GET /api/v1/panels/515/?version=1.2
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{
    "id": 515,
    "name": "Iron metabolism disorders",
    "strs": [],
    "genes": [
        {
            "tags": [],
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                "Expert Review Green",
                "NHS GMS",
                "Wessex and West Midlands GLH"
            ],
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            "penetrance": null,
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                "301310 Anemia, sideroblastic, with ataxia"
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            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "mode_of_pathogenicity": ""
        },
        {
            "tags": [],
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                "Expert Review Green",
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                "hgnc_symbol": "ALAS2",
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            "penetrance": null,
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                "300752 Protoporphyria, erythropoietic, X-linked",
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            "entity_name": "ALAS2",
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            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
            "mode_of_pathogenicity": ""
        },
        {
            "tags": [],
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                "Expert Review Green",
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                "Yorkshire and North East GLH",
                "NHS GMS",
                "Wessex and West Midlands GLH"
            ],
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                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:870",
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                "omim_gene": [
                    "606882"
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                "alias_name": [
                    "Wilson disease",
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                    "copper-transporting ATPase 2"
                ],
                "gene_symbol": "ATP7B",
                "hgnc_symbol": "ATP7B",
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                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "penetrance": null,
            "phenotypes": [
                "277900 WILSON DISEASE"
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            "transcript": null,
            "entity_name": "ATP7B",
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            "confidence_level": "3",
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            "mode_of_pathogenicity": ""
        },
        {
            "tags": [],
            "evidence": [
                "North West GLH",
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                "London South GLH",
                "NHS GMS",
                "Expert Review Green",
                "Wessex and West Midlands GLH"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1073",
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                "omim_gene": [
                    "112266"
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                "alias_name": null,
                "gene_symbol": "BMP6",
                "hgnc_symbol": "BMP6",
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                    "GRch37": {
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                    },
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                    }
                },
                "hgnc_date_symbol_changed": "1991-06-05"
            },
            "penetrance": null,
            "phenotypes": [
                "NA IRON OVERLOAD",
                "112266 Mild to moderate iron overload",
                "Iron overload"
            ],
            "transcript": null,
            "entity_name": "BMP6",
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            ],
            "confidence_level": "3",
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
            "mode_of_pathogenicity": ""
        },
        {
            "tags": [],
            "evidence": [
                "North West GLH",
                "Yorkshire and North East GLH",
                "London South GLH",
                "NHS GMS",
                "Expert Review Green",
                "Wessex and West Midlands GLH"
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            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2295",
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                "omim_gene": [
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                "alias_name": [
                    "ferroxidase"
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                "gene_symbol": "CP",
                "hgnc_symbol": "CP",
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                "ensembl_genes": {
                    "GRch37": {
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                            "location": "3:148880197-148939842",
                            "ensembl_id": "ENSG00000047457"
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                    },
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                    }
                },
                "hgnc_date_symbol_changed": "1986-01-01"
            },
            "penetrance": null,
            "phenotypes": [
                "604290 Hemosiderosis, systemic, due to aceruloplasminemia",
                "604290 ACERULOPLASMINEMIA"
            ],
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            "entity_name": "CP",
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            "confidence_level": "3",
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "mode_of_pathogenicity": ""
        },
        {
            "tags": [],
            "evidence": [
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                "Yorkshire and North East GLH",
                "NHS GMS",
                "Expert Review Green",
                "Wessex and West Midlands GLH"
            ],
            "gene_data": {
                "alias": [
                    "DCYTB",
                    "FLJ23462",
                    "FRRS3",
                    "CYB561A2"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:20797",
                "gene_name": "cytochrome b reductase 1",
                "omim_gene": [
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                "alias_name": [
                    "ferric-chelate reductase 3",
                    "cytochrome b561 family, member A2"
                ],
                "gene_symbol": "CYBRD1",
                "hgnc_symbol": "CYBRD1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "2:172378757-172414643",
                            "ensembl_id": "ENSG00000071967"
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                    },
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                },
                "hgnc_date_symbol_changed": "2003-07-16"
            },
            "penetrance": null,
            "phenotypes": [
                "NA IRON OVERLOAD",
                "N/A Primary iron overload",
                "Iron overload"
            ],
            "transcript": null,
            "entity_name": "CYBRD1",
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            "mode_of_pathogenicity": ""
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        {
            "tags": [],
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            "gene_data": {
                "alias": [
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                "biotype": "protein_coding",
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                "omim_gene": [
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                "alias_name": [
                    "ferritin light polypeptide-like 3",
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                    "ferritin light chain",
                    "ferritin L-chain",
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                "gene_symbol": "FTL",
                "hgnc_symbol": "FTL",
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                "23940258",
                "23421845",
                "19176363"
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            "mode_of_pathogenicity": ""
        },
        {
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                "biotype": "protein_coding",
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                "omim_gene": [
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                            "location": "1:155204243-155214490",
                            "ensembl_id": "ENSG00000177628"
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            "phenotypes": [
                "230900 Gaucher disease, type II",
                "231005 Gaucher disease, type IIIC",
                "231000 Gaucher disease, type III",
                "230800 Gaucher disease, type I"
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                "27816428",
                "20575041"
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        {
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                "Expert Review Green",
                "London South GLH",
                "NHS GMS",
                "Wessex and West Midlands GLH"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:20134",
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            "phenotypes": [
                "616860 Anemia, sideroblastic, 3, pyridoxine-refractory",
                "Sideroblastic anaemia - increased serum ferritin"
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            "entity_name": "GLRX5",
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                "25342667"
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        },
        {
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                "Expert Review Green",
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                    "HEPC",
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            "penetrance": null,
            "phenotypes": [
                "613313 Hemochromatosis, type 2B",
                "613313 HEMOCHROMATOSIS, TYPE 2B",
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                "12915468"
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            "mode_of_pathogenicity": ""
        },
        {
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            "evidence": [
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                "London South GLH",
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            "gene_data": {
                "alias": [
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:4886",
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                "omim_gene": [
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                "alias_name": [
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                "hgnc_symbol": "HFE",
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            "penetrance": null,
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                "235200 Hemochromatosis",
                "235200HEMOCHROMATOSIS, TYPE 1"
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                "Yorkshire and North East GLH",
                "London South GLH",
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                "Expert Review Green",
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            "gene_data": {
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                    "haemojuvelin"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:4887",
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                "alias_name": [
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                "hgnc_symbol": "HFE2",
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            "phenotypes": [
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                "602390 HEMOCHROMATOSIS, TYPE 2A",
                "602390 Hemochromatosis, type 2A"
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        },
        {
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                "Yorkshire and North East GLH",
                "London South GLH",
                "NHS GMS",
                "Expert Review Green",
                "Wessex and West Midlands GLH"
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            "gene_data": {
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            "penetrance": null,
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                "206100 Anemia, hypochromic microcytic, with iron overload 1",
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            "mode_of_pathogenicity": ""
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        {
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:26054",
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                "alias_name": null,
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                "IRIDA",
                "206200 IRON-REFRACTORY IRON DEFICIENCY ANEMIA"
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