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{
"count": 220423,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1507",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1505",
"results": [
{
"created": "2020-11-10T20:47:17.059734+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OCLN as ready",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:47:17.039530+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ocln has been classified as Green List (High Evidence).",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:47:13.349339+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5344",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OCLN: Rating: GREEN; Mode of pathogenicity: None; Publications: 20727516, 32240828, 29192239, 28386946; Phenotypes: Pseudo-TORCH syndrome 1, MIM#251290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:44:38.392511+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OCLN were changed from to Pseudo-TORCH syndrome 1, MIM#251290",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:43:56.027885+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OCLN were set to ",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:43:22.766668+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: OCLN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:42:50.357606+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: OCLN: Rating: GREEN; Mode of pathogenicity: None; Publications: 20727516, 32240828, 29192239, 28386946; Phenotypes: Pseudo-TORCH syndrome 1, MIM#251290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:38:12.457411+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ERCC6 as ready",
"entity_name": "ERCC6",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:38:12.446122+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ercc6 has been classified as Green List (High Evidence).",
"entity_name": "ERCC6",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:38:09.230647+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ERCC6 were changed from to Cockayne syndrome, type B, MIM#133540",
"entity_name": "ERCC6",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:37:35.487570+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ERCC6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ERCC6",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:37:00.454956+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ERCC6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Cockayne syndrome, type B, MIM#133540; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ERCC6",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:33:02.378802+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: JAM3 as ready",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:33:02.366882+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jam3 has been classified as Green List (High Evidence).",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:32:51.942391+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: JAM3 were changed from to Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:32:17.251706+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: JAM3 were set to ",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:31:45.908438+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: JAM3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:31:11.537274+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: JAM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23255084, 21109224; Phenotypes: Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:30:24.910867+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5344",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: JAM3 as ready",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:30:24.902703+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5344",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jam3 has been classified as Green List (High Evidence).",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:30:17.114993+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5344",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: JAM3 were changed from to Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:29:58.032002+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5343",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: JAM3 were set to ",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:29:34.576674+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5342",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: JAM3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:29:16.174396+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5341",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: JAM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23255084, 21109224; Phenotypes: Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:28:31.481109+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: JAM3 as ready",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:28:31.470593+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jam3 has been classified as Green List (High Evidence).",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:28:28.809950+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.243",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: JAM3 were changed from to Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:28:01.599576+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: JAM3 were set to ",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:27:24.112201+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.241",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: JAM3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:26:49.500403+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.240",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: JAM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23255084, 21109224; Phenotypes: Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:25:50.162538+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: JAM3 as ready",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:25:50.151145+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: jam3 has been classified as Green List (High Evidence).",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:25:47.267766+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: JAM3 were changed from to Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:25:15.649953+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: JAM3 were set to ",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:24:43.185163+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: JAM3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:24:09.773511+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: JAM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 23255084, 21109224; Phenotypes: Hemorrhagic destruction of the brain, subependymal calcification, and cataracts, MIM# 613730; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "JAM3",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:21:11.901782+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFIH1 as ready",
"entity_name": "IFIH1",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:21:11.889374+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ifih1 has been classified as Green List (High Evidence).",
"entity_name": "IFIH1",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:21:08.075746+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFIH1 were changed from to Aicardi-Goutieres syndrome 7, MIM#615846",
"entity_name": "IFIH1",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:20:35.560582+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: IFIH1 were set to ",
"entity_name": "IFIH1",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:20:06.422725+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: IFIH1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "IFIH1",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:19:30.178069+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: IFIH1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24686847; Phenotypes: Aicardi-Goutieres syndrome 7, MIM#615846; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "IFIH1",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:17:18.655298+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADAR as ready",
"entity_name": "ADAR",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:17:18.647135+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adar has been classified as Green List (High Evidence).",
"entity_name": "ADAR",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:17:14.874266+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADAR were changed from to Aicardi-Goutieres syndrome 6, MIM#615010",
"entity_name": "ADAR",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:16:42.759748+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ADAR were set to ",
"entity_name": "ADAR",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:16:10.687696+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ADAR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADAR",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:15:37.585094+11:00",
"panel_name": "Brain Calcification",
"panel_id": 58,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ADAR: Rating: GREEN; Mode of pathogenicity: None; Publications: 23001123, 24262145; Phenotypes: Aicardi-Goutieres syndrome 6, MIM#615010; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ADAR",
"entity_type": "gene"
},
{
"created": "2020-11-10T20:07:56.698442+11:00",
"panel_name": "Bardet Biedl syndrome",
"panel_id": 53,
"panel_version": "1.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "promoted panel to version 1.0",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-11-10T17:15:47.977918+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: POLE: Changed rating: GREEN",
"entity_name": "POLE",
"entity_type": "gene"
},
{
"created": "2020-11-10T17:15:32.823019+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POLE as ready",
"entity_name": "POLE",
"entity_type": "gene"
},
{
"created": "2020-11-10T17:15:32.817742+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment when marking as ready: The association with microcephaly relates to IMAGE-I syndrome.",
"entity_name": "POLE",
"entity_type": "gene"
},
{
"created": "2020-11-10T17:15:32.780994+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pole has been classified as Green List (High Evidence).",
"entity_name": "POLE",
"entity_type": "gene"
},
{
"created": "2020-11-10T17:15:03.227532+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POLE were changed from FILS syndrome 615139; IMAGE-I syndrome 618336 to IMAGE-I syndrome, MIM# 618336",
"entity_name": "POLE",
"entity_type": "gene"
},
{
"created": "2020-11-10T17:13:42.123058+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.497",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: POLE as Green List (high evidence)",
"entity_name": "POLE",
"entity_type": "gene"
},
{
"created": "2020-11-10T17:13:42.114044+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.497",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pole has been classified as Green List (High Evidence).",
"entity_name": "POLE",
"entity_type": "gene"
},
{
"created": "2020-11-10T12:21:15.217384+11:00",
"panel_name": "Microcephaly",
"panel_id": 138,
"panel_version": "0.496",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "gene: POLE was added\ngene: POLE was added to Microcephaly. Sources: Literature\nMode of inheritance for gene: POLE was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: POLE were set to PMID: 30503519\nPhenotypes for gene: POLE were set to FILS syndrome 615139; IMAGE-I syndrome 618336\nReview for gene: POLE was set to GREEN\nAdded comment: PMID: 30503519 - microcephaly reported in multiple patients with biallelic LOF variants \nSources: Literature",
"entity_name": "POLE",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:18:53.717867+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCKAP1 as ready",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:18:53.705769+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nckap1 has been classified as Green List (High Evidence).",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:18:50.848899+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NCKAP1 were changed from to Intellectual disability; autism",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:18:21.399475+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NCKAP1 were set to ",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:17:09.207588+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NCKAP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:16:37.654405+11:00",
"panel_name": "Autism",
"panel_id": 51,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NCKAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 33157009; Phenotypes: Intellectual disability, autism; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:15:55.569553+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5341",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCKAP1 as ready",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:15:55.558755+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5341",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nckap1 has been classified as Green List (High Evidence).",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:15:48.064053+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5341",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NCKAP1 were changed from to Intellectual disability; autism",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:15:24.951278+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5340",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NCKAP1 were set to ",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:14:58.358643+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5339",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NCKAP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:14:35.916051+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5338",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NCKAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 33157009; Phenotypes: Intellectual disability, autism; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:13:47.565550+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NCKAP1 as ready",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:13:47.545257+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nckap1 has been classified as Green List (High Evidence).",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:13:41.866269+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NCKAP1 were changed from to Intellectual disability; autism",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:12:51.547101+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NCKAP1 were set to ",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:11:15.888788+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NCKAP1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T18:10:22.729354+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.3181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NCKAP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 33157009; Phenotypes: Intellectual disability, autism; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "NCKAP1",
"entity_type": "gene"
},
{
"created": "2020-11-09T17:14:44.280048+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to New South Wales Health Pathology",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-11-09T16:42:05.130205+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ZBTB16 was added\ngene: ZBTB16 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: ZBTB16 was set to Unknown",
"entity_name": "ZBTB16",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:05.077410+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VHL was added\ngene: VHL was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: VHL was set to Unknown",
"entity_name": "VHL",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:05.012582+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TRIM33 was added\ngene: TRIM33 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TRIM33 was set to Unknown",
"entity_name": "TRIM33",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.945609+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TRIM27 was added\ngene: TRIM27 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TRIM27 was set to Unknown",
"entity_name": "TRIM27",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.863950+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TRIM24 was added\ngene: TRIM24 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TRIM24 was set to Unknown",
"entity_name": "TRIM24",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.780045+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TPR was added\ngene: TPR was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TPR was set to Unknown",
"entity_name": "TPR",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.728023+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TP53 was added\ngene: TP53 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TP53 was set to Unknown",
"entity_name": "TP53",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.675274+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TGFBR2 was added\ngene: TGFBR2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TGFBR2 was set to Unknown",
"entity_name": "TGFBR2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.623127+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TFG was added\ngene: TFG was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TFG was set to Unknown",
"entity_name": "TFG",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.570365+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TET2 was added\ngene: TET2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TET2 was set to Unknown",
"entity_name": "TET2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.517968+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TCF12 was added\ngene: TCF12 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TCF12 was set to Unknown",
"entity_name": "TCF12",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.464123+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TBL1XR1 was added\ngene: TBL1XR1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TBL1XR1 was set to Unknown",
"entity_name": "TBL1XR1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.411027+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TAF15 was added\ngene: TAF15 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TAF15 was set to Unknown",
"entity_name": "TAF15",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.360055+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TACC3 was added\ngene: TACC3 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TACC3 was set to Unknown",
"entity_name": "TACC3",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.307708+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TACC1 was added\ngene: TACC1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: TACC1 was set to Unknown",
"entity_name": "TACC1",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.256264+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SUFU was added\ngene: SUFU was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SUFU was set to Unknown",
"entity_name": "SUFU",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.204487+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: STAT5B was added\ngene: STAT5B was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: STAT5B was set to Unknown",
"entity_name": "STAT5B",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.153641+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SRD5A2 was added\ngene: SRD5A2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SRD5A2 was set to Unknown",
"entity_name": "SRD5A2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.102152+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SMAD4 was added\ngene: SMAD4 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SMAD4 was set to Unknown",
"entity_name": "SMAD4",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:04.042418+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SDHD was added\ngene: SDHD was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SDHD was set to Unknown",
"entity_name": "SDHD",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:03.989969+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SDHC was added\ngene: SDHC was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SDHC was set to Unknown",
"entity_name": "SDHC",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:03.933305+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SDHB was added\ngene: SDHB was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SDHB was set to Unknown",
"entity_name": "SDHB",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:03.875822+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SDHAF2 was added\ngene: SDHAF2 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SDHAF2 was set to Unknown",
"entity_name": "SDHAF2",
"entity_type": "gene"
},
{
"created": "2020-11-09T16:42:03.805848+11:00",
"panel_name": "Incidentalome_NSW",
"panel_id": 3437,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SDHA was added\ngene: SDHA was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology\nMode of inheritance for gene: SDHA was set to Unknown",
"entity_name": "SDHA",
"entity_type": "gene"
}
]
}