{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=656","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=654","results":[{"created":"2022-12-24T17:13:10.499432+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1677","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deafness tag was added to gene: CDC14A.","entity_name":"CDC14A","entity_type":"gene"},{"created":"2022-12-24T17:12:39.712575+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1677","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CDAN1 as ready","entity_name":"CDAN1","entity_type":"gene"},{"created":"2022-12-24T17:12:39.658901+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1677","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdan1 has been classified as Red List (Low Evidence).","entity_name":"CDAN1","entity_type":"gene"},{"created":"2022-12-24T17:12:36.391436+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1677","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CDAN1 were changed from Anemia, congenital dyserythropoietic, type I to Dyserythropoietic anaemia, congenital, type Ia, MIM#224120","entity_name":"CDAN1","entity_type":"gene"},{"created":"2022-12-24T17:12:15.435737+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1676","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CDAN1 as Red List (low evidence)","entity_name":"CDAN1","entity_type":"gene"},{"created":"2022-12-24T17:12:15.422892+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1676","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdan1 has been classified as Red List (Low Evidence).","entity_name":"CDAN1","entity_type":"gene"},{"created":"2022-12-24T17:11:58.126120+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CDAN1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Dyserythropoietic anaemia, congenital, type Ia, 224120; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CDAN1","entity_type":"gene"},{"created":"2022-12-24T17:10:15.272503+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: CDAN1.\nTag haematological tag was added to gene: CDAN1.","entity_name":"CDAN1","entity_type":"gene"},{"created":"2022-12-24T17:09:47.081695+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: CD79B.","entity_name":"CD79B","entity_type":"gene"},{"created":"2022-12-24T17:09:22.848752+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: CD79A.","entity_name":"CD79A","entity_type":"gene"},{"created":"2022-12-24T17:08:36.639133+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: CD40LG.","entity_name":"CD40LG","entity_type":"gene"},{"created":"2022-12-24T17:06:37.580762+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: CD3E.\nTag immunological tag was added to gene: CD3E.","entity_name":"CD3E","entity_type":"gene"},{"created":"2022-12-24T17:06:14.207038+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: CD3D.","entity_name":"CD3D","entity_type":"gene"},{"created":"2022-12-24T17:03:42.145369+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag endocrine tag was added to gene: CAVIN1.","entity_name":"CAVIN1","entity_type":"gene"},{"created":"2022-12-24T17:03:15.222226+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: CASR.\nTag endocrine tag was added to gene: CASR.","entity_name":"CASR","entity_type":"gene"},{"created":"2022-12-24T17:01:04.845476+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: CARD11.\nTag immunological tag was added to gene: CARD11.","entity_name":"CARD11","entity_type":"gene"},{"created":"2022-12-24T17:00:34.221015+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag deafness tag was added to gene: CABP2.","entity_name":"CABP2","entity_type":"gene"},{"created":"2022-12-24T17:00:08.082614+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: CA5A.","entity_name":"CA5A","entity_type":"gene"},{"created":"2022-12-24T16:59:45.932295+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag skeletal tag was added to gene: CA2.","entity_name":"CA2","entity_type":"gene"},{"created":"2022-12-24T16:59:25.922435+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: C9.","entity_name":"C9","entity_type":"gene"},{"created":"2022-12-24T16:58:48.729530+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: C8B.\nTag immunological tag was added to gene: C8B.","entity_name":"C8B","entity_type":"gene"},{"created":"2022-12-24T16:58:25.884136+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: C7.","entity_name":"C7","entity_type":"gene"},{"created":"2022-12-24T16:58:05.483394+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: C6.","entity_name":"C6","entity_type":"gene"},{"created":"2022-12-24T16:54:32.351539+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: C5.","entity_name":"C5","entity_type":"gene"},{"created":"2022-12-24T16:53:50.657483+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.570","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GOSR2 were changed from Epilepsy, progressive myoclonic 6 , MIM#614018 to Epilepsy, progressive myoclonic 6 , MIM#614018; Muscular dystrophy, congenital, with or without seizures, MIM# 620166","entity_name":"GOSR2","entity_type":"gene"},{"created":"2022-12-24T16:53:25.089532+11:00","panel_name":"Muscular dystrophy_Paediatric","panel_id":141,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GOSR2 were changed from Epilepsy, progressive myoclonic 6\t614018 to Muscular dystrophy, congenital, with or without seizures, MIM# 620166","entity_name":"GOSR2","entity_type":"gene"},{"created":"2022-12-24T16:52:16.056729+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.569","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: GOSR2: Added comment: PMIDs 29855340; 33639315: at least three families reported with a muscular dystrophy presentation as well as seizures.; Changed publications: 21549339, 24458321, 30363482, 29855340, 33639315; Changed phenotypes: Epilepsy, progressive myoclonic 6 , MIM#614018, Muscular dystrophy, congenital, with or without seizures, MIM# 620166","entity_name":"GOSR2","entity_type":"gene"},{"created":"2022-12-24T15:05:46.820740+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"John Christodoulou","item_type":"entity","text":"reviewed gene: GCH1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 32456656, PMID: 20301681; Phenotypes: dystonia, truncal hypotonia, peripheral hypertonia, seizures, ID, fever; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"GCH1","entity_type":"gene"},{"created":"2022-12-24T14:48:46.736303+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"John Christodoulou","item_type":"entity","text":"reviewed gene: UROS: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 30685241; Phenotypes: hydros, photosensitivity, erythrodontia, corneal scarring, haemolytic anaemia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"UROS","entity_type":"gene"},{"created":"2022-12-24T14:37:28.024864+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"John Christodoulou","item_type":"entity","text":"reviewed gene: TRMU: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 33485800, PMID: 33365252; Phenotypes: liver failure, Leigh syndrome, cardiomyopathy' myopathy; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRMU","entity_type":"gene"},{"created":"2022-12-24T14:31:13.471629+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"John Christodoulou","item_type":"entity","text":"reviewed gene: TPP1: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 30783219, PMID: 32280231; Phenotypes: neruodegeneration, seizures, loss of vision, loss of language; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TPP1","entity_type":"gene"},{"created":"2022-12-24T13:32:22.054385+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.569","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TNNC2 were changed from Congenital myopathy, MONDO:0019952, TNNC2-related to Myopathy, congenital, with neonatal respiratory insufficiency, MIM# 620161","entity_name":"TNNC2","entity_type":"gene"},{"created":"2022-12-24T13:31:58.724917+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.568","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TNNC2: Changed phenotypes: Myopathy, congenital, with neonatal respiratory insufficiency, MIM# 620161","entity_name":"TNNC2","entity_type":"gene"},{"created":"2022-12-23T17:56:20.831526+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: BTK.","entity_name":"BTK","entity_type":"gene"},{"created":"2022-12-23T17:56:00.873981+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: BTD.","entity_name":"BTD","entity_type":"gene"},{"created":"2022-12-23T17:55:40.141319+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag renal tag was added to gene: BSND.","entity_name":"BSND","entity_type":"gene"},{"created":"2022-12-23T17:55:17.571922+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag endocrine tag was added to gene: BSCL2.","entity_name":"BSCL2","entity_type":"gene"},{"created":"2022-12-23T17:54:42.729905+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag haematological tag was added to gene: BRIP1.","entity_name":"BRIP1","entity_type":"gene"},{"created":"2022-12-23T17:54:17.593400+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag immunological tag was added to gene: BLNK.","entity_name":"BLNK","entity_type":"gene"},{"created":"2022-12-23T17:53:56.445017+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: BCKDK.","entity_name":"BCKDK","entity_type":"gene"},{"created":"2022-12-23T17:53:35.454452+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: BCKDHB.","entity_name":"BCKDHB","entity_type":"gene"},{"created":"2022-12-23T17:49:58.695747+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag metabolic tag was added to gene: BCKDHA.","entity_name":"BCKDHA","entity_type":"gene"},{"created":"2022-12-23T17:47:17.857787+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TFG as ready","entity_name":"TFG","entity_type":"gene"},{"created":"2022-12-23T17:47:17.836991+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tfg has been classified as Red List (Low Evidence).","entity_name":"TFG","entity_type":"gene"},{"created":"2022-12-23T17:47:14.511695+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TFG were changed from Hereditary motor and sensory neuropathy to Hereditary motor and sensory neuropathy, Okinawa type, MIM# 604484; Spastic paraplegia 57, autosomal recessive, MIM# 615658","entity_name":"TFG","entity_type":"gene"},{"created":"2022-12-23T17:47:03.254478+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1674","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TFG was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"TFG","entity_type":"gene"},{"created":"2022-12-23T17:46:52.678902+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1673","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TFG as Red List (low evidence)","entity_name":"TFG","entity_type":"gene"},{"created":"2022-12-23T17:46:52.662051+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1673","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tfg has been classified as Red List (Low Evidence).","entity_name":"TFG","entity_type":"gene"},{"created":"2022-12-23T17:46:40.696954+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1672","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TFG: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hereditary motor and sensory neuropathy, Okinawa type, MIM# 604484, Spastic paraplegia 57, autosomal recessive, MIM# 615658; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"TFG","entity_type":"gene"},{"created":"2022-12-23T17:44:19.766602+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1672","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TG as ready","entity_name":"TG","entity_type":"gene"},{"created":"2022-12-23T17:44:19.753565+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1672","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tg has been classified as Green List (High Evidence).","entity_name":"TG","entity_type":"gene"},{"created":"2022-12-23T17:44:15.838196+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1672","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TG were changed from Thyroid dyshormonogenesis 3 to Thyroid dyshormonogenesis 3, MIM# 274700","entity_name":"TG","entity_type":"gene"},{"created":"2022-12-23T17:44:03.839046+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1671","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TG were set to ","entity_name":"TG","entity_type":"gene"},{"created":"2022-12-23T17:43:51.040866+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1670","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: TG.\nTag endocrine tag was added to gene: TG.","entity_name":"TG","entity_type":"gene"},{"created":"2022-12-23T17:43:34.874174+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1670","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TG: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Thyroid dyshormonogenesis 3, MIM# 274700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TG","entity_type":"gene"},{"created":"2022-12-23T17:42:48.500121+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1670","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGM5 as ready","entity_name":"TGM5","entity_type":"gene"},{"created":"2022-12-23T17:42:48.483924+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1670","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgm5 has been classified as Red List (Low Evidence).","entity_name":"TGM5","entity_type":"gene"},{"created":"2022-12-23T17:42:43.198612+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1670","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGM5 were changed from Peeling skin syndrome, acral type to Peeling skin syndrome 2, MIM# 609796","entity_name":"TGM5","entity_type":"gene"},{"created":"2022-12-23T17:42:30.985627+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1669","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TGM5 as Red List (low evidence)","entity_name":"TGM5","entity_type":"gene"},{"created":"2022-12-23T17:42:30.972707+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1669","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgm5 has been classified as Red List (Low Evidence).","entity_name":"TGM5","entity_type":"gene"},{"created":"2022-12-23T17:42:19.584118+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1668","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TGM5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Peeling skin syndrome 2, MIM# 609796; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TGM5","entity_type":"gene"},{"created":"2022-12-23T17:40:57.944214+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1668","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGM1 as ready","entity_name":"TGM1","entity_type":"gene"},{"created":"2022-12-23T17:40:57.932445+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1668","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgm1 has been classified as Red List (Low Evidence).","entity_name":"TGM1","entity_type":"gene"},{"created":"2022-12-23T17:40:53.650787+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1668","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGM1 were changed from Ichthyosis, congenital, autosomal recessive to Ichthyosis, congenital, autosomal recessive 1 (MIM#242300)","entity_name":"TGM1","entity_type":"gene"},{"created":"2022-12-23T17:40:40.978377+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1667","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TGM1 as Red List (low evidence)","entity_name":"TGM1","entity_type":"gene"},{"created":"2022-12-23T17:40:40.965143+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1667","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgm1 has been classified as Red List (Low Evidence).","entity_name":"TGM1","entity_type":"gene"},{"created":"2022-12-23T17:40:26.340112+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1666","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TGM1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ichthyosis, congenital, autosomal recessive 1 (MIM#242300); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TGM1","entity_type":"gene"},{"created":"2022-12-23T17:38:28.385350+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1666","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFBR2 as ready","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-12-23T17:38:28.371567+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1666","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfbr2 has been classified as Green List (High Evidence).","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-12-23T17:38:24.044988+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1666","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFBR2 were changed from Loeys-Dietz syndrome to Loeys-Dietz syndrome 2, MIM# 610168","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-12-23T17:38:11.462573+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1665","user_name":"Zornitza Stark","item_type":"entity","text":"Tag cardiac tag was added to gene: TGFBR2.\nTag treatable tag was added to gene: TGFBR2.","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-12-23T17:37:55.169234+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1665","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TGFBR2: Changed phenotypes: Loeys-Dietz syndrome 2, MIM# 610168","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-12-23T17:37:41.041537+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1665","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TGFBR2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2022-12-23T17:36:53.316623+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1665","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFBR1 as ready","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2022-12-23T17:36:53.305147+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1665","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfbr1 has been classified as Green List (High Evidence).","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2022-12-23T17:36:49.982843+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1665","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFBR1 were changed from Loeys-Dietz syndrome to Loeys-Dietz syndrome 1, MIM# 609192","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2022-12-23T17:36:37.425267+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1664","user_name":"Zornitza Stark","item_type":"entity","text":"Tag cardiac tag was added to gene: TGFBR1.\nTag treatable tag was added to gene: TGFBR1.","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2022-12-23T17:36:21.745070+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1664","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TGFBR1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Loeys-Dietz syndrome 1, MIM# 609192; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2022-12-23T17:32:32.575158+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1664","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TH as ready","entity_name":"TH","entity_type":"gene"},{"created":"2022-12-23T17:32:32.561894+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1664","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: th has been classified as Green List (High Evidence).","entity_name":"TH","entity_type":"gene"},{"created":"2022-12-23T17:32:28.779963+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1664","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TH were set to ","entity_name":"TH","entity_type":"gene"},{"created":"2022-12-23T17:32:17.160520+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1663","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: TH.\nTag endocrine tag was added to gene: TH.","entity_name":"TH","entity_type":"gene"},{"created":"2022-12-23T17:30:20.015904+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1663","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: THRA as ready","entity_name":"THRA","entity_type":"gene"},{"created":"2022-12-23T17:30:19.998093+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1663","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thra has been classified as Green List (High Evidence).","entity_name":"THRA","entity_type":"gene"},{"created":"2022-12-23T17:30:16.509954+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1663","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: THRA were changed from Hypothyroidism, congenital, nongoitrous, 6 to Hypothyroidism, congenital, nongoitrous, 6, MIM# 614450","entity_name":"THRA","entity_type":"gene"},{"created":"2022-12-23T17:30:04.508005+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1662","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: THRA were set to ","entity_name":"THRA","entity_type":"gene"},{"created":"2022-12-23T17:29:49.157975+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1661","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: THRA.\nTag endocrine tag was added to gene: THRA.","entity_name":"THRA","entity_type":"gene"},{"created":"2022-12-23T17:29:34.414861+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1661","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: THRA: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypothyroidism, congenital, nongoitrous, 6, MIM# 614450; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"THRA","entity_type":"gene"},{"created":"2022-12-23T17:26:12.309348+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1661","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: THRB as ready","entity_name":"THRB","entity_type":"gene"},{"created":"2022-12-23T17:26:12.296902+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1661","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thrb has been classified as Red List (Low Evidence).","entity_name":"THRB","entity_type":"gene"},{"created":"2022-12-23T17:25:57.751482+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1661","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: THRB were changed from Thyroid hormone resistance to Thyroid hormone resistance, MIM# 188570; Thyroid hormone resistance, autosomal recessive, MIM# 274300; Thyroid hormone resistance, selective pituitary, MIM# 145650","entity_name":"THRB","entity_type":"gene"},{"created":"2022-12-23T17:25:43.674604+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1660","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: THRB was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"THRB","entity_type":"gene"},{"created":"2022-12-23T17:25:29.226707+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1659","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: THRB as Red List (low evidence)","entity_name":"THRB","entity_type":"gene"},{"created":"2022-12-23T17:25:29.214068+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1659","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: thrb has been classified as Red List (Low Evidence).","entity_name":"THRB","entity_type":"gene"},{"created":"2022-12-23T17:25:17.349156+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1658","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: THRB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Thyroid hormone resistance, MIM# 188570, Thyroid hormone resistance, autosomal recessive, MIM# 274300, Thyroid hormone resistance, selective pituitary, MIM# 145650; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"THRB","entity_type":"gene"},{"created":"2022-12-23T17:23:19.903698+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1658","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TIMM8A as ready","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2022-12-23T17:23:19.885774+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1658","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: timm8a has been classified as Red List (Low Evidence).","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2022-12-23T17:23:15.296382+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1658","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TIMM8A were changed from Mohr-Tranebjaerg syndrome to Mohr-Tranebjaerg syndrome MIM#304700","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2022-12-23T17:23:03.658475+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1657","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TIMM8A were set to ","entity_name":"TIMM8A","entity_type":"gene"},{"created":"2022-12-23T17:22:52.027814+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.1656","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TIMM8A as Red List (low evidence)","entity_name":"TIMM8A","entity_type":"gene"}]}