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                "hgnc_date_symbol_changed": "2003-10-08"
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            "penetrance": null,
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            "mode_of_pathogenicity": ""
        },
        {
            "tags": [],
            "evidence": [
                "Expert Review Red",
                "South West GLH",
                "South West GLH"
            ],
            "gene_data": {
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                    "TNXBS",
                    "XBS",
                    "XB"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:11976",
                "gene_name": "tenascin XB",
                "omim_gene": [
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                "alias_name": null,
                "gene_symbol": "TNXB",
                "hgnc_symbol": "TNXB",
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                "ensembl_genes": {
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                },
                "hgnc_date_symbol_changed": "2000-07-25"
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            "entity_type": "gene",
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            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "mode_of_pathogenicity": ""
        },
        {
            "tags": [],
            "evidence": [
                "Expert Review Red",
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                "South West GLH"
            ],
            "gene_data": {
                "alias": [
                    "KIAA1858"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:23216",
                "gene_name": "zinc finger protein 469",
                "omim_gene": [
                    "612078"
                ],
                "alias_name": null,
                "gene_symbol": "ZNF469",
                "hgnc_symbol": "ZNF469",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
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                            "ensembl_id": "ENSG00000225614"
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                "hgnc_date_symbol_changed": "2003-10-15"
            },
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            "phenotypes": [],
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            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "mode_of_pathogenicity": ""
        }
    ],
    "stats": {
        "number_of_strs": 0,
        "number_of_genes": 62,
        "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 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": "2020-02-19T14:31:36.806820Z",
    "disease_sub_group": "",
    "relevant_disorders": [
        "R125"
    ],
    "signed_off": "2020-02-19"
}