{"count":220497,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=89","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=87","results":[{"created":"2025-12-16T08:36:34.170863+11:00","panel_name":"Pulmonary Arterial Hypertension","panel_id":3095,"panel_version":"1.50","user_name":"Chirag Patel","item_type":"entity","text":"gene: NF1 was added\ngene: NF1 was added to Pulmonary Arterial Hypertension. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NF1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NF1 were set to 33446201; 32742882; 32437637\nPhenotypes for gene: NF1 were set to Neurofibromatosis, type 1, MIM# 162200; Diffuse interstitial lung disease; Pulmonary hypertension","entity_name":"NF1","entity_type":"gene"},{"created":"2025-12-16T08:36:23.614758+11:00","panel_name":"Pulmonary Arterial Hypertension","panel_id":3095,"panel_version":"1.49","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HRAS from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:36:23.571297+11:00","panel_name":"Pulmonary Arterial Hypertension","panel_id":3095,"panel_version":"1.49","user_name":"Chirag Patel","item_type":"entity","text":"gene: HRAS was added\ngene: HRAS was added to Pulmonary Arterial Hypertension. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HRAS was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: HRAS were set to 18039947; 18978662; 27102959\nPhenotypes for gene: HRAS were set to Costello syndrome\t218040; chILD, pulmonary arterial hypertension\nMode of pathogenicity for gene: HRAS was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments","entity_name":"HRAS","entity_type":"gene"},{"created":"2025-12-16T08:35:51.940629+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.121","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: KCNK3 as Green List (high evidence)","entity_name":"KCNK3","entity_type":"gene"},{"created":"2025-12-16T08:35:51.930243+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.121","user_name":"Chirag Patel","item_type":"entity","text":"Gene: kcnk3 has been classified as Green List (High Evidence).","entity_name":"KCNK3","entity_type":"gene"},{"created":"2025-12-16T08:35:34.889112+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.121","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: KCNK3 as Green List (high evidence)","entity_name":"KCNK3","entity_type":"gene"},{"created":"2025-12-16T08:35:34.879192+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.121","user_name":"Chirag Patel","item_type":"entity","text":"Gene: kcnk3 has been classified as Green List (High Evidence).","entity_name":"KCNK3","entity_type":"gene"},{"created":"2025-12-16T08:34:24.588857+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.120","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene NF1 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:33:47.785776+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.120","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene HRAS from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:33:00.595467+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.119","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene KCNK3 from panel Pulmonary Arterial Hypertension","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:23:31.262349+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.118","user_name":"Chirag Patel","item_type":"entity","text":"Publications for gene: TINF2 were set to 18252230; 21477109; 18979121; 18669893; 21199492; 33097095","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-12-16T08:23:13.853258+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.118","user_name":"Chirag Patel","item_type":"entity","text":"Publications for gene: TINF2 were set to ","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-12-16T08:23:07.339495+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: ZBTB7B as ready","entity_name":"ZBTB7B","entity_type":"gene"},{"created":"2025-12-16T08:23:07.327279+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"entity","text":"Gene: zbtb7b has been classified as Amber List (Moderate Evidence).","entity_name":"ZBTB7B","entity_type":"gene"},{"created":"2025-12-16T08:23:02.132458+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: ZNF341 as ready","entity_name":"ZNF341","entity_type":"gene"},{"created":"2025-12-16T08:23:02.119897+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"entity","text":"Gene: znf341 has been classified as Red List (Low Evidence).","entity_name":"ZNF341","entity_type":"gene"},{"created":"2025-12-16T08:22:35.676048+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: TINF2 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-12-16T08:22:18.082715+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene ZBTB7B from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:22:17.936278+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"entity","text":"gene: ZBTB7B was added\ngene: ZBTB7B was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Amber,Literature\nMode of inheritance for gene: ZBTB7B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: ZBTB7B were set to PMID: 40392549\nPhenotypes for gene: ZBTB7B were set to Inborn error of immunity, MONDO:0003778, ZBTB7B-related\nMode of pathogenicity for gene: ZBTB7B was set to Other","entity_name":"ZBTB7B","entity_type":"gene"},{"created":"2025-12-16T08:21:41.559531+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene ZNF341 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:21:41.412601+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.117","user_name":"Chirag Patel","item_type":"entity","text":"gene: ZNF341 was added\ngene: ZNF341 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Red,Expert list\nMode of inheritance for gene: ZNF341 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ZNF341 were set to 29907691; 29907690\nPhenotypes for gene: ZNF341 were set to Hyper-IgE recurrent infection syndrome 3, autosomal recessive, MIM# 618282; Bronchiectasis","entity_name":"ZNF341","entity_type":"gene"},{"created":"2025-12-16T08:21:39.580807+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.116","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: STAT1 as ready","entity_name":"STAT1","entity_type":"gene"},{"created":"2025-12-16T08:21:39.567340+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.116","user_name":"Chirag Patel","item_type":"entity","text":"Gene: stat1 has been classified as Green List (High Evidence).","entity_name":"STAT1","entity_type":"gene"},{"created":"2025-12-16T08:21:03.486205+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.116","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: TINF2 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-12-16T08:20:43.987237+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.116","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: TINF2 were changed from Dyskeratosis congenita, autosomal dominant 3, MIM# 613990; Revesz syndrome, MIM# 268130 to Dyskeratosis congenita, autosomal dominant 3, MIM# 613990; Revesz syndrome, MIM# 268130","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-12-16T08:20:26.745916+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.116","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: TINF2 were changed from  to Dyskeratosis congenita, autosomal dominant 3, MIM# 613990; Revesz syndrome, MIM# 268130","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-12-16T08:20:09.334088+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.116","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: TINF2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-12-16T08:19:55.669589+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.115","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: TINF2 as ready","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-12-16T08:19:55.658057+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.115","user_name":"Chirag Patel","item_type":"entity","text":"Gene: tinf2 has been classified as Green List (High Evidence).","entity_name":"TINF2","entity_type":"gene"},{"created":"2025-12-16T08:19:51.802732+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.115","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene STAT1 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:19:51.672476+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.115","user_name":"Chirag Patel","item_type":"entity","text":"gene: STAT1 was added\ngene: STAT1 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: STAT1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: STAT1 were set to 28427548; 28367431; 21727188; 27379765; 26732859; 27114460\nPhenotypes for gene: STAT1 were set to Immunodeficiency 31A, mycobacteriosis, autosomal dominant, MIM#\t614892; Childhood bronchiectasis","entity_name":"STAT1","entity_type":"gene"},{"created":"2025-12-16T08:19:36.080791+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.115","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: STRA6 as ready","entity_name":"STRA6","entity_type":"gene"},{"created":"2025-12-16T08:19:36.065644+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.115","user_name":"Chirag Patel","item_type":"entity","text":"Gene: stra6 has been classified as Green List (High Evidence).","entity_name":"STRA6","entity_type":"gene"},{"created":"2025-12-16T08:19:15.820216+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.115","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene STRA6 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:19:15.664928+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.115","user_name":"Chirag Patel","item_type":"entity","text":"gene: STRA6 was added\ngene: STRA6 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: STRA6 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: STRA6 were set to 17273977; 17503335; 19213032; 26373900; 30880327; 26373900; 25457163\nPhenotypes for gene: STRA6 were set to Microphthalmia, syndromic 9, MIM# 601186","entity_name":"STRA6","entity_type":"gene"},{"created":"2025-12-16T08:18:14.023051+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.114","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene TINF2 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:18:02.414026+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.113","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: TBX4 as ready","entity_name":"TBX4","entity_type":"gene"},{"created":"2025-12-16T08:18:02.401793+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.113","user_name":"Chirag Patel","item_type":"entity","text":"Gene: tbx4 has been classified as Green List (High Evidence).","entity_name":"TBX4","entity_type":"gene"},{"created":"2025-12-16T08:16:41.523649+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.113","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene TBX4 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:16:41.358502+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.113","user_name":"Chirag Patel","item_type":"entity","text":"gene: TBX4 was added\ngene: TBX4 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Expert list,Victorian Clinical Genetics Services\nMode of inheritance for gene: TBX4 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal\nPublications for gene: TBX4 were set to 31761294; 31965066; 29631995; 23592887; 30578383\nPhenotypes for gene: TBX4 were set to Ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension MIM#147891; Amelia, posterior, with pelvic and pulmonary hypoplasia syndrome, MIM# 601360","entity_name":"TBX4","entity_type":"gene"},{"created":"2025-12-16T08:15:22.909892+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.112","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: STAT3 as ready","entity_name":"STAT3","entity_type":"gene"},{"created":"2025-12-16T08:15:22.901452+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.112","user_name":"Chirag Patel","item_type":"entity","text":"Gene: stat3 has been classified as Green List (High Evidence).","entity_name":"STAT3","entity_type":"gene"},{"created":"2025-12-16T08:15:11.708039+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.112","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: SOX18 as ready","entity_name":"SOX18","entity_type":"gene"},{"created":"2025-12-16T08:15:11.701096+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.112","user_name":"Chirag Patel","item_type":"entity","text":"Gene: sox18 has been classified as Green List (High Evidence).","entity_name":"SOX18","entity_type":"gene"},{"created":"2025-12-16T08:15:03.820590+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.112","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: SMAD9 as ready","entity_name":"SMAD9","entity_type":"gene"},{"created":"2025-12-16T08:15:03.812286+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.112","user_name":"Chirag Patel","item_type":"entity","text":"Gene: smad9 has been classified as Green List (High Evidence).","entity_name":"SMAD9","entity_type":"gene"},{"created":"2025-12-16T08:14:49.862553+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.112","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene STAT3 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:14:49.774687+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.111","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: PGM3 as ready","entity_name":"PGM3","entity_type":"gene"},{"created":"2025-12-16T08:14:49.750064+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.111","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pgm3 has been classified as Amber List (Moderate Evidence).","entity_name":"PGM3","entity_type":"gene"},{"created":"2025-12-16T08:14:49.480746+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.112","user_name":"Chirag Patel","item_type":"entity","text":"gene: STAT3 was added\ngene: STAT3 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: STAT3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: STAT3 were set to 17881745; 14566054; 25349174; 25038750; 25359994\nPhenotypes for gene: STAT3 were set to Hyper-IgE recurrent infection syndrome MIM# 147060; Autoimmune disease, multisystem, infantile-onset, 1 MIM# 615952; Childhood bronchiectasis, interstitial lung disease or pneumatocele\nMode of pathogenicity for gene: STAT3 was set to Other","entity_name":"STAT3","entity_type":"gene"},{"created":"2025-12-16T08:14:13.541147+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.111","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SOX18 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:14:13.369182+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.111","user_name":"Chirag Patel","item_type":"entity","text":"gene: SOX18 was added\ngene: SOX18 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: SOX18 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SOX18 were set to 30549413; 33851505\nPhenotypes for gene: SOX18 were set to Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome, MIM#\t137940","entity_name":"SOX18","entity_type":"gene"},{"created":"2025-12-16T08:13:35.310082+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.111","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SMAD9 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:13:35.141094+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.111","user_name":"Chirag Patel","item_type":"entity","text":"gene: SMAD9 was added\ngene: SMAD9 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Expert list,Victorian Clinical Genetics Services\nMode of inheritance for gene: SMAD9 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SMAD9 were set to 29844917; 21920918; 19211612; 21898662\nPhenotypes for gene: SMAD9 were set to Pulmonary hypertension, primary, 2 MIM#615342","entity_name":"SMAD9","entity_type":"gene"},{"created":"2025-12-16T08:12:34.992233+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.110","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene PGM3 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:12:34.843147+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.110","user_name":"Chirag Patel","item_type":"entity","text":"gene: PGM3 was added\ngene: PGM3 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Amber,Expert list\nMode of inheritance for gene: PGM3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PGM3 were set to 24698316; 24589341; 28704707; 30264496\nPhenotypes for gene: PGM3 were set to Immunodeficiency 23, MIM#\t615816; HIES (Job syndrome); Bronchiectasis","entity_name":"PGM3","entity_type":"gene"},{"created":"2025-12-16T08:11:21.134434+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: RET as ready","entity_name":"RET","entity_type":"gene"},{"created":"2025-12-16T08:11:21.124195+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ret has been classified as Red List (Low Evidence).","entity_name":"RET","entity_type":"gene"},{"created":"2025-12-16T08:11:13.050221+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: PHOX2B as ready","entity_name":"PHOX2B","entity_type":"gene"},{"created":"2025-12-16T08:11:13.040006+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"entity","text":"Gene: phox2b has been classified as Green List (High Evidence).","entity_name":"PHOX2B","entity_type":"gene"},{"created":"2025-12-16T08:11:03.923677+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: NF1 as ready","entity_name":"NF1","entity_type":"gene"},{"created":"2025-12-16T08:11:03.913856+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"entity","text":"Gene: nf1 has been classified as Green List (High Evidence).","entity_name":"NF1","entity_type":"gene"},{"created":"2025-12-16T08:10:56.570608+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: LTBP4 as ready","entity_name":"LTBP4","entity_type":"gene"},{"created":"2025-12-16T08:10:56.563173+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ltbp4 has been classified as Green List (High Evidence).","entity_name":"LTBP4","entity_type":"gene"},{"created":"2025-12-16T08:09:43.809890+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene RET from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:09:43.642440+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.109","user_name":"Chirag Patel","item_type":"entity","text":"gene: RET was added\ngene: RET was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Red,Victorian Clinical Genetics Services\nMode of inheritance for gene: RET was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: RET were set to 18438890; 16443855; 12566528; 12086152\nPhenotypes for gene: RET were set to Central hypoventilation syndrome, congenital, MIM#209880","entity_name":"RET","entity_type":"gene"},{"created":"2025-12-16T08:09:00.331192+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.108","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene PHOX2B from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:09:00.111242+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.108","user_name":"Chirag Patel","item_type":"entity","text":"gene: PHOX2B was added\ngene: PHOX2B was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Victorian Clinical Genetics Services,Victorian Clinical Genetics Services\nMode of inheritance for gene: PHOX2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PHOX2B were set to 20301600\nPhenotypes for gene: PHOX2B were set to Central hypoventilation syndrome, congenital, with or without Hirschsprung disease, MIM# 209880","entity_name":"PHOX2B","entity_type":"gene"},{"created":"2025-12-16T08:08:19.740201+11:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"1.68","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene NME8 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:07:46.775440+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.107","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene NF1 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:07:46.478506+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.107","user_name":"Chirag Patel","item_type":"entity","text":"gene: NF1 was added\ngene: NF1 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: NF1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NF1 were set to 33446201; 32742882; 32437637\nPhenotypes for gene: NF1 were set to Neurofibromatosis, type 1, MIM# 162200; Diffuse interstitial lung disease; Pulmonary hypertension","entity_name":"NF1","entity_type":"gene"},{"created":"2025-12-16T08:06:41.231041+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.106","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene LTBP4 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:06:41.064925+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.106","user_name":"Chirag Patel","item_type":"entity","text":"gene: LTBP4 was added\ngene: LTBP4 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LTBP4 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: LTBP4 were set to 22829427; 19836010; 28684544\nPhenotypes for gene: LTBP4 were set to Cutis laxa, autosomal recessive, type IC, MIM#\t613177; Urban-Rifkin-Davis Syndrome – cutis laxa; Infant/Childhood emphysema","entity_name":"LTBP4","entity_type":"gene"},{"created":"2025-12-16T08:06:33.103812+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.105","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: LRBA as ready","entity_name":"LRBA","entity_type":"gene"},{"created":"2025-12-16T08:06:33.091867+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.105","user_name":"Chirag Patel","item_type":"entity","text":"Gene: lrba has been classified as Green List (High Evidence).","entity_name":"LRBA","entity_type":"gene"},{"created":"2025-12-16T08:06:24.295643+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.105","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: KCNK3 as ready","entity_name":"KCNK3","entity_type":"gene"},{"created":"2025-12-16T08:06:24.287290+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.105","user_name":"Chirag Patel","item_type":"entity","text":"Gene: kcnk3 has been classified as Amber List (Moderate Evidence).","entity_name":"KCNK3","entity_type":"gene"},{"created":"2025-12-16T08:06:00.305293+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.105","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene LRBA from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:06:00.091223+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.105","user_name":"Chirag Patel","item_type":"entity","text":"gene: LRBA was added\ngene: LRBA was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: LRBA was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: LRBA were set to 25468195; 30479781; 26768763; 28956255; 28512785\nPhenotypes for gene: LRBA were set to Immunodeficiency, common variable, 8, with autoimmunity, MIM#\t614700; Immunodysregulation polyendocrinopathy enteropathy X-linked (IPEX) -like; Childhood bronchiectasis and GLILD (Granulomatous and Lymphocytic interstitial lung disease)","entity_name":"LRBA","entity_type":"gene"},{"created":"2025-12-16T08:05:39.916218+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.104","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: HRAS as ready","entity_name":"HRAS","entity_type":"gene"},{"created":"2025-12-16T08:05:39.905630+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.104","user_name":"Chirag Patel","item_type":"entity","text":"Gene: hras has been classified as Green List (High Evidence).","entity_name":"HRAS","entity_type":"gene"},{"created":"2025-12-16T08:05:23.008023+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.104","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene KCNK3 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:05:22.810799+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.104","user_name":"Chirag Patel","item_type":"entity","text":"gene: KCNK3 was added\ngene: KCNK3 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Amber,Expert list\nMode of inheritance for gene: KCNK3 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal\nPublications for gene: KCNK3 were set to 23883380; 27649371\nPhenotypes for gene: KCNK3 were set to Pulmonary hypertension, primary, 4 MIM#615344","entity_name":"KCNK3","entity_type":"gene"},{"created":"2025-12-16T08:04:57.176970+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.104","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: HPS6 as ready","entity_name":"HPS6","entity_type":"gene"},{"created":"2025-12-16T08:04:57.168522+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.104","user_name":"Chirag Patel","item_type":"entity","text":"Gene: hps6 has been classified as Red List (Low Evidence).","entity_name":"HPS6","entity_type":"gene"},{"created":"2025-12-16T08:04:45.834827+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.104","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HPS6 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:04:45.703911+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.104","user_name":"Chirag Patel","item_type":"entity","text":"gene: HPS6 was added\ngene: HPS6 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Red,Victorian Clinical Genetics Services\nMode of inheritance for gene: HPS6 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: HPS6 were set to Hermansky-Pudlak syndrome 6, MIM#\t614075","entity_name":"HPS6","entity_type":"gene"},{"created":"2025-12-16T08:04:38.656639+11:00","panel_name":"Pulmonary Arterial Hypertension","panel_id":3095,"panel_version":"1.48","user_name":"Chirag Patel","item_type":"panel","text":"Added reviews for gene KCNK3 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:03:51.385370+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.103","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: GATA2 as ready","entity_name":"GATA2","entity_type":"gene"},{"created":"2025-12-16T08:03:51.378007+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.103","user_name":"Chirag Patel","item_type":"entity","text":"Gene: gata2 has been classified as Green List (High Evidence).","entity_name":"GATA2","entity_type":"gene"},{"created":"2025-12-16T08:03:26.889092+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.103","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene GATA2 from panel Interstitial Lung Disease","entity_name":null,"entity_type":null},{"created":"2025-12-16T08:03:26.675942+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.103","user_name":"Chirag Patel","item_type":"entity","text":"gene: GATA2 was added\ngene: GATA2 was added to Pulmonary Fibrosis_Interstitial Lung Disease. Sources: Expert Review Green,Victorian Clinical Genetics Services,Victorian Clinical Genetics Services\ntreatable tags were added to gene: GATA2.\nMode of inheritance for gene: GATA2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: GATA2 were set to 21670465; 21242295; 21892158; 25707267; 6577833; 24345756; 24227816\nPhenotypes for gene: GATA2 were set to Immunodeficiency 21, MIM# 614172; MONDO:0042982; Emberger syndrome, MIM# 614038; MONDO:0013540; chILD, childhood pulmonary alveolar proteinosis","entity_name":"GATA2","entity_type":"gene"},{"created":"2025-12-16T08:03:17.991093+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.102","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: GDNF as ready","entity_name":"GDNF","entity_type":"gene"},{"created":"2025-12-16T08:03:17.981424+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.102","user_name":"Chirag Patel","item_type":"entity","text":"Gene: gdnf has been classified as Red List (Low Evidence).","entity_name":"GDNF","entity_type":"gene"},{"created":"2025-12-16T08:01:51.552906+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.102","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: FOXP1 as ready","entity_name":"FOXP1","entity_type":"gene"},{"created":"2025-12-16T08:01:51.546025+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.102","user_name":"Chirag Patel","item_type":"entity","text":"Gene: foxp1 has been classified as Red List (Low Evidence).","entity_name":"FOXP1","entity_type":"gene"},{"created":"2025-12-16T08:01:08.941403+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.102","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: FOXC2 as ready","entity_name":"FOXC2","entity_type":"gene"},{"created":"2025-12-16T08:01:08.934787+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.102","user_name":"Chirag Patel","item_type":"entity","text":"Gene: foxc2 has been classified as Amber List (Moderate Evidence).","entity_name":"FOXC2","entity_type":"gene"},{"created":"2025-12-16T08:00:56.164637+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.102","user_name":"Chirag Patel","item_type":"entity","text":"Mode of inheritance for gene: FGFR2 was changed from BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"FGFR2","entity_type":"gene"},{"created":"2025-12-16T08:00:47.073374+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.101","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: FOXC2 as ready","entity_name":"FOXC2","entity_type":"gene"}]}