{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=139","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=137","results":[{"created":"2025-10-30T16:27:48.868212+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.386","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: recql4 has been classified as Green List (High Evidence).","entity_name":"RECQL4","entity_type":"gene"},{"created":"2025-10-30T16:27:30.702022+11:00","panel_name":"Hypophosphataemia or rickets","panel_id":122,"panel_version":"0.45","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: FGF23: Rating: GREEN; Mode of pathogenicity: Other; Publications: 11062477, 34444516; Phenotypes: Autosomal dominant hypophosphatemic rickets MONDO:0008660; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGF23","entity_type":"gene"},{"created":"2025-10-30T16:27:11.216221+11:00","panel_name":"Neurodegeneration with brain iron accumulation","panel_id":3438,"panel_version":"1.2","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC27A3 as ready","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:27:11.208823+11:00","panel_name":"Neurodegeneration with brain iron accumulation","panel_id":3438,"panel_version":"1.2","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc27a3 has been classified as Red List (Low Evidence).","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:27:02.408882+11:00","panel_name":"Neurodegeneration with brain iron accumulation","panel_id":3438,"panel_version":"1.2","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC27A3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:25:59.734046+11:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"1.59","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC27A3 as ready","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:25:59.724186+11:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"1.59","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc27a3 has been classified as Red List (Low Evidence).","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:25:55.244650+11:00","panel_name":"Hypophosphataemia or rickets","panel_id":122,"panel_version":"0.45","user_name":"Chirag Patel","item_type":"entity","text":"Source Victorian Clinical Genetics Services was removed from CYP27B1.\nSource Expert List was added to CYP27B1.\nMode of inheritance for gene CYP27B1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: CYP27B1 were changed from  to Vitamin D-dependent rickets, type I MIM#264700\nPublications for gene CYP27B1 were changed from 9486994, 9415400, 12050193, 27473561, 34492747, 33823104 to 9486994, 9415400, 12050193, 27473561, 34492747, 33823104","entity_name":"CYP27B1","entity_type":"gene"},{"created":"2025-10-30T16:25:44.388245+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.408","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC27A3 as ready","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:25:44.380324+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.408","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc27a3 has been classified as Red List (Low Evidence).","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:25:29.679329+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.594","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC27A3 as ready","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:25:29.672199+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.594","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc27a3 has been classified as Red List (Low Evidence).","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:25:21.443722+11:00","panel_name":"Hypophosphataemia or rickets","panel_id":122,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: CYP27B1: Rating: ; Mode of pathogenicity: None; Publications: 9486994, 9415400, 12050193, 27473561, 34492747, 33823104; Phenotypes: Vitamin D-dependent rickets, type I MIM#264700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CYP27B1","entity_type":"gene"},{"created":"2025-10-30T16:25:10.249990+11:00","panel_name":"Optic Atrophy","panel_id":149,"panel_version":"1.54","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC27A3 as ready","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:25:10.243012+11:00","panel_name":"Optic Atrophy","panel_id":149,"panel_version":"1.54","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc27a3 has been classified as Red List (Low Evidence).","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:24:57.070604+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3505","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC27A3 as ready","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:24:57.060820+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3505","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc27a3 has been classified as Red List (Low Evidence).","entity_name":"SLC27A3","entity_type":"gene"},{"created":"2025-10-30T16:23:59.646033+11:00","panel_name":"Infertility and Recurrent Pregnancy Loss","panel_id":4455,"panel_version":"1.50","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: YTHDC2 as ready","entity_name":"YTHDC2","entity_type":"gene"},{"created":"2025-10-30T16:23:59.638482+11:00","panel_name":"Infertility and Recurrent Pregnancy Loss","panel_id":4455,"panel_version":"1.50","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ythdc2 has been classified as Green List (High Evidence).","entity_name":"YTHDC2","entity_type":"gene"},{"created":"2025-10-30T16:23:46.500639+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3505","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: YTHDC2 as ready","entity_name":"YTHDC2","entity_type":"gene"},{"created":"2025-10-30T16:23:46.493738+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3505","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ythdc2 has been classified as Green List (High Evidence).","entity_name":"YTHDC2","entity_type":"gene"},{"created":"2025-10-30T16:23:40.695644+11:00","panel_name":"Hypophosphataemia or rickets","panel_id":122,"panel_version":"0.44","user_name":"Chirag Patel","item_type":"entity","text":"Source Victorian Clinical Genetics Services was removed from DMP1.\nSource Expert List was added to DMP1.\nMode of inheritance for gene DMP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: DMP1 were changed from  to Hypophosphatemic rickets MIM#241520\nPublications for gene DMP1 were changed from 17033625, 22695891, 20213538, 17033621, 32920683, 15590631 to 17033625, 22695891, 20213538, 17033621, 32920683, 15590631","entity_name":"DMP1","entity_type":"gene"},{"created":"2025-10-30T16:23:15.452914+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3505","user_name":"Zornitza Stark","item_type":"panel","text":"Copied gene YTHDC2 from panel Primary Ovarian Insufficiency_Premature Ovarian Failure","entity_name":null,"entity_type":null},{"created":"2025-10-30T16:23:14.893607+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3505","user_name":"Zornitza Stark","item_type":"entity","text":"gene: YTHDC2 was added\ngene: YTHDC2 was added to Mendeliome. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: YTHDC2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: YTHDC2 were set to 29033321, 29360036, 35138268\nPhenotypes for gene: YTHDC2 were set to Primary ovarian failure, MONDO:0005387","entity_name":"YTHDC2","entity_type":"gene"},{"created":"2025-10-30T16:23:11.493658+11:00","panel_name":"Infertility and Recurrent Pregnancy Loss","panel_id":4455,"panel_version":"1.50","user_name":"Zornitza Stark","item_type":"panel","text":"Copied gene YTHDC2 from panel Primary Ovarian Insufficiency_Premature Ovarian Failure","entity_name":null,"entity_type":null},{"created":"2025-10-30T16:23:11.447554+11:00","panel_name":"Infertility and Recurrent Pregnancy Loss","panel_id":4455,"panel_version":"1.50","user_name":"Zornitza Stark","item_type":"entity","text":"gene: YTHDC2 was added\ngene: YTHDC2 was added to Infertility and Recurrent Pregnancy Loss. Sources: Expert Review Green,Genomics England PanelApp\nMode of inheritance for gene: YTHDC2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: YTHDC2 were set to 29033321, 29360036, 35138268\nPhenotypes for gene: YTHDC2 were set to Primary ovarian failure, MONDO:0005387","entity_name":"YTHDC2","entity_type":"gene"},{"created":"2025-10-30T16:23:08.132963+11:00","panel_name":"Hypophosphataemia or rickets","panel_id":122,"panel_version":"0.43","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: DMP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17033625, 22695891, 20213538, 17033621, 32920683, 15590631; Phenotypes: Hypophosphatemic rickets MIM#241520; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DMP1","entity_type":"gene"},{"created":"2025-10-30T16:22:56.580077+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.386","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: YTHDC2 as ready","entity_name":"YTHDC2","entity_type":"gene"},{"created":"2025-10-30T16:22:56.570491+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.386","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ythdc2 has been classified as Green List (High Evidence).","entity_name":"YTHDC2","entity_type":"gene"},{"created":"2025-10-30T16:22:17.224259+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.386","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZSWIM7 as ready","entity_name":"ZSWIM7","entity_type":"gene"},{"created":"2025-10-30T16:22:17.214240+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.386","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zswim7 has been classified as Green List (High Evidence).","entity_name":"ZSWIM7","entity_type":"gene"},{"created":"2025-10-30T16:22:14.676009+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.386","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZSWIM7 were set to 40991243, 34402903","entity_name":"ZSWIM7","entity_type":"gene"},{"created":"2025-10-30T16:18:06.836321+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.267","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OTUD7A were set to 31997314; 29395075; 29395074; 33381903","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:17:39.140509+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.266","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: OTUD7A as Green List (high evidence)","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:17:39.130739+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.266","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otud7a has been classified as Green List (High Evidence).","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:17:14.736135+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.265","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: OTUD7A.","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:16:56.068414+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.408","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OTUD7A were set to 31997314; 29395075; 29395074; 33381903","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:16:28.520616+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.407","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: OTUD7A as Green List (high evidence)","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:16:28.508331+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.407","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otud7a has been classified as Green List (High Evidence).","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:16:06.671589+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.406","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: OTUD7A.","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:15:37.164797+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3504","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OTUD7A were set to 31997314; 29395075; 29395074; 33381903","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:15:11.329807+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3503","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: OTUD7A as Green List (high evidence)","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:15:11.322348+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otud7a has been classified as Green List (High Evidence).","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:13:59.488256+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.385","user_name":"Chirag Patel","item_type":"entity","text":"Source NHS GMS was removed from FSHB.\nSource Expert List was added to FSHB.\nPhenotypes for gene: FSHB were changed from Hypogonadotropic hypogonadism 24 without anosmia 229070 to Hypogonadotropic hypogonadism 24 without anosmia, MIM# 229070\nPublications for gene FSHB were changed from 8220432, 8220432, 9624193, 9806482, 12161499 to 8220432, 8220432, 9624193, 9806482, 12161499","entity_name":"FSHB","entity_type":"gene"},{"created":"2025-10-30T16:13:39.924506+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.384","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: FSHB: Rating: GREEN; Mode of pathogenicity: None; Publications: 8220432, 8220432, 9624193, 9806482, 12161499; Phenotypes: Hypogonadotropic hypogonadism 24 without anosmia, MIM# 229070; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"FSHB","entity_type":"gene"},{"created":"2025-10-30T16:12:05.629156+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.384","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: FSHR: Rating: GREEN; Mode of pathogenicity: None; Publications: 7553856, 9769327, 11889179, 20087398, 36704038; Phenotypes: Ovarian dysgenesis 1, MIM# 233300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FSHR","entity_type":"gene"},{"created":"2025-10-30T16:11:18.077037+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.384","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from FSHR.\nSource Expert List was added to FSHR.\nPhenotypes for gene: FSHR were changed from Ovarian dysgenesis 1 233300; Ovarian response to FSH stimulation 276400 to Ovarian dysgenesis 1 MONDO:0024463\nPublications for gene FSHR were changed from 7553856, 9769327, 11889179, 20087398, 36704038 to 7553856, 9769327, 11889179, 20087398, 36704038","entity_name":"FSHR","entity_type":"gene"},{"created":"2025-10-30T16:09:54.782919+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.383","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from GALT.\nSource Expert List was added to GALT.\nPhenotypes for gene: GALT were changed from Galactosemia, 230400 to Primary ovarian failure, MONDO:0005387; Galactosemia MIM#230400\nPublications for gene GALT were changed from 39440457, 19733849, 34433538, 31042289, 34730073 to 39440457, 19733849, 34433538, 31042289, 34730073","entity_name":"GALT","entity_type":"gene"},{"created":"2025-10-30T16:09:34.931685+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.382","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: GALT: Rating: GREEN; Mode of pathogenicity: None; Publications: 39440457, 19733849, 34433538, 31042289, 34730073; Phenotypes: Primary ovarian failure, MONDO:0005387, Galactosemia MIM#230400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GALT","entity_type":"gene"},{"created":"2025-10-30T16:09:11.704915+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3502","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: OTUD7A.","entity_name":"OTUD7A","entity_type":"gene"},{"created":"2025-10-30T16:08:03.616042+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.382","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: HSD17B4: Rating: GREEN; Mode of pathogenicity: None; Publications: 20673864, 28830375; Phenotypes: Perrault syndrome 1, #MIM 233400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"HSD17B4","entity_type":"gene"},{"created":"2025-10-30T16:07:46.684418+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.382","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from HSD17B4.\nSource Expert List was added to HSD17B4.\nPhenotypes for gene: HSD17B4 were changed from Perrault syndrome 1 233400 to Perrault syndrome 1, #MIM 233400\nPublications for gene HSD17B4 were changed from 20673864, 28830375 to 20673864, 28830375","entity_name":"HSD17B4","entity_type":"gene"},{"created":"2025-10-30T16:06:47.948427+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.381","user_name":"Chirag Patel","item_type":"entity","text":"Source NHS GMS was removed from PMM2.\nSource Expert List was added to PMM2.\nPhenotypes for gene: PMM2 were changed from Congenital disorder of glycosylation, type Ia 212065 to Primary ovarian failure, MONDO:0005387; Congenital disorder of glycosylation, type Ia 212065\nPublications for gene PMM2 were changed from 20301289, 31902100, 25497157, 33583911 to 20301289, 31902100, 25497157, 33583911","entity_name":"PMM2","entity_type":"gene"},{"created":"2025-10-30T16:06:21.014382+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.380","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PMM2: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301289, 31902100, 25497157, 33583911; Phenotypes: Primary ovarian failure, MONDO:0005387, Congenital disorder of glycosylation, type Ia 212065; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PMM2","entity_type":"gene"},{"created":"2025-10-30T16:03:01.689644+11:00","panel_name":"Primary pigmented nodular adrenocortical disease","panel_id":4488,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDE11A as ready","entity_name":"PDE11A","entity_type":"gene"},{"created":"2025-10-30T16:03:01.678623+11:00","panel_name":"Primary pigmented nodular adrenocortical disease","panel_id":4488,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde11a has been classified as Green List (High Evidence).","entity_name":"PDE11A","entity_type":"gene"},{"created":"2025-10-30T16:02:54.497704+11:00","panel_name":"Primary pigmented nodular adrenocortical disease","panel_id":4488,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDE8B as ready","entity_name":"PDE8B","entity_type":"gene"},{"created":"2025-10-30T16:02:54.490854+11:00","panel_name":"Primary pigmented nodular adrenocortical disease","panel_id":4488,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pde8b has been classified as Green List (High Evidence).","entity_name":"PDE8B","entity_type":"gene"},{"created":"2025-10-30T16:02:47.224677+11:00","panel_name":"Primary pigmented nodular adrenocortical disease","panel_id":4488,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKACA as ready","entity_name":"PRKACA","entity_type":"gene"},{"created":"2025-10-30T16:02:47.217125+11:00","panel_name":"Primary pigmented nodular adrenocortical disease","panel_id":4488,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkaca has been classified as Green List (High Evidence).","entity_name":"PRKACA","entity_type":"gene"},{"created":"2025-10-30T16:02:15.153494+11:00","panel_name":"Hypertension and Aldosterone disorders","panel_id":190,"panel_version":"1.16","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC5 as ready","entity_name":"ARMC5","entity_type":"gene"},{"created":"2025-10-30T16:02:15.144267+11:00","panel_name":"Hypertension and Aldosterone disorders","panel_id":190,"panel_version":"1.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc5 has been classified as Red List (Low Evidence).","entity_name":"ARMC5","entity_type":"gene"},{"created":"2025-10-30T16:01:51.458468+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3502","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC5 as ready","entity_name":"ARMC5","entity_type":"gene"},{"created":"2025-10-30T16:01:51.448542+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.3502","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc5 has been classified as Green List (High Evidence).","entity_name":"ARMC5","entity_type":"gene"},{"created":"2025-10-30T16:01:30.648254+11:00","panel_name":"Primary pigmented nodular adrenocortical disease","panel_id":4488,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC5 as ready","entity_name":"ARMC5","entity_type":"gene"},{"created":"2025-10-30T16:01:30.641126+11:00","panel_name":"Primary pigmented nodular adrenocortical disease","panel_id":4488,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc5 has been classified as Green List (High Evidence).","entity_name":"ARMC5","entity_type":"gene"},{"created":"2025-10-30T16:01:20.962623+11:00","panel_name":"Primary pigmented nodular adrenocortical disease","panel_id":4488,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKAR1A as ready","entity_name":"PRKAR1A","entity_type":"gene"},{"created":"2025-10-30T16:01:20.955562+11:00","panel_name":"Primary pigmented nodular adrenocortical disease","panel_id":4488,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkar1a has been classified as Green List (High Evidence).","entity_name":"PRKAR1A","entity_type":"gene"},{"created":"2025-10-30T15:59:26.745295+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.380","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from WT1.\nSource Expert List was added to WT1.\nMode of inheritance for gene WT1 was changed from  to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: WT1 were changed from  to Primary ovarian failure, MONDO:0005387\nPublications for gene WT1 were changed from 26358501, 34845858 to 26358501, 34845858","entity_name":"WT1","entity_type":"gene"},{"created":"2025-10-30T15:59:08.446094+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.379","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: WT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 26358501, 34845858; Phenotypes: Primary ovarian failure, MONDO:0005387; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WT1","entity_type":"gene"},{"created":"2025-10-30T15:58:22.150456+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.379","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from WDR11.\nSource Expert List was added to WDR11.\nMode of inheritance for gene WDR11 was changed from  to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: WDR11 were changed from  to Hypogonadotropic hypogonadism 14 with or without anosmia, MIM# 614858\nPublications for gene WDR11 were changed from 20887964, 37988663, 36130823, 35722485, 32982993, 29263200 to 20887964, 37988663, 36130823, 35722485, 32982993, 29263200","entity_name":"WDR11","entity_type":"gene"},{"created":"2025-10-30T15:58:09.152738+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.406","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AUTS2 were set to 23332918; 25205402; 31474318; 39953909","entity_name":"AUTS2","entity_type":"gene"},{"created":"2025-10-30T15:58:06.790638+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.378","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: WDR11: Rating: GREEN; Mode of pathogenicity: None; Publications: 20887964, 37988663, 36130823, 35722485, 32982993, 29263200; Phenotypes: Hypogonadotropic hypogonadism 14 with or without anosmia, MIM# 614858; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"WDR11","entity_type":"gene"},{"created":"2025-10-30T15:57:16.995666+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.405","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: AUTS2 were set to 23332918; 25205402; 31474318","entity_name":"AUTS2","entity_type":"gene"},{"created":"2025-10-30T15:57:16.601952+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.378","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: TACR3: Rating: GREEN; Mode of pathogenicity: None; Publications: 22031817, 20332248, 20194706, 20395662, 19755480, 28915117, 19079066; Phenotypes: Hypogonadotropic hypogonadism 11 with or without anosmia, MIM# 61484; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TACR3","entity_type":"gene"},{"created":"2025-10-30T15:57:00.763581+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.378","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from TACR3.\nSource Expert List was added to TACR3.\nMode of inheritance for gene TACR3 was changed from  to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TACR3 were changed from  to Hypogonadotropic hypogonadism 11 with or without anosmia, MIM# 614840\nPublications for gene TACR3 were changed from 22031817, 20332248, 20194706, 20395662, 19755480, 28915117, 19079066 to 22031817, 20332248, 20194706, 20395662, 19755480, 28915117, 19079066","entity_name":"TACR3","entity_type":"gene"},{"created":"2025-10-30T15:56:32.881368+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.377","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from TAC3.\nSource Expert List was added to TAC3.\nMode of inheritance for gene TAC3 was changed from  to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: TAC3 were changed from  to Hypogonadotropic hypogonadism 10 with or without anosmia, MIM# 614839\nPublications for gene TAC3 were changed from 20332248, 20194706, 34403359, 19079066 to 20332248, 20194706, 34403359, 19079066","entity_name":"TAC3","entity_type":"gene"},{"created":"2025-10-30T15:56:14.960344+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.376","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: TAC3: Rating: GREEN; Mode of pathogenicity: None; Publications: 20332248, 20194706, 34403359, 19079066; Phenotypes: Hypogonadotropic hypogonadism 10 with or without anosmia, MIM# 614839; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TAC3","entity_type":"gene"},{"created":"2025-10-30T15:55:53.968037+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.278","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KDM1A as ready","entity_name":"KDM1A","entity_type":"gene"},{"created":"2025-10-30T15:55:53.957292+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.278","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kdm1a has been classified as Green List (High Evidence).","entity_name":"KDM1A","entity_type":"gene"},{"created":"2025-10-30T15:55:33.112801+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"1.7","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: JAG1 as Green List (high evidence)","entity_name":"JAG1","entity_type":"gene"},{"created":"2025-10-30T15:55:33.102018+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"1.7","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: jag1 has been classified as Green List (High Evidence).","entity_name":"JAG1","entity_type":"gene"},{"created":"2025-10-30T15:55:26.980843+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: JAG1 as ready","entity_name":"JAG1","entity_type":"gene"},{"created":"2025-10-30T15:55:26.972120+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: jag1 has been classified as Green List (High Evidence).","entity_name":"JAG1","entity_type":"gene"},{"created":"2025-10-30T15:55:25.190213+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.376","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from STAR.\nSource Expert List was added to STAR.\nMode of inheritance for gene STAR was changed from  to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: STAR were changed from  to Lipoid adrenal hyperplasia, MIM# 201710\nPublications for gene STAR were changed from 38913505, 36733346 to 38913505, 36733346","entity_name":"STAR","entity_type":"gene"},{"created":"2025-10-30T15:55:01.023794+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.375","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: STAR: Rating: GREEN; Mode of pathogenicity: None; Publications: 38913505, 36733346; Phenotypes: Lipoid adrenal hyperplasia, MIM# 201710; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"STAR","entity_type":"gene"},{"created":"2025-10-30T15:54:44.870924+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: JAG1 as Green List (high evidence)","entity_name":"JAG1","entity_type":"gene"},{"created":"2025-10-30T15:54:44.863198+11:00","panel_name":"Renal Tubulointerstitial Disease","panel_id":199,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: jag1 has been classified as Green List (High Evidence).","entity_name":"JAG1","entity_type":"gene"},{"created":"2025-10-30T15:53:24.203405+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.375","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from SEMA3A.\nSource Expert List was added to SEMA3A.\nMode of inheritance for gene SEMA3A was changed from  to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: SEMA3A were changed from  to Hypogonadotropic hypogonadism 16 with or without anosmia, MIM# 614897\nPublications for gene SEMA3A were changed from 22416012, 22927827, 32060892, 31200363, 33819414 to 22416012, 22927827, 32060892, 31200363, 33819414","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2025-10-30T15:53:02.194309+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.374","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SEMA3A: Rating: GREEN; Mode of pathogenicity: None; Publications: 22416012, 22927827, 32060892, 31200363, 33819414; Phenotypes: Hypogonadotropic hypogonadism 16 with or without anosmia, MIM# 614897; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SEMA3A","entity_type":"gene"},{"created":"2025-10-30T15:51:59.377497+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.374","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from PROK2.\nSource Expert List was added to PROK2.\nMode of inheritance for gene PROK2 was changed from  to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPhenotypes for gene: PROK2 were changed from  to Hypogonadotropic hypogonadism 4 with or without anosmia, MIM# 610628\nPublications for gene PROK2 were changed from 23341491, 18559922, 17959774, 17054399, 31200363, 33819414 to 23341491, 18559922, 17959774, 17054399, 31200363, 33819414","entity_name":"PROK2","entity_type":"gene"},{"created":"2025-10-30T15:51:25.543651+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.373","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PROK2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"PROK2","entity_type":"gene"},{"created":"2025-10-30T15:50:45.817999+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.373","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: KISS1R: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"KISS1R","entity_type":"gene"},{"created":"2025-10-30T15:50:37.618130+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.373","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from KISS1R.\nSource Expert List was added to KISS1R.\nMode of inheritance for gene KISS1R was changed from  to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: KISS1R were changed from  to Hypogonadotropic hypogonadism 8 with or without anosmia, MIM# 614837\nPublications for gene KISS1R were changed from 23349759, 22619348, 21193544, 17164310, 14573733, 27094476, 33819414 to 23349759, 22619348, 21193544, 17164310, 14573733, 27094476, 33819414","entity_name":"KISS1R","entity_type":"gene"},{"created":"2025-10-30T15:46:56.520606+11:00","panel_name":"Metal Metabolism Disorders","panel_id":3469,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC31A1 were set to 35913762, 36562171","entity_name":"SLC31A1","entity_type":"gene"},{"created":"2025-10-30T15:46:28.933741+11:00","panel_name":"Metal Metabolism Disorders","panel_id":3469,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC31A1 as Green List (high evidence)","entity_name":"SLC31A1","entity_type":"gene"},{"created":"2025-10-30T15:46:28.923379+11:00","panel_name":"Metal Metabolism Disorders","panel_id":3469,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc31a1 has been classified as Green List (High Evidence).","entity_name":"SLC31A1","entity_type":"gene"},{"created":"2025-10-30T15:44:18.767435+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.372","user_name":"Chirag Patel","item_type":"entity","text":"Source Royal Melbourne Hospital was removed from GNAS.\nSource Expert Review was added to GNAS.\nMode of inheritance for gene GNAS was changed from  to Other\nPhenotypes for gene: GNAS were changed from  to Pseudohypoparathyroidism Ia (103580) AD; Pseudohypoparathyroidism Ib (603233) AD; Pseudohypoparathyroidism Ic (612462) AD; Pseudopseudohypoparathyroidism (612463); Osseous heteroplasia, progressive (166350) AD; Pituitary adenoma 3, multiple types, somatic (617686)","entity_name":"GNAS","entity_type":"gene"},{"created":"2025-10-30T15:43:53.894394+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.371","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: GNAS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pseudohypoparathyroidism Ia (103580) AD, Pseudohypoparathyroidism Ib (603233) AD, Pseudohypoparathyroidism Ic (612462) AD, Pseudopseudohypoparathyroidism (612463), Osseous heteroplasia, progressive (166350) AD, Pituitary adenoma 3, multiple types, somatic (617686); Mode of inheritance: Other","entity_name":"GNAS","entity_type":"gene"},{"created":"2025-10-30T15:33:23.962956+11:00","panel_name":"Primary Ovarian Insufficiency_Premature Ovarian Failure","panel_id":3166,"panel_version":"0.371","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: LMNA as Amber List (moderate evidence)","entity_name":"LMNA","entity_type":"gene"}]}