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                    "factor H related protein 5"
                ],
                "gene_symbol": "CFHR5",
                "hgnc_symbol": "CFHR5",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:196946667-196978804",
                            "ensembl_id": "ENSG00000134389"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:196977556-197009674",
                            "ensembl_id": "ENSG00000134389"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2006-02-28"
            },
            "penetrance": null,
            "phenotypes": [
                "Nephropathy due to CFHR5 deficiency, MIM#\t614809"
            ],
            "transcript": null,
            "entity_name": "CFHR5",
            "entity_type": "gene",
            "publications": [
                "22622361"
            ],
            "confidence_level": "0",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "mode_of_pathogenicity": null
        }
    ],
    "stats": {
        "number_of_strs": 0,
        "number_of_genes": 15,
        "number_of_regions": 0
    },
    "types": [
        {
            "name": "Rare Disease 100K",
            "slug": "rare-disease-100k",
            "description": "Rare Disease 100K"
        },
        {
            "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": "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": "563248da22c1fc58285b283a",
    "regions": [],
    "version": "2.2",
    "disease_group": "Renal and urinary tract disorders",
    "version_created": "2020-02-13T11:31:11.314498Z",
    "disease_sub_group": "Syndromes with prominent renal abnormalities",
    "relevant_disorders": [
        "R201"
    ],
    "signed_off": "2020-02-13"
}