{"count":220377,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=48","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=46","results":[{"created":"2026-01-29T14:32:48.153006+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.30","user_name":"Chirag Patel","item_type":"entity","text":"gene: KCNQ1 was added\ngene: KCNQ1 was added to Adrenal insufficiency. Sources: Expert Review Amber,Genomics England PanelApp\nMode of inheritance for gene: KCNQ1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: KCNQ1 were set to 29097701\nPhenotypes for gene: KCNQ1 were set to Hypopituitarism, MONDO:0005152; Long QT syndrome 1 (192500)","entity_name":"KCNQ1","entity_type":"gene"},{"created":"2026-01-29T14:32:16.331078+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.29","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene ESRP2 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:32:16.276795+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.29","user_name":"Chirag Patel","item_type":"entity","text":"gene: ESRP2 was added\ngene: ESRP2 was added to Adrenal insufficiency. Sources: Expert Review Amber,Expert list\nMode of inheritance for gene: ESRP2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: ESRP2 were set to 29805042\nPhenotypes for gene: ESRP2 were set to Cleft palate, MONDO:0016064; Hypopituitarism MONDO:0005152","entity_name":"ESRP2","entity_type":"gene"},{"created":"2026-01-29T14:31:42.726807+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.28","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CDON from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:31:42.652332+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.28","user_name":"Chirag Patel","item_type":"entity","text":"gene: CDON was added\ngene: CDON was added to Adrenal insufficiency. Sources: Expert Review Amber,Genomics England PanelApp\nMode of inheritance for gene: CDON was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: CDON were set to 21802063; 29749693; 32729136; 33270637; 26529631; 27974186\nPhenotypes for gene: CDON were set to Holoprosencephaly 11 (614226)","entity_name":"CDON","entity_type":"gene"},{"created":"2026-01-29T14:30:52.073945+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.27","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene ARNT2 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:30:52.002552+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.27","user_name":"Chirag Patel","item_type":"entity","text":"gene: ARNT2 was added\ngene: ARNT2 was added to Adrenal insufficiency. Sources: Expert Review Amber,Literature,Genomics England PanelApp,Genetic Health Queensland\nMode of inheritance for gene: ARNT2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ARNT2 were set to 24022475, 11381139\nPhenotypes for gene: ARNT2 were set to Webb-Dattani syndrome 615926","entity_name":"ARNT2","entity_type":"gene"},{"created":"2026-01-29T14:28:36.774159+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.26","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene ZRSR2 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:28:36.703039+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.26","user_name":"Chirag Patel","item_type":"entity","text":"gene: ZRSR2 was added\ngene: ZRSR2 was added to Adrenal insufficiency. Sources: Expert Review Green,Literature\nMode of inheritance for gene: ZRSR2 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: ZRSR2 were set to 38158857\nPhenotypes for gene: ZRSR2 were set to Orofaciodigital syndrome XXI, MIM# 301132","entity_name":"ZRSR2","entity_type":"gene"},{"created":"2026-01-29T14:27:51.743838+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.25","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene TBX19 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:27:51.692336+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.25","user_name":"Chirag Patel","item_type":"entity","text":"gene: TBX19 was added\ngene: TBX19 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: TBX19 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TBX19 were set to 15613420, 31998673, 11290323, 15476446, 22170728\nPhenotypes for gene: TBX19 were set to Adrenocorticotropic hormone deficiency, 201400","entity_name":"TBX19","entity_type":"gene"},{"created":"2026-01-29T14:27:11.570444+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.24","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene TBC1D32 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:27:11.503681+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.24","user_name":"Chirag Patel","item_type":"entity","text":"gene: TBC1D32 was added\ngene: TBC1D32 was added to Adrenal insufficiency. Sources: Expert Review Green,Literature\nMode of inheritance for gene: TBC1D32 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TBC1D32 were set to 32573025; 32060556; 24285566; 31130284; 36826837; 40319332\nPhenotypes for gene: TBC1D32 were set to Syndromic hypopituitarism","entity_name":"TBC1D32","entity_type":"gene"},{"created":"2026-01-29T14:26:46.317284+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.23","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene SOX3 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:26:46.258365+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.23","user_name":"Chirag Patel","item_type":"entity","text":"gene: SOX3 was added\ngene: SOX3 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\nSV/CNV tags were added to gene: SOX3.\nMode of inheritance for gene: SOX3 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: SOX3 were set to 24346842; 15800844; 21289259; 24737742\nPhenotypes for gene: SOX3 were set to Panhypopituitarism, X-linked (312000); Mental retardation, X-linked, with isolated growth hormone deficiency (300123)","entity_name":"SOX3","entity_type":"gene"},{"created":"2026-01-29T14:24:12.557438+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.22","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene ROBO1 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:24:12.498803+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.22","user_name":"Chirag Patel","item_type":"entity","text":"gene: ROBO1 was added\ngene: ROBO1 was added to Adrenal insufficiency. Sources: Expert Review Green,Literature\nMode of inheritance for gene: ROBO1 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal\nPublications for gene: ROBO1 were set to PMID: 30530901; 30692597; 33270637; 28402530\nPhenotypes for gene: ROBO1 were set to Pituitary hormone deficiency, combined or isolated, 8, MIM#\t620303","entity_name":"ROBO1","entity_type":"gene"},{"created":"2026-01-29T14:22:24.161239+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.21","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HESX1 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:22:24.046610+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.21","user_name":"Chirag Patel","item_type":"entity","text":"gene: HESX1 was added\ngene: HESX1 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: HESX1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: HESX1 were set to 14561704; 26781211; 11136712; 16940453\nPhenotypes for gene: HESX1 were set to Growth hormone deficiency with pituitary anomalies (182230); Pituitary hormone deficiency, combined, 5 (182230)","entity_name":"HESX1","entity_type":"gene"},{"created":"2026-01-29T14:20:19.580520+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.20","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene OTX2 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:20:19.529354+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.20","user_name":"Chirag Patel","item_type":"entity","text":"gene: OTX2 was added\ngene: OTX2 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: OTX2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: OTX2 were set to 19965921; 22715480; 18628516; 18728160\nPhenotypes for gene: OTX2 were set to Pituitary hormone deficiency, combined, 6 (613986); Microphthalmia, syndromic 5 (610125)","entity_name":"OTX2","entity_type":"gene"},{"created":"2026-01-29T14:19:46.618873+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.19","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene LHX4 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:19:46.569066+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.19","user_name":"Chirag Patel","item_type":"entity","text":"gene: LHX4 was added\ngene: LHX4 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\ntreatable tags were added to gene: LHX4.\nMode of inheritance for gene: LHX4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: LHX4 were set to 18073311; 18445675; 11567216\nPhenotypes for gene: LHX4 were set to Pituitary hormone deficiency, combined, 4 (262700)","entity_name":"LHX4","entity_type":"gene"},{"created":"2026-01-29T14:19:40.164321+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.18","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene LHX3 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:19:40.105209+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.18","user_name":"Chirag Patel","item_type":"entity","text":"gene: LHX3 was added\ngene: LHX3 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp\ntreatable tags were added to gene: LHX3.\nMode of inheritance for gene: LHX3 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: LHX3 were set to Pituitary hormone deficiency, combined, 3 (221750)","entity_name":"LHX3","entity_type":"gene"},{"created":"2026-01-29T14:19:21.832568+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.17","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HID1 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:19:21.778710+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.17","user_name":"Chirag Patel","item_type":"entity","text":"gene: HID1 was added\ngene: HID1 was added to Adrenal insufficiency. Sources: Expert Review Green,Literature\nMode of inheritance for gene: HID1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HID1 were set to 33999436\nPhenotypes for gene: HID1 were set to Developmental and epileptic encephalopathy 105 with hypopituitarism MIM#619983","entity_name":"HID1","entity_type":"gene"},{"created":"2026-01-29T14:17:01.453844+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.16","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene GLI3 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:17:01.388270+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.16","user_name":"Chirag Patel","item_type":"entity","text":"gene: GLI3 was added\ngene: GLI3 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp,Genomics England PanelApp\nMode of inheritance for gene: GLI3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: GLI3 were set to 24736735; 15739154; 9054938 10945658 11693785\nPhenotypes for gene: GLI3 were set to Greig cephalopolysyndactyly syndrome (175700); Pallister-Hall syndrome (146510)","entity_name":"GLI3","entity_type":"gene"},{"created":"2026-01-29T14:16:11.947099+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.15","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene GLI2 from panel Pituitary hormone deficiency","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:16:11.892489+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.15","user_name":"Chirag Patel","item_type":"entity","text":"gene: GLI2 was added\ngene: GLI2 was added to Adrenal insufficiency. Sources: Expert Review Green,Genomics England PanelApp,Victorian Clinical Genetics Services\nMode of inheritance for gene: GLI2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown\nPublications for gene: GLI2 were set to 14581620; 17096318; 33235745; 27585885; 15994174; 20685856; 30629636; 30583238\nPhenotypes for gene: GLI2 were set to Culler-Jones syndrome (615849); Holoprosencephaly 9 (610829)","entity_name":"GLI2","entity_type":"gene"},{"created":"2026-01-29T14:12:03.428421+11:00","panel_name":"Pituitary hormone deficiency","panel_id":3236,"panel_version":"0.172","user_name":"Chirag Patel","item_type":"entity","text":"Phenotypes for gene: FGF17 were changed from  to Hypogonadotropic hypogonadism 20 with or without anosmia, MIM# 615270","entity_name":"FGF17","entity_type":"gene"},{"created":"2026-01-29T14:09:32.393669+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.14","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene NR0B1 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:09:32.333145+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.14","user_name":"Chirag Patel","item_type":"entity","text":"gene: NR0B1 was added\ngene: NR0B1 was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services\nSV/CNV tags were added to gene: NR0B1.\nMode of inheritance for gene: NR0B1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: NR0B1 were set to 19508677; 26030781\nPhenotypes for gene: NR0B1 were set to Adrenal hypoplasia, congenital (MIM# 300200); 46XY sex reversal 2, dosage-sensitive, MIM#\t300018","entity_name":"NR0B1","entity_type":"gene"},{"created":"2026-01-29T14:03:02.031700+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.13","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CYP11B2 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:03:01.944243+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.13","user_name":"Chirag Patel","item_type":"entity","text":"gene: CYP11B2 was added\ngene: CYP11B2 was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services\ntreatable tags were added to gene: CYP11B2.\nMode of inheritance for gene: CYP11B2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP11B2 were set to 8439335; 9360501; 15240589; 9814506; 12788848; 8772616\nPhenotypes for gene: CYP11B2 were set to Hypoaldosteronism, congenital, due to CMO I deficiency (MIM#203400) or due to CMO II deficiency (MIM#610600).","entity_name":"CYP11B2","entity_type":"gene"},{"created":"2026-01-29T14:01:15.622762+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.12","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene STAR from panel Congenital adrenal hyperplasia","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:01:15.568489+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.12","user_name":"Chirag Patel","item_type":"entity","text":"gene: STAR was added\ngene: STAR was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services,Victorian Clinical Genetics Services\nMode of inheritance for gene: STAR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: STAR were set to 7892608; 8634702\nPhenotypes for gene: STAR were set to Lipoid adrenal hyperplasia (MIM#201710)","entity_name":"STAR","entity_type":"gene"},{"created":"2026-01-29T14:01:11.068122+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.11","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene POR from panel Congenital adrenal hyperplasia","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:01:11.014060+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.11","user_name":"Chirag Patel","item_type":"entity","text":"gene: POR was added\ngene: POR was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services,Victorian Clinical Genetics Services\nMode of inheritance for gene: POR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: POR were set to 27068427\nPhenotypes for gene: POR were set to Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, MIM#201750; Disordered steroidogenesis due to cytochrome P450 oxidoreductase, MIM#613571","entity_name":"POR","entity_type":"gene"},{"created":"2026-01-29T14:01:04.122197+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.10","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HSD3B2 from panel Congenital adrenal hyperplasia","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:01:04.067309+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.10","user_name":"Chirag Patel","item_type":"entity","text":"gene: HSD3B2 was added\ngene: HSD3B2 was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services,Victorian Clinical Genetics Services\nMode of inheritance for gene: HSD3B2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HSD3B2 were set to 1363812; 18252794\nPhenotypes for gene: HSD3B2 were set to Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency, MIM# 201810","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2026-01-29T14:01:00.257197+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.9","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CYP21A2 from panel Congenital adrenal hyperplasia","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:01:00.192089+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.9","user_name":"Chirag Patel","item_type":"entity","text":"gene: CYP21A2 was added\ngene: CYP21A2 was added to Adrenal insufficiency. Sources: Expert Review Green,Expert list,Expert list\nMode of inheritance for gene: CYP21A2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CYP21A2 were set to Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, 201910; Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency, 201910","entity_name":"CYP21A2","entity_type":"gene"},{"created":"2026-01-29T14:00:55.510625+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.8","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CYP17A1 from panel Congenital adrenal hyperplasia","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:00:55.456531+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.8","user_name":"Chirag Patel","item_type":"entity","text":"gene: CYP17A1 was added\ngene: CYP17A1 was added to Adrenal insufficiency. Sources: Expert Review Green,Expert list,Expert list\nMode of inheritance for gene: CYP17A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP17A1 were set to PMID: 2843762, 14671162, 2026124\nPhenotypes for gene: CYP17A1 were set to 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110","entity_name":"CYP17A1","entity_type":"gene"},{"created":"2026-01-29T14:00:06.373843+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CYP11B1 from panel Congenital adrenal hyperplasia","entity_name":null,"entity_type":null},{"created":"2026-01-29T14:00:06.182729+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"gene: CYP11B1 was added\ngene: CYP11B1 was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services,Victorian Clinical Genetics Services\ntreatable tags were added to gene: CYP11B1.\nMode of inheritance for gene: CYP11B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP11B1 were set to 8768848\nPhenotypes for gene: CYP11B1 were set to Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, MIM# 202010","entity_name":"CYP11B1","entity_type":"gene"},{"created":"2026-01-29T13:56:32.553649+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.6","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CYP11A1 from panel Differences of Sex Development","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:56:32.501860+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.6","user_name":"Chirag Patel","item_type":"entity","text":"gene: CYP11A1 was added\ngene: CYP11A1 was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CYP11A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP11A1 were set to 12161514; 16705068; 18182448; 28425981\nPhenotypes for gene: CYP11A1 were set to Adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete, MIM# 613743","entity_name":"CYP11A1","entity_type":"gene"},{"created":"2026-01-29T13:56:07.417180+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.5","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CDKN1C from panel Differences of Sex Development","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:56:07.364749+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.5","user_name":"Chirag Patel","item_type":"entity","text":"gene: CDKN1C was added\ngene: CDKN1C was added to Adrenal insufficiency. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: CDKN1C was set to MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)\nPublications for gene: CDKN1C were set to 22634751; 33076988; 31976094; 31497289\nPhenotypes for gene: CDKN1C were set to IMAGe syndrome, MIM# 614732\nMode of pathogenicity for gene: CDKN1C 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":"CDKN1C","entity_type":"gene"},{"created":"2026-01-29T13:53:50.605237+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.4","user_name":"Chirag Patel","item_type":"panel","text":"Panel types changed to Victorian Clinical Genetics Services; Genetic Health Queensland; Rare Disease","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:53:38.917657+11:00","panel_name":"Adrenal insufficiency","panel_id":4523,"panel_version":"0.3","user_name":"Chirag Patel","item_type":"panel","text":"HPO terms changed from  to Adrenal insufficiency, HP:0000846; Congenital adrenal hypoplasia, HP:0008244","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:38:25.722886+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.8","user_name":"Chirag Patel","item_type":"panel","text":"Panel status changed from internal to public","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:38:02.357025+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: STAR as ready","entity_name":"STAR","entity_type":"gene"},{"created":"2026-01-29T13:38:02.346186+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Gene: star has been classified as Green List (High Evidence).","entity_name":"STAR","entity_type":"gene"},{"created":"2026-01-29T13:37:57.322054+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: POR as ready","entity_name":"POR","entity_type":"gene"},{"created":"2026-01-29T13:37:57.312137+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Gene: por has been classified as Green List (High Evidence).","entity_name":"POR","entity_type":"gene"},{"created":"2026-01-29T13:37:50.862715+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: HSD3B2 as ready","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2026-01-29T13:37:50.851689+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Gene: hsd3b2 has been classified as Green List (High Evidence).","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2026-01-29T13:37:40.461243+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: CYP21A2 as ready","entity_name":"CYP21A2","entity_type":"gene"},{"created":"2026-01-29T13:37:40.451403+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Gene: cyp21a2 has been classified as Green List (High Evidence).","entity_name":"CYP21A2","entity_type":"gene"},{"created":"2026-01-29T13:37:28.019100+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: CYP11B1 as ready","entity_name":"CYP11B1","entity_type":"gene"},{"created":"2026-01-29T13:37:28.011983+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"Gene: cyp11b1 has been classified as Green List (High Evidence).","entity_name":"CYP11B1","entity_type":"gene"},{"created":"2026-01-29T13:36:31.497141+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene STAR from panel Differences of Sex Development","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:36:31.444954+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.7","user_name":"Chirag Patel","item_type":"entity","text":"gene: STAR was added\ngene: STAR was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: STAR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: STAR were set to 7892608; 8634702\nPhenotypes for gene: STAR were set to Lipoid adrenal hyperplasia (MIM#201710)","entity_name":"STAR","entity_type":"gene"},{"created":"2026-01-29T13:36:28.535918+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.6","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene POR from panel Differences of Sex Development","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:36:28.481869+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.6","user_name":"Chirag Patel","item_type":"entity","text":"gene: POR was added\ngene: POR was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: POR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: POR were set to 27068427\nPhenotypes for gene: POR were set to Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis, MIM#201750; Disordered steroidogenesis due to cytochrome P450 oxidoreductase, MIM#613571","entity_name":"POR","entity_type":"gene"},{"created":"2026-01-29T13:27:09.210315+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.5","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CYP11B1 from panel Differences of Sex Development","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:27:09.154615+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.5","user_name":"Chirag Patel","item_type":"entity","text":"gene: CYP11B1 was added\ngene: CYP11B1 was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Victorian Clinical Genetics Services\ntreatable tags were added to gene: CYP11B1.\nMode of inheritance for gene: CYP11B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP11B1 were set to 8768848\nPhenotypes for gene: CYP11B1 were set to Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, MIM# 202010","entity_name":"CYP11B1","entity_type":"gene"},{"created":"2026-01-29T13:24:52.008229+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.4","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: HSD3B2 as ready","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2026-01-29T13:24:51.996561+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.4","user_name":"Chirag Patel","item_type":"entity","text":"Gene: hsd3b2 has been classified as Green List (High Evidence).","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2026-01-29T13:24:48.071163+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.4","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: CYP17A1 as ready","entity_name":"CYP17A1","entity_type":"gene"},{"created":"2026-01-29T13:24:48.061170+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.4","user_name":"Chirag Patel","item_type":"entity","text":"Gene: cyp17a1 has been classified as Green List (High Evidence).","entity_name":"CYP17A1","entity_type":"gene"},{"created":"2026-01-29T13:23:52.632963+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.4","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene HSD3B2 from panel Mendeliome","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:23:52.553300+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.4","user_name":"Chirag Patel","item_type":"entity","text":"gene: HSD3B2 was added\ngene: HSD3B2 was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: HSD3B2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: HSD3B2 were set to 1363812; 18252794\nPhenotypes for gene: HSD3B2 were set to Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency, MIM# 201810","entity_name":"HSD3B2","entity_type":"gene"},{"created":"2026-01-29T13:22:50.856185+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.3","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CYP17A1 from panel Hypertension and Aldosterone disorders","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:22:50.802923+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.3","user_name":"Chirag Patel","item_type":"entity","text":"gene: CYP17A1 was added\ngene: CYP17A1 was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: CYP17A1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CYP17A1 were set to PMID: 2843762, 14671162, 2026124\nPhenotypes for gene: CYP17A1 were set to 17-alpha-hydroxylase/17,20-lyase deficiency, MIM# 202110","entity_name":"CYP17A1","entity_type":"gene"},{"created":"2026-01-29T13:20:30.259236+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.2","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene CYP21A2 from panel Hypertension and Aldosterone disorders","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:20:30.206423+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.2","user_name":"Chirag Patel","item_type":"entity","text":"gene: CYP21A2 was added\ngene: CYP21A2 was added to Congenital adrenal hyperplasia. Sources: Expert Review Green,Expert list\nMode of inheritance for gene: CYP21A2 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CYP21A2 were set to Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, 201910; Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency, 201910","entity_name":"CYP21A2","entity_type":"gene"},{"created":"2026-01-29T13:16:34.528976+11:00","panel_name":"Congenital adrenal hyperplasia","panel_id":4522,"panel_version":"0.1","user_name":"Chirag Patel","item_type":"panel","text":"HPO terms changed from  to Congenital adrenal hyperplasia, HP:0008258\nPanel types changed to Victorian Clinical Genetics Services; Genetic Health Queensland; Rare Disease","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:12:40.628930+11:00","panel_name":"Familial hypocalciuric hypercalcaemia","panel_id":4525,"panel_version":"0.6","user_name":"Chirag Patel","item_type":"panel","text":"Panel status changed from internal to public","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:12:30.827510+11:00","panel_name":"Familial hypocalciuric hypercalcaemia","panel_id":4525,"panel_version":"0.5","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: GNA11 as ready","entity_name":"GNA11","entity_type":"gene"},{"created":"2026-01-29T13:12:30.817039+11:00","panel_name":"Familial hypocalciuric hypercalcaemia","panel_id":4525,"panel_version":"0.5","user_name":"Chirag Patel","item_type":"entity","text":"Gene: gna11 has been classified as Green List (High Evidence).","entity_name":"GNA11","entity_type":"gene"},{"created":"2026-01-29T13:12:13.555132+11:00","panel_name":"Familial hypocalciuric hypercalcaemia","panel_id":4525,"panel_version":"0.5","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: AP2S1 as ready","entity_name":"AP2S1","entity_type":"gene"},{"created":"2026-01-29T13:12:13.547831+11:00","panel_name":"Familial hypocalciuric hypercalcaemia","panel_id":4525,"panel_version":"0.5","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ap2s1 has been classified as Green List (High Evidence).","entity_name":"AP2S1","entity_type":"gene"},{"created":"2026-01-29T13:11:29.688649+11:00","panel_name":"Familial hypocalciuric hypercalcaemia","panel_id":4525,"panel_version":"0.5","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene GNA11 from panel Hypercalcaemia","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:11:29.626408+11:00","panel_name":"Familial hypocalciuric hypercalcaemia","panel_id":4525,"panel_version":"0.5","user_name":"Chirag Patel","item_type":"entity","text":"gene: GNA11 was added\ngene: GNA11 was added to Familial hypocalciuric hypercalcaemia. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: GNA11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: GNA11 were set to 23802516; 28833550; 27913609\nPhenotypes for gene: GNA11 were set to Hypocalciuric hypercalcaemia, type II, MIM# 145981; MONDO:0007792","entity_name":"GNA11","entity_type":"gene"},{"created":"2026-01-29T13:10:52.945485+11:00","panel_name":"Familial hypocalciuric hypercalcaemia","panel_id":4525,"panel_version":"0.4","user_name":"Chirag Patel","item_type":"panel","text":"Copied gene AP2S1 from panel Hypercalcaemia","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:10:52.887414+11:00","panel_name":"Familial hypocalciuric hypercalcaemia","panel_id":4525,"panel_version":"0.4","user_name":"Chirag Patel","item_type":"entity","text":"gene: AP2S1 was added\ngene: AP2S1 was added to Familial hypocalciuric hypercalcaemia. Sources: Expert Review Green,Victorian Clinical Genetics Services\nMode of inheritance for gene: AP2S1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: AP2S1 were set to 23222959; 33729479; 33168530; 3204769; 31723423; 29479578\nPhenotypes for gene: AP2S1 were set to Hypocalciuric hypercalcaemia, type III, MIM# 600740; MONDO:0010926","entity_name":"AP2S1","entity_type":"gene"},{"created":"2026-01-29T13:09:43.256498+11:00","panel_name":"Hyperparathyroidism","panel_id":4526,"panel_version":"0.10","user_name":"Chirag Patel","item_type":"panel","text":"Panel status changed from internal to public","entity_name":null,"entity_type":null},{"created":"2026-01-29T13:08:58.984834+11:00","panel_name":"Hyperparathyroidism","panel_id":4526,"panel_version":"0.9","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: RET as ready","entity_name":"RET","entity_type":"gene"},{"created":"2026-01-29T13:08:58.977495+11:00","panel_name":"Hyperparathyroidism","panel_id":4526,"panel_version":"0.9","user_name":"Chirag Patel","item_type":"entity","text":"Gene: ret has been classified as Green List (High Evidence).","entity_name":"RET","entity_type":"gene"},{"created":"2026-01-29T13:08:51.012599+11:00","panel_name":"Hyperparathyroidism","panel_id":4526,"panel_version":"0.9","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: MEN1 as ready","entity_name":"MEN1","entity_type":"gene"},{"created":"2026-01-29T13:08:51.005052+11:00","panel_name":"Hyperparathyroidism","panel_id":4526,"panel_version":"0.9","user_name":"Chirag Patel","item_type":"entity","text":"Gene: men1 has been classified as Green List (High Evidence).","entity_name":"MEN1","entity_type":"gene"},{"created":"2026-01-29T13:08:47.324403+11:00","panel_name":"Hyperparathyroidism","panel_id":4526,"panel_version":"0.9","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: GCM2 as ready","entity_name":"GCM2","entity_type":"gene"},{"created":"2026-01-29T13:08:47.314683+11:00","panel_name":"Hyperparathyroidism","panel_id":4526,"panel_version":"0.9","user_name":"Chirag Patel","item_type":"entity","text":"Gene: gcm2 has been classified as Green List (High Evidence).","entity_name":"GCM2","entity_type":"gene"},{"created":"2026-01-29T13:08:41.668788+11:00","panel_name":"Hyperparathyroidism","panel_id":4526,"panel_version":"0.9","user_name":"Chirag Patel","item_type":"entity","text":"Marked gene: CDKN1B as ready","entity_name":"CDKN1B","entity_type":"gene"},{"created":"2026-01-29T13:08:41.656248+11:00","panel_name":"Hyperparathyroidism","panel_id":4526,"panel_version":"0.9","user_name":"Chirag Patel","item_type":"entity","text":"Gene: cdkn1b has been classified as Green List (High Evidence).","entity_name":"CDKN1B","entity_type":"gene"}]}