{"count":221272,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=221","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=219","results":[{"created":"2025-05-27T20:04:50.240590+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1025","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SERPINH1 as ready","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2025-05-27T20:04:50.233149+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1025","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: serpinh1 has been classified as Green List (High Evidence).","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2025-05-27T20:04:45.301978+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1025","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SERPINH1 were changed from Orofaciodigital syndrome VI, 277170 (3) to Osteogenesis imperfecta, type X, MIM# 613848; Osteogenesis imperfecta type 10, MONDO:0013459","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2025-05-27T20:04:34.285941+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1024","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SERPINH1 were set to ","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2025-05-27T20:02:00.996539+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1023","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SERAC1 as ready","entity_name":"SERAC1","entity_type":"gene"},{"created":"2025-05-27T20:02:00.989053+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1023","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: serac1 has been classified as Green List (High Evidence).","entity_name":"SERAC1","entity_type":"gene"},{"created":"2025-05-27T20:01:55.283725+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1023","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SERAC1 were changed from 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, 614739 (3) to 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, MIM# 614739","entity_name":"SERAC1","entity_type":"gene"},{"created":"2025-05-27T20:01:35.581259+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1022","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SERAC1 were set to ","entity_name":"SERAC1","entity_type":"gene"},{"created":"2025-05-27T20:01:06.674459+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1021","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SEPSECS as ready","entity_name":"SEPSECS","entity_type":"gene"},{"created":"2025-05-27T20:01:06.667189+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1021","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sepsecs has been classified as Green List (High Evidence).","entity_name":"SEPSECS","entity_type":"gene"},{"created":"2025-05-27T20:00:59.581012+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1021","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SEPSECS were changed from Pontocerebellar hypoplasia type 2D, 613811 (3) to Pontocerebellar hypoplasia type 2D, MIM# 613811","entity_name":"SEPSECS","entity_type":"gene"},{"created":"2025-05-27T20:00:47.039126+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1020","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SEPSECS were set to ","entity_name":"SEPSECS","entity_type":"gene"},{"created":"2025-05-27T19:59:56.378185+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1019","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SEC23B as ready","entity_name":"SEC23B","entity_type":"gene"},{"created":"2025-05-27T19:59:56.370984+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1019","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sec23b has been classified as Green List (High Evidence).","entity_name":"SEC23B","entity_type":"gene"},{"created":"2025-05-27T19:59:51.674544+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1019","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SEC23B were changed from Dyserythropoietic anemia, congenital, type II, 224100 (3) to Dyserythropoietic anemia, congenital, type II MIM#224100","entity_name":"SEC23B","entity_type":"gene"},{"created":"2025-05-27T19:59:39.800157+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1018","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SEC23B were set to ","entity_name":"SEC23B","entity_type":"gene"},{"created":"2025-05-27T19:59:04.531795+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1017","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SDCCAG8 as ready","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2025-05-27T19:59:04.524386+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1017","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sdccag8 has been classified as Green List (High Evidence).","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2025-05-27T19:58:59.071601+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1017","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SDCCAG8 were changed from Bardet-Biedl syndrome 16, 615993 (3) to Bardet-Biedl syndrome 16 (MIM# 615993); Senior-Loken syndrome 7 (MIM# 613615)","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2025-05-27T19:58:44.798808+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1016","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SDCCAG8 were set to ","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2025-05-27T19:58:20.387647+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1015","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SCO2 as ready","entity_name":"SCO2","entity_type":"gene"},{"created":"2025-05-27T19:58:20.377912+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1015","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sco2 has been classified as Green List (High Evidence).","entity_name":"SCO2","entity_type":"gene"},{"created":"2025-05-27T19:58:15.950462+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1015","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SCO2 were changed from Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1, 604377 (3) to Mitochondrial complex IV deficiency, nuclear type 2 MIM#604377","entity_name":"SCO2","entity_type":"gene"},{"created":"2025-05-27T19:55:32.011109+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1014","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SCO2 were set to ","entity_name":"SCO2","entity_type":"gene"},{"created":"2025-05-27T19:55:08.343342+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1013","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SC5D as ready","entity_name":"SC5D","entity_type":"gene"},{"created":"2025-05-27T19:55:08.336196+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1013","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sc5d has been classified as Green List (High Evidence).","entity_name":"SC5D","entity_type":"gene"},{"created":"2025-05-27T19:55:04.487029+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1013","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SC5D were changed from Lathosterolosis, 607330 (3) to Lathosterolosis, MIM#607330","entity_name":"SC5D","entity_type":"gene"},{"created":"2025-05-27T19:54:54.665023+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1012","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SC5D were set to ","entity_name":"SC5D","entity_type":"gene"},{"created":"2025-05-27T19:54:20.959065+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1011","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SAMHD1 as ready","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2025-05-27T19:54:20.949783+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1011","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: samhd1 has been classified as Green List (High Evidence).","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2025-05-27T19:54:15.984580+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1011","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SAMHD1 were changed from Aicardi-Goutieres syndrome 5, 612952 (3) to Aicardi-Goutieres syndrome 5, MIM# 612952","entity_name":"SAMHD1","entity_type":"gene"},{"created":"2025-05-27T19:53:51.949310+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1010","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SACS as ready","entity_name":"SACS","entity_type":"gene"},{"created":"2025-05-27T19:53:51.942468+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1010","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sacs has been classified as Green List (High Evidence).","entity_name":"SACS","entity_type":"gene"},{"created":"2025-05-27T19:53:47.480379+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1010","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SACS were changed from Spastic ataxia, Charlevoix-Saguenay type, 270550 (3) to Spastic ataxia, Charlevoix-Saguenay type, MIM#270550","entity_name":"SACS","entity_type":"gene"},{"created":"2025-05-27T19:53:35.208749+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1009","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SACS were set to ","entity_name":"SACS","entity_type":"gene"},{"created":"2025-05-27T19:53:22.541428+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1008","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: SACS.","entity_name":"SACS","entity_type":"gene"},{"created":"2025-05-27T19:52:53.968895+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1008","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RYR1 as ready","entity_name":"RYR1","entity_type":"gene"},{"created":"2025-05-27T19:52:53.960554+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1008","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ryr1 has been classified as Green List (High Evidence).","entity_name":"RYR1","entity_type":"gene"},{"created":"2025-05-27T19:52:49.886465+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1008","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RYR1 were changed from Central core disease, MIM# 117000; Neuromuscular disease, congenital, with uniform type 1 fiber, MIM# 117000 to Central core disease (MIM#117000); Minicore myopathy with external ophthalmoplegia (MIM#255320); Neuromuscular disease, congenital, with uniform type 1 fiber (MIM#117000)","entity_name":"RYR1","entity_type":"gene"},{"created":"2025-05-27T19:52:05.482888+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1007","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RTEL1 as ready","entity_name":"RTEL1","entity_type":"gene"},{"created":"2025-05-27T19:52:05.476239+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1007","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rtel1 has been classified as Green List (High Evidence).","entity_name":"RTEL1","entity_type":"gene"},{"created":"2025-05-27T19:52:00.686594+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1007","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RTEL1 were changed from Dyskeratosis congenita, autosomal recessive 5, 615190 (3) to Dyskeratosis congenita, autosomal recessive 5, MIM#615190","entity_name":"RTEL1","entity_type":"gene"},{"created":"2025-05-27T19:51:48.710035+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1006","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RTEL1 were set to ","entity_name":"RTEL1","entity_type":"gene"},{"created":"2025-05-27T19:51:23.001388+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1005","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS6KA3 as ready","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2025-05-27T19:51:22.987831+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1005","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps6ka3 has been classified as Green List (High Evidence).","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2025-05-27T19:51:04.460684+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1005","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS6KA3 was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2025-05-27T19:50:53.010517+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1004","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS6KA3 were changed from Coffin-Lowry syndrome to Coffin-Lowry syndrome, MIM#303600; Intellectual developmental disorder, X-linked 19; MIM#300844","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2025-05-27T19:50:42.699426+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1003","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS6KA3 were set to ","entity_name":"RPS6KA3","entity_type":"gene"},{"created":"2025-05-27T19:50:19.021019+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1002","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPGRIP1L as ready","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2025-05-27T19:50:19.012911+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1002","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpgrip1l has been classified as Green List (High Evidence).","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2025-05-27T19:50:14.868018+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1002","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPGRIP1L were changed from Meckel syndrome 5, 611561 (3) to Joubert syndrome 7, MIM# 611560; Meckel syndrome 5, MIM# 611561; COACH syndrome 3, MIM# 619113; Ciliopathy, RPGRIP1L-related, MONDO:0005308","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2025-05-27T19:50:02.171738+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1001","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPGRIP1L were set to ","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2025-05-27T19:49:37.192047+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1000","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPE65 as ready","entity_name":"RPE65","entity_type":"gene"},{"created":"2025-05-27T19:49:37.182728+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1000","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpe65 has been classified as Green List (High Evidence).","entity_name":"RPE65","entity_type":"gene"},{"created":"2025-05-27T19:49:31.350388+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.1000","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPE65 were changed from Leber congenital amaurosis 2, 204100 (3) to Retinitis pigmentosa 20, MIM#613794; Leber congenital amaurosis 2, MIM#204100","entity_name":"RPE65","entity_type":"gene"},{"created":"2025-05-27T19:49:05.807761+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.999","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RP2 as ready","entity_name":"RP2","entity_type":"gene"},{"created":"2025-05-27T19:49:05.792309+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.999","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rp2 has been classified as Green List (High Evidence).","entity_name":"RP2","entity_type":"gene"},{"created":"2025-05-27T19:47:36.692846+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.999","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RP2 were changed from Retinitis pigmentosa 2, 312600 (3) to Retinitis pigmentosa 2, MIM #312600","entity_name":"RP2","entity_type":"gene"},{"created":"2025-05-27T19:47:25.950177+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.998","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RP2 were set to ","entity_name":"RP2","entity_type":"gene"},{"created":"2025-05-27T19:46:57.443436+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.997","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNASEH2C as ready","entity_name":"RNASEH2C","entity_type":"gene"},{"created":"2025-05-27T19:46:57.436153+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.997","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnaseh2c has been classified as Green List (High Evidence).","entity_name":"RNASEH2C","entity_type":"gene"},{"created":"2025-05-27T19:46:53.253847+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.997","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RNASEH2C were changed from Aicardi-Goutieres syndrome 3, 610329 (3) to Aicardi-Goutieres syndrome 3, MIM# 610329","entity_name":"RNASEH2C","entity_type":"gene"},{"created":"2025-05-27T19:46:36.602145+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.996","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RNASEH2C were set to ","entity_name":"RNASEH2C","entity_type":"gene"},{"created":"2025-05-27T19:46:12.837278+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.995","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNASEH2B as ready","entity_name":"RNASEH2B","entity_type":"gene"},{"created":"2025-05-27T19:46:12.827921+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.995","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnaseh2b has been classified as Green List (High Evidence).","entity_name":"RNASEH2B","entity_type":"gene"},{"created":"2025-05-27T19:46:09.026025+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.995","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RNASEH2B were changed from Aicardi-Goutieres syndrome 2, 610181 (3) to Aicardi-Goutieres syndrome 2 MIM#610181","entity_name":"RNASEH2B","entity_type":"gene"},{"created":"2025-05-27T19:45:58.195239+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.994","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RNASEH2B were set to ","entity_name":"RNASEH2B","entity_type":"gene"},{"created":"2025-05-27T19:45:24.050954+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.993","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RNASEH2A as ready","entity_name":"RNASEH2A","entity_type":"gene"},{"created":"2025-05-27T19:45:24.044094+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.993","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rnaseh2a has been classified as Green List (High Evidence).","entity_name":"RNASEH2A","entity_type":"gene"},{"created":"2025-05-27T19:45:16.703971+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.993","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RNASEH2A were changed from Aicardi-Goutieres syndrome 4, 610333 (3) to Aicardi-Goutieres syndrome 4 MIM#610333; RNASEH2A-related type 1 interferonopathy MONDO:0700259","entity_name":"RNASEH2A","entity_type":"gene"},{"created":"2025-05-27T19:45:07.109796+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.992","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RNASEH2A were set to ","entity_name":"RNASEH2A","entity_type":"gene"},{"created":"2025-05-27T19:44:27.058788+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.991","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RMRP as ready","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-05-27T19:44:27.051743+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.991","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rmrp has been classified as Green List (High Evidence).","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-05-27T19:44:18.826978+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.991","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RMRP were changed from Cartilage-hair hypoplasia, 250250 (3) to Cartilage-hair hypoplasia MIM#250250; Anauxetic dysplasia 1, MIM#607095; Metaphyseal dysplasia without hypotrichosis MIM#250460","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-05-27T19:44:06.077551+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.990","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RMRP were set to ","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-05-27T19:43:23.533197+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.989","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RMND1 as ready","entity_name":"RMND1","entity_type":"gene"},{"created":"2025-05-27T19:43:23.523598+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.989","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rmnd1 has been classified as Green List (High Evidence).","entity_name":"RMND1","entity_type":"gene"},{"created":"2025-05-27T19:43:17.019149+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.989","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RMND1 were changed from Combined oxidative phosphorylation deficiency 11, 614922 (3) to Combined oxidative phosphorylation deficiency 11, MIM#614922","entity_name":"RMND1","entity_type":"gene"},{"created":"2025-05-27T19:43:06.205934+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.988","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RMND1 were set to ","entity_name":"RMND1","entity_type":"gene"},{"created":"2025-05-27T19:42:40.827456+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.987","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RDH12 as ready","entity_name":"RDH12","entity_type":"gene"},{"created":"2025-05-27T19:42:40.817606+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.987","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rdh12 has been classified as Green List (High Evidence).","entity_name":"RDH12","entity_type":"gene"},{"created":"2025-05-27T19:42:35.015228+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.987","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RDH12 were changed from Leber congenital amaurosis 13, 612712 (3) to Leber congenital amaurosis 13, MIM#612712","entity_name":"RDH12","entity_type":"gene"},{"created":"2025-05-27T19:42:24.035277+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.986","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RDH12 were set to ","entity_name":"RDH12","entity_type":"gene"},{"created":"2025-05-27T19:41:58.685442+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.985","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RBBP8 as ready","entity_name":"RBBP8","entity_type":"gene"},{"created":"2025-05-27T19:41:58.678201+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.985","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rbbp8 has been classified as Green List (High Evidence).","entity_name":"RBBP8","entity_type":"gene"},{"created":"2025-05-27T19:41:55.584992+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.985","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RBBP8 were changed from Seckel syndrome 2, 606744 (3) to Jawad syndrome MIM#251255; Seckel syndrome 2 MIM#606744","entity_name":"RBBP8","entity_type":"gene"},{"created":"2025-05-27T19:41:43.535729+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.984","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RBBP8 were set to ","entity_name":"RBBP8","entity_type":"gene"},{"created":"2025-05-27T19:41:19.793579+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.983","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAX as ready","entity_name":"RAX","entity_type":"gene"},{"created":"2025-05-27T19:41:19.750707+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.983","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rax has been classified as Green List (High Evidence).","entity_name":"RAX","entity_type":"gene"},{"created":"2025-05-27T19:41:16.396433+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.983","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAX were changed from Microphthalmia, isolated 3, 611038 (3) to Microphthalmia, syndromic 16, MIM #611038","entity_name":"RAX","entity_type":"gene"},{"created":"2025-05-27T19:41:04.574822+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.982","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAX were set to ","entity_name":"RAX","entity_type":"gene"},{"created":"2025-05-27T19:40:41.439973+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.981","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RARS2 as ready","entity_name":"RARS2","entity_type":"gene"},{"created":"2025-05-27T19:40:41.433180+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.981","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rars2 has been classified as Green List (High Evidence).","entity_name":"RARS2","entity_type":"gene"},{"created":"2025-05-27T19:40:37.642493+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.981","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RARS2 were changed from Pontocerebellar hypoplasia, type 6, 611523 (3) to Pontocerebellar hypoplasia, type 6, MIM#611523","entity_name":"RARS2","entity_type":"gene"},{"created":"2025-05-27T19:40:26.663334+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.980","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RARS2 were set to ","entity_name":"RARS2","entity_type":"gene"},{"created":"2025-05-27T19:40:03.632131+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.979","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAPSN as ready","entity_name":"RAPSN","entity_type":"gene"},{"created":"2025-05-27T19:40:03.621571+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.979","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rapsn has been classified as Green List (High Evidence).","entity_name":"RAPSN","entity_type":"gene"},{"created":"2025-05-27T19:39:59.514602+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.979","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAPSN were changed from Fetal akinesia deformation sequence, 208150 (3) to Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency MIM#616326; Fetal akinesia deformation sequence 2 MIM#618388","entity_name":"RAPSN","entity_type":"gene"},{"created":"2025-05-27T19:39:48.485848+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.978","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAPSN were set to ","entity_name":"RAPSN","entity_type":"gene"},{"created":"2025-05-27T19:39:23.560695+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.977","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAG2 as ready","entity_name":"RAG2","entity_type":"gene"}]}