{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=322","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=320","results":[{"created":"2024-12-13T15:57:46.719337+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.821","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: WHRN were changed from Usher syndrome, type 2D, 611383 (3) to Usher syndrome, type 2D, MIM#611383","entity_name":"WHRN","entity_type":"gene"},{"created":"2024-12-13T15:57:19.201265+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.820","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: WHRN were set to ","entity_name":"WHRN","entity_type":"gene"},{"created":"2024-12-13T15:56:56.925958+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.819","user_name":"Lucy Spencer","item_type":"entity","text":"reviewed gene: FERMT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26937547; Phenotypes: Kindler syndrome MIM#173650; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FERMT1","entity_type":"gene"},{"created":"2024-12-13T15:56:53.287389+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.819","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYMK as ready","entity_name":"MYMK","entity_type":"gene"},{"created":"2024-12-13T15:56:53.275261+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.819","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mymk has been classified as Green List (High Evidence).","entity_name":"MYMK","entity_type":"gene"},{"created":"2024-12-13T15:56:49.927108+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.819","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYMK were changed from Carey-Fineman-Ziter syndrome, 254940 (3), Autosomal recessive to Carey-Fineman-Ziter syndrome, MIM#254940","entity_name":"MYMK","entity_type":"gene"},{"created":"2024-12-13T15:56:30.313268+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.818","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYMK were set to ","entity_name":"MYMK","entity_type":"gene"},{"created":"2024-12-13T15:55:59.568960+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.817","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MED25 as ready","entity_name":"MED25","entity_type":"gene"},{"created":"2024-12-13T15:55:59.539254+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.817","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: med25 has been classified as Green List (High Evidence).","entity_name":"MED25","entity_type":"gene"},{"created":"2024-12-13T15:55:56.127342+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.817","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MED25 were changed from Basel-Vanagait-Smirin-Yosef syndrome, 616449 (3) to Basel-Vanagait-Smirin-Yosef syndrome, MIM# 616449; congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome MONDO:0014643","entity_name":"MED25","entity_type":"gene"},{"created":"2024-12-13T15:55:41.454744+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.816","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MED25 were set to ","entity_name":"MED25","entity_type":"gene"},{"created":"2024-12-13T15:55:00.439260+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.815","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MED17 as ready","entity_name":"MED17","entity_type":"gene"},{"created":"2024-12-13T15:55:00.401757+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.815","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: med17 has been classified as Green List (High Evidence).","entity_name":"MED17","entity_type":"gene"},{"created":"2024-12-13T15:54:48.504059+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.815","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MED17 were changed from Microcephaly, postnatal progressive, with seizures and brain atrophy, 613668 (3) to Microcephaly, postnatal progressive, with seizures and brain atrophy, MIM#613668","entity_name":"MED17","entity_type":"gene"},{"created":"2024-12-13T15:54:32.058773+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.814","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MED17 were set to ","entity_name":"MED17","entity_type":"gene"},{"created":"2024-12-13T15:51:00.312029+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.813","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DOCK8 as ready","entity_name":"DOCK8","entity_type":"gene"},{"created":"2024-12-13T15:51:00.291517+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.813","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dock8 has been classified as Green List (High Evidence).","entity_name":"DOCK8","entity_type":"gene"},{"created":"2024-12-13T15:50:50.475883+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.813","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DOCK8 were changed from Hyper-IgE recurrent infection syndrome, autosomal recessive, 243700 (3) to Hyper-IgE recurrent infection syndrome, autosomal recessive, MIM#243700","entity_name":"DOCK8","entity_type":"gene"},{"created":"2024-12-13T15:50:34.647649+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.812","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DOCK8 were set to ","entity_name":"DOCK8","entity_type":"gene"},{"created":"2024-12-13T15:50:08.197170+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.811","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MANBA as ready","entity_name":"MANBA","entity_type":"gene"},{"created":"2024-12-13T15:50:08.183077+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.811","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: manba has been classified as Green List (High Evidence).","entity_name":"MANBA","entity_type":"gene"},{"created":"2024-12-13T15:50:03.833857+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.811","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MANBA were changed from Mannosidosis, beta, 248510 (3) to Mannosidosis, beta, MIM#248510","entity_name":"MANBA","entity_type":"gene"},{"created":"2024-12-13T15:49:37.650906+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.810","user_name":"Lucy Spencer","item_type":"entity","text":"reviewed gene: ZNHIT3: Rating: GREEN; Mode of pathogenicity: None; Publications: 39252897; Phenotypes: PEHO syndrome MIM#260565; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZNHIT3","entity_type":"gene"},{"created":"2024-12-13T15:49:31.214814+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.810","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAI1 as ready","entity_name":"DNAI1","entity_type":"gene"},{"created":"2024-12-13T15:49:31.204317+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.810","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnai1 has been classified as Green List (High Evidence).","entity_name":"DNAI1","entity_type":"gene"},{"created":"2024-12-13T15:49:24.732811+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.810","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAI1 were changed from Ciliary dyskinesia, primary, 1, with or without situs inversus, 244400 (3) to Ciliary dyskinesia, primary, 1, with or without situs inversus, MIM#244400","entity_name":"DNAI1","entity_type":"gene"},{"created":"2024-12-13T15:49:10.587303+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.809","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAI1 were set to ","entity_name":"DNAI1","entity_type":"gene"},{"created":"2024-12-13T15:48:39.435898+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.808","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUSC3 as ready","entity_name":"TUSC3","entity_type":"gene"},{"created":"2024-12-13T15:48:39.424529+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.808","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tusc3 has been classified as Green List (High Evidence).","entity_name":"TUSC3","entity_type":"gene"},{"created":"2024-12-13T15:48:35.811891+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.808","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUSC3 were changed from Mental retardation, autosomal recessive 7, 611093 (3) to Intellectual developmental disorder, autosomal recessive 7 MIM#611093","entity_name":"TUSC3","entity_type":"gene"},{"created":"2024-12-13T15:48:21.515510+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.807","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUSC3 were set to ","entity_name":"TUSC3","entity_type":"gene"},{"created":"2024-12-13T15:47:36.651907+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.806","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNAH11 as ready","entity_name":"DNAH11","entity_type":"gene"},{"created":"2024-12-13T15:47:36.636691+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.806","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnah11 has been classified as Green List (High Evidence).","entity_name":"DNAH11","entity_type":"gene"},{"created":"2024-12-13T15:47:32.622329+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.806","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DNAH11 were changed from Ciliary dyskinesia, primary, 7, with or without situs inversus, 611884 (3) to Ciliary dyskinesia, primary, 7, with or without situs inversus, MIM#611884","entity_name":"DNAH11","entity_type":"gene"},{"created":"2024-12-13T15:47:17.364928+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.805","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DNAH11 were set to ","entity_name":"DNAH11","entity_type":"gene"},{"created":"2024-12-13T15:46:06.383999+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.804","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LYRM7 as ready","entity_name":"LYRM7","entity_type":"gene"},{"created":"2024-12-13T15:46:06.365064+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.804","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lyrm7 has been classified as Green List (High Evidence).","entity_name":"LYRM7","entity_type":"gene"},{"created":"2024-12-13T15:46:02.561235+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.804","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LYRM7 were changed from Mitochondrial complex III deficiency, nuclear type 8, 615838 (3), Autosomal recessive to Mitochondrial complex III deficiency, nuclear type 8, MIM#615838, Autosomal recessive","entity_name":"LYRM7","entity_type":"gene"},{"created":"2024-12-13T15:45:44.257867+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.803","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LYRM7 were set to ","entity_name":"LYRM7","entity_type":"gene"},{"created":"2024-12-13T15:44:37.097498+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.802","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DLG3 as ready","entity_name":"DLG3","entity_type":"gene"},{"created":"2024-12-13T15:44:37.069444+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.802","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dlg3 has been classified as Green List (High Evidence).","entity_name":"DLG3","entity_type":"gene"},{"created":"2024-12-13T15:44:32.847873+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.802","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DLG3 were changed from Mental retardation, X-linked 90, 300850 (3) to Intellectual developmental disorder, X-linked 90 MIM#300850","entity_name":"DLG3","entity_type":"gene"},{"created":"2024-12-13T15:44:08.256308+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.801","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DLG3 were set to ","entity_name":"DLG3","entity_type":"gene"},{"created":"2024-12-13T15:43:06.757033+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.800","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBA8 as ready","entity_name":"TUBA8","entity_type":"gene"},{"created":"2024-12-13T15:43:06.740055+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.800","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tuba8 has been classified as Red List (Low Evidence).","entity_name":"TUBA8","entity_type":"gene"},{"created":"2024-12-13T15:42:56.527234+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.800","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBA8 were changed from Polymicrogyria with optic nerve hypoplasia, 613180 (3) to Polymicrogyria with optic nerve hypoplasia MONDO:0013172","entity_name":"TUBA8","entity_type":"gene"},{"created":"2024-12-13T15:42:42.814765+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.799","user_name":"Lucy Spencer","item_type":"entity","text":"reviewed gene: ZBTB24: Rating: GREEN; Mode of pathogenicity: None; Publications: 23486536; Phenotypes: Immunodeficiency-centromeric instability-facial anomalies syndrome 2, MIM# 614069, MONDO:0013553; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZBTB24","entity_type":"gene"},{"created":"2024-12-13T15:42:42.185382+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.799","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBA8 were set to ","entity_name":"TUBA8","entity_type":"gene"},{"created":"2024-12-13T15:41:07.465175+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.798","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRPPRC as ready","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2024-12-13T15:41:07.454288+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.798","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrpprc has been classified as Green List (High Evidence).","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2024-12-13T15:41:03.052792+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.798","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRPPRC were changed from Leigh syndrome, French-Canadian type, 220111 (3) to Mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian) MIM#220111","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2024-12-13T15:40:19.655861+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.797","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LRPPRC were set to ","entity_name":"LRPPRC","entity_type":"gene"},{"created":"2024-12-13T15:36:55.543366+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.796","user_name":"Lucy Spencer","item_type":"entity","text":"reviewed gene: WNT10A: Rating: RED; Mode of pathogenicity: None; Publications: 19559398, 30426266; Phenotypes: Ectodermal dysplasia 16 (odontoonychodermal dysplasia) MIM#257980, Schopf-Schulz-Passarge syndrome MIM#224750, Tooth agenesis, selective, 4 MIM#150400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"WNT10A","entity_type":"gene"},{"created":"2024-12-13T15:34:42.826862+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.796","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DDHD2 as ready","entity_name":"DDHD2","entity_type":"gene"},{"created":"2024-12-13T15:34:42.812025+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.796","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ddhd2 has been classified as Green List (High Evidence).","entity_name":"DDHD2","entity_type":"gene"},{"created":"2024-12-13T15:34:38.236310+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.796","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DDHD2 were changed from Spastic paraplegia 54, autosomal recessive, 615033 (3) to Spastic paraplegia 54, autosomal recessive, MIM#615033","entity_name":"DDHD2","entity_type":"gene"},{"created":"2024-12-13T15:34:22.688230+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.795","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DDHD2 were set to ","entity_name":"DDHD2","entity_type":"gene"},{"created":"2024-12-13T15:33:54.458969+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.794","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRDN as ready","entity_name":"TRDN","entity_type":"gene"},{"created":"2024-12-13T15:33:54.446831+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.794","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: trdn has been classified as Green List (High Evidence).","entity_name":"TRDN","entity_type":"gene"},{"created":"2024-12-13T15:33:48.159303+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.794","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRDN were changed from Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness, 615441 (3) to Cardiac arrhythmia syndrome, with or without skeletal muscle weakness MIM#615441; Catecholaminergic polymorphic ventricular tachycardia MONDO:0017990","entity_name":"TRDN","entity_type":"gene"},{"created":"2024-12-13T15:33:33.064688+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.793","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRDN were set to ","entity_name":"TRDN","entity_type":"gene"},{"created":"2024-12-13T15:33:04.482852+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.792","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MARS2 as ready","entity_name":"MARS2","entity_type":"gene"},{"created":"2024-12-13T15:33:04.457245+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.792","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mars2 has been classified as Green List (High Evidence).","entity_name":"MARS2","entity_type":"gene"},{"created":"2024-12-13T15:33:00.672599+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.792","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MARS2 were changed from Spastic ataxia 3, autosomal recessive, 611390 (3) to Combined oxidative phosphorylation deficiency 25; MIM #616430, MONDO:0014636; Spastic ataxia 3, autosomal recessive, MIM #611390, MONDO:0012664","entity_name":"MARS2","entity_type":"gene"},{"created":"2024-12-13T15:32:47.417753+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.791","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MARS2 were set to ","entity_name":"MARS2","entity_type":"gene"},{"created":"2024-12-13T15:30:52.137925+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.790","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TNFSF11 as ready","entity_name":"TNFSF11","entity_type":"gene"},{"created":"2024-12-13T15:30:52.100128+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.790","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tnfsf11 has been classified as Green List (High Evidence).","entity_name":"TNFSF11","entity_type":"gene"},{"created":"2024-12-13T15:30:46.672151+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.790","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TNFSF11 were changed from Osteopetrosis, autosomal recessive 2, 259710 (3) to Osteopetrosis, autosomal recessive 2, MIM#259710","entity_name":"TNFSF11","entity_type":"gene"},{"created":"2024-12-13T15:30:32.329543+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.789","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TNFSF11 were set to ","entity_name":"TNFSF11","entity_type":"gene"},{"created":"2024-12-13T15:30:00.719120+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.788","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMEM70 as ready","entity_name":"TMEM70","entity_type":"gene"},{"created":"2024-12-13T15:30:00.698971+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.788","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmem70 has been classified as Green List (High Evidence).","entity_name":"TMEM70","entity_type":"gene"},{"created":"2024-12-13T15:29:56.633453+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.788","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMEM70 were changed from Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2, 614052 (3) to Mitochondrial disease MONDO:0044970","entity_name":"TMEM70","entity_type":"gene"},{"created":"2024-12-13T15:29:38.307348+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.787","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMEM70 were set to ","entity_name":"TMEM70","entity_type":"gene"},{"created":"2024-12-13T15:28:52.578603+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.786","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LINS1 as ready","entity_name":"LINS1","entity_type":"gene"},{"created":"2024-12-13T15:28:52.566828+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.786","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lins1 has been classified as Green List (High Evidence).","entity_name":"LINS1","entity_type":"gene"},{"created":"2024-12-13T15:28:41.425285+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.786","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LINS1 were changed from Mental retardation, autosomal recessive 27, 614340 (3) to Intellectual developmental disorder, autosomal recessive 2, MIM#614340","entity_name":"LINS1","entity_type":"gene"},{"created":"2024-12-13T15:28:17.728009+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.785","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LINS1 were set to ","entity_name":"LINS1","entity_type":"gene"},{"created":"2024-12-13T15:28:01.549718+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.784","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LINS1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LINS1","entity_type":"gene"},{"created":"2024-12-13T15:27:09.181227+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.784","user_name":"Lucy Spencer","item_type":"entity","text":"reviewed gene: VPS45: Rating: GREEN; Mode of pathogenicity: None; Publications: 30294941; Phenotypes: Neutropaenia, severe congenital, 5, autosomal recessive, MIM# 615285; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VPS45","entity_type":"gene"},{"created":"2024-12-13T15:26:07.293685+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.784","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF1A as ready","entity_name":"KIF1A","entity_type":"gene"},{"created":"2024-12-13T15:26:07.276821+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.784","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif1a has been classified as Green List (High Evidence).","entity_name":"KIF1A","entity_type":"gene"},{"created":"2024-12-13T15:25:54.218752+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.784","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF1A were changed from Spastic paraplegia 30, autosomal recessive, 610357 (3) to Spastic paraplegia 30, autosomal recessive, MIM#610357","entity_name":"KIF1A","entity_type":"gene"},{"created":"2024-12-13T15:25:41.563703+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.783","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF1A were set to ","entity_name":"KIF1A","entity_type":"gene"},{"created":"2024-12-13T15:24:53.537795+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.782","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TIMM8A as ready","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2024-12-13T15:24:53.527136+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.782","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: timm8a has been classified as Green List (High Evidence).","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2024-12-13T15:24:45.180582+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.782","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TIMM8A were changed from Jensen syndrome, 311150 (3) to Mohr-Tranebjaerg syndrome MIM#304700","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2024-12-13T15:24:19.806771+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.781","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TIMM8A were set to ","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2024-12-13T15:23:48.386919+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.780","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STXBP2 as ready","entity_name":"STXBP2","entity_type":"gene"},{"created":"2024-12-13T15:23:48.369275+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.780","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stxbp2 has been classified as Green List (High Evidence).","entity_name":"STXBP2","entity_type":"gene"},{"created":"2024-12-13T15:23:44.701072+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.780","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: STXBP2 were changed from Hemophagocytic lymphohistiocytosis, familial, 5, 613101 (3) to Haemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease MIM#613101","entity_name":"STXBP2","entity_type":"gene"},{"created":"2024-12-13T15:23:21.464621+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.779","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: STXBP2 were set to ","entity_name":"STXBP2","entity_type":"gene"},{"created":"2024-12-13T15:22:54.299346+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.778","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LZTFL1 as ready","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2024-12-13T15:22:54.286168+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.778","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lztfl1 has been classified as Green List (High Evidence).","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2024-12-13T15:22:50.392146+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.778","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LZTFL1 were changed from Bardet-Biedl syndrome 17, 615994 (3) to Bardet-Biedl syndrome 17 MIM#615994; MONDO:0014445","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2024-12-13T15:22:37.359502+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.777","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LZTFL1 were set to ","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2024-12-13T15:22:08.423277+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.776","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMS as ready","entity_name":"SMS","entity_type":"gene"},{"created":"2024-12-13T15:22:08.408065+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.776","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sms has been classified as Green List (High Evidence).","entity_name":"SMS","entity_type":"gene"},{"created":"2024-12-13T15:22:04.580039+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.776","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMS were changed from Mental retardation, X-linked, Snyder-Robinson type, 309583 (3) to Intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type MIM#309583","entity_name":"SMS","entity_type":"gene"},{"created":"2024-12-13T15:21:46.136478+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.775","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMS were set to ","entity_name":"SMS","entity_type":"gene"},{"created":"2024-12-13T15:21:18.928500+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.774","user_name":"Lucy Spencer","item_type":"entity","text":"reviewed gene: VARS2: Rating: GREEN; Mode of pathogenicity: None; Publications: 31064326; Phenotypes: Combined oxidative phosphorylation deficiency 20 MIM#615917; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"VARS2","entity_type":"gene"}]}