GET /api/v1/panels/224/?version=2.4
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{
    "id": 224,
    "name": "Short QT syndrome",
    "strs": [],
    "genes": [
        {
            "tags": [
                "for-review"
            ],
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                "West Midlands, Oxford and Wessex GLH",
                "South West GLH",
                "London South GLH",
                "North West GLH",
                "Brugada syndrome (Version 1.7)",
                "UKGTN",
                "Expert Review Green",
                "Long QT syndrome (Version 1.5)",
                "Emory Genetics Laboratory",
                "Literature"
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            "gene_data": {
                "alias": [
                    "Cav1.2",
                    "CACH2",
                    "CACN2",
                    "TS",
                    "LQT8"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1390",
                "gene_name": "calcium voltage-gated channel subunit alpha1 C",
                "omim_gene": [
                    "114205"
                ],
                "alias_name": null,
                "gene_symbol": "CACNA1C",
                "hgnc_symbol": "CACNA1C",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:2079952-2802108",
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                    }
                },
                "hgnc_date_symbol_changed": "1991-01-30"
            },
            "penetrance": null,
            "phenotypes": [
                "Brugada syndrome 3 611875",
                "syncope",
                "brugada syndrome",
                "scd",
                "Brugada syndrome 3 (611875)",
                "short qt",
                "Timothy syndrome (601005)"
            ],
            "transcript": null,
            "entity_name": "CACNA1C",
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                "24291113",
                "16301704",
                "30027834",
                "30279520",
                "17224476",
                "28427417",
                "28490369",
                "29759541",
                "29697308"
            ],
            "confidence_level": "3",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "mode_of_pathogenicity": null
        },
        {
            "tags": [],
            "evidence": [
                "West Midlands, Oxford and Wessex GLH",
                "South West GLH",
                "London South GLH",
                "North West GLH",
                "Long QT syndrome (Version 1.5)",
                "Brugada syndrome (Version 1.7)",
                "Expert Review Green",
                "Emory Genetics Laboratory",
                "Radboud University Medical Center, Nijmegen",
                "UKGTN",
                "Literature"
            ],
            "gene_data": {
                "alias": [
                    "Kv11.1",
                    "HERG",
                    "erg1"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6251",
                "gene_name": "potassium voltage-gated channel subfamily H member 2",
                "omim_gene": [
                    "152427"
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                "alias_name": null,
                "gene_symbol": "KCNH2",
                "hgnc_symbol": "KCNH2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "7:150642049-150675403",
                            "ensembl_id": "ENSG00000055118"
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                            "location": "7:150944961-150978315",
                            "ensembl_id": "ENSG00000055118"
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                    }
                },
                "hgnc_date_symbol_changed": "1993-03-22"
            },
            "penetrance": null,
            "phenotypes": [
                "Brugada",
                "Short QT syndrome 1 (609620)",
                "ventricular fibrillation",
                "cardiac arrest",
                "Short QT syndrome 1 609620",
                "Long QT syndrome-2 (613688)",
                "short qt",
                "atrial fibrillation"
            ],
            "transcript": null,
            "entity_name": "KCNH2",
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                "16301704",
                "4676148",
                "15828882",
                "19340359",
                "18692916",
                "21130771",
                "25974115",
                "29016797",
                "29759541",
                "16011830",
                "19439805",
                "22194679",
                "16039272",
                "29085299"
            ],
            "confidence_level": "3",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "mode_of_pathogenicity": "Other"
        },
        {
            "tags": [],
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                "West Midlands, Oxford and Wessex GLH",
                "South West GLH",
                "London South GLH",
                "North West GLH",
                "Radboud University Medical Center, Nijmegen",
                "UKGTN",
                "Expert Review Green",
                "Long QT syndrome (Version 1.5)",
                "Emory Genetics Laboratory",
                "Literature"
            ],
            "gene_data": {
                "alias": [
                    "Kir2.1",
                    "IRK1",
                    "LQT7"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6263",
                "gene_name": "potassium voltage-gated channel subfamily J member 2",
                "omim_gene": [
                    "600681"
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                "alias_name": null,
                "gene_symbol": "KCNJ2",
                "hgnc_symbol": "KCNJ2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "17:68164814-68176189",
                            "ensembl_id": "ENSG00000123700"
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                    },
                    "GRch38": {
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                            "location": "17:70168673-70180048",
                            "ensembl_id": "ENSG00000123700"
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                    }
                },
                "hgnc_date_symbol_changed": "1994-02-08"
            },
            "penetrance": null,
            "phenotypes": [
                "Atrial fibrillation, familial, 9 (613980)",
                "Short QT syndrome 3 609622",
                "Short QT syndrome 3 (609622)",
                "Andersen syndrome (170390)",
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                "short qt",
                "atrial fibrillation"
            ],
            "transcript": null,
            "entity_name": "KCNJ2",
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                "16301704",
                "15761194",
                "22155372",
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                "24794859",
                "22311718",
                "22308236",
                "19285083",
                "19710529",
                "25691870"
            ],
            "confidence_level": "3",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "mode_of_pathogenicity": "Other"
        },
        {
            "tags": [],
            "evidence": [
                "West Midlands, Oxford and Wessex GLH",
                "Expert Review Green",
                "South West GLH",
                "London South GLH",
                "North West GLH",
                "Radboud University Medical Center, Nijmegen",
                "UKGTN",
                "Long QT syndrome (Version 1.5)",
                "Emory Genetics Laboratory",
                "Other"
            ],
            "gene_data": {
                "alias": [
                    "Kv7.1",
                    "KCNA8",
                    "KVLQT1",
                    "JLNS1",
                    "LQT1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6294",
                "gene_name": "potassium voltage-gated channel subfamily Q member 1",
                "omim_gene": [
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                "alias_name": [
                    "Jervell and Lange-Nielsen syndrome 1"
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                "gene_symbol": "KCNQ1",
                "hgnc_symbol": "KCNQ1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "11:2465914-2870339",
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                },
                "hgnc_date_symbol_changed": "1997-02-05"
            },
            "penetrance": "unknown",
            "phenotypes": [
                "Short QT syndrome 2 609621",
                "Long QT syndrome-1 (192500)",
                "Atrial fibrillation, familial, 3 (607554)",
                "Short QT syndrome 2 (609621)",
                "Idiopathic Ventricular Fibrillation",
                "Short QT-interval syndrome",
                "Jervell and Lange-Nielsen syndrome (220400)"
            ],
            "transcript": null,
            "entity_name": "KCNQ1",
            "entity_type": "gene",
            "publications": [
                "16226079",
                "16301704",
                "15159330",
                "16109388",
                "26168993",
                "26346102",
                "25974115",
                "29697308"
            ],
            "confidence_level": "3",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "mode_of_pathogenicity": null
        },
        {
            "tags": [
                "watchlist"
            ],
            "evidence": [
                "Expert Review Amber",
                "South West GLH",
                "London South GLH",
                "North West GLH",
                "UKGTN",
                "Brugada syndrome (Version 1.7)",
                "Literature"
            ],
            "gene_data": {
                "alias": [
                    "lncRNA-N3"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1399",
                "gene_name": "calcium voltage-gated channel auxiliary subunit alpha2delta 1",
                "omim_gene": [
                    "114204"
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                "alias_name": null,
                "gene_symbol": "CACNA2D1",
                "hgnc_symbol": "CACNA2D1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                "hgnc_date_symbol_changed": "1992-03-27"
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            "penetrance": null,
            "phenotypes": [
                "short qt",
                "Brugada syndrome",
                "aborted sudden death",
                "Short QT syndrome 6"
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            "transcript": null,
            "entity_name": "CACNA2D1",
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            "confidence_level": "2",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
            "mode_of_pathogenicity": null
        },
        {
            "tags": [
                "watchlist"
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                "South West GLH",
                "London South GLH",
                "North West GLH",
                "Expert Review Amber",
                "UKGTN",
                "Brugada syndrome (Version 1.7)",
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            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1402",
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                "alias_name": null,
                "gene_symbol": "CACNB2",
                "hgnc_symbol": "CACNB2",
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                "Brugada syndrome 4 (611876)",
                "Short QT syndrome 5",
                "brugada syndrome",
                "Brugada syndrome 4 611876",
                "short qt"
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            "entity_name": "CACNB2",
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            "mode_of_pathogenicity": null
        },
        {
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                "Brugada syndrome (Version 1.7)",
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                    "IVF",
                    "HB2",
                    "HH1",
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                    "ICCD"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:10593",
                "gene_name": "sodium voltage-gated channel alpha subunit 5",
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                "alias_name": [
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                "Long QT syndrome-3 (603830)",
                "Cardiomyopathy, dilated, 1E (601154)",
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            "transcript": null,
            "entity_name": "SCN5A",
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                "22490985"
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            "mode_of_pathogenicity": null
        },
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                "Expert Review Amber",
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                "alias_name": [
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            "phenotypes": [
                "short QT",
                "ventricular fibrillation",
                "cardiac arrest"
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            "mode_of_pathogenicity": null
        },
        {
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                "Expert Review Red",
                "Brugada syndrome (Version 1.7)",
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                "alias": [
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:60",
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            "penetrance": null,
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        {
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            "penetrance": null,
            "phenotypes": [
                "Long QT syndrome-11 (611820)",
                "?Long QT syndrome-11 611820"
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            "entity_name": "AKAP9",
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            "confidence_level": "1",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
            "mode_of_pathogenicity": ""
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        {
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            "evidence": [
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            "penetrance": null,
            "phenotypes": [
                "{Long QT syndrome, acquired, reduced susceptibility to} 613688"
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            "mode_of_pathogenicity": ""
        },
        {
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            "evidence": [
                "North West GLH",
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                "Long QT syndrome (Version 1.5)",
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            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:493",
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                "alias_name": null,
                "gene_symbol": "ANK2",
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            "phenotypes": [
                "Long QT syndrome 4 (600919)",
                "Long QT syndrome 4 600919",
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                "Cardiac arrhythmia, ankyrin-B-related 600919"
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