HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=307",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=305",
"results": [
{
"created": "2025-01-17T11:17:19.817939+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NAA10 were changed from N-terminal acetyltransferase deficiency, 300855 (3) to Ogden syndrome (MIM#300855); Syndromic microphthalmia 1 (MIM#309800)",
"entity_name": "NAA10",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:17:07.161306+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NAA10 were set to ",
"entity_name": "NAA10",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:16:26.664162+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBC1D24 as ready",
"entity_name": "TBC1D24",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:16:26.651186+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbc1d24 has been classified as Green List (High Evidence).",
"entity_name": "TBC1D24",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:16:22.825182+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TBC1D24 were changed from Epileptic encephalopathy, early infantile, 16, 615338 (3) to Deafness, autosomal recessive 86 MIM#614617; Developmental and epileptic encephalopathy 16 MIM#615338; DOORS syndrome MIM#220500; Epilepsy, rolandic, with proxysmal exercise-induce dystonia and writer's cramp MIM#608105; Myoclonic epilepsy, infantile, familial MIM#605021",
"entity_name": "TBC1D24",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:15:56.018805+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TBC1D24 were set to ",
"entity_name": "TBC1D24",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:15:32.531093+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NALCN as ready",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:15:32.519815+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nalcn has been classified as Green List (High Evidence).",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:15:29.278916+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NALCN were changed from Hypotonia, infantile, with psychomotor retardation and characteristic facies, 615419 (3) to Hypotonia, infantile, with psychomotor retardation and characteristic facies 1 (MIM#615419)",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:15:17.442698+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NALCN were set to ",
"entity_name": "NALCN",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:14:53.807311+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NANS as ready",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:14:53.794925+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nans has been classified as Green List (High Evidence).",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:14:50.959627+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NANS were changed from Spondyloepimetaphyseal dysplasia, Camera-Genevieve type, 610442 (3), Autosomal recessive to Spondyloepimetaphyseal dysplasia, Camera-Genevieve type (MIM#610442)",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:14:38.411876+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NANS were set to ",
"entity_name": "NANS",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:14:09.720927+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TCAP as ready",
"entity_name": "TCAP",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:14:09.697758+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tcap has been classified as Green List (High Evidence).",
"entity_name": "TCAP",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:14:06.288030+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TCAP were changed from Muscular dystrophy, limb-girdle, type 2G, 601954 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 7, MIM#601954",
"entity_name": "TCAP",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:13:54.141516+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TCAP were set to ",
"entity_name": "TCAP",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:13:25.945889+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NBN as ready",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:13:25.934269+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nbn has been classified as Green List (High Evidence).",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:13:22.841985+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NBN were changed from Nijmegen breakage syndrome, 251260 (3) to Nijmegen breakage syndrome, MIM#251260",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:13:11.202360+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NBN were set to ",
"entity_name": "NBN",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:12:49.109316+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS6 as ready",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:12:49.094082+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs6 has been classified as Green List (High Evidence).",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:12:45.823668+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS6 were changed from Mitochondrial complex I deficiency, 252010 (3) to Mitochondrial complex I deficiency, nuclear type 9 (MIM#618232)",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:12:34.151514+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS6 were set to ",
"entity_name": "NDUFS6",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:12:05.966575+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEK1 as ready",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:12:05.939262+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nek1 has been classified as Green List (High Evidence).",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:12:02.440212+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEK1 were changed from Short-rib thoracic dysplasia 6 with or without polydactyly, 263520 (3) to Short-rib thoracic dysplasia 6 with or without polydactyly, MIM#263520",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:11:49.799805+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEK1 were set to ",
"entity_name": "NEK1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:11:18.186991+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CFI as ready",
"entity_name": "CFI",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:11:18.174127+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cfi has been classified as Green List (High Evidence).",
"entity_name": "CFI",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:11:08.364329+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CFI were changed from Complement factor I deficiency, 610984 (3) to Complement factor I deficiency, MIM#610984",
"entity_name": "CFI",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:10:55.307995+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CFI were set to ",
"entity_name": "CFI",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:10:16.757932+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NFU1 as ready",
"entity_name": "NFU1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:10:16.745711+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nfu1 has been classified as Green List (High Evidence).",
"entity_name": "NFU1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:10:10.254691+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NFU1 were changed from Multiple mitochondrial dysfunctions syndrome 1, 605711 (3) to Multiple mitochondrial dysfunctions syndrome 1, MIM#605711",
"entity_name": "NFU1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:09:53.893076+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NFU1 were set to ",
"entity_name": "NFU1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:09:15.882154+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHST14 as ready",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:09:15.869612+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chst14 has been classified as Green List (High Evidence).",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:09:12.945347+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CHST14 were changed from Ehlers-Danlos syndrome, musculocontractural type 1, 601776 (3) to Ehlers-Danlos syndrome, musculocontractural type 1, MIM#601776",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:09:00.781455+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CHST14 were set to ",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:08:18.804540+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NMNAT1 as ready",
"entity_name": "NMNAT1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:08:18.780764+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nmnat1 has been classified as Green List (High Evidence).",
"entity_name": "NMNAT1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:08:15.315297+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NMNAT1 were changed from Leber congenital amaurosis 9, 608553 (3) to Leber congenital amaurosis 9, MIM#608553",
"entity_name": "NMNAT1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:08:03.594309+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NMNAT1 were set to ",
"entity_name": "NMNAT1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:05:08.200028+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NPR2 as ready",
"entity_name": "NPR2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:05:08.168447+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: npr2 has been classified as Green List (High Evidence).",
"entity_name": "NPR2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:05:03.698029+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NPR2 were set to ",
"entity_name": "NPR2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:02:52.206448+11:00",
"panel_name": "Hydrocephalus_Ventriculomegaly",
"panel_id": 115,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ARID1B as ready",
"entity_name": "ARID1B",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:02:52.194561+11:00",
"panel_name": "Hydrocephalus_Ventriculomegaly",
"panel_id": 115,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: arid1b has been classified as Green List (High Evidence).",
"entity_name": "ARID1B",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:02:16.295353+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PC as ready",
"entity_name": "PC",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:02:16.261144+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pc has been classified as Green List (High Evidence).",
"entity_name": "PC",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:00:15.032999+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PC were changed from Pyruvate carboxylase deficiency, 266150 (3) to Pyruvate carboxylase deficiency (MIM#266150)",
"entity_name": "PC",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:00:03.213292+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PC were set to ",
"entity_name": "PC",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:59:35.770845+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PCDH12 as ready",
"entity_name": "PCDH12",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:59:35.753493+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pcdh12 has been classified as Green List (High Evidence).",
"entity_name": "PCDH12",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:59:31.917598+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PCDH12 were changed from Microcephaly, seizures, spasticity, and brain calcification, 251280 (3), Autosomal recessive to Diencephalic-mesencephalic junction dysplasia syndrome 1 (MIM# 251280)",
"entity_name": "PCDH12",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:59:03.411813+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PCDH12 were set to ",
"entity_name": "PCDH12",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:58:36.788840+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PCNT as ready",
"entity_name": "PCNT",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:58:36.744932+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pcnt has been classified as Green List (High Evidence).",
"entity_name": "PCNT",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:58:33.123560+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PCNT were changed from Microcephalic osteodysplastic primordial dwarfism, type II, 210720 (3) to Microcephalic osteodysplastic primordial dwarfism, type II, MIM# 210720; MONDO:0008872",
"entity_name": "PCNT",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:58:19.604006+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PCNT were set to ",
"entity_name": "PCNT",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:57:50.181210+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGT as ready",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:57:50.161076+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigt has been classified as Green List (High Evidence).",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:57:46.823073+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGT were changed from Multiple congenital anomalies-hypotonia-seizures syndrome 3 to Multiple congenital anomalies-hypotonia-seizures syndrome 3, MIM# 615398, MONDO:0014165",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:57:34.410097+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGT were set to ",
"entity_name": "PIGT",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:57:08.840884+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PKLR as ready",
"entity_name": "PKLR",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:57:08.828638+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pklr has been classified as Green List (High Evidence).",
"entity_name": "PKLR",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:57:04.757906+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PKLR were changed from Pyruvate kinase deficiency, 266200 (3) to Pyruvate kinase deficiency, MIM#266200",
"entity_name": "PKLR",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:56:52.725749+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PKLR were set to ",
"entity_name": "PKLR",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:56:12.913022+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PMPCA were changed from Spinocerebellar ataxia, autosomal recessive 2, MIM#213200 to Spinocerebellar ataxia 2, MIM#213200",
"entity_name": "PMPCA",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:55:34.786784+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PMPCA as ready",
"entity_name": "PMPCA",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:55:34.765094+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pmpca has been classified as Green List (High Evidence).",
"entity_name": "PMPCA",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:55:31.708022+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PMPCA were changed from Spinocerebellar ataxia, autosomal recessive 2, 213200 (3) to Spinocerebellar ataxia, autosomal recessive 2, MIM#213200",
"entity_name": "PMPCA",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:55:20.443551+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PMPCA were set to ",
"entity_name": "PMPCA",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:54:52.931479+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PYCR2 as ready",
"entity_name": "PYCR2",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:54:52.917345+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pycr2 has been classified as Green List (High Evidence).",
"entity_name": "PYCR2",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:54:45.988806+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PYCR2 were changed from Leukodystrophy, hypomyelinating, 10, 616420 (3) to Leukodystrophy, hypomyelinating, 10, MIM#616420",
"entity_name": "PYCR2",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:54:32.944186+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PYCR2 were set to ",
"entity_name": "PYCR2",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:54:03.576385+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POR as ready",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:54:03.559473+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: por has been classified as Green List (High Evidence).",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:53:59.812275+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: POR were set to ",
"entity_name": "POR",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:53:33.623137+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PTH1R as ready",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:53:33.606498+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pth1r has been classified as Green List (High Evidence).",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:53:30.233562+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PTH1R were changed from Chondrodysplasia, Blomstrand type, 215045 (3) to Chondrodysplasia, Blomstrand type (MIM#215045); Eiken syndrome (MIM#600002)",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:53:17.532770+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PTH1R were set to ",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:53:06.370294+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: PTH1R was changed from to None",
"entity_name": "PTH1R",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:52:21.729453+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Tag for review tag was added to gene: RCBTB1.",
"entity_name": "RCBTB1",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:50:53.900310+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COL6A3 as ready",
"entity_name": "COL6A3",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:50:53.886813+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: col6a3 has been classified as Green List (High Evidence).",
"entity_name": "COL6A3",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:50:50.505282+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COL6A3 were changed from Ullrich congenital muscular dystrophy 1, 254090 (3) to Ullrich congenital muscular dystrophy 1, MIM#254090",
"entity_name": "COL6A3",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:50:15.267339+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COL6A3 were set to ",
"entity_name": "COL6A3",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:49:32.864247+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1099",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CEP78 as ready",
"entity_name": "CEP78",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:49:32.849970+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1099",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep78 has been classified as Green List (High Evidence).",
"entity_name": "CEP78",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:49:29.645558+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1099",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CEP78 were changed from Cone-rod dystrophy and hearing loss, 617236 (3), Autosomal recessive to Cone-rod dystrophy and hearing loss, MIM#617236",
"entity_name": "CEP78",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:49:14.642529+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1098",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CEP78 were set to ",
"entity_name": "CEP78",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:48:28.236270+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1097",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CYP4F22 as ready",
"entity_name": "CYP4F22",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:48:28.223594+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1097",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cyp4f22 has been classified as Green List (High Evidence).",
"entity_name": "CYP4F22",
"entity_type": "gene"
},
{
"created": "2025-01-17T10:48:21.114328+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1097",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CYP4F22 were changed from Ichthyosis, congenital, autosomal recessive 5, 604777 (3) to Ichthyosis, congenital, autosomal recessive 5, MIM#604777",
"entity_name": "CYP4F22",
"entity_type": "gene"
}
]
}