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{
"count": 220314,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=841",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=839",
"results": [
{
"created": "2022-05-14T17:52:46.483514+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14282",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MXI1 as Red List (low evidence)",
"entity_name": "MXI1",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:52:46.469830+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14282",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mxi1 has been classified as Red List (Low Evidence).",
"entity_name": "MXI1",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:51:48.136379+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14281",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MXI1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "MXI1",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:50:57.015533+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYD88 as ready",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:50:57.004693+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myd88 has been classified as Green List (High Evidence).",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:50:53.684366+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYD88 were changed from to Immunodeficiency 68, MIM# 612260",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:50:21.751747+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYD88 were set to ",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:49:51.306915+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYD88 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:49:20.577614+10:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYD88: Rating: GREEN; Mode of pathogenicity: None; Publications: 18669862, 20538326, 31301515; Phenotypes: Immunodeficiency 68, MIM# 612260; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:48:34.179929+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14281",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYD88 as ready",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:48:34.169624+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14281",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myd88 has been classified as Green List (High Evidence).",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:48:24.627807+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14281",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYD88 were changed from to Immunodeficiency 68, MIM# 612260",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:48:03.889514+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14280",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYD88 were set to ",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:47:41.780815+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14279",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYD88 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T17:47:16.778282+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14278",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYD88: Rating: GREEN; Mode of pathogenicity: None; Publications: 18669862, 20538326, 31301515; Phenotypes: Immunodeficiency 68, MIM# 612260; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYD88",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:46:17.600941+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14278",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYH14 as ready",
"entity_name": "MYH14",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:46:17.587492+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14278",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myh14 has been classified as Green List (High Evidence).",
"entity_name": "MYH14",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:34:00.418985+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14278",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYH14 were changed from to Deafness, autosomal dominant 4A, MIM# 600652; Peripheral neuropathy, myopathy, hoarseness, and hearing loss 614369",
"entity_name": "MYH14",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:33:36.442408+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14277",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYH14 were set to ",
"entity_name": "MYH14",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:33:16.595009+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14276",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYH14 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYH14",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:32:56.235651+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14275",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYH14: Rating: GREEN; Mode of pathogenicity: None; Publications: 15015131, 25719458, 31045651, 28221712, 34681017, 21480433, 31653586, 31631044, 31231018; Phenotypes: Deafness, autosomal dominant 4A, MIM# 600652, Peripheral neuropathy, myopathy, hoarseness, and hearing loss 614369; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "MYH14",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:22:17.566194+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14275",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYH3 as ready",
"entity_name": "MYH3",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:22:17.552517+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14275",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myh3 has been classified as Green List (High Evidence).",
"entity_name": "MYH3",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:22:05.737227+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14275",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYH3 were changed from to Arthrogryposis, distal, type 2A (Freeman-Sheldon) 193700; Arthrogryposis, distal, type 2B3 (Sheldon-Hall) 618436; Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A 178110; Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B 618469",
"entity_name": "MYH3",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:21:38.614398+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14274",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYH3 were set to ",
"entity_name": "MYH3",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:21:16.059091+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14273",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYH3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MYH3",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:20:55.352196+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYH3: Rating: GREEN; Mode of pathogenicity: None; Publications: 25957469, 26544689, 21531865, 18695058; Phenotypes: Arthrogryposis, distal, type 2A (Freeman-Sheldon) 193700, Arthrogryposis, distal, type 2B3 (Sheldon-Hall) 618436, Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A 178110, Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B 618469; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "MYH3",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:19:02.423963+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO1E as ready",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:19:02.406253+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo1e has been classified as Green List (High Evidence).",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:18:57.621111+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYO1E as ready",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:18:57.610306+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: myo1e has been classified as Green List (High Evidence).",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:18:45.240888+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO1E were changed from to Glomerulosclerosis, focal segmental, 6, MIM# 614131",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:18:37.523446+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MYO1E were changed from to Glomerulosclerosis, focal segmental, 6, MIM# 614131",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:18:13.085347+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.199",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO1E were set to ",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:17:40.010433+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYO1E was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:17:06.601274+10:00",
"panel_name": "Proteinuria",
"panel_id": 144,
"panel_version": "0.197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYO1E: Rating: GREEN; Mode of pathogenicity: None; Publications: 21756023, 31520189, 25739341, 23977349; Phenotypes: Glomerulosclerosis, focal segmental, 6, MIM# 614131; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:16:50.961632+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14271",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MYO1E were set to ",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:16:29.926894+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14270",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MYO1E was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:15:49.183583+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MYO1E: Rating: GREEN; Mode of pathogenicity: None; Publications: 21756023, 31520189, 25739341, 23977349; Phenotypes: Glomerulosclerosis, focal segmental, 6, MIM# 614131; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MYO1E",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:10:16.633530+10:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WNT1 as ready",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:10:16.623085+10:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnt1 has been classified as Green List (High Evidence).",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:10:11.697241+10:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WNT1 were changed from to Osteogenesis imperfecta, type XV, MIM# 615220",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:09:42.682536+10:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WNT1 were set to ",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:09:09.167850+10:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WNT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:08:09.507375+10:00",
"panel_name": "Osteogenesis Imperfecta",
"panel_id": 147,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WNT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23499309, 23499310, 23656646, 26671912; Phenotypes: Osteogenesis imperfecta, type XV, MIM# 615220; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:06:20.302420+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WNT1 as ready",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:06:20.293157+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnt1 has been classified as Green List (High Evidence).",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:06:08.641642+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WNT1 were changed from to Osteogenesis imperfecta, type XV, MIM# 615220",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:05:47.973880+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14268",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WNT1 were set to ",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:05:27.612624+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WNT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T13:05:04.861754+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14266",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WNT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23499309, 23499310, 23656646, 26671912; Phenotypes: Osteogenesis imperfecta, type XV, MIM# 615220; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WNT1",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:55:36.178649+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14266",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WNK4 as ready",
"entity_name": "WNK4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:55:36.165719+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14266",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnk4 has been classified as Green List (High Evidence).",
"entity_name": "WNK4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:55:27.563344+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14266",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WNK4 were changed from to Pseudohypoaldosteronism, type IIB, MIM# 614491",
"entity_name": "WNK4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:55:00.307922+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WNK4 were set to ",
"entity_name": "WNK4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:54:38.982322+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WNK4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WNK4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:54:18.971383+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14263",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WNK4: Rating: GREEN; Mode of pathogenicity: None; Publications: 22266938, 31044551; Phenotypes: Pseudohypoaldosteronism, type IIB, MIM# 614491; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WNK4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:52:42.635483+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14263",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WNK1 as ready",
"entity_name": "WNK1",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:52:42.625930+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14263",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wnk1 has been classified as Green List (High Evidence).",
"entity_name": "WNK1",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:52:33.836726+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14263",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WNK1 were changed from to Neuropathy, hereditary sensory and autonomic, type II, MIM# 201300; MONDO:0024309; Pseudohypoaldosteronism, type IIC, MIM# 614492",
"entity_name": "WNK1",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:52:12.345363+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WNK1 were set to ",
"entity_name": "WNK1",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:51:48.358683+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WNK1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "WNK1",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:51:04.998740+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Well established gene-disease association.\r\n\r\nNote mono-allelic variants are associated with pseudohypoaldosteronism; to: Well established gene-disease associations.\r\n",
"entity_name": "WNK1",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:44:32.971139+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: WNK1: Changed phenotypes: Neuropathy, hereditary sensory and autonomic, type II, MIM# 201300, MONDO:0024309, Pseudohypoaldosteronism, type IIC, MIM# 614492; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "WNK1",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:42:24.398585+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR4 as ready",
"entity_name": "WDR4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:42:24.375033+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr4 has been classified as Green List (High Evidence).",
"entity_name": "WDR4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:42:13.897733+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR4 were changed from to Galloway-Mowat syndrome 6, OMIM #618347; Microcephaly, growth deficiency, seizures, and brain malformations, OMIM #618346",
"entity_name": "WDR4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:36:13.201254+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14259",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDR4 were set to ",
"entity_name": "WDR4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:35:52.901269+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14258",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:35:25.171934+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14257",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WDR4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26416026, 30079490, 29597095, 28617965; Phenotypes: Galloway-Mowat syndrome 6, OMIM #618347, Microcephaly, growth deficiency, seizures, and brain malformations, OMIM #618346; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WDR4",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:32:33.601331+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14257",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: WDR36 as Amber List (moderate evidence)",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:32:33.590029+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14257",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr36 has been classified as Amber List (Moderate Evidence).",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:32:10.619586+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Multiple individuals reported.\r\n\r\nHowever, note one of the earliest reported variants p.Asp658Gly is present in >1,000 individuals in gnomad, and another, p.Ala449Thr is present in >2000.; to: Multiple individuals reported. Adult-onset.\r\n\r\nHowever, note one of the earliest reported variants p.Asp658Gly is present in >1,000 individuals in gnomad, and another, p.Ala449Thr is present in >2000.",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:31:59.362816+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: WDR36: Changed rating: AMBER",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:31:00.644437+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: WDR36: Changed publications: 15677485, 18172102, 20813748, 34681019, 29540704",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:28:23.952286+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Multiple individuals reported.\r\n\r\nHowever, note one of the earliest reported variants p.Asp658Gly is present in >1,000 individuals in gnomad.; to: Multiple individuals reported.\r\n\r\nHowever, note one of the earliest reported variants p.Asp658Gly is present in >1,000 individuals in gnomad, and another, p.Ala449Thr is present in >2000.",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:26:32.739591+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR36 as ready",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:26:32.728351+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr36 has been classified as Green List (High Evidence).",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:26:24.390820+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14256",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR36 were changed from to Glaucoma 1, open angle, G, MIM# 609887",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:26:04.048540+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14255",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WDR36 were set to ",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:25:44.115099+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14254",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WDR36 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:25:23.022838+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14253",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WDR36: Rating: GREEN; Mode of pathogenicity: None; Publications: 15677485, 18172102, 20813748; Phenotypes: Glaucoma 1, open angle, G, MIM# 609887; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WDR36",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:21:27.703668+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14253",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WASHC5 as ready",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:21:27.692401+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14253",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: washc5 has been classified as Green List (High Evidence).",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:21:19.402983+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14253",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WASHC5 were changed from to Ritscher-Schinzel syndrome 1, MIM# 220210; Spastic paraplegia 8, autosomal dominant, MIM# 603563",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:20:50.865641+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14252",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WASHC5 were set to ",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:20:25.472610+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14251",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WASHC5 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-05-14T12:19:54.998917+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WASHC5: Rating: GREEN; Mode of pathogenicity: None; Publications: 17160902, 23455931, 30778698, 24065355, 33456446; Phenotypes: Ritscher-Schinzel syndrome 1, MIM# 220210, Spastic paraplegia 8, autosomal dominant, MIM# 603563; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "WASHC5",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:11:26.048973+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WASF1 were changed from to Neurodevelopmental disorder with absent language and variable seizures , MIM#618707",
"entity_name": "WASF1",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:10:52.531457+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4769",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WASF1 were set to PMID: 29961568",
"entity_name": "WASF1",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:10:13.207745+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WASF1 as ready",
"entity_name": "WASF1",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:10:13.196077+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wasf1 has been classified as Green List (High Evidence).",
"entity_name": "WASF1",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:10:03.070252+10:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4768",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WASF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 29961568, 34845217, 34478686, 34356165; Phenotypes: Neurodevelopmental disorder with absent language and variable seizures , MIM#618707; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WASF1",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:09:57.331269+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14250",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WASF1 were changed from to Neurodevelopmental disorder with absent language and variable seizures , MIM#618707",
"entity_name": "WASF1",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:09:39.060767+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14249",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WASF1 were set to ",
"entity_name": "WASF1",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:09:11.239556+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14248",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WASF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WASF1",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:08:52.275412+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WASF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 29961568, 34845217, 34478686, 34356165; Phenotypes: Neurodevelopmental disorder with absent language and variable seizures , MIM#618707; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "WASF1",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:05:59.013111+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WAC as ready",
"entity_name": "WAC",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:05:58.999994+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wac has been classified as Green List (High Evidence).",
"entity_name": "WAC",
"entity_type": "gene"
},
{
"created": "2022-05-13T19:05:49.916138+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14247",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WAC were changed from to Desanto-Shinawi syndrome, MIM# 616708",
"entity_name": "WAC",
"entity_type": "gene"
}
]
}