GET /api/v1/panels/546/?format=api
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{
    "id": 546,
    "hash_id": null,
    "name": "Lipodystrophy - childhood onset",
    "disease_group": "",
    "disease_sub_group": "",
    "status": "public",
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    "version_created": "2024-05-03T19:50:34.781116Z",
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        "R158"
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        "number_of_strs": 0,
        "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."
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                "Lipodystrophy, congenital generalized, type 1, 608594"
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                "Alstrom syndrome, OMIM:203800"
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                "Expert Review Green",
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            "penetrance": "Complete",
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                "Expert Review Green",
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        {
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            "entity_type": "gene",
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            "penetrance": null,
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        {
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                "Expert Review Green",
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                "Expert Review Green"
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                "Diabetes mellitus, insulin-resistant, with acanthosis nigricans, OMIM:610549"
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                "Expert Review Green",
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        {
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                            "location": "5:14664664-14699711",
                            "ensembl_id": "ENSG00000154124"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2014-03-11"
            },
            "entity_type": "gene",
            "entity_name": "OTULIN",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "27523608",
                "27559085"
            ],
            "evidence": [
                "NHS GMS",
                "Expert Review Green",
                "Expert Review"
            ],
            "phenotypes": [
                "Autoinflammation, panniculitis, and dermatosis syndrome, OMIM:617099"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "KEN",
                    "KIAA0402",
                    "PCN",
                    "PCNTB",
                    "SCKL4"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:16068",
                "gene_name": "pericentrin",
                "omim_gene": [
                    "605925"
                ],
                "alias_name": [
                    "kendrin",
                    "Seckel syndrome 4"
                ],
                "gene_symbol": "PCNT",
                "hgnc_symbol": "PCNT",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "21:47744036-47865682",
                            "ensembl_id": "ENSG00000160299"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "21:46324122-46445769",
                            "ensembl_id": "ENSG00000160299"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2005-11-03"
            },
            "entity_type": "gene",
            "entity_name": "PCNT",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "21270239"
            ],
            "evidence": [
                "Expert Review Green",
                "NHS GMS",
                "Expert list"
            ],
            "phenotypes": [
                "Microcephalic osteodysplastic primordial dwarfism, type II, OMIM:210720",
                "Insulin resistance, HP:0000855"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CT",
                    "CTPCT"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:8754",
                "gene_name": "phosphate cytidylyltransferase 1, choline, alpha",
                "omim_gene": [
                    "123695"
                ],
                "alias_name": [
                    "phosphate cytidylyltransferase 1, choline, alpha isoform"
                ],
                "gene_symbol": "PCYT1A",
                "hgnc_symbol": "PCYT1A",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:195941093-196014828",
                            "ensembl_id": "ENSG00000161217"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:196214222-196287957",
                            "ensembl_id": "ENSG00000161217"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1999-05-05"
            },
            "entity_type": "gene",
            "entity_name": "PCYT1A",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "18955728",
                "24889630"
            ],
            "evidence": [
                "Expert Review Green",
                "NHS GMS",
                "Expert list"
            ],
            "phenotypes": [
                "Spondylometaphyseal dysplasia with cone-rod dystrophy, OMIM:608940",
                "congenital generalized lipodystrophy, MONDO:0006536",
                "Insulin resistance, HP:0000855"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "GRB1",
                    "p85-ALPHA",
                    "p85"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:8979",
                "gene_name": "phosphoinositide-3-kinase regulatory subunit 1",
                "omim_gene": [
                    "171833"
                ],
                "alias_name": [
                    "phosphoinositide-3-kinase regulatory subunit alpha"
                ],
                "gene_symbol": "PIK3R1",
                "hgnc_symbol": "PIK3R1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "5:67511548-67597649",
                            "ensembl_id": "ENSG00000145675"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "5:68215720-68301821",
                            "ensembl_id": "ENSG00000145675"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-12-08"
            },
            "entity_type": "gene",
            "entity_name": "PIK3R1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Other",
            "publications": [
                "23810378",
                "26497935",
                "27710244",
                "27766312"
            ],
            "evidence": [
                "Expert Review Green",
                "NHS GMS",
                "Expert list"
            ],
            "phenotypes": [
                "SHORT syndrome, OMIM:269880"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9076",
                "gene_name": "perilipin 1",
                "omim_gene": [
                    "170290"
                ],
                "alias_name": null,
                "gene_symbol": "PLIN1",
                "hgnc_symbol": "PLIN1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "15:90207596-90222658",
                            "ensembl_id": "ENSG00000166819"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "15:89664365-89679427",
                            "ensembl_id": "ENSG00000166819"
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                    }
                },
                "hgnc_date_symbol_changed": "2009-08-12"
            },
            "entity_type": "gene",
            "entity_name": "PLIN1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments",
            "publications": [
                "21345103",
                "30020498",
                "11371650",
                "25695774",
                "25114292",
                "29747582"
            ],
            "evidence": [
                "Expert Review Green",
                "Radboud University Medical Center, Nijmegen"
            ],
            "phenotypes": [
                "Lipodystrophy, familial partial, type 4, 613877"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "DKFZP434C245"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:24488",
                "gene_name": "POC1 centriolar protein A",
                "omim_gene": [
                    "614783"
                ],
                "alias_name": null,
                "gene_symbol": "POC1A",
                "hgnc_symbol": "POC1A",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:52109269-52188706",
                            "ensembl_id": "ENSG00000164087"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:52075253-52154690",
                            "ensembl_id": "ENSG00000164087"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "2010-03-26"
            },
            "entity_type": "gene",
            "entity_name": "POC1A",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "22440536",
                "26336158",
                "28819016",
                "33372278",
                "35234134"
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            "evidence": [
                "Expert Review Green",
                "NHS GMS",
                "Expert list"
            ],
            "phenotypes": [
                "Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis, OMIM:614813",
                "Insulin resistance, HP:0000855"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CDC2"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9175",
                "gene_name": "DNA polymerase delta 1, catalytic subunit",
                "omim_gene": [
                    "174761"
                ],
                "alias_name": [
                    "CDC2 homolog (S. cerevisiae)"
                ],
                "gene_symbol": "POLD1",
                "hgnc_symbol": "POLD1",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "19:50887461-50921273",
                            "ensembl_id": "ENSG00000062822"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "19:50384204-50418018",
                            "ensembl_id": "ENSG00000062822"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-02-06"
            },
            "entity_type": "gene",
            "entity_name": "POLD1",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "25131834",
                "26172944",
                "23770608"
            ],
            "evidence": [
                "Expert Review Green",
                "Radboud University Medical Center, Nijmegen"
            ],
            "phenotypes": [
                "Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome, 615381"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "PPARG1",
                    "PPARG2",
                    "NR1C3",
                    "PPARgamma"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9236",
                "gene_name": "peroxisome proliferator activated receptor gamma",
                "omim_gene": [
                    "601487"
                ],
                "alias_name": null,
                "gene_symbol": "PPARG",
                "hgnc_symbol": "PPARG",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:12328867-12475855",
                            "ensembl_id": "ENSG00000132170"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "3:12287368-12434356",
                            "ensembl_id": "ENSG00000132170"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1996-03-12"
            },
            "entity_type": "gene",
            "entity_name": "PPARG",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [],
            "evidence": [
                "Expert Review Green",
                "Illumina TruGenome Clinical Sequencing Services",
                "UKGTN",
                "Radboud University Medical Center, Nijmegen"
            ],
            "phenotypes": [
                "Insulin resistance, severe, digenic 604367",
                "Lipodystrophy, familial partial, type 3 604367"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "HN3",
                    "PROS26"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9541",
                "gene_name": "proteasome subunit beta 4",
                "omim_gene": [
                    "602177"
                ],
                "alias_name": null,
                "gene_symbol": "PSMB4",
                "hgnc_symbol": "PSMB4",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:151372010-151374420",
                            "ensembl_id": "ENSG00000159377"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:151399534-151401944",
                            "ensembl_id": "ENSG00000159377"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1995-05-03"
            },
            "entity_type": "gene",
            "entity_name": "PSMB4",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "26524591",
                "34416217"
            ],
            "evidence": [
                "Expert Review Green",
                "NHS GMS",
                "Expert list"
            ],
            "phenotypes": [
                "?Proteasome-associated autoinflammatory syndrome 3 and digenic forms, OMIM:617591"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "digenic"
            ],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "RING10",
                    "D6S216E",
                    "PSMB5i",
                    "beta5i"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9545",
                "gene_name": "proteasome subunit beta 8",
                "omim_gene": [
                    "177046"
                ],
                "alias_name": null,
                "gene_symbol": "PSMB8",
                "hgnc_symbol": "PSMB8",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "6:32808494-32812480",
                            "ensembl_id": "ENSG00000204264"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "6:32840717-32844703",
                            "ensembl_id": "ENSG00000204264"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1992-06-25"
            },
            "entity_type": "gene",
            "entity_name": "PSMB8",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "20534754",
                "21129723",
                "21953331",
                "26524591"
            ],
            "evidence": [
                "Expert Review Green",
                "NHS GMS",
                "Expert list"
            ],
            "phenotypes": [
                "Proteasome-associated autoinflammatory syndrome 1 and digenic forms, OMIM:256040"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "digenic"
            ],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "RECQL2",
                    "RECQ3"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12791",
                "gene_name": "Werner syndrome RecQ like helicase",
                "omim_gene": [
                    "604611"
                ],
                "alias_name": null,
                "gene_symbol": "WRN",
                "hgnc_symbol": "WRN",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "8:30891317-31031285",
                            "ensembl_id": "ENSG00000165392"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "8:31033801-31173769",
                            "ensembl_id": "ENSG00000165392"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1991-08-21"
            },
            "entity_type": "gene",
            "entity_name": "WRN",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "22654791",
                "23849162",
                "27710244",
                "35780059"
            ],
            "evidence": [
                "Expert Review Green",
                "NHS GMS",
                "Expert list"
            ],
            "phenotypes": [
                "Werner syndrome, OMIM:277700"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "FACE-1",
                    "Ste24p",
                    "STE24",
                    "HGPS",
                    "PRO1"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12877",
                "gene_name": "zinc metallopeptidase STE24",
                "omim_gene": [
                    "606480"
                ],
                "alias_name": [
                    "Hutchinson-Gilford progeria syndrome",
                    "CAAX prenyl protease 1 homolog"
                ],
                "gene_symbol": "ZMPSTE24",
                "hgnc_symbol": "ZMPSTE24",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "1:40723779-40759856",
                            "ensembl_id": "ENSG00000084073"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "1:40258107-40294184",
                            "ensembl_id": "ENSG00000084073"
                        }
                    }
                },
                "hgnc_date_symbol_changed": "1999-09-17"
            },
            "entity_type": "gene",
            "entity_name": "ZMPSTE24",
            "confidence_level": "3",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "18435794",
                "16297189",
                "20034068",
                "12913070",
                "15317753"
            ],
            "evidence": [
                "Expert Review Green",
                "Radboud University Medical Center, Nijmegen"
            ],
            "phenotypes": [
                "Mandibuloacral dysplasia with type B lipodystrophy, 608612"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:392",
                "gene_name": "AKT serine/threonine kinase 2",
                "omim_gene": [
                    "164731"
                ],
                "alias_name": null,
                "gene_symbol": "AKT2",
                "hgnc_symbol": "AKT2",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "19:40736224-40791443",
                            "ensembl_id": "ENSG00000105221"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "19:40230317-40285536",
                            "ensembl_id": "ENSG00000105221"
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                    }
                },
                "hgnc_date_symbol_changed": "1992-11-05"
            },
            "entity_type": "gene",
            "entity_name": "AKT2",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "12843127",
                "15166380",
                "17327441",
                "27710244"
            ],
            "evidence": [
                "Expert Review Amber",
                "Expert list"
            ],
            "phenotypes": [
                "Diabetes mellitus, type II, OMIM:125853",
                "Type 2 diabetes mellitus, MONDO:0005148",
                "Hypoinsulinemic hypoglycemia with hemihypertrophy, OMIM:240900",
                "Hypoinsulinemic hypoglycemia and body hemihypertrophy, MONDO:0009416",
                "Partial lipodystrophy"
            ],
            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "CIDE-3",
                    "FLJ20871",
                    "Fsp27"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:24229",
                "gene_name": "cell death inducing DFFA like effector c",
                "omim_gene": [
                    "612120"
                ],
                "alias_name": null,
                "gene_symbol": "CIDEC",
                "hgnc_symbol": "CIDEC",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "3:9908398-9921938",
                            "ensembl_id": "ENSG00000187288"
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                    },
                    "GRch38": {
                        "90": {
                            "location": "3:9866711-9880254",
                            "ensembl_id": "ENSG00000187288"
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                    }
                },
                "hgnc_date_symbol_changed": "2004-07-26"
            },
            "entity_type": "gene",
            "entity_name": "CIDEC",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": null,
            "publications": [
                "20049731",
                "25565658",
                "27710244"
            ],
            "evidence": [
                "Expert Review Amber",
                "Expert list"
            ],
            "phenotypes": [
                "?Lipodystrophy, familial partial, type 5, OMIM:615238"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [
                    "HC8"
                ],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:9532",
                "gene_name": "proteasome subunit alpha 3",
                "omim_gene": [
                    "176843"
                ],
                "alias_name": null,
                "gene_symbol": "PSMA3",
                "hgnc_symbol": "PSMA3",
                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
                        "82": {
                            "location": "14:58711549-58738730",
                            "ensembl_id": "ENSG00000100567"
                        }
                    },
                    "GRch38": {
                        "90": {
                            "location": "14:58244831-58272012",
                            "ensembl_id": "ENSG00000100567"
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                    }
                },
                "hgnc_date_symbol_changed": "1995-05-03"
            },
            "entity_type": "gene",
            "entity_name": "PSMA3",
            "confidence_level": "2",
            "penetrance": null,
            "mode_of_pathogenicity": "",
            "publications": [
                "26524591"
            ],
            "evidence": [
                "Expert Review Amber",
                "NHS GMS",
                "Expert list"
            ],
            "phenotypes": [
                "Proteasome associated autoinflammatory syndrome-1, CANDLES (Chronic, atypical, neutrophillic dermatosis with lipodystrophy and elevated temperature syndrome), Joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy (JMP syndrome)"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [
                "digenic"
            ],
            "transcript": null
        },
        {
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                "hgnc_symbol": "ADRA2A",
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                            "location": "10:112836790-112840658",
                            "ensembl_id": "ENSG00000150594"
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                    },
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                    }
                },
                "hgnc_date_symbol_changed": "1990-09-10"
            },
            "entity_type": "gene",
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            "mode_of_pathogenicity": null,
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            ],
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                "No OMIM number",
                "familial partial lipodystrophy"
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            "mode_of_inheritance": "MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
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        },
        {
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                "alias": [
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                    "617457"
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                "hgnc_symbol": "POLR3GL",
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                            "location": "1:145456236-145470388",
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                    }
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                "hgnc_date_symbol_changed": "2005-02-02"
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                "31695177"
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                "Expert Review Red",
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            ],
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                "endosteal hyperostosis",
                "oligodontia",
                "growth retardation",
                "facial dysmorphisms",
                "lipodystrophy"
            ],
            "mode_of_inheritance": "BIALLELIC, autosomal or pseudoautosomal",
            "tags": [],
            "transcript": null
        },
        {
            "gene_data": {
                "alias": [],
                "biotype": "protein_coding",
                "hgnc_id": "HGNC:12692",
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                "omim_gene": [
                    "193060"
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                "alias_name": null,
                "gene_symbol": "VIM",
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                "hgnc_release": "2017-11-03",
                "ensembl_genes": {
                    "GRch37": {
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                            "location": "10:17270258-17279592",
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                    }
                },
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            "entity_type": "gene",
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                "32066935"
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                "lipodystrophy HP:0009125"
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            "transcript": []
        }
    ],
    "strs": [],
    "regions": []
}