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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=915",
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"results": [
{
"created": "2022-03-26T09:30:04.017583+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11951",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBCK were set to ",
"entity_name": "TBCK",
"entity_type": "gene"
},
{
"created": "2022-03-26T09:29:44.421514+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11950",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBCK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBCK",
"entity_type": "gene"
},
{
"created": "2022-03-26T09:29:26.747412+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11949",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TBCK: Rating: GREEN; Mode of pathogenicity: None; Publications: 27040692, 30103036, 27040691; Phenotypes: Hypotonia, infantile, with psychomotor retardation and characteristic facies 3, MIM# 616900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBCK",
"entity_type": "gene"
},
{
"created": "2022-03-26T09:13:08.417897+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4604",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBC1D23 as ready",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T09:13:08.407307+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4604",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d23 has been classified as Green List (High Evidence).",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T09:13:04.290197+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4604",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBC1D23 were changed from to Pontocerebellar hypoplasia, type 11, MIM# 617695",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T09:12:12.458166+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4603",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBC1D23 were set to ",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T09:11:30.369711+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4602",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBC1D23 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T09:10:56.803758+11:00",
"panel_name": "Intellectual disability syndromic and non-syndromic",
"panel_id": 250,
"panel_version": "0.4601",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TBC1D23: Rating: GREEN; Mode of pathogenicity: None; Publications: 28823707, 28823706; Phenotypes: Pontocerebellar hypoplasia, type 11, MIM# 617695; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:42:20.541788+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11949",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBC1D23 as ready",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:42:20.530663+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11949",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d23 has been classified as Green List (High Evidence).",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:42:11.851898+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11949",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBC1D23 were changed from to Pontocerebellar hypoplasia, type 11, MIM# 617695",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:41:52.173215+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11948",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBC1D23 were set to ",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:41:32.847926+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11947",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBC1D23 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBC1D23",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:40:46.481148+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBC1D1 as ready",
"entity_name": "TBC1D1",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:40:46.469661+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d1 has been classified as Green List (High Evidence).",
"entity_name": "TBC1D1",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:40:38.951473+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11946",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBC1D1 were changed from to CAKUT; Non-syndromic renal or urinary tract malformation, MONDO:0019720",
"entity_name": "TBC1D1",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:40:20.801919+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11945",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBC1D1 were set to ",
"entity_name": "TBC1D1",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:40:00.515574+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11944",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TBC1D1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBC1D1",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:39:39.303154+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TBC1D1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26572137; Phenotypes: CAKUT, Non-syndromic renal or urinary tract malformation, MONDO:0019720; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TBC1D1",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:33:19.966210+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAZ as ready",
"entity_name": "TAZ",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:33:19.952671+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: taz has been classified as Green List (High Evidence).",
"entity_name": "TAZ",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:33:10.215277+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11943",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAZ were changed from to Barth syndrome, MIM# 302060",
"entity_name": "TAZ",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:32:47.589217+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11942",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TAZ was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TAZ",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:32:27.352506+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11941",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TAZ: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Barth syndrome, MIM# 302060; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "TAZ",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:31:28.740805+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11941",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAT were changed from Tyrosinemia, type II, MIM# 276600 to Tyrosinaemia, type II, MIM# 276600",
"entity_name": "TAT",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:31:07.151555+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAT as ready",
"entity_name": "TAT",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:31:07.140139+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tat has been classified as Green List (High Evidence).",
"entity_name": "TAT",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:30:57.161853+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11940",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAT were changed from to Tyrosinemia, type II, MIM# 276600",
"entity_name": "TAT",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:30:37.160730+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11939",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAT",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:29:44.637919+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11938",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAS2R38 as ready",
"entity_name": "TAS2R38",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:29:44.626715+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11938",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tas2r38 has been classified as Red List (Low Evidence).",
"entity_name": "TAS2R38",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:25:12.898531+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11938",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAS2R38 were changed from to [Phenylthiocarbamide tasting] 171200",
"entity_name": "TAS2R38",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:24:52.356517+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11937",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TAS2R38 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TAS2R38",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:23:42.557041+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TAS2R38 as Red List (low evidence)",
"entity_name": "TAS2R38",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:23:42.544752+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11936",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tas2r38 has been classified as Red List (Low Evidence).",
"entity_name": "TAS2R38",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:23:23.704662+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11935",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TAS2R38: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: [Phenylthiocarbamide tasting] 171200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TAS2R38",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:22:32.757450+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11935",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAS2R16 as ready",
"entity_name": "TAS2R16",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:22:32.746574+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11935",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tas2r16 has been classified as Red List (Low Evidence).",
"entity_name": "TAS2R16",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:22:23.460353+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11935",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAS2R16 were changed from to [Beta-glycopyranoside tasting], (3) {Alcohol dependence, susceptibility to} 617956",
"entity_name": "TAS2R16",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:22:03.533806+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11934",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TAS2R16 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TAS2R16",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:21:45.293968+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TAS2R16 as Red List (low evidence)",
"entity_name": "TAS2R16",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:21:45.282615+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11933",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tas2r16 has been classified as Red List (Low Evidence).",
"entity_name": "TAS2R16",
"entity_type": "gene"
},
{
"created": "2022-03-26T08:21:26.996309+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11932",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TAS2R16: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: [Beta-glycopyranoside tasting], (3) {Alcohol dependence, susceptibility to} 617956; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TAS2R16",
"entity_type": "gene"
},
{
"created": "2022-03-25T23:21:54.109915+11:00",
"panel_name": "Leukodystrophy - paediatric",
"panel_id": 298,
"panel_version": "0.246",
"user_name": "Arina Puzriakova",
"item_type": "entity",
"text": "reviewed gene: ACER3: Rating: GREEN; Mode of pathogenicity: None; Publications: 34281620; Phenotypes: Leukodystrophy, progressive, early childhood-onset, OMIM:617762; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ACER3",
"entity_type": "gene"
},
{
"created": "2022-03-25T18:57:01.827333+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11932",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TANGO2 as ready",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-03-25T18:57:01.815011+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11932",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tango2 has been classified as Green List (High Evidence).",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-03-25T18:56:53.999109+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11932",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TANGO2 were changed from to Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration, MIM# 616878",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-03-25T18:56:35.723955+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11931",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TANGO2 were set to ",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-03-25T18:56:12.664905+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11930",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TANGO2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:31:42.854789+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11929",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TANGO2: Rating: GREEN; Mode of pathogenicity: None; Publications: 26805782, 30245509; Phenotypes: Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration, MIM# 616878; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TANGO2",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:29:13.374812+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11929",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TACR3 as ready",
"entity_name": "TACR3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:29:13.364902+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11929",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tacr3 has been classified as Green List (High Evidence).",
"entity_name": "TACR3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:29:04.991812+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11929",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TACR3 were changed from to Hypogonadotropic hypogonadism 11 with or without anosmia, MIM# 614840",
"entity_name": "TACR3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:28:43.333362+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11928",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TACR3 were set to ",
"entity_name": "TACR3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:28:23.154355+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11927",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TACR3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TACR3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:28:00.338417+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11926",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TACR3: Rating: GREEN; Mode of pathogenicity: None; Publications: 20332248, 19079066; Phenotypes: Hypogonadotropic hypogonadism 11 with or without anosmia, MIM# 614840; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TACR3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:24:28.279349+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11926",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAC3 as ready",
"entity_name": "TAC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:24:28.267736+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11926",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tac3 has been classified as Green List (High Evidence).",
"entity_name": "TAC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:24:19.117015+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11926",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAC3 were changed from to Hypogonadotropic hypogonadism 10 with or without anosmia, MIM# 614839",
"entity_name": "TAC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:22:17.148007+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11925",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TAC3 were set to ",
"entity_name": "TAC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:21:57.053909+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11924",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TAC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:21:38.150217+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11923",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TAC3: Rating: GREEN; Mode of pathogenicity: None; Publications: 19079066, 20332248, 23329188, 22031817; Phenotypes: Hypogonadotropic hypogonadism 10 with or without anosmia, MIM# 614839; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TAC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:19:51.571111+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11923",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: T as ready",
"entity_name": "T",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:19:51.558097+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11923",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: t has been classified as Red List (Low Evidence).",
"entity_name": "T",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:18:25.727710+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11923",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: T were changed from to Sacral agenesis with vertebral anomalies, MIM# 615709",
"entity_name": "T",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:18:02.319693+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11922",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: T were set to ",
"entity_name": "T",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:17:42.661174+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11921",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: T was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "T",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:17:23.013098+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11920",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: T as Red List (low evidence)",
"entity_name": "T",
"entity_type": "gene"
},
{
"created": "2022-03-25T15:17:23.001264+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11920",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: t has been classified as Red List (Low Evidence).",
"entity_name": "T",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:56:52.624942+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11919",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: T: Rating: RED; Mode of pathogenicity: None; Publications: 24253444, 28116192; Phenotypes: Sacral agenesis with vertebral anomalies 615709; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "T",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:52:18.530906+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11919",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAT were set to ",
"entity_name": "LAT",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:51:27.911472+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EPHB4 as ready",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:51:27.900498+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ephb4 has been classified as Green List (High Evidence).",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:16:29.944101+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.238",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EPHB4 were changed from to Lymphatic malformation 7 (MIM#617300), AD",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:15:56.842892+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.237",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EPHB4 were set to ",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:15:03.323133+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.236",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EPHB4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EPHB4",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:14:03.232068+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GUSB as ready",
"entity_name": "GUSB",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:14:03.220802+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gusb has been classified as Green List (High Evidence).",
"entity_name": "GUSB",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:13:54.176832+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GUSB were changed from to Mucopolysaccharidosis VII, MIM# 253220; MONDO:0009662",
"entity_name": "GUSB",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:13:31.588795+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.234",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GUSB were set to ",
"entity_name": "GUSB",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:12:58.891907+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GUSB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GUSB",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:12:28.845707+11:00",
"panel_name": "Hydrops fetalis",
"panel_id": 116,
"panel_version": "0.232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GUSB: Rating: GREEN; Mode of pathogenicity: None; Publications: 34302381; Phenotypes: Mucopolysaccharidosis VII, MIM# 253220, MONDO:0009662; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GUSB",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:10:40.367345+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11918",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TCF20 were set to 30739909; 30819258; 25228304",
"entity_name": "TCF20",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:08:46.192899+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11917",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAS1L were set to 25644381; 34653234; 26358559",
"entity_name": "LAS1L",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:07:06.874569+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11916",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: LAS1L: Changed rating: GREEN; Changed phenotypes: Wilson-Turner syndrome, MIM# 309585, congenital lethal motor neuron disease",
"entity_name": "LAS1L",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:06:17.806229+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11916",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LARGE1 were set to ",
"entity_name": "LARGE1",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:05:53.123142+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11915",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LARGE1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LARGE1",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:05:10.474177+11:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMC3 as ready",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:05:10.459974+11:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamc3 has been classified as Green List (High Evidence).",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:05:07.605851+11:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LAMC3 were changed from to Cortical malformations, occipital, MIM#614115",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:03:54.964492+11:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAMC3 were set to ",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:03:23.784439+11:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: LAMC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:02:53.785532+11:00",
"panel_name": "Polymicrogyria and Schizencephaly",
"panel_id": 18,
"panel_version": "0.172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: LAMC3: Rating: GREEN; Mode of pathogenicity: None; Publications: 21572413, 34354730; Phenotypes: Cortical malformations, occipital, MIM#614115; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:02:37.590867+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11914",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LAMC3 were changed from to Cortical malformations, occipital, MIM#614115",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:02:12.805026+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LAMC3 as ready",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:02:12.793681+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamc3 has been classified as Green List (High Evidence).",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:02:07.978154+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: LAMC3 as Green List (high evidence)",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:02:07.967971+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "0.1508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lamc3 has been classified as Green List (High Evidence).",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2022-03-25T14:01:18.280517+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.11913",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LAMC3 were set to ",
"entity_name": "LAMC3",
"entity_type": "gene"
}
]
}