{"count":220313,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=867","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=865","results":[{"created":"2022-04-30T17:46:38.434835+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13480","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GALT1 were set to ","entity_name":"B4GALT1","entity_type":"gene"},{"created":"2022-04-30T17:46:16.597573+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13479","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B4GALT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GALT1","entity_type":"gene"},{"created":"2022-04-30T17:45:58.155500+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13478","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Intellectual disability is part of CDG, although non-neurological forms of this CDG have been described. \nSources: Expert list; to: At least 3 unrelated families.\r\nSources: Expert list","entity_name":"B4GALT1","entity_type":"gene"},{"created":"2022-04-30T17:44:17.890084+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13478","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B4GALNT1 as ready","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2022-04-30T17:44:17.875169+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13478","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b4galnt1 has been classified as Green List (High Evidence).","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2022-04-30T17:44:09.551763+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13478","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B4GALNT1 were changed from  to Spastic paraplegia 26, autosomal recessive (MIM #609195)","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2022-04-30T17:43:49.044156+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13477","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GALNT1 were set to 23746551 24103911","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2022-04-30T17:42:02.203368+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13476","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B4GALNT1 were set to ","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2022-04-30T17:41:41.170217+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13475","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B4GALNT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2022-04-30T17:41:16.088933+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13474","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: B4GALNT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 23746551 24103911; Phenotypes: Spastic paraplegia 26, autosomal recessive (MIM #609195); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"B4GALNT1","entity_type":"gene"},{"created":"2022-04-30T17:39:47.031644+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13474","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: B3GLCT as ready","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2022-04-30T17:39:47.018675+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13474","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: b3glct has been classified as Green List (High Evidence).","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2022-04-30T17:39:37.996914+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13474","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: B3GLCT were changed from  to Peters-plus syndrome, MIM#261540","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2022-04-30T17:39:17.069482+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13473","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: B3GLCT were set to ","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2022-04-30T17:38:55.707285+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13472","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: B3GLCT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2022-04-30T17:38:33.409919+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13471","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: B3GLCT: Rating: GREEN; Mode of pathogenicity: None; Publications: 18798333, 19796186, 32533185, 32204707, 31795264; Phenotypes: Peters-plus syndrome, MIM#261540; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"B3GLCT","entity_type":"gene"},{"created":"2022-04-30T17:36:02.228847+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13471","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: APOA5 as ready","entity_name":"APOA5","entity_type":"gene"},{"created":"2022-04-30T17:36:02.214032+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13471","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: apoa5 has been classified as Green List (High Evidence).","entity_name":"APOA5","entity_type":"gene"},{"created":"2022-04-30T17:34:24.357573+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4710","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AP1S2 as ready","entity_name":"AP1S2","entity_type":"gene"},{"created":"2022-04-30T17:34:24.340783+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4710","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ap1s2 has been classified as Green List (High Evidence).","entity_name":"AP1S2","entity_type":"gene"},{"created":"2022-04-30T17:34:20.622524+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4710","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AP1S2 were changed from  to Pettigrew syndrome, MIM# 304340","entity_name":"AP1S2","entity_type":"gene"},{"created":"2022-04-30T17:33:44.644587+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4709","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AP1S2 were set to ","entity_name":"AP1S2","entity_type":"gene"},{"created":"2022-04-30T17:25:50.045257+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4708","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AP1S2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"AP1S2","entity_type":"gene"},{"created":"2022-04-30T17:25:12.525027+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4707","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: AP1S2: Rating: GREEN; Mode of pathogenicity: None; Publications: 17186471, 17617514, 19377476, 30714330, 23756445; Phenotypes: Pettigrew syndrome, MIM# 304340; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"AP1S2","entity_type":"gene"},{"created":"2022-04-30T17:24:26.031017+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13471","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AP1S2 were changed from Mental retardation, X-linked syndromic 5, MIM#304340 to Pettigrew syndrome, MIM# 304340","entity_name":"AP1S2","entity_type":"gene"},{"created":"2022-04-30T17:24:03.436735+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13470","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AP1S2 were set to ","entity_name":"AP1S2","entity_type":"gene"},{"created":"2022-04-30T17:23:40.356045+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13469","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: AP1S2: Rating: GREEN; Mode of pathogenicity: None; Publications: 17186471, 17617514, 19377476, 30714330, 23756445; Phenotypes: Pettigrew syndrome, MIM# 304340; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"AP1S2","entity_type":"gene"},{"created":"2022-04-30T17:20:35.965241+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13469","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: APCDD1 as ready","entity_name":"APCDD1","entity_type":"gene"},{"created":"2022-04-30T17:20:35.954966+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13469","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: apcdd1 has been classified as Green List (High Evidence).","entity_name":"APCDD1","entity_type":"gene"},{"created":"2022-04-30T17:20:20.325496+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13469","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: APCDD1 were changed from  to Hypotrichosis 1, MIM#605389","entity_name":"APCDD1","entity_type":"gene"},{"created":"2022-04-30T17:19:59.215760+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13468","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: APCDD1 were set to ","entity_name":"APCDD1","entity_type":"gene"},{"created":"2022-04-30T17:19:39.497620+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13467","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: APCDD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"APCDD1","entity_type":"gene"},{"created":"2022-04-30T17:19:19.766224+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13466","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: APCDD1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypotrichosis 1, MIM#605389; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"APCDD1","entity_type":"gene"},{"created":"2022-04-30T17:17:22.338395+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13466","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ANO10 were changed from Spinocerebellar ataxia, autosomal recessive 10 MIM#613728 to Spinocerebellar ataxia, autosomal recessive 10, MIM#613728","entity_name":"ANO10","entity_type":"gene"},{"created":"2022-04-30T17:17:07.221028+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13465","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ANO10 were set to ","entity_name":"ANO10","entity_type":"gene"},{"created":"2022-04-30T17:16:44.442012+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13464","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ANO10: Rating: GREEN; Mode of pathogenicity: None; Publications: 21092923, 25182700; Phenotypes: Spinocerebellar ataxia, autosomal recessive 10, MIM#613728; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ANO10","entity_type":"gene"},{"created":"2022-04-30T17:15:09.370330+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13464","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PHOX2B as ready","entity_name":"PHOX2B","entity_type":"gene"},{"created":"2022-04-30T17:15:09.347232+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13464","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: phox2b has been classified as Green List (High Evidence).","entity_name":"PHOX2B","entity_type":"gene"},{"created":"2022-04-30T17:15:00.024691+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13464","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PHOX2B were changed from  to Central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease - MIM#209880; Neuroblastoma with Hirschsprung disease - MIM#613013","entity_name":"PHOX2B","entity_type":"gene"},{"created":"2022-04-30T17:14:40.630631+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13463","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PHOX2B were set to ","entity_name":"PHOX2B","entity_type":"gene"},{"created":"2022-04-30T17:14:20.722141+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13462","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PHOX2B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PHOX2B","entity_type":"gene"},{"created":"2022-04-30T17:13:37.826894+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13461","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX26 as ready","entity_name":"PEX26","entity_type":"gene"},{"created":"2022-04-30T17:13:37.814464+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13461","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex26 has been classified as Green List (High Evidence).","entity_name":"PEX26","entity_type":"gene"},{"created":"2022-04-30T17:13:29.194117+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13461","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX26 were changed from  to Peroxisome biogenesis disorder 7A (Zellweger) - MIM#614872; Peroxisome biogenesis disorder 7B - MIM#614873","entity_name":"PEX26","entity_type":"gene"},{"created":"2022-04-30T17:13:08.247063+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13460","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX26 were set to ","entity_name":"PEX26","entity_type":"gene"},{"created":"2022-04-30T17:12:47.600826+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13459","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX26 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX26","entity_type":"gene"},{"created":"2022-04-30T17:12:13.926323+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13458","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX2 as ready","entity_name":"PEX2","entity_type":"gene"},{"created":"2022-04-30T17:12:13.913111+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13458","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex2 has been classified as Green List (High Evidence).","entity_name":"PEX2","entity_type":"gene"},{"created":"2022-04-30T17:11:50.289937+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13458","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX2 were changed from  to Peroxisome biogenesis disorder 5A (Zellweger) - MIM#614866; Peroxisome biogenesis disorder 5B - MIM#614867","entity_name":"PEX2","entity_type":"gene"},{"created":"2022-04-30T17:11:28.082507+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13457","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX2 were set to ","entity_name":"PEX2","entity_type":"gene"},{"created":"2022-04-30T17:11:07.367653+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13456","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX2","entity_type":"gene"},{"created":"2022-04-30T17:10:24.873647+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13455","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX19 as ready","entity_name":"PEX19","entity_type":"gene"},{"created":"2022-04-30T17:10:24.863718+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13455","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex19 has been classified as Green List (High Evidence).","entity_name":"PEX19","entity_type":"gene"},{"created":"2022-04-30T17:09:52.808542+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13455","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX19 were changed from  to Peroxisome biogenesis disorder 12A (Zellweger) - MIM#614886","entity_name":"PEX19","entity_type":"gene"},{"created":"2022-04-29T18:25:50.823453+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13454","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX16 as ready","entity_name":"PEX16","entity_type":"gene"},{"created":"2022-04-29T18:25:50.812740+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13454","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":"2022-04-29T18:25:42.231405+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13454","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX16 were changed from  to Peroxisome biogenesis disorder 8A (Zellweger) - MIM#614876; Peroxisome biogenesis disorder 8B - MIM#614877","entity_name":"PEX16","entity_type":"gene"},{"created":"2022-04-29T18:25:21.462715+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13453","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX16 were set to ","entity_name":"PEX16","entity_type":"gene"},{"created":"2022-04-29T18:25:00.577035+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13452","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":"2022-04-29T18:21:38.879136+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13451","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX14 as ready","entity_name":"PEX14","entity_type":"gene"},{"created":"2022-04-29T18:21:38.867006+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13451","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex14 has been classified as Green List (High Evidence).","entity_name":"PEX14","entity_type":"gene"},{"created":"2022-04-29T18:21:29.929621+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13451","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":"2022-04-29T18:20:53.547422+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13450","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX14 were set to ","entity_name":"PEX14","entity_type":"gene"},{"created":"2022-04-29T18:20:34.069111+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13449","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":"2022-04-29T18:20:02.328739+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13448","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX13 as ready","entity_name":"PEX13","entity_type":"gene"},{"created":"2022-04-29T18:20:02.317687+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13448","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex13 has been classified as Green List (High Evidence).","entity_name":"PEX13","entity_type":"gene"},{"created":"2022-04-29T18:19:52.518804+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13448","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX13 were changed from  to Peroxisome biogenesis disorder 11A (Zellweger) - MIM#614883; Peroxisome biogenesis disorder 11B - MIM#614885","entity_name":"PEX13","entity_type":"gene"},{"created":"2022-04-29T18:19:30.878343+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13447","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":"2022-04-29T18:18:57.238765+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13446","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX12 as ready","entity_name":"PEX12","entity_type":"gene"},{"created":"2022-04-29T18:18:57.229039+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13446","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex12 has been classified as Green List (High Evidence).","entity_name":"PEX12","entity_type":"gene"},{"created":"2022-04-29T18:18:44.644680+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13446","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PEX12 were changed from  to Peroxisome biogenesis disorder 3A (Zellweger) - MIM#614859; Peroxisome biogenesis disorder 3B - MIM#266510","entity_name":"PEX12","entity_type":"gene"},{"created":"2022-04-29T18:14:26.320039+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13445","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PEX12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX12","entity_type":"gene"},{"created":"2022-04-29T18:12:02.832401+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13444","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ENTPD1 were set to 24482476; 30652007","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:11:39.707434+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13443","user_name":"Zornitza Stark","item_type":"entity","text":"commented on gene: ENTPD1: PMID  35471564: 27 individuals from 17 families published, expanding the phenotype to a complex neurodevelopmental disorder characterised by ID, white matter abnormalities and spastic paraplegia.","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:11:19.465876+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13443","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: ENTPD1: Changed publications: 24482476, 30652007, 35471564","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:10:42.070203+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.263","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ENTPD1 as ready","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:10:42.059787+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.263","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: entpd1 has been classified as Green List (High Evidence).","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:10:38.397682+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.263","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ENTPD1 as Green List (high evidence)","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:10:38.384293+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.263","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: entpd1 has been classified as Green List (High Evidence).","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:10:23.264130+10:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.262","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ENTPD1 was added\ngene: ENTPD1 was added to Leukodystrophy - paediatric. Sources: Literature\nMode of inheritance for gene: ENTPD1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ENTPD1 were set to 35471564\nPhenotypes for gene: ENTPD1 were set to Spastic paraplegia 64, autosomal recessive, MIM# 615683\nReview for gene: ENTPD1 was set to GREEN\nAdded comment: 27 individuals from 17 families published, expanding the phenotype to a complex neurodevelopmental disorder characterised by ID, white matter abnormalities and spastic paraplegia. \nSources: Literature","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:10:03.871706+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4707","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ENTPD1 as ready","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:10:03.858876+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4707","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: entpd1 has been classified as Green List (High Evidence).","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:10:02.741807+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4707","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ENTPD1 as Green List (high evidence)","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:10:02.724357+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4707","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: entpd1 has been classified as Green List (High Evidence).","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:09:14.431271+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4706","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ENTPD1 was added\ngene: ENTPD1 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature\nMode of inheritance for gene: ENTPD1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ENTPD1 were set to 35471564\nPhenotypes for gene: ENTPD1 were set to Spastic paraplegia 64, autosomal recessive, MIM#\t615683\nReview for gene: ENTPD1 was set to GREEN\nAdded comment: 27 individuals from 17 families published, expanding the phenotype to a complex neurodevelopmental disorder characterised by ID, white matter abnormalities and spastic paraplegia. \nSources: Literature","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:06:19.155036+10:00","panel_name":"Hereditary Spastic Paraplegia - paediatric","panel_id":317,"panel_version":"1.26","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ENTPD1 were set to 24482476; 30652007","entity_name":"ENTPD1","entity_type":"gene"},{"created":"2022-04-29T18:05:04.322101+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13443","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RSPH1 as ready","entity_name":"RSPH1","entity_type":"gene"},{"created":"2022-04-29T18:05:04.308808+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13443","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rsph1 has been classified as Green List (High Evidence).","entity_name":"RSPH1","entity_type":"gene"},{"created":"2022-04-29T18:04:56.384610+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13443","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RSPH1 were changed from  to Ciliary dyskinesia, primary, 24 MIM#615481","entity_name":"RSPH1","entity_type":"gene"},{"created":"2022-04-29T18:04:35.321518+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13442","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RSPH1 were set to ","entity_name":"RSPH1","entity_type":"gene"},{"created":"2022-04-29T18:04:15.065056+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13441","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RSPH1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RSPH1","entity_type":"gene"},{"created":"2022-04-29T18:02:34.543854+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CNGB1 as ready","entity_name":"CNGB1","entity_type":"gene"},{"created":"2022-04-29T18:02:34.525205+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cngb1 has been classified as Green List (High Evidence).","entity_name":"CNGB1","entity_type":"gene"},{"created":"2022-04-29T18:02:25.753198+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CNGB1 were changed from Retinitis pigmentosa 45, 613767 to Retinitis pigmentosa 45, MIM#613767","entity_name":"CNGB1","entity_type":"gene"},{"created":"2022-04-29T18:02:17.414650+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CNGB1 were set to ","entity_name":"CNGB1","entity_type":"gene"},{"created":"2022-04-29T18:02:03.140459+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CNGB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 11379879, 15557452, 23661369, 33847019; Phenotypes: Retinitis pigmentosa 45 MIM#613767; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CNGB1","entity_type":"gene"},{"created":"2022-04-29T18:00:48.794077+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CNGA1 as ready","entity_name":"CNGA1","entity_type":"gene"},{"created":"2022-04-29T18:00:48.779848+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cnga1 has been classified as Green List (High Evidence).","entity_name":"CNGA1","entity_type":"gene"},{"created":"2022-04-29T18:00:42.153632+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CNGA1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CNGA1","entity_type":"gene"},{"created":"2022-04-29T18:00:16.093077+10:00","panel_name":"Retinitis pigmentosa_Autosomal Recessive/X-linked","panel_id":277,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CNGA1 were set to ","entity_name":"CNGA1","entity_type":"gene"}]}