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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=835",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=833",
"results": [
{
"created": "2022-05-18T17:03:17.719407+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MET was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MET",
"entity_type": "gene"
},
{
"created": "2022-05-18T17:02:55.680304+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: MET: Changed phenotypes: Renal cell carcinoma, papillary, 1, familial and somatic, MIM# 605074, Papillary renal cell carcinoma MONDO:0017884",
"entity_name": "MET",
"entity_type": "gene"
},
{
"created": "2022-05-18T17:02:31.900346+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MET: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Papillary renal cell carcinoma MONDO:0017884; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MET",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:59:39.532991+10:00",
"panel_name": "Retinitis pigmentosa_Autosomal Recessive/X-linked",
"panel_id": 277,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MERTK as ready",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:59:39.518965+10:00",
"panel_name": "Retinitis pigmentosa_Autosomal Recessive/X-linked",
"panel_id": 277,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mertk has been classified as Green List (High Evidence).",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:59:34.142305+10:00",
"panel_name": "Retinitis pigmentosa_Autosomal Recessive/X-linked",
"panel_id": 277,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MERTK were changed from childhood onset rod-cone dystrophy with early macular atrophy; Leber congenital amaurosisRetinitis pigmentosa 38, 613862 to Retinitis pigmentosa 38, MIM# 613862",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:59:20.644198+10:00",
"panel_name": "Retinitis pigmentosa_Autosomal Recessive/X-linked",
"panel_id": 277,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MERTK were set to ",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:58:39.756335+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14486",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Marked gene: ATG16L1 as ready",
"entity_name": "ATG16L1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:58:39.746730+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14486",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Gene: atg16l1 has been classified as Red List (Low Evidence).",
"entity_name": "ATG16L1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:56:53.607980+10:00",
"panel_name": "Retinitis pigmentosa_Autosomal Recessive/X-linked",
"panel_id": 277,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MERTK: Rating: GREEN; Mode of pathogenicity: None; Publications: 11062461, 17301963, 20300561, 22180149; Phenotypes: Retinitis pigmentosa 38, MIM# 613862; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:56:05.748955+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MERTK as ready",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:56:05.736185+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mertk has been classified as Green List (High Evidence).",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:55:54.205867+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MERTK were changed from to Retinitis pigmentosa 38, MIM# 613862",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:55:28.025331+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MERTK were set to ",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:55:02.261288+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MERTK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:54:37.430555+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MERTK: Rating: GREEN; Mode of pathogenicity: None; Publications: 11062461, 17301963, 20300561, 22180149; Phenotypes: Retinitis pigmentosa 38, MIM# 613862; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MERTK",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:52:21.403693+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MEIS1 as ready",
"entity_name": "MEIS1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:52:21.391727+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: meis1 has been classified as Red List (Low Evidence).",
"entity_name": "MEIS1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:52:04.387110+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MEIS1 as Red List (low evidence)",
"entity_name": "MEIS1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:52:04.369007+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: meis1 has been classified as Red List (Low Evidence).",
"entity_name": "MEIS1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:51:17.811123+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MEIS1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "MEIS1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:44:57.098142+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14482",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Phenotypes for gene: ATP1A1 were changed from Charcot-Marie-Tooth disease, axonal, type 2DD MIM#618036; Hypomagnesemia, seizures, and mental retardation 2 MIM#618314 to Charcot-Marie-Tooth disease, axonal, type 2DD MIM#618036; Hypomagnesemia, seizures, and mental retardation 2 MIM#618314",
"entity_name": "ATP1A1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:42:45.936742+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14481",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Marked gene: ATP2A2 as ready",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:42:45.926360+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14481",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Gene: atp2a2 has been classified as Green List (High Evidence).",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:41:09.286093+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14481",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Phenotypes for gene: ATG16L1 were changed from to {Inflammatory bowel disease (Crohn disease) 10} MIM#611081",
"entity_name": "ATG16L1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:40:58.689666+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14480",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Publications for gene: ATG16L1 were set to ",
"entity_name": "ATG16L1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:40:50.475923+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14480",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Classified gene: ATG16L1 as Red List (low evidence)",
"entity_name": "ATG16L1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:40:50.452506+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14480",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Gene: atg16l1 has been classified as Red List (Low Evidence).",
"entity_name": "ATG16L1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:34:39.171235+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14479",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Phenotypes for gene: ATL3 were changed from Neuropathy, hereditary sensory, type IF, MIM# 615632 to Neuropathy, hereditary sensory, type IF, MIM# 615632",
"entity_name": "ATL3",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:34:02.254313+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14478",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Phenotypes for gene: ATP2A2 were changed from to Acrokeratosis verruciformis MIM#101900; Darier disease MIM#124200",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:33:57.871818+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14477",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Publications for gene: ATP2A2 were set to ",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:33:51.547032+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14477",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATP2A2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:31:23.888158+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14476",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Phenotypes for gene: ATP1A1 were changed from to Charcot-Marie-Tooth disease, axonal, type 2DD MIM#618036; Hypomagnesemia, seizures, and mental retardation 2 MIM#618314",
"entity_name": "ATP1A1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:31:10.827100+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14475",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Marked gene: ATP1A1 as ready",
"entity_name": "ATP1A1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:31:10.811952+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14475",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Gene: atp1a1 has been classified as Green List (High Evidence).",
"entity_name": "ATP1A1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:29:02.678226+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14475",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "reviewed gene: ATG16L1: Rating: ; Mode of pathogenicity: None; Publications: PMID: 20602997; Phenotypes: {Inflammatory bowel disease (Crohn disease) 10} MIM#611081; Mode of inheritance: None",
"entity_name": "ATG16L1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:27:26.549963+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14475",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Phenotypes for gene: ATL3 were changed from to Neuropathy, hereditary sensory, type IF, MIM# 615632",
"entity_name": "ATL3",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:27:25.363081+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14474",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Marked gene: ATL3 as ready",
"entity_name": "ATL3",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:27:25.350098+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14474",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Gene: atl3 has been classified as Green List (High Evidence).",
"entity_name": "ATL3",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:27:10.422854+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14474",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "reviewed gene: ATP2A2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 24336169; Phenotypes: Acrokeratosis verruciformis MIM#101900, Darier disease MIM#124200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "ATP2A2",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:24:12.988192+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14474",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Publications for gene: ATP1A1 were set to ",
"entity_name": "ATP1A1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:24:04.972066+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14474",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATP1A1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "ATP1A1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:21:59.254916+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14473",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Publications for gene: ATL3 were set to ",
"entity_name": "ATL3",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:21:46.944394+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14473",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATL3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown",
"entity_name": "ATL3",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:09:00.152042+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14472",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Marked gene: ATF1 as ready",
"entity_name": "ATF1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:09:00.134022+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14472",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Gene: atf1 has been classified as Red List (Low Evidence).",
"entity_name": "ATF1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:00:58.014416+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14472",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Classified gene: ATF1 as Red List (low evidence)",
"entity_name": "ATF1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:00:58.001756+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14472",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Gene: atf1 has been classified as Red List (Low Evidence).",
"entity_name": "ATF1",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:00:53.944473+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MEIOB as ready",
"entity_name": "MEIOB",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:00:53.928680+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: meiob has been classified as Green List (High Evidence).",
"entity_name": "MEIOB",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:00:37.881341+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14471",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Marked gene: ASPN as ready",
"entity_name": "ASPN",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:00:37.868860+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14471",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Gene: aspn has been classified as Red List (Low Evidence).",
"entity_name": "ASPN",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:00:11.897592+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MEGF8 as ready",
"entity_name": "MEGF8",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:00:11.885720+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: megf8 has been classified as Green List (High Evidence).",
"entity_name": "MEGF8",
"entity_type": "gene"
},
{
"created": "2022-05-18T16:00:01.108956+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14471",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MEGF8 were changed from to Carpenter syndrome, MIM#614976",
"entity_name": "MEGF8",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:59:36.632101+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14470",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MEGF8 were set to ",
"entity_name": "MEGF8",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:59:12.896019+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14469",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MEGF8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MEGF8",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:58:50.920536+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14468",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MEGF8: Rating: GREEN; Mode of pathogenicity: None; Publications: 23063620; Phenotypes: Carpenter syndrome, MIM#614976; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MEGF8",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:56:01.390964+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14468",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MEFV as ready",
"entity_name": "MEFV",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:56:01.374543+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14468",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mefv has been classified as Green List (High Evidence).",
"entity_name": "MEFV",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:55:50.576875+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14468",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Publications for gene: ASPN were set to ",
"entity_name": "ASPN",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:55:35.062376+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14467",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MEFV were changed from to Familial Mediterranean fever MIM# 249100",
"entity_name": "MEFV",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:55:09.890875+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14466",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MEFV was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MEFV",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:54:47.464646+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14465",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MEFV: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Familial Mediterranean fever MIM# 249100; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MEFV",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:53:16.390177+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14465",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MED23 as ready",
"entity_name": "MED23",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:53:16.380138+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14465",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: med23 has been classified as Green List (High Evidence).",
"entity_name": "MED23",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:53:05.173358+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14465",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MED23 were changed from to Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy, MIM# 614249",
"entity_name": "MED23",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:52:41.541040+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14464",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MED23 were set to ",
"entity_name": "MED23",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:52:18.284739+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14463",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MED23 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MED23",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:51:56.530724+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MED23: Rating: GREEN; Mode of pathogenicity: None; Publications: 21868677, 25845469, 27311965, 30847200, 31164858; Phenotypes: Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy, MIM# 614249; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MED23",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:49:16.203074+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MED13 as ready",
"entity_name": "MED13",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:49:16.188217+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: med13 has been classified as Green List (High Evidence).",
"entity_name": "MED13",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:49:06.129690+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14462",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MED13 were changed from to Intellectual developmental disorder, autosomal dominant 61, MIM# 618009",
"entity_name": "MED13",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:48:41.406695+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14461",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MED13 were set to ",
"entity_name": "MED13",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:48:19.038845+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14460",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MED13 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MED13",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:47:56.440823+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14459",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MED13: Rating: GREEN; Mode of pathogenicity: None; Publications: 29740699; Phenotypes: Intellectual developmental disorder, autosomal dominant 61, MIM# 618009; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MED13",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:43:59.382774+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14459",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MECP2 as ready",
"entity_name": "MECP2",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:43:59.367112+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14459",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mecp2 has been classified as Green List (High Evidence).",
"entity_name": "MECP2",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:43:42.248238+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14459",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MECP2 were changed from to Rett syndrome, MIM# 312750; Intellectual developmental disorder, X-linked, syndromic 13, MIM# 300055; Encephalopathy, neonatal severe, MIM# 300673",
"entity_name": "MECP2",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:43:18.080557+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14458",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MECP2 were set to ",
"entity_name": "MECP2",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:42:47.679710+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14457",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MECP2 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "MECP2",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:42:23.948957+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MECP2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Rett syndrome, MIM# 312750, Intellectual developmental disorder, X-linked, syndromic 13, MIM# 300055, Encephalopathy, neonatal severe, MIM# 300673; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)",
"entity_name": "MECP2",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:40:40.574919+10:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MCM9 as ready",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:40:40.562821+10:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mcm9 has been classified as Green List (High Evidence).",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:40:37.731472+10:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MCM9 were changed from Ovarian dysgenesis 4, 616185 to Ovarian dysgenesis 4, MIM#616185",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:40:29.982719+10:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.299",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MCM9 were set to ",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:40:17.718645+10:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.298",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MCM9: Rating: GREEN; Mode of pathogenicity: None; Publications: 25480036, 26771056, 33538981, 33095795; Phenotypes: Ovarian dysgenesis 4, MIM# 616185; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:39:25.325006+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MCM9 as ready",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:39:25.312355+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mcm9 has been classified as Green List (High Evidence).",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:39:14.408006+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MCM9 were changed from to Ovarian dysgenesis 4, MIM# 616185",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:38:48.066953+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14455",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MCM9 were set to ",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:38:16.352870+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14454",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MCM9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:37:54.122970+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MCM9: Rating: GREEN; Mode of pathogenicity: None; Publications: 25480036, 26771056, 33538981, 33095795; Phenotypes: Ovarian dysgenesis 4, MIM# 616185; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MCM9",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:34:47.497925+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MCM8 as ready",
"entity_name": "MCM8",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:34:47.475034+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mcm8 has been classified as Green List (High Evidence).",
"entity_name": "MCM8",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:19:08.784652+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14453",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Phenotypes for gene: ASPN were changed from {Lumbar disc degeneration} MIM#603932; {Osteoarthritis susceptibility 3} MIM#607850 to {Lumbar disc degeneration} MIM#603932; {Osteoarthritis susceptibility 3} MIM#607850",
"entity_name": "ASPN",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:19:08.552111+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14453",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Phenotypes for gene: ASPN were changed from to {Lumbar disc degeneration} MIM#603932; {Osteoarthritis susceptibility 3} MIM#607850",
"entity_name": "ASPN",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:17:35.355002+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14452",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Classified gene: ASPN as Red List (low evidence)",
"entity_name": "ASPN",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:17:35.341978+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14452",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Gene: aspn has been classified as Red List (Low Evidence).",
"entity_name": "ASPN",
"entity_type": "gene"
},
{
"created": "2022-05-18T15:17:21.894361+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14451",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Marked gene: ARV1 as ready",
"entity_name": "ARV1",
"entity_type": "gene"
}
]
}