{"count":221277,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=230","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=228","results":[{"created":"2025-05-09T14:38:47.396627+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.707","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufs4 has been classified as Green List (High Evidence).","entity_name":"NDUFS4","entity_type":"gene"},{"created":"2025-05-09T14:38:45.349666+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.707","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFS4 were changed from Leigh syndrome, 256000 (3) to Mitochondrial complex I deficiency, nuclear type 1, MIM#252010","entity_name":"NDUFS4","entity_type":"gene"},{"created":"2025-05-09T14:38:18.403418+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.706","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF5 as ready","entity_name":"NDUFAF5","entity_type":"gene"},{"created":"2025-05-09T14:38:18.392654+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.706","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf5 has been classified as Green List (High Evidence).","entity_name":"NDUFAF5","entity_type":"gene"},{"created":"2025-05-09T14:38:15.596405+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.706","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF5 were changed from Mitochondrial complex 1 deficiency, 252010 (3) to Mitochondrial complex I deficiency, nuclear type 16 MIM#618238","entity_name":"NDUFAF5","entity_type":"gene"},{"created":"2025-05-09T14:37:55.679701+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.705","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDUFAF2 as ready","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2025-05-09T14:37:55.669602+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.705","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndufaf2 has been classified as Green List (High Evidence).","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2025-05-09T14:37:53.310617+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.705","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDUFAF2 were changed from Leigh syndrome, 256000 (3) to Mitochondrial complex I deficiency, nuclear type 10, MIM#618233","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2025-05-09T14:37:42.650274+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.704","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDUFAF2 were set to ","entity_name":"NDUFAF2","entity_type":"gene"},{"created":"2025-05-09T14:37:23.571720+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.703","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDRG1 as ready","entity_name":"NDRG1","entity_type":"gene"},{"created":"2025-05-09T14:37:23.565468+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.703","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndrg1 has been classified as Green List (High Evidence).","entity_name":"NDRG1","entity_type":"gene"},{"created":"2025-05-09T14:37:21.464513+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.703","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDRG1 were changed from Charcot-Marie-Tooth disease, type 4D, 601455 (3) to Charcot-Marie-Tooth disease, type 4D MIM#601455","entity_name":"NDRG1","entity_type":"gene"},{"created":"2025-05-09T14:36:58.742377+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.702","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDP as ready","entity_name":"NDP","entity_type":"gene"},{"created":"2025-05-09T14:36:58.734983+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.702","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndp has been classified as Green List (High Evidence).","entity_name":"NDP","entity_type":"gene"},{"created":"2025-05-09T14:36:55.617537+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.702","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDP were changed from Norrie disease, 310600 (3) to Norrie disease, MIM# 310600","entity_name":"NDP","entity_type":"gene"},{"created":"2025-05-09T14:36:45.224268+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.701","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDP were set to ","entity_name":"NDP","entity_type":"gene"},{"created":"2025-05-09T14:36:23.449167+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.700","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDE1 as ready","entity_name":"NDE1","entity_type":"gene"},{"created":"2025-05-09T14:36:23.441787+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.700","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nde1 has been classified as Green List (High Evidence).","entity_name":"NDE1","entity_type":"gene"},{"created":"2025-05-09T14:36:20.857165+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.700","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDE1 were changed from Lissencephaly 4 (with microcephaly), 614019 (3) to Lissencephaly 4 (with microcephaly), MIM#614019","entity_name":"NDE1","entity_type":"gene"},{"created":"2025-05-09T14:36:08.095009+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.699","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDE1 were set to ","entity_name":"NDE1","entity_type":"gene"},{"created":"2025-05-09T14:35:47.967346+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.698","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCF2 as ready","entity_name":"NCF2","entity_type":"gene"},{"created":"2025-05-09T14:35:47.957245+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.698","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncf2 has been classified as Green List (High Evidence).","entity_name":"NCF2","entity_type":"gene"},{"created":"2025-05-09T14:35:45.496505+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.698","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NCF2 were changed from Chronic granulomatous disease due to deficiency of NCF-2, 233710 (3) to Chronic granulomatous disease 2, autosomal recessive, MIM# 233710","entity_name":"NCF2","entity_type":"gene"},{"created":"2025-05-09T14:35:34.881088+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.697","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NCF2 were set to ","entity_name":"NCF2","entity_type":"gene"},{"created":"2025-05-09T14:34:01.272625+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.696","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NBN as ready","entity_name":"NBN","entity_type":"gene"},{"created":"2025-05-09T14:34:01.265782+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.696","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":"2025-05-09T14:33:58.461898+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.696","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":"2025-05-09T14:33:49.281778+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.695","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NBN were set to ","entity_name":"NBN","entity_type":"gene"},{"created":"2025-05-09T14:33:27.333962+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.694","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NARS2 as ready","entity_name":"NARS2","entity_type":"gene"},{"created":"2025-05-09T14:33:27.324164+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.694","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nars2 has been classified as Green List (High Evidence).","entity_name":"NARS2","entity_type":"gene"},{"created":"2025-05-09T14:33:22.918470+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.694","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NARS2 were changed from Combined oxidative phosphorylation deficiency 24, 616239 (3) to Combined oxidative phosphorylation deficiency 24 - MIM#616239, MONDO:0014547","entity_name":"NARS2","entity_type":"gene"},{"created":"2025-05-09T14:33:12.617529+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.693","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NARS2 were set to ","entity_name":"NARS2","entity_type":"gene"},{"created":"2025-05-09T14:32:01.824599+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.692","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NALCN as ready","entity_name":"NALCN","entity_type":"gene"},{"created":"2025-05-09T14:32:01.817460+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.692","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":"2025-05-09T14:31:29.860766+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.692","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":"2025-05-09T14:31:17.754625+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.691","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NALCN were set to ","entity_name":"NALCN","entity_type":"gene"},{"created":"2025-05-09T14:30:38.896893+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.690","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NAGS as ready","entity_name":"NAGS","entity_type":"gene"},{"created":"2025-05-09T14:30:38.889791+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.690","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nags has been classified as Green List (High Evidence).","entity_name":"NAGS","entity_type":"gene"},{"created":"2025-05-09T14:30:17.312807+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.690","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NAGS were changed from N-acetylglutamate synthase deficiency, 237310 (3) to N-acetylglutamate synthase deficiency MIM#237310","entity_name":"NAGS","entity_type":"gene"},{"created":"2025-05-09T14:29:55.551190+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.689","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NAGS were set to ","entity_name":"NAGS","entity_type":"gene"},{"created":"2025-05-09T14:29:36.161468+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.688","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NAGLU as ready","entity_name":"NAGLU","entity_type":"gene"},{"created":"2025-05-09T14:29:36.151646+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.688","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: naglu has been classified as Green List (High Evidence).","entity_name":"NAGLU","entity_type":"gene"},{"created":"2025-05-09T14:29:34.029959+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.688","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NAGLU were changed from Mucopolysaccharidosis type IIIB (Sanfilippo B), 252920 (3) to Mucopolysaccharidosis type IIIB (Sanfilippo B) MIM#252920","entity_name":"NAGLU","entity_type":"gene"},{"created":"2025-05-09T14:29:23.944463+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.687","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NAGLU were set to ","entity_name":"NAGLU","entity_type":"gene"},{"created":"2025-05-09T14:29:01.437200+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.686","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NAGA as ready","entity_name":"NAGA","entity_type":"gene"},{"created":"2025-05-09T14:29:01.426331+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.686","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: naga has been classified as Green List (High Evidence).","entity_name":"NAGA","entity_type":"gene"},{"created":"2025-05-09T14:28:58.832326+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.686","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NAGA were changed from Schindler disease, type I, 609241 (3) to Schindler disease, type I MIM#609241; Schindler disease, type III MIM#609241","entity_name":"NAGA","entity_type":"gene"},{"created":"2025-05-09T14:28:38.370792+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.685","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NAGA were set to ","entity_name":"NAGA","entity_type":"gene"},{"created":"2025-05-09T14:27:39.250179+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.684","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO7A as ready","entity_name":"MYO7A","entity_type":"gene"},{"created":"2025-05-09T14:27:39.240162+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.684","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo7a has been classified as Green List (High Evidence).","entity_name":"MYO7A","entity_type":"gene"},{"created":"2025-05-09T14:27:34.997888+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.684","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYO7A were changed from Usher syndrome, type 1B, 276900 (3) to Usher syndrome, type 1B, MIM# 276900","entity_name":"MYO7A","entity_type":"gene"},{"created":"2025-05-09T14:27:25.544188+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.683","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO7A were set to ","entity_name":"MYO7A","entity_type":"gene"},{"created":"2025-05-09T14:27:00.560891+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.682","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYO5B as ready","entity_name":"MYO5B","entity_type":"gene"},{"created":"2025-05-09T14:27:00.553714+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.682","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myo5b has been classified as Green List (High Evidence).","entity_name":"MYO5B","entity_type":"gene"},{"created":"2025-05-09T14:26:58.261132+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.682","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYO5B were changed from Microvillus inclusion disease, 251850 (3) to Cholestasis, progressive familial intrahepatic, 10, MIM#619868; Diarrhea 2, with microvillus atrophy, with or without cholestasis, MIM#251850","entity_name":"MYO5B","entity_type":"gene"},{"created":"2025-05-09T14:26:45.186678+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.681","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYO5B were set to ","entity_name":"MYO5B","entity_type":"gene"},{"created":"2025-05-09T14:26:22.631843+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.680","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MVK as ready","entity_name":"MVK","entity_type":"gene"},{"created":"2025-05-09T14:26:22.621674+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.680","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mvk has been classified as Green List (High Evidence).","entity_name":"MVK","entity_type":"gene"},{"created":"2025-05-09T14:26:20.454312+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.680","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MVK were changed from Mevalonic aciduria, 610377 (3) to Mevalonic aciduria, MIM#610377; Hyper-IgD syndrome, MIM#260920","entity_name":"MVK","entity_type":"gene"},{"created":"2025-05-09T14:26:09.752986+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.679","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MVK were set to ","entity_name":"MVK","entity_type":"gene"},{"created":"2025-05-09T14:25:46.087913+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.678","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MUT as ready","entity_name":"MUT","entity_type":"gene"},{"created":"2025-05-09T14:25:46.081503+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.678","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mut has been classified as Green List (High Evidence).","entity_name":"MUT","entity_type":"gene"},{"created":"2025-05-09T14:25:40.471384+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.678","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MUT were changed from Methylmalonic aciduria, mut(0) type, 251000 (3) to Methylmalonic aciduria, mut(0) type, MIM# 251000","entity_name":"MUT","entity_type":"gene"},{"created":"2025-05-09T14:25:17.653787+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.677","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MUSK as ready","entity_name":"MUSK","entity_type":"gene"},{"created":"2025-05-09T14:25:17.641094+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.677","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: musk has been classified as Green List (High Evidence).","entity_name":"MUSK","entity_type":"gene"},{"created":"2025-05-09T14:25:15.333979+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.677","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MUSK were changed from Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency, 616325 (3) to Fetal akinesia deformation sequence 1 MIM#208150; Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency MIM#616325","entity_name":"MUSK","entity_type":"gene"},{"created":"2025-05-09T14:25:04.757777+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.676","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MUSK were set to ","entity_name":"MUSK","entity_type":"gene"},{"created":"2025-05-09T14:24:38.749828+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.675","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTTP as ready","entity_name":"MTTP","entity_type":"gene"},{"created":"2025-05-09T14:24:38.743279+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.675","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mttp has been classified as Green List (High Evidence).","entity_name":"MTTP","entity_type":"gene"},{"created":"2025-05-09T14:24:35.732225+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.675","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MTTP were changed from Abetalipoproteinemia, 200100 (3) to Abetalipoproteinaemia MIM#200100","entity_name":"MTTP","entity_type":"gene"},{"created":"2025-05-09T14:24:24.728946+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.674","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MTTP were set to ","entity_name":"MTTP","entity_type":"gene"},{"created":"2025-05-09T14:23:04.153750+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.673","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTRR as ready","entity_name":"MTRR","entity_type":"gene"},{"created":"2025-05-09T14:23:04.147399+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.673","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mtrr has been classified as Green List (High Evidence).","entity_name":"MTRR","entity_type":"gene"},{"created":"2025-05-09T14:22:31.323440+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.673","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MTRR were changed from Homocystinuria-megaloblastic anemia, cbl E type, 236270 (3) to Homocystinuria-megaloblastic anemia, cbl E type, MIM #236270","entity_name":"MTRR","entity_type":"gene"},{"created":"2025-05-09T14:22:20.674608+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.672","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MTRR were set to ","entity_name":"MTRR","entity_type":"gene"},{"created":"2025-05-09T14:21:54.542611+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.671","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTR as ready","entity_name":"MTR","entity_type":"gene"},{"created":"2025-05-09T14:21:54.535703+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.671","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mtr has been classified as Green List (High Evidence).","entity_name":"MTR","entity_type":"gene"},{"created":"2025-05-09T14:21:51.184822+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.671","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MTR were changed from Homocystinuria-megaloblastic anemia, cblG complementation type, 250940 (3) to Homocystinuria-megaloblastic anaemia, cblG complementation type, MIM# 250940","entity_name":"MTR","entity_type":"gene"},{"created":"2025-05-09T14:21:39.627451+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.670","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MTR were set to ","entity_name":"MTR","entity_type":"gene"},{"created":"2025-05-09T14:21:18.016796+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.669","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTMR2 as ready","entity_name":"MTMR2","entity_type":"gene"},{"created":"2025-05-09T14:21:18.006353+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.669","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mtmr2 has been classified as Green List (High Evidence).","entity_name":"MTMR2","entity_type":"gene"},{"created":"2025-05-09T14:21:15.522844+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.669","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MTMR2 were changed from Charcot-Marie-Tooth disease, type 4B1, 601382 (3) to Charcot-Marie-Tooth disease, type 4B1, MIM#601382","entity_name":"MTMR2","entity_type":"gene"},{"created":"2025-05-09T14:20:45.406881+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.668","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTM1 as ready","entity_name":"MTM1","entity_type":"gene"},{"created":"2025-05-09T14:20:45.396876+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.668","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mtm1 has been classified as Green List (High Evidence).","entity_name":"MTM1","entity_type":"gene"},{"created":"2025-05-09T14:20:43.199334+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.668","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MTM1 were changed from Myotubular myopathy, X-linked, 310400 (3) to Myopathy, centronuclear, X-linked MIM#310400","entity_name":"MTM1","entity_type":"gene"},{"created":"2025-05-09T14:20:33.937807+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.667","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MTM1 were set to ","entity_name":"MTM1","entity_type":"gene"},{"created":"2025-05-09T14:20:10.859806+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.666","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTHFR as ready","entity_name":"MTHFR","entity_type":"gene"},{"created":"2025-05-09T14:20:10.850686+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.666","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mthfr has been classified as Green List (High Evidence).","entity_name":"MTHFR","entity_type":"gene"},{"created":"2025-05-09T14:19:57.280528+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.666","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MTHFR were changed from Homocystinuria due to MTHFR deficiency, 236250 (3) to Homocystinuria due to MTHFR deficiency, MIM# 236250","entity_name":"MTHFR","entity_type":"gene"},{"created":"2025-05-09T14:19:47.025019+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.665","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MTHFR were set to ","entity_name":"MTHFR","entity_type":"gene"},{"created":"2025-05-09T13:59:06.493770+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.664","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MTFMT as ready","entity_name":"MTFMT","entity_type":"gene"},{"created":"2025-05-09T13:59:06.484650+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.664","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mtfmt has been classified as Green List (High Evidence).","entity_name":"MTFMT","entity_type":"gene"},{"created":"2025-05-09T13:59:02.245667+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.664","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MTFMT were changed from Combined oxidative phosphorylation deficiency 15, 614947 (3) to Combined oxidative phosphorylation deficiency 15, MIM#614947","entity_name":"MTFMT","entity_type":"gene"},{"created":"2025-05-09T13:58:52.109333+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.663","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MTFMT were set to ","entity_name":"MTFMT","entity_type":"gene"},{"created":"2025-05-09T13:58:31.142445+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.662","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MRE11 as ready","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-05-09T13:58:31.132613+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.662","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mre11 has been classified as Green List (High Evidence).","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-05-09T13:58:27.252658+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.662","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MRE11 were changed from Ataxia-telangiectasia-like disorder, 604391 (3) to Ataxia-telangiectasia-like disorder, MIM#604391","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-05-09T13:58:15.630601+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.661","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MRE11 were set to ","entity_name":"MRE11","entity_type":"gene"},{"created":"2025-05-09T13:57:55.885901+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.660","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MPV17 as ready","entity_name":"MPV17","entity_type":"gene"},{"created":"2025-05-09T13:57:55.876232+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.660","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mpv17 has been classified as Green List (High Evidence).","entity_name":"MPV17","entity_type":"gene"}]}