{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=242","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=240","results":[{"created":"2025-04-30T15:36:09.027706+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.391","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAT4 were set to ","entity_name":"FAT4","entity_type":"gene"},{"created":"2025-04-30T15:35:31.317128+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.390","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCL as ready","entity_name":"FANCL","entity_type":"gene"},{"created":"2025-04-30T15:35:31.310500+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.390","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancl has been classified as Green List (High Evidence).","entity_name":"FANCL","entity_type":"gene"},{"created":"2025-04-30T15:35:27.453877+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.390","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCL were changed from Fanconi anemia, complementation group L, 614083 (3) to Fanconi anaemia, complementation group L MIM#614083","entity_name":"FANCL","entity_type":"gene"},{"created":"2025-04-30T15:35:15.327154+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.389","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCL were set to ","entity_name":"FANCL","entity_type":"gene"},{"created":"2025-04-30T15:34:57.759456+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.388","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCI as ready","entity_name":"FANCI","entity_type":"gene"},{"created":"2025-04-30T15:34:57.752441+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.388","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fanci has been classified as Green List (High Evidence).","entity_name":"FANCI","entity_type":"gene"},{"created":"2025-04-30T15:34:55.662764+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.388","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCI were changed from Fanconi anemia, complementation group I, 609053 (3) to Fanconi anaemia, complementation group I, MIM#609053","entity_name":"FANCI","entity_type":"gene"},{"created":"2025-04-30T15:34:40.010689+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.387","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCI were set to ","entity_name":"FANCI","entity_type":"gene"},{"created":"2025-04-30T15:34:21.737261+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.386","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCG as ready","entity_name":"FANCG","entity_type":"gene"},{"created":"2025-04-30T15:34:21.731060+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.386","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancg has been classified as Green List (High Evidence).","entity_name":"FANCG","entity_type":"gene"},{"created":"2025-04-30T15:34:19.655897+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.386","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCG were changed from Fanconi anemia, complementation group G, 614082 (3) to Fanconi anaemia, complementation group G, MIM#614082","entity_name":"FANCG","entity_type":"gene"},{"created":"2025-04-30T15:34:06.890865+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.385","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCG were set to ","entity_name":"FANCG","entity_type":"gene"},{"created":"2025-04-30T15:33:49.482099+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.384","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCF as ready","entity_name":"FANCF","entity_type":"gene"},{"created":"2025-04-30T15:33:49.475252+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.384","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancf has been classified as Green List (High Evidence).","entity_name":"FANCF","entity_type":"gene"},{"created":"2025-04-30T15:33:46.934446+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.384","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCF were changed from Fanconi anemia, complementation group F, 603467 (3) to Fanconi anaemia, complementation group F, MIM#603467","entity_name":"FANCF","entity_type":"gene"},{"created":"2025-04-30T15:33:33.147649+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.383","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCF were set to ","entity_name":"FANCF","entity_type":"gene"},{"created":"2025-04-30T15:33:04.234344+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.382","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCE as ready","entity_name":"FANCE","entity_type":"gene"},{"created":"2025-04-30T15:33:04.224391+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.382","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fance has been classified as Green List (High Evidence).","entity_name":"FANCE","entity_type":"gene"},{"created":"2025-04-30T15:33:01.232919+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.382","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCE were changed from Fanconi anemia, complementation group E, 600901 (3) to Fanconi anaemia, complementation group E, MIM#600901","entity_name":"FANCE","entity_type":"gene"},{"created":"2025-04-30T15:32:43.437395+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.381","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCE were set to ","entity_name":"FANCE","entity_type":"gene"},{"created":"2025-04-30T15:32:23.171494+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.380","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCD2 as ready","entity_name":"FANCD2","entity_type":"gene"},{"created":"2025-04-30T15:32:23.165061+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.380","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancd2 has been classified as Green List (High Evidence).","entity_name":"FANCD2","entity_type":"gene"},{"created":"2025-04-30T15:32:21.114493+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.380","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCD2 were changed from Fanconi anemia, complementation group D2, 227646 (3) to Fanconi anaemia, complementation group D2, MIM#227646","entity_name":"FANCD2","entity_type":"gene"},{"created":"2025-04-30T15:32:06.188027+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.379","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCD2 were set to ","entity_name":"FANCD2","entity_type":"gene"},{"created":"2025-04-30T15:31:48.140200+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.378","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCC as ready","entity_name":"FANCC","entity_type":"gene"},{"created":"2025-04-30T15:31:48.128021+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.378","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancc has been classified as Green List (High Evidence).","entity_name":"FANCC","entity_type":"gene"},{"created":"2025-04-30T15:31:41.940097+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.378","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCC were changed from Fanconi anemia, complementation group C, 227645 (3) to Fanconi anaemia, complementation group C, MIM#227645","entity_name":"FANCC","entity_type":"gene"},{"created":"2025-04-30T15:31:24.528240+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.377","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCC were set to ","entity_name":"FANCC","entity_type":"gene"},{"created":"2025-04-30T15:31:04.009779+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.376","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCB as ready","entity_name":"FANCB","entity_type":"gene"},{"created":"2025-04-30T15:31:04.000358+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.376","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancb has been classified as Green List (High Evidence).","entity_name":"FANCB","entity_type":"gene"},{"created":"2025-04-30T15:31:01.842376+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.376","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCB were changed from Fanconi anemia, complementation group B, 300514 (3) to Fanconi anaemia, complementation group B, MIM#300514","entity_name":"FANCB","entity_type":"gene"},{"created":"2025-04-30T15:30:34.443272+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.375","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCA as ready","entity_name":"FANCA","entity_type":"gene"},{"created":"2025-04-30T15:30:34.432806+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.375","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fanca has been classified as Green List (High Evidence).","entity_name":"FANCA","entity_type":"gene"},{"created":"2025-04-30T15:30:31.473097+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.375","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCA were changed from Fanconi anemia, complementation group A, 227650 (3) to Fanconi anaemia, complementation group A, MIM# 227650; MONDO:0009215","entity_name":"FANCA","entity_type":"gene"},{"created":"2025-04-30T15:30:10.160655+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.374","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAM126A as ready","entity_name":"FAM126A","entity_type":"gene"},{"created":"2025-04-30T15:30:10.153942+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.374","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fam126a has been classified as Green List (High Evidence).","entity_name":"FAM126A","entity_type":"gene"},{"created":"2025-04-30T15:30:07.914314+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.374","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAM126A were changed from Leukodystrophy, hypomyelinating, 5, 610532 (3) to Leukodystrophy, hypomyelinating, 5 MIM#610532","entity_name":"FAM126A","entity_type":"gene"},{"created":"2025-04-30T15:29:58.173767+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.373","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAM126A were set to ","entity_name":"FAM126A","entity_type":"gene"},{"created":"2025-04-30T15:29:40.009864+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.372","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FAH as ready","entity_name":"FAH","entity_type":"gene"},{"created":"2025-04-30T15:29:39.995703+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.372","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fah has been classified as Green List (High Evidence).","entity_name":"FAH","entity_type":"gene"},{"created":"2025-04-30T15:29:37.926900+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.372","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FAH were changed from Tyrosinemia, type I, 276700 (3) to Tyrosinaemia, type I, MIM# 276700","entity_name":"FAH","entity_type":"gene"},{"created":"2025-04-30T15:29:22.749899+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.371","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FAH were set to ","entity_name":"FAH","entity_type":"gene"},{"created":"2025-04-30T15:29:03.636855+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.370","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: F2 as ready","entity_name":"F2","entity_type":"gene"},{"created":"2025-04-30T15:29:03.630350+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.370","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: f2 has been classified as Green List (High Evidence).","entity_name":"F2","entity_type":"gene"},{"created":"2025-04-30T15:29:01.191691+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.370","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: F2 were changed from Hypoprothrombinaemia (MIM#613679); Dysprothrombinaemia, 613679 to Hypoprothrombinaemia (MIM#613679)","entity_name":"F2","entity_type":"gene"},{"created":"2025-04-30T15:28:41.198853+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.369","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: F2 were set to ","entity_name":"F2","entity_type":"gene"},{"created":"2025-04-30T15:27:59.758891+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.368","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EXOSC8 as ready","entity_name":"EXOSC8","entity_type":"gene"},{"created":"2025-04-30T15:27:59.749697+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.368","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: exosc8 has been classified as Green List (High Evidence).","entity_name":"EXOSC8","entity_type":"gene"},{"created":"2025-04-30T15:27:57.513478+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.368","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EXOSC8 were changed from Pontocerebellar hypoplasia, type 1C, 616081 (3) to Pontocerebellar hypoplasia, type 1C, MIM#616081","entity_name":"EXOSC8","entity_type":"gene"},{"created":"2025-04-30T15:18:23.520066+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.367","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EXOSC8 were set to ","entity_name":"EXOSC8","entity_type":"gene"},{"created":"2025-04-30T15:15:06.954322+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.366","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EXOSC3 as ready","entity_name":"EXOSC3","entity_type":"gene"},{"created":"2025-04-30T15:15:06.946487+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.366","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: exosc3 has been classified as Green List (High Evidence).","entity_name":"EXOSC3","entity_type":"gene"},{"created":"2025-04-30T15:15:04.842631+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.366","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EXOSC3 were changed from Pontocerebellar hypoplasia, type 1B, 614678 (3) to Pontocerebellar hypoplasia, type 1B, MIM# 614678","entity_name":"EXOSC3","entity_type":"gene"},{"created":"2025-04-30T15:14:54.072023+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.365","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EXOSC3 were set to ","entity_name":"EXOSC3","entity_type":"gene"},{"created":"2025-04-30T15:14:34.680960+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.364","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EVC2 as ready","entity_name":"EVC2","entity_type":"gene"},{"created":"2025-04-30T15:14:34.673311+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.364","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: evc2 has been classified as Green List (High Evidence).","entity_name":"EVC2","entity_type":"gene"},{"created":"2025-04-30T15:14:20.123687+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.364","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EVC2 were changed from Ellis-van Creveld syndrome, 225500 (3) to Ellis-van Creveld syndrome MIM#225500","entity_name":"EVC2","entity_type":"gene"},{"created":"2025-04-30T15:14:10.271501+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.363","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EVC2 were set to ","entity_name":"EVC2","entity_type":"gene"},{"created":"2025-04-30T15:13:40.086871+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.362","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EVC as ready","entity_name":"EVC","entity_type":"gene"},{"created":"2025-04-30T15:13:40.080246+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.362","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: evc has been classified as Green List (High Evidence).","entity_name":"EVC","entity_type":"gene"},{"created":"2025-04-30T15:13:38.074327+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.362","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EVC were changed from Ellis-van Creveld syndrome, 225500 (3) to Ellis-van Creveld syndrome, MIM# 225500","entity_name":"EVC","entity_type":"gene"},{"created":"2025-04-30T15:13:26.549694+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.361","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EVC were set to ","entity_name":"EVC","entity_type":"gene"},{"created":"2025-04-30T15:10:55.611010+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.360","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ETHE1 as ready","entity_name":"ETHE1","entity_type":"gene"},{"created":"2025-04-30T15:10:55.604122+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.360","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ethe1 has been classified as Green List (High Evidence).","entity_name":"ETHE1","entity_type":"gene"},{"created":"2025-04-30T15:10:53.318844+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.360","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ETHE1 were changed from Ethylmalonic encephalopathy, 602473 (3) to Ethylmalonic encephalopathy, MIM#602473","entity_name":"ETHE1","entity_type":"gene"},{"created":"2025-04-30T15:10:31.083776+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.359","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ETHE1 were set to ","entity_name":"ETHE1","entity_type":"gene"},{"created":"2025-04-30T15:10:12.991068+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.358","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ETFDH as ready","entity_name":"ETFDH","entity_type":"gene"},{"created":"2025-04-30T15:10:12.983047+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.358","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: etfdh has been classified as Green List (High Evidence).","entity_name":"ETFDH","entity_type":"gene"},{"created":"2025-04-30T15:10:10.685976+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.358","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ETFDH were changed from Glutaric acidemia IIC, 231680 (3) to Glutaric acidemia IIC, MIM# 231680","entity_name":"ETFDH","entity_type":"gene"},{"created":"2025-04-30T15:09:58.546277+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.357","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ETFDH were set to ","entity_name":"ETFDH","entity_type":"gene"},{"created":"2025-04-30T15:09:32.508654+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.356","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ETFB as ready","entity_name":"ETFB","entity_type":"gene"},{"created":"2025-04-30T15:09:32.501310+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.356","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: etfb has been classified as Green List (High Evidence).","entity_name":"ETFB","entity_type":"gene"},{"created":"2025-04-30T15:09:29.924755+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.356","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ETFB were changed from Glutaric acidemia IIB, 231680 (3) to Glutaric acidemia IIB, MIM# 231680","entity_name":"ETFB","entity_type":"gene"},{"created":"2025-04-30T15:09:19.728764+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.355","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ETFB were set to ","entity_name":"ETFB","entity_type":"gene"},{"created":"2025-04-30T15:07:14.570067+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.354","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ETFA as ready","entity_name":"ETFA","entity_type":"gene"},{"created":"2025-04-30T15:07:14.560484+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.354","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: etfa has been classified as Green List (High Evidence).","entity_name":"ETFA","entity_type":"gene"},{"created":"2025-04-30T15:07:12.243983+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.354","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ETFA were changed from Glutaric acidemia IIA, 231680 (3) to Glutaric acidemia IIA, MIM# 231680","entity_name":"ETFA","entity_type":"gene"},{"created":"2025-04-30T15:07:02.603406+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.353","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ETFA were set to ","entity_name":"ETFA","entity_type":"gene"},{"created":"2025-04-30T15:06:43.990412+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.352","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ESCO2 as ready","entity_name":"ESCO2","entity_type":"gene"},{"created":"2025-04-30T15:06:43.980594+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.352","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: esco2 has been classified as Green List (High Evidence).","entity_name":"ESCO2","entity_type":"gene"},{"created":"2025-04-30T15:06:41.395654+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.352","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ESCO2 were changed from SC phocomelia syndrome, 269000 (3) to Roberts-SC phocomelia syndrome (MIM#268300)","entity_name":"ESCO2","entity_type":"gene"},{"created":"2025-04-30T15:06:31.242829+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.351","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ESCO2 were set to ","entity_name":"ESCO2","entity_type":"gene"},{"created":"2025-04-30T15:06:08.786237+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.350","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC8 as ready","entity_name":"ERCC8","entity_type":"gene"},{"created":"2025-04-30T15:06:08.780000+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.350","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc8 has been classified as Green List (High Evidence).","entity_name":"ERCC8","entity_type":"gene"},{"created":"2025-04-30T15:06:04.748820+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.350","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC8 were changed from Cockayne syndrome, type A, 216400 (3) to Cockayne syndrome, type A, MIM#216400","entity_name":"ERCC8","entity_type":"gene"},{"created":"2025-04-30T15:05:44.450934+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.349","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC6 as ready","entity_name":"ERCC6","entity_type":"gene"},{"created":"2025-04-30T15:05:44.444772+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.349","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc6 has been classified as Green List (High Evidence).","entity_name":"ERCC6","entity_type":"gene"},{"created":"2025-04-30T15:05:42.223742+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.349","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC6 were changed from Cockayne syndrome, type B, 133540 (3) to Cockayne spectrum with or without cerebrooculofacioskeletal syndrome MONDO:0100506","entity_name":"ERCC6","entity_type":"gene"},{"created":"2025-04-30T15:05:33.475735+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.348","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ERCC6 were set to ","entity_name":"ERCC6","entity_type":"gene"},{"created":"2025-04-30T15:05:16.208563+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.347","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC5 as ready","entity_name":"ERCC5","entity_type":"gene"},{"created":"2025-04-30T15:05:16.202140+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.347","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc5 has been classified as Green List (High Evidence).","entity_name":"ERCC5","entity_type":"gene"},{"created":"2025-04-30T15:05:14.334961+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.347","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC5 were changed from Xeroderma pigmentosum, group G, 278780 (3) to Cerebrooculofacioskeletal syndrome 3, MIM# 616570; MONDO:0014696; Xeroderma pigmentosum, group G, MIM# 278780; MONDO:0010216","entity_name":"ERCC5","entity_type":"gene"},{"created":"2025-04-30T15:05:04.207320+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.346","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ERCC5 were set to ","entity_name":"ERCC5","entity_type":"gene"},{"created":"2025-04-30T15:04:37.421446+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.345","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC4 as ready","entity_name":"ERCC4","entity_type":"gene"},{"created":"2025-04-30T15:04:37.414471+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.345","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc4 has been classified as Green List (High Evidence).","entity_name":"ERCC4","entity_type":"gene"},{"created":"2025-04-30T15:04:35.504380+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.345","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC4 were changed from Fanconi anemia, complementation group Q, 615272 (3) to Fanconi anemia, complementation group Q, MIM# 615272 MONDO:0014108; Xeroderma pigmentosum, group F, MIM# 278760 MONDO:0010215; XFE progeroid syndrome, MIM# 610965 MONDO:0012590","entity_name":"ERCC4","entity_type":"gene"},{"created":"2025-04-30T15:04:14.875636+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.344","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERCC2 as ready","entity_name":"ERCC2","entity_type":"gene"},{"created":"2025-04-30T15:04:14.869064+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.344","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ercc2 has been classified as Green List (High Evidence).","entity_name":"ERCC2","entity_type":"gene"},{"created":"2025-04-30T15:04:12.598104+10:00","panel_name":"Prepair 500+","panel_id":4225,"panel_version":"1.344","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ERCC2 were changed from Cerebrooculofacioskeletal syndrome 2, 610756 (3) to Cerebrooculofacioskeletal syndrome 2, MIM# 610756; Trichothiodystrophy 1, photosensitive, MIM# 601675; Xeroderma pigmentosum, group D, MIM# 278730","entity_name":"ERCC2","entity_type":"gene"}]}