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{
"count": 221272,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1037",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1035",
"results": [
{
"created": "2022-01-20T18:33:24.091528+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PITX1 were set to ",
"entity_name": "PITX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:32:56.673729+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PITX1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PITX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:32:29.028342+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PITX1: Rating: GREEN; Mode of pathogenicity: None; Publications: 21775501, 22258522, 18950742; Phenotypes: Brachydactyly-elbow wrist dysplasia syndrome, MONDO:0008520, Clubfoot, MONDO:0007342, Liebenberg syndrome, OMIM:186550, Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly, OMIM:119800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PITX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:31:22.139098+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2550",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PITX1 as ready",
"entity_name": "PITX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:31:22.124979+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2550",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pitx1 has been classified as Green List (High Evidence).",
"entity_name": "PITX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:31:13.962269+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2550",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PITX1 were set to ",
"entity_name": "PITX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:30:54.306979+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2549",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PITX1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PITX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:30:16.270076+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ICAM1 as ready",
"entity_name": "ICAM1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:30:16.258872+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: icam1 has been classified as Red List (Low Evidence).",
"entity_name": "ICAM1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:30:07.644080+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ICAM1 as Red List (low evidence)",
"entity_name": "ICAM1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:30:07.628713+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: icam1 has been classified as Red List (Low Evidence).",
"entity_name": "ICAM1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:29:32.100813+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IRAK3 as ready",
"entity_name": "IRAK3",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:29:32.085663+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: irak3 has been classified as Red List (Low Evidence).",
"entity_name": "IRAK3",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:27:19.781889+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: IRAK3 as Red List (low evidence)",
"entity_name": "IRAK3",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:27:19.763430+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: irak3 has been classified as Red List (Low Evidence).",
"entity_name": "IRAK3",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:20:50.639373+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2548",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FEZF1 as ready",
"entity_name": "FEZF1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:20:50.630079+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2548",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fezf1 has been classified as Red List (Low Evidence).",
"entity_name": "FEZF1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:20:46.439820+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2548",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FEZF1 were changed from Hypogonadotropic hypogonadism 22, with or without anosmia, MIM#\t616030 to Hypogonadotropic hypogonadism 22, with or without anosmia, MIM#\t616030",
"entity_name": "FEZF1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:17:57.237230+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2547",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FEZF1 as ready",
"entity_name": "FEZF1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:17:57.212145+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2547",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fezf1 has been classified as Red List (Low Evidence).",
"entity_name": "FEZF1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:17:53.273529+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2547",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FEZF1 were changed from HYPOGONADOTROPIC HYPOGONADISM WITH OR WITHOUT ANOSMIA to Hypogonadotropic hypogonadism 22, with or without anosmia, MIM#\t616030",
"entity_name": "FEZF1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:17:12.325396+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2546",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NAXE as ready",
"entity_name": "NAXE",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:17:12.312852+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2546",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: naxe has been classified as Red List (Low Evidence).",
"entity_name": "NAXE",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:17:08.446787+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2546",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NAXE were changed from Lethal Neurometabolic Disorder of Early Childhood to Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy\t, MIM#617186",
"entity_name": "NAXE",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:15:45.304923+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2545",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRMT10C as ready",
"entity_name": "TRMT10C",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:15:45.294459+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2545",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trmt10c has been classified as Amber List (Moderate Evidence).",
"entity_name": "TRMT10C",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:15:37.260122+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2545",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TRMT10C were set to ",
"entity_name": "TRMT10C",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:15:22.947857+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2544",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TRMT10C: Changed publications: 27132592",
"entity_name": "TRMT10C",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:15:02.644660+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2544",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRMT10C were changed from Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies to Combined oxidative phosphorylation deficiency 30, MIM# 616974",
"entity_name": "TRMT10C",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:14:44.964434+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2543",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRMT10C as Amber List (moderate evidence)",
"entity_name": "TRMT10C",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:14:44.952435+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2543",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trmt10c has been classified as Amber List (Moderate Evidence).",
"entity_name": "TRMT10C",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:14:33.605519+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2542",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRMT10C: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Combined oxidative phosphorylation deficiency 30, MIM# 616974; Mode of inheritance: None",
"entity_name": "TRMT10C",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:13:14.236442+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2542",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PBX1 as ready",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:13:14.226886+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2542",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pbx1 has been classified as Green List (High Evidence).",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:13:09.263059+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2542",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PBX1 were set to ",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:12:56.421581+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2541",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PBX1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:12:32.788697+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic",
"panel_id": 63,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PBX1 as ready",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:12:32.779172+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic",
"panel_id": 63,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pbx1 has been classified as Green List (High Evidence).",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:12:29.547962+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic",
"panel_id": 63,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PBX1 were changed from to Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay, OMIM #617641",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:12:04.247565+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic",
"panel_id": 63,
"panel_version": "0.104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PBX1 were set to ",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:11:21.795930+11:00",
"panel_name": "Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic",
"panel_id": 63,
"panel_version": "0.103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PBX1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PBX1",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:10:33.381288+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2540",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PFKM as ready",
"entity_name": "PFKM",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:10:33.363362+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2540",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pfkm has been classified as Red List (Low Evidence).",
"entity_name": "PFKM",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:09:49.728621+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2540",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TRPM7 as Amber List (moderate evidence)",
"entity_name": "TRPM7",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:09:49.719071+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2540",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trpm7 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TRPM7",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:09:37.776807+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: 4 variants identified in a stillbirth cohort. Some supportive evidence that these variants alter channel function.; to: 4 variants identified in a stillbirth cohort.\r\n\r\nIon channel expressed in the nervous and cardiac systems. The variant associated with ALS/dementia in the Guam population, p.Thr1482Ile is present in >23,000 hets in gnomad, which is out of keeping for a rare Mendelian disorder. Note recent publication associating missense variants with cardiac arrhythmia and stillbirth, with some functional data provided to substantiate effect of variant on protein function but not necessarily establish gene-disease association.",
"entity_name": "TRPM7",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:09:05.311366+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: TRPM7: Changed rating: AMBER",
"entity_name": "TRPM7",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:08:11.807713+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRPM7 as ready",
"entity_name": "TRPM7",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:08:11.796546+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trpm7 has been classified as Red List (Low Evidence).",
"entity_name": "TRPM7",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:07:54.523440+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TRPM7: Rating: RED; Mode of pathogenicity: None; Publications: 31423533; Phenotypes: Arrhythmia, stillbirth; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TRPM7",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:03:32.136424+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTH as ready",
"entity_name": "PTH",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:03:32.123418+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pth has been classified as Red List (Low Evidence).",
"entity_name": "PTH",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:03:24.412268+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2539",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTH were changed from FAMILIAL ISOLATED HYPOPARATHYROIDISM to Hypoparathyroidism, familial isolated 1, MIM#\t146200",
"entity_name": "PTH",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:02:21.537542+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SET as ready",
"entity_name": "SET",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:02:21.519348+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: set has been classified as Red List (Low Evidence).",
"entity_name": "SET",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:02:17.155675+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SET were changed from SET syndrome to Mental retardation, autosomal dominant 58, MIM#\t618106",
"entity_name": "SET",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:01:17.102876+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CAPN10 as ready",
"entity_name": "CAPN10",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:01:17.083861+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: capn10 has been classified as Red List (Low Evidence).",
"entity_name": "CAPN10",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:01:08.774346+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CAPN10 were changed from to {Diabetes mellitus, noninsulin-dependent 1}\t601283",
"entity_name": "CAPN10",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:00:46.964263+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CAPN10 were set to ",
"entity_name": "CAPN10",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:00:29.150832+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CAPN10 as Red List (low evidence)",
"entity_name": "CAPN10",
"entity_type": "gene"
},
{
"created": "2022-01-20T18:00:29.138366+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: capn10 has been classified as Red List (Low Evidence).",
"entity_name": "CAPN10",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:59:15.675306+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPARC as ready",
"entity_name": "SPARC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:59:15.655740+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sparc has been classified as Green List (High Evidence).",
"entity_name": "SPARC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:59:07.784429+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SPARC were changed from to Osteogenesis imperfecta, type XVII, MIM# 616507",
"entity_name": "SPARC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:58:50.261181+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SPARC were set to ",
"entity_name": "SPARC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:58:31.682015+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SPARC was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPARC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:58:15.297420+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: SPARC: Rating: GREEN; Mode of pathogenicity: None; Publications: 26027498, 34462290; Phenotypes: Osteogenesis imperfecta, type XVII, MIM# 616507; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SPARC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:54:51.997950+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPARC as ready",
"entity_name": "SPARC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:54:51.987162+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sparc has been classified as Red List (Low Evidence).",
"entity_name": "SPARC",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:53:46.960107+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MESD as ready",
"entity_name": "MESD",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:53:46.946330+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mesd has been classified as Green List (High Evidence).",
"entity_name": "MESD",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:52:55.286478+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SLC39A7: Changed rating: GREEN",
"entity_name": "SLC39A7",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:52:43.281898+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: SLC39A7: Changed rating: RED",
"entity_name": "SLC39A7",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:51:47.067736+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: ALOXE3: Changed rating: RED",
"entity_name": "ALOXE3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:51:24.810579+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: ALOX12B: Changed rating: RED",
"entity_name": "ALOX12B",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:50:14.557443+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NUAK2 as ready",
"entity_name": "NUAK2",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:50:14.546816+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nuak2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NUAK2",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:50:04.918448+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NUAK2 as Amber List (moderate evidence)",
"entity_name": "NUAK2",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:50:04.907289+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nuak2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NUAK2",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:49:43.775651+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2536",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NUAK2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NUAK2",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:48:57.588435+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2536",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NUAK2 were changed from Anencephaly to Anencephaly 2, OMIM #619452",
"entity_name": "NUAK2",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:48:20.978592+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2535",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FZD2 as ready",
"entity_name": "FZD2",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:48:20.967540+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2535",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fzd2 has been classified as Green List (High Evidence).",
"entity_name": "FZD2",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:48:13.581434+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2535",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FZD2 were set to ",
"entity_name": "FZD2",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:47:51.382724+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2534",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FZD2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "FZD2",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:47:23.802417+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2533",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TRPV3 as ready",
"entity_name": "TRPV3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:47:23.788207+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2533",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: trpv3 has been classified as Red List (Low Evidence).",
"entity_name": "TRPV3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:47:20.722163+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2533",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TRPV3 were changed from OLMSTED SYNDROME to Olmsted syndrome 1, MIM#\t614594",
"entity_name": "TRPV3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:46:10.370778+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2532",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TSFM as ready",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:46:10.358800+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2532",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tsfm has been classified as Green List (High Evidence).",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:46:06.065847+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2532",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TSFM were changed from Combined oxidative phosphorylation deficiency 3 to Combined oxidative phosphorylation deficiency 3, MIM#610505",
"entity_name": "TSFM",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:45:22.902823+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBB3 as ready",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:45:22.891642+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubb3 has been classified as Green List (High Evidence).",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:45:18.663952+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBB3 were changed from CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1; CONGENITAL FIBROSIS OF THE EXTRAOCULAR MUSCLES to Cortical dysplasia, complex, with other brain malformations 1, OMIM # 614039",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:44:59.264978+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBB3 were set to 32573066",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:44:33.064229+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2529",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TUBB3 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:43:54.436073+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBG1 as ready",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:43:54.422460+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubg1 has been classified as Green List (High Evidence).",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2022-01-20T17:43:50.765369+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.2528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBG1 were changed from Posteriorly predominant pachygyria and severe microcephaly to Cortical dysplasia, complex, with other brain malformations 4, OMIM #615412",
"entity_name": "TUBG1",
"entity_type": "gene"
}
]
}