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{
"count": 220864,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1960",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1958",
"results": [
{
"created": "2020-01-26T20:39:09.548209+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1696",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC39A8 were changed from Congenital disorder of glycosylation, type IIn , MIM#16721 to Congenital disorder of glycosylation, type IIn , MIM#16721",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:38:48.125392+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1695",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC39A8 as ready",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:38:48.117097+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1695",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc39a8 has been classified as Green List (High Evidence).",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:38:42.022131+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: STT3B as Red List (low evidence)",
"entity_name": "STT3B",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:38:40.664746+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.27",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stt3b has been classified as Red List (Low Evidence).",
"entity_name": "STT3B",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:37:54.478389+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STT3B: Rating: RED; Mode of pathogenicity: None; Publications: 23842455; Phenotypes: Congenital disorder of glycosylation, type Ix 615597; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STT3B",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:35:26.564764+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC39A8 as ready",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:35:26.557210+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc39a8 has been classified as Green List (High Evidence).",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:33:59.463943+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.547",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC39A8 as ready",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:33:59.457208+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.547",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc39a8 has been classified as Green List (High Evidence).",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:32:13.318353+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.963",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC39A8 were changed from to Congenital disorder of glycosylation, type IIn , MIM#16721",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:32:12.523826+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.547",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC39A8 as Green List (high evidence)",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:32:12.515653+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.547",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc39a8 has been classified as Green List (High Evidence).",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:31:50.449688+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.962",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC39A8 were set to ",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:31:11.379078+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.961",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC39A8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:31:09.586159+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.546",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC39A8 was added\ngene: SLC39A8 was added to Genetic Epilepsy. Sources: Expert Review\nMode of inheritance for gene: SLC39A8 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC39A8 were set to 26637978; 26637979\nPhenotypes for gene: SLC39A8 were set to Congenital disorder of glycosylation, type IIn , MIM#16721\nReview for gene: SLC39A8 was set to GREEN\nAdded comment: 6 individuals from Hutterite descent and two other unrelated families reported. Seizures reported in 2 Hutterite individuals and also in the other two unrelated families. \nSources: Expert Review",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:28:59.453809+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.545",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services; Rare Disease",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-26T20:28:53.725621+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC39A8 as ready",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:28:53.717105+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc39a8 has been classified as Green List (High Evidence).",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:28:40.130208+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC39A8 as Green List (high evidence)",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:28:39.922040+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.26",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc39a8 has been classified as Green List (High Evidence).",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:28:14.026421+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1695",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC39A8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:27:52.409677+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.25",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC39A8 was added\ngene: SLC39A8 was added to Congenital Disorders of Glycosylation. Sources: Expert Review\nMode of inheritance for gene: SLC39A8 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC39A8 were set to 26637978; 26637979\nPhenotypes for gene: SLC39A8 were set to Congenital disorder of glycosylation, type IIn , MIM#16721\nReview for gene: SLC39A8 was set to GREEN\ngene: SLC39A8 was marked as current diagnostic\nAdded comment: 6 individuals from Hutterite descent and two other unrelated families reported. \nSources: Expert Review",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:27:40.137731+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1694",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC39A8 were changed from to Congenital disorder of glycosylation, type IIn , MIM#16721",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:26:48.776966+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1694",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC39A8 were set to ",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:24:56.191081+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1693",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC39A8: Rating: GREEN; Mode of pathogenicity: None; Publications: 26637978, 26637979; Phenotypes: Congenital disorder of glycosylation, type IIn , MIM#16721; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC39A8",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:22:02.060478+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.544",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC35A3 as ready",
"entity_name": "SLC35A3",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:22:02.052608+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.544",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc35a3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SLC35A3",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:21:35.265483+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.544",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC35A3 as Amber List (moderate evidence)",
"entity_name": "SLC35A3",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:21:35.258418+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.544",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc35a3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SLC35A3",
"entity_type": "gene"
},
{
"created": "2020-01-26T20:20:32.833261+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.543",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC35A3 was added\ngene: SLC35A3 was added to Genetic Epilepsy. Sources: Expert Review\nMode of inheritance for gene: SLC35A3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC35A3 were set to 28328131; 24031089; 28777481\nPhenotypes for gene: SLC35A3 were set to Arthrogryposis, mental retardation, and seizures; OMIM #615553\nReview for gene: SLC35A3 was set to AMBER\nAdded comment: Three families reported; seizures in two. \nSources: Expert Review",
"entity_name": "SLC35A3",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:53:39.479677+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.542",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC35A1 as ready",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:53:39.469302+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.542",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc35a1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:53:17.596535+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC35A1 as ready",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:53:17.589591+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc35a1 has been classified as Green List (High Evidence).",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:51:33.061278+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGM1 as ready",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:51:33.052761+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgm1 has been classified as Green List (High Evidence).",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:49:23.556698+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.24",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PGM1 were changed from to Congenital disorder of glycosylation, type It 614921",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:49:00.915640+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.542",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SLC35A1 as Amber List (moderate evidence)",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:49:00.136631+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.542",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc35a1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:47:57.467281+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.541",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SLC35A1 was added\ngene: SLC35A1 was added to Genetic Epilepsy. Sources: Expert Review\nMode of inheritance for gene: SLC35A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SLC35A1 were set to 28856833; 23873973; 11157507\nPhenotypes for gene: SLC35A1 were set to Congenital disorder of glycosylation, type IIf, MIM# 603585\nReview for gene: SLC35A1 was set to AMBER\nAdded comment: Three unrelated families reported, neurological presentation including seizures in two. \nSources: Expert Review",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:47:03.797321+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC35A1 were changed from to Congenital disorder of glycosylation, type IIf, MIM# 603585",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:45:51.471636+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC35A1 were set to ",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:45:36.841049+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1693",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGS as ready",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:45:36.832290+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1693",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigs has been classified as Green List (High Evidence).",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:45:16.012352+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC35A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:44:33.213436+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SLC35A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28856833, 23873973, 11157507; Phenotypes: Congenital disorder of glycosylation, type IIf, MIM# 603585; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC35A1",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:38:09.975897+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.540",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGS as ready",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:38:09.967143+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.540",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigs has been classified as Green List (High Evidence).",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:37:02.297822+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1693",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PIGS as Green List (high evidence)",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:37:02.290673+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1693",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigs has been classified as Green List (High Evidence).",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:35:59.942532+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1692",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PIGS was added\ngene: PIGS was added to Intellectual disability syndromic and non-syndromic. Sources: Expert Review\nMode of inheritance for gene: PIGS was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PIGS were set to 30269814\nPhenotypes for gene: PIGS were set to Glycosylphosphatidylinositol biosynthesis defect 18, MIM#\t618143\nReview for gene: PIGS was set to GREEN\nAdded comment: Three unrelated families reported. Severe neurological phenotype ranging from fetal akinesia to ID/EE. \nSources: Expert Review",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:34:40.261173+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.540",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PIGS as Green List (high evidence)",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:34:40.254501+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.540",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigs has been classified as Green List (High Evidence).",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:33:01.172755+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PIGS was added\ngene: PIGS was added to Genetic Epilepsy. Sources: Expert Review\nMode of inheritance for gene: PIGS was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PIGS were set to 30269814\nPhenotypes for gene: PIGS were set to Glycosylphosphatidylinositol biosynthesis defect 18\t618143\nReview for gene: PIGS was set to GREEN\nAdded comment: Three unrelated families reported. Severe neurological phenotype ranging from fetal akinesia to ID/EE. \nSources: Expert Review",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:32:46.910254+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGS as ready",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:32:46.902294+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigs has been classified as Green List (High Evidence).",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:32:01.901210+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PIGS as Green List (high evidence)",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:32:01.892900+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.960",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigs has been classified as Green List (High Evidence).",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:30:57.362870+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGS as ready",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:30:57.356141+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigs has been classified as Green List (High Evidence).",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:30:42.076130+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.959",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PIGS was added\ngene: PIGS was added to Mendeliome. Sources: Expert Review\nMode of inheritance for gene: PIGS was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PIGS were set to 30269814\nPhenotypes for gene: PIGS were set to Glycosylphosphatidylinositol biosynthesis defect 18\t618143\nReview for gene: PIGS was set to GREEN\nAdded comment: Three unrelated families reported. Severe neurological phenotype ranging from fetal akinesia to ID/EE \nSources: Expert Review",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:30:41.646294+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PIGS as Green List (high evidence)",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:30:41.637328+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigs has been classified as Green List (High Evidence).",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T19:28:24.053544+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PIGS was added\ngene: PIGS was added to Congenital Disorders of Glycosylation. Sources: Expert Review\nMode of inheritance for gene: PIGS was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PIGS were set to 30269814,\nPhenotypes for gene: PIGS were set to Glycosylphosphatidylinositol biosynthesis defect 18\t618143\nReview for gene: PIGS was set to GREEN\nAdded comment: Three unrelated families reported. Severe neurological phenotype ranging from fetal akinesia to ID/EE. \nSources: Expert Review",
"entity_name": "PIGS",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:31:09.576998+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PGM1 were set to ",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:30:28.347036+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PGM1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:30:25.157647+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1691",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FUK as ready",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:30:25.149053+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1691",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fuk has been classified as Amber List (Moderate Evidence).",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:29:43.572229+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PGM1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24499211; Phenotypes: Congenital disorder of glycosylation, type It 614921; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PGM1",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:28:38.834763+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1691",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FUK as Amber List (moderate evidence)",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:28:38.828125+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1691",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fuk has been classified as Amber List (Moderate Evidence).",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:27:27.157040+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1690",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FUK was added\ngene: FUK was added to Intellectual disability syndromic and non-syndromic. Sources: Literature\nMode of inheritance for gene: FUK was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FUK were set to 30503518\nPhenotypes for gene: FUK were set to Congenital disorder of glycosylation with defective fucosylation 2, MIM# 618324\nReview for gene: FUK was set to AMBER\nAdded comment: Two unrelated individuals reported. \nSources: Literature",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:26:39.746563+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FUK as ready",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:26:39.739654+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fuk has been classified as Amber List (Moderate Evidence).",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:25:46.736859+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FUK as Amber List (moderate evidence)",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:25:46.729850+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.958",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fuk has been classified as Amber List (Moderate Evidence).",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:25:27.500740+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FUK as ready",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:25:27.493490+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fuk has been classified as Amber List (Moderate Evidence).",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:25:20.984516+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.957",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FUK was added\ngene: FUK was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: FUK was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FUK were set to 30503518\nPhenotypes for gene: FUK were set to Congenital disorder of glycosylation with defective fucosylation 2, MIM# 618324\nReview for gene: FUK was set to AMBER\nAdded comment: Two unrelated individuals reported. \nSources: Literature",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:25:05.227289+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FUK as Amber List (moderate evidence)",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:25:05.220482+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fuk has been classified as Amber List (Moderate Evidence).",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:23:39.974201+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FUK was added\ngene: FUK was added to Genetic Epilepsy. Sources: Literature\nMode of inheritance for gene: FUK was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FUK were set to 30503518\nPhenotypes for gene: FUK were set to Congenital disorder of glycosylation with defective fucosylation 2, MIM# 618324\nReview for gene: FUK was set to AMBER\nAdded comment: Two unrelated individuals reported; seizures prominent part of the clinical presentation in both. \nSources: Literature",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:23:25.020910+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FUK as ready",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:23:25.010731+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fuk has been classified as Amber List (Moderate Evidence).",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:22:53.696276+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FUK as Amber List (moderate evidence)",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:22:53.689034+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fuk has been classified as Amber List (Moderate Evidence).",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:21:31.817911+11:00",
"panel_name": "Congenital Disorders of Glycosylation",
"panel_id": 68,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FUK was added\ngene: FUK was added to Congenital Disorders of Glycosylation. Sources: Literature\nMode of inheritance for gene: FUK was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FUK were set to 30503518\nPhenotypes for gene: FUK were set to Congenital disorder of glycosylation with defective fucosylation 2, MIM#\t618324\nReview for gene: FUK was set to AMBER\nAdded comment: Two unrelated individuals reported. \nSources: Literature",
"entity_name": "FUK",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:13:47.774974+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.536",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR62 as ready",
"entity_name": "WDR62",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:13:47.766957+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.536",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr62 has been classified as Green List (High Evidence).",
"entity_name": "WDR62",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:13:28.612260+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.956",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF142 as ready",
"entity_name": "ZNF142",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:13:28.605076+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.956",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf142 has been classified as Green List (High Evidence).",
"entity_name": "ZNF142",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:13:17.499488+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.956",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF142 as Green List (high evidence)",
"entity_name": "ZNF142",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:13:17.493003+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.956",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf142 has been classified as Green List (High Evidence).",
"entity_name": "ZNF142",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:12:59.278067+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.955",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ZNF142 was added\ngene: ZNF142 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: ZNF142 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ZNF142 were set to 31036918\nPhenotypes for gene: ZNF142 were set to Neurodevelopmental disorder with impaired speech and hyperkinetic movements, MIM#618425\nReview for gene: ZNF142 was set to GREEN\ngene: ZNF142 was marked as current diagnostic\nAdded comment: 7 individuals from 4 unrelated families reported. \nSources: Expert list",
"entity_name": "ZNF142",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:12:33.470132+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1689",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF142 as ready",
"entity_name": "ZNF142",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:12:33.463262+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1689",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf142 has been classified as Green List (High Evidence).",
"entity_name": "ZNF142",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:12:05.684713+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1689",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF142 as Green List (high evidence)",
"entity_name": "ZNF142",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:12:05.677611+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1689",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf142 has been classified as Green List (High Evidence).",
"entity_name": "ZNF142",
"entity_type": "gene"
},
{
"created": "2020-01-26T18:11:15.391703+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.1688",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ZNF142 was added\ngene: ZNF142 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert list\nMode of inheritance for gene: ZNF142 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ZNF142 were set to 31036918\nPhenotypes for gene: ZNF142 were set to Neurodevelopmental disorder with impaired speech and hyperkinetic movements, MIM#618425\nReview for gene: ZNF142 was set to GREEN\ngene: ZNF142 was marked as current diagnostic\nAdded comment: 7 individuals from 4 unrelated families reported. \nSources: Expert list",
"entity_name": "ZNF142",
"entity_type": "gene"
}
]
}