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                    "number_of_regions": 1
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                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
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        },
        {
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            "entity_type": "gene",
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            "mode_of_pathogenicity": "",
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            "evidence": [
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            ],
            "phenotypes": [],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
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            ],
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        },
        {
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            "entity_type": "gene",
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                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
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                        "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
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        },
        {
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                "Vazza G (2000)"
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                "Expert Review Removed",
                "Expert list"
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                "version_created": "2024-04-16T23:15:54.219280Z",
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                "types": [
                    {
                        "name": "Rare Disease 100K",
                        "slug": "rare-disease-100k",
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            "transcript": []
        },
        {
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                    "LERK2",
                    "Elk-L"
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                "hgnc_symbol": "EFNB1",
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                "Expert Review Removed",
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                        "name": "Rare Disease 100K",
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                    {
                        "name": "GMS Rare Disease Virtual",
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                    {
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        {
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            "entity_type": "gene",
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                        "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
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                        "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
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                        "slug": "gms-rare-disease-virtual",
                        "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                    },
                    {
                        "name": "Component Of Super Panel",
                        "slug": "component-of-super-panel",
                        "description": "This panel is a component of a Super Panel"
                    },
                    {
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                        "slug": "gms-signed-off",
                        "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
                    }
                ]
            },
            "transcript": null
        },
        {
            "gene_data": {
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                    "P-450AROM",
                    "CPV1",
                    "ARO1",
                    "CYAR",
                    "aromatase"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2594",
                "gene_name": "cytochrome P450 family 19 subfamily A member 1",
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                "hgnc_date_symbol_changed": "2003-02-28"
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            "evidence": [
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                "PAGE Additional Gene List"
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                    {
                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
                        "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                    },
                    {
                        "name": "GMS signed-off",
                        "slug": "gms-signed-off",
                        "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
                    },
                    {
                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
                        "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
                    }
                ]
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:8009",
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                "omim_gene": [
                    "600566"
                ],
                "alias_name": [
                    "neurexin II"
                ],
                "gene_symbol": "NRXN2",
                "hgnc_symbol": "NRXN2",
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                            "location": "11:64373646-64490660",
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                            "location": "11:64606174-64723188",
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                },
                "hgnc_date_symbol_changed": "1998-10-14"
            },
            "entity_type": "gene",
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            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
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                "PAGE DD-Gene2Phenotype"
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                        "slug": "gms-rare-disease-virtual",
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                    },
                    {
                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
                        "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
                    }
                ]
            },
            "transcript": null
        },
        {
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                    "ALK6",
                    "CDw293"
                ],
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                    "603248"
                ],
                "alias_name": null,
                "gene_symbol": "BMPR1B",
                "hgnc_symbol": "BMPR1B",
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                "ensembl_genes": {
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                            "location": "4:95679119-96079599",
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                "Expert Review Removed",
                "Emory Genetics Laboratory"
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            "tags": [
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                },
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                    {
                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
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                    },
                    {
                        "name": "GMS signed-off",
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                        "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
                    },
                    {
                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
                        "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                    }
                ]
            },
            "transcript": null
        },
        {
            "gene_data": {
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                    "CLG3"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7159",
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                "omim_gene": [
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                "alias_name": [
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                ],
                "gene_symbol": "MMP13",
                "hgnc_symbol": "MMP13",
                "hgnc_release": "2017-11-03T00:00:00",
                "ensembl_genes": {
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                            "location": "11:102813724-102826463",
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                },
                "hgnc_date_symbol_changed": "1994-11-20"
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            "entity_type": "gene",
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                "Expert Review Removed",
                "Emory Genetics Laboratory"
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                    {
                        "name": "GMS Rare Disease",
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                    },
                    {
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                    },
                    {
                        "name": "GMS Rare Disease Virtual",
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                    }
                ]
            },
            "transcript": null
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        {
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                    "TABP",
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                "alias_name": [
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                "hgnc_date_symbol_changed": "1997-06-20"
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                "Emory Genetics Laboratory"
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                    {
                        "name": "GMS Rare Disease",
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                    },
                    {
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                    {
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        {
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                    {
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                    {
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        {
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                "alias_name": [
                    "steroidogenic factor 1"
                ],
                "gene_symbol": "NR5A1",
                "hgnc_symbol": "NR5A1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "9:127243516-127269709",
                            "ensembl_id": "ENSG00000136931"
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                    },
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                        "90": {
                            "location": "9:124481236-124507430",
                            "ensembl_id": "ENSG00000136931"
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                    }
                },
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            },
            "entity_type": "gene",
            "entity_name": "NR5A1",
            "confidence_level": "0",
            "penetrance": null,
            "mode_of_pathogenicity": "Other - please provide details in the comments",
            "publications": [],
            "evidence": [
                "Expert Review Removed",
                "DD-Gene2Phenotype"
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            "tags": [
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                },
                "types": [
                    {
                        "name": "Component Of Super Panel",
                        "slug": "component-of-super-panel",
                        "description": "This panel is a component of a Super Panel"
                    },
                    {
                        "name": "GMS signed-off",
                        "slug": "gms-signed-off",
                        "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
                    },
                    {
                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
                        "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
                    }
                ]
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "hCAP-D3",
                    "CAP-D3",
                    "hHCP-6",
                    "KIAA0056",
                    "FLJ42888",
                    "hcp-6"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:28952",
                "gene_name": "non-SMC condensin II complex subunit D3",
                "omim_gene": [
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                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "11:134020014-134095348",
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                "Expert Review Red"
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                "hash_id": null,
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                        "description": "This panel is a component of a Super Panel"
                    },
                    {
                        "name": "GMS signed-off",
                        "slug": "gms-signed-off",
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                    },
                    {
                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
                        "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
                    }
                ]
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FLJ46629"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:25099",
                "gene_name": "protein arginine methyltransferase 9",
                "omim_gene": [
                    "616125"
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                    "GRch37": {
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                            "location": "4:148558936-148605381",
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                "DD-Gene2Phenotype",
                "Expert Review Red"
            ],
            "phenotypes": [
                "AUTOSOMAL RECESSIVE MENTAL RETARDATION"
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            "panel": {
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                        "name": "Component Of Super Panel",
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                    {
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                    },
                    {
                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
                        "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
                    }
                ]
            },
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        },
        {
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                    "HsT19662"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6825",
                "gene_name": "mannosidase alpha class 2A member 2",
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                "hgnc_symbol": "MAN2A2",
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                    }
                },
                "hgnc_date_symbol_changed": "1997-07-01"
            },
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            "mode_of_pathogenicity": "Other",
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                "DD-Gene2Phenotype"
            ],
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            ],
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                "disease_sub_group": "",
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                },
                "types": [
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                        "name": "Component Of Super Panel",
                        "slug": "component-of-super-panel",
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                    {
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                    },
                    {
                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
                        "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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        {
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                "biotype": "Mt_tRNA",
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                "hgnc_date_symbol_changed": "2005-02-16"
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                "DD-Gene2Phenotype"
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                    {
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                        "slug": "gms-rare-disease",
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                        "slug": "gms-rare-disease",
                        "description": "This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"
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                    {
                        "name": "GMS Rare Disease",
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                        "slug": "gms-rare-disease-virtual",
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                    "Genetic Epilepsies with Febrile Seizures Plus (GEFS+)",
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                    "number_of_regions": 18
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                "types": [
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                        "name": "Rare Disease 100K",
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                    {
                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
                        "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                    },
                    {
                        "name": "GMS signed-off",
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                        "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
                    },
                    {
                        "name": "Component Of Super Panel",
                        "slug": "component-of-super-panel",
                        "description": "This panel is a component of a Super Panel"
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                ]
            },
            "transcript": []
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        {
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                        "name": "GMS Rare Disease Virtual",
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                    {
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