{"count":220463,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=962","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=960","results":[{"created":"2022-02-28T18:26:13.800570+11:00","panel_name":"Congenital nystagmus","panel_id":3762,"panel_version":"1.5","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AP3D1 as Green List (high evidence)","entity_name":"AP3D1","entity_type":"gene"},{"created":"2022-02-28T18:26:13.788740+11:00","panel_name":"Congenital nystagmus","panel_id":3762,"panel_version":"1.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ap3d1 has been classified as Green List (High Evidence).","entity_name":"AP3D1","entity_type":"gene"},{"created":"2022-02-28T18:25:56.583292+11:00","panel_name":"Congenital nystagmus","panel_id":3762,"panel_version":"1.4","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: AP3D1: Now four affected individuals from two unrelated families, with a mouse model that recapitulates the human phenotype.","entity_name":"AP3D1","entity_type":"gene"},{"created":"2022-02-28T18:25:42.736914+11:00","panel_name":"Congenital nystagmus","panel_id":3762,"panel_version":"1.4","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: AP3D1: Changed rating: GREEN; Changed publications: 26744459, 9697856, 30472485","entity_name":"AP3D1","entity_type":"gene"},{"created":"2022-02-28T18:25:19.950740+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11079","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AP3D1 as Green List (high evidence)","entity_name":"AP3D1","entity_type":"gene"},{"created":"2022-02-28T18:25:19.938200+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11079","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ap3d1 has been classified as Green List (High Evidence).","entity_name":"AP3D1","entity_type":"gene"},{"created":"2022-02-28T18:24:38.261366+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11078","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: AP3D1: Added comment: Now four affected individuals from two unrelated families, with a mouse model that recapitulates the human phenotype.; Changed rating: GREEN; Changed publications: 26744459, 9697856, 30472485; Changed phenotypes: Hermansky-Pudlak syndrome 10, MIM# 617050, Oculocutaneous albinism, Severe neutropaenia, Recurrent infections, Seizures, Hearing loss, Neurodevelopmental delay","entity_name":"AP3D1","entity_type":"gene"},{"created":"2022-02-28T18:20:43.933849+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: YIPF5 as ready","entity_name":"YIPF5","entity_type":"gene"},{"created":"2022-02-28T18:20:43.924548+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: yipf5 has been classified as Green List (High Evidence).","entity_name":"YIPF5","entity_type":"gene"},{"created":"2022-02-28T18:20:20.373717+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR4 as ready","entity_name":"WDR4","entity_type":"gene"},{"created":"2022-02-28T18:20:20.359096+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr4 has been classified as Green List (High Evidence).","entity_name":"WDR4","entity_type":"gene"},{"created":"2022-02-28T18:19:57.701118+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: WDR37 as ready","entity_name":"WDR37","entity_type":"gene"},{"created":"2022-02-28T18:19:57.670139+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: wdr37 has been classified as Green List (High Evidence).","entity_name":"WDR37","entity_type":"gene"},{"created":"2022-02-28T18:19:36.057906+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VPS51 as ready","entity_name":"VPS51","entity_type":"gene"},{"created":"2022-02-28T18:19:36.042172+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps51 has been classified as Amber List (Moderate Evidence).","entity_name":"VPS51","entity_type":"gene"},{"created":"2022-02-28T18:19:08.072951+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VPS50 as ready","entity_name":"VPS50","entity_type":"gene"},{"created":"2022-02-28T18:19:08.061784+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps50 has been classified as Amber List (Moderate Evidence).","entity_name":"VPS50","entity_type":"gene"},{"created":"2022-02-28T18:18:43.096013+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VPS4A as ready","entity_name":"VPS4A","entity_type":"gene"},{"created":"2022-02-28T18:18:43.085819+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps4a has been classified as Green List (High Evidence).","entity_name":"VPS4A","entity_type":"gene"},{"created":"2022-02-28T18:18:05.058382+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBGCP2 as ready","entity_name":"TUBGCP2","entity_type":"gene"},{"created":"2022-02-28T18:18:05.040558+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubgcp2 has been classified as Green List (High Evidence).","entity_name":"TUBGCP2","entity_type":"gene"},{"created":"2022-02-28T18:17:18.218449+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HEXB as ready","entity_name":"HEXB","entity_type":"gene"},{"created":"2022-02-28T18:17:18.197819+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hexb has been classified as Red List (Low Evidence).","entity_name":"HEXB","entity_type":"gene"},{"created":"2022-02-28T18:17:06.759394+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HEXB as Red List (low evidence)","entity_name":"HEXB","entity_type":"gene"},{"created":"2022-02-28T18:17:06.749134+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hexb has been classified as Red List (Low Evidence).","entity_name":"HEXB","entity_type":"gene"},{"created":"2022-02-28T18:16:29.233758+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4342","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GTPBP2 as ready","entity_name":"GTPBP2","entity_type":"gene"},{"created":"2022-02-28T18:16:29.222665+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4342","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gtpbp2 has been classified as Green List (High Evidence).","entity_name":"GTPBP2","entity_type":"gene"},{"created":"2022-02-28T18:16:21.836815+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4342","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GTPBP2 as Green List (high evidence)","entity_name":"GTPBP2","entity_type":"gene"},{"created":"2022-02-28T18:16:21.823836+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4342","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gtpbp2 has been classified as Green List (High Evidence).","entity_name":"GTPBP2","entity_type":"gene"},{"created":"2022-02-28T18:15:53.444121+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4341","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MCF2 as ready","entity_name":"MCF2","entity_type":"gene"},{"created":"2022-02-28T18:15:53.428242+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4341","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcf2 has been classified as Red List (Low Evidence).","entity_name":"MCF2","entity_type":"gene"},{"created":"2022-02-28T18:15:48.617681+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4341","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MCF2 as Red List (low evidence)","entity_name":"MCF2","entity_type":"gene"},{"created":"2022-02-28T18:15:48.608235+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4341","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mcf2 has been classified as Red List (Low Evidence).","entity_name":"MCF2","entity_type":"gene"},{"created":"2022-02-28T18:15:23.768772+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4340","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAN2C1 as ready","entity_name":"MAN2C1","entity_type":"gene"},{"created":"2022-02-28T18:15:23.755896+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4340","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: man2c1 has been classified as Green List (High Evidence).","entity_name":"MAN2C1","entity_type":"gene"},{"created":"2022-02-28T18:15:18.444202+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4340","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MAN2C1 as Green List (high evidence)","entity_name":"MAN2C1","entity_type":"gene"},{"created":"2022-02-28T18:15:18.433148+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4340","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: man2c1 has been classified as Green List (High Evidence).","entity_name":"MAN2C1","entity_type":"gene"},{"created":"2022-02-28T18:14:46.656998+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4339","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: INTS8 as ready","entity_name":"INTS8","entity_type":"gene"},{"created":"2022-02-28T18:14:46.645312+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4339","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ints8 has been classified as Red List (Low Evidence).","entity_name":"INTS8","entity_type":"gene"},{"created":"2022-02-28T18:14:41.819668+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4339","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: INTS8 as Red List (low evidence)","entity_name":"INTS8","entity_type":"gene"},{"created":"2022-02-28T18:14:41.809586+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4339","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ints8 has been classified as Red List (Low Evidence).","entity_name":"INTS8","entity_type":"gene"},{"created":"2022-02-28T18:14:17.064853+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4338","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GRM7 as ready","entity_name":"GRM7","entity_type":"gene"},{"created":"2022-02-28T18:14:17.041621+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4338","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grm7 has been classified as Green List (High Evidence).","entity_name":"GRM7","entity_type":"gene"},{"created":"2022-02-28T18:14:12.121684+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4338","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GRM7 as Green List (high evidence)","entity_name":"GRM7","entity_type":"gene"},{"created":"2022-02-28T18:14:12.112219+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4338","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grm7 has been classified as Green List (High Evidence).","entity_name":"GRM7","entity_type":"gene"},{"created":"2022-02-28T18:13:43.316124+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4337","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ERMARD as ready","entity_name":"ERMARD","entity_type":"gene"},{"created":"2022-02-28T18:13:43.304730+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4337","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ermard has been classified as Red List (Low Evidence).","entity_name":"ERMARD","entity_type":"gene"},{"created":"2022-02-28T18:13:37.466450+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4337","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ERMARD as Red List (low evidence)","entity_name":"ERMARD","entity_type":"gene"},{"created":"2022-02-28T18:13:37.456165+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4337","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ermard has been classified as Red List (Low Evidence).","entity_name":"ERMARD","entity_type":"gene"},{"created":"2022-02-28T18:13:02.227318+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4336","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GPT2 as ready","entity_name":"GPT2","entity_type":"gene"},{"created":"2022-02-28T18:13:02.213626+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4336","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gpt2 has been classified as Red List (Low Evidence).","entity_name":"GPT2","entity_type":"gene"},{"created":"2022-02-28T18:12:56.904442+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4336","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GPT2 as Red List (low evidence)","entity_name":"GPT2","entity_type":"gene"},{"created":"2022-02-28T18:12:56.892992+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4336","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gpt2 has been classified as Red List (Low Evidence).","entity_name":"GPT2","entity_type":"gene"},{"created":"2022-02-28T18:12:26.857567+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4335","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GON7 as ready","entity_name":"GON7","entity_type":"gene"},{"created":"2022-02-28T18:12:26.845821+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4335","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gon7 has been classified as Amber List (Moderate Evidence).","entity_name":"GON7","entity_type":"gene"},{"created":"2022-02-28T18:12:21.242133+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4335","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GON7 as Amber List (moderate evidence)","entity_name":"GON7","entity_type":"gene"},{"created":"2022-02-28T18:12:21.230763+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4335","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gon7 has been classified as Amber List (Moderate Evidence).","entity_name":"GON7","entity_type":"gene"},{"created":"2022-02-28T18:12:09.298887+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4334","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GON7: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Galloway-Mowat syndrome 9, MIM# 619603; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GON7","entity_type":"gene"},{"created":"2022-02-28T18:10:35.940431+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4334","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EOMES as ready","entity_name":"EOMES","entity_type":"gene"},{"created":"2022-02-28T18:10:35.926860+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4334","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2022-02-28T18:10:29.974291+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4334","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EOMES as Red List (low evidence)","entity_name":"EOMES","entity_type":"gene"},{"created":"2022-02-28T18:10:29.962430+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4334","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eomes has been classified as Red List (Low Evidence).","entity_name":"EOMES","entity_type":"gene"},{"created":"2022-02-28T18:09:51.163489+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4333","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: GOLGA2: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GOLGA2","entity_type":"gene"},{"created":"2022-02-28T18:09:42.442090+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4333","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GOLGA2 as ready","entity_name":"GOLGA2","entity_type":"gene"},{"created":"2022-02-28T18:09:42.430907+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4333","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: golga2 has been classified as Amber List (Moderate Evidence).","entity_name":"GOLGA2","entity_type":"gene"},{"created":"2022-02-28T18:09:39.028384+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4333","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GOLGA2 were changed from  to neuromuscular disease, GOLGA2-related MONDO#0019056","entity_name":"GOLGA2","entity_type":"gene"},{"created":"2022-02-28T18:09:12.709034+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4332","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GOLGA2 as Amber List (moderate evidence)","entity_name":"GOLGA2","entity_type":"gene"},{"created":"2022-02-28T18:09:12.672682+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4332","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: golga2 has been classified as Amber List (Moderate Evidence).","entity_name":"GOLGA2","entity_type":"gene"},{"created":"2022-02-28T18:08:59.755395+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4331","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GOLGA2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: neuromuscular disease, GOLGA2-related MONDO#0019056; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GOLGA2","entity_type":"gene"},{"created":"2022-02-28T18:07:48.786440+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4331","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ENO1 as ready","entity_name":"ENO1","entity_type":"gene"},{"created":"2022-02-28T18:07:48.767615+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4331","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eno1 has been classified as Red List (Low Evidence).","entity_name":"ENO1","entity_type":"gene"},{"created":"2022-02-28T18:07:42.979503+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4331","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ENO1 as Red List (low evidence)","entity_name":"ENO1","entity_type":"gene"},{"created":"2022-02-28T18:07:42.966096+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4331","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eno1 has been classified as Red List (Low Evidence).","entity_name":"ENO1","entity_type":"gene"},{"created":"2022-02-28T18:07:00.456742+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4330","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP85L as ready","entity_name":"CEP85L","entity_type":"gene"},{"created":"2022-02-28T18:07:00.423509+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4330","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep85l has been classified as Green List (High Evidence).","entity_name":"CEP85L","entity_type":"gene"},{"created":"2022-02-28T18:06:53.879325+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4330","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CEP85L as Green List (high evidence)","entity_name":"CEP85L","entity_type":"gene"},{"created":"2022-02-28T18:06:53.870079+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4330","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep85l has been classified as Green List (High Evidence).","entity_name":"CEP85L","entity_type":"gene"},{"created":"2022-02-28T18:06:42.600538+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4329","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CEP85L: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Lissencephaly 10, posterior predominant (MIM618873); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CEP85L","entity_type":"gene"},{"created":"2022-02-28T18:06:00.180676+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4329","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HEXA as ready","entity_name":"HEXA","entity_type":"gene"},{"created":"2022-02-28T18:06:00.163968+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4329","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hexa has been classified as Red List (Low Evidence).","entity_name":"HEXA","entity_type":"gene"},{"created":"2022-02-28T18:05:55.486440+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4329","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HEXA as Red List (low evidence)","entity_name":"HEXA","entity_type":"gene"},{"created":"2022-02-28T18:05:55.474134+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4329","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hexa has been classified as Red List (Low Evidence).","entity_name":"HEXA","entity_type":"gene"},{"created":"2022-02-28T18:05:29.886490+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4328","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXR1 as ready","entity_name":"FOXR1","entity_type":"gene"},{"created":"2022-02-28T18:05:29.876438+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4328","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxr1 has been classified as Red List (Low Evidence).","entity_name":"FOXR1","entity_type":"gene"},{"created":"2022-02-28T18:05:24.359689+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4328","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FOXR1 as Red List (low evidence)","entity_name":"FOXR1","entity_type":"gene"},{"created":"2022-02-28T18:05:24.348384+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4328","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxr1 has been classified as Red List (Low Evidence).","entity_name":"FOXR1","entity_type":"gene"},{"created":"2022-02-28T18:05:09.999759+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4327","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FOXR1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"FOXR1","entity_type":"gene"},{"created":"2022-02-28T18:04:41.991732+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4327","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HERC1 as ready","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-02-28T18:04:41.976230+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4327","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: herc1 has been classified as Green List (High Evidence).","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-02-28T18:04:28.048031+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4327","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HERC1 as Green List (high evidence)","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-02-28T18:04:28.037808+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4327","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: herc1 has been classified as Green List (High Evidence).","entity_name":"HERC1","entity_type":"gene"},{"created":"2022-02-28T18:03:47.053319+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4326","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FDXR as ready","entity_name":"FDXR","entity_type":"gene"},{"created":"2022-02-28T18:03:47.041763+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4326","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fdxr has been classified as Red List (Low Evidence).","entity_name":"FDXR","entity_type":"gene"},{"created":"2022-02-28T18:03:41.425777+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4326","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: FDXR as Red List (low evidence)","entity_name":"FDXR","entity_type":"gene"},{"created":"2022-02-28T18:03:41.414532+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4326","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fdxr has been classified as Red List (Low Evidence).","entity_name":"FDXR","entity_type":"gene"},{"created":"2022-02-28T18:03:13.216962+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4325","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CDK5 as ready","entity_name":"CDK5","entity_type":"gene"},{"created":"2022-02-28T18:03:13.204169+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4325","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdk5 has been classified as Red List (Low Evidence).","entity_name":"CDK5","entity_type":"gene"},{"created":"2022-02-28T18:02:41.076532+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4325","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CDK5 as Red List (low evidence)","entity_name":"CDK5","entity_type":"gene"},{"created":"2022-02-28T18:02:41.064629+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4325","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdk5 has been classified as Red List (Low Evidence).","entity_name":"CDK5","entity_type":"gene"},{"created":"2022-02-28T18:01:26.644704+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.4324","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EXOC7 as ready","entity_name":"EXOC7","entity_type":"gene"}]}