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            "phenotypes": [],
            "transcript": null,
            "entity_name": "PPOX",
            "entity_type": "gene",
            "publications": [],
            "confidence_level": "1",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
            "mode_of_pathogenicity": ""
        },
        {
            "tags": [],
            "evidence": [
                "London North GLH",
                "Expert Review Red",
                "NHS GMS"
            ],
            "gene_data": {
                "alias": [
                    "VEGF-A",
                    "VPF"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12680",
                "gene_name": "vascular endothelial growth factor A",
                "omim_gene": [
                    "192240"
                ],
                "alias_name": null,
                "gene_symbol": "VEGFA",
                "hgnc_symbol": "VEGFA",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:43737921-43754224",
                            "ensembl_id": "ENSG00000112715"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "6:43770184-43786487",
                            "ensembl_id": "ENSG00000112715"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2006-10-31"
            },
            "penetrance": null,
            "phenotypes": [
                "Association with POEMS syndrome"
            ],
            "transcript": null,
            "entity_name": "VEGFA",
            "entity_type": "gene",
            "publications": [],
            "confidence_level": "1",
            "mode_of_inheritance": "",
            "mode_of_pathogenicity": ""
        },
        {
            "tags": [],
            "evidence": [
                "Expert Review Removed",
                "London North GLH",
                "NHS GMS"
            ],
            "gene_data": {
                "alias": [
                    "FBH",
                    "FBH2",
                    "FHH2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:4379",
                "gene_name": "G protein subunit alpha 11",
                "omim_gene": [
                    "139313"
                ],
                "alias_name": null,
                "gene_symbol": "GNA11",
                "hgnc_symbol": "GNA11",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "19:3094408-3124002",
                            "ensembl_id": "ENSG00000088256"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "19:3094410-3124004",
                            "ensembl_id": "ENSG00000088256"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-07-20"
            },
            "penetrance": null,
            "phenotypes": [
                "Phakomatosis pigmentovascularis",
                "Extensive dermal melanocytosis"
            ],
            "transcript": null,
            "entity_name": "GNA11",
            "entity_type": "gene",
            "publications": [],
            "confidence_level": "0",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "mode_of_pathogenicity": ""
        },
        {
            "tags": [],
            "evidence": [
                "Expert Review Removed",
                "London North GLH",
                "NHS GMS"
            ],
            "gene_data": {
                "alias": [
                    "G-ALPHA-q",
                    "GAQ"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:4390",
                "gene_name": "G protein subunit alpha q",
                "omim_gene": [
                    "600998"
                ],
                "alias_name": null,
                "gene_symbol": "GNAQ",
                "hgnc_symbol": "GNAQ",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "9:80331003-80646374",
                            "ensembl_id": "ENSG00000156052"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "9:77716087-78031458",
                            "ensembl_id": "ENSG00000156052"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-12-15"
            },
            "penetrance": null,
            "phenotypes": [
                "Phakomatosis pigmentovascularis",
                "Extensive dermal melanocytosis",
                "Sturge Weber syndrome"
            ],
            "transcript": null,
            "entity_name": "GNAQ",
            "entity_type": "gene",
            "publications": [],
            "confidence_level": "0",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "mode_of_pathogenicity": ""
        }
    ],
    "stats": {
        "number_of_strs": 0,
        "number_of_genes": 35,
        "number_of_regions": 0
    },
    "types": [
        {
            "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 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)"
        },
        {
            "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."
        }
    ],
    "status": "public",
    "hash_id": null,
    "regions": [],
    "version": "1.2",
    "disease_group": "",
    "version_created": "2020-02-19T11:59:59.965778Z",
    "disease_sub_group": "",
    "relevant_disorders": [
        "R326"
    ],
    "signed_off": null
}