{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=222","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=220","results":[{"created":"2025-05-27T19:39:23.552070+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.977","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rag2 has been classified as Green List (High Evidence).","entity_name":"RAG2","entity_type":"gene"},{"created":"2025-05-27T19:39:19.109829+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.977","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAG2 were changed from Severe combined immunodeficiency, B cell-negative, 601457 (3) to Combined cellular and humoral immune defects with granulomas (MIM#233650); Omenn syndrome (MIM#603554); Severe combined immunodeficiency, B cell-negative (MIM#601457)","entity_name":"RAG2","entity_type":"gene"},{"created":"2025-05-27T19:38:50.562875+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.976","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAG1 as ready","entity_name":"RAG1","entity_type":"gene"},{"created":"2025-05-27T19:38:50.555706+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.976","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rag1 has been classified as Green List (High Evidence).","entity_name":"RAG1","entity_type":"gene"},{"created":"2025-05-27T19:38:46.405791+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.976","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAG1 were changed from Severe combined immunodeficiency, B cell-negative, 601457 (3) to Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, and autoimmunity MIM# 609889; Combined cellular and humoral immune defects with granulomas MIM# 233650; Omenn syndrome MIM# 603554; Severe combined immunodeficiency, B cell-negative MIM# 601457","entity_name":"RAG1","entity_type":"gene"},{"created":"2025-05-27T19:38:19.520514+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.975","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB3GAP2 as ready","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2025-05-27T19:38:19.513677+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.975","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab3gap2 has been classified as Green List (High Evidence).","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2025-05-27T19:38:15.366131+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.975","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB3GAP2 were changed from Warburg micro syndrome 2, 614225 (3) to Warburg micro syndrome MONDO:0016649","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2025-05-27T19:38:04.892518+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.974","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB3GAP2 were set to ","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2025-05-27T19:37:40.148637+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.973","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB3GAP1 as ready","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2025-05-27T19:37:40.142247+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.973","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab3gap1 has been classified as Green List (High Evidence).","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2025-05-27T19:37:36.011277+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.973","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB3GAP1 were changed from Warburg micro syndrome 1, 600118 (3) to Warburg micro syndrome 1, MIM# 600118; Martsolf syndrome 2, MIM# 619420","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2025-05-27T19:37:25.764766+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.972","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB3GAP1 were set to ","entity_name":"RAB3GAP1","entity_type":"gene"},{"created":"2025-05-27T19:37:00.995684+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.971","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB23 as ready","entity_name":"RAB23","entity_type":"gene"},{"created":"2025-05-27T19:37:00.988850+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.971","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab23 has been classified as Green List (High Evidence).","entity_name":"RAB23","entity_type":"gene"},{"created":"2025-05-27T19:36:56.654810+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.971","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB23 were changed from Carpenter syndrome, 201000 (3) to Carpenter syndrome MIM#201000","entity_name":"RAB23","entity_type":"gene"},{"created":"2025-05-27T19:36:46.816057+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.970","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB23 were set to ","entity_name":"RAB23","entity_type":"gene"},{"created":"2025-05-27T19:36:23.320414+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.969","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB18 as ready","entity_name":"RAB18","entity_type":"gene"},{"created":"2025-05-27T19:36:23.314181+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.969","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab18 has been classified as Green List (High Evidence).","entity_name":"RAB18","entity_type":"gene"},{"created":"2025-05-27T19:36:19.564017+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.969","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB18 were changed from Warburg micro syndrome 3, 614222 (3) to Warburg micro syndrome 3 MIM#614222","entity_name":"RAB18","entity_type":"gene"},{"created":"2025-05-27T19:36:09.533673+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.968","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB18 were set to ","entity_name":"RAB18","entity_type":"gene"},{"created":"2025-05-26T23:56:39.565605+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.967","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TMEM231 as ready","entity_name":"TMEM231","entity_type":"gene"},{"created":"2025-05-26T23:56:39.558380+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.967","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tmem231 has been classified as Green List (High Evidence).","entity_name":"TMEM231","entity_type":"gene"},{"created":"2025-05-26T23:56:32.252317+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.967","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TMEM231 were changed from Joubert syndrome 20, 614970 (3) to Joubert syndrome 20, MIM#614970; Meckel syndrome 11, MIM#615397","entity_name":"TMEM231","entity_type":"gene"},{"created":"2025-05-26T23:56:04.682941+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.966","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TMEM231 were set to ","entity_name":"TMEM231","entity_type":"gene"},{"created":"2025-05-26T23:27:44.966634+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.965","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TMEM237 as ready","entity_name":"TMEM237","entity_type":"gene"},{"created":"2025-05-26T23:27:44.959299+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.965","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tmem237 has been classified as Green List (High Evidence).","entity_name":"TMEM237","entity_type":"gene"},{"created":"2025-05-26T23:27:21.965648+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.965","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TMEM237 were changed from Joubert syndrome 14, 614424 (3) to Joubert syndrome 14, MIM#614424","entity_name":"TMEM237","entity_type":"gene"},{"created":"2025-05-26T23:27:11.603681+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.964","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TMEM237 were set to ","entity_name":"TMEM237","entity_type":"gene"},{"created":"2025-05-26T23:26:39.936182+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.963","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TMEM67 as ready","entity_name":"TMEM67","entity_type":"gene"},{"created":"2025-05-26T23:26:39.927053+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.963","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tmem67 has been classified as Green List (High Evidence).","entity_name":"TMEM67","entity_type":"gene"},{"created":"2025-05-26T23:26:35.369785+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.963","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TMEM67 were changed from Joubert syndrome 6, 610688 (3) to COACH syndrome 1 MIM#216360; Joubert syndrome 6 MIM#610688; Meckel syndrome 3 MIM#607361; Nephronophthisis 11 MIM#613550","entity_name":"TMEM67","entity_type":"gene"},{"created":"2025-05-26T23:26:29.274892+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.962","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TMEM67 were set to ","entity_name":"TMEM67","entity_type":"gene"},{"created":"2025-05-26T23:26:12.029866+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.961","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TMTC3 as ready","entity_name":"TMTC3","entity_type":"gene"},{"created":"2025-05-26T23:26:12.023332+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.961","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tmtc3 has been classified as Green List (High Evidence).","entity_name":"TMTC3","entity_type":"gene"},{"created":"2025-05-26T23:22:22.644205+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.961","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TMTC3 were changed from Lissencephaly 8, 617255 (3), Autosomal recessive to Lissencephaly 8 MIM#617255, MONDO:0014992","entity_name":"TMTC3","entity_type":"gene"},{"created":"2025-05-26T23:22:16.775324+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.960","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TMTC3 were set to ","entity_name":"TMTC3","entity_type":"gene"},{"created":"2025-05-26T23:22:01.544477+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.959","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TOE1 as ready","entity_name":"TOE1","entity_type":"gene"},{"created":"2025-05-26T23:22:01.537272+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.959","user_name":"Seb Lunke","item_type":"entity","text":"Gene: toe1 has been classified as Green List (High Evidence).","entity_name":"TOE1","entity_type":"gene"},{"created":"2025-05-26T23:21:56.851439+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.959","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TOE1 were changed from Pontocerebellar hypoplasia, type 7, 614969 (3), Autosomal recessive to Pontocerebellar hypoplasia, type 7 MIM#614969","entity_name":"TOE1","entity_type":"gene"},{"created":"2025-05-26T23:21:47.953965+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.958","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TOE1 were set to ","entity_name":"TOE1","entity_type":"gene"},{"created":"2025-05-26T23:18:55.928573+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.957","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TPP1 as ready","entity_name":"TPP1","entity_type":"gene"},{"created":"2025-05-26T23:18:55.921544+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.957","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tpp1 has been classified as Green List (High Evidence).","entity_name":"TPP1","entity_type":"gene"},{"created":"2025-05-26T23:18:51.844075+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.957","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TPP1 were changed from Ceroid lipofuscinosis, neuronal, 2, 204500 (3) to Ceroid lipofuscinosis, neuronal, 2 MIM#204500; Spinocerebellar ataxia, autosomal recessive 7 MIM#609270","entity_name":"TPP1","entity_type":"gene"},{"created":"2025-05-26T23:18:44.040582+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.956","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TPP1 were set to ","entity_name":"TPP1","entity_type":"gene"},{"created":"2025-05-26T23:18:18.973101+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.955","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TRDN as ready","entity_name":"TRDN","entity_type":"gene"},{"created":"2025-05-26T23:18:18.966694+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.955","user_name":"Seb Lunke","item_type":"entity","text":"Gene: trdn has been classified as Green List (High Evidence).","entity_name":"TRDN","entity_type":"gene"},{"created":"2025-05-26T23:18:15.403590+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.955","user_name":"Seb Lunke","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":"2025-05-26T23:17:54.303898+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.954","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TRDN were set to ","entity_name":"TRDN","entity_type":"gene"},{"created":"2025-05-26T23:17:40.415989+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.953","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TREX1 as ready","entity_name":"TREX1","entity_type":"gene"},{"created":"2025-05-26T23:17:40.408607+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.953","user_name":"Seb Lunke","item_type":"entity","text":"Gene: trex1 has been classified as Green List (High Evidence).","entity_name":"TREX1","entity_type":"gene"},{"created":"2025-05-26T23:17:24.875834+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.953","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TREX1 were changed from Aicardi-Goutieres syndrome 1, dominant and recessive, 225750 (3) to Aicardi-Goutieres syndrome 1, dominant and recessive, MIM# 225750, MONDO:0009165","entity_name":"TREX1","entity_type":"gene"},{"created":"2025-05-26T23:17:16.142649+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.952","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TREX1 were set to ","entity_name":"TREX1","entity_type":"gene"},{"created":"2025-05-26T23:14:40.165173+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.951","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TRIM32 as ready","entity_name":"TRIM32","entity_type":"gene"},{"created":"2025-05-26T23:14:40.158727+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.951","user_name":"Seb Lunke","item_type":"entity","text":"Gene: trim32 has been classified as Green List (High Evidence).","entity_name":"TRIM32","entity_type":"gene"},{"created":"2025-05-26T23:14:29.844340+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.951","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TRIM32 were set to 9634523; 10399877; 17994549; 25351777; 19492423, 19303295, 31309175","entity_name":"TRIM32","entity_type":"gene"},{"created":"2025-05-26T23:14:16.369918+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.950","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TRIM32 were changed from Muscular dystrophy, limb-girdle, type 2H, 254110 (3) to Muscular dystrophy, limb-girdle, autosomal recessive 8 MIM#254110","entity_name":"TRIM32","entity_type":"gene"},{"created":"2025-05-26T23:14:08.486293+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.949","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TRIM32 were set to ","entity_name":"TRIM32","entity_type":"gene"},{"created":"2025-05-26T23:08:05.759398+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.948","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TRIM37 as ready","entity_name":"TRIM37","entity_type":"gene"},{"created":"2025-05-26T23:08:05.752383+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.948","user_name":"Seb Lunke","item_type":"entity","text":"Gene: trim37 has been classified as Green List (High Evidence).","entity_name":"TRIM37","entity_type":"gene"},{"created":"2025-05-26T23:08:01.242018+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.948","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TRIM37 were changed from Mulibrey nanism, 253250 (3) to Mulibrey nanism MIM#253250","entity_name":"TRIM37","entity_type":"gene"},{"created":"2025-05-26T23:07:53.105941+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.947","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TRIM37 were set to ","entity_name":"TRIM37","entity_type":"gene"},{"created":"2025-05-26T23:07:23.436170+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.946","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TRMU as ready","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-05-26T23:07:23.428932+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.946","user_name":"Seb Lunke","item_type":"entity","text":"Gene: trmu has been classified as Green List (High Evidence).","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-05-26T23:07:19.366895+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.946","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TRMU were changed from Liver failure, transient infantile, 613070 (3) to Liver failure, transient infantile MIM# 613070; acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins MONDO:0013111","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-05-26T23:07:12.028585+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.945","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TRMU were set to ","entity_name":"TRMU","entity_type":"gene"},{"created":"2025-05-26T23:06:57.759814+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.944","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TRPM6 as ready","entity_name":"TRPM6","entity_type":"gene"},{"created":"2025-05-26T23:06:57.753229+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.944","user_name":"Seb Lunke","item_type":"entity","text":"Gene: trpm6 has been classified as Green List (High Evidence).","entity_name":"TRPM6","entity_type":"gene"},{"created":"2025-05-26T23:06:53.826862+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.944","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TRPM6 were changed from Hypomagnesemia 1, intestinal, 602014 (3) to Hypomagnesemia 1, intestinal MIM#602014","entity_name":"TRPM6","entity_type":"gene"},{"created":"2025-05-26T23:06:29.786354+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.943","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TRPM6 were set to ","entity_name":"TRPM6","entity_type":"gene"},{"created":"2025-05-26T23:05:54.945980+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.942","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TSEN2 as ready","entity_name":"TSEN2","entity_type":"gene"},{"created":"2025-05-26T23:05:54.934069+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.942","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tsen2 has been classified as Green List (High Evidence).","entity_name":"TSEN2","entity_type":"gene"},{"created":"2025-05-26T23:05:51.206921+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.942","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TSEN2 were changed from Pontocerebellar hypoplasia type 2B, 612389 (3) to Pontocerebellar hypoplasia type 2B, MIM #612389","entity_name":"TSEN2","entity_type":"gene"},{"created":"2025-05-26T23:05:42.865357+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.941","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TSEN2 were set to ","entity_name":"TSEN2","entity_type":"gene"},{"created":"2025-05-26T23:03:58.949370+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.940","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TSEN54 as ready","entity_name":"TSEN54","entity_type":"gene"},{"created":"2025-05-26T23:03:58.942240+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.940","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tsen54 has been classified as Green List (High Evidence).","entity_name":"TSEN54","entity_type":"gene"},{"created":"2025-05-26T23:03:35.974715+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.940","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TSEN54 were changed from Pontocerebellar hypoplasia type 2A, 277470 (3) to Pontocerebellar hypoplasia type 2A (MIM#277470); Pontocerebellar hypoplasia type 4 (MIM#225753); ?Pontocerebellar hypoplasia type 5 (MIM#610204)","entity_name":"TSEN54","entity_type":"gene"},{"created":"2025-05-26T23:03:27.498569+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.939","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TSEN54 were set to ","entity_name":"TSEN54","entity_type":"gene"},{"created":"2025-05-26T23:03:08.615769+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.938","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TSFM as ready","entity_name":"TSFM","entity_type":"gene"},{"created":"2025-05-26T23:03:08.609326+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.938","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tsfm has been classified as Green List (High Evidence).","entity_name":"TSFM","entity_type":"gene"},{"created":"2025-05-26T23:02:35.603560+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.938","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TSFM were changed from Combined oxidative phosphorylation deficiency 3, 610505 (3) to Combined oxidative phosphorylation deficiency 3, MIM#610505","entity_name":"TSFM","entity_type":"gene"},{"created":"2025-05-26T23:02:28.822067+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.937","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TSFM were set to ","entity_name":"TSFM","entity_type":"gene"},{"created":"2025-05-26T23:01:53.816926+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.936","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TSHB as ready","entity_name":"TSHB","entity_type":"gene"},{"created":"2025-05-26T23:01:53.805366+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.936","user_name":"Seb Lunke","item_type":"entity","text":"Gene: tshb has been classified as Green List (High Evidence).","entity_name":"TSHB","entity_type":"gene"},{"created":"2025-05-26T23:01:49.498420+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.936","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TSHB were changed from Hypothryoidism, congenital, nongoitrous 4, 275100 (3) to Hypothyroidism, congenital, nongoitrous 4 MIM#275100","entity_name":"TSHB","entity_type":"gene"},{"created":"2025-05-26T23:01:40.351196+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.935","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TSHB were set to ","entity_name":"TSHB","entity_type":"gene"},{"created":"2025-05-26T22:55:09.147782+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.934","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TTC37 as ready","entity_name":"TTC37","entity_type":"gene"},{"created":"2025-05-26T22:55:09.138825+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.934","user_name":"Seb Lunke","item_type":"entity","text":"Gene: ttc37 has been classified as Green List (High Evidence).","entity_name":"TTC37","entity_type":"gene"},{"created":"2025-05-26T22:54:45.888845+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.934","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TTC37 were changed from Trichohepatoenteric syndrome 1, 222470 (3) to Trichohepatoenteric syndrome 1 MIM#222470","entity_name":"TTC37","entity_type":"gene"},{"created":"2025-05-26T22:54:34.517170+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.933","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TTC37 were set to ","entity_name":"TTC37","entity_type":"gene"},{"created":"2025-05-26T22:54:06.326086+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.932","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TTC7A as ready","entity_name":"TTC7A","entity_type":"gene"},{"created":"2025-05-26T22:54:06.318704+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.932","user_name":"Seb Lunke","item_type":"entity","text":"Gene: ttc7a has been classified as Green List (High Evidence).","entity_name":"TTC7A","entity_type":"gene"},{"created":"2025-05-26T22:54:00.815940+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.932","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TTC7A were set to ","entity_name":"TTC7A","entity_type":"gene"},{"created":"2025-05-26T22:53:33.075279+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.931","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TTC8 as ready","entity_name":"TTC8","entity_type":"gene"},{"created":"2025-05-26T22:53:33.067591+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.931","user_name":"Seb Lunke","item_type":"entity","text":"Gene: ttc8 has been classified as Green List (High Evidence).","entity_name":"TTC8","entity_type":"gene"},{"created":"2025-05-26T22:53:25.603113+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.931","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TTC8 were changed from Bardet-Biedl syndrome 8, 615985 (3) to Bardet-Biedl syndrome 8, MIM #615985","entity_name":"TTC8","entity_type":"gene"},{"created":"2025-05-26T22:53:19.307738+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.930","user_name":"Seb Lunke","item_type":"entity","text":"Publications for gene: TTC8 were set to ","entity_name":"TTC8","entity_type":"gene"},{"created":"2025-05-26T22:52:21.269522+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.929","user_name":"Seb Lunke","item_type":"entity","text":"Marked gene: TTPA as ready","entity_name":"TTPA","entity_type":"gene"},{"created":"2025-05-26T22:52:21.258951+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.929","user_name":"Seb Lunke","item_type":"entity","text":"Gene: ttpa has been classified as Green List (High Evidence).","entity_name":"TTPA","entity_type":"gene"},{"created":"2025-05-26T22:52:16.851270+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.929","user_name":"Seb Lunke","item_type":"entity","text":"Phenotypes for gene: TTPA were changed from Ataxia with isolated vitamin E deficiency, 277460 (3) to Ataxia with isolated vitamin E deficiency MIM#277460","entity_name":"TTPA","entity_type":"gene"}]}