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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=306",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=304",
"results": [
{
"created": "2025-01-17T11:37:42.072242+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1195",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NARS2 were set to ",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:37:15.133006+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NNT as ready",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:37:15.119979+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nnt has been classified as Green List (High Evidence).",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:37:08.427412+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1194",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NNT were changed from Glucocorticoid deficiency 4, 614736 (3) to Glucocorticoid deficiency 4, with or without mineralocorticoid deficiency MIM#614736; MONDO:0013874",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:36:56.374053+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1193",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NNT were set to ",
"entity_name": "NNT",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:36:24.278230+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PSAP as ready",
"entity_name": "PSAP",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:36:24.266299+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: psap has been classified as Green List (High Evidence).",
"entity_name": "PSAP",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:36:20.543553+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1192",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PSAP were changed from Metachromatic leukodystrophy due to SAP-b deficiency, 249900 (3) to Metachromatic leukodystrophy due to SAP-b deficiency, MIM#249900",
"entity_name": "PSAP",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:36:08.166700+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1191",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PSAP were set to ",
"entity_name": "PSAP",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:35:40.909918+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAB33B as ready",
"entity_name": "RAB33B",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:35:40.896770+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rab33b has been classified as Green List (High Evidence).",
"entity_name": "RAB33B",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:35:37.654377+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1190",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAB33B were changed from Smith-McCort dysplasia 2, 615222 (3) to Smith-McCort dysplasia 2, MIM #615222",
"entity_name": "RAB33B",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:35:16.837418+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1189",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAB33B were set to ",
"entity_name": "RAB33B",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:34:25.812541+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAB39B as ready",
"entity_name": "RAB39B",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:34:25.800669+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rab39b has been classified as Green List (High Evidence).",
"entity_name": "RAB39B",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:34:22.552380+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1188",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAB39B were changed from Mental retardation, X-linked 72, 300271 (3) to Intellectual developmental disorder, X-linked 72, MIM #300271",
"entity_name": "RAB39B",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:34:10.512582+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1187",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAB39B were set to ",
"entity_name": "RAB39B",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:33:45.628851+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RARS as ready",
"entity_name": "RARS",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:33:45.617132+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rars has been classified as Green List (High Evidence).",
"entity_name": "RARS",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:33:42.326991+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1186",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RARS were changed from Leukodystrophy, hypomyelinating, 9, 616140 (3) to Leukodystrophy, hypomyelinating, 9, MIM#616140",
"entity_name": "RARS",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:33:29.973411+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1185",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RARS were set to ",
"entity_name": "RARS",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:33:06.432597+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RAX as ready",
"entity_name": "RAX",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:33:06.420359+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rax has been classified as Green List (High Evidence).",
"entity_name": "RAX",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:33:02.428904+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1184",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RAX were changed from Microphthalmia, isolated 3, 611038 (3) to Microphthalmia, syndromic 16, MIM #611038",
"entity_name": "RAX",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:32:49.963848+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RAX were set to ",
"entity_name": "RAX",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:32:19.613311+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RBCK1 as ready",
"entity_name": "RBCK1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:32:19.600034+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rbck1 has been classified as Green List (High Evidence).",
"entity_name": "RBCK1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:32:14.929444+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RBCK1 were changed from Polyglucosan body myopathy 1 with or without immunodeficiency, 615895 (3) to Polyglucosan body myopathy 1 with or without immunodeficiency, MIM #615895",
"entity_name": "RBCK1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:32:02.325821+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RBCK1 were set to ",
"entity_name": "RBCK1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:31:32.056337+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RP2 as ready",
"entity_name": "RP2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:31:32.027875+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rp2 has been classified as Green List (High Evidence).",
"entity_name": "RP2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:31:29.002700+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RP2 were changed from Retinitis pigmentosa 2, 312600 (3) to Retinitis pigmentosa 2, MIM#312600",
"entity_name": "RP2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:31:17.269159+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RP2 were set to ",
"entity_name": "RP2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:30:50.820139+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC16A2 as ready",
"entity_name": "SLC16A2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:30:50.806595+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc16a2 has been classified as Green List (High Evidence).",
"entity_name": "SLC16A2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:30:42.668010+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1178",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC16A2 were changed from Allan-Herndon-Dudley syndrome to Allan-Herndon-Dudley syndrome, MIM #300523",
"entity_name": "SLC16A2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:30:30.785942+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC16A2 were set to ",
"entity_name": "SLC16A2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:30:05.591064+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC25A38 as ready",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:30:05.577070+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc25a38 has been classified as Green List (High Evidence).",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:30:01.223919+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC25A38 were changed from Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive, 205950 (3) to Anaemia, sideroblastic, 1, MIM #300751",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:29:46.940628+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC25A38 were set to ",
"entity_name": "SLC25A38",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:29:20.626457+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC35D1 as ready",
"entity_name": "SLC35D1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:29:20.613385+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc35d1 has been classified as Green List (High Evidence).",
"entity_name": "SLC35D1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:29:17.788466+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC35D1 were changed from Schneckenbecken dysplasia, 269250 (3) to Schneckenbecken dysplasia, MIM#269250",
"entity_name": "SLC35D1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:29:05.842714+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1173",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC35D1 were set to ",
"entity_name": "SLC35D1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:28:22.412030+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPATA7 as ready",
"entity_name": "SPATA7",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:28:22.396417+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spata7 has been classified as Green List (High Evidence).",
"entity_name": "SPATA7",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:28:17.350023+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1172",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SPATA7 were changed from Leber congenital amaurosis 3, 604232 (3) to Leber congenital amaurosis 3, MIM #604232; Retinitis pigmentosa 94, variable age at onset, autosomal recessive, MIM #604232",
"entity_name": "SPATA7",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:28:05.746053+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1171",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SPATA7 were set to ",
"entity_name": "SPATA7",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:27:39.810187+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAP1 as ready",
"entity_name": "TAP1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:27:39.800394+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tap1 has been classified as Green List (High Evidence).",
"entity_name": "TAP1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:27:36.825017+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TAP1 were changed from Bare lymphocyte syndrome, type I, 604571 (3) to MHC class I deficiency 1, MIM #604571",
"entity_name": "TAP1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:27:24.782374+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1169",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TAP1 were set to ",
"entity_name": "TAP1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:26:53.424350+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TMEM107 as ready",
"entity_name": "TMEM107",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:26:53.407488+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tmem107 has been classified as Green List (High Evidence).",
"entity_name": "TMEM107",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:26:50.307354+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1168",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TMEM107 were changed from Orofaciodigital syndrome XVI, 617563 (3), Autosomal recessive to Orofaciodigital syndrome XVI, MIM#617563",
"entity_name": "TMEM107",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:26:35.807403+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TMEM107 were set to ",
"entity_name": "TMEM107",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:25:25.974930+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1166",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RARS2 as ready",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:25:25.962547+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1166",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rars2 has been classified as Green List (High Evidence).",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:25:22.476394+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1166",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RARS2 were changed from Pontocerebellar hypoplasia, type 6, 611523 (3) to Pontocerebellar hypoplasia, type 6, MIM#611523",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:25:07.936501+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RARS2 were set to ",
"entity_name": "RARS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:24:40.671594+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MOCS1 as ready",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:24:40.661549+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mocs1 has been classified as Green List (High Evidence).",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:24:37.034458+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MOCS1 were changed from Molybdenum cofactor deficiency A, 252150 (3) to Molybdenum cofactor deficiency A, MIM#252150",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:24:25.413513+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1163",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MOCS1 were set to ",
"entity_name": "MOCS1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:23:59.841043+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RDH12 as ready",
"entity_name": "RDH12",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:23:59.824252+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rdh12 has been classified as Green List (High Evidence).",
"entity_name": "RDH12",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:23:56.195099+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RDH12 were changed from Leber congenital amaurosis 13, 612712 (3) to Leber congenital amaurosis 13, MIM#612712",
"entity_name": "RDH12",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:23:43.878459+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RDH12 were set to ",
"entity_name": "RDH12",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:23:18.080458+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1160",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RFXANK as ready",
"entity_name": "RFXANK",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:23:18.068363+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1160",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rfxank has been classified as Green List (High Evidence).",
"entity_name": "RFXANK",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:23:15.178182+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1160",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RFXANK were changed from MHC class II deficiency, complementation group B, 209920 (3) to MHC class II deficiency 2, MIM#620815",
"entity_name": "RFXANK",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:23:00.803397+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RFXANK were set to ",
"entity_name": "RFXANK",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:22:38.330189+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1158",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MTR as ready",
"entity_name": "MTR",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:22:38.316394+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1158",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mtr has been classified as Green List (High Evidence).",
"entity_name": "MTR",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:22:35.205200+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1158",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MTR were changed from Homocystinuria-megaloblastic anemia, cblG complementation type, 250940 (3) to Homocystinuria-megaloblastic anaemia, cblG complementation type, MIM# 250940",
"entity_name": "MTR",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:22:21.487528+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MTR were set to ",
"entity_name": "MTR",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:21:53.138637+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: RMND1 as ready",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:21:53.126151+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: rmnd1 has been classified as Green List (High Evidence).",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:21:50.107957+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: RMND1 were changed from Combined oxidative phosphorylation deficiency 11, 614922 (3) to Combined oxidative phosphorylation deficiency 11, MIM#614922",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:21:37.783432+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1155",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: RMND1 were set to ",
"entity_name": "RMND1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:21:09.193750+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1154",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SDHAF1 as ready",
"entity_name": "SDHAF1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:21:09.178023+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1154",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sdhaf1 has been classified as Green List (High Evidence).",
"entity_name": "SDHAF1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:20:49.156956+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1154",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SDHAF1 were changed from Mitochondrial complex II deficiency, 252011 (3) to Mitochondrial complex II deficiency, nuclear type 2, MIM#619166",
"entity_name": "SDHAF1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:20:36.953412+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SDHAF1 were set to ",
"entity_name": "SDHAF1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:20:10.933242+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC12A6 as ready",
"entity_name": "SLC12A6",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:20:10.918883+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc12a6 has been classified as Green List (High Evidence).",
"entity_name": "SLC12A6",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:20:07.603348+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC12A6 were changed from Agenesis of the corpus callosum with peripheral neuropathy, 218000 (3) to Agenesis of the corpus callosum with peripheral neuropathy, MIM#218000",
"entity_name": "SLC12A6",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:19:54.595470+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1151",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC12A6 were set to ",
"entity_name": "SLC12A6",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:19:30.008603+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SQSTM1 as ready",
"entity_name": "SQSTM1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:19:29.988027+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sqstm1 has been classified as Green List (High Evidence).",
"entity_name": "SQSTM1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:18:48.700503+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SQSTM1 were changed from Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset, 617145 (3), Autosomal recessive to Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset, MIM#617145",
"entity_name": "SQSTM1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:18:35.528314+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SQSTM1 were set to ",
"entity_name": "SQSTM1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:18:13.917245+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STX11 as ready",
"entity_name": "STX11",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:18:13.897505+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stx11 has been classified as Green List (High Evidence).",
"entity_name": "STX11",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:18:10.834854+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STX11 were changed from Hemophagocytic lymphohistiocytosis, familial, 4, MIM#603552 to Haemophagocytic lymphohistiocytosis, familial, 4, MIM#603552",
"entity_name": "STX11",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:17:59.324664+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STX11 were changed from Hemophagocytic lymphohistiocytosis, familial, 4, 603552 (3) to Hemophagocytic lymphohistiocytosis, familial, 4, MIM#603552",
"entity_name": "STX11",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:17:48.012612+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STX11 were set to ",
"entity_name": "STX11",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:17:23.054435+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NAA10 as ready",
"entity_name": "NAA10",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:17:23.040840+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: naa10 has been classified as Green List (High Evidence).",
"entity_name": "NAA10",
"entity_type": "gene"
}
]
}