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{
"count": 220313,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=866",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=864",
"results": [
{
"created": "2022-05-01T18:06:28.003087+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bpgm has been classified as Amber List (Moderate Evidence).",
"entity_name": "BPGM",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:06:10.074742+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BPGM: Rating: AMBER; Mode of pathogenicity: None; Publications: 1421379, 27651169, 25015942; Phenotypes: Erythrocytosis, familial, 8, MIM# 222800; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "BPGM",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:04:48.284470+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BMPR1A as ready",
"entity_name": "BMPR1A",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:04:48.271977+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bmpr1a has been classified as Green List (High Evidence).",
"entity_name": "BMPR1A",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:04:40.118687+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BMPR1A were changed from to Polyposis, juvenile intestinal, MIM# 174900",
"entity_name": "BMPR1A",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:04:20.472638+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13524",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BMPR1A were set to ",
"entity_name": "BMPR1A",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:04:00.604482+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BMPR1A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BMPR1A",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:03:40.804713+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BMPR1A: Rating: GREEN; Mode of pathogenicity: None; Publications: 11381269; Phenotypes: Polyposis, juvenile intestinal, MIM# 174900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BMPR1A",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:01:39.440605+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BLVRA as ready",
"entity_name": "BLVRA",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:01:39.421761+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: blvra has been classified as Amber List (Moderate Evidence).",
"entity_name": "BLVRA",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:01:31.157718+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BLVRA were changed from to Hyperbiliverdinaemia , MIM#614156",
"entity_name": "BLVRA",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:01:09.769953+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BLVRA were set to ",
"entity_name": "BLVRA",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:00:48.176584+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BLVRA was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "BLVRA",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:00:28.572874+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13519",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BLVRA as Amber List (moderate evidence)",
"entity_name": "BLVRA",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:00:28.560819+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13519",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: blvra has been classified as Amber List (Moderate Evidence).",
"entity_name": "BLVRA",
"entity_type": "gene"
},
{
"created": "2022-05-01T18:00:05.189682+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BLVRA: Rating: AMBER; Mode of pathogenicity: None; Publications: 19580635, 21278388; Phenotypes: Hyperbiliverdinaemia , MIM#614156; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "BLVRA",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:56:26.332903+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BLK as ready",
"entity_name": "BLK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:56:26.319359+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: blk has been classified as Amber List (Moderate Evidence).",
"entity_name": "BLK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:56:16.782763+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BLK were changed from to Common variable immunodeficiency, MONDO:0015517",
"entity_name": "BLK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:55:58.964703+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13517",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BLK were set to ",
"entity_name": "BLK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:55:32.183530+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BLK was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BLK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:55:11.664088+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BLK as Amber List (moderate evidence)",
"entity_name": "BLK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:55:11.651910+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: blk has been classified as Amber List (Moderate Evidence).",
"entity_name": "BLK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:54:52.313054+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BLK: Rating: AMBER; Mode of pathogenicity: None; Publications: 25926555; Phenotypes: Common variable immunodeficiency, MONDO:0015517; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BLK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:50:52.627285+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BHLHE41 as ready",
"entity_name": "BHLHE41",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:50:52.613797+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bhlhe41 has been classified as Red List (Low Evidence).",
"entity_name": "BHLHE41",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:50:40.494449+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BHLHE41 were changed from to [Short sleep, familial natural, 1] 612975",
"entity_name": "BHLHE41",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:50:18.611861+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13513",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BHLHE41 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BHLHE41",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:49:56.476248+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BHLHE41 as Red List (low evidence)",
"entity_name": "BHLHE41",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:49:56.463051+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bhlhe41 has been classified as Red List (Low Evidence).",
"entity_name": "BHLHE41",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:49:36.560425+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BHLHE41: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: [Short sleep, familial natural, 1] 612975; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BHLHE41",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:47:57.564601+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BFSP1 as ready",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:47:57.554288+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bfsp1 has been classified as Green List (High Evidence).",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:44:10.229939+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BFSP1 were changed from to Cataract 33, multiple types, MIM# 611391",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:43:54.698501+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.330",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BFSP1 as ready",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:43:54.688407+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.330",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bfsp1 has been classified as Green List (High Evidence).",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:43:51.856963+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.330",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BFSP1 were changed from to Cataract 33, multiple types, MIM# 611391",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:43:23.552311+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.329",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BFSP1 were set to ",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:42:54.701501+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.328",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BFSP1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:42:23.419727+10:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.327",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BFSP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17225135, 26694549, 24379646, 28450710, 31842807, 26694549; Phenotypes: Cataract 33, multiple types, MIM# 611391; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:42:19.681919+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13510",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BFSP1 were set to ",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:41:51.244081+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13509",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BFSP1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:41:17.914453+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BFSP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17225135, 26694549, 24379646, 28450710, 31842807, 26694549; Phenotypes: Cataract 33, multiple types, MIM# 611391; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "BFSP1",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:36:54.211840+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BCL2 as ready",
"entity_name": "BCL2",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:36:54.200763+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bcl2 has been classified as Red List (Low Evidence).",
"entity_name": "BCL2",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:36:45.367376+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BCL2 as Red List (low evidence)",
"entity_name": "BCL2",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:36:45.354499+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bcl2 has been classified as Red List (Low Evidence).",
"entity_name": "BCL2",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:36:25.135502+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13507",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BCL2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "BCL2",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:35:31.517730+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13507",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BCKDK as ready",
"entity_name": "BCKDK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:35:31.487918+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13507",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bckdk has been classified as Green List (High Evidence).",
"entity_name": "BCKDK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:35:23.745919+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13507",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BCKDK were changed from to Branched-chain ketoacid dehydrogenase kinase deficiency MIM#614923; disorder of branched-chain amino acid metabolism",
"entity_name": "BCKDK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:35:04.177145+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13506",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BCKDK were set to ",
"entity_name": "BCKDK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:34:44.271645+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13505",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BCKDK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BCKDK",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:34:01.036311+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BCL10 as ready",
"entity_name": "BCL10",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:34:01.023437+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bcl10 has been classified as Green List (High Evidence).",
"entity_name": "BCL10",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:33:49.915377+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BCL10 were changed from to Immunodeficiency 37, MIM# 616098",
"entity_name": "BCL10",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:33:28.942834+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BCL10 were set to ",
"entity_name": "BCL10",
"entity_type": "gene"
},
{
"created": "2022-05-01T17:33:08.427645+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BCL10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BCL10",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:24:57.581195+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13501",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BCHE as ready",
"entity_name": "BCHE",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:24:57.561103+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13501",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bche has been classified as Green List (High Evidence).",
"entity_name": "BCHE",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:24:48.931320+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13501",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BCHE were changed from to Butyrylcholinesterase deficiency, MIM# 617936",
"entity_name": "BCHE",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:24:26.052436+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BCHE was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BCHE",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:24:04.149502+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13499",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BCHE: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Butyrylcholinesterase deficiency, MIM# 617936; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BCHE",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:22:20.643934+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13499",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS2 as ready",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:22:20.633648+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13499",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs2 has been classified as Green List (High Evidence).",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:22:12.084549+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13499",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS2 were changed from to Bardet-Biedl syndrome 2, MIM# 615981; Retinitis pigmentosa 74, MIM# 616562",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:21:51.366026+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS2 were set to ",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:21:22.527206+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13497",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS2",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:20:34.360901+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS12 as ready",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:20:34.350612+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs12 has been classified as Green List (High Evidence).",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:20:20.345582+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS12 were changed from to Bardet-Biedl syndrome 12, MIM# 615989",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:19:54.746752+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13495",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS12 were set to ",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:19:31.591374+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS12",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:18:37.483834+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS10 as ready",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:18:37.469565+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs10 has been classified as Green List (High Evidence).",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:18:27.154672+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS10 were changed from to Bardet-Biedl syndrome 10, MIM# 615987",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:17:56.364634+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13492",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS10 were set to ",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:17:35.117299+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13491",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS10",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:16:31.490241+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BBS1 as ready",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:16:31.480141+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bbs1 has been classified as Green List (High Evidence).",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:16:22.659139+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BBS1 were changed from to Bardet-Biedl syndrome 1, MIM# 209900",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:16:00.746098+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BBS1 were set to ",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2022-04-30T18:15:34.303949+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13488",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BBS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BBS1",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:54:57.408358+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BAG3 as ready",
"entity_name": "BAG3",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:54:57.394686+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bag3 has been classified as Green List (High Evidence).",
"entity_name": "BAG3",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:54:42.015617+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BAG3 were changed from to Cardiomyopathy, dilated, 1HH, MIM# 613881; Myopathy, myofibrillar, 6, MIM# 612954",
"entity_name": "BAG3",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:54:21.085832+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BAG3 were set to ",
"entity_name": "BAG3",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:53:56.584905+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BAG3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BAG3",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:53:34.514697+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BAG3: Rating: GREEN; Mode of pathogenicity: None; Publications: 21353195, 25008357, 25448463, 24623017, 27391596, 28211974, 30442290, 31983221, 28737513, 29323723, 33947203, 25208129, 32453099, 22734908; Phenotypes: Cardiomyopathy, dilated, 1HH, MIM# 613881, Myopathy, myofibrillar, 6, MIM# 612954; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BAG3",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:51:08.657408+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Deleted their comment",
"entity_name": "BACH2",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:51:02.517048+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "commented on gene: BACH2: Two families and a mouse model.",
"entity_name": "BACH2",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:50:04.175830+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BACH2 as ready",
"entity_name": "BACH2",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:50:04.155621+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bach2 has been classified as Green List (High Evidence).",
"entity_name": "BACH2",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:49:46.865862+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BACH2 were changed from to Immunodeficiency 60 and autoimmunity, MIM# 618394",
"entity_name": "BACH2",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:49:24.441240+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BACH2 were set to ",
"entity_name": "BACH2",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:49:03.805253+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BACH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BACH2",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:48:23.324458+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13481",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BACH2: Rating: GREEN; Mode of pathogenicity: None; Publications: 28530713; Phenotypes: Immunodeficiency 60 and autoimmunity, MIM# 618394; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BACH2",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:47:07.116523+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13481",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B4GALT1 as ready",
"entity_name": "B4GALT1",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:47:07.103564+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13481",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b4galt1 has been classified as Green List (High Evidence).",
"entity_name": "B4GALT1",
"entity_type": "gene"
},
{
"created": "2022-04-30T17:46:58.749653+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.13481",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B4GALT1 were changed from to Congenital disorder of glycosylation, type Iid, MIM#607091",
"entity_name": "B4GALT1",
"entity_type": "gene"
}
]
}