{"count":220497,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1548","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1546","results":[{"created":"2020-10-08T17:19:19.329606+11:00","panel_name":"Achromatopsia","panel_id":3149,"panel_version":"1.0","user_name":"Bryony Thompson","item_type":"panel","text":"promoted panel to version 1.0","entity_name":null,"entity_type":null},{"created":"2020-10-08T15:52:38.158466+11:00","panel_name":"Hyperthyroidism","panel_id":3372,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"panel","text":"Panel types changed to Victorian Clinical Genetics Services; Rare Disease","entity_name":null,"entity_type":null},{"created":"2020-10-08T15:50:03.785668+11:00","panel_name":"Hyperthyroidism","panel_id":3372,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSHR as ready","entity_name":"TSHR","entity_type":"gene"},{"created":"2020-10-08T15:50:03.777879+11:00","panel_name":"Hyperthyroidism","panel_id":3372,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tshr has been classified as Green List (High Evidence).","entity_name":"TSHR","entity_type":"gene"},{"created":"2020-10-08T15:50:01.056900+11:00","panel_name":"Hyperthyroidism","panel_id":3372,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TSHR were changed from Hyperthyroidism, nonautoimmune, 609152; Congenital, nonautoimmune hyperthyroidism to Hyperthyroidism, nonautoimmune, MIM# 609152","entity_name":"TSHR","entity_type":"gene"},{"created":"2020-10-08T15:49:47.155417+11:00","panel_name":"Hyperthyroidism","panel_id":3372,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TSHR were set to ","entity_name":"TSHR","entity_type":"gene"},{"created":"2020-10-08T15:49:38.096745+11:00","panel_name":"Hyperthyroidism","panel_id":3372,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TSHR was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TSHR","entity_type":"gene"},{"created":"2020-10-08T15:49:22.525868+11:00","panel_name":"Hyperthyroidism","panel_id":3372,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TSHR: Rating: GREEN; Mode of pathogenicity: None; Publications: 7920658, 7800007, 8964822; Phenotypes: Hyperthyroidism, nonautoimmune, MIM# 609152; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TSHR","entity_type":"gene"},{"created":"2020-10-08T15:27:04.468427+11:00","panel_name":"Additional findings_Paediatric","panel_id":3302,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Additional findings Paediatric to Additional findings_Paediatric","entity_name":null,"entity_type":null},{"created":"2020-10-08T15:25:40.388083+11:00","panel_name":"Additional findings Paediatric","panel_id":3302,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"panel","text":"Panel name changed from Newborn Screening_BabySeq to Additional findings Paediatric\nPanel types changed to Australian Genomics","entity_name":null,"entity_type":null},{"created":"2020-10-08T15:18:21.677993+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LZTFL1 as ready","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2020-10-08T15:18:21.669782+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lztfl1 has been classified as Green List (High Evidence).","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2020-10-08T15:18:18.270431+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LZTFL1 were changed from  to Bardet-Biedl syndrome 17 (MIM#615994)","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2020-10-08T15:17:47.868697+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LZTFL1 were set to ","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2020-10-08T15:17:19.190746+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LZTFL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2020-10-08T15:07:28.582736+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP290 as ready","entity_name":"CEP290","entity_type":"gene"},{"created":"2020-10-08T15:07:28.571847+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep290 has been classified as Green List (High Evidence).","entity_name":"CEP290","entity_type":"gene"},{"created":"2020-10-08T15:07:24.861498+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CEP290 were changed from  to Bardet-Biedl syndrome 14, MIM# 615991","entity_name":"CEP290","entity_type":"gene"},{"created":"2020-10-08T15:07:00.607010+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEP290 were set to 18327255; 20690115","entity_name":"CEP290","entity_type":"gene"},{"created":"2020-10-08T15:06:40.342834+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEP290 were set to ","entity_name":"CEP290","entity_type":"gene"},{"created":"2020-10-08T15:06:16.128425+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CEP290 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP290","entity_type":"gene"},{"created":"2020-10-08T15:05:45.295671+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CEP290: Rating: GREEN; Mode of pathogenicity: None; Publications: 18327255, 20690115; Phenotypes: Bardet-Biedl syndrome 14, MIM# 615991; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP290","entity_type":"gene"},{"created":"2020-10-08T14:57:27.021801+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Three families reported with a BBS phenotype, although this association is not listed in OMIM. Gene is associated with other ciliopathies as well.; to: Three families reported with a BBS phenotype, although this association is not listed in OMIM or MONDO. Gene is associated with other ciliopathies as well.","entity_name":"IFT172","entity_type":"gene"},{"created":"2020-10-08T14:56:44.701179+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IFT172: Rating: GREEN; Mode of pathogenicity: None; Publications: 30761183, 26763875, 25168386; Phenotypes: Bardet-Biedl syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT172","entity_type":"gene"},{"created":"2020-10-08T14:54:28.473357+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS12 as ready","entity_name":"BBS12","entity_type":"gene"},{"created":"2020-10-08T14:54:28.465623+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs12 has been classified as Green List (High Evidence).","entity_name":"BBS12","entity_type":"gene"},{"created":"2020-10-08T14:54:25.769902+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS12 were changed from  to Bardet-Biedl syndrome 12, MIM# 615989","entity_name":"BBS12","entity_type":"gene"},{"created":"2020-10-08T14:53:56.463686+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS12 were set to ","entity_name":"BBS12","entity_type":"gene"},{"created":"2020-10-08T14:53:28.541977+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS12","entity_type":"gene"},{"created":"2020-10-08T14:52:58.941781+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BBS12: Rating: GREEN; Mode of pathogenicity: None; Publications: 19797195, 29633607, 26082521; Phenotypes: Bardet-Biedl syndrome 12, MIM# 615989; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS12","entity_type":"gene"},{"created":"2020-10-08T14:46:47.004898+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS10 as ready","entity_name":"BBS10","entity_type":"gene"},{"created":"2020-10-08T14:46:46.991634+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs10 has been classified as Green List (High Evidence).","entity_name":"BBS10","entity_type":"gene"},{"created":"2020-10-08T14:46:40.420248+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS10 were changed from  to Bardet-Biedl syndrome 10, MIM# 615987","entity_name":"BBS10","entity_type":"gene"},{"created":"2020-10-08T14:46:13.526845+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS10 were set to ","entity_name":"BBS10","entity_type":"gene"},{"created":"2020-10-08T14:45:45.816062+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS10","entity_type":"gene"},{"created":"2020-10-08T14:45:15.270798+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BBS10: Rating: GREEN; Mode of pathogenicity: None; Publications: 16582908, 19252258; Phenotypes: Bardet-Biedl syndrome 10, MIM# 615987; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS10","entity_type":"gene"},{"created":"2020-10-08T14:40:44.327453+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SDCCAG8 as ready","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2020-10-08T14:40:44.313114+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sdccag8 has been classified as Green List (High Evidence).","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2020-10-08T14:40:36.095336+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SDCCAG8 were changed from  to Bardet-Biedl syndrome 16, MIM# 615993","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2020-10-08T14:40:03.528689+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SDCCAG8 were set to ","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2020-10-08T14:39:15.426087+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SDCCAG8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2020-10-08T14:38:46.320023+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SDCCAG8: Rating: GREEN; Mode of pathogenicity: None; Publications: 20835237, 22626039, 22626039; Phenotypes: Bardet-Biedl syndrome 16, MIM# 615993; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2020-10-08T14:34:39.835368+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TTC8 as ready","entity_name":"TTC8","entity_type":"gene"},{"created":"2020-10-08T14:34:39.815958+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ttc8 has been classified as Green List (High Evidence).","entity_name":"TTC8","entity_type":"gene"},{"created":"2020-10-08T14:34:33.191825+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TTC8 were changed from  to Bardet-Biedl syndrome 8, MIM# 615985","entity_name":"TTC8","entity_type":"gene"},{"created":"2020-10-08T14:34:01.084977+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TTC8 were set to ","entity_name":"TTC8","entity_type":"gene"},{"created":"2020-10-08T14:33:21.640978+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC8","entity_type":"gene"},{"created":"2020-10-08T14:32:52.316735+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TTC8: Rating: GREEN; Mode of pathogenicity: None; Publications: 14520415, 19797195; Phenotypes: Bardet-Biedl syndrome 8, MIM# 615985; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC8","entity_type":"gene"},{"created":"2020-10-08T14:30:52.267165+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALMS1 as ready","entity_name":"ALMS1","entity_type":"gene"},{"created":"2020-10-08T14:30:52.205924+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alms1 has been classified as Green List (High Evidence).","entity_name":"ALMS1","entity_type":"gene"},{"created":"2020-10-08T14:30:47.643613+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ALMS1 were changed from  to Alstrom syndrome, MIM# 203800","entity_name":"ALMS1","entity_type":"gene"},{"created":"2020-10-08T14:30:19.612416+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALMS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ALMS1","entity_type":"gene"},{"created":"2020-10-08T14:29:33.031356+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BBS1 as ready","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-10-08T14:29:33.018030+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bbs1 has been classified as Green List (High Evidence).","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-10-08T14:29:30.084673+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BBS1 were changed from  to Bardet-Biedl syndrome 1, MIM# 209900","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-10-08T14:28:55.906390+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BBS1 were set to ","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-10-08T14:28:27.219142+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BBS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-10-08T14:27:58.675054+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BBS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 20177705; Phenotypes: Bardet-Biedl syndrome 1, MIM# 209900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BBS1","entity_type":"gene"},{"created":"2020-10-08T14:25:15.358627+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARL6 as ready","entity_name":"ARL6","entity_type":"gene"},{"created":"2020-10-08T14:25:15.345212+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arl6 has been classified as Green List (High Evidence).","entity_name":"ARL6","entity_type":"gene"},{"created":"2020-10-08T14:25:12.329769+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ARL6 were changed from  to Bardet-Biedl syndrome 3, MIM# 600151","entity_name":"ARL6","entity_type":"gene"},{"created":"2020-10-08T14:24:38.872514+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ARL6 were set to ","entity_name":"ARL6","entity_type":"gene"},{"created":"2020-10-08T14:24:09.376012+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.32","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ARL6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARL6","entity_type":"gene"},{"created":"2020-10-08T14:23:33.233480+11:00","panel_name":"Bardet Biedl syndrome","panel_id":53,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ARL6: Rating: GREEN; Mode of pathogenicity: None; Publications: 15258860, 32361989, 31888296, 25402481; Phenotypes: Bardet-Biedl syndrome 3, MIM# 600151; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARL6","entity_type":"gene"},{"created":"2020-10-08T14:19:26.017533+11:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"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":"2020-10-08T14:16:50.373288+11:00","panel_name":"Craniosynostosis","panel_id":93,"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":"2020-10-08T14:15:07.430170+11:00","panel_name":"Glaucoma congenital","panel_id":105,"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":"2020-10-08T14:14:05.044484+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PITX2 as ready","entity_name":"PITX2","entity_type":"gene"},{"created":"2020-10-08T14:14:05.030768+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pitx2 has been classified as Green List (High Evidence).","entity_name":"PITX2","entity_type":"gene"},{"created":"2020-10-08T14:14:01.627588+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PITX2 were changed from  to Axenfeld-Rieger syndrome, type 1, MIM# 180500","entity_name":"PITX2","entity_type":"gene"},{"created":"2020-10-08T14:13:35.256706+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PITX2 were set to ","entity_name":"PITX2","entity_type":"gene"},{"created":"2020-10-08T14:13:07.568130+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PITX2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PITX2","entity_type":"gene"},{"created":"2020-10-08T14:12:38.571415+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PITX2: Rating: GREEN; Mode of pathogenicity: None; Publications: 8944018, 31185933, 29023440; Phenotypes: Axenfeld-Rieger syndrome, type 1, MIM# 180500; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PITX2","entity_type":"gene"},{"created":"2020-10-08T14:10:04.331676+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYOC as ready","entity_name":"MYOC","entity_type":"gene"},{"created":"2020-10-08T14:10:04.323839+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myoc has been classified as Green List (High Evidence).","entity_name":"MYOC","entity_type":"gene"},{"created":"2020-10-08T14:09:58.731423+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYOC were changed from  to Glaucoma 1A, primary open angle, MIM# 137750","entity_name":"MYOC","entity_type":"gene"},{"created":"2020-10-08T14:05:25.659889+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYOC were set to ","entity_name":"MYOC","entity_type":"gene"},{"created":"2020-10-08T11:30:24.902022+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYOC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYOC","entity_type":"gene"},{"created":"2020-10-08T11:29:58.149493+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MYOC: Rating: GREEN; Mode of pathogenicity: None; Publications: 9535666; Phenotypes: Glaucoma 1A, primary open angle, MIM# 137750; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYOC","entity_type":"gene"},{"created":"2020-10-08T11:27:12.474143+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4837","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LTBP2 as ready","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:27:12.462981+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4837","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ltbp2 has been classified as Green List (High Evidence).","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:27:02.888609+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4837","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LTBP2 were changed from  to Glaucoma 3, primary congenital, D 613086; Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma, MIM# 251750","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:26:45.754226+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4836","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LTBP2 were set to ","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:26:27.625227+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4835","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LTBP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:26:09.229154+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4834","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LTBP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 19656777, 19361779, 20617341, 32165823, 30380740, 30565850; Phenotypes: Glaucoma 3, primary congenital, D 613086, Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma, MIM# 251750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:25:27.720263+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LTBP2: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:24:52.264002+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LTBP2 as ready","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:24:52.256041+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ltbp2 has been classified as Green List (High Evidence).","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:24:48.471020+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LTBP2 were changed from  to Glaucoma 3, primary congenital, D 613086; Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma, MIM# 251750","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:24:25.862178+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LTBP2 were set to ","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:23:58.333070+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LTBP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:23:29.677854+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LTBP2: Changed rating: GREEN","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:23:23.163746+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LTBP2: Rating: ; Mode of pathogenicity: None; Publications: 19656777, 19361779, 20617341, 32165823, 30380740, 30565850; Phenotypes: Glaucoma 3, primary congenital, D 613086, Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma, MIM# 251750; Mode of inheritance: None","entity_name":"LTBP2","entity_type":"gene"},{"created":"2020-10-08T11:18:59.735336+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LMX1B as ready","entity_name":"LMX1B","entity_type":"gene"},{"created":"2020-10-08T11:18:59.718997+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lmx1b has been classified as Green List (High Evidence).","entity_name":"LMX1B","entity_type":"gene"},{"created":"2020-10-08T11:18:55.412664+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LMX1B were changed from  to Nail-patella syndrome, MIM# 161200","entity_name":"LMX1B","entity_type":"gene"},{"created":"2020-10-08T11:18:26.319419+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LMX1B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LMX1B","entity_type":"gene"},{"created":"2020-10-08T11:17:59.043423+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LMX1B: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Nail-patella syndrome, MIM# 161200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LMX1B","entity_type":"gene"},{"created":"2020-10-08T11:17:16.856031+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXC1 as ready","entity_name":"FOXC1","entity_type":"gene"},{"created":"2020-10-08T11:17:16.844316+11:00","panel_name":"Glaucoma congenital","panel_id":105,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxc1 has been classified as Green List (High Evidence).","entity_name":"FOXC1","entity_type":"gene"}]}