HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=935",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=933",
"results": [
{
"created": "2022-03-16T18:28:31.775470+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndst1 has been classified as Green List (High Evidence).",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:28:22.975235+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11456",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDST1 were changed from to Mental retardation, autosomal recessive 46 - MIM#616116",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:27:52.548629+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11455",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDST1 were set to ",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:27:28.044324+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11454",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDST1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:25:42.304874+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4575",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDST1 as ready",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:25:42.294128+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4575",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndst1 has been classified as Green List (High Evidence).",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:25:23.616145+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4575",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDST1 were changed from to Mental retardation, autosomal recessive 46 - MIM#616116",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:24:48.881654+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4574",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDST1 were set to ",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:24:03.584073+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4573",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NDST1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:23:18.203064+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDST1 as ready",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:23:18.193461+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndst1 has been classified as Green List (High Evidence).",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:23:15.087955+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDST1 as Green List (high evidence)",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:23:15.078608+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndst1 has been classified as Green List (High Evidence).",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:21:41.932155+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NDST1 as Green List (high evidence)",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:21:41.922359+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndst1 has been classified as Green List (High Evidence).",
"entity_name": "NDST1",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:20:08.983640+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCR3 as ready",
"entity_name": "NCR3",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:20:08.972552+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncr3 has been classified as Red List (Low Evidence).",
"entity_name": "NCR3",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:19:59.031123+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NCR3 as Red List (low evidence)",
"entity_name": "NCR3",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:19:59.021984+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11453",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncr3 has been classified as Red List (Low Evidence).",
"entity_name": "NCR3",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:18:53.649605+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11452",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCOA4 as ready",
"entity_name": "NCOA4",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:18:53.638458+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11452",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncoa4 has been classified as Red List (Low Evidence).",
"entity_name": "NCOA4",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:18:43.775293+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11452",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NCOA4 as Red List (low evidence)",
"entity_name": "NCOA4",
"entity_type": "gene"
},
{
"created": "2022-03-16T18:18:43.764585+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11452",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncoa4 has been classified as Red List (Low Evidence).",
"entity_name": "NCOA4",
"entity_type": "gene"
},
{
"created": "2022-03-16T17:21:21.969772+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11451",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCF4 as ready",
"entity_name": "NCF4",
"entity_type": "gene"
},
{
"created": "2022-03-16T17:21:21.959477+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11451",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncf4 has been classified as Green List (High Evidence).",
"entity_name": "NCF4",
"entity_type": "gene"
},
{
"created": "2022-03-16T17:20:31.071812+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11451",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NCF4 were changed from to Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III MIM#613960",
"entity_name": "NCF4",
"entity_type": "gene"
},
{
"created": "2022-03-16T17:20:08.878797+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11450",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NCF4 were set to ",
"entity_name": "NCF4",
"entity_type": "gene"
},
{
"created": "2022-03-16T17:19:45.839244+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11449",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NCF4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NCF4",
"entity_type": "gene"
},
{
"created": "2022-03-16T17:15:16.606521+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCF2 as ready",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-03-16T17:15:16.588205+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncf2 has been classified as Green List (High Evidence).",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-03-16T17:11:30.344558+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.70",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NCF2 were changed from to Chronic granulomatous disease 2, autosomal recessive, MIM# 233710",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-03-16T17:10:56.199765+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.69",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NCF2 were set to ",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-03-16T17:07:40.416266+11:00",
"panel_name": "Inflammatory bowel disease",
"panel_id": 123,
"panel_version": "0.68",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NCF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:56:14.876261+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11448",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCF2 as ready",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:56:14.865263+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11448",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ncf2 has been classified as Green List (High Evidence).",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:54:30.807256+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11448",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NCF2 were changed from to Chronic granulomatous disease 2, autosomal recessive, MIM# 233710",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:54:08.975819+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11447",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NCF2 were set to ",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:53:48.867345+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11446",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NCF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NCF2",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:52:48.731957+11:00",
"panel_name": "Amelogenesis imperfecta",
"panel_id": 3564,
"panel_version": "1.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DSPP as ready",
"entity_name": "DSPP",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:52:48.721305+11:00",
"panel_name": "Amelogenesis imperfecta",
"panel_id": 3564,
"panel_version": "1.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dspp has been classified as Green List (High Evidence).",
"entity_name": "DSPP",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:52:08.184067+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SALL4 as ready",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:52:08.171174+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sall4 has been classified as Green List (High Evidence).",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:51:58.363904+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11445",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SALL4 were changed from to Duane-radial ray syndrome, MIM# 607323; MONDO:0011812; IVIC syndrome, MIM# 147750; MONDO:0007836",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:51:35.926069+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11444",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SALL4 were set to ",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:44:44.702209+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11443",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SALL4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:44:22.019411+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SALL4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Duane-radial ray syndrome, MIM# 607323, MONDO:0011812, IVIC syndrome, MIM# 147750, MONDO:0007836; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SALL4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:39:14.890077+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TYROBP as ready",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:39:14.879632+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tyrobp has been classified as Green List (High Evidence).",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:38:59.884781+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11442",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TYROBP were changed from to Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, MIM# 221770",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:38:29.868655+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11441",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TYROBP were set to ",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:37:36.665131+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11440",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TYROBP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:37:12.785333+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11439",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TYROBP: Rating: GREEN; Mode of pathogenicity: None; Publications: 10888890, 12370476, 27904822; Phenotypes: Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, MIM# 221770; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TYROBP",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:32:08.316336+11:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IRAK4 as ready",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:32:08.306275+11:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: irak4 has been classified as Green List (High Evidence).",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:30:26.985361+11:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IRAK4 were changed from to Immunodeficiency 67, MIM# 607676",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:29:48.231029+11:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IRAK4 were set to ",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:29:18.503365+11:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IRAK4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:28:47.373451+11:00",
"panel_name": "Defects of innate immunity",
"panel_id": 231,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IRAK4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26825884, 17878374, 17544092, 16950813; Phenotypes: Immunodeficiency 67, MIM# 607676; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:28:00.964830+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11439",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IRAK4 as ready",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:28:00.951680+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11439",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: irak4 has been classified as Green List (High Evidence).",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:27:52.422213+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11439",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IRAK4 were changed from to Immunodeficiency 67, MIM# 607676",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:27:29.913964+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11438",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IRAK4 were set to ",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:26:44.186387+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11437",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IRAK4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:26:25.971277+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IRAK4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26825884, 17878374, 17544092, 16950813; Phenotypes: Immunodeficiency 67, MIM# 607676; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IRAK4",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:24:40.551625+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11436",
"user_name": "Manny Jacobs",
"item_type": "entity",
"text": "reviewed gene: TYK2: Rating: GREEN; Mode of pathogenicity: None; Publications: 17088085, 17521577, 26304966; Phenotypes: # 611521 IMMUNODEFICIENCY 35; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TYK2",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:23:22.261378+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: INSR as ready",
"entity_name": "INSR",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:23:22.247243+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: insr has been classified as Green List (High Evidence).",
"entity_name": "INSR",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:22:36.397195+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11436",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: INSR were changed from to Hyperinsulinemic hypoglycemia, familial, 5, MIM# 609968; Leprechaunism, MIM# 246200; Rabson-Mendenhall syndrome, MIM# 262190",
"entity_name": "INSR",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:22:15.223541+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11435",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: INSR were set to ",
"entity_name": "INSR",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:21:56.530601+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11434",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: INSR was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "INSR",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:21:35.700493+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: INSR: Rating: GREEN; Mode of pathogenicity: None; Publications: 34965699; Phenotypes: Hyperinsulinemic hypoglycemia, familial, 5, MIM# 609968, Leprechaunism, MIM# 246200, Rabson-Mendenhall syndrome, MIM# 262190; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "INSR",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:17:54.326718+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: INS as ready",
"entity_name": "INS",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:17:54.316517+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ins has been classified as Green List (High Evidence).",
"entity_name": "INS",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:17:40.134945+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11433",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: INS were changed from to Diabetes mellitus, insulin-dependent, 2, MIM# 125852; Diabetes mellitus, permanent neonatal 4, MIM# 618858; Maturity-onset diabetes of the young, type 10, MIM# 613370",
"entity_name": "INS",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:17:17.617111+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11432",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: INS were set to ",
"entity_name": "INS",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:16:55.622731+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11431",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: INS was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "INS",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:16:37.186488+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: INS: Rating: GREEN; Mode of pathogenicity: None; Publications: 18162506; Phenotypes: Diabetes mellitus, insulin-dependent, 2, MIM# 125852, Diabetes mellitus, permanent neonatal 4, MIM# 618858, Maturity-onset diabetes of the young, type 10, MIM# 613370; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "INS",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:14:08.784277+11:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: INO80 as ready",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:14:08.772710+11:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ino80 has been classified as Amber List (Moderate Evidence).",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:13:58.036083+11:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: INO80 were changed from to Primary immunodeficiency, MONDO:0003778",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:13:28.745043+11:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: INO80 were set to ",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:12:49.530355+11:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: INO80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:10:03.355866+11:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: INO80 as Amber List (moderate evidence)",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:10:03.341836+11:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ino80 has been classified as Amber List (Moderate Evidence).",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:09:02.390766+11:00",
"panel_name": "Predominantly Antibody Deficiency",
"panel_id": 222,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: INO80: Rating: AMBER; Mode of pathogenicity: None; Publications: 25312759; Phenotypes: Primary immunodeficiency, MONDO:0003778; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:08:39.572351+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: INO80 as ready",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:08:39.562392+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ino80 has been classified as Amber List (Moderate Evidence).",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:08:25.784066+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: INO80 were changed from to Primary immunodeficiency, MONDO:0003778",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:08:00.529250+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11429",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: INO80 were set to ",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:07:39.052860+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11428",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: INO80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:07:20.535100+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: INO80 as Amber List (moderate evidence)",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:07:20.523640+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11427",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ino80 has been classified as Amber List (Moderate Evidence).",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:07:17.361803+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11426",
"user_name": "Manny Jacobs",
"item_type": "entity",
"text": "reviewed gene: TYMP: Rating: GREEN; Mode of pathogenicity: None; Publications: 21933806; Phenotypes: # 603041 MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TYMP",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:06:56.549791+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: INO80: Rating: AMBER; Mode of pathogenicity: None; Publications: 25312759; Phenotypes: Primary immunodeficiency, MONDO:0003778; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "INO80",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:02:29.657327+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IMPAD1 as ready",
"entity_name": "IMPAD1",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:02:29.647611+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: impad1 has been classified as Green List (High Evidence).",
"entity_name": "IMPAD1",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:02:12.409327+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11426",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IMPAD1 were changed from to Chondrodysplasia with joint dislocations, GPAPP type MIM#614078",
"entity_name": "IMPAD1",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:01:45.137245+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11425",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IMPAD1 were set to ",
"entity_name": "IMPAD1",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:01:24.343186+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11424",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IMPAD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "IMPAD1",
"entity_type": "gene"
},
{
"created": "2022-03-16T16:01:02.161695+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11423",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Deleted their review",
"entity_name": "IMPAD1",
"entity_type": "gene"
}
]
}