GET /api/v1/panels/Hereditary%20ataxia/
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{
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                ]
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        },
        {
            "gene_data": {
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                "alias_name": [
                    "Cayman ataxia",
                    "caytaxin"
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                "hgnc_symbol": "ATCAY",
                "gene_name": "ATCAY, caytaxin",
                "ensembl_genes": {
                    "GRch37": {
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            "entity_type": "gene",
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                ]
            }
        },
        {
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                    "607585"
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                "alias_name": [
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            "entity_type": "gene",
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                ]
            }
        },
        {
            "gene_data": {
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                    "182350"
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                "alias_name": [
                    "sodium/potassium-transporting ATPase subunit alpha-3",
                    "sodium pump subunit alpha-3",
                    "sodium-potassium ATPase catalytic subunit alpha-3"
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                "hgnc_symbol": "ATP1A3",
                "gene_name": "ATPase Na+/K+ transporting subunit alpha 3",
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                ]
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        },
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                ]
            }
        },
        {
            "gene_data": {
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                ]
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        },
        {
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                "alias_name": null,
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                "Expert Review Green",
                "Expert Review"
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                        "description": "Rare Disease 100K"
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                ]
            }
        },
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                "alias_name": [
                    "protein phosphatase 1, regulatory subunit 85"
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                    "mGlu1",
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                    }
                ]
            }
        },
        {
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                    "GM2 gangliosidosis",
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                    }
                ]
            }
        },
        {
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                    "606873"
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                "alias": []
            },
            "entity_type": "gene",
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                "UKGTN"
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                        "name": "Rare Disease 100K",
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                        "description": "Rare Disease 100K"
                    }
                ]
            }
        },
        {
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                "omim_gene": [
                    "147265"
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                "alias_name": [
                    "protein phosphatase 1, regulatory subunit 94"
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                "gene_name": "inositol 1,4,5-trisphosphate receptor type 1",
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                    "Insp3r1",
                    "IP3R1",
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            },
            "entity_type": "gene",
            "entity_name": "ITPR1",
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            "penetrance": "Complete",
            "mode_of_pathogenicity": "Other - please provide details in the comments",
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                ]
            }
        },
        {
            "gene_data": {
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                    "RBK1",
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            "entity_type": "gene",
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                ]
            }
        },
        {
            "gene_data": {
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                "alias_name": null,
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                "ensembl_genes": {
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            },
            "entity_type": "gene",
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                ]
            }
        },
        {
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            "entity_type": "gene",
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                ]
            }
        },
        {
            "gene_data": {
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                "omim_gene": [
                    "602208"
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                "alias_name": null,
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                "ensembl_genes": {
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                "hgnc_id": "HGNC:6256",
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                    "Kir4.1",
                    "Kir1.2"
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            },
            "entity_type": "gene",
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            "penetrance": "Complete",
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                "Illumina TruGenome Clinical Sequencing Services",
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            }
        },
        {
            "gene_data": {
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                "alias_name": null,
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                "gene_name": "kinesin family member 1C",
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            },
            "entity_type": "gene",
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            "penetrance": "Complete",
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                ]
            }
        },
        {
            "gene_data": {
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                "alias_name": [
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            "entity_type": "gene",
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            "penetrance": "Complete",
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                    "WFS"
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                "UKGTN"
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                        "name": "Rare Disease 100K",
                        "slug": "rare-disease-100k",
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                ]
            }
        },
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            "entity_type": "gene",
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:14857",
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            "entity_type": "gene",
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                "types": [
                    {
                        "name": "Rare Disease 100K",
                        "slug": "rare-disease-100k",
                        "description": "Rare Disease 100K"
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                ]
            }
        },
        {
            "gene_data": {
                "gene_symbol": "DMXL2",
                "omim_gene": [
                    "612186"
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                "alias_name": [
                    "rabconnectin 3"
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                "gene_name": "Dmx like 2",
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                "hgnc_date_symbol_changed": "1998-04-27",
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                "hgnc_id": "HGNC:2938",
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                    "KIAA0856",
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            },
            "entity_type": "gene",
            "entity_name": "DMXL2",
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                ]
            }
        },
        {
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                "alias_name": [
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            "entity_type": "gene",
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                        "name": "Rare Disease 100K",
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                ]
            }
        },
        {
            "gene_data": {
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                "alias_name": null,
                "hgnc_symbol": "VAMP1",
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            "entity_type": "gene",
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                ]
            }
        },
        {
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                "alias_name": [
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            "entity_type": "gene",
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                ]
            }
        },
        {
            "gene_data": {
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                "alias_name": [
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                "ensembl_genes": {
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            "entity_type": "gene",
            "entity_name": "ALAS2",
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            "penetrance": "Complete",
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                ]
            }
        },
        {
            "gene_data": {
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                "gene_name": "atrophin 1",
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            "entity_type": "gene",
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                ]
            }
        },
        {
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            "entity_type": "gene",
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                ]
            }
        },
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                    "ATPIB",
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            },
            "entity_type": "gene",
            "entity_name": "ATP8A2",
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            "penetrance": "Complete",
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                "Expert Review Red",
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                "biotype": "protein_coding",
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                    "CST6",
                    "PME"
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            },
            "entity_type": "gene",
            "entity_name": "CSTB",
            "confidence_level": "1",
            "penetrance": "Complete",
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
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            "phenotypes": [
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                    "number_of_strs": 12
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                "types": [
                    {
                        "name": "Rare Disease 100K",
                        "slug": "rare-disease-100k",
                        "description": "Rare Disease 100K"
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                ]
            }
        },
        {
            "gene_data": {
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                "omim_gene": [
                    "603448"
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                "alias_name": null,
                "hgnc_symbol": "DAB1",
                "gene_name": "DAB1, reelin adaptor protein",
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                    "GRch37": {
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2661",
                "alias": []
            },
            "entity_type": "gene",
            "entity_name": "DAB1",
            "confidence_level": "1",
            "penetrance": "Complete",
            "mode_of_pathogenicity": "Other - please provide details in the comments",
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                    "number_of_strs": 12
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                        "name": "Rare Disease 100K",
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                ]
            }
        },
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            "gene_data": {
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                "omim_gene": [
                    "600112"
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                "alias_name": null,
                "hgnc_symbol": "DYNC1H1",
                "gene_name": "dynein cytoplasmic 1 heavy chain 1",
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                "hgnc_date_symbol_changed": "2005-11-24",
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2961",
                "alias": [
                    "Dnchc1",
                    "HL-3",
                    "p22",
                    "DHC1",
                    "CMT2O"
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            },
            "entity_type": "gene",
            "entity_name": "DYNC1H1",
            "confidence_level": "1",
            "penetrance": "Complete",
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            "publications": [],
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                "Illumina TruGenome Clinical Sequencing Services"
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            "phenotypes": [
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                    "number_of_strs": 12
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                "types": [
                    {
                        "name": "Rare Disease 100K",
                        "slug": "rare-disease-100k",
                        "description": "Rare Disease 100K"
                    }
                ]
            }
        },
        {
            "gene_data": {
                "gene_symbol": "ELOVL5",
                "omim_gene": [
                    "611805"
                ],
                "alias_name": null,
                "hgnc_symbol": "ELOVL5",
                "gene_name": "ELOVL fatty acid elongase 5",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "ensembl_id": "ENSG00000012660",
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                    },
                    "GRch38": {
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                "hgnc_release": "2017-11-03T00:00:00",
                "hgnc_date_symbol_changed": "2003-06-12",
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:21308",
                "alias": [
                    "HELO1",
                    "dJ483K16.1"
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            },
            "entity_type": "gene",
            "entity_name": "ELOVL5",
            "confidence_level": "1",
            "penetrance": "Complete",
            "mode_of_pathogenicity": "Other - please provide details in the comments ",
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                "Expert Review Red",
                "Expert Review"
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                "Spinocerebellar ataxia 36 (#615957)"
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                "version_created": "2018-11-16T13:52:37.045805Z",
                "relevant_disorders": [],
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                "types": [
                    {
                        "name": "Rare Disease 100K",
                        "slug": "rare-disease-100k",
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                ]
            }
        },
        {
            "gene_data": {
                "gene_symbol": "MTPAP",
                "omim_gene": [
                    "613669"
                ],
                "alias_name": [
                    "TUTase1"
                ],
                "hgnc_symbol": "MTPAP",
                "gene_name": "mitochondrial poly(A) polymerase",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "ensembl_id": "ENSG00000107951",
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                "hgnc_release": "2017-11-03T00:00:00",
                "hgnc_date_symbol_changed": "2009-01-12",
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                "hgnc_id": "HGNC:25532",
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                    "mtPAP",
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                ]
            },
            "entity_type": "gene",
            "entity_name": "MTPAP",
            "confidence_level": "1",
            "penetrance": "Complete",
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                "Expert Review Red",
                "UKGTN",
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                "relevant_disorders": [],
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                "types": [
                    {
                        "name": "Rare Disease 100K",
                        "slug": "rare-disease-100k",
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                ]
            }
        },
        {
            "gene_data": {
                "gene_symbol": "NAGLU",
                "omim_gene": [
                    "609701"
                ],
                "alias_name": [
                    "Sanfilippo disease IIIB"
                ],
                "hgnc_symbol": "NAGLU",
                "gene_name": "N-acetyl-alpha-glucosaminidase",
                "ensembl_genes": {
                    "GRch37": {
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                    },
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                "hgnc_release": "2017-11-03T00:00:00",
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7632",
                "alias": [
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            },
            "entity_type": "gene",
            "entity_name": "NAGLU",
            "confidence_level": "1",
            "penetrance": "Complete",
            "mode_of_pathogenicity": "Other - please provide details in the comments ",
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                "Expert Review Red",
                "Expert review"
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                    "number_of_strs": 12
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                        "slug": "rare-disease-100k",
                        "description": "Rare Disease 100K"
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                ]
            }
        },
        {
            "gene_data": {
                "gene_symbol": "NOP56",
                "omim_gene": [
                    "614154"
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                "alias_name": [
                    "spinocerebellar ataxia 36"
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                "hgnc_symbol": "NOP56",
                "gene_name": "NOP56 ribonucleoprotein",
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                "hgnc_date_symbol_changed": "2009-01-13",
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                "hgnc_id": "HGNC:15911",
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            },
            "entity_type": "gene",
            "entity_name": "NOP56",
            "confidence_level": "1",
            "penetrance": "Complete",
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
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                "Spinocerebellarataxia36,614153"
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            "mode_of_inheritance": "Other - please specifiy in evaluation comments",
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                ]
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        },
        {
            "gene_data": {
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                "omim_gene": [
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                "alias_name": null,
                "hgnc_symbol": "PAX2",
                "gene_name": "paired box 2",
                "ensembl_genes": {
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:8616",
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            "entity_type": "gene",
            "entity_name": "PAX2",
            "confidence_level": "1",
            "penetrance": "Complete",
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                "Expert Review Red",
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                ]
            }
        },
        {
            "gene_data": {
                "gene_symbol": "PCLO",
                "omim_gene": [
                    "604918"
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                "alias_name": [
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                "hgnc_symbol": "PCLO",
                "gene_name": "piccolo presynaptic cytomatrix protein",
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            },
            "entity_type": "gene",
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            "penetrance": "Complete",
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                "Expert Review Red",
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                        "description": "Rare Disease 100K"
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        },
        {
            "gene_data": {
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                "alias_name": null,
                "hgnc_symbol": "PIK3R5",
                "gene_name": "phosphoinositide-3-kinase regulatory subunit 5",
                "ensembl_genes": {
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                    "p101"
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            },
            "entity_type": "gene",
            "entity_name": "PIK3R5",
            "confidence_level": "1",
            "penetrance": "Complete",
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Red",
                "UKGTN",
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                "id": 20,
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                ]
            }
        },
        {
            "gene_data": {
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                "alias_name": [
                    "PP2A subunit B isoform beta"
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                "hgnc_symbol": "PPP2R2B",
                "gene_name": "protein phosphatase 2 regulatory subunit Bbeta",
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9305",
                "alias": [
                    "PR55-BETA",
                    "PR52B",
                    "B55beta"
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            },
            "entity_type": "gene",
            "entity_name": "PPP2R2B",
            "confidence_level": "1",
            "penetrance": "Complete",
            "mode_of_pathogenicity": "Other - please provide details in the comments",
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                "Expert Review Red",
                "Radboud University Medical Center, Nijmegen",
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