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[
{
"created": "2024-04-15T16:49:59.605836Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.6",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Publications for gene: CYBRD1 were set to 15338274; 27884173",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2024-04-15T16:48:12.280288Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.5",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of gene: CYBRD1: Added comment: It would appear that there are no CYBRD1 rare SNVs associated with iron metabolism. However, PMID: 37632052 concludes that the coexistence of minor alleles of HDAC3 rs976552 and CYBRD1 rs884409 is linked with higher prevalence of hepatocellular carcinoma.\r\n\r\nFurthermore, HFE p.C282Y variant together with the CYBRD1 polymorphism rs884409 reduces CYBRD1 promoter activity by 30% (PMID: 19673882).; Changed rating: AMBER",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2024-03-11T14:29:52.077389Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.5",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "Phenotypes for gene: ALAS2 were changed from Protoporphyria, erythropoietic, X-linked OMIM:300752; Anemia, sideroblastic, 1 OMIM:300751; X-linked erythropoietic protoporphyria MONDO:0010420; X-linked sideroblastic anemia 1 MONDO:0020721 to Anemia, sideroblastic, 1, OMIM:300751",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2024-01-24T21:57:07.931452Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.4",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "Classified gene: STAB1 as Amber List (moderate evidence)",
"entity_name": "STAB1",
"entity_type": "gene"
},
{
"created": "2024-01-24T21:57:07.927053Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.4",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "Added comment: Comment on list classification: There is sufficient evidence available for the promotion of STAB1 gene to green rating in the next GMS review.",
"entity_name": "STAB1",
"entity_type": "gene"
},
{
"created": "2024-01-24T21:57:07.891758Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.4",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "Gene: stab1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "STAB1",
"entity_type": "gene"
},
{
"created": "2024-01-24T21:55:22.933821Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.3",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "changed review comment from: PMID:37490907 reported the identification of biallelic variants in STAB10 gene in 10 individuals from 7 families with unexplained hyperferritinaemia without iron overload. All of them were in good health and had no dysmorphologies, psycho-motor development abnormalities, hearing or vision disorders, or other pathologies.; to: PMID:37490907 reported the identification of biallelic variants in STAB10 gene in 10 individuals from 7 families with unexplained hyperferritinaemia without iron overload. All of them were in good health and had no dysmorphologies, psycho-motor development abnormalities, hearing or vision disorders, or other pathologies.\r\n\r\nThis gene has not yet been associated with relevant phenotypes either in OMIM or in Gene2Phenotype.",
"entity_name": "STAB1",
"entity_type": "gene"
},
{
"created": "2024-01-24T21:54:46.509189Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.3",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "commented on gene: STAB1: PMID:37490907 reported the identification of biallelic variants in STAB10 gene in 10 individuals from 7 families with unexplained hyperferritinaemia without iron overload. All of them were in good health and had no dysmorphologies, psycho-motor development abnormalities, hearing or vision disorders, or other pathologies.",
"entity_name": "STAB1",
"entity_type": "gene"
},
{
"created": "2024-01-24T21:04:32.781247Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.3",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "Tag Q1_24_promote_green tag was added to gene: STAB1.",
"entity_name": "STAB1",
"entity_type": "gene"
},
{
"created": "2024-01-24T20:31:23.956824Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.3",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "reviewed gene: STAB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 37490907; Phenotypes: Genetic hyperferritinemia without iron overload (disorder), SNOMED:766929007; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STAB1",
"entity_type": "gene"
},
{
"created": "2023-12-01T21:05:33.615900Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.3",
"user_name": "Edoardo Monfrini",
"item_type": "entity",
"text": "gene: STAB1 was added\ngene: STAB1 was added to Iron metabolism disorders - NOT common HFE mutations. Sources: Literature\nMode of inheritance for gene: STAB1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: STAB1 were set to 37490907\nPhenotypes for gene: STAB1 were set to Hyperferritinemia without iron overload\nPenetrance for gene: STAB1 were set to Complete\nReview for gene: STAB1 was set to GREEN\nAdded comment: Sources: Literature",
"entity_name": "STAB1",
"entity_type": "gene"
},
{
"created": "2023-03-22T15:33:13.980384Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.1",
"user_name": "Catherine Snow",
"item_type": "panel",
"text": "Panel version 2.0 has been signed off on 2023-03-22",
"entity_name": null,
"entity_type": null
},
{
"created": "2023-03-22T15:32:37.588218Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "2.0",
"user_name": "Catherine Snow",
"item_type": "panel",
"text": "promoted panel to version 2.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2023-03-22T13:21:43.717341Z",
"panel_name": "Iron metabolism disorders - NOT common HFE mutations",
"panel_id": 515,
"panel_version": "1.41",
"user_name": "Eleanor Williams",
"item_type": "panel",
"text": "Panel name changed from Iron metabolism disorders to Iron metabolism disorders - NOT common HFE mutations\nList of related panels changed from R96 to Iron metabolism disorders; R96",
"entity_name": null,
"entity_type": null
},
{
"created": "2023-02-07T11:40:35.403589Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.40",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "Tag gene-checked was removed from gene: BMP6.",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2023-02-07T11:40:15.366744Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.40",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "Phenotypes for gene: BMP6 were changed from {Iron overload, susceptibility to}, OMIM:620121; Hemochromatosis type 5 ORPHA:447792 to {Iron overload, susceptibility to}, OMIM:620121",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2023-02-07T11:38:23.551527Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.39",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "Phenotypes for gene: BMP6 were changed from Hemochromatosis type 5 ORPHA:447792 to {Iron overload, susceptibility to}, OMIM:620121; Hemochromatosis type 5 ORPHA:447792",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2023-02-01T09:04:26.372322Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.38",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "Tag Q2_21_MOI was removed from gene: FTL.",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2023-02-01T09:02:54.159415Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.38",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "commented on gene: FTL",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2023-02-01T09:02:40.824022Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.37",
"user_name": "Achchuthan Shanmugasundram",
"item_type": "entity",
"text": "Mode of inheritance for gene FTL was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2022-11-03T11:29:31.362921Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.36",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "Phenotypes for gene: HFE were changed from 235200 HEMOCHROMATOSIS, TYPE 1; HFE1; 235200 Hemochromatosis; 235200HEMOCHROMATOSIS, TYPE 1 to Hemochromatosis, OMIM:235200",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2022-07-29T13:47:58.237149Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.35",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "commented on gene: HEPH",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2022-07-29T13:47:58.221806Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.35",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "commented on gene: FTH1",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2022-07-29T10:53:27.998055Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.34",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "Source Expert Review Red was added to HEPH.\nRating Changed from Amber List (moderate evidence) to Red List (low evidence)",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2022-07-29T10:53:27.922933Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.34",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "Source Expert Review Red was added to FTH1.\nRating Changed from Amber List (moderate evidence) to Red List (low evidence)",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2022-06-30T16:15:06.954406Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.33",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "changed review comment from: The new_gene_name tag has been added. The new name for GBA is GBA1.; to: Added new-gene-name tag, new approved HGNC gene symbol for GBA is GBA1.",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2022-06-30T15:22:22.513494Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.33",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Tag new-gene-name tag was added to gene: GBA.",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2022-06-30T15:18:11.949778Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.33",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "commented on gene: GBA",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2022-05-03T14:40:29.213462Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.33",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Tag gene-checked tag was added to gene: CYBRD1.",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2022-05-03T10:56:32.380340Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.33",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Tag gene-checked tag was added to gene: BMP6.",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2021-03-03T10:27:31.485046Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.33",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: SERPINA1 were changed from ALPHA-1-ANTITRYPSIN DEFICIENCY OMIM:613490; alpha 1-antitrypsin deficiency MONDO:0013282 to Emphysema due to AAT deficiency OMIM:613490; alpha 1-antitrypsin deficiency MONDO:0013282",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2021-03-03T10:26:56.921886Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.32",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: SERPINA1 were changed from ALPHA-1-ANTITRYPSIN DEFICIENCY P to ALPHA-1-ANTITRYPSIN DEFICIENCY OMIM:613490; alpha 1-antitrypsin deficiency MONDO:0013282",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2021-03-03T10:25:52.620494Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.31",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: SERPINA1 were changed from A1ATD; 613490 ALPHA-1-ANTITRYPSIN DEFICIENCY to ALPHA-1-ANTITRYPSIN DEFICIENCY P",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2021-03-03T10:23:13.771377Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.30",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: SEC23B were changed from 224100 Dyserythropoietic anemia, congenital, type II to Dyserythropoietic anemia, congenital, type II OMIM:224100; congenital dyserythropoietic anemia type 2 MONDO:0009134",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2021-03-03T10:15:48.677007Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.29",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Added comment: Comment on phenotypes: This phenotype does not appear to be relevant to this panel.",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2021-03-03T10:15:48.657118Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.29",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: ACVR1 were changed from new type of IRIDA; IRIDA to Fibrodysplasia ossificans progressiva OMIM:135100",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2021-03-03T10:08:52.822742Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.28",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: STEAP3 were changed from 615234 ?Anemia, hypochromic microcytic, with iron overload 2 to ?Anemia, hypochromic microcytic, with iron overload 2 OMIM:615234; severe congenital hypochromic anemia with ringed sideroblasts MONDO:0014094",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2021-03-03T09:57:11.826280Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.27",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Publications for gene: HEPH were set to ",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2021-03-03T09:55:05.722131Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.26",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: FTH1 were changed from 615517 ?Hemochromatosis, type 5; HFE5; 615517 HEMOCHROMATOSIS, TYPE 5 to ?Hemochromatosis, type 5 OMIM:615517; hemochromatosis type 5 MONDO:0014225",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2021-03-03T07:13:26.914736Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.25",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: FECH were changed from EPP1; 177000 PROTOPORPHYRIA, ERYTHROPOIETIC, 1 to Protoporphyria, erythropoietic, 1 OMIM:177000; protoporphyria, erythropoietic, 1 MONDO:0008319",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2021-03-03T07:10:08.963553Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.24",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: TFR2 were changed from 604250 HEMOCHROMATOSIS, TYPE 3; 604250 Hemochromatosis, type 3; HFE3 to Hemochromatosis, type 3 OMIM:604250; hemochromatosis type 3 MONDO:0011417",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2021-03-03T07:07:42.128614Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.23",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: TF were changed from 209300 Atransferrinemia, Hypoferritinaemia; 209300 Atransferrinemia to Atransferrinemia OMIM:209300; atransferrinemia MONDO:0008846",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2021-03-03T07:05:22.092172Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.22",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: SLC40A1 were changed from HFE4; 606069 Hemochromatosis, type 4; 606069 HEMOCHROMATOSIS, TYPE 4 to Hemochromatosis, type 4 OMIM:606069; hemochromatosis type 4 MONDO:0011631",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2021-03-03T06:59:29.584846Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.21",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A38 were changed from 205950 Anemia, sideroblastic, 2, pyridoxine-refractory; Sideroblastic anaemia - increased serum ferritin to Anemia, sideroblastic, 2, pyridoxine-refractory OMIM:205950; sideroblastic anemia 2 MONDO:0008785",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2021-03-03T06:56:28.049454Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.20",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: SLC11A2 were changed from Anemia, hypochromic microcytic, with iron overload 1 OMIM:206100 to Anemia, hypochromic microcytic, with iron overload 1 OMIM:206100; microcytic anemia with liver iron overload MONDO:0008787",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2021-03-03T06:55:17.119623Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.19",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: SLC11A2 were changed from 206100 ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1; DMT1-related anemia; 206100 Anemia, hypochromic microcytic, with iron overload 1; AHMIO1 DMT1-related anemia to Anemia, hypochromic microcytic, with iron overload 1 OMIM:206100",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2021-03-03T06:52:28.598112Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.18",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: HFE2 were changed from HFE2A; 602390 HEMOCHROMATOSIS, TYPE 2A; 602390 Hemochromatosis, type 2A to Hemochromatosis, type 2A OMIM:602390",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2021-03-02T18:31:49.938827Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.17",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: HAMP were changed from 613313 Hemochromatosis, type 2B; 613313 HEMOCHROMATOSIS, TYPE 2B; HFE2B to Hemochromatosis, type 2B OMIM:613313",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2021-03-02T18:23:50.790704Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.16",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: GLRX5 were changed from 616860 Anemia, sideroblastic, 3, pyridoxine-refractory; Sideroblastic anaemia - increased serum ferritin to Anemia, sideroblastic, 3, pyridoxine-refractory OMIM:616860",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2021-03-02T18:00:18.257245Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.15",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: GBA were changed from 230900 Gaucher disease, type II; 231005 Gaucher disease, type IIIC; 231000 Gaucher disease, type III; 230800 Gaucher disease, type I to Gaucher disease, type II OMIM:230900; Gaucher disease, type IIIC OMIM:231005; Gaucher disease, type III OMIM:231000; Gaucher disease, type I OMIM:230800",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2021-03-02T17:41:30.505074Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.14",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "edited their review of gene: FTL: Added comment: The MOI for FTL should be \"BOTH monoallelic and biallelic, autosomal or pseudoautosomal\" to detect biallielic variants found in L-ferritin deficiency, dominant and recessive OMIM:615604.; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2021-03-02T17:37:45.059511Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.14",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Tag Q2_21_MOI tag was added to gene: FTL.",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2021-03-02T17:29:39.071822Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.14",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: FTL were changed from Hyperferritinemia-cataract syndrome OIMM:600886; L-ferritin deficiency, dominant and recessive OMIM:615604; Neurodegeneration with brain iron accumulation 3 606159 to Hyperferritinemia-cataract syndrome OIMM:600886; L-ferritin deficiency, dominant and recessive OMIM:615604; Neurodegeneration with brain iron accumulation 3 OMIM:606159",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2021-03-02T17:28:50.224030Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.13",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2021-03-02T17:28:39.960349Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.13",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: FTL were changed from NBIA3; 615604 L-FERRITIN DEFICIENCY; LFTD; 600886 Hyperferritinemia-cataract syndrome; HRFTC; 600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT; 615604 L-ferritin deficiency, dominant and recessive; 606159 Neurodegeneration with brain iron accumulation 3; 606159 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3 to Hyperferritinemia-cataract syndrome OIMM:600886; L-ferritin deficiency, dominant and recessive OMIM:615604; Neurodegeneration with brain iron accumulation 3 606159",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2021-03-02T17:27:00.213735Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.12",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Added comment: Comment on phenotypes: L-ferritin deficiency, dominant and recessive OMIM:615604;Hyperferritinemia-cataract syndrome OMIM:600886;Neurodegeneration with brain iron accumulation 3 OMIM:606159",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2021-03-02T17:27:00.184435Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.12",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: FTL were changed from NBIA3; 615604 L-FERRITIN DEFICIENCY; LFTD; 600886 Hyperferritinemia-cataract syndrome; HRFTC; 600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT; 615604 L-ferritin deficiency, dominant and recessive; 606159 Neurodegeneration with brain iron accumulation 3; 606159 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3 to NBIA3; 615604 L-FERRITIN DEFICIENCY; LFTD; 600886 Hyperferritinemia-cataract syndrome; HRFTC; 600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT; 615604 L-ferritin deficiency, dominant and recessive; 606159 Neurodegeneration with brain iron accumulation 3; 606159 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2021-03-02T17:17:37.538131Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.11",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Added comment: Comment on phenotypes: There is no OMIM, MONDO or ORPHANET disease association to this gene. The term hereditary hemochromatosis MONDO:0006507 was chosen as it represent the general disease described in the limited literature associated with this gene.",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2021-03-02T17:17:37.515036Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.11",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: CYBRD1 were changed from hereditary hemochromatosis MONDO:0006507 to hereditary hemochromatosis MONDO:0006507",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2021-03-02T17:15:28.440541Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.10",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: CYBRD1 were changed from NA IRON OVERLOAD; N/A Primary iron overload; Iron overload to hereditary hemochromatosis MONDO:0006507",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2021-03-02T16:36:42.994980Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.9",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: CP were changed from 604290 Hemosiderosis, systemic, due to aceruloplasminemia; 604290 ACERULOPLASMINEMIA to aceruloplasminemia MONDO:0011426; Hemosiderosis, systemic, due to aceruloplasminemia OMIM:604290",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2021-03-02T16:24:00.329967Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.8",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: BMP6 were changed from NA IRON OVERLOAD; 112266 Mild to moderate iron overload; Iron overload to Hemochromatosis type 5 ORPHA:447792",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2021-03-02T16:11:13.146879Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.7",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Publications for gene: BMP6 were set to 26582087",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2021-03-02T15:53:31.758386Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.6",
"user_name": "Sarah Leigh",
"item_type": "entity",
"text": "Phenotypes for gene: ALAS2 were changed from 300752 Protoporphyria, erythropoietic, X-linked; 300751 Anemia, sideroblastic, 1; Sideroblastic anaemia - increased serum ferritin to Protoporphyria, erythropoietic, X-linked OMIM:300752; Anemia, sideroblastic, 1 OMIM:300751; X-linked erythropoietic protoporphyria MONDO:0010420; X-linked sideroblastic anemia 1 MONDO:0020721",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2021-03-02T10:37:18.981141Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.5",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "Phenotypes for gene: CDAN1 were changed from 224120 Dyserythropoietic anemia, congenital, type Ia to Dyserythropoietic anemia, congenital, type Ia, OMIM:224120; Anemia, congenital dyserythropoietic, type 1a, MONDO:0009135",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2021-01-22T08:01:42.930455Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HEPH: Rating: RED; Mode of pathogenicity: None; Publications: 30182051, 30060949; Phenotypes: Iron metabolism defect; Mode of inheritance: None",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2021-01-22T07:43:11.167066Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FTH1: Rating: RED; Mode of pathogenicity: None; Publications: 11389486; Phenotypes: Hemochromatosis, type 5, MIM# 615517; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2021-01-22T07:33:20.974533Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CYBRD1: Rating: RED; Mode of pathogenicity: None; Publications: 15338274; Phenotypes: Iron overload; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2020-03-03T16:57:45.252560Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.3",
"user_name": "Catherine Snow",
"item_type": "panel",
"text": "Panel version has been signed off",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-03-03T16:56:11.712179Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.2",
"user_name": "Catherine Snow",
"item_type": "panel",
"text": "Panel types changed to GMS Rare Disease Virtual; GMS Rare Disease; GMS signed-off",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-09-23T14:30:42.966801Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "1.0",
"user_name": "Louise Daugherty",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-09-23T14:29:33.738416Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.55",
"user_name": "Louise Daugherty",
"item_type": "panel",
"text": "Panel types changed to GMS Rare Disease; GMS signed-off",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-08-22T12:50:21.148274Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.54",
"user_name": "Louise Daugherty",
"item_type": "panel",
"text": "List of related panels changed from to R96",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-07-22T15:17:09.722041Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.53",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: ATP7B as Green List (high evidence)",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:17:09.719357Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.53",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:17:09.699453Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.53",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: atp7b has been classified as Green List (High Evidence).",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:16:52.139107Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.52",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: ABCB7 as Green List (high evidence)",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:16:52.135304Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.52",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:16:52.115006Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.52",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: abcb7 has been classified as Green List (High Evidence).",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:16:32.037119Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.51",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: ALAS2 as Green List (high evidence)",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:16:32.034387Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.51",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:16:32.019630Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.51",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: alas2 has been classified as Green List (High Evidence).",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:16:17.289981Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.50",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: GLRX5 as Green List (high evidence)",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:16:17.287171Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.50",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:16:17.270162Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.50",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: glrx5 has been classified as Green List (High Evidence).",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:15:48.431414Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.49",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: SLC25A38 as Green List (high evidence)",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:15:48.428240Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.49",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:15:48.412416Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.49",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: slc25a38 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:14:37.068653Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.48",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: FECH as Amber List (moderate evidence)",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:14:37.065740Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.48",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Downgraded from Green to Amber. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene to Amber.",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:14:37.045869Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.48",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: fech has been classified as Amber List (Moderate Evidence).",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:13:59.979851Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.47",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: SERPINA1 as Red List (low evidence)",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:13:59.976758Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.47",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Downgraded from Green to Red. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene to Red.",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:13:59.958795Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.47",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: serpina1 has been classified as Red List (Low Evidence).",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:11:33.518427Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.46",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "changed review comment from: Comment on list classification: Downgraded from Green to Amber. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene to Amber.; to: Comment on list classification: Downgraded from Green to Amber. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene to Amber.\r\n\r\nDiscrepant reviews, to be discussed at July workshop to agree rating.",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:11:13.224425Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.46",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: HEPH as Amber List (moderate evidence)",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:11:13.221261Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.46",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Downgraded from Green to Amber. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene to Amber.",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:11:13.194767Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.46",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: heph has been classified as Amber List (Moderate Evidence).",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:10:09.953853Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.45",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: SEC23B as Red List (low evidence)",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:10:09.950886Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.45",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Downgraded from Green to Red. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene to Red. It is Green on the rare anaemias panel",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:10:09.914627Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.45",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: sec23b has been classified as Red List (Low Evidence).",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:09:22.366172Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.44",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "changed review comment from: Comment on list classification: Downgraded from Green to Amber. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene to Amber.; to: Comment on list classification: Downgraded from Green to Amber. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene to Amber.",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:07:17.591027Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.44",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: CDAN1 as Red List (low evidence)",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:07:17.588213Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.44",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Downgraded from Green to Red. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene to Red. YNEGLH noted that it is Green on the Rare Anaemia panel.",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:07:17.551526Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.44",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: cdan1 has been classified as Red List (Low Evidence).",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:06:00.268772Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.43",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: CDAN1: Discrepant reviews, to be discussed at July workshop to agree rating.",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:05:23.503414Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.43",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: FTH1 as Amber List (moderate evidence)",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:05:23.500849Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.43",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Downgraded from Green to Amber. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene to Amber.",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:05:23.483200Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.43",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: fth1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-07-22T15:04:17.757549Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.42",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FTH1: Discrepant reviews, to be discussed at July workshop to agree rating.",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-05-29T14:04:18.576682Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.41",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-05-29T14:00:38.310836Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.41",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-05-29T13:59:08.675644Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.41",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: STEAP3 as Amber List (moderate evidence)",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2019-05-29T13:59:08.673112Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.41",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Demoted from Green to Amber. Initial Green gene submitted by one GLH (Carl Fratter Wessex and the West Midlands GLH), subsequently after the GMS Haematology Specialist Test Group webex call 8th March 2019 Patricia Bignell (Wessex and the West Midlands GLH) reviewed gene again and suggested downgrading to Amber (webex 8.03.19 WWMGLH comments v1.doc).",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2019-05-29T13:59:08.658323Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.41",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: steap3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2019-05-29T13:30:00.035029Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.40",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: ACVR1 as Red List (low evidence)",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-05-29T13:30:00.032574Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.40",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Demoted from Green to Red. Initial Green gene submitted by one GLH (Carl Fratter Wessex and the West Midlands GLH), subsequently after the GMS Haematology Specialist Test Group webex call 8th March 2019 Patricia Bignell (Wessex and the West Midlands GLH) reviewed gene again and suggested downgrading to Red (webex 8.03.19 WWMGLH comments v1.doc). This is supported by the other GLHs in the Haematology Specialist Test Group",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-05-29T13:30:00.015695Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.40",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: acvr1 has been classified as Red List (Low Evidence).",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.906929Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ABCB7: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.890272Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ALAS2: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.877025Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: GLRX5: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.865059Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SLC25A38: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.853333Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ATP7B: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.841925Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: CYBRD1: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.828969Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FECH: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Amber",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.817364Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: GBA: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.805864Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HEPH: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Amber",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.793706Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SERPINA1: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Red",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.782748Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ABCB7: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.771368Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ALAS2: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.760042Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: GLRX5: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.748618Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SLC25A38: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.737297Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: STEAP3: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Amber",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.725633Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SEC23B: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Red",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.713286Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: CDAN1: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Red",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.702357Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FTH1: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Amber",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.690364Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: BMP6: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Green",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-05-28T14:08:10.678259Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.39",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ACVR1: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Red",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:16:37.659776Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.38",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Wessex and West Midlands GLH was added to SEC23B.\nRating Changed from Green List (high evidence) to Green List (high evidence)",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:16:37.582671Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.38",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Wessex and West Midlands GLH was added to CDAN1.\nRating Changed from Green List (high evidence) to Green List (high evidence)",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.489224Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "commented on gene: ABCB7: I had a discussion with Cambridge and Dr WJH Griffiths to see what he recommends for patients with iron overload; advice was to include SLC25A38, GLRX5, ALAS2 and ABCB7. We have found 8 patients with Iron overload that have a variant in the above genes.",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.476606Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "commented on gene: ALAS2: I had a discussion with Cambridge and Dr WJH Griffiths to see what he recommends for patients with iron overload; advice was to include SLC25A38, GLRX5, ALAS2 and ABCB7. We have found 8 patients with Iron overload that have a variant in the above genes.",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.465570Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "commented on gene: GLRX5: I had a discussion with Cambridge and Dr WJH Griffiths to see what he recommends for patients with iron overload; advice was to include SLC25A38, GLRX5, ALAS2 and ABCB7. We have found 8 patients with Iron overload that have a variant in the above genes.",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.453556Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "commented on gene: SLC25A38: I had a discussion with Cambridge and Dr WJH Griffiths to see what he recommends for patients with iron overload; advice was to include SLC25A38, GLRX5, ALAS2 and ABCB7. We have found 8 patients with Iron overload that have a variant in the above genes.",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.438871Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: ATP7B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.427667Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: CYBRD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.416612Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: FECH: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.404023Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: GBA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.390292Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: HEPH: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.379606Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: SERPINA1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.366139Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: ABCB7: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.352118Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: ALAS2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.338630Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: GLRX5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.325210Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: SLC25A38: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.311315Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: STEAP3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.299695Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: SEC23B: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.286684Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: CDAN1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.275545Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: FTH1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.260568Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: BMP6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-05-28T13:11:42.239174Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.37",
"user_name": "PATRICIA BIGNELL",
"item_type": "entity",
"text": "reviewed gene: ACVR1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-05-28T12:08:02.809424Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.36",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Wessex and West Midlands GLH was added to SERPINA1.",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-05-28T12:08:02.729979Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.36",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to SERPINA1.",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-05-28T12:08:02.654503Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.36",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to SERPINA1.",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-05-28T12:08:02.564894Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.36",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to SERPINA1.",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-05-28T10:12:03.578861Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.35",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SERPINA1: Changed gene listed on panel from SERPINC1 to SERPINA1, incorrect gene listed by North West GLH, Yorkshire and North East GLH and Wessex and the West Midlands GLH. The phenotype is 613490 ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD which matches SERPINA1. Gene changed after comments from Carl Fratter and Patrica Bignell highlighting the error.",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-05-28T10:02:58.698611Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.35",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "SERPINC1 was changed to SERPINA1",
"entity_name": "SERPINA1",
"entity_type": "gene"
},
{
"created": "2019-05-28T10:02:58.625815Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.35",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was removed from SERPINC1.\nSource Yorkshire and North East GLH was removed from SERPINC1.\nSource NHS GMS was removed from SERPINC1.\nSource Wessex and West Midlands GLH was removed from SERPINC1.\nSource Expert list was added to SERPINC1.",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-05-04T21:25:02.455790Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.34",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to CYBRD1.",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-05-04T21:25:02.382780Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.34",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to ALAS2.",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-05-04T21:25:02.310841Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.34",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to GLRX5.",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-05-04T21:25:02.234599Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.34",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to SLC25A38.",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-05-04T20:55:51.739836Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.33",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: CYBRD1: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-05-04T20:55:51.728739Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.33",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ALAS2: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-05-04T20:55:51.716960Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.33",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: GLRX5: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-05-04T20:55:51.703655Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.33",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SLC25A38: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-05-04T20:55:51.692640Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.33",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: BMP6: Review/rating updated by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) from initial review February 2019, on behalf of London South GLH for the GMS Haematology specialist test group. Gene rating upgraded from Red to Green.",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-05-04T20:54:21.828835Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.32",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: CYBRD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-05-04T20:54:21.814511Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.32",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: ALAS2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-05-04T20:54:21.798156Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.32",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: GLRX5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-05-04T20:54:21.785784Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.32",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: SLC25A38: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-05-04T20:54:21.772699Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.32",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "edited their review of gene: BMP6: Changed rating: GREEN",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-05-04T19:55:03.327559Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.31",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A38 were changed from 205950 Anemia, sideroblastic, 2, pyridoxine-refractory to 205950 Anemia, sideroblastic, 2, pyridoxine-refractory; Sideroblastic anaemia - increased serum ferritin",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-05-04T19:54:03.109043Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.30",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Publications for gene: GLRX5 were set to 30401706; 24003969; 30098397",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-05-04T19:53:14.312950Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.29",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Phenotypes for gene: GLRX5 were changed from 616860 Anemia, sideroblastic, 3, pyridoxine-refractory to 616860 Anemia, sideroblastic, 3, pyridoxine-refractory; Sideroblastic anaemia - increased serum ferritin",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-05-04T19:51:24.997333Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.28",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Publications for gene: ALAS2 were set to 30401706; 24003969; 30098397",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-05-04T19:51:03.403690Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.27",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Phenotypes for gene: ALAS2 were changed from 300752 Protoporphyria, erythropoietic, X-linked; 300751 Anemia, sideroblastic, 1 to 300752 Protoporphyria, erythropoietic, X-linked; 300751 Anemia, sideroblastic, 1; Sideroblastic anaemia - increased serum ferritin",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-05-04T19:49:53.041142Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.26",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Phenotypes for gene: CYBRD1 were changed from NA IRON OVERLOAD; N/A Primary iron overload to NA IRON OVERLOAD; N/A Primary iron overload; Iron overload",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-03-11T11:51:11.238529Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: SEC23B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-03-11T11:47:49.631795Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: CDAN1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.360383Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: TMPRSS6: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TMPRSS6; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 206200.IRON-REFRACTORY IRON DEFICIENCY ANEMIA; IRIDA; PMID(s): none submitted",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.346355Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: TFR2: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TFR2; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 604250.HEMOCHROMATOSIS, TYPE 3; HFE3; PMID(s): none submitted",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.332645Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: TF: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TF; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 209300 Atransferrinemia, Hypoferritinaemia; PMID(s): none submitted",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.318833Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SLC40A1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SLC40A1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: 606069.HEMOCHROMATOSIS, TYPE 4; HFE4; PMID(s): none submitted",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.302900Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SLC11A2: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SLC11A2; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 206100 ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1 DMT1-related anemia (OMIM entry 600523); PMID(s): none submitted",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.289283Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SERPINC1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SERPINC1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 613490 ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD; PMID(s): none submitted",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.274695Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HFE2: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HJV; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 602390.HEMOCHROMATOSIS, TYPE 2A; HFE2A; PMID(s): none submitted",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.257938Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HFE: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HFE; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 235200.HEMOCHROMATOSIS, TYPE 1; HFE1; PMID(s): none submitted",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.240246Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HEPH: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HEPH; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: Not submitted; PMID(s): none submitted",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.224334Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HAMP: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HAMP; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 613313.HEMOCHROMATOSIS, TYPE 2B; HFE2B; PMID(s): none submitted",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.210869Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: GBA: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: GBA; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 230800 Gaucher disease, type I, 230900 Gaucher disease, type II, 231000 Gaucher disease, type III, 231005 Gaucher disease, type IIIC; PMID(s): none submitted",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.198546Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FTL: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FTL; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: 600886.HYPERFERRITINEMIA WITH OR WITHOUT CATARACT; HRFTC, 606159. NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3 , 615604. L-FERRITIN DEFICIENCY; LFTD; PMID(s): none submitted",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.185415Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FTH1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FTH1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: 615517 HEMOCHROMATOSIS, TYPE 5; HFE5; PMID(s): none submitted",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.169511Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FECH: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FECH; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 177000.PROTOPORPHYRIA, ERYTHROPOIETIC, 1; EPP1; PMID(s): none submitted",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.153585Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: CYBRD1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CYBRD1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: NA IRON OVERLOAD; PMID(s): none submitted",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.137063Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: CP: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CP; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 604290.ACERULOPLASMINEMIA; PMID(s): none submitted",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.121116Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: BMP6: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: BMP6; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: NA IRON OVERLOAD; PMID(s): none submitted",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.107361Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ATP7B: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ATP7B; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 277900.WILSON DISEASE; PMID(s): none submitted",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:49:44.089458Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.25",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ACVR1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ACVR1; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: IRIDA; PMID(s): none submitted",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.710378Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: TMPRSS6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 206200 IRON-REFRACTORY IRON DEFICIENCY ANEMIA, IRIDA; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.694663Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: TFR2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 604250 HEMOCHROMATOSIS, TYPE 3, HFE3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.680157Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: TF: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 209300 Atransferrinemia, Hypoferritinaemia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.664646Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: SLC40A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 606069 HEMOCHROMATOSIS, TYPE 4, HFE4; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.648336Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: SLC11A2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 206100 ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1, AHMIO1 DMT1-related anemia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.629261Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: SERPINC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 613490 ALPHA-1-ANTITRYPSIN DEFICIENCY, A1ATD; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.611521Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: HFE2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 602390 HEMOCHROMATOSIS, TYPE 2A, HFE2A; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.594743Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: HFE: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 235200HEMOCHROMATOSIS, TYPE 1, HFE1; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.580143Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: HEPH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.563781Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: HAMP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 613313 HEMOCHROMATOSIS, TYPE 2B, HFE2B; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.544058Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: GBA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 230800 Gaucher disease, type I, 230900 Gaucher disease, type II, 231000 Gaucher disease, type III, 231005 Gaucher disease, type IIIC; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.515960Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: FTL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT, HRFTC, 606159 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3, NBIA3, 615604 L-FERRITIN DEFICIENCY, LFTD; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.501151Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: FTH1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 615517 HEMOCHROMATOSIS, TYPE 5, HFE5; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.486556Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: FECH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 177000 PROTOPORPHYRIA, ERYTHROPOIETIC, 1, EPP1; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.472072Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: CYBRD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: NA IRON OVERLOAD; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.457332Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: CP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 604290 ACERULOPLASMINEMIA; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.443035Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: BMP6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: NA IRON OVERLOAD; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.428231Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: ATP7B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 277900 WILSON DISEASE; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:45:45.412427Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.24",
"user_name": "Steve Keeney",
"item_type": "entity",
"text": "reviewed gene: ACVR1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: IRIDA; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:39.051229Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes IRIDA; 206200 IRON-REFRACTORY IRON DEFICIENCY ANEMIA for gene: TMPRSS6",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.984036Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 604250 HEMOCHROMATOSIS, TYPE 3; HFE3 for gene: TFR2",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.917236Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 209300 Atransferrinemia, Hypoferritinaemia for gene: TF",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.848244Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes HFE4; 606069 HEMOCHROMATOSIS, TYPE 4 for gene: SLC40A1",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.780919Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 206100 ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1 DMT1-related anemia for gene: SLC11A2",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.713131Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes A1ATD; 613490 ALPHA-1-ANTITRYPSIN DEFICIENCY for gene: SERPINC1",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.641400Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes HFE2A; 602390 HEMOCHROMATOSIS, TYPE 2A for gene: HFE2",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.571555Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes HFE1; 235200HEMOCHROMATOSIS, TYPE 1 for gene: HFE",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.361492Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 613313 HEMOCHROMATOSIS, TYPE 2B; HFE2B for gene: HAMP",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.290915Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 230900 Gaucher disease, type II; 231005 Gaucher disease, type IIIC; 231000 Gaucher disease, type III; 230800 Gaucher disease, type I for gene: GBA",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.223649Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes NBIA3; 615604 L-FERRITIN DEFICIENCY; HRFTC; 600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT; LFTD; 606159 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3 for gene: FTL",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.156566Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes HFE5; 615517 HEMOCHROMATOSIS, TYPE 5 for gene: FTH1",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.088393Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes EPP1; 177000 PROTOPORPHYRIA, ERYTHROPOIETIC, 1 for gene: FECH",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:38.005022Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes NA IRON OVERLOAD for gene: CYBRD1",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:37.929291Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 604290 ACERULOPLASMINEMIA for gene: CP",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:37.857069Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes NA IRON OVERLOAD for gene: BMP6",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:37.788953Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 277900 WILSON DISEASE for gene: ATP7B",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:42:37.723462Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.23",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes IRIDA for gene: ACVR1",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:31.704395Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to TMPRSS6.",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:31.632067Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to TFR2.",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:31.548498Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to TF.",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:31.475951Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to SLC40A1.",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:31.407563Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to SLC11A2.",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:31.337266Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to SERPINC1.",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:31.253033Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to HFE2.",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:31.178869Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to HFE.",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:31.107538Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to HEPH.",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:31.032598Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to HAMP.",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:30.957409Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to GBA.",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:30.878662Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to FTL.",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:30.806333Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to FTH1.",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:30.732840Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to FECH.",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:30.647425Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to CYBRD1.",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:30.569537Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to CP.",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:30.494071Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to BMP6.",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:30.416225Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to ATP7B.",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-18T11:37:30.331570Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.21",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source North West GLH was added to ACVR1.",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.774955Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: TMPRSS6: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TMPRSS6; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 206200 IRON-REFRACTORY IRON DEFICIENCY ANEMIA; IRIDA; PMID(s): none submitted",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.763618Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: TFR2: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TFR2; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 604250 HEMOCHROMATOSIS, TYPE 3; HFE3; PMID(s): none submitted",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.751650Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: TF: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TF; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 209300 Atransferrinemia, Hypoferritinaemia; PMID(s): none submitted",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.739627Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SLC40A1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SLC40A1; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: 606069 HEMOCHROMATOSIS, TYPE 4; HFE4; PMID(s): none submitted",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.727500Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SLC11A2: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SLC11A2; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 206100 ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1 DMT1-related anemia; PMID(s): none submitted",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.715216Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SERPINC1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SERPINC1; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 613490 ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD; PMID(s): none submitted",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.703661Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: SEC23B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.688487Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HFE2: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HJV; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 602390 HEMOCHROMATOSIS, TYPE 2A; HFE2A; PMID(s): none submitted",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.675424Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HFE: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HFE; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 235200 HEMOCHROMATOSIS, TYPE 1; HFE1; PMID(s): none submitted",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.664039Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HEPH: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HEPH; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: N/A; PMID(s): none submitted",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.652396Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HAMP: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HAMP; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 613313 HEMOCHROMATOSIS, TYPE 2B; HFE2B; PMID(s): none submitted",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.639011Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: GBA: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: GBA; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 230800 Gaucher disease, type I;230900 Gaucher disease, type II;231000 Gaucher disease, type III;231005 Gaucher disease, type IIIC; PMID(s): none submitted",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.626417Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FTL: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FTL; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: 600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT; HRFTC; 606159 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3; 615604 L-FERRITIN DEFICIENCY; LFTD; PMID(s): none submitted",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.615661Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FTH1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FTH1; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: 615517 HEMOCHROMATOSIS, TYPE 5; HFE5; PMID(s): none submitted",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.593060Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FECH: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FECH; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 177000 PROTOPORPHYRIA, ERYTHROPOIETIC, 1; EPP1; PMID(s): none submitted",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.581967Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: CYBRD1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CYBRD1; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: N/A Primary iron overload; PMID(s): 15338274",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.570552Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: CP: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CP; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 604290 ACERULOPLASMINEMIA; PMID(s): none submitted",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.547383Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: CDAN1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.532610Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: BMP6: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: BMP6; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: N/A Iron overload; PMID(s): none submitted",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.519787Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ATP7B: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ATP7B; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 277900 WILSON DISEASE; PMID(s): none submitted",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:39:41.502511Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.20",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: ACVR1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ACVR1; Suggested intial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: N/A IRIDA; PMID(s): none submitted",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:56.222299Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.19",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Mode of inheritance for gene: SEC23B was changed from to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:45.630495Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.18",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: SEC23B as Green List (high evidence)",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:45.624871Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.18",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: sec23b has been classified as Green List (High Evidence).",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:34.906620Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.17",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Mode of inheritance for gene: CDAN1 was changed from to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:27.112458Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.16",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Classified gene: CDAN1 as Green List (high evidence)",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:27.104963Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.16",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Gene: cdan1 has been classified as Green List (High Evidence).",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.934155Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: TMPRSS6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 206200 IRON-REFRACTORY IRON DEFICIENCY ANEMIA, IRIDA; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.920712Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: TFR2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 604250 HEMOCHROMATOSIS, TYPE 3, HFE3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.901255Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: TF: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 209300 Atransferrinemia, Hypoferritinaemia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.885133Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: SLC40A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 606069 HEMOCHROMATOSIS, TYPE 4, HFE4; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.869313Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: SLC11A2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 206100 ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1, AHMIO1 DMT1-related anemia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.855094Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: SERPINC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 613490 ALPHA-1-ANTITRYPSIN DEFICIENCY, A1ATD; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.842386Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: SEC23B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 224100 Dyserythropoietic anemia, congenital, type II; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.826479Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: HFE2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 602390 HEMOCHROMATOSIS, TYPE 2A, HFE2A; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.812647Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: HFE: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 235200 HEMOCHROMATOSIS, TYPE 1, HFE1; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.799849Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: HEPH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.786637Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: HAMP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 613313 HEMOCHROMATOSIS, TYPE 2B, HFE2B; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.770599Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: GBA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 230800 Gaucher disease, type I, 230900 Gaucher disease, type II, 231000 Gaucher disease, type III, 231005 Gaucher disease, type IIIC; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.758164Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: FTL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT, HRFTC, 606159 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3, NBIA3, 615604 L-FERRITIN DEFICIENCY, LFTD; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.741697Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: FTH1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 615517 HEMOCHROMATOSIS, TYPE 5, HFE5; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.724773Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: FECH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 177000 PROTOPORPHYRIA, ERYTHROPOIETIC, 1, EPP1; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.710703Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: CYBRD1: Rating: GREEN; Mode of pathogenicity: ; Publications: 15338274; Phenotypes: N/A Primary iron overload; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.695225Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: CP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 604290 ACERULOPLASMINEMIA; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.679113Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: CDAN1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 224120 Dyserythropoietic anemia, congenital, type Ia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.665053Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: BMP6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Iron overload; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.652605Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: ATP7B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 277900 WILSON DISEASE; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:36:10.638607Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.15",
"user_name": "Mandy nesbitt",
"item_type": "entity",
"text": "reviewed gene: ACVR1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: IRIDA; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:08.174756Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes IRIDA; 206200 IRON-REFRACTORY IRON DEFICIENCY ANEMIA for gene: TMPRSS6",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:08.112457Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 604250 HEMOCHROMATOSIS, TYPE 3; HFE3 for gene: TFR2",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:08.048155Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 209300 Atransferrinemia, Hypoferritinaemia for gene: TF",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.986656Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes HFE4; 606069 HEMOCHROMATOSIS, TYPE 4 for gene: SLC40A1",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.922255Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 206100 ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1 DMT1-related anemia for gene: SLC11A2",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.862035Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes A1ATD; 613490 ALPHA-1-ANTITRYPSIN DEFICIENCY for gene: SERPINC1",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.803745Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 224100 Dyserythropoietic anemia, congenital, type II for gene: SEC23B",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.735623Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes HFE2A; 602390 HEMOCHROMATOSIS, TYPE 2A for gene: HFE2",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.675711Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 235200 HEMOCHROMATOSIS, TYPE 1; HFE1 for gene: HFE",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.565020Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 613313 HEMOCHROMATOSIS, TYPE 2B; HFE2B for gene: HAMP",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.503902Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 230900 Gaucher disease, type II; 231005 Gaucher disease, type IIIC; 231000 Gaucher disease, type III; 230800 Gaucher disease, type I for gene: GBA",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.441811Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes NBIA3; 615604 L-FERRITIN DEFICIENCY; HRFTC; 600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT; LFTD; 606159 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3 for gene: FTL",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.382061Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes HFE5; 615517 HEMOCHROMATOSIS, TYPE 5 for gene: FTH1",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.319113Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes EPP1; 177000 PROTOPORPHYRIA, ERYTHROPOIETIC, 1 for gene: FECH",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.253556Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes N/A Primary iron overload for gene: CYBRD1",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.184256Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 604290 ACERULOPLASMINEMIA for gene: CP\nPublications for gene CP were changed from 8641692; 8789443; 11756598(potentially evidence for AD inheritance) to 15338274",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.089211Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 224120 Dyserythropoietic anemia, congenital, type Ia for gene: CDAN1",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:07.016981Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes Iron overload for gene: BMP6",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:06.959920Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 277900 WILSON DISEASE for gene: ATP7B",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:32:06.900955Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.14",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes IRIDA for gene: ACVR1",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:29:39.659182Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.13",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to SEC23B.",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:29:39.076992Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.13",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to CDAN1.",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:28.020377Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to TMPRSS6.",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.954966Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to TFR2.",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.890857Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to TF.",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.825008Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to SLC40A1.",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.758936Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to SLC11A2.",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.695610Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to SERPINC1.",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.647677Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: SEC23B was added\ngene: SEC23B was added to Iron metabolism disorders. Sources: Yorkshire and North East GLH\nMode of inheritance for gene: SEC23B was set to ",
"entity_name": "SEC23B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.591330Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to HFE2.",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.525273Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to HFE.",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.461138Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to HEPH.",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.396710Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to HAMP.",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.334543Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to GBA.",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.263215Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to FTL.",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.187370Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to FTH1.",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.117223Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to FECH.",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:27.042598Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to CYBRD1.",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:26.977255Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to CP.",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:26.930393Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: CDAN1 was added\ngene: CDAN1 was added to Iron metabolism disorders. Sources: Yorkshire and North East GLH\nMode of inheritance for gene: CDAN1 was set to ",
"entity_name": "CDAN1",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:26.870978Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to BMP6.",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:26.809867Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to ATP7B.",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-13T12:28:26.745180Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.12",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Yorkshire and North East GLH was added to ACVR1.",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.651604Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: TMPRSS6: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TMPRSS6; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 206200 Iron-refractory iron deficiency anemia; PMID(s): 18408718; 19357398",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.639360Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: TFR2: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TFR2; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 604250 Hemochromatosis, type 3; PMID(s): 10802645; 11313241",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.626803Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: TF: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TF; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 209300 Atransferrinemia; PMID(s): 11110675; 15466165",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.614124Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SLC40A1: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SLC40A1; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 606069 Hemochromatosis, type 4; PMID(s): 11431687; 16351644",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.600847Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: SLC11A2: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SLC11A2; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 206100 Anemia, hypochromic microcytic, with iron overload 1; PMID(s): 15459009; 16160008; 16439678",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.585464Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HFE2: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HJV(HFE2); Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 602390 Hemochromatosis, type 2A; PMID(s): 14982873. ",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.572766Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HFE: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HFE; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 235200 Hemochromatosis; PMID(s): 18199861",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.561154Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HAMP: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HAMP; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 613313 Hemochromatosis, type 2B; PMID(s): 12469120; 15198949; 12915468",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.549651Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FTL: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FTL; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 600886 Hyperferritinemia-cataract syndrome; 615604 L-ferritin deficiency, dominant and recessive; 606159 Neurodegeneration with brain iron accumulation 3; PMID(s): 23421845; 19176363; 23940258; 18413574",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.538682Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: FTH1: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FTH1; Suggested intial gene rating: Red List (low evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 615517 ?Hemochromatosis, type 5; PMID(s): 11389486",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.524798Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: CP: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CP; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 604290 Hemosiderosis, systemic, due to aceruloplasminemia; PMID(s): 8641692; 8789443; 11756598(potentially evidence for AD inheritance)",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:25:58.511854Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.11",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: BMP6: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: BMP6; Suggested intial gene rating: Red List (low evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 112266 Mild to moderate iron overload; PMID(s): 26582087",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.426983Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: TMPRSS6: Rating: GREEN; Mode of pathogenicity: ; Publications: 18408718, 19357398; Phenotypes: 206200 Iron-refractory iron deficiency anemia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.412547Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: TFR2: Rating: GREEN; Mode of pathogenicity: ; Publications: 10802645, 11313241; Phenotypes: 604250 Hemochromatosis, type 3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.397589Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: TF: Rating: GREEN; Mode of pathogenicity: ; Publications: 11110675, 15466165; Phenotypes: 209300 Atransferrinemia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.383073Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: SLC40A1: Rating: GREEN; Mode of pathogenicity: ; Publications: 11431687, 16351644; Phenotypes: 606069 Hemochromatosis, type 4; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.368717Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: SLC11A2: Rating: GREEN; Mode of pathogenicity: ; Publications: 15459009, 16160008, 16439678; Phenotypes: 206100 Anemia, hypochromic microcytic, with iron overload 1; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.348365Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: HFE2: Rating: GREEN; Mode of pathogenicity: ; Publications: 14982873; Phenotypes: 602390 Hemochromatosis, type 2A; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.331077Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: HFE: Rating: GREEN; Mode of pathogenicity: ; Publications: 18199861; Phenotypes: 235200 Hemochromatosis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.315041Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: HAMP: Rating: GREEN; Mode of pathogenicity: ; Publications: 12469120, 15198949, 12915468; Phenotypes: 613313 Hemochromatosis, type 2B; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.295920Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: FTL: Rating: GREEN; Mode of pathogenicity: ; Publications: 23421845, 19176363, 23940258, 18413574; Phenotypes: 600886 Hyperferritinemia-cataract syndrome, 615604 L-ferritin deficiency, dominant and recessive, 606159 Neurodegeneration with brain iron accumulation 3; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.279930Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: FTH1: Rating: RED; Mode of pathogenicity: ; Publications: 11389486; Phenotypes: 615517 ?Hemochromatosis, type 5; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.261757Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: CP: Rating: GREEN; Mode of pathogenicity: ; Publications: 8641692, 8789443, 11756598(potentially evidence for AD inheritance); Phenotypes: 604290 Hemosiderosis, systemic, due to aceruloplasminemia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:24:37.237567Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.10",
"user_name": "Frances Smith",
"item_type": "entity",
"text": "reviewed gene: BMP6: Rating: RED; Mode of pathogenicity: ; Publications: 26582087; Phenotypes: 112266 Mild to moderate iron overload; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.778458Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 206200 Iron-refractory iron deficiency anemia for gene: TMPRSS6\nPublications for gene TMPRSS6 were changed from 25588876; 28476747; 23729726 to 19357398; 18408718",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.712033Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 604250 Hemochromatosis, type 3 for gene: TFR2\nPublications for gene TFR2 were changed from 24055163; 18094142; 26029709 to 10802645; 11313241",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.647458Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 209300 Atransferrinemia for gene: TF\nPublications for gene TF were changed from 23888904; 25486930; 11110675 to 15466165; 11110675",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.574539Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 606069 Hemochromatosis, type 4 for gene: SLC40A1\nPublications for gene SLC40A1 were changed from 19846751 to 16351644; 11431687",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.500107Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 206100 Anemia, hypochromic microcytic, with iron overload 1 for gene: SLC11A2\nPublications for gene SLC11A2 were changed from 29178181; 21871825 to 16160008; 16439678; 15459009",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.435503Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 602390 Hemochromatosis, type 2A for gene: HFE2\nPublications for gene HFE2 were changed from 30166352; 14982873; 19342478; 14647275 to 14982873",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.368574Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 235200 Hemochromatosis for gene: HFE\nPublications for gene HFE were changed from 27518069; 18210110; 24266916 to 18199861",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.294995Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 613313 Hemochromatosis, type 2B for gene: HAMP\nPublications for gene HAMP were changed from 22297252; 14630809 to 12469120; 15198949; 12915468",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.226009Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 606159 Neurodegeneration with brain iron accumulation 3; 615604 L-ferritin deficiency, dominant and recessive; 600886 Hyperferritinemia-cataract syndrome for gene: FTL\nPublications for gene FTL were changed from 20511138; 29797321; 12547246; Neuroferritinopathy GeneReviews 2018; 23421845 to 18413574; 23940258; 23421845; 19176363",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.146918Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 615517 ?Hemochromatosis, type 5 for gene: FTH1",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:30.072340Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 604290 Hemosiderosis, systemic, due to aceruloplasminemia for gene: CP\nPublications for gene CP were changed from 16629161; Aceruloplasminemia GeneReviews 2018; 24002824; 29503155 to 8641692; 8789443; 11756598(potentially evidence for AD inheritance)",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:20:29.997444Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.9",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Added phenotypes 112266 Mild to moderate iron overload for gene: BMP6\nPublications for gene BMP6 were changed from 28335084; 26582087 to 26582087",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:23.556139Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to TMPRSS6.",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:23.482100Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to TFR2.",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:23.413629Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to TF.",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:23.346549Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to SLC40A1.",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:23.280165Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to SLC11A2.",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:23.209872Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to HFE2.",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:23.145364Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to HFE.",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:23.076302Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to HAMP.",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:23.009017Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to FTL.",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:22.939803Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to FTH1.",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:22.869423Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to CP.",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-08T17:17:22.785718Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.7",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source London South GLH was added to BMP6.",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-08T14:58:16.376905Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "commented on gene: HFE2: New HGNC approved gene symbol for HFE2 is HJV",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-08T14:58:03.263252Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Tag new-gene-name tag was added to gene: HFE2.",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.387317Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: TMPRSS6: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.373972Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: TFR2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.361429Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: TF: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.348019Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: STEAP3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.334911Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: SLC40A1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.322339Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: SLC25A38: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.309458Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: SLC11A2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.296374Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: SERPINC1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.283352Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: HFE2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.270675Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: HFE: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.258067Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: HEPH: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.245269Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: HAMP: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.232860Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: GLRX5: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.219867Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: GBA: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.206425Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: FTL: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.192919Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: FTH1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.179833Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: FECH: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.166842Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: CYBRD1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.153239Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: CP: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.140391Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: BMP6: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.127035Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: ATP7B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.109565Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: ALAS2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.092912Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: ACVR1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:51:27.074538Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.6",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "reviewed gene: ABCB7: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:30.092289Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: TMPRSS6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:30.080321Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: TFR2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:30.068162Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: TF: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:30.054555Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: STEAP3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:30.040365Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: SLC40A1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:30.027270Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: SLC25A38: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:30.014161Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: SLC11A2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:30.000918Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: SERPINC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.986696Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: HFE2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.973731Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: HFE: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.955995Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: HEPH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.942356Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: HAMP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.929964Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: GLRX5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.917121Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: GBA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.903689Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: FTL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.890494Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: FTH1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.878137Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: FECH: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.861136Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: CYBRD1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.847211Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: CP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.833722Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: BMP6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.819456Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: ATP7B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.806277Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: ALAS2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.792988Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: ACVR1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:50:29.780184Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.5",
"user_name": "Carl Fratter",
"item_type": "entity",
"text": "reviewed gene: ABCB7: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.923159Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to TMPRSS6.",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.863868Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to TFR2.",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.804325Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to TF.",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.742605Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to STEAP3.",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.681764Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to SLC40A1.",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.618118Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to SLC25A38.",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.554968Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to SLC11A2.",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.490875Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to SERPINC1.",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.429528Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to HFE2.",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.363167Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to HFE.",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.306951Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to HEPH.",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.252851Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to HAMP.",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.192003Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to GLRX5.",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.125425Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to GBA.",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.069334Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to FTL.",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:26.013818Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to FTH1.",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:25.954127Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to FECH.",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:25.893783Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to CYBRD1.",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:25.837048Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to CP.",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:25.782536Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to BMP6.",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:25.725637Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to ATP7B.",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:25.669035Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to ALAS2.",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:25.613509Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to ACVR1.",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:48:25.556113Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.4",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source NHS GMS was added to ABCB7.",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:27.443430Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to TMPRSS6.\nMode of inheritance for gene TMPRSS6 was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes IRIDA; 206200 IRON-REFRACTORY IRON DEFICIENCY ANEMIA for gene: TMPRSS6\nPublications for gene TMPRSS6 were changed from to 25588876; 28476747; 23729726\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:27.378812Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to TFR2.\nMode of inheritance for gene TFR2 was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes 604250 HEMOCHROMATOSIS, TYPE 3; HFE3 for gene: TFR2\nPublications for gene TFR2 were changed from to 24055163; 18094142; 26029709\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:27.312213Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to TF.\nMode of inheritance for gene TF was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes 209300 Atransferrinemia, Hypoferritinaemia for gene: TF\nPublications for gene TF were changed from to 23888904; 25486930; 11110675\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:27.251651Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to STEAP3.\nMode of inheritance for gene STEAP3 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nAdded phenotypes 615234 ?Anemia, hypochromic microcytic, with iron overload 2 for gene: STEAP3\nPublications for gene STEAP3 were changed from to 22031863\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:27.190794Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to SLC40A1.\nMode of inheritance for gene SLC40A1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nAdded phenotypes HFE4; 606069 HEMOCHROMATOSIS, TYPE 4 for gene: SLC40A1\nPublications for gene SLC40A1 were changed from to 19846751\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:27.130157Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to SLC25A38.\nMode of inheritance for gene SLC25A38 was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes 205950 Anemia, sideroblastic, 2, pyridoxine-refractory for gene: SLC25A38\nPublications for gene SLC25A38 were changed from to 19412178; 24323989; 21393332\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:27.073832Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to SLC11A2.\nMode of inheritance for gene SLC11A2 was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes 206100 ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1; DMT1-related anemia for gene: SLC11A2\nPublications for gene SLC11A2 were changed from to 29178181; 21871825\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:27.000858Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to SERPINC1.\nMode of inheritance for gene SERPINC1 was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes A1ATD; 613490 ALPHA-1-ANTITRYPSIN DEFICIENCY for gene: SERPINC1\nPublications for gene SERPINC1 were changed from to 18210110; 27296815\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.937742Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to HFE2.\nMode of inheritance for gene HFE2 was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes HFE2A; 602390 HEMOCHROMATOSIS, TYPE 2A for gene: HFE2\nPublications for gene HFE2 were changed from to 30166352; 14982873; 19342478; 14647275\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.877587Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to HFE.\nMode of inheritance for gene HFE was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes 235200 HEMOCHROMATOSIS, TYPE 1; HFE1 for gene: HFE\nPublications for gene HFE were changed from to 27518069; 18210110; 24266916\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.816198Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to HEPH.\nMode of inheritance for gene HEPH was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.760012Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to HAMP.\nMode of inheritance for gene HAMP was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes 613313 HEMOCHROMATOSIS, TYPE 2B; HFE2B for gene: HAMP\nPublications for gene HAMP were changed from to 22297252; 14630809\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.691861Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to GLRX5.\nMode of inheritance for gene GLRX5 was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes 616860 Anemia, sideroblastic, 3, pyridoxine-refractory for gene: GLRX5\nPublications for gene GLRX5 were changed from to 30401706; 24003969; 30098397\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.628188Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to GBA.\nMode of inheritance for gene GBA was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes 230900 Gaucher disease, type II; 231005 Gaucher disease, type IIIC; 231000 Gaucher disease, type III; 230800 Gaucher disease, type I for gene: GBA\nPublications for gene GBA were changed from to 27265538; 27816428; 20575041\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.570459Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to FTL.\nMode of inheritance for gene FTL was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nAdded phenotypes NBIA3; 615604 L-FERRITIN DEFICIENCY; HRFTC; 600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT; LFTD; 606159 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3 for gene: FTL\nPublications for gene FTL were changed from to 20511138; 29797321; 12547246; Neuroferritinopathy GeneReviews 2018; 23421845\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.516094Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to FTH1.\nMode of inheritance for gene FTH1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nAdded phenotypes HFE5; 615517 HEMOCHROMATOSIS, TYPE 5 for gene: FTH1\nPublications for gene FTH1 were changed from to 11389486\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.461885Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to FECH.\nMode of inheritance for gene FECH was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes EPP1; 177000 PROTOPORPHYRIA, ERYTHROPOIETIC, 1 for gene: FECH\nPublications for gene FECH were changed from to 26387792; 20857522; 28614581\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.398118Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to CYBRD1.\nMode of inheritance for gene CYBRD1 was changed from to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene CYBRD1 were changed from to 15338274; 27884173\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.334132Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to CP.\nMode of inheritance for gene CP was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes 604290 ACERULOPLASMINEMIA for gene: CP\nPublications for gene CP were changed from to 16629161; Aceruloplasminemia GeneReviews 2018; 24002824; 29503155\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.280709Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to BMP6.\nMode of inheritance for gene BMP6 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nAdded phenotypes Iron overload for gene: BMP6\nPublications for gene BMP6 were changed from to 28335084; 26582087\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.227606Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to ATP7B.\nMode of inheritance for gene ATP7B was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes 277900 WILSON DISEASE for gene: ATP7B\nPublications for gene ATP7B were changed from to 24002824; 18210110; 27982432; 24266916; 28433102\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.173351Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to ALAS2.\nMode of inheritance for gene ALAS2 was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nAdded phenotypes 300752 Protoporphyria, erythropoietic, X-linked; 300751 Anemia, sideroblastic, 1 for gene: ALAS2\nPublications for gene ALAS2 were changed from to 30401706; 24003969; 30098397\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.114772Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to ACVR1.\nMode of inheritance for gene ACVR1 was changed from to BIALLELIC, autosomal or pseudoautosomal\nAdded phenotypes new type of IRIDA for gene: ACVR1\nPublications for gene ACVR1 were changed from to 28476747\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:47:26.052250Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.3",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "Source Expert Review Green was added to ABCB7.\nMode of inheritance for gene ABCB7 was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nAdded phenotypes 301310 Anemia, sideroblastic, with ataxia for gene: ABCB7\nPublications for gene ABCB7 were changed from to 30401706; 10196363; 29787825\nRating Changed from Red List (low evidence) to Green List (high evidence)",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.993684Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: TMPRSS6 was added\ngene: TMPRSS6 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: TMPRSS6 was set to ",
"entity_name": "TMPRSS6",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.956071Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: TFR2 was added\ngene: TFR2 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: TFR2 was set to ",
"entity_name": "TFR2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.921391Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: TF was added\ngene: TF was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: TF was set to ",
"entity_name": "TF",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.886535Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: STEAP3 was added\ngene: STEAP3 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: STEAP3 was set to ",
"entity_name": "STEAP3",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.850837Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: SLC40A1 was added\ngene: SLC40A1 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: SLC40A1 was set to ",
"entity_name": "SLC40A1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.815811Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: SLC25A38 was added\ngene: SLC25A38 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: SLC25A38 was set to ",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.780463Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: SLC11A2 was added\ngene: SLC11A2 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: SLC11A2 was set to ",
"entity_name": "SLC11A2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.743084Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: SERPINC1 was added\ngene: SERPINC1 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: SERPINC1 was set to ",
"entity_name": "SERPINC1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.706812Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: HFE2 was added\ngene: HFE2 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: HFE2 was set to ",
"entity_name": "HFE2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.671444Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: HFE was added\ngene: HFE was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: HFE was set to ",
"entity_name": "HFE",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.635987Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: HEPH was added\ngene: HEPH was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: HEPH was set to ",
"entity_name": "HEPH",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.594044Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: HAMP was added\ngene: HAMP was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: HAMP was set to ",
"entity_name": "HAMP",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.557892Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: GLRX5 was added\ngene: GLRX5 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: GLRX5 was set to ",
"entity_name": "GLRX5",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.523598Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: GBA was added\ngene: GBA was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: GBA was set to ",
"entity_name": "GBA",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.489258Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: FTL was added\ngene: FTL was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: FTL was set to ",
"entity_name": "FTL",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.455824Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: FTH1 was added\ngene: FTH1 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: FTH1 was set to ",
"entity_name": "FTH1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.422391Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: FECH was added\ngene: FECH was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: FECH was set to ",
"entity_name": "FECH",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.387026Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: CYBRD1 was added\ngene: CYBRD1 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: CYBRD1 was set to ",
"entity_name": "CYBRD1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.351663Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: CP was added\ngene: CP was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: CP was set to ",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.317267Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: BMP6 was added\ngene: BMP6 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: BMP6 was set to ",
"entity_name": "BMP6",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.283307Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: ATP7B was added\ngene: ATP7B was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: ATP7B was set to ",
"entity_name": "ATP7B",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.249558Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: ALAS2 was added\ngene: ALAS2 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: ALAS2 was set to ",
"entity_name": "ALAS2",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.214745Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: ACVR1 was added\ngene: ACVR1 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: ACVR1 was set to ",
"entity_name": "ACVR1",
"entity_type": "gene"
},
{
"created": "2019-02-05T17:44:59.178202Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.2",
"user_name": "Louise Daugherty",
"item_type": "entity",
"text": "gene: ABCB7 was added\ngene: ABCB7 was added to Iron metabolism disorders. Sources: Wessex and West Midlands GLH\nMode of inheritance for gene: ABCB7 was set to ",
"entity_name": "ABCB7",
"entity_type": "gene"
},
{
"created": "2018-11-16T09:35:02.079493Z",
"panel_name": "Iron metabolism disorders",
"panel_id": 515,
"panel_version": "0.0",
"user_name": "Ellen McDonagh",
"item_type": "panel",
"text": "Added Panel Iron metabolism disorders\nSet panel types to: GMS Rare Disease",
"entity_name": null,
"entity_type": null
}
]