{"count":221276,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=227","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=225","results":[{"created":"2025-05-09T16:53:11.903098+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.841","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRDM5 were changed from Brittle cornea syndrome 2, 614170 (3) to Brittle cornea syndrome 2, MIM#614170","entity_name":"PRDM5","entity_type":"gene"},{"created":"2025-05-09T16:53:00.584580+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.840","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRDM5 were set to ","entity_name":"PRDM5","entity_type":"gene"},{"created":"2025-05-09T16:52:40.468255+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.839","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PQBP1 as ready","entity_name":"PQBP1","entity_type":"gene"},{"created":"2025-05-09T16:52:40.458309+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.839","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pqbp1 has been classified as Green List (High Evidence).","entity_name":"PQBP1","entity_type":"gene"},{"created":"2025-05-09T16:52:38.655139+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.839","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PQBP1 were changed from Renpenning syndrome, 309500 (3) to Renpenning syndrome MIM#309500","entity_name":"PQBP1","entity_type":"gene"},{"created":"2025-05-09T16:52:30.436202+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.838","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PQBP1 were set to ","entity_name":"PQBP1","entity_type":"gene"},{"created":"2025-05-09T16:52:01.767720+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.837","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PPT1 as ready","entity_name":"PPT1","entity_type":"gene"},{"created":"2025-05-09T16:52:01.760127+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.837","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppt1 has been classified as Green List (High Evidence).","entity_name":"PPT1","entity_type":"gene"},{"created":"2025-05-09T16:51:59.783029+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.837","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PPT1 were changed from Ceroid lipofuscinosis, neuronal, 1, 256730 (3) to Ceroid lipofuscinosis, neuronal, 1, MIM# 256730","entity_name":"PPT1","entity_type":"gene"},{"created":"2025-05-09T16:51:50.518547+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.836","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PPT1 were set to ","entity_name":"PPT1","entity_type":"gene"},{"created":"2025-05-09T16:51:27.685678+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.835","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POU1F1 as ready","entity_name":"POU1F1","entity_type":"gene"},{"created":"2025-05-09T16:51:27.675040+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.835","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pou1f1 has been classified as Green List (High Evidence).","entity_name":"POU1F1","entity_type":"gene"},{"created":"2025-05-09T16:51:25.492449+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.835","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POU1F1 were changed from Pituitary hormone deficiency, combined, 1, 613038 (3) to Pituitary hormone deficiency, combined or isolated, 1, MIM#613038","entity_name":"POU1F1","entity_type":"gene"},{"created":"2025-05-09T16:51:16.251653+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.834","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POU1F1 were set to ","entity_name":"POU1F1","entity_type":"gene"},{"created":"2025-05-09T16:50:55.416632+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.833","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POR as ready","entity_name":"POR","entity_type":"gene"},{"created":"2025-05-09T16:50:55.407147+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.833","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":"2025-05-09T16:50:53.134026+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.833","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POR were changed from Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, 201750 (3) to Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis (MIM#201750)","entity_name":"POR","entity_type":"gene"},{"created":"2025-05-09T16:50:41.624232+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.832","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POR were set to ","entity_name":"POR","entity_type":"gene"},{"created":"2025-05-09T16:50:22.795581+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.831","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POMT2 as ready","entity_name":"POMT2","entity_type":"gene"},{"created":"2025-05-09T16:50:22.788155+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.831","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomt2 has been classified as Green List (High Evidence).","entity_name":"POMT2","entity_type":"gene"},{"created":"2025-05-09T16:50:20.348818+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.831","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POMT2 were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, 613150 (3) to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2, MIM# 613150; Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 2, MIM# 613156","entity_name":"POMT2","entity_type":"gene"},{"created":"2025-05-09T16:50:09.073730+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.830","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POMT2 were set to ","entity_name":"POMT2","entity_type":"gene"},{"created":"2025-05-09T16:49:46.392574+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.829","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POMT1 as ready","entity_name":"POMT1","entity_type":"gene"},{"created":"2025-05-09T16:49:46.375674+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.829","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomt1 has been classified as Green List (High Evidence).","entity_name":"POMT1","entity_type":"gene"},{"created":"2025-05-09T16:49:43.816155+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.829","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POMT1 were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1, 236670 (3) to Myopathy caused by variation in POMT1 MONDO:0700070","entity_name":"POMT1","entity_type":"gene"},{"created":"2025-05-09T16:49:33.086420+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.828","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POMT1 were set to ","entity_name":"POMT1","entity_type":"gene"},{"created":"2025-05-09T16:49:14.863951+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.827","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POMGNT1 as ready","entity_name":"POMGNT1","entity_type":"gene"},{"created":"2025-05-09T16:49:14.857054+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.827","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pomgnt1 has been classified as Green List (High Evidence).","entity_name":"POMGNT1","entity_type":"gene"},{"created":"2025-05-09T16:49:12.219966+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.827","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POMGNT1 were changed from Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3, 253280 (3) to Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3, MIM#253280; Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B3, MIM#61315","entity_name":"POMGNT1","entity_type":"gene"},{"created":"2025-05-09T16:48:37.666699+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.826","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POMGNT1 were set to ","entity_name":"POMGNT1","entity_type":"gene"},{"created":"2025-05-09T16:48:08.346529+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.825","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POLR3B as ready","entity_name":"POLR3B","entity_type":"gene"},{"created":"2025-05-09T16:48:08.339609+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.825","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: polr3b has been classified as Green List (High Evidence).","entity_name":"POLR3B","entity_type":"gene"},{"created":"2025-05-09T16:48:06.256181+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.825","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POLR3B were changed from Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism, 614381 (3) to Leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism,MIM#614381","entity_name":"POLR3B","entity_type":"gene"},{"created":"2025-05-09T16:47:55.394765+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.824","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POLR3B were set to ","entity_name":"POLR3B","entity_type":"gene"},{"created":"2025-05-09T16:47:34.467851+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.823","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POLR1C as ready","entity_name":"POLR1C","entity_type":"gene"},{"created":"2025-05-09T16:47:34.460720+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.823","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: polr1c has been classified as Green List (High Evidence).","entity_name":"POLR1C","entity_type":"gene"},{"created":"2025-05-09T16:47:32.580053+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.823","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POLR1C were changed from Treacher Collins syndrome 3, 248390 (3) to Leukodystrophy, hypomyelinating, 11 MIM#616494; Treacher Collins syndrome 3 MIM#248390","entity_name":"POLR1C","entity_type":"gene"},{"created":"2025-05-09T16:47:15.184972+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.822","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: POLR1C were set to ","entity_name":"POLR1C","entity_type":"gene"},{"created":"2025-05-09T16:46:49.340622+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.821","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POLG as ready","entity_name":"POLG","entity_type":"gene"},{"created":"2025-05-09T16:46:49.329985+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.821","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: polg has been classified as Green List (High Evidence).","entity_name":"POLG","entity_type":"gene"},{"created":"2025-05-09T16:46:47.299569+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.821","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POLG were changed from Mitochondrial DNA depletion syndrome 4A (Alpers type), 203700 (3) to Mitochondrial DNA depletion syndrome 4A (Alpers type), MIM# 203700; Mitochondrial DNA depletion syndrome 4B (MNGIE type), MIM#613662","entity_name":"POLG","entity_type":"gene"},{"created":"2025-05-09T16:46:25.020336+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.820","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PNPO as ready","entity_name":"PNPO","entity_type":"gene"},{"created":"2025-05-09T16:46:25.012833+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.820","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pnpo has been classified as Green List (High Evidence).","entity_name":"PNPO","entity_type":"gene"},{"created":"2025-05-09T16:46:23.079428+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.820","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PNPO were changed from Pyridoxamine 5'-phosphate oxidase deficiency, 610090 (3) to Pyridoxamine 5'-phosphate oxidase deficiency MIM#610090","entity_name":"PNPO","entity_type":"gene"},{"created":"2025-05-09T16:46:14.295296+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.819","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PNPO were set to ","entity_name":"PNPO","entity_type":"gene"},{"created":"2025-05-09T16:45:22.729751+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.818","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PNKP as ready","entity_name":"PNKP","entity_type":"gene"},{"created":"2025-05-09T16:45:22.722794+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.818","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pnkp has been classified as Green List (High Evidence).","entity_name":"PNKP","entity_type":"gene"},{"created":"2025-05-09T16:45:20.796368+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.818","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PNKP were changed from Microcephaly, seizures, and developmental delay, 613402 (3) to Ataxia-oculomotor apraxia 4, MIM# 616267; Microcephaly, seizures, and developmental delay, MIM# 613402","entity_name":"PNKP","entity_type":"gene"},{"created":"2025-05-09T16:44:56.107052+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.817","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PNKP were set to ","entity_name":"PNKP","entity_type":"gene"},{"created":"2025-05-09T16:44:35.721844+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.816","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PMM2 as ready","entity_name":"PMM2","entity_type":"gene"},{"created":"2025-05-09T16:44:35.715564+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.816","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pmm2 has been classified as Green List (High Evidence).","entity_name":"PMM2","entity_type":"gene"},{"created":"2025-05-09T16:44:33.816443+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.816","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PMM2 were changed from Congenital disorder of glycosylation, type Ia, 212065 (3) to Congenital disorder of glycosylation, type Ia (MIM#212065)","entity_name":"PMM2","entity_type":"gene"},{"created":"2025-05-09T16:44:11.340406+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.815","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLPBP as ready","entity_name":"PLPBP","entity_type":"gene"},{"created":"2025-05-09T16:44:11.330834+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.815","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plpbp has been classified as Green List (High Evidence).","entity_name":"PLPBP","entity_type":"gene"},{"created":"2025-05-09T16:44:09.230854+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.815","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PLPBP were changed from Epilepsy, early-onset, vitamin B6-dependent, 617290 (3), Autosomal recessive to Epilepsy, early-onset, vitamin B6-dependent, MIM#617290","entity_name":"PLPBP","entity_type":"gene"},{"created":"2025-05-09T16:43:59.551640+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.814","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PLPBP were set to ","entity_name":"PLPBP","entity_type":"gene"},{"created":"2025-05-09T16:43:03.503409+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.813","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLP1 as ready","entity_name":"PLP1","entity_type":"gene"},{"created":"2025-05-09T16:43:03.493458+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.813","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plp1 has been classified as Green List (High Evidence).","entity_name":"PLP1","entity_type":"gene"},{"created":"2025-05-09T16:43:00.883761+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.813","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PLP1 were changed from Pelizaeus-Merzbacher disease, 312080 (3) to Pelizaeus-Merzbacher disease MIM#312080, Pelizeaus-Merzbacher spectrum disorder MONDO:0010714; Spastic paraplegia 2, X-linked MIM#312920, hereditary spastic paraplegia 2 MONDO:0010733","entity_name":"PLP1","entity_type":"gene"},{"created":"2025-05-09T16:42:45.204306+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.812","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PLP1 were set to ","entity_name":"PLP1","entity_type":"gene"},{"created":"2025-05-09T16:42:25.861084+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.811","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLOD1 as ready","entity_name":"PLOD1","entity_type":"gene"},{"created":"2025-05-09T16:42:25.851336+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.811","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: plod1 has been classified as Green List (High Evidence).","entity_name":"PLOD1","entity_type":"gene"},{"created":"2025-05-09T16:42:23.662466+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.811","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PLOD1 were changed from Ehlers-Danlos syndrome, type VI, 225400 (3) to Ehlers-Danlos syndrome, kyphoscoliotic type, 1, MIM# 225400","entity_name":"PLOD1","entity_type":"gene"},{"created":"2025-05-09T16:42:13.768560+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.810","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PLOD1 were set to ","entity_name":"PLOD1","entity_type":"gene"},{"created":"2025-05-09T16:41:52.646772+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.809","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PLA2G6 as ready","entity_name":"PLA2G6","entity_type":"gene"},{"created":"2025-05-09T16:41:52.639669+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.809","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pla2g6 has been classified as Green List (High Evidence).","entity_name":"PLA2G6","entity_type":"gene"},{"created":"2025-05-09T16:41:38.201137+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.809","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PKHD1 as ready","entity_name":"PKHD1","entity_type":"gene"},{"created":"2025-05-09T16:41:38.194651+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.809","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pkhd1 has been classified as Green List (High Evidence).","entity_name":"PKHD1","entity_type":"gene"},{"created":"2025-05-09T16:41:07.159746+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.809","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PKHD1 were changed from Polycystic kidney and hepatic disease, 263200 (3) to Polycystic kidney disease 4, with or without hepatic disease MIM#263200","entity_name":"PKHD1","entity_type":"gene"},{"created":"2025-05-09T16:40:56.934966+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.808","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PKHD1 were set to ","entity_name":"PKHD1","entity_type":"gene"},{"created":"2025-05-09T16:40:31.013065+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.807","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIGT as ready","entity_name":"PIGT","entity_type":"gene"},{"created":"2025-05-09T16:40:31.003391+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.807","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":"2025-05-09T16:40:28.864471+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.807","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":"2025-05-09T16:40:17.155346+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.806","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PIGT were set to ","entity_name":"PIGT","entity_type":"gene"},{"created":"2025-05-09T16:39:55.350167+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.805","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIGN as ready","entity_name":"PIGN","entity_type":"gene"},{"created":"2025-05-09T16:39:55.340410+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.805","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pign has been classified as Green List (High Evidence).","entity_name":"PIGN","entity_type":"gene"},{"created":"2025-05-09T16:39:53.400226+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.805","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PIGN were changed from Multiple congenital anomalies-hypotonia-seizures syndrome 1, 614080 (3) to Multiple congenital anomalies-hypotonia-seizures syndrome 1,MIM#614080","entity_name":"PIGN","entity_type":"gene"},{"created":"2025-05-09T16:39:42.295036+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.804","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PIGN were set to ","entity_name":"PIGN","entity_type":"gene"},{"created":"2025-05-09T16:39:21.116063+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.803","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIGG as ready","entity_name":"PIGG","entity_type":"gene"},{"created":"2025-05-09T16:39:21.100402+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.803","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pigg has been classified as Green List (High Evidence).","entity_name":"PIGG","entity_type":"gene"},{"created":"2025-05-09T16:39:01.902065+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.803","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PIGG were set to ","entity_name":"PIGG","entity_type":"gene"},{"created":"2025-05-09T16:38:43.761503+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.802","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIBF1 as ready","entity_name":"PIBF1","entity_type":"gene"},{"created":"2025-05-09T16:38:43.750457+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.802","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pibf1 has been classified as Green List (High Evidence).","entity_name":"PIBF1","entity_type":"gene"},{"created":"2025-05-09T16:38:28.981400+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.802","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PHYH as ready","entity_name":"PHYH","entity_type":"gene"},{"created":"2025-05-09T16:38:28.970497+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.802","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: phyh has been classified as Green List (High Evidence).","entity_name":"PHYH","entity_type":"gene"},{"created":"2025-05-09T16:38:17.055961+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.802","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PHYH were changed from Refsum disease, 266500 (3) to Refsum disease MIM#266500","entity_name":"PHYH","entity_type":"gene"},{"created":"2025-05-09T16:38:07.321716+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.801","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PHYH were set to ","entity_name":"PHYH","entity_type":"gene"},{"created":"2025-05-09T16:37:39.385580+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.800","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PHGDH as ready","entity_name":"PHGDH","entity_type":"gene"},{"created":"2025-05-09T16:37:39.370101+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.800","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: phgdh has been classified as Green List (High Evidence).","entity_name":"PHGDH","entity_type":"gene"},{"created":"2025-05-09T16:37:36.669686+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.800","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PHGDH were changed from Neu-Laxova syndrome1, 256520 (3) to Neu-Laxova syndrome 1 MIM#256520; Phosphoglycerate dehydrogenase deficiency MIM#601815","entity_name":"PHGDH","entity_type":"gene"},{"created":"2025-05-09T16:37:28.722288+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.799","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PHGDH were set to ","entity_name":"PHGDH","entity_type":"gene"},{"created":"2025-05-09T16:37:07.087626+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.798","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PHF8 as ready","entity_name":"PHF8","entity_type":"gene"},{"created":"2025-05-09T16:37:07.080334+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.798","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: phf8 has been classified as Green List (High Evidence).","entity_name":"PHF8","entity_type":"gene"},{"created":"2025-05-09T16:37:05.159132+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.798","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PHF8 were changed from Mental retardation syndrome, X-linked, Siderius type, 300263 (3) to Intellectual developmental disorder, X-linked syndromic, Siderius type, MIM#\t300263","entity_name":"PHF8","entity_type":"gene"},{"created":"2025-05-09T16:36:37.518529+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.797","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PHF8 were set to ","entity_name":"PHF8","entity_type":"gene"},{"created":"2025-05-09T16:36:16.090784+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.796","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PGM3 as ready","entity_name":"PGM3","entity_type":"gene"},{"created":"2025-05-09T16:36:16.083798+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.796","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pgm3 has been classified as Green List (High Evidence).","entity_name":"PGM3","entity_type":"gene"},{"created":"2025-05-09T16:36:13.902277+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.796","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PGM3 were changed from Immunodeficiency 23, 615816 (3) to Immunodeficiency 23, MIM# 615816","entity_name":"PGM3","entity_type":"gene"},{"created":"2025-05-09T16:36:05.685489+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.795","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PGM3 were set to ","entity_name":"PGM3","entity_type":"gene"},{"created":"2025-05-09T16:35:45.634570+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.794","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PGM1 as ready","entity_name":"PGM1","entity_type":"gene"}]}