{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1341","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1339","results":[{"created":"2021-04-24T14:37:52.901254+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SALL4 were changed from  to Duane-radial ray syndrome, MIM# 607323; MONDO:0011812; IVIC syndrome, MIM# 147750; MONDO:0007836","entity_name":"SALL4","entity_type":"gene"},{"created":"2021-04-24T14:37:28.847113+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SALL4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL4","entity_type":"gene"},{"created":"2021-04-24T14:36:58.974042+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SALL4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Duane-radial ray syndrome, MIM# 607323, MONDO:0011812, IVIC syndrome, MIM# 147750, MONDO:0007836; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL4","entity_type":"gene"},{"created":"2021-04-24T14:34:51.451266+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7322","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SALL1 as ready","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:34:51.437451+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7322","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sall1 has been classified as Green List (High Evidence).","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:34:42.970640+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7322","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SALL1 were changed from  to Townes-Brocks syndrome 1, MIM#107480; MONDO:0054581","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:34:22.373850+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7321","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SALL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:34:01.258157+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7320","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SALL1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Townes-Brocks syndrome 1, MIM#107480, MONDO:0054581; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:33:09.723525+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SALL1 as ready","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:33:09.711435+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sall1 has been classified as Green List (High Evidence).","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:33:06.169805+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SALL1 were changed from  to Townes-Brocks syndrome 1, MIM#107480; MONDO:0054581","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:32:31.218323+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SALL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:32:05.071706+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: SALL1: Added comment: Well established gene-disease association.; Changed phenotypes: Townes-Brocks syndrome 1,  MIM#107480, MONDO:0054581","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:31:07.912384+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SALL1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Townes-Brocks syndrome 1,  107480; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL1","entity_type":"gene"},{"created":"2021-04-24T14:30:35.366930+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS7 as ready","entity_name":"RPS7","entity_type":"gene"},{"created":"2021-04-24T14:30:35.357141+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps7 has been classified as Green List (High Evidence).","entity_name":"RPS7","entity_type":"gene"},{"created":"2021-04-24T14:30:31.236501+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS7 were changed from  to Diamond-Blackfan anaemia 8, MIM# 612563; MONDO:0012939","entity_name":"RPS7","entity_type":"gene"},{"created":"2021-04-24T14:30:03.597192+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS7 were set to ","entity_name":"RPS7","entity_type":"gene"},{"created":"2021-04-24T14:29:38.385653+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS7 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS7","entity_type":"gene"},{"created":"2021-04-24T12:00:38.689722+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS26 as ready","entity_name":"RPS26","entity_type":"gene"},{"created":"2021-04-24T12:00:38.679952+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps26 has been classified as Green List (High Evidence).","entity_name":"RPS26","entity_type":"gene"},{"created":"2021-04-24T12:00:33.510467+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS26 were changed from  to Diamond-Blackfan anaemia 10, MIM# 613309; MONDO:0013217","entity_name":"RPS26","entity_type":"gene"},{"created":"2021-04-24T11:58:41.944430+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS26 were set to ","entity_name":"RPS26","entity_type":"gene"},{"created":"2021-04-24T11:58:19.813673+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS26 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS26","entity_type":"gene"},{"created":"2021-04-24T11:57:16.039041+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS24 as ready","entity_name":"RPS24","entity_type":"gene"},{"created":"2021-04-24T11:57:16.029813+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps24 has been classified as Green List (High Evidence).","entity_name":"RPS24","entity_type":"gene"},{"created":"2021-04-24T11:57:03.471448+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS24 were changed from  to Diamond-blackfan anaemia 3, MIM# 610629; MONDO:0012529","entity_name":"RPS24","entity_type":"gene"},{"created":"2021-04-24T11:56:32.542431+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS24 were set to ","entity_name":"RPS24","entity_type":"gene"},{"created":"2021-04-24T11:56:03.416876+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS24 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS24","entity_type":"gene"},{"created":"2021-04-24T11:55:38.756671+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: At least 3 unrelated individuals reported.; to: At least 3 unrelated individuals reported. Thumb abnormalities are a feature.","entity_name":"RPS24","entity_type":"gene"},{"created":"2021-04-24T11:55:27.246000+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RPS24: Changed phenotypes: Diamond-blackfan anaemia 3, MIM# 610629, MONDO:0012529","entity_name":"RPS24","entity_type":"gene"},{"created":"2021-04-24T11:54:52.077660+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS19 were changed from Diamond-Blackfan anemia 1, MIM# 105650; MONDO:0007110 to Diamond-Blackfan anaemia 1, MIM# 105650; MONDO:0007110","entity_name":"RPS19","entity_type":"gene"},{"created":"2021-04-24T11:54:06.442557+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.217","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS17 were changed from Diamond-Blackfan anemia 4, MIM#\t612527 to Diamond-Blackfan anaemia 4, MIM#\t612527; MONDO:0012924","entity_name":"RPS17","entity_type":"gene"},{"created":"2021-04-24T11:53:20.764037+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7320","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS17 were changed from Diamond-Blackfan anemia 4, MIM# 612527 to Diamond-Blackfan anaemia 4, MIM# 612527; MONDO:0012924","entity_name":"RPS17","entity_type":"gene"},{"created":"2021-04-24T11:52:42.086387+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS17 were changed from Diamond-Blackfan anemia 4, MIM# 612527 to Diamond-Blackfan anaemia 4, MIM# 612527; MONDO:0012924","entity_name":"RPS17","entity_type":"gene"},{"created":"2021-04-24T11:51:44.361714+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPS10 as ready","entity_name":"RPS10","entity_type":"gene"},{"created":"2021-04-24T11:51:44.351887+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rps10 has been classified as Green List (High Evidence).","entity_name":"RPS10","entity_type":"gene"},{"created":"2021-04-24T11:51:34.025297+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPS10 were changed from  to Diamond-Blackfan anemia 9, MIM# 613308; MONDO:0013216","entity_name":"RPS10","entity_type":"gene"},{"created":"2021-04-24T11:50:52.266521+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPS10 were set to ","entity_name":"RPS10","entity_type":"gene"},{"created":"2021-04-24T11:50:23.255316+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPS10 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPS10","entity_type":"gene"},{"created":"2021-04-24T11:49:47.941810+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL5 as ready","entity_name":"RPL5","entity_type":"gene"},{"created":"2021-04-24T11:49:47.926510+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl5 has been classified as Green List (High Evidence).","entity_name":"RPL5","entity_type":"gene"},{"created":"2021-04-24T11:49:44.696275+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL5 were changed from  to Diamond-Blackfan anaemia 6, MIM# 612561; MONDO:0012937","entity_name":"RPL5","entity_type":"gene"},{"created":"2021-04-24T11:49:13.541251+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPL5 were set to ","entity_name":"RPL5","entity_type":"gene"},{"created":"2021-04-24T11:48:49.808813+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPL5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPL5","entity_type":"gene"},{"created":"2021-04-24T11:48:21.013843+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL35A as ready","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:48:21.003101+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl35a has been classified as Green List (High Evidence).","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:48:09.083154+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.216","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL35A were changed from Diamond-Blackfan anemia 5, MIM# 612528 to Diamond-Blackfan anemia 5, MIM# 612528; MONDO:0012925","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:47:40.640182+10:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"0.215","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: RPL35A.","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:47:24.197973+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7319","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL35A were changed from Diamond-Blackfan anemia 5, MIM# 612528 to Diamond-Blackfan anemia 5, MIM# 612528; MONDO:0012925","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:47:06.220525+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7318","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: RPL35A: Changed phenotypes: Diamond-Blackfan anemia 5, MIM# 612528, MONDO:0012925","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:47:01.910845+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL35A were changed from Diamond-Blackfan anaemia 5, MIM# 612528 to Diamond-Blackfan anaemia 5, MIM# 612528; MONDO:0012925","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:46:25.105751+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL35A were changed from  to Diamond-Blackfan anaemia 5, MIM# 612528","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:46:00.474048+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPL35A were set to ","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:45:35.336833+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPL35A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:45:07.704793+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: RPL35A.","entity_name":"RPL35A","entity_type":"gene"},{"created":"2021-04-24T11:44:38.817144+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Well established gene-disease association.; to: Well established gene-disease association, thumb abnormalities are a feature.","entity_name":"RPL11","entity_type":"gene"},{"created":"2021-04-24T11:44:24.567213+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RPL11 as ready","entity_name":"RPL11","entity_type":"gene"},{"created":"2021-04-24T11:44:24.557251+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rpl11 has been classified as Green List (High Evidence).","entity_name":"RPL11","entity_type":"gene"},{"created":"2021-04-24T11:44:21.373275+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RPL11 were changed from  to Diamond-Blackfan anaemia 7, MIM# 612562; MONDO:0012938","entity_name":"RPL11","entity_type":"gene"},{"created":"2021-04-24T11:43:49.603433+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RPL11 were set to ","entity_name":"RPL11","entity_type":"gene"},{"created":"2021-04-24T11:43:27.832109+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPL11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RPL11","entity_type":"gene"},{"created":"2021-04-24T11:42:26.618653+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PALB2 as ready","entity_name":"PALB2","entity_type":"gene"},{"created":"2021-04-24T11:42:26.609024+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: palb2 has been classified as Green List (High Evidence).","entity_name":"PALB2","entity_type":"gene"},{"created":"2021-04-24T11:41:59.484352+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PALB2 were changed from  to Fanconi anaemia, complementation group N, MIM# 610832","entity_name":"PALB2","entity_type":"gene"},{"created":"2021-04-24T11:41:28.921855+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PALB2 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PALB2","entity_type":"gene"},{"created":"2021-04-24T11:41:13.578479+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PALB2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PALB2","entity_type":"gene"},{"created":"2021-04-24T11:39:12.593061+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCI as ready","entity_name":"FANCI","entity_type":"gene"},{"created":"2021-04-24T11:39:12.583244+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fanci has been classified as Green List (High Evidence).","entity_name":"FANCI","entity_type":"gene"},{"created":"2021-04-24T11:38:52.155920+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCL as ready","entity_name":"FANCL","entity_type":"gene"},{"created":"2021-04-24T11:38:52.114872+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancl has been classified as Green List (High Evidence).","entity_name":"FANCL","entity_type":"gene"},{"created":"2021-04-24T11:38:49.533222+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCL were changed from  to Fanconi anemia, complementation group L, MIM# 614083; MONDO:0013566","entity_name":"FANCL","entity_type":"gene"},{"created":"2021-04-24T11:38:34.324605+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCI were changed from  to Fanconi anemia, complementation group I, MIM# 609053; MONDO:0012186","entity_name":"FANCI","entity_type":"gene"},{"created":"2021-04-24T11:38:09.048102+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCL were set to ","entity_name":"FANCL","entity_type":"gene"},{"created":"2021-04-24T11:37:51.908441+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCI were set to ","entity_name":"FANCI","entity_type":"gene"},{"created":"2021-04-24T11:37:31.546570+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCL","entity_type":"gene"},{"created":"2021-04-24T11:37:11.170058+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCI was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCI","entity_type":"gene"},{"created":"2021-04-24T11:36:43.329891+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCF as ready","entity_name":"FANCF","entity_type":"gene"},{"created":"2021-04-24T11:36:43.315433+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancf has been classified as Green List (High Evidence).","entity_name":"FANCF","entity_type":"gene"},{"created":"2021-04-24T11:36:37.127576+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCG as ready","entity_name":"FANCG","entity_type":"gene"},{"created":"2021-04-24T11:36:37.114956+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancg has been classified as Green List (High Evidence).","entity_name":"FANCG","entity_type":"gene"},{"created":"2021-04-24T11:36:28.257750+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCG were changed from  to Fanconi anaemia, complementation group G, MIM# 614082; MONDO:0013565","entity_name":"FANCG","entity_type":"gene"},{"created":"2021-04-24T11:35:58.106932+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCF were changed from  to Fanconi anaemia, complementation group F 603467; MONDO:0011325","entity_name":"FANCF","entity_type":"gene"},{"created":"2021-04-24T11:35:42.845597+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCG were set to ","entity_name":"FANCG","entity_type":"gene"},{"created":"2021-04-24T11:35:22.079376+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCF were set to ","entity_name":"FANCF","entity_type":"gene"},{"created":"2021-04-24T11:35:07.160446+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCG was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCG","entity_type":"gene"},{"created":"2021-04-24T11:34:43.606769+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCF was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCF","entity_type":"gene"},{"created":"2021-04-24T11:34:12.859305+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCE as ready","entity_name":"FANCE","entity_type":"gene"},{"created":"2021-04-24T11:34:12.849246+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fance has been classified as Green List (High Evidence).","entity_name":"FANCE","entity_type":"gene"},{"created":"2021-04-24T11:34:01.410396+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCE were changed from  to Fanconi anaemia, complementation group E, MIM# 600901; MONDO:0010953","entity_name":"FANCE","entity_type":"gene"},{"created":"2021-04-24T11:33:33.026295+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.104","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCE were set to ","entity_name":"FANCE","entity_type":"gene"},{"created":"2021-04-24T11:33:08.721079+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCE was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCE","entity_type":"gene"},{"created":"2021-04-24T11:32:13.201682+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.7318","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCD2 were changed from Fanconi anemia, complementation group D2, MIM#227646 to Fanconi anemia, complementation group D2, MIM#227646; MONDO:0009214","entity_name":"FANCD2","entity_type":"gene"},{"created":"2021-04-24T11:31:45.835517+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCD2 as ready","entity_name":"FANCD2","entity_type":"gene"},{"created":"2021-04-24T11:31:45.825825+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fancd2 has been classified as Green List (High Evidence).","entity_name":"FANCD2","entity_type":"gene"},{"created":"2021-04-24T11:31:38.879535+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCD2 were changed from Fanconi anaemia, complementation group D2, MIM# 227646 to Fanconi anaemia, complementation group D2, MIM# 227646; MONDO:0009214","entity_name":"FANCD2","entity_type":"gene"},{"created":"2021-04-24T11:31:06.721379+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FANCD2 were changed from  to Fanconi anaemia, complementation group D2, MIM# 227646","entity_name":"FANCD2","entity_type":"gene"},{"created":"2021-04-24T11:30:37.492417+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FANCD2 were set to ","entity_name":"FANCD2","entity_type":"gene"},{"created":"2021-04-24T11:30:14.637469+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FANCD2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FANCD2","entity_type":"gene"},{"created":"2021-04-24T11:29:40.744222+10:00","panel_name":"Radial Ray Abnormalities","panel_id":163,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FANCC as ready","entity_name":"FANCC","entity_type":"gene"}]}