{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=307","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&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"}]}