{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1443","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1441","results":[{"created":"2021-01-16T21:07:47.380837+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBB3 were changed from  to Cortical dysplasia, complex, with other brain malformations 1, MIM# 614039","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T21:07:12.350732+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB3 were set to ","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T21:06:36.225115+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBB3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T21:06:06.395125+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TUBB3: Rating: GREEN; Mode of pathogenicity: None; Publications: 20829227, 25059107, 33318778; Phenotypes: Cortical dysplasia, complex, with other brain malformations 1, MIM# 614039; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB3","entity_type":"gene"},{"created":"2021-01-16T21:02:02.403813+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB2B as ready","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:02:02.394337+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb2b has been classified as Green List (High Evidence).","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:01:59.493949+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBB2B were changed from  to Cortical dysplasia, complex, with other brain malformations 7, MIM# 610031","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:01:29.253200+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB2B were set to ","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:01:01.413592+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBB2B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T21:00:29.106955+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TUBB2B: Rating: GREEN; Mode of pathogenicity: None; Publications: 19465910, 22333901, 26732629, 33082561; Phenotypes: Cortical dysplasia, complex, with other brain malformations 7, MIM# 610031; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB2B","entity_type":"gene"},{"created":"2021-01-16T20:56:55.582279+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBB as ready","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T20:56:55.573671+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubb has been classified as Green List (High Evidence).","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T20:56:52.802878+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TUBB were changed from  to Cortical dysplasia, complex, with other brain malformations 6, MIM# 615771","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T20:56:25.932518+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB were set to ","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T20:55:58.115412+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBB was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T20:55:27.786217+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TUBB: Rating: GREEN; Mode of pathogenicity: None; Publications: 23246003, 32085672; Phenotypes: Cortical dysplasia, complex, with other brain malformations 6, MIM# 615771; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBB","entity_type":"gene"},{"created":"2021-01-16T20:49:37.084551+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TUBA1A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBA1A","entity_type":"gene"},{"created":"2021-01-16T20:49:05.491880+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TUBA1A: Rating: GREEN; Mode of pathogenicity: None; Publications: 17218254, 17584854, 18728072; Phenotypes: Lissencephaly 3, MIM# 611603; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TUBA1A","entity_type":"gene"},{"created":"2021-01-16T20:46:08.709106+11:00","panel_name":"Tubulinopathies","panel_id":21,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"panel","text":"Panel types changed to Australian Genomics; Victorian Clinical Genetics Services; Rare Disease","entity_name":null,"entity_type":null},{"created":"2021-01-16T20:38:05.917858+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"1.0","user_name":"Zornitza Stark","item_type":"panel","text":"promoted panel to version 1.0","entity_name":null,"entity_type":null},{"created":"2021-01-16T20:35:59.251327+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6055","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FZD4 as ready","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:35:59.238306+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6055","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fzd4 has been classified as Green List (High Evidence).","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:35:52.322084+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6055","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FZD4 were changed from  to Exudative vitreoretinopathy 1, MIM# 133780","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:35:33.060615+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6054","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FZD4 were set to ","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:35:15.307642+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6053","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FZD4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:34:53.863909+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6052","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FZD4: Rating: GREEN; Mode of pathogenicity: None; Publications: 21097938, 33302760, 31999491; Phenotypes: Exudative vitreoretinopathy 1, MIM# 133780; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:34:16.016442+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FZD4 as ready","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:34:16.008446+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fzd4 has been classified as Green List (High Evidence).","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:34:14.034666+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FZD4 were changed from  to Exudative vitreoretinopathy 1, MIM# 133780","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:34:06.551001+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FZD4 were set to ","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:33:58.879802+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FZD4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:33:49.102886+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: FZD4: Rating: GREEN; Mode of pathogenicity: None; Publications: 21097938, 33302760, 31999491; Phenotypes: Exudative vitreoretinopathy 1, MIM# 133780; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FZD4","entity_type":"gene"},{"created":"2021-01-16T20:31:37.948099+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KCNJ13 as ready","entity_name":"KCNJ13","entity_type":"gene"},{"created":"2021-01-16T20:31:37.937315+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnj13 has been classified as Amber List (Moderate Evidence).","entity_name":"KCNJ13","entity_type":"gene"},{"created":"2021-01-16T20:31:19.822791+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KCNJ13 were changed from  to Snowflake vitreoretinal degeneration, MIM# 193230","entity_name":"KCNJ13","entity_type":"gene"},{"created":"2021-01-16T20:31:09.471263+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KCNJ13 were set to ","entity_name":"KCNJ13","entity_type":"gene"},{"created":"2021-01-16T20:30:48.716330+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KCNJ13 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"KCNJ13","entity_type":"gene"},{"created":"2021-01-16T20:30:38.329160+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KCNJ13 as Amber List (moderate evidence)","entity_name":"KCNJ13","entity_type":"gene"},{"created":"2021-01-16T20:30:38.321356+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnj13 has been classified as Amber List (Moderate Evidence).","entity_name":"KCNJ13","entity_type":"gene"},{"created":"2021-01-16T20:30:29.063713+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KCNJ13: Rating: AMBER; Mode of pathogenicity: None; Publications: 18179896, 23255580, 31647904; Phenotypes: Snowflake vitreoretinal degeneration, MIM# 193230; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"KCNJ13","entity_type":"gene"},{"created":"2021-01-16T20:25:23.078271+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF11 as ready","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-01-16T20:25:23.065879+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif11 has been classified as Green List (High Evidence).","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-01-16T20:25:21.028468+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KIF11 were changed from  to Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation, MIM# 152950","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-01-16T20:25:13.236816+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KIF11 were set to ","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-01-16T20:25:05.567565+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF11 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-01-16T20:24:55.566755+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KIF11: Rating: GREEN; Mode of pathogenicity: None; Publications: 22284827; Phenotypes: Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation, MIM# 152950; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KIF11","entity_type":"gene"},{"created":"2021-01-16T20:23:40.149586+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRP5 as ready","entity_name":"LRP5","entity_type":"gene"},{"created":"2021-01-16T20:23:40.141783+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrp5 has been classified as Green List (High Evidence).","entity_name":"LRP5","entity_type":"gene"},{"created":"2021-01-16T20:23:28.508883+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRP5 were changed from  to Exudative vitreoretinopathy 4, MIM# 601813","entity_name":"LRP5","entity_type":"gene"},{"created":"2021-01-16T20:23:19.471918+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LRP5 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LRP5","entity_type":"gene"},{"created":"2021-01-16T20:23:09.307844+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LRP5: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Exudative vitreoretinopathy 4, MIM# 601813; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LRP5","entity_type":"gene"},{"created":"2021-01-16T20:20:19.675094+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDP as ready","entity_name":"NDP","entity_type":"gene"},{"created":"2021-01-16T20:20:19.656282+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndp has been classified as Green List (High Evidence).","entity_name":"NDP","entity_type":"gene"},{"created":"2021-01-16T20:20:16.788159+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDP were changed from  to Exudative vitreoretinopathy 2, X-linked, MIM# 305390; Norrie disease, MIM# 310600","entity_name":"NDP","entity_type":"gene"},{"created":"2021-01-16T20:20:00.970664+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDP was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"NDP","entity_type":"gene"},{"created":"2021-01-16T20:19:49.808900+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NDP: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Exudative vitreoretinopathy 2, X-linked, MIM# 305390, Norrie disease, MIM# 310600; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"NDP","entity_type":"gene"},{"created":"2021-01-16T20:18:11.501226+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NR2E3 as ready","entity_name":"NR2E3","entity_type":"gene"},{"created":"2021-01-16T20:18:11.493560+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nr2e3 has been classified as Green List (High Evidence).","entity_name":"NR2E3","entity_type":"gene"},{"created":"2021-01-16T20:18:08.926688+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NR2E3 were changed from  to Enhanced S-cone syndrome, MIM# 268100","entity_name":"NR2E3","entity_type":"gene"},{"created":"2021-01-16T20:17:55.984984+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NR2E3 were set to ","entity_name":"NR2E3","entity_type":"gene"},{"created":"2021-01-16T20:17:48.397613+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NR2E3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NR2E3","entity_type":"gene"},{"created":"2021-01-16T20:17:38.343452+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NR2E3: Rating: GREEN; Mode of pathogenicity: None; Publications: 10655056, 11071390, 18294254; Phenotypes: Enhanced S-cone syndrome 268100; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NR2E3","entity_type":"gene"},{"created":"2021-01-16T20:14:47.285890+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6052","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSPAN12 as ready","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:14:47.269342+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6052","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tspan12 has been classified as Green List (High Evidence).","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:14:39.322954+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6052","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSPAN12 were changed from  to Exudative vitreoretinopathy 5, MIM# 613310","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:14:21.603470+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6051","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TSPAN12 were set to ","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:14:03.970462+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6050","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TSPAN12 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:13:46.037150+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6049","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TSPAN12: Rating: GREEN; Mode of pathogenicity: None; Publications: 20159111, 20159112, 21334594; Phenotypes: Exudative vitreoretinopathy 5, MIM# 613310; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:13:38.108850+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSPAN12 as ready","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:13:38.098165+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tspan12 has been classified as Green List (High Evidence).","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:13:33.063740+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSPAN12 were changed from  to Exudative vitreoretinopathy 5, MIM# 613310","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:13:23.378795+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TSPAN12 were set to ","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:13:16.758003+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TSPAN12 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:12:43.783162+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TSPAN12: Rating: GREEN; Mode of pathogenicity: None; Publications: 20159111, 20159112, 21334594; Phenotypes: Exudative vitreoretinopathy 5, MIM# 613310; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TSPAN12","entity_type":"gene"},{"created":"2021-01-16T20:10:42.857510+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNNB1 as ready","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:10:42.849649+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnb1 has been classified as Green List (High Evidence).","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:10:39.042387+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CTNNB1 as Green List (high evidence)","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:10:39.035001+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnb1 has been classified as Green List (High Evidence).","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:10:29.247162+11:00","panel_name":"Syndromic Retinopathy","panel_id":3099,"panel_version":"0.158","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CTNNB1 was added\ngene: CTNNB1 was added to Syndromic Retinopathy. Sources: Expert Review\nMode of inheritance for gene: CTNNB1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: CTNNB1 were set to 33350591\nPhenotypes for gene: CTNNB1 were set to Neurodevelopmental disorder with spastic diplegia and visual defects, MIM# 615075\nReview for gene: CTNNB1 was set to GREEN\nAdded comment: Multiple ocular defects reported in the context of this neurodevelopmental disorder, including vitreoretinopathy. \nSources: Expert Review","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:08:04.856267+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTNNB1 as ready","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:08:04.843366+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctnnb1 has been classified as Green List (High Evidence).","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:08:02.205186+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CTNNB1 were changed from  to Exudative vitreoretinopathy 7, MIM# 617572; Neurodevelopmental disorder with spastic diplegia and visual defects, MIM# 615075","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:07:54.266502+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CTNNB1 were set to ","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:07:46.077461+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CTNNB1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:07:35.732521+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CTNNB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28575650, 33350591, 32039639; Phenotypes: Exudative vitreoretinopathy 7, MIM# 617572, Neurodevelopmental disorder with spastic diplegia and visual defects, MIM# 615075; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CTNNB1","entity_type":"gene"},{"created":"2021-01-16T20:04:38.873329+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL18A1 as ready","entity_name":"COL18A1","entity_type":"gene"},{"created":"2021-01-16T20:04:38.865821+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col18a1 has been classified as Green List (High Evidence).","entity_name":"COL18A1","entity_type":"gene"},{"created":"2021-01-16T20:04:36.320413+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL18A1 were changed from  to Knobloch syndrome, type 1, MIM# 267750","entity_name":"COL18A1","entity_type":"gene"},{"created":"2021-01-16T20:04:26.570853+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL18A1 were set to ","entity_name":"COL18A1","entity_type":"gene"},{"created":"2021-01-16T20:04:17.344623+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL18A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"COL18A1","entity_type":"gene"},{"created":"2021-01-16T20:04:07.233088+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COL18A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27259167, 25456301; Phenotypes: Knobloch syndrome, type 1, MIM# 267750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"COL18A1","entity_type":"gene"},{"created":"2021-01-16T18:25:31.389284+11:00","panel_name":"Vascular Malformations_Germline","panel_id":300,"panel_version":"1.0","user_name":"Zornitza Stark","item_type":"panel","text":"promoted panel to version 1.0","entity_name":null,"entity_type":null},{"created":"2021-01-16T18:25:05.701991+11:00","panel_name":"Vascular Malformations_Germline","panel_id":300,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TEK were set to ","entity_name":"TEK","entity_type":"gene"},{"created":"2021-01-16T18:24:54.430669+11:00","panel_name":"Vascular Malformations_Germline","panel_id":300,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TEK: Rating: GREEN; Mode of pathogenicity: None; Publications: 19888299; Phenotypes: Venous malformations, multiple cutaneous and mucosal, MIM# 600195; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TEK","entity_type":"gene"},{"created":"2021-01-16T18:23:21.861467+11:00","panel_name":"Vascular Malformations_Germline","panel_id":300,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMAD4 as ready","entity_name":"SMAD4","entity_type":"gene"},{"created":"2021-01-16T18:23:21.850176+11:00","panel_name":"Vascular Malformations_Germline","panel_id":300,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smad4 has been classified as Green List (High Evidence).","entity_name":"SMAD4","entity_type":"gene"},{"created":"2021-01-16T18:23:10.649301+11:00","panel_name":"Vascular Malformations_Germline","panel_id":300,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMAD4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome, MIM# 175050; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SMAD4","entity_type":"gene"},{"created":"2021-01-16T18:22:20.404551+11:00","panel_name":"Vascular Malformations_Germline","panel_id":300,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PTEN as ready","entity_name":"PTEN","entity_type":"gene"},{"created":"2021-01-16T18:22:20.393574+11:00","panel_name":"Vascular Malformations_Germline","panel_id":300,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pten has been classified as Green List (High Evidence).","entity_name":"PTEN","entity_type":"gene"},{"created":"2021-01-16T18:22:17.677794+11:00","panel_name":"Vascular Malformations_Germline","panel_id":300,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PTEN were changed from Cowden syndrome; Bannayan-Riley-Ruvalcaba syndrome; Lhermitte-Duclos syndrome to Cowden syndrome 1, MIM# 158350; Bannayan-Riley-Ruvalcaba syndrome; Lhermitte-Duclos syndrome","entity_name":"PTEN","entity_type":"gene"}]}