
        },
        {
            "name": "Ether-a-go-go-related gene potassium channel 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "O08962"
        },
        {
            "name": "Ether-a-go-go-related protein 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "O08962"
        },
        {
            "name": "RERG; r-ERG; eag-related protein 1; ether-a-go-go-related protein 1; ether-a-go-go-related gene potassium channel 1; voltage-gated potassium channel subunit Kv11.1; potassium channel, voltage gated eag related subfamily H, member 2; ERG-1; potassium voltage-gated channel, subfamily H (eag-related), member 2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_446401",
            "id": "NP_446401"
        },
        {
            "name": "RERG",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "O08962"
        },
        {
            "name": "Voltage-gated potassium channel subunit Kv11.1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "O08962"
        },
        {
            "name": "potassium voltage-gated channel subfamily H member 2 isoform X3",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/XP_008760852",
            "id": "XP_008760852"
        },
        {
            "name": "potassium voltage-gated channel subfamily H member 2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_446401",
            "id": "NP_446401"
        },
        {
            "name": "r-ERG",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "O08962"
        }
    ],
    "function": [
        {
            "annotation": "Comparative Study of the Effect of Macrolide Antibiotics Erythromycin, Clarithromycin, and Azithromycin on the ERG1 Gene Expression in H9c2 Cardiomyoblast Cells.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_446401",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_446401"
                },
                {
                    "database": "PubMed",
                    "id": "32559772",
                    "url": "https://glygen.org/publication/PubMed/32559772"
                }
            ]
        },
        {
            "annotation": "ERG1 plays an essential role in rat cardiomyocyte fate decision by mediating AKT signaling.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_446401",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_446401"
                },
                {
                    "database": "PubMed",
                    "id": "33426760",
                    "url": "https://glygen.org/publication/PubMed/33426760"
                }
            ]
        },
        {
            "annotation": "ERK-dependent induction of the immediate-early gene Egr1 and the late gene Gpr50 contribute to two distinct phases of PACAP Gs-GPCR signaling for neuritogenesis.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_446401",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_446401"
                },
                {
                    "database": "PubMed",
                    "id": "35841324",
                    "url": "https://glygen.org/publication/PubMed/35841324"
                }
            ]
        },
        {
            "annotation": "Kcnh2 mediates FAK/AKT-FOXO3A pathway to attenuate sepsis-induced cardiac dysfunction.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_446401",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_446401"
                },
                {
                    "database": "PubMed",
                    "id": "33263944",
                    "url": "https://glygen.org/publication/PubMed/33263944"
                }
            ]
        },
        {
            "annotation": "Mu opioid receptors in the medial preoptic area govern social play behavior in adolescent male rats.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_446401",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_446401"
                },
                {
                    "database": "PubMed",
                    "id": "32388931",
                    "url": "https://glygen.org/publication/PubMed/32388931"
                }
            ]
        },
        {
            "annotation": "Pore-forming (alpha) subunit of voltage-gated inwardly rectifying potassium channel. Channel properties are modulated by cAMP and subunit assembly. Mediates the rapidly activating component of the delayed rectifying potassium current in heart (IKr) (By similarity).",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962#function"
                },
                {
                    "database": "UniProtKB",
                    "id": "Q12809",
                    "url": "https://www.uniprot.org/uniprot/Q12809#function"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0050793",
            "recommended_name": {
                "id": "DOID:0050793",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0050793",
                "name": "short QT syndrome",
                "description": "A heart conduction disease that is characterized by heart arrhythmia defined as a short QT interval on an EKG (less than 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart."
            },
            "synonyms": [
                {
                    "id": "MONDO:0012314",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012314",
                    "name": "short QT syndrome type 3",
                    "description": "Any short QT syndrome in which the cause of the disease is a mutation in the KCNJ2 gene."
                },
                {
                    "id": "MONDO:0012314",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012314",
                    "name": "KCNJ2 short QT syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0012314",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012314",
                    "name": "short QT syndrome caused by mutation in KCNJ2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012314",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012314",
                    "name": "short QT syndrome type 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012314",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012314",
                    "name": "SQT3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012314",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012314",
                    "name": "short QT syndrome 3",
                    "description": ""
                },
                {
                    "id": "MONDO:0012313",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012313",
                    "name": "short QT syndrome type 2",
                    "description": "Any short QT syndrome in which the cause of the disease is a mutation in the KCNQ1 gene."
                },
                {
                    "id": "MONDO:0012313",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012313",
                    "name": "KCNQ1 short QT syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0012313",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012313",
                    "name": "short QT syndrome caused by mutation in KCNQ1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012313",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012313",
                    "name": "short QT syndrome type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012313",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012313",
                    "name": "SQT2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012313",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012313",
                    "name": "short QT syndrome 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012312",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012312",
                    "name": "short QT syndrome type 1",
                    "description": "Any short QT syndrome in which the cause of the disease is a mutation in the KCNH2 gene."
                },
                {
                    "id": "MONDO:0012312",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012312",
                    "name": "KCNH2 short QT syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0012312",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012312",
                    "name": "SQTS",
                    "description": ""
                },
                {
                    "id": "MONDO:0012312",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012312",
                    "name": "short QT syndrome caused by mutation in KCNH2",
                    "description": ""
                },
                {
                    "id": "MONDO:0012312",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012312",
                    "name": "short QT syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012312",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012312",
                    "name": "SQT1",
                    "description": ""
                },
                {
                    "id": "MONDO:0012312",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012312",
                    "name": "short QT syndrome 1",
                    "description": ""
                },
                {
                    "id": "MIM:609622",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/609622",
                    "name": "Short QT syndrome 3",
                    "description": "Short QT syndrome 3"
                },
                {
                    "id": "MIM:609621",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/609621",
                    "name": "Short QT syndrome 2",
                    "description": "Short QT syndrome 2"
                },
                {
                    "id": "MIM:609620",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/609620",
                    "name": "Short QT syndrome 1",
                    "description": "Short QT syndrome 1"
                }
            ],
            "evidence": [
                {
                    "id": "0050793",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0050793"
                }
            ]
        },
        {
            "disease_id": "DOID:0110645",
            "recommended_name": {
                "id": "DOID:0110645",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110645",
                "name": "long QT syndrome 2",
                "description": "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1."
            },
            "synonyms": [
                {
                    "id": "DOID:0110645",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110645",
                    "name": "LQT2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013367",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013367",
                    "name": "long QT syndrome 2",
                    "description": "An autosomal dominant condition caused by mutation(s) in the KCNH2 gene, encoding potassium voltage-gated channel subfamily H member 2. It is characterized by a prolonged QT interval that may result in torsade de pointes, ventricular fibrillation and/or sudden cardiac death."
                },
                {
                    "id": "MONDO:0013367",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013367",
                    "name": "LQT2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013367",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013367",
                    "name": "Long QT syndrome, acquired, reduced susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0013367",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013367",
                    "name": "long QT syndrome 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013367",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013367",
                    "name": "long QT syndrome type 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0013367",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013367",
                    "name": "long QT syndrome 1/2, digenic",
                    "description": ""
                },
                {
                    "id": "MONDO:0013367",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013367",
                    "name": "long QT syndrome 2, acquired, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0013367",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013367",
                    "name": "long QT syndrome 2/3, digenic",
                    "description": ""
                },
                {
                    "id": "MONDO:0013367",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013367",
                    "name": "long QT syndrome 2/5, digenic",
                    "description": ""
                },
                {
                    "id": "MONDO:0013367",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013367",
                    "name": "long QT syndrome 2/9, digenic",
                    "description": ""
                },
                {
                    "id": "MIM:613688",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/613688",
                    "name": "Long QT syndrome 2",
                    "description": "Long QT syndrome 2"
                }
            ],
            "evidence": [
                {
                    "id": "0110645",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110645"
                }
            ]
        },
        {
            "disease_id": "DOID:10273",
            "recommended_name": {
                "id": "DOID:10273",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10273",
                "name": "heart conduction disease",
                "description": "A cardiovascular system disease that involves the heart's electrical conduction system."
            },
            "synonyms": [
                {
                    "id": "DOID:10273",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10273",
                    "name": "heart rhythm disease",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "10273",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10273"
                }
            ]
        },
        {
            "disease_id": "DOID:1826",
            "recommended_name": {
                "id": "DOID:1826",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1826",
                "name": "epilepsy",
                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions."
            },
            "synonyms": [
                {
                    "id": "DOID:1826",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1826",
                    "name": "epilepsy syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:1826",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1826",
                    "name": "epileptic syndrome",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1826",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1826"
                }
            ]
        },
        {
            "disease_id": "DOID:2843",
            "recommended_name": {
                "id": "DOID:2843",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2843",
                "name": "long QT syndrome",
                "description": "An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles)."
            },
            "synonyms": [
                {
                    "id": "DOID:2843",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2843",
                    "name": "LQT",
                    "description": ""
                },
                {
                    "id": "DOID:2843",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2843",
                    "name": "Romano-Ward syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:2843",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2843",
                    "name": "long Q-T syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0100316",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100316",
                    "name": "long QT syndrome 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0100316",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100316",
                    "name": "LQT1",
                    "description": ""
                },
                {
                    "id": "MONDO:0100316",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100316",
                    "name": "long QT syndrome 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0100316",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100316",
                    "name": "long QT syndrome type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0100316",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100316",
                    "name": "ventricular fibrillation with prolonged QT interval",
                    "description": ""
                },
                {
                    "id": "MONDO:0100316",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100316",
                    "name": "long QT syndrome 1, acquired, susceptibility to",
                    "description": ""
                },
                {
                    "id": "MONDO:0100316",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100316",
                    "name": "long QT syndrome 1/2, digenic",
                    "description": ""
                },
                {
                    "id": "MIM:192500",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/192500",
                    "name": "Long QT syndrome 1",
                    "description": "Long QT syndrome 1"
                }
            ],
            "evidence": [
                {
                    "id": "2843",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2843"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [
        {
            "start_pos": 630,
            "end_pos": 630,
            "sequence_org": "G",
            "sequence_mut": "S",
            "comment": "Dominant negative mutant; abolishes ERG current.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                },
                {
                    "database": "PubMed",
                    "id": "11212207",
                    "url": "https://glygen.org/publication/PubMed/11212207"
                }
            ]
        }
    ],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Rattus norvegicus",
            "taxid": 10116,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "gene": [
        {
            "name": "Kcnh2",
            "url": "https://www.uniprot.org/uniprot/O08962",
            "locus": {
                "chromosome": "4",
                "start_pos": 10859008,
                "end_pos": 10826928,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSRNOG00000009872",
                        "url": "https://www.ensembl.org/id/ENSRNOG00000009872"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "ENSRNOG00000009872",
            "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000009872",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "cd00038",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd00038",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "cd00130",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd00130",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "117018",
            "url": "https://www.ncbi.nlm.nih.gov/gene/117018",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "O08962",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:O08962*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "IPR000014",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR000014",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR000595",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR000595",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR000700",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR000700",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR001610",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001610",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR003938",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR003938",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR003967",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR003967",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR005821",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR005821",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR014710",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR014710",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR018490",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR018490",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR035965",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR035965",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "rno:117018",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+rno:117018",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "TEDCEKR",
            "url": "https://omabrowser.org/oma/group/TEDCEKR/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "66005at2759",
            "url": "http://www.orthodb.org/?query=66005at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10217",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10217",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR10217:SF506",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10217:SF506",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00027",
            "url": "http://pfam.xfam.org/family/PF00027",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00520",
            "url": "http://pfam.xfam.org/family/PF00520",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF13426",
            "url": "http://pfam.xfam.org/family/PF13426",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PR_O08962",
            "url": "http://purl.obolibrary.org/obo/PR_O08962",
            "database": "PRO",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "R-RNO-1296072",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-1296072",
            "database": "Reactome",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "R-RNO-5576890",
            "url": "https://www.reactome.org/PathwayBrowser/#R-RNO-5576890",
            "database": "Reactome",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "NP_446401",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_446401",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "621414",
            "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=621414",
            "database": "RGD",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "A6K570",
            "url": "https://www.uniprot.org/uniprot/A6K570",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A6K570-1",
            "url": "https://www.uniprot.org/uniprot/A6K570-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "F1LN86",
            "url": "https://www.uniprot.org/uniprot/F1LN86",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "F1LN86-1",
            "url": "https://www.uniprot.org/uniprot/F1LN86-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "O08962",
            "url": "https://www.uniprot.org/uniprot/O08962",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "O08962-1",
            "url": "https://www.uniprot.org/uniprot/O08962-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MPVRRGHVAPQNTFLDTIIRKFEGQSRKFIIANARVENCAVIYCNDGFCELCGYSRAEVMQRPCTCDFLHGPRTQRRAAAQIAQALLGAEERKVEIAFYRKDGSCFLCLVDVVPVKNEDGAVIMFILNFEVVMEKDMVGSPAHDTNHRGPSTSWLASGRAKTFRLKLPALLALTARESPMRTGSTGSPGAPGAVVVDVDLTPAAPSSESLALDEVSAMDNHVAGLGPAEERRALVGPASASPVASIPGPHPSPRAQSLNPDASGSSCSLARTRSRESCASVRRASSADDIEAMRAGALPLPPRHASTGAMHPLRSGLLNSTSDSDLVRYRTISKIPQITLNFVDLKGDPFLASPTSDREIIAPKIKERTHNVTEKVTQVLSLGADVLPEYKLQAPRIHRWTILHYSPFKAVWDWLILLLVIYTAVFTPYSAAFLLKETEDGSQAPDCGYACQPLAVVDLLVDIMFIVDILINFRTTYVNANEEVVSHPGRIAVHYFKGWFLIDMVAAIPFDLLIFGSGSEELIGLLKTARLLRLVRVARKLDRYSEYGAAVLFLLMCTFALIAHWLACIWYAIGNMEQPHMDSHIGWLHNLGDQIGKPYNSSGLGGPSIKDKYVTALYFTFSSLTSVGFGNVSPNTNSEKIFSICVMLIGSLMYASIFGNVSAIIQRLYSGTARYHTQMLRVREFIRFHQIPNPLRQRLEEYFQHAWSYTNGIDMNAVLKGFPECLQADICLHLNRSLLQHCKPFRGATKGCLRALAMKFKTTHAPPGDTLVHAGDLLTALYFISRGSIEILRGDVVVAILGKNDIFGEPLNLYARPGKSNGDVRALTYCDLHKIHRDDLLEVLDMYPEFSDHFWSSLEITFNLRDTNMIPGSPSSAELESGFNRQRKRKLSFRRRTDKDTEQPGEVSALGQGPARVGPGPSCRGQPGGPWGESPSSGPSSPESSEDEGPGRSSSPLRLVPFSSPRPPGDSPGGEPLTEDGEKSSDTCNPLSGAFSGVSNIFSFWGDSRGRQYQELPRCPAPAPSLLNIPLSSPGRRSRGDVESRLDALQRQLNRLETRLSADMATVLQLLQRQMTLVPPAYSAVTTPGPGPTSTSPLLPVGPVPTLTLDSLSQVSQFVAFEELPAGAPELPQDGPTRRLSLPGQLGALTSQPLHRHGSDPGS",
        "length": 1163,
        "header": "sp|O08962-1|KCNH2_RAT Isoform 1 of Potassium voltage-gated channel subfamily H member 2  OS=Rattus norvegicus OX=10116 GN=Kcnh2 PE=1 SV=1 CANONICAL=O08962-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A6K570-1",
            "url": "",
            "sequence": {
                "sequence": "MAIPAGKESRTGALQTRAQKGRVRRAVRISSLVAQEVLSLGADVLPEYKLQAPRIHRWTILHYSPFKAVWDWLILLLVIYTAVFTPYSAAFLLKETEDGSQAPDCGYACQPLAVVDLLVDIMFIVDILINFRTTYVNANEEVVSHPGRIAVHYFKGWFLIDMVAAIPFDLLIFGSGSEELIGLLKTARLLRLVRVARKLDRYSEYGAAVLFLLMCTFALIAHWLACIWYAIGNMEQPHMDSHIGWLHNLGDQIGKPYNSSGLGGPSIKDKYVTALYFTFSSLTSVGFGNVSPNTNSEKIFSICVMLIGSLMYASIFGNVSAIIQRLYSGTARYHTQMLRVREFIRFHQIPNPLRQRLEEYFQHAWSYTNGIDMNAVLKGFPECLQADICLHLNRSLLQHCKPFRGATKGCLRALAMKFKTTHAPPGDTLVHAGDLLTALYFISRGSIEILRGDVVVAILGKNDIFGEPLNLYARPGKSNGDVRALTYCDLHKIHRDDLLEVLDMYPEFSDHFWSSLEITFNLRDTNMIPGSPSSAELESGFNRQRKRKLSFRRRTDKDTEQPGEVSALGQGPARVGPGPSCRGQPGGPWGESPSSGPSSPESSEDEGPGRSSSPLRLVPFSSPRPPGDSPGGEPLTEDGEKSSDTCNPLSGAFSGVSNIFSFWGDSRGRQYQELPRCPAPAPSLLNIPLSSPGRRSRGDVESRLDALQRQLNRLETRLSADMATVLQLLQRQMTLVPPAYSAVTTPGPGPTSTSPLLPVGPVPTLTLDSLSQVSQFVAFEELPAGAPELPQDGPTRRLSLPGQLGALTSQPLHRHGSDPGS",
                "length": 821,
                "header": "tr|A6K570-1|A6K570_RAT Computationally mapped isoform of Potassium voltage-gated channel subfamily H member 2  OS=Rattus norvegicus OX=10116 GN=Kcnh2 PE=2 SV=1 CANONICAL=O08962-1"
            },
            "locus": {
                "chromosome": "4",
                "start_pos": 10858617,
                "end_pos": 10849331,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000084826.2",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000084826.2"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000073593.1",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000073593.1"
                    }
                ]
            }
        },
        {
            "isoform_ac": "F1LN86-1",
            "url": "",
            "sequence": {
                "sequence": "MPVRRGHVAPQNTFLDTIIRKFEGQSRKFIIANARVENCAVIYCNDGFCELCGYSRAEVMQRPCTCDFLHGPRTQRRAAAQIAQALLGAEERKVEIAFYRKDGSCFLCLVDVVPVKNEDGAVIMFILNFEVVMEKDMVGSPAHDTNHRGPSTSWLASGRAKTFRLKLPALLALTARESPMRTGSTGSPGAPGAVVVDVDLTPAAPSSESLALDEVSAMDNHVAGLGPAEERRALVGPASASPVASIRGPHPSPPAQSLNPDASGSSCSLARTRSRESCASVRRASSADDIEAMRAGALPPPPRHASTGAMHPLRSGLLNSTSDSDLVRYRTISKIPQITLNFVDLKGDPFLASPTSDREIIAPKIKERTHNVTEKVTQVLSLGADVLPEYKLQAPRIHRWTILHYSPFKAVWDWLILLLVIYTAVFTPYSAAFLLKETEDGSQAPDCGYACQPLAVVDLLVDIMFIVDILINFRTTYVNANEEVVSHPGRIAVHYFKGWFLIDMVAAIPFDLLIFGSGSEELIGLLKTARLLRLVRVARKLDRYSEYGAAVLFLLMCTFALIAHWLACIWYAIGNMEQPHMDSHIGWLHNLGDQIGKPYNSSGLGGPSIKDKYVTALYFTFSSLTSVGFGNVSPNTNSEKIFSICVMLIGSLMYASIFGNVSAIIQRLYSGTARYHTQMLRVREFIRFHQIPNPLRQRLEEYFQHAWSYTNGIDMNAVLKGFPECLQADICLHLNRSLLQHCKPFRGATKGCLRALAMKFKTTHAPPGDTLVHAGDLLTALYFISRGSIEILRGDVVVAILGKNDIFGEPLNLYARPGKSNGDVRALTYCDLHKIHRDDLLEVLDMYPEFSDHFWSSLEITFNLRDTNMIPGSPSSAELESGFNRQRKRKLSFRRRTDKDTEQPGEVSALGQGPARVGPGPSCRGQPGGPWGESPSSGPSSPESSEDEGPGRSSSPLRLVPFSSPRPPGDSPGGEPLTEDGEKSSDTCNPLSGAFSGVSNIFSFWGDSRGRQYQELPRCPAPAPSLLNIPLSSPGRRSRGDVESRLDALQRQLNRLETRLSADMATVLQLLQRQMTLVPPAYSAVTTPGPGPTSTSPLLPVGPVPTLTLDSLSQVSQFVAFEELPAGAPELPQDGPTRRLSLPGQLGALTSQPLHRHGSDPGS",
                "length": 1163,
                "header": "tr|F1LN86-1|F1LN86_RAT Computationally mapped isoform of Potassium voltage-gated channel subfamily H member 2  OS=Rattus norvegicus OX=10116 GN=Kcnh2 PE=1 SV=1 CANONICAL=O08962-1"
            },
            "locus": {
                "chromosome": "4",
                "start_pos": 10858617,
                "end_pos": 10827369,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSRNOT00000013800.5",
                        "url": "https://www.ensembl.org/id/ENSRNOT00000013800.5"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSRNOP00000013800.3",
                        "url": "https://www.ensembl.org/id/ENSRNOP00000013800.3"
                    }
                ]
            }
        },
        {
            "isoform_ac": "O08962-1",
            "url": "",
            "sequence": {
                "sequence": "MPVRRGHVAPQNTFLDTIIRKFEGQSRKFIIANARVENCAVIYCNDGFCELCGYSRAEVMQRPCTCDFLHGPRTQRRAAAQIAQALLGAEERKVEIAFYRKDGSCFLCLVDVVPVKNEDGAVIMFILNFEVVMEKDMVGSPAHDTNHRGPSTSWLASGRAKTFRLKLPALLALTARESPMRTGSTGSPGAPGAVVVDVDLTPAAPSSESLALDEVSAMDNHVAGLGPAEERRALVGPASASPVASIPGPHPSPRAQSLNPDASGSSCSLARTRSRESCASVRRASSADDIEAMRAGALPLPPRHASTGAMHPLRSGLLNSTSDSDLVRYRTISKIPQITLNFVDLKGDPFLASPTSDREIIAPKIKERTHNVTEKVTQVLSLGADVLPEYKLQAPRIHRWTILHYSPFKAVWDWLILLLVIYTAVFTPYSAAFLLKETEDGSQAPDCGYACQPLAVVDLLVDIMFIVDILINFRTTYVNANEEVVSHPGRIAVHYFKGWFLIDMVAAIPFDLLIFGSGSEELIGLLKTARLLRLVRVARKLDRYSEYGAAVLFLLMCTFALIAHWLACIWYAIGNMEQPHMDSHIGWLHNLGDQIGKPYNSSGLGGPSIKDKYVTALYFTFSSLTSVGFGNVSPNTNSEKIFSICVMLIGSLMYASIFGNVSAIIQRLYSGTARYHTQMLRVREFIRFHQIPNPLRQRLEEYFQHAWSYTNGIDMNAVLKGFPECLQADICLHLNRSLLQHCKPFRGATKGCLRALAMKFKTTHAPPGDTLVHAGDLLTALYFISRGSIEILRGDVVVAILGKNDIFGEPLNLYARPGKSNGDVRALTYCDLHKIHRDDLLEVLDMYPEFSDHFWSSLEITFNLRDTNMIPGSPSSAELESGFNRQRKRKLSFRRRTDKDTEQPGEVSALGQGPARVGPGPSCRGQPGGPWGESPSSGPSSPESSEDEGPGRSSSPLRLVPFSSPRPPGDSPGGEPLTEDGEKSSDTCNPLSGAFSGVSNIFSFWGDSRGRQYQELPRCPAPAPSLLNIPLSSPGRRSRGDVESRLDALQRQLNRLETRLSADMATVLQLLQRQMTLVPPAYSAVTTPGPGPTSTSPLLPVGPVPTLTLDSLSQVSQFVAFEELPAGAPELPQDGPTRRLSLPGQLGALTSQPLHRHGSDPGS",
                "length": 1163,
                "header": "sp|O08962-1|KCNH2_RAT Isoform 1 of Potassium voltage-gated channel subfamily H member 2  OS=Rattus norvegicus OX=10116 GN=Kcnh2 PE=1 SV=1 CANONICAL=O08962-1"
            },
            "locus": {}
        }
    ],
    "glycosylation": [
        {
            "glytoucan_ac": "",
            "type": "N-linked",
            "subtype": "",
            "site_category": "predicted",
            "site_seq": "N",
            "relation": "attached",
            "comment": "N-linked (GlcNAc...) asparagine",
            "start_pos": 600,
            "start_aa": "Asn",
            "end_pos": 600,
            "end_aa": "Asn",
            "residue": "Asn",
            "site_lbl": "Asn600",
            "evidence": [
                {
                    "id": "O08962",
                    "database": "UniProtKB",
                    "url": "https://www.uniprot.org/uniprot/O08962#ptm_processing"
                }
            ]
        }
    ],
    "phosphorylation": [
        {
            "start_pos": 1141,
            "end_pos": 1141,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                }
            ],
            "site_lbl": "Ser1141"
        },
        {
            "start_pos": 239,
            "end_pos": 239,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                }
            ],
            "site_lbl": "Ser239"
        },
        {
            "start_pos": 245,
            "end_pos": 245,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                }
            ],
            "site_lbl": "Ser245"
        },
        {
            "start_pos": 285,
            "end_pos": 285,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                },
                {
                    "database": "PubMed",
                    "id": "22673903",
                    "url": "https://glygen.org/publication/PubMed/22673903"
                },
                {
                    "database": "iPTMnet",
                    "id": "O08962",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/O08962"
                }
            ],
            "site_lbl": "Ser285"
        },
        {
            "start_pos": 286,
            "end_pos": 286,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                },
                {
                    "database": "PubMed",
                    "id": "22673903",
                    "url": "https://glygen.org/publication/PubMed/22673903"
                },
                {
                    "database": "iPTMnet",
                    "id": "O08962",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/O08962"
                }
            ],
            "site_lbl": "Ser286"
        },
        {
            "start_pos": 322,
            "end_pos": 322,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                }
            ],
            "site_lbl": "Ser322"
        },
        {
            "start_pos": 353,
            "end_pos": 353,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                },
                {
                    "database": "PubMed",
                    "id": "22673903",
                    "url": "https://glygen.org/publication/PubMed/22673903"
                },
                {
                    "database": "iPTMnet",
                    "id": "O08962",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/O08962"
                }
            ],
            "site_lbl": "Ser353"
        },
        {
            "start_pos": 873,
            "end_pos": 873,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                }
            ],
            "site_lbl": "Ser873"
        },
        {
            "start_pos": 876,
            "end_pos": 876,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "Phosphoserine",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                }
            ],
            "site_lbl": "Ser876"
        }
    ],
    "glycation": [],
    "keywords": [
        "glycoprotein",
        "glycoprotein_predicted"
    ],
    "publication": [
        {
            "title": "Expression of mRNA for voltage-dependent and inward-rectifying K channels in GH3/B6 cells and rat pituitary.",
            "journal": "J. Neuroendocrinol.",
            "date": "2000",
            "authors": "Wulfsen I, Hauber HP, Schiemann D, Bauer CK, Schwarz JR",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "O08962",
                    "url": "https://www.uniprot.org/uniprot/O08962"
                }
            ],
            "reference": [
                {
                    "type": "PubMed",
                    "id": "10718922",
                    "url": "https://glygen.org/publication/PubMed/10718922"
                }
            ]
        },
        {
            "title": "Erg1, erg2 and erg3 K channel subunits are able to form heteromultimers.",
            "journal": "Pflugers Arch.",
            "date": "2001",
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        {
            "title": "The IKr drug response is modulated by KCR1 in transfected cardiac and noncardiac cell lines.",
            "journal": "FASEB J.",
            "date": "2003",
            "authors": "Hayashi K., Balser J.R., Chanthaphaychith S., George A.L. Jr., Johns D.C., Kupershmidt S., Petersen C.I., Roden D.M., Wei J., Yang I.C.-H.",
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        {
            "title": "Fast erg K+ currents in rat embryonic serotonergic neurones.",
            "journal": "J. Physiol. (Lond.)",
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            "authors": "Hirdes W, Schweizer M, Schuricht KS, Guddat SS, Wulfsen I, Bauer CK, Schwarz JR",
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            "title": "Quantitative maps of protein phosphorylation sites across 14 different rat organs and tissues.",
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            "title": "Mu opioid receptors in the medial preoptic area govern social play behavior in adolescent male rats.",
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            "title": "ERG1 plays an essential role in rat cardiomyocyte fate decision by mediating AKT signaling.",
            "journal": "Stem cells (Dayton, Ohio)",
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            "authors": "Wang D, Liu C, Liu H, Meng Y, Lin F, Gu Y, Wang H, Shang M, Tong C, Sachinidis A, Ying Q, Li L, Peng L",
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            "title": "ERK-dependent induction of the immediate-early gene Egr1 and the late gene Gpr50 contribute to two distinct phases of PACAP Gs-GPCR signaling for neuritogenesis.",
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        {
            "title": "Tissue and species distribution of mRNA for the IKr-like K+ channel, erg.",
            "journal": "Circ. Res.",
            "date": "1997",
            "authors": "Dixon J.E., Cohen I.S., McKinnon D., Wymore R.S., Wymore R.T., Gintant G.A.",
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        {
            "title": "RERG is a molecular correlate of the inward-rectifying K current in clonal rat pituitary cells.",
            "journal": "Recept. Channels",
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            "authors": "Wulfsen I., Pongs O., Ludwig J., Bauer C.K., Schwarz J.R., Engeland B.",
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                    "id": "9664620",
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            ]
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        {
            "id": "rno:117018",
            "name": "",
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            "resource": "KEGG Pathway"
        },
        {
            "id": "R-RNO-1296072",
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            "description": "Voltage gated Potassium channels"
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        {
            "id": "R-RNO-5576890",
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            "description": "Phase 3 - rapid repolarisation"
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        {
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            "tax_id": 10090,
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                "length": 1162
            },
            "evidence": [
                {
                    "id": "45229700",
                    "url": "http://www.informatics.jax.org/homology/45229700",
                    "database": "MGI"
                }
            ],
            "common_name": "Mouse"
        },
        {
            "uniprot_canonical_ac": "Q12809-1",
            "protein_name": "Potassium voltage-gated channel subfamily H member 2",
            "gene_name": "KCNH2",
            "tax_id": 9606,
            "organism": "Homo sapiens",
            "sequence": {
                "sequence": "MPVRRGHVAPQNTFLDTIIRKFEGQSRKFIIANARVENCAVIYCNDGFCELCGYSRAEVMQRPCTCDFLHGPRTQRRAAAQIAQALLGAEERKVEIAFYRKDGSCFLCLVDVVPVKNEDGAVIMFILNFEVVMEKDMVGSPAHDTNHRGPPTSWLAPGRAKTFRLKLPALLALTARESSVRSGGAGGAGAPGAVVVDVDLTPAAPSSESLALDEVTAMDNHVAGLGPAEERRALVGPGSPPRSAPGQLPSPRAHSLNPDASGSSCSLARTRSRESCASVRRASSADDIEAMRAGVLPPPPRHASTGAMHPLRSGLLNSTSDSDLVRYRTISKIPQITLNFVDLKGDPFLASPTSDREIIAPKIKERTHNVTEKVTQVLSLGADVLPEYKLQAPRIHRWTILHYSPFKAVWDWLILLLVIYTAVFTPYSAAFLLKETEEGPPATECGYACQPLAVVDLIVDIMFIVDILINFRTTYVNANEEVVSHPGRIAVHYFKGWFLIDMVAAIPFDLLIFGSGSEELIGLLKTARLLRLVRVARKLDRYSEYGAAVLFLLMCTFALIAHWLACIWYAIGNMEQPHMDSRIGWLHNLGDQIGKPYNSSGLGGPSIKDKYVTALYFTFSSLTSVGFGNVSPNTNSEKIFSICVMLIGSLMYASIFGNVSAIIQRLYSGTARYHTQMLRVREFIRFHQIPNPLRQRLEEYFQHAWSYTNGIDMNAVLKGFPECLQADICLHLNRSLLQHCKPFRGATKGCLRALAMKFKTTHAPPGDTLVHAGDLLTALYFISRGSIEILRGDVVVAILGKNDIFGEPLNLYARPGKSNGDVRALTYCDLHKIHRDDLLEVLDMYPEFSDHFWSSLEITFNLRDTNMIPGSPGSTELEGGFSRQRKRKLSFRRRTDKDTEQPGEVSALGPGRAGAGPSSRGRPGGPWGESPSSGPSSPESSEDEGPGRSSSPLRLVPFSSPRPPGEPPGGEPLMEDCEKSSDTCNPLSGAFSGVSNIFSFWGDSRGRQYQELPRCPAPTPSLLNIPLSSPGRRPRGDVESRLDALQRQLNRLETRLSADMATVLQLLQRQMTLVPPAYSAVTTPGPGPTSTSPLLPVSPLPTLTLDSLSQVSQFMACEELPPGAPELPQEGPTRRLSLPGQLGALTSQPLHRHGSDPGS",
                "length": 1159
            },
            "evidence": [
                {
                    "id": "45229700",
                    "url": "http://www.informatics.jax.org/homology/45229700",
                    "database": "MGI"
                }
            ],
            "common_name": "Human"
        }
    ],
    "go_annotation": {
        "categories": [
            {
                "name": "Cellular Component",
                "total": 8,
                "go_terms": [
                    {
                        "name": "membrane",
                        "id": "GO:0016020",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "inward rectifier potassium channel complex",
                        "id": "GO:1902937",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902937",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "nuclear envelope",
                        "id": "GO:0005635",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005635",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cytoplasm",
                        "id": "GO:0005737",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "plasma membrane",
                        "id": "GO:0005886",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cell surface",
                        "id": "GO:0009986",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009986",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "perinuclear region of cytoplasm",
                        "id": "GO:0048471",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048471",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "voltage-gated potassium channel complex",
                        "id": "GO:0008076",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008076",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 13,
                "go_terms": [
                    {
                        "name": "voltage-gated potassium channel activity",
                        "id": "GO:0005249",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005249",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "delayed rectifier potassium channel activity",
                        "id": "GO:0005251",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005251",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization",
                        "id": "GO:1902282",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902282",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "C3HC4-type RING finger domain binding",
                        "id": "GO:0055131",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055131",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "monoatomic ion channel activity",
                        "id": "GO:0005216",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005216",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "identical protein binding",
                        "id": "GO:0042802",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042802",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "protein homodimerization activity",
                        "id": "GO:0042803",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0042803",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "ubiquitin protein ligase binding",
                        "id": "GO:0031625",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031625",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "protein-containing complex binding",
                        "id": "GO:0044877",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0044877",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "potassium channel activity",
                        "id": "GO:0005267",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005267",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "transcription cis-regulatory region binding",
                        "id": "GO:0000976",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000976",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "scaffold protein binding",
                        "id": "GO:0097110",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097110",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "inward rectifier potassium channel activity",
                        "id": "GO:0005242",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005242",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Biological Process",
                "total": 24,
                "go_terms": [
                    {
                        "name": "regulation of potassium ion transmembrane transport",
                        "id": "GO:1901379",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1901379",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "negative regulation of potassium ion transmembrane transport",
                        "id": "GO:1901380",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1901380",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
                                "url": "https://www.uniprot.org/uniprot/O08962"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "membrane repolarization during action potential",
                        "id": "GO:0086011",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0086011",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "O08962",
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