{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1680","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1678","results":[{"created":"2020-08-09T20:58:57.820587+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC30A10: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypermanganesemia with dystonia 1, MIM# 613280; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC30A10","entity_type":"gene"},{"created":"2020-08-09T20:53:46.441847+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: POLG as ready","entity_name":"POLG","entity_type":"gene"},{"created":"2020-08-09T20:53:46.432660+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: polg has been classified as Red List (Low Evidence).","entity_name":"POLG","entity_type":"gene"},{"created":"2020-08-09T20:53:40.731592+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: POLG were changed from  to Mitochondrial DNA depletion syndrome 4A (Alpers type), MIM# 203700","entity_name":"POLG","entity_type":"gene"},{"created":"2020-08-09T20:53:14.188240+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: POLG was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"POLG","entity_type":"gene"},{"created":"2020-08-09T20:52:53.839754+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.155","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: POLG as Red List (low evidence)","entity_name":"POLG","entity_type":"gene"},{"created":"2020-08-09T20:52:53.829817+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.155","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: polg has been classified as Red List (Low Evidence).","entity_name":"POLG","entity_type":"gene"},{"created":"2020-08-09T20:52:16.456708+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: POLG: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Mitochondrial DNA depletion syndrome 4A (Alpers type), MIM# 203700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"POLG","entity_type":"gene"},{"created":"2020-08-09T20:48:33.580386+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PKHD1 as ready","entity_name":"PKHD1","entity_type":"gene"},{"created":"2020-08-09T20:48:33.570393+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.154","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":"2020-08-09T20:48:14.165922+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PKHD1 were changed from  to Polycystic kidney disease 4, with or without hepatic disease, MIM# 263200","entity_name":"PKHD1","entity_type":"gene"},{"created":"2020-08-09T20:47:42.982459+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.153","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PKHD1 were set to ","entity_name":"PKHD1","entity_type":"gene"},{"created":"2020-08-09T20:47:20.697502+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.152","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PKHD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PKHD1","entity_type":"gene"},{"created":"2020-08-09T20:46:53.066646+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PKHD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 30366773, 25771912, 8616994; Phenotypes: Polycystic kidney disease 4, with or without hepatic disease, MIM# 263200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PKHD1","entity_type":"gene"},{"created":"2020-08-09T20:42:37.266664+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX7 as ready","entity_name":"PEX7","entity_type":"gene"},{"created":"2020-08-09T20:42:37.255913+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex7 has been classified as Red List (Low Evidence).","entity_name":"PEX7","entity_type":"gene"},{"created":"2020-08-09T20:42:30.185065+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX7 were changed from  to Peroxisome biogenesis disorder 2A (Zellweger), MIM# 214110","entity_name":"PEX7","entity_type":"gene"},{"created":"2020-08-09T20:42:16.418673+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX7 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX7","entity_type":"gene"},{"created":"2020-08-09T20:41:59.028319+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX7","entity_type":"gene"},{"created":"2020-08-09T20:41:34.540323+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.149","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PEX7 as Red List (low evidence)","entity_name":"PEX7","entity_type":"gene"},{"created":"2020-08-09T20:41:34.532547+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.149","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex7 has been classified as Red List (Low Evidence).","entity_name":"PEX7","entity_type":"gene"},{"created":"2020-08-09T20:41:11.821463+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 2A (Zellweger), MIM# 214110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX7","entity_type":"gene"},{"created":"2020-08-09T20:39:35.838894+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX5 as ready","entity_name":"PEX5","entity_type":"gene"},{"created":"2020-08-09T20:39:35.828512+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex5 has been classified as Red List (Low Evidence).","entity_name":"PEX5","entity_type":"gene"},{"created":"2020-08-09T20:39:31.987374+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX5 were changed from  to Peroxisome biogenesis disorder 10A (Zellweger), MIM# 614882","entity_name":"PEX5","entity_type":"gene"},{"created":"2020-08-09T20:39:09.639062+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX5","entity_type":"gene"},{"created":"2020-08-09T20:38:49.438912+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PEX5 as Red List (low evidence)","entity_name":"PEX5","entity_type":"gene"},{"created":"2020-08-09T20:38:49.430440+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex5 has been classified as Red List (Low Evidence).","entity_name":"PEX5","entity_type":"gene"},{"created":"2020-08-09T20:38:26.687252+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 10A (Zellweger), MIM# 614882; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX5","entity_type":"gene"},{"created":"2020-08-09T20:36:41.846236+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX3 as ready","entity_name":"PEX3","entity_type":"gene"},{"created":"2020-08-09T20:36:41.837644+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex3 has been classified as Red List (Low Evidence).","entity_name":"PEX3","entity_type":"gene"},{"created":"2020-08-09T20:36:39.549597+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX3 were changed from  to Peroxisome biogenesis disorder 12A (Zellweger), MIM# 614886","entity_name":"PEX3","entity_type":"gene"},{"created":"2020-08-09T20:36:17.475021+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX3","entity_type":"gene"},{"created":"2020-08-09T20:35:49.535144+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PEX3 as Red List (low evidence)","entity_name":"PEX3","entity_type":"gene"},{"created":"2020-08-09T20:35:49.524501+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex3 has been classified as Red List (Low Evidence).","entity_name":"PEX3","entity_type":"gene"},{"created":"2020-08-09T20:35:23.227803+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 12A (Zellweger), MIM# 614886; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX3","entity_type":"gene"},{"created":"2020-08-09T20:32:15.150594+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX19 as ready","entity_name":"PEX19","entity_type":"gene"},{"created":"2020-08-09T20:32:15.140944+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex19 has been classified as Red List (Low Evidence).","entity_name":"PEX19","entity_type":"gene"},{"created":"2020-08-09T20:32:12.251462+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX19 were changed from  to Peroxisome biogenesis disorder 8A (Zellweger), MIM# 614876","entity_name":"PEX19","entity_type":"gene"},{"created":"2020-08-09T20:31:36.548760+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX19 were set to ","entity_name":"PEX19","entity_type":"gene"},{"created":"2020-08-09T20:31:16.485852+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX19 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX19","entity_type":"gene"},{"created":"2020-08-09T20:30:54.476926+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PEX19 as Red List (low evidence)","entity_name":"PEX19","entity_type":"gene"},{"created":"2020-08-09T20:30:54.468261+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex19 has been classified as Red List (Low Evidence).","entity_name":"PEX19","entity_type":"gene"},{"created":"2020-08-09T20:30:31.513985+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX19: Rating: RED; Mode of pathogenicity: None; Publications: 20683989; Phenotypes: Peroxisome biogenesis disorder 8A (Zellweger), MIM# 614876; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX19","entity_type":"gene"},{"created":"2020-08-09T20:26:12.166449+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PEX16 as Red List (low evidence)","entity_name":"PEX16","entity_type":"gene"},{"created":"2020-08-09T20:26:12.158760+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex16 has been classified as Red List (Low Evidence).","entity_name":"PEX16","entity_type":"gene"},{"created":"2020-08-09T20:25:50.152750+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX16 as ready","entity_name":"PEX16","entity_type":"gene"},{"created":"2020-08-09T20:25:50.144400+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex16 has been classified as Green List (High Evidence).","entity_name":"PEX16","entity_type":"gene"},{"created":"2020-08-09T20:25:47.193977+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX16 were changed from  to Peroxisome biogenesis disorder 13A (Zellweger), MIM# 614887","entity_name":"PEX16","entity_type":"gene"},{"created":"2020-08-09T20:25:19.538947+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX16 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX16","entity_type":"gene"},{"created":"2020-08-09T20:24:53.180974+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX16: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 13A (Zellweger), MIM# 614887; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX16","entity_type":"gene"},{"created":"2020-08-09T20:23:16.306906+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX14 as ready","entity_name":"PEX14","entity_type":"gene"},{"created":"2020-08-09T20:23:16.297133+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex14 has been classified as Amber List (Moderate Evidence).","entity_name":"PEX14","entity_type":"gene"},{"created":"2020-08-09T20:22:46.456917+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX14 were changed from  to Peroxisome biogenesis disorder 13A (Zellweger), MIM# 614887","entity_name":"PEX14","entity_type":"gene"},{"created":"2020-08-09T20:22:19.620685+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX14 were set to ","entity_name":"PEX14","entity_type":"gene"},{"created":"2020-08-09T20:21:59.438897+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX14","entity_type":"gene"},{"created":"2020-08-09T20:21:24.274310+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PEX14 as Amber List (moderate evidence)","entity_name":"PEX14","entity_type":"gene"},{"created":"2020-08-09T20:21:24.265868+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex14 has been classified as Amber List (Moderate Evidence).","entity_name":"PEX14","entity_type":"gene"},{"created":"2020-08-09T20:21:03.011945+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX14: Rating: AMBER; Mode of pathogenicity: None; Publications: 21686775, 18285423; Phenotypes: Peroxisome biogenesis disorder 13A (Zellweger), MIM# 614887; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX14","entity_type":"gene"},{"created":"2020-08-09T20:18:56.970394+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX13 as ready","entity_name":"PEX13","entity_type":"gene"},{"created":"2020-08-09T20:18:56.959827+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex13 has been classified as Red List (Low Evidence).","entity_name":"PEX13","entity_type":"gene"},{"created":"2020-08-09T20:18:53.933935+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX13 were changed from  to Peroxisome biogenesis disorder 11A (Zellweger), MIM# 614883","entity_name":"PEX13","entity_type":"gene"},{"created":"2020-08-09T20:18:31.652914+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX13 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX13","entity_type":"gene"},{"created":"2020-08-09T20:18:07.051490+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PEX13 as Red List (low evidence)","entity_name":"PEX13","entity_type":"gene"},{"created":"2020-08-09T20:18:07.041987+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex13 has been classified as Red List (Low Evidence).","entity_name":"PEX13","entity_type":"gene"},{"created":"2020-08-09T20:17:43.590009+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX13: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 11A (Zellweger), MIM# 614883; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX13","entity_type":"gene"},{"created":"2020-08-09T20:15:39.422434+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX11B as ready","entity_name":"PEX11B","entity_type":"gene"},{"created":"2020-08-09T20:15:39.413544+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex11b has been classified as Red List (Low Evidence).","entity_name":"PEX11B","entity_type":"gene"},{"created":"2020-08-09T20:15:36.618532+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX11B were changed from  to Peroxisome biogenesis disorder 14B, MIM# 614920","entity_name":"PEX11B","entity_type":"gene"},{"created":"2020-08-09T20:15:10.375229+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX11B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX11B","entity_type":"gene"},{"created":"2020-08-09T20:14:45.524277+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PEX11B as Red List (low evidence)","entity_name":"PEX11B","entity_type":"gene"},{"created":"2020-08-09T20:14:45.514098+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex11b has been classified as Red List (Low Evidence).","entity_name":"PEX11B","entity_type":"gene"},{"created":"2020-08-09T20:14:19.503840+10:00","panel_name":"Cholestasis","panel_id":78,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX11B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Peroxisome biogenesis disorder 14B, MIM# 614920; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX11B","entity_type":"gene"},{"created":"2020-08-09T18:05:49.105393+10:00","panel_name":"Melanoma","panel_id":3279,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"panel","text":"Panel types changed to Cancer Germline; SA Pathology","entity_name":null,"entity_type":null},{"created":"2020-08-09T18:04:33.219152+10:00","panel_name":"Medulloblastoma","panel_id":3280,"panel_version":"0.1","user_name":"Zornitza Stark","item_type":"panel","text":"Panel types changed to Cancer Germline; SA Pathology","entity_name":null,"entity_type":null},{"created":"2020-08-09T18:01:37.377898+10:00","panel_name":"Medulloblastoma","panel_id":3280,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PHOX2B was added\ngene: PHOX2B was added to Medulloblastoma. Sources: SA Pathology,Expert Review Green\nMode of inheritance for gene: PHOX2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PHOX2B","entity_type":"gene"},{"created":"2020-08-09T18:01:37.334264+10:00","panel_name":"Medulloblastoma","panel_id":3280,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ALK was added\ngene: ALK was added to Medulloblastoma. Sources: SA Pathology,Expert Review Green\nMode of inheritance for gene: ALK was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ALK","entity_type":"gene"},{"created":"2020-08-09T18:01:37.290560+10:00","panel_name":"Medulloblastoma","panel_id":3280,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TP53 was added\ngene: TP53 was added to Medulloblastoma. Sources: SA Pathology,Expert Review Green\nMode of inheritance for gene: TP53 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TP53","entity_type":"gene"},{"created":"2020-08-09T18:01:37.247000+10:00","panel_name":"Medulloblastoma","panel_id":3280,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SUFU was added\ngene: SUFU was added to Medulloblastoma. Sources: SA Pathology,Expert Review Green\nMode of inheritance for gene: SUFU was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SUFU","entity_type":"gene"},{"created":"2020-08-09T18:01:37.198837+10:00","panel_name":"Medulloblastoma","panel_id":3280,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PTCH1 was added\ngene: PTCH1 was added to Medulloblastoma. Sources: SA Pathology,Expert Review Green\nMode of inheritance for gene: PTCH1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PTCH1","entity_type":"gene"},{"created":"2020-08-09T18:01:37.155496+10:00","panel_name":"Medulloblastoma","panel_id":3280,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: APC was added\ngene: APC was added to Medulloblastoma. Sources: SA Pathology,Expert Review Green\nMode of inheritance for gene: APC was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"APC","entity_type":"gene"},{"created":"2020-08-09T18:01:37.108952+10:00","panel_name":"Melanoma","panel_id":3279,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CDKN2A was added\ngene: CDKN2A was added to Melanoma. Sources: SA Pathology,Expert Review Green\nMode of inheritance for gene: CDKN2A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CDKN2A","entity_type":"gene"},{"created":"2020-08-09T18:01:37.066139+10:00","panel_name":"Melanoma","panel_id":3279,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CDK4 was added\ngene: CDK4 was added to Melanoma. Sources: SA Pathology,Expert Review Green\nMode of inheritance for gene: CDK4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: CDK4 were set to Melanoma, cutaneous malignant, MIM#609408","entity_name":"CDK4","entity_type":"gene"},{"created":"2020-08-09T18:01:37.015889+10:00","panel_name":"Melanoma","panel_id":3279,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BAP1 was added\ngene: BAP1 was added to Melanoma. Sources: SA Pathology,Expert Review Green\nMode of inheritance for gene: BAP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: BAP1 were set to Tumour predisposition syndrome, MIM#614327","entity_name":"BAP1","entity_type":"gene"},{"created":"2020-08-09T18:01:36.479775+10:00","panel_name":"Medulloblastoma","panel_id":3280,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Medulloblastoma","entity_name":null,"entity_type":null},{"created":"2020-08-09T18:01:36.471767+10:00","panel_name":"Melanoma","panel_id":3279,"panel_version":"0.0","user_name":"Zornitza Stark","item_type":"panel","text":"Added panel Melanoma","entity_name":null,"entity_type":null},{"created":"2020-08-09T17:37:51.063959+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2835","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC5A6 were changed from Developmental delay; epilepsy; neurodegeneration to Developmental delay; epilepsy; neurodegeneration; Neurodegeneration, infantile-onset, biotin-responsive, MIM#\t618973","entity_name":"SLC5A6","entity_type":"gene"},{"created":"2020-08-09T17:37:16.426444+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC5A6 were changed from Developmental delay; epilepsy; neurodegeneration to Developmental delay; epilepsy; neurodegeneration; Neurodegeneration, infantile-onset, biotin-responsive, MIM#\t618973","entity_name":"SLC5A6","entity_type":"gene"},{"created":"2020-08-09T17:36:47.419405+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SLC5A6: Changed phenotypes: Developmental delay, epilepsy, neurodegeneration, Neurodegeneration, infantile-onset, biotin-responsive, MIM# 618973","entity_name":"SLC5A6","entity_type":"gene"},{"created":"2020-08-09T17:36:32.779868+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.774","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC5A6 were changed from Developmental delay; epilepsy; neurodegeneration to Developmental delay; epilepsy; neurodegeneration; Neurodegeneration, infantile-onset, biotin-responsive, MIM#\t618973","entity_name":"SLC5A6","entity_type":"gene"},{"created":"2020-08-09T17:35:47.878748+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3737","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC5A6 were changed from Developmental delay; epilepsy; neurodegeneration to Developmental delay; epilepsy; neurodegeneration; Neurodegeneration, infantile-onset, biotin-responsive, MIM#\t618973","entity_name":"SLC5A6","entity_type":"gene"},{"created":"2020-08-09T17:35:31.369947+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3736","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SLC5A6: Changed phenotypes: Developmental delay, epilepsy, neurodegeneration, Neurodegeneration, infantile-onset, biotin-responsive, MIM# 618973","entity_name":"SLC5A6","entity_type":"gene"},{"created":"2020-08-09T17:34:37.943590+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMO were changed from Microcephaly, congenital heart disease, polydactyly, aganglionosis; Curry-Jones syndrome, somatic mosaic 601707 to Microcephaly, congenital heart disease, polydactyly, aganglionosis; Pallister-Hall-like syndrome\t, MIM#241800; Curry-Jones syndrome, somatic mosaic 601707","entity_name":"SMO","entity_type":"gene"},{"created":"2020-08-09T17:33:57.721666+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SMO: Changed phenotypes: Microcephaly, congenital heart disease, polydactyly, aganglionosis, Pallister-Hall-like syndrome, MIM# 241800, Curry-Jones syndrome, somatic mosaic 601707","entity_name":"SMO","entity_type":"gene"},{"created":"2020-08-09T17:33:07.427870+10:00","panel_name":"Microcephaly","panel_id":138,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMO were changed from Microcephaly, congenital heart disease, polydactyly, aganglionosis to Microcephaly, congenital heart disease, polydactyly, aganglionosis; Pallister-Hall-like syndrome\t, MIM#241800","entity_name":"SMO","entity_type":"gene"},{"created":"2020-08-09T17:32:16.006381+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3736","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMO were changed from Microcephaly, congenital heart disease, polydactyly, aganglionosis; Curry-Jones syndrome, somatic mosaic 601707 to Microcephaly, congenital heart disease, polydactyly, aganglionosis, Pallister-Hall-like syndrome, MIM#\t241800; Curry-Jones syndrome, somatic mosaic 601707","entity_name":"SMO","entity_type":"gene"},{"created":"2020-08-09T17:31:37.954434+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3735","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SMO: Changed phenotypes: Microcephaly, congenital heart disease, polydactyly, aganglionosis, Pallister-Hall-like syndrome, MIM# 241800, Curry-Jones syndrome, somatic mosaic 601707","entity_name":"SMO","entity_type":"gene"},{"created":"2020-08-09T17:31:02.853576+10:00","panel_name":"Hirschsprung disease","panel_id":110,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMO were changed from Microcephaly, congenital heart disease, polydactyly, aganglionosis to Microcephaly, congenital heart disease, polydactyly, aganglionosis; Pallister-Hall-like syndrome\t, MIM#241800","entity_name":"SMO","entity_type":"gene"},{"created":"2020-08-09T17:30:38.425965+10:00","panel_name":"Hirschsprung disease","panel_id":110,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SMO: Changed phenotypes: Microcephaly, congenital heart disease, polydactyly, aganglionosis, Pallister-Hall-like syndrome , MIM#241800","entity_name":"SMO","entity_type":"gene"},{"created":"2020-08-09T17:30:20.841319+10:00","panel_name":"Craniosynostosis","panel_id":93,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: SMO.","entity_name":"SMO","entity_type":"gene"}]}