Search Entities

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                "alias": [
                    "SDR21C1"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1548",
                "gene_name": "carbonyl reductase 1",
                "omim_gene": [
                    "114830"
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                "alias_name": [
                    "short chain dehydrogenase/reductase family 21C, member 1"
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                "gene_symbol": "CBR1",
                "hgnc_symbol": "CBR1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "21:37442239-37445464",
                            "ensembl_id": "ENSG00000159228"
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                "hgnc_date_symbol_changed": "1991-02-20"
            },
            "entity_type": "gene",
            "entity_name": "CBR1",
            "confidence_level": "1",
            "penetrance": null,
            "mode_of_pathogenicity": "",
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                "30794780",
                "27843122"
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                "Literature"
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                "id": 227,
                "hash_id": "590b12638f6203169828a560",
                "name": "Genomic imprinting",
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                "disease_sub_group": "",
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                    {
                        "name": "Research",
                        "slug": "research",
                        "description": "This is a gene panel used for research."
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            "gene_data": {
                "alias": [
                    "B7323"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:15718",
                "gene_name": "APC down-regulated 1",
                "omim_gene": [
                    "607479"
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                "alias_name": null,
                "gene_symbol": "APCDD1",
                "hgnc_symbol": "APCDD1",
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                        "82": {
                            "location": "18:10454625-10489945",
                            "ensembl_id": "ENSG00000154856"
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                "hgnc_date_symbol_changed": "2001-06-21"
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            "entity_name": "APCDD1",
            "confidence_level": "3",
            "penetrance": "Complete",
            "mode_of_pathogenicity": "",
            "publications": [
                "22512811",
                "20393562"
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            "evidence": [
                "Expert Review Green",
                "Radboud University Medical Center, Nijmegen",
                "Other"
            ],
            "phenotypes": [
                "Hereditary hypotrichosis simplex (HHS)",
                "Hypotrichosis simplex (HS)",
                "Hypotrichosis 1",
                "non-syndromic hereditary hypotrichosis",
                "Hypotrichosis 1, 605389"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
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                "id": 189,
                "hash_id": "56937d0d22c1fc25158f3c9e",
                "name": "Non-syndromic hypotrichosis",
                "disease_group": "Dermatological disorders",
                "disease_sub_group": "Skin adnexa disorders",
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                "version_created": "2024-01-24T12:04:27.219717Z",
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        {
            "gene_data": {
                "alias": [
                    "DBM"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2689",
                "gene_name": "dopamine beta-hydroxylase",
                "omim_gene": [
                    "609312"
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                "alias_name": [
                    "dopamine beta-monooxygenase"
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                "hgnc_symbol": "DBH",
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                            "location": "9:136501482-136524466",
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                "hgnc_date_symbol_changed": "2001-06-22"
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            "entity_name": "DBH",
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                "27604308",
                "27778639",
                "27830117"
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                "Radboud University Medical Center, Nijmegen",
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                "Literature"
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                "Dopamine beta-hydroxylase deficiency, 223360"
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            "tags": [
                "treatable"
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                "name": "Neurotransmitter disorders",
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                "disease_sub_group": "Motor Disorders of the CNS",
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                "version": "1.9",
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            "gene_data": {
                "alias": [
                    "FMF",
                    "TRIM20"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6998",
                "gene_name": "MEFV, pyrin innate immunity regulator",
                "omim_gene": [
                    "608107"
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                "alias_name": [
                    "marenostrin"
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                "gene_symbol": "MEFV",
                "hgnc_symbol": "MEFV",
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                "ensembl_genes": {
                    "GRch37": {
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                            "location": "16:3292028-3306627",
                            "ensembl_id": "ENSG00000103313"
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                "hgnc_date_symbol_changed": "1989-10-30"
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            "mode_of_pathogenicity": "",
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                "UKGTN",
                "Emory Genetics Laboratory",
                "Illumina TruGenome Clinical Sequencing Services",
                "Radboud University Medical Center, Nijmegen",
                "Expert list"
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                "Familial Mediterranean fever, AD, OMIM:134610",
                "Familial Mediterranean fever, AR, OMIM:249100"
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                "version": "1.43",
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        {
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                "alias": [
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                    "PIDX",
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                "gene_name": "forkhead box P3",
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            "entity_name": "FOXP3",
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                "Expert Review Green",
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                "Radboud University Medical Center, Nijmegen"
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                "Immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, 304790",
                "{Diabetes mellitus, type I, susceptibility to}, 222100",
                "Neonatal Diabetes"
            ],
            "mode_of_inheritance": "X-LINKED: hemizygous mutation in males, biallelic mutations in females",
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            "panel": {
                "id": 87,
                "hash_id": "55d1e3f522c1fc237fbd46e9",
                "name": "Multi-organ autoimmune diabetes",
                "disease_group": "Endocrine disorders",
                "disease_sub_group": "Disorders of unusual phenotypes",
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                "version": "1.11",
                "version_created": "2022-06-07T10:32:58.649996Z",
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                "stats": {
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                        "slug": "rare-disease-100k",
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            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "PTS2R",
                    "RD"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:8860",
                "gene_name": "peroxisomal biogenesis factor 7",
                "omim_gene": [
                    "601757"
                ],
                "alias_name": [
                    "Refsum disease"
                ],
                "gene_symbol": "PEX7",
                "hgnc_symbol": "PEX7",
                "hgnc_release": "2017-11-03T00:00:00",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:137143717-137235075",
                            "ensembl_id": "ENSG00000112357"
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                "hgnc_date_symbol_changed": "1997-05-22"
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            "entity_name": "PEX7",
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            "penetrance": "Complete",
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            "evidence": [
                "NHS GMS",
                "Emory Genetics Laboratory"
            ],
            "phenotypes": [
                "Eye Disorders"
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            "panel": {
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                "hash_id": "55507b25bb5a161bf644a3b2",
                "name": "Glaucoma (developmental)",
                "disease_group": "Ophthalmological disorders",
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                "version": "1.45",
                "version_created": "2024-02-20T15:55:53.657622Z",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 232,
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                "types": [
                    {
                        "name": "Rare Disease 100K",
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                        "description": "Rare Disease 100K"
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                ]
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "Kv1.1",
                    "RBK1",
                    "HUK1",
                    "MBK1"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:6218",
                "gene_name": "potassium voltage-gated channel subfamily A member 1",
                "omim_gene": [
                    "176260"
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                "alias_name": null,
                "gene_symbol": "KCNA1",
                "hgnc_symbol": "KCNA1",
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                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "12:5019071-5040527",
                            "ensembl_id": "ENSG00000111262"
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                "28787010"
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                "hash_id": null,
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        {
            "gene_data": {
                "alias": [
                    "FAF"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:3587",
                "gene_name": "Fanconi anemia complementation group F",
                "omim_gene": [
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                            "location": "11:22644079-22647387",
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                            "location": "11:22622519-22626787",
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                "hgnc_date_symbol_changed": "1998-08-26"
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                "28297620",
                "Cancer Gene Census"
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                "Curated sources",
                "Expert Review Green"
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                "Class: BM failure FA, (typ AR)",
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                "Fanconi anaemia F",
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                "AML, Leukaemia",
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                "name": "Haematological malignancies for rare disease",
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        {
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                "alias_name": [
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        {
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        {
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            "entity_type": "gene",
            "entity_name": "FANCC",
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            "evidence": [
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                "Expert list"
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                "Fanconi Anemia"
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                "version_created": "2024-03-26T14:49:24.653790Z",
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                    "Childhood solid tumours pertinent cancer susceptibility"
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                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [
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                        "name": "Cancer Germline 100K",
                        "slug": "cancer-germline-100k",
                        "description": "Cancer Germline 100K"
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                ]
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        },
        {
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                    "LKB1"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:11389",
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                "alias_name": [
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                "hgnc_symbol": "STK11",
                "hgnc_release": "2017-11-03T00:00:00",
                "ensembl_genes": {
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                            "location": "19:1189406-1228428",
                            "ensembl_id": "ENSG00000118046"
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                        "90": {
                            "location": "19:1177558-1228435",
                            "ensembl_id": "ENSG00000118046"
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                },
                "hgnc_date_symbol_changed": "1998-01-21"
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            "penetrance": "Complete",
            "mode_of_pathogenicity": null,
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                "Expert Review Green",
                "Expert list"
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            "phenotypes": [
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            "panel": {
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                "hash_id": "595ce30f8f62036352471f39",
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                "disease_sub_group": "Pertinent cancer susceptibility gene panel",
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                "version": "2.29",
                "version_created": "2024-01-24T18:24:52.770842Z",
                "relevant_disorders": [
                    "Carcinoma of unknown primary",
                    "Other",
                    "Adult solid tumours pertinent cancer susceptibility"
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                    "number_of_strs": 0,
                    "number_of_regions": 0
                },
                "types": [
                    {
                        "name": "Cancer Germline 100K",
                        "slug": "cancer-germline-100k",
                        "description": "Cancer Germline 100K"
                    },
                    {
                        "name": "GMS Cancer Germline Virtual",
                        "slug": "gms-cancer-germline-virtual",
                        "description": "This is a panel used for WGS germline analysis for the GMS."
                    },
                    {
                        "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."
                    }
                ]
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "PKD4",
                    "PC2",
                    "Pc-2",
                    "TRPP2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9009",
                "gene_name": "polycystin 2, transient receptor potential cation channel",
                "omim_gene": [
                    "173910"
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                "alias_name": [
                    "transient receptor potential cation channel, subfamily P, member 2"
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                "gene_symbol": "PKD2",
                "hgnc_symbol": "PKD2",
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                "ensembl_genes": {
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                            "location": "4:88928820-88998929",
                            "ensembl_id": "ENSG00000118762"
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                    "GRch38": {
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                            "location": "4:88007668-88077777",
                            "ensembl_id": "ENSG00000118762"
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                "hgnc_date_symbol_changed": "1988-08-07"
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            "entity_type": "gene",
            "entity_name": "PKD2",
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            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
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                "Expert Review Red",
                "South West GLH"
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            "phenotypes": [
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                "Polycystic kidney disease 2, 613095"
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            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
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            "panel": {
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                "hash_id": null,
                "name": "Thoracic aortic aneurysm or dissection (GMS)",
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                "disease_sub_group": "",
                "status": "public",
                "version": "3.11",
                "version_created": "2024-04-10T17:56:14.551936Z",
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                    "Thoracic aortic aneurysm and dissection",
                    "R125"
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                "stats": {
                    "number_of_genes": 70,
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                    "number_of_regions": 0
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                "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."
                    }
                ]
            },
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:10896",
                "gene_name": "SKI proto-oncogene",
                "omim_gene": [
                    "164780"
                ],
                "alias_name": null,
                "gene_symbol": "SKI",
                "hgnc_symbol": "SKI",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:2160134-2241558",
                            "ensembl_id": "ENSG00000157933"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "1:2228695-2310119",
                            "ensembl_id": "ENSG00000157933"
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                "hgnc_date_symbol_changed": "2001-06-22"
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            "publications": [
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                "Expert Review Green",
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                "London South GLH",
                "North West GLH"
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            "phenotypes": [
                "Shprintzen-Goldberg Craniosynostosis Syndrome, 182212",
                "Shprintzen-Goldberg syndrome (182212)",
                "Marfan Syndrome, Thoracic Aortic Aneurysm & Dissection (TAAD), and Related Disorders"
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            "panel": {
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                "disease_sub_group": "",
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                    "R125"
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                "stats": {
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                    "number_of_regions": 0
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                "types": [
                    {
                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
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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."
                    }
                ]
            },
            "transcript": null
        },
        {
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                "alias": [
                    "LH1"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9081",
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                "omim_gene": [
                    "153454"
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                "alias_name": [
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                "gene_symbol": "PLOD1",
                "hgnc_symbol": "PLOD1",
                "hgnc_release": "2017-11-03T00:00:00",
                "ensembl_genes": {
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                        "82": {
                            "location": "1:11994262-12035595",
                            "ensembl_id": "ENSG00000083444"
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                    "GRch38": {
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                            "location": "1:11934205-11975538",
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                "hgnc_date_symbol_changed": "2004-12-14"
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            "entity_type": "gene",
            "entity_name": "PLOD1",
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            "penetrance": "Complete",
            "mode_of_pathogenicity": "",
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                "15666309"
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                "South West GLH",
                "London South GLH",
                "Expert Review Green",
                "Other"
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                "Ehlers-Danlos syndrome, type VI, 225400",
                "kyphoscoliotic EDS"
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                "status": "public",
                "version": "1.127",
                "version_created": "2024-01-24T10:52:51.597959Z",
                "relevant_disorders": [
                    "Familial retinal arteriolar tortuosity",
                    "FTAAD",
                    "Familial Thoracic Aortic Aneurysm Disease"
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                "stats": {
                    "number_of_genes": 65,
                    "number_of_strs": 0,
                    "number_of_regions": 0
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                "types": [
                    {
                        "name": "Rare Disease 100K",
                        "slug": "rare-disease-100k",
                        "description": "Rare Disease 100K"
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                ]
            },
            "transcript": null
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        {
            "gene_data": {
                "alias": [
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                    "muCL",
                    "CANP",
                    "CANPL1"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:1476",
                "gene_name": "calpain 1",
                "omim_gene": [
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                            "location": "11:64948037-64979477",
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                "hgnc_date_symbol_changed": "1989-06-30"
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                "Expert Review Green",
                "Expert list"
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                "Spastic paraplegia 76 autosomal recessive\t616907"
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            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
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            "panel": {
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                "hash_id": "55ad019f22c1fc7042059038",
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                "disease_group": "Neurology and neurodevelopmental disorders",
                "disease_sub_group": "Motor Disorders of the CNS",
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                "version": "1.311",
                "version_created": "2024-04-16T23:15:54.219280Z",
                "relevant_disorders": [],
                "stats": {
                    "number_of_genes": 115,
                    "number_of_strs": 10,
                    "number_of_regions": 0
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                "types": [
                    {
                        "name": "Rare Disease 100K",
                        "slug": "rare-disease-100k",
                        "description": "Rare Disease 100K"
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                ]
            },
            "transcript": null
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        {
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                "alias": [
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                    "HL-3",
                    "p22",
                    "DHC1",
                    "CMT2O"
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2961",
                "gene_name": "dynein cytoplasmic 1 heavy chain 1",
                "omim_gene": [
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                "gene_symbol": "DYNC1H1",
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                    "Arthrogrythsis",
                    "R83"
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                "types": [
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                        "name": "Rare Disease 100K",
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                        "description": "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."
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                    {
                        "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."
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                ]
            },
            "transcript": null
        },
        {
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:492",
                "gene_name": "ankyrin 1",
                "omim_gene": [
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                "types": [
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                        "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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                        "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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                "Expert Review Red",
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                    {
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                "alias_name": [
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        },
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                    {
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        {
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                    {
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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)"
                    },
                    {
                        "name": "GMS signed-off",
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                    {
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            "transcript": null
        },
        {
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                "hgnc_id": "HGNC:10808",
                "gene_name": "sarcoglycan epsilon",
                "omim_gene": [
                    "604149"
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                "alias_name": null,
                "gene_symbol": "SGCE",
                "hgnc_symbol": "SGCE",
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                            "location": "7:94214542-94285521",
                            "ensembl_id": "ENSG00000127990"
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                    "GRch38": {
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                            "ensembl_id": "ENSG00000127990"
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                    }
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                "hgnc_date_symbol_changed": "1999-01-11"
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            "entity_type": "gene",
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            "mode_of_pathogenicity": "",
            "publications": [
                "12325078",
                "11528394",
                "http://www.ncbi.nlm.nih.gov/books/NBK1155/",
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                "22626943"
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            "evidence": [
                "Expert Review Red",
                "Wessex and West Midlands GLH",
                "Yorkshire and North East GLH",
                "NHS GMS",
                "London North GLH"
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                "hash_id": null,
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                "version_created": "2024-04-15T09:57:08.902052Z",
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                    "R58"
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                    "number_of_strs": 16,
                    "number_of_regions": 4
                },
                "types": [
                    {
                        "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."
                    },
                    {
                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
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                ]
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            "transcript": null
        },
        {
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                    "GEFSP2",
                    "HBSCI",
                    "NAC1",
                    "SMEI"
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                "hgnc_id": "HGNC:10585",
                "gene_name": "sodium voltage-gated channel alpha subunit 1",
                "omim_gene": [
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                "alias_name": null,
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                "hgnc_symbol": "SCN1A",
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                            "location": "2:166845670-166984523",
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                "Wessex and West Midlands GLH",
                "Yorkshire and North East GLH",
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                "London North GLH"
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                "familial hemiplegic migraine 3",
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                    "R58"
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                "types": [
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                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
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                    },
                    {
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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."
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                    {
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                        "slug": "gms-rare-disease-virtual",
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                "omim_gene": [
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                "hgnc_symbol": "SLC19A3",
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                    "R58"
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                "types": [
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                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
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                        "name": "GMS Rare Disease Virtual",
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                "alias_name": null,
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                "hgnc_date_symbol_changed": "2005-02-16"
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                "types": [
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                        "name": "Rare Disease 100K",
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                    "MITRAC15"
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                "hash_id": null,
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                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
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                    {
                        "name": "Component Of Super Panel",
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                ]
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        {
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                    "MPPP52"
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                "alias_name": null,
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                    "R98"
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                "types": [
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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."
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                    {
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                    {
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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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        {
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        {
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            "tags": [],
            "panel": {
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                "hash_id": null,
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                    "R21",
                    "Fetal anomalies with a likely genetic cause",
                    "Fetal anomalies with a likely genetic cause - non urgent",
                    "R412"
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                },
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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
        },
        {
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                "alias": [
                    "HDR"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:4172",
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                "omim_gene": [
                    "131320"
                ],
                "alias_name": null,
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                            "location": "10:8095567-8117161",
                            "ensembl_id": "ENSG00000107485"
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            "entity_type": "gene",
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                "Expert list"
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            "panel": {
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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
        },
        {
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                    "HOT7T175",
                    "AXOR12"
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                "alias_name": null,
                "gene_symbol": "KISS1R",
                "hgnc_symbol": "KISS1R",
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                "hgnc_date_symbol_changed": "2006-02-15"
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                "PAGE Additional Gene List"
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                    "number_of_strs": 2,
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                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
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                    {
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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",
                        "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": [
                    "HSS",
                    "MPS3A",
                    "SFMD"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:10818",
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                "omim_gene": [
                    "605270"
                ],
                "alias_name": [
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                    "mucopolysaccharidosis type IIIA"
                ],
                "gene_symbol": "SGSH",
                "hgnc_symbol": "SGSH",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
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                            "location": "17:78180515-78194722",
                            "ensembl_id": "ENSG00000181523"
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                    },
                    "GRch38": {
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                            "location": "17:80206716-80220923",
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                    }
                },
                "hgnc_date_symbol_changed": "1997-06-24"
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            "entity_type": "gene",
            "entity_name": "SGSH",
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            "evidence": [
                "Expert Review Amber",
                "PAGE DD-Gene2Phenotype"
            ],
            "phenotypes": [
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            "tags": [],
            "panel": {
                "id": 478,
                "hash_id": null,
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                "disease_sub_group": "",
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                    "Fetal anomalies with a likely genetic cause - non urgent",
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                "types": [
                    {
                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
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                    },
                    {
                        "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": [
                    "Dnahc9",
                    "KIAA0357",
                    "HL20",
                    "HL-20",
                    "DNAL1",
                    "DYH9"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:2953",
                "gene_name": "dynein axonemal heavy chain 9",
                "omim_gene": [
                    "603330"
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                "alias_name": null,
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                "hgnc_symbol": "DNAH9",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
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                            "location": "17:11501748-11873065",
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                            "location": "17:11598431-11969748",
                            "ensembl_id": "ENSG00000007174"
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                    }
                },
                "hgnc_date_symbol_changed": "1997-02-05"
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            "entity_type": "gene",
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                "DD-Gene2Phenotype"
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            "panel": {
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                    {
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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",
                        "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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                ]
            },
            "transcript": null
        },
        {
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                ]
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        },
        {
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                "hgnc_id": "HGNC:13771",
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                    {
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                    {
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                        "slug": "gms-rare-disease",
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                ]
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                    {
                        "name": "GMS Rare Disease",
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                    "Leber Congenital Amaurosis Early-Onset Severe Retinal Dystrophy",
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                    "R32"
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                "types": [
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                "omim_gene": [
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                "ensembl_genes": {
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                            "location": "5:149237519-149324356",
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                "hgnc_date_symbol_changed": "1990-03-20"
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            "entity_type": "gene",
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                "Expert Review Red"
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            "phenotypes": [
                "Retinitis pigmentosa 43, 613810",
                "Eye Disorders"
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            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
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            "panel": {
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                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
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                    {
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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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                    {
                        "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."
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            },
            "transcript": null
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        {
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12601",
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                "omim_gene": [
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                "Emory Genetics Laboratory"
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            "panel": {
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                "disease_sub_group": "Congenital malformations caused by ciliopathies",
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                "relevant_disorders": [
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                    "Bardet-Biedl Syndrome"
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                "stats": {
                    "number_of_genes": 205,
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                    "number_of_regions": 2
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                "types": [
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                        "name": "Rare Disease 100K",
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                        "description": "Rare Disease 100K"
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        {
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                "alias_name": [
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                "hgnc_symbol": "NDUFB8",
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                            "location": "10:102267203-102289757",
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                    }
                },
                "hgnc_date_symbol_changed": "1996-10-18"
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                "27290639"
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            "evidence": [
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                "MetBioNet",
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                    "R135"
                ],
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                },
                "types": [
                    {
                        "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 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": "Component Of Super Panel",
                        "slug": "component-of-super-panel",
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                ]
            },
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        },
        {
            "gene_data": {
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                "biotype": "protein_coding",
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                "omim_gene": [
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                    "histidine tRNA ligase 1, cytoplasmic"
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                "hgnc_symbol": "HARS",
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                "ensembl_genes": {
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                            "location": "5:140052758-140071609",
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                    "GRch38": {
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                "hgnc_date_symbol_changed": "2001-06-22"
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                "Expert Review Green",
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                    "Hereditary neuropathy or pain disorder - NOT PMP22 copy number",
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                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
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                    {
                        "name": "GMS signed-off",
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                    {
                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
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                    }
                ]
            },
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        },
        {
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:119",
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                "omim_gene": [
                    "609751"
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                "alias_name": [
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                "gene_symbol": "ACOX1",
                "hgnc_symbol": "ACOX1",
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                "hgnc_date_symbol_changed": "1994-02-11"
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                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
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                    {
                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
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            },
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        {
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:7193",
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                "alias_name": null,
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                "hgnc_symbol": "MOCS2",
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                "hgnc_date_symbol_changed": "1998-07-23"
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                "types": [
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                        "name": "GMS Rare Disease",
                        "slug": "gms-rare-disease",
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                    {
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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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                    {
                        "name": "GMS Rare Disease Virtual",
                        "slug": "gms-rare-disease-virtual",
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                    }
                ]
            },
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        {
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                "biotype": "protein_coding",
                "hgnc_id": "HGNC:18550",
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                "omim_gene": [
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                "alias_name": null,
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                "hgnc_symbol": "IER3IP1",
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                "hgnc_date_symbol_changed": "2005-01-18"
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                "London North GLH"
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        {
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                "hgnc_symbol": "PEX14",
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                "hgnc_date_symbol_changed": "1998-08-21"
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                        "description": "This is a gene panel used for research."
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                "Expert Review Green",
                "Expert list"
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                        "slug": "research",
                        "description": "This is a gene panel used for research."
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