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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=656",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&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"
}
]
}